This document describes a pigment composition and process for its manufacture. Specifically, it involves treating an aqueous pigment precipitate to coat the pigment particles with a water-insoluble diacid salt of an N-aliphatic alkylene diamine. This coating allows the pigment to be more easily dispersed in oil-based vehicles. Test results showed the coated pigments required less time and passes to achieve proper dispersion compared to uncoated pigments. The coating did not impair the hardness of finished paint films.
The document discusses using iron(II) salt complexes as reducing agents for dyeing cotton with vat dyes as an alternative to sodium hydrosulfite. Single ligand systems of iron(II) complexes were ineffective at reducing anthraquinoid vat dyes except with gluconic acid. A two ligand system using tartaric acid, triethanolamine or citric acid, triethanolamine complexes iron(II) more stably and effectively reduces and dyes cotton with various vat dyes at room temperature, comparable to sodium hydrosulfite. The stability and dyeing effectiveness depends on maximizing the complexation of iron(II).
Removal of Harmful Textile Dye Congo Red from Aqueous Solution Using Chitosan...IJERA Editor
Color is an important aspect of human life. Textile industries are the major consumers of dye stuffs. During coloration process, 10 to 15 percent of the dyes will be lost and this will be discharged with the effluents coming from textile industries. These are very difficult to degrade and they may degrade to form products that are highly toxic to human. Today, methods such as coagulation, flocculation, activated carbon adsorption, etc. are available for the removal of dyes. These are all quite expensive and difficult to degrade. Chitosan is a natural hetero polymer derived from chitin. Chitosan has proved to be effective in removing hazardous compounds from environment due to its multiple functional groups. It is available as flakes and powder. In the present work, chitosan beads were prepared and modified with a cationic surfactant CTAB for the removal of dye Congo Red. Batch experiments were conducted to study the effect of CTAB concentration, contact time, agitation speed, adsorbent dosage, initial dye concentration and pH. Batch equilibrium data were analyzed using Langmuir and Freundlich isotherm. Bach kinetic data were analyzed using Pseudo first order kinetic model and pseudo second order kinetic model.
This document describes new basic phthalocyanine dyestuffs and a process for their production. Specifically, it details reacting a phthalocyanine dyestuff containing replaceable halogen atoms with a tertiary amine to produce new basic dyestuffs. Examples are provided of suitable starting materials and reaction conditions to yield dyestuffs that are soluble in dilute acids and useful for dyeing various materials like cotton, wool and cellulose.
This document summarizes a study on the sorption and transport of Crystal Violet dye in and through biobased cryogel membranes made of poly(vinyl alcohol) blended with various biopolymers. The cryogels were characterized using techniques like SEM, DSC, and FTIR. Sorption isotherms and diffusion/permeability coefficients were determined for Crystal Violet dye diffusion into and out of the cryogels. The highest sorption capacity and removal efficiency for Crystal Violet from aqueous solutions was found for cryogels containing scleroglucan bioinsertions.
Effect of hardness of water on fixation and total wash off percentage of reac...Elias Khalil (ইলিয়াস খলিল)
Dye-house water quality is the most important parameter to be confirmed before dyeing; precisely the presence of metal content i.e. Hardness. This research will investigate & analyses the impact of separate hardness (i.e. Calcium, Magnesium & Iron) on particular „Turquoise‟ (C.I. Reactive Blue 21) & a „High Exhaustion‟ class (C.I. HE Red 120, C.I. HE Yellow 84) of Reactive dye on cotton knitted-fabric. From evaluation of dyed fabric the range of metal content is sorted out where the quality starts to fluctuate as distinctive visible & spectral change of shade & fixation rate of the dye molecules has been found. The result of the work will help for further projection about water quality degradation in upcoming years & its effect on dyeing behavior, also the sustainability of present dyeing process to cope with the ever degrading quality of water.
The document discusses salt-free dyeing of cotton with reactive dyes using cationic agents. It aims to study the feasibility of using cationic agents instead of salt for dyeing cotton with reactive dyes. Various cationic agents are used to pretreat cotton via exhaust and pad-dry methods, followed by exhaust dyeing without salt. Dye exhaustion and color yield are compared for different cationic agents and pretreatment methods. Results show that pretreatment with cationic agents increases dye exhaustion and color yield compared to dyeing with salt. Tinofix ECO gives the highest dye exhaustion and color yield for most dyes tested. The study suggests cationic agents can enable salt-free dyeing of cotton with reactive
This document describes a chemistry student's organic synthesis project on preparing pure 1,4-dioxan and synthesizing various polycyclic aromatic hydrocarbons including pyrene, 1,3,6,8-tetraphenylpyrene, and 1,3,6,8-tetrakis(4-ethoxyphenyl)pyrene using Suzuki coupling reactions. The student acknowledges the guidance received from their project mentor and other professors. The document provides details on the preparation, reaction mechanisms, and isolation of products for the various compounds synthesized as part of the project.
The document discusses using iron(II) salt complexes as reducing agents for dyeing cotton with vat dyes as an alternative to sodium hydrosulfite. Single ligand systems of iron(II) complexes were ineffective at reducing anthraquinoid vat dyes except with gluconic acid. A two ligand system using tartaric acid, triethanolamine or citric acid, triethanolamine complexes iron(II) more stably and effectively reduces and dyes cotton with various vat dyes at room temperature, comparable to sodium hydrosulfite. The stability and dyeing effectiveness depends on maximizing the complexation of iron(II).
Removal of Harmful Textile Dye Congo Red from Aqueous Solution Using Chitosan...IJERA Editor
Color is an important aspect of human life. Textile industries are the major consumers of dye stuffs. During coloration process, 10 to 15 percent of the dyes will be lost and this will be discharged with the effluents coming from textile industries. These are very difficult to degrade and they may degrade to form products that are highly toxic to human. Today, methods such as coagulation, flocculation, activated carbon adsorption, etc. are available for the removal of dyes. These are all quite expensive and difficult to degrade. Chitosan is a natural hetero polymer derived from chitin. Chitosan has proved to be effective in removing hazardous compounds from environment due to its multiple functional groups. It is available as flakes and powder. In the present work, chitosan beads were prepared and modified with a cationic surfactant CTAB for the removal of dye Congo Red. Batch experiments were conducted to study the effect of CTAB concentration, contact time, agitation speed, adsorbent dosage, initial dye concentration and pH. Batch equilibrium data were analyzed using Langmuir and Freundlich isotherm. Bach kinetic data were analyzed using Pseudo first order kinetic model and pseudo second order kinetic model.
This document describes new basic phthalocyanine dyestuffs and a process for their production. Specifically, it details reacting a phthalocyanine dyestuff containing replaceable halogen atoms with a tertiary amine to produce new basic dyestuffs. Examples are provided of suitable starting materials and reaction conditions to yield dyestuffs that are soluble in dilute acids and useful for dyeing various materials like cotton, wool and cellulose.
This document summarizes a study on the sorption and transport of Crystal Violet dye in and through biobased cryogel membranes made of poly(vinyl alcohol) blended with various biopolymers. The cryogels were characterized using techniques like SEM, DSC, and FTIR. Sorption isotherms and diffusion/permeability coefficients were determined for Crystal Violet dye diffusion into and out of the cryogels. The highest sorption capacity and removal efficiency for Crystal Violet from aqueous solutions was found for cryogels containing scleroglucan bioinsertions.
Effect of hardness of water on fixation and total wash off percentage of reac...Elias Khalil (ইলিয়াস খলিল)
Dye-house water quality is the most important parameter to be confirmed before dyeing; precisely the presence of metal content i.e. Hardness. This research will investigate & analyses the impact of separate hardness (i.e. Calcium, Magnesium & Iron) on particular „Turquoise‟ (C.I. Reactive Blue 21) & a „High Exhaustion‟ class (C.I. HE Red 120, C.I. HE Yellow 84) of Reactive dye on cotton knitted-fabric. From evaluation of dyed fabric the range of metal content is sorted out where the quality starts to fluctuate as distinctive visible & spectral change of shade & fixation rate of the dye molecules has been found. The result of the work will help for further projection about water quality degradation in upcoming years & its effect on dyeing behavior, also the sustainability of present dyeing process to cope with the ever degrading quality of water.
The document discusses salt-free dyeing of cotton with reactive dyes using cationic agents. It aims to study the feasibility of using cationic agents instead of salt for dyeing cotton with reactive dyes. Various cationic agents are used to pretreat cotton via exhaust and pad-dry methods, followed by exhaust dyeing without salt. Dye exhaustion and color yield are compared for different cationic agents and pretreatment methods. Results show that pretreatment with cationic agents increases dye exhaustion and color yield compared to dyeing with salt. Tinofix ECO gives the highest dye exhaustion and color yield for most dyes tested. The study suggests cationic agents can enable salt-free dyeing of cotton with reactive
This document describes a chemistry student's organic synthesis project on preparing pure 1,4-dioxan and synthesizing various polycyclic aromatic hydrocarbons including pyrene, 1,3,6,8-tetraphenylpyrene, and 1,3,6,8-tetrakis(4-ethoxyphenyl)pyrene using Suzuki coupling reactions. The student acknowledges the guidance received from their project mentor and other professors. The document provides details on the preparation, reaction mechanisms, and isolation of products for the various compounds synthesized as part of the project.
This document summarizes a study on dispersing reduced graphene in organic solvents through noncovalent functionalization with end-functional polymers. The researchers prepared an aqueous dispersion of reduced graphene oxide through chemical reduction, then tested its dispersibility in various organic solvents. To disperse the graphene in nonsolvents, they noncovalently functionalized it with amine-terminated polymers via sonication. FTIR and Raman spectroscopy confirmed the amine groups on the polymers interacted with carboxyl groups on the graphene surface, enhancing dispersibility in organic media.
Dyeing of polyester with disperse reactive dyesIIT DELHI
Disperse dyes are used to dye polyester fabrics. They are insoluble in water but can be dispersed onto fibers using dispersing agents. This document discusses the characteristics of disperse dyes and examples of common disperse dyes. It also examines using disperse reactive dyes for dyeing polyester, which have properties of both disperse and reactive dyes, and can provide improved fastness. The dyeing process for polyester using disperse reactive dyes is outlined, and effects of pH and dye concentration on dye uptake are analyzed.
Azoic dyes are produced by reacting a diazo-component or base salt with a coupling component like naphthol. This reaction forms an insoluble azo group that produces the dye within the fiber, resulting in excellent washing fastness. Azoic dyes can be used to dye cellulose fibers like cotton. The dyeing process involves three steps: naphtholation, diazotization, and coupling. Azoic dyes form an insoluble color product within the fabric, making them different from azo dyes which use a soluble azo group.
Latex ingredients and compounding with formulations of products with brief ma...PRIYABRATA GHOSH
This document provides information on latex ingredients and compounding formulations for rubber products. It discusses the composition of natural rubber latex and factors contributing to its colloidal stability. Methods for concentrating latex include evaporation, creaming, centrifuging, and electro-decantation. Latex is commonly preserved with ammonia and bactericides. The document also covers the production of synthetic latex dispersions through emulsion polymerization and their applications. Steps for preparing solid dispersions and liquid emulsions are outlined. Finally, auxiliary chemicals and compounding ingredients used in latex formulations are described.
The document summarizes a study on using solid waste from the leather industry as an adsorbent for removing dye from wastewater. Some key findings:
1) The leather waste was processed into activated carbon and used to adsorb Acid Red 131 dye from an aqueous solution.
2) Batch adsorption experiments showed equilibrium was reached after 180 minutes and adsorption capacity increased with initial dye concentration and adsorbent dose.
3) The Langmuir isotherm model provided the best fit for the equilibrium adsorption data, indicating monolayer adsorption onto the activated carbon surface.
4) The study demonstrates the potential of utilizing a solid waste to treat wastewater contaminated
Thiourea mediated regioselective synthesis of symmetrical and unsymmetrical d...Science Padayatchi
This document describes a method for the regioselective synthesis of symmetrical and unsymmetrical thioethers from chloroisoquinolines using thiourea. The reaction produces isoquinoline-1-thiols under optimized thiourea conditions, and varying the amount of thiourea allows for the selective formation of either symmetrical thioethers or unsymmetrical thioethers. A proposed mechanism indicates that thiourea acts as a sulfur source in an aromatic nucleophilic substitution reaction to form an isothiouronium salt intermediate, which then produces the thiol or thioether products. This method avoids byproduct formation and provides a simplified and environmentally friendly approach for synthesizing various organosulfur
property of Tris(acetylacetonato)manganese(III) MUKULsethi5
this presentation useful for discussing #chemical and #physical property and application of ..
#Manganese(III)acetylacetonate
#Manganicacetylacetonate
#3-Penten-2-one,4-hydroxy-,manganese(3+) salt
#Mangan(3+)tris[(2Z)-4-oxo-2-penten-2-olat]
#3-Penten-2-one,4-hydroxy-,manganese(3+)salt,(3Z)-(3:1)
in this I discuss chemical and physical property, #spectra, application, #harmness etc
Thin layer chromatography (TLC) is a simple technique used to separate mixtures and identify compounds. It works by distributing compounds between two phases - a stationary phase coated on a plate and a mobile phase, which is a solvent that travels up the plate. Key aspects of TLC include the stationary phase, usually silica gel or alumina; the mobile phase solvent or solvent mixture; and detection of spots under UV light or after spraying reagents. TLC allows for rapid separation and quantification of compounds in a mixture based on the retardation factor (Rf) value, which is a measure of how far each compound travels up the plate relative to the solvent front.
Adsorptive Removal of Methylene Blue Using Groundnut Shell Activated Carbon C...IOSRJAC
In this work, activated carbon prepared from groundnut shells (GSAC) by sulphuric acid treatment was coated with Fe3O4(GSAC- Fe3O4) and tested for its efficiency as an adsorbentfor the removal of methylene blue (MB) dye from aqueous solution. The structural morphology and functional groups present were investigated using scanning electron microscope (SEM) and Fourier transform infrared (FTIR) spectroscopy. Various sorption parameters such as effect of pH, contact time, initial dye concentration and adsorbent dosage were studied. The percentage removal of methylene blue increased with decrease in initial methylene blue concentration and increased with increase in contact time and dose of the adsorbent. Equilibrium data were analysed using Langmuir and Freundlich isotherm models. Kinetic data were studied using pseudo-first order and pseudo-second order kinetic models.
This document provides answers to questions about various methods for treating hazardous waste and petroleum refining processes. It discusses chemical treatment methods, gravity settling, electric desalting, dehydration, atmospheric distillation units, vacuum distillation units, top tray reflux, blending processes, line blending, gasoline blending, the chemical structure of asphalt, the effects of heat on asphalt, types of asphalt, and air blowing of asphalt. The document appears to be fully solved assignments for petroleum management students. It provides contact information at the end for obtaining additional assignments.
Dyeing of cotton with reactive dyes quality q&aAdane Nega
The document discusses several key aspects of dyeing cotton with reactive dyes, including:
1) Dye quality can vary depending on the manufacturer and factors like impurities. Quality checks are important to evaluate dye concentration and color properties.
2) Proper dyeing conditions like temperature, pH, salt concentration, and alkali levels are important for ensuring level dyeing and reproducibility.
3) Dyeing properties vary for different dyes, fiber types (e.g. mercerized cotton), and dye classes like phthalocyanine dyes. Incremental addition of materials is often needed to control dye exhaustion.
Thin layer chromatography (TLC) is a simple, inexpensive technique used to separate and identify components in organic compounds. In TLC, compounds are distributed between a stationary phase, like silica gel, and a mobile phase, like a solvent or solvent mixture. As the mobile phase travels up the plate, different components travel at different rates depending on their solubility, allowing separation. Common adsorbents and solvent systems used for lipid separation are described. Various detection reagents can be used to visualize separated components under UV light or by producing colored spots. Examples are given of separations achieved for different lipid classes and subclasses using TLC.
Thin layer chromatography (TLC) is a technique used to separate chemical compounds. It involves a stationary phase, consisting of a thin layer of adsorbent material like silica gel coated on a flat surface, and a mobile phase of solvent that travels up the stationary phase via capillary action. TLC is useful for determining and detecting pigments, pesticides, insecticides, and for identifying compounds in forensic analysis and chemical reactions. It requires small amounts of sample and solvent and allows for fast separation of compounds.
This document describes British patent GB785288 (A) which was filed on June 12, 1953 and published on October 23, 1957. It relates to an air heating apparatus for motor vehicles that has its own heat source. The apparatus includes a combustion chamber, combustion air blower driven by a motor, and a pre-combustion chamber with an ignition plug and fuel feed device. It also includes means to keep the blower motor running after fuel supply is cut off to allow the apparatus to cool to a predetermined temperature.
This document describes British patent GB785283 (A) for shaped carbon or graphite bodies with high bending strength and tensile strength. The bodies consist of a graphite or carbon basic body reinforced with iron, steel, or nickel steel elements bonded with synthetic resins. The basic body is made from coke, anthracite or other carbonaceous materials shaped and heat treated. Reinforcing elements can be rods, wires or strips inserted into or on the surface of the basic body and bonded with resins like phenol-formaldehyde or furan resins. The reinforced bodies have applications like heat exchange tubes or rods.
This document provides details of a bearing quality testing machine that tests roller thrust bearings for manufacturing inaccuracies. It includes diagrams of the machine and descriptions of its components. The machine applies a gradually increasing axial thrust to the bearing while it rotates to test the percentage of surface contact between its rollers and races under load. It measures the resulting torque on the driving motor to determine if the bearing meets quality standards.
The document describes experiments comparing the effectiveness of using lead salts alone, chelate organometallic compounds alone, and mixtures of lead salts with chelate compounds for sweetening petroleum fractions. The results showed that lead salts alone had little effect, chelate compounds required higher amounts to fully sweeten, but mixtures of lead salts with chelate compounds achieved full sweetening using lower amounts of chelate compounds, demonstrating improved efficiency.
This document describes improvements to cyanine dyestuffs, specifically those useful for sensitizing photographic silver halide emulsions. The cyanine dyestuffs are obtained by reacting a terazole quaternary salt with a 5 or 6-membered heterocyclic nitrogen compound or a heterocyclic nitrogen ketomethylene nucleus. The resulting products have general formulas IV or V, representing cyanine dyes that may exist in different resonance forms. The dyes described contain substituents like alkyl, cycloalkyl, aryl, and heterocyclic groups.
This document describes a patent for an apparatus that detects foreign bodies on the bottoms of transparent vessels like milk bottles. The apparatus uses a cathode ray tube located below a knife-edged grid that supports the vessel to scan the bottom with a light beam. A light responsive device above the vessel detects reductions in light caused by foreign bodies. The grid and adjustable scanning allow vessels of different sizes to be scanned without dismantling the apparatus.
This document describes a patent for a method of controlling the rate of oxidation in an autogenetic oxidation process. The key aspects of the control method are: (1) leading at least part of the effluent from the oxidation reactor in a heat exchange with the influent liquor to heat and concentrate the influent, (2) maintaining a minimum temperature of around 3000 British Thermal Units per gallon for the influent liquor entering the reactor to sustain the reaction. The heat exchange concentrates the influent liquor through evaporation without causing excessive heating that could lead to "gunking" or solidification of the flowing liquor.
This document summarizes a study on dispersing reduced graphene in organic solvents through noncovalent functionalization with end-functional polymers. The researchers prepared an aqueous dispersion of reduced graphene oxide through chemical reduction, then tested its dispersibility in various organic solvents. To disperse the graphene in nonsolvents, they noncovalently functionalized it with amine-terminated polymers via sonication. FTIR and Raman spectroscopy confirmed the amine groups on the polymers interacted with carboxyl groups on the graphene surface, enhancing dispersibility in organic media.
Dyeing of polyester with disperse reactive dyesIIT DELHI
Disperse dyes are used to dye polyester fabrics. They are insoluble in water but can be dispersed onto fibers using dispersing agents. This document discusses the characteristics of disperse dyes and examples of common disperse dyes. It also examines using disperse reactive dyes for dyeing polyester, which have properties of both disperse and reactive dyes, and can provide improved fastness. The dyeing process for polyester using disperse reactive dyes is outlined, and effects of pH and dye concentration on dye uptake are analyzed.
Azoic dyes are produced by reacting a diazo-component or base salt with a coupling component like naphthol. This reaction forms an insoluble azo group that produces the dye within the fiber, resulting in excellent washing fastness. Azoic dyes can be used to dye cellulose fibers like cotton. The dyeing process involves three steps: naphtholation, diazotization, and coupling. Azoic dyes form an insoluble color product within the fabric, making them different from azo dyes which use a soluble azo group.
Latex ingredients and compounding with formulations of products with brief ma...PRIYABRATA GHOSH
This document provides information on latex ingredients and compounding formulations for rubber products. It discusses the composition of natural rubber latex and factors contributing to its colloidal stability. Methods for concentrating latex include evaporation, creaming, centrifuging, and electro-decantation. Latex is commonly preserved with ammonia and bactericides. The document also covers the production of synthetic latex dispersions through emulsion polymerization and their applications. Steps for preparing solid dispersions and liquid emulsions are outlined. Finally, auxiliary chemicals and compounding ingredients used in latex formulations are described.
The document summarizes a study on using solid waste from the leather industry as an adsorbent for removing dye from wastewater. Some key findings:
1) The leather waste was processed into activated carbon and used to adsorb Acid Red 131 dye from an aqueous solution.
2) Batch adsorption experiments showed equilibrium was reached after 180 minutes and adsorption capacity increased with initial dye concentration and adsorbent dose.
3) The Langmuir isotherm model provided the best fit for the equilibrium adsorption data, indicating monolayer adsorption onto the activated carbon surface.
4) The study demonstrates the potential of utilizing a solid waste to treat wastewater contaminated
Thiourea mediated regioselective synthesis of symmetrical and unsymmetrical d...Science Padayatchi
This document describes a method for the regioselective synthesis of symmetrical and unsymmetrical thioethers from chloroisoquinolines using thiourea. The reaction produces isoquinoline-1-thiols under optimized thiourea conditions, and varying the amount of thiourea allows for the selective formation of either symmetrical thioethers or unsymmetrical thioethers. A proposed mechanism indicates that thiourea acts as a sulfur source in an aromatic nucleophilic substitution reaction to form an isothiouronium salt intermediate, which then produces the thiol or thioether products. This method avoids byproduct formation and provides a simplified and environmentally friendly approach for synthesizing various organosulfur
property of Tris(acetylacetonato)manganese(III) MUKULsethi5
this presentation useful for discussing #chemical and #physical property and application of ..
#Manganese(III)acetylacetonate
#Manganicacetylacetonate
#3-Penten-2-one,4-hydroxy-,manganese(3+) salt
#Mangan(3+)tris[(2Z)-4-oxo-2-penten-2-olat]
#3-Penten-2-one,4-hydroxy-,manganese(3+)salt,(3Z)-(3:1)
in this I discuss chemical and physical property, #spectra, application, #harmness etc
Thin layer chromatography (TLC) is a simple technique used to separate mixtures and identify compounds. It works by distributing compounds between two phases - a stationary phase coated on a plate and a mobile phase, which is a solvent that travels up the plate. Key aspects of TLC include the stationary phase, usually silica gel or alumina; the mobile phase solvent or solvent mixture; and detection of spots under UV light or after spraying reagents. TLC allows for rapid separation and quantification of compounds in a mixture based on the retardation factor (Rf) value, which is a measure of how far each compound travels up the plate relative to the solvent front.
Adsorptive Removal of Methylene Blue Using Groundnut Shell Activated Carbon C...IOSRJAC
In this work, activated carbon prepared from groundnut shells (GSAC) by sulphuric acid treatment was coated with Fe3O4(GSAC- Fe3O4) and tested for its efficiency as an adsorbentfor the removal of methylene blue (MB) dye from aqueous solution. The structural morphology and functional groups present were investigated using scanning electron microscope (SEM) and Fourier transform infrared (FTIR) spectroscopy. Various sorption parameters such as effect of pH, contact time, initial dye concentration and adsorbent dosage were studied. The percentage removal of methylene blue increased with decrease in initial methylene blue concentration and increased with increase in contact time and dose of the adsorbent. Equilibrium data were analysed using Langmuir and Freundlich isotherm models. Kinetic data were studied using pseudo-first order and pseudo-second order kinetic models.
This document provides answers to questions about various methods for treating hazardous waste and petroleum refining processes. It discusses chemical treatment methods, gravity settling, electric desalting, dehydration, atmospheric distillation units, vacuum distillation units, top tray reflux, blending processes, line blending, gasoline blending, the chemical structure of asphalt, the effects of heat on asphalt, types of asphalt, and air blowing of asphalt. The document appears to be fully solved assignments for petroleum management students. It provides contact information at the end for obtaining additional assignments.
Dyeing of cotton with reactive dyes quality q&aAdane Nega
The document discusses several key aspects of dyeing cotton with reactive dyes, including:
1) Dye quality can vary depending on the manufacturer and factors like impurities. Quality checks are important to evaluate dye concentration and color properties.
2) Proper dyeing conditions like temperature, pH, salt concentration, and alkali levels are important for ensuring level dyeing and reproducibility.
3) Dyeing properties vary for different dyes, fiber types (e.g. mercerized cotton), and dye classes like phthalocyanine dyes. Incremental addition of materials is often needed to control dye exhaustion.
Thin layer chromatography (TLC) is a simple, inexpensive technique used to separate and identify components in organic compounds. In TLC, compounds are distributed between a stationary phase, like silica gel, and a mobile phase, like a solvent or solvent mixture. As the mobile phase travels up the plate, different components travel at different rates depending on their solubility, allowing separation. Common adsorbents and solvent systems used for lipid separation are described. Various detection reagents can be used to visualize separated components under UV light or by producing colored spots. Examples are given of separations achieved for different lipid classes and subclasses using TLC.
Thin layer chromatography (TLC) is a technique used to separate chemical compounds. It involves a stationary phase, consisting of a thin layer of adsorbent material like silica gel coated on a flat surface, and a mobile phase of solvent that travels up the stationary phase via capillary action. TLC is useful for determining and detecting pigments, pesticides, insecticides, and for identifying compounds in forensic analysis and chemical reactions. It requires small amounts of sample and solvent and allows for fast separation of compounds.
This document describes British patent GB785288 (A) which was filed on June 12, 1953 and published on October 23, 1957. It relates to an air heating apparatus for motor vehicles that has its own heat source. The apparatus includes a combustion chamber, combustion air blower driven by a motor, and a pre-combustion chamber with an ignition plug and fuel feed device. It also includes means to keep the blower motor running after fuel supply is cut off to allow the apparatus to cool to a predetermined temperature.
This document describes British patent GB785283 (A) for shaped carbon or graphite bodies with high bending strength and tensile strength. The bodies consist of a graphite or carbon basic body reinforced with iron, steel, or nickel steel elements bonded with synthetic resins. The basic body is made from coke, anthracite or other carbonaceous materials shaped and heat treated. Reinforcing elements can be rods, wires or strips inserted into or on the surface of the basic body and bonded with resins like phenol-formaldehyde or furan resins. The reinforced bodies have applications like heat exchange tubes or rods.
This document provides details of a bearing quality testing machine that tests roller thrust bearings for manufacturing inaccuracies. It includes diagrams of the machine and descriptions of its components. The machine applies a gradually increasing axial thrust to the bearing while it rotates to test the percentage of surface contact between its rollers and races under load. It measures the resulting torque on the driving motor to determine if the bearing meets quality standards.
The document describes experiments comparing the effectiveness of using lead salts alone, chelate organometallic compounds alone, and mixtures of lead salts with chelate compounds for sweetening petroleum fractions. The results showed that lead salts alone had little effect, chelate compounds required higher amounts to fully sweeten, but mixtures of lead salts with chelate compounds achieved full sweetening using lower amounts of chelate compounds, demonstrating improved efficiency.
This document describes improvements to cyanine dyestuffs, specifically those useful for sensitizing photographic silver halide emulsions. The cyanine dyestuffs are obtained by reacting a terazole quaternary salt with a 5 or 6-membered heterocyclic nitrogen compound or a heterocyclic nitrogen ketomethylene nucleus. The resulting products have general formulas IV or V, representing cyanine dyes that may exist in different resonance forms. The dyes described contain substituents like alkyl, cycloalkyl, aryl, and heterocyclic groups.
This document describes a patent for an apparatus that detects foreign bodies on the bottoms of transparent vessels like milk bottles. The apparatus uses a cathode ray tube located below a knife-edged grid that supports the vessel to scan the bottom with a light beam. A light responsive device above the vessel detects reductions in light caused by foreign bodies. The grid and adjustable scanning allow vessels of different sizes to be scanned without dismantling the apparatus.
This document describes a patent for a method of controlling the rate of oxidation in an autogenetic oxidation process. The key aspects of the control method are: (1) leading at least part of the effluent from the oxidation reactor in a heat exchange with the influent liquor to heat and concentrate the influent, (2) maintaining a minimum temperature of around 3000 British Thermal Units per gallon for the influent liquor entering the reactor to sustain the reaction. The heat exchange concentrates the influent liquor through evaporation without causing excessive heating that could lead to "gunking" or solidification of the flowing liquor.
The document describes a method for activating clay by mixing it with concentrated sulfuric acid to form a free-flowing mixture with insufficient water to promote activation. This mixture is then brought into contact with live steam to activate the clay. The method provides advantages over prior methods by being neater, more rapid, and allowing improved clay activation with less acid and water used. Several examples demonstrate treating clay samples by this method and testing the activated clays' effectiveness at decolorizing mineral oil.
This document describes a process for producing substituted pteridine derivatives. Specifically, it involves condensing a 2-halo-3,3-dialkoxy-propionaldehyde with a 2,4,5-triamino-6-hydroxypyrimidine to form a 2-amino-5,6-dihydropteridine. This intermediate is then oxidized to remove hydrogen atoms and form a 2-amino pteridine. The pteridine can be further derivatized by acylation to form novel 2-acylamino pteridines. An example reaction is provided to synthesize 2-amino-4-benzyloxy-6-diethoxymethyl-5,6-
This document describes a patent for improving the vacuum carbonate process for separating acid gases like hydrogen sulfide from coal carbonization gases. Specifically, it addresses three problems with the existing process: vacuum pump plugging due to polymer formation, ammonia contamination of separated gases, and clogging of condenser lines by high melting point hydrocarbons like naphthalene. The invention reduces vacuum pump compression ratios to eliminate hard polymer formation and introduces solvent oil vapors to dissolve contaminants and prevent clogging of condensers. This results in continuous operation of the vacuum carbonate plant for ten months without shutdowns for pump cleaning.
1) The document describes a process for polymerizing olefins by bringing the olefin into contact with a reaction medium containing a transition metal halide that has been reacted with an organometallic compound.
2) The transition metal halides used are halides of Group IV to VI transition metals, and the organometallic compounds used include alkali metal alkyls, alkenyls, alkynyls, aryls, and aralkyls.
3) The polymerizations produce polymers with higher molecular weights suitable for films and fibers or lower molecular weights suitable as chemical intermediates.
This document describes a patent from 1957 for an improved connection for lagging irons used in underground mine workings. The connection involves a tongue on one lagging iron that extends into a forked end of the other iron. A pivot pin passes through bores in the fork prongs and tongue to connect the irons. A clamping wedge can be inserted to rigidly secure the connection and allow angular deflection of the irons. The improvement involves orienting the irons so the tongue points toward the work face, and extending the fork prongs so the tongue can fully extend without projecting over the previous iron. This allows the inserted iron to be immediately connected by the pivot pin without needing an auxiliary pin.
This document describes a process for producing subtiltryptasin, a therapeutically valuable substance, by cultivating Bacillus subtilis var. indolasus or a mutant thereof in a protein-free culture medium. The culture medium contains a carbon source such as dextrose or glycerol and a nitrogen source such as an ammonium salt. The cultivation is continued until consumption of the nutrients and forms a substance with therapeutic properties containing at least 10,000 bacilli per cc. The active substance is produced during growth of the bacteria.
This document describes a patent for an automatic control system for a vehicle's variable-speed transmission mechanism. The system uses electromagnets to actuate the gear-changing components and relays to control the electromagnets. A moving coil actuates switches that control the relays based on vehicle speed. As speed increases, it causes the gears to change automatically from first to second to third. This allows for fully automatic shifting of the vehicle's transmission based on speed.
This document describes a process for producing condensation products by reacting polyalkylene oxides or their derivatives with polybasic carboxylic acids. The polyalkylene oxides must have a molecular weight over 1000 and contain both a lipophilic group and a free hydroxyl group. The polybasic carboxylic acids must contain at least three carboxyl groups and a lipophilic group. The resulting condensation products can be water-soluble or water-insoluble and are suitable for use as dispersing, emulsifying, thickening agents and in other applications.
This document summarizes a patent for an electrical heating panel assembly. It describes a frame that holds a panel made of two bonded sheets of insulating material with an electrical heating resistance in between. The panel is set back from the frame edges to allow air circulation behind the panel and between panels when multiple units are installed together. The heating resistance takes a sinuous path between the panel sheets for even heat distribution.
The document describes a patent for a method of preparing hydrofining catalysts. The method involves reacting sodium aluminate, aluminum sulfate, and sodium silicate in an aqueous solution at pH 9-10 to form an alumina-silica precipitate. This precipitate is then dried, heated, and impregnated with an active hydrofining catalyst like cobalt molybdate. Experiments show this catalyst is very effective at hydrofining heating oil fractions, significantly reducing carbon residue and sulfur levels. It performs particularly well by further reducing carbon residue levels when the hydrofined oils are blended with untreated oils.
This patent document describes a high-speed sheet feeding mechanism for folding box machines. It summarizes improvements made to blank feeding mechanisms in previous patents, with the primary objective of modifying the action of the mechanism that controls the motion of the pneumatic feeder. This allows for greatly increased machine speeds without objectionable vibration. The improved feeder control mechanism reduces the peak velocity reached by the feeder midway through its oscillatory motion by continuously varying the radius of oscillation in a controlled fashion. This reduces angular acceleration of the suction feeder without shortening its travel path or impairing other qualities.
This document describes a patent for covers for motor vehicles. Specifically, it details covers that are tailored to fit the shape of the vehicle. The covers have an opening with fastening means, such that when fastened the cover fits snugly over the entire vehicle and cannot be removed without unfastening. Examples are provided for covers tailored to fit a motorcycle and a motor car. The covers are designed to protect vehicles parked outdoors from deterioration in a way that is easier to use than loose covers that must be tied or weighted down.
This document describes a process for producing hydrocarbon drying oils through the polymerization of butadiene and styrene monomers in the presence of sodium catalyst. It discusses conducting the reaction in a reactor, then treating the product solution with an organic acid to convert the sodium into a filterable salt. The process aims to improve upon previous large-scale methods by addressing issues like sodium handling hazards and slow reaction rates due to induction periods through continuous treatment of the product solution directly in the reactor with excess acid.
This document describes a process for producing hydrocarbon drying oils through the polymerization of butadiene and styrene monomers in the presence of sodium catalyst. It discusses conducting the reaction in a reactor, then treating the product solution with an organic acid to convert the sodium into a filterable salt. The process aims to improve upon large-scale production by continuously feeding reagents to a reactor while removing the polymerized product, and pre-treating make-up materials to improve reaction efficiency.
Done by ABJ_ platinum8, Ali Bin Jassim Secondary Independent School for Boys.
Environmental Catalysis Module: Students examines different types of catalytic systems, including heterogeneous and homogeneous catalysis. Depending on the knowledge they gained during activities, the students are then asked to design their projects.
Our Project: using Cheap Catalyst in car exhaust: Using cheap converter for most of the cars in place of that high price converters to get clean environment.
Difference between reactive dye and disperse dye on fabricAzmir Latif Beg
We are introducing about reactive dye and disperse dye on fabric. At present reactive dye and disperse dyes is not a single word globally now it achieved vast sector in dyeing sector. I just try to make a different reactive dye and disperse dye on fabric application based.
Id 120303045 (chemials use in bangladesh textile industry)Sarif Md. Al amin
This document discusses chemicals used in the Bangladesh textile industry. It provides details on size chemicals such as starches, PVA, and tallow used to improve yarn strength and smoothness. Basic chemicals like acetic acid, oxalic acid, and soda ash are explained along with their uses to maintain pH levels. Bleaching agents including hydrogen peroxide and its environmental benefits over chlorine are covered. The roles of salts like sodium sulfate and sodium chloride as electrolytes to increase dye affinity are summarized. Finally, scouring agents used to remove oils and dirt from fabrics are presented.
This document describes a method of applying a protective resinous coating to heat-sensitive electrical elements by polymerizing polymerizable organic compounds using high energy electrons or cathode rays. Specifically, it involves surrounding the electrical element with a monomeric compound and irradiating it with high energy electrons to polymerize the monomer into a solid polymer coating without damaging the heat-sensitive component inside. This allows for rapid encapsulation of elements like resistors, capacitors, transistors, and diodes without impairing their properties through the application of heat.
This document summarizes a study on using biodegradable organic salts as alternatives to inorganic salts and alkalis in the reactive dyeing of cotton textiles. The study found that three biodegradable polycarboxylic sodium salts - sodium edate, trisodium NTA, and tetrasodium GLDA - can provide color yields and fastness properties comparable to traditional inorganic salts and alkalis when used in pad-steam dyeing. Tetrasodium GLDA particularly increased color yield for one reactive dye. Using the organic salts also reduced the total dissolved solids in the dyeing effluent, offering environmental benefits over conventional reactive dyeing methods.
This document describes several British patents from 1957 related to cleaning devices, detergents, and fertilizers. It provides details of GB785643 (A) which describes a cleaning device for printing presses, GB785644 (A) which describes improvements to saponaceous detergents incorporating ethylene diamine tetra-acetic acid, and GB785645 (A) which describes a method for preventing caking of granulated fertilizers using a urea-formaldehyde condensation product coating.
This document describes improvements to producing borated dextrines that can be dispersed in cold water without agglomerating. Specifically, it involves treating dextrine by moistening it to 9-18% moisture, then blending it with at least 7% borax and a hydroscopic chemical like potassium acetate that can absorb water. This produces a dextrine that is dry, sand-like grains that readily absorb water and disperse individually without lump formation when mixed with water.
This document discusses the analysis and characterization of petroleum and petroleum products. It begins with an introduction to the constituents of petroleum and the fractional distillation process used to separate petroleum into fractions. It then describes several key tests used to analyze petroleum products, including tests to determine specific gravity, viscosity, aniline point, color, cloud point, pour point, and tests to detect water, acid/base content, ash, and metals. The document provides details on the principles and procedures for each test method. It concludes with discussions of petroleum fractionation and the typical composition of crude petroleum.
The document discusses pH and its importance in the dyeing process. It explains that pH must be properly maintained throughout dyeing for effective exhaustion and fixation of dyes to the fabric. The document then discusses three techniques for controlling pH: maintaining high acidity/alkalinity, controlling pH within a narrow neutral range, and gradually shifting pH as dyeing proceeds. It also provides details on dye types, dyeing processes, chemicals used, and other parameters important for successful dyeing.
Presence of volatile organic compounds in fine coat paint used in house dec...Alexander Decker
This document analyzes paint samples commonly used for house painting in Nigeria. Chemical tests found the presence of alcohols, ketones, and aldehydes in the samples. Specifically, the maximum levels detected were 0.65 ppm of formaldehyde, 0.60 ppm of acetone, and 0.75 ppm of alcohol. While not acutely toxic, long-term exposure to these volatile organic compounds (VOCs) can have compounding health effects due to their ability to cause irritation and potentially cancer. The document also provides background on the typical chemical composition of paint, including binders, resins, pigments, and solvents which contribute most to VOC levels.
The patent describes unsaturated polyester resins with higher molecular weight, low viscosity, and high solubility in reactive diluents. The resins are prepared from a combination of unsaturated carboxylic acids, aromatic carboxylic acids, specific aliphatic branched diols, monoalcohols, and optionally other components. They have reduced volatile organic compound emissions. The resins and methods allow for products with good physical properties for applications like marine uses that have strict requirements.
Ecofriendly Stain Remover Based on Sugar Based Polymeric SurfactantsIRJET Journal
1. Sugar-based polymers containing citric acid, maleic anhydride, and phthalic anhydride were synthesized to develop stain-removing surfactants.
2. Two polymers were analyzed and found to differ in acid value, viscosity, surface tension, and HLB ratio. Polymer P1 containing citric acid performed better in stain removal.
3. Stain removers were formulated using Polymer P1 and conventional surfactants. Analysis found the stain removers were comparable to a commercial brand in pH, viscosity, surface tension, and stain removal of soils, turmeric, and ink.
IRJET- Preparation of Activated Carbon from PolystyreneIRJET Journal
This document summarizes research on preparing activated carbon from polystyrene waste. The researchers used polystyrene waste to create activated carbon via pyrolysis followed by thermal activation. They tested the activated carbon produced for characteristics like moisture content, ash content, density, solubility in water and acid, pH, decolorizing power, phenol number, and iron content. Batch experiments showed the polystyrene-derived activated carbon effectively removed pollutants like chloride from water, with around 80-85% removal achieved within 5 hours. The activated carbon produced adsorption properties similar to commercially available activated carbon. The study thus provides an effective way to utilize polystyrene waste through conversion to useful activated carbon.
IRJET- Preparation of Activated Carbon from PolystyreneIRJET Journal
This document summarizes research on preparing activated carbon from polystyrene waste. The researchers used polystyrene waste to create activated carbon via pyrolysis followed by thermal activation. They tested the activated carbon produced for characteristics like moisture content, ash content, density, solubility in water and acid, pH, decolorizing power, phenol number, and iron content. Batch experiments showed the polystyrene-derived activated carbon effectively removed pollutants like acetone acid and HCL from water, with over 80% removal achieved. The activated carbon produced from waste polystyrene provides an environmentally friendly use of this non-biodegradable material.
This document describes an ink composition for ink jet printers. It contains an aqueous carrier medium, a pigment dispersion or dye, and a special type of penetrant. The penetrant is an aliphatic diol with at least 6 carbon atoms, high water solubility, and is selected from compounds with 2 or more carbon substituents or hexene diols. These penetrants increase ink drying speed without destabilizing pigment dispersions or reducing reliability. The inks exhibit rapid drying, storage stability, reliable performance, and good print quality.
This document provides an overview of dyes and pigments, with a focus on reactive dyes. It defines dyes and pigments, describes their classification and color-producing factors. Reactive dyes are discussed in more detail, including their classification based on reactivity and reactive groups. The process of reactive dyeing is summarized, including dyeing conditions, the approach of reactive dyes to fibers, and their chemical reaction with cellulose fibers. A sample process curve is also shown. Finally, the document provides a profile of a wet processing plant to illustrate dyeing operations.
This document provides a 3-sentence summary of GB784603 (A) which describes a fuel feeding apparatus for pressure burners. The apparatus includes a valve body with passages that selectively connect a mixture tube, air passage, and fuel passages. A stationary rubber disk member and rotatable disk valve member control the connections between passages for starting, running, and shutting off the burner. The valve members and passages allow the burner to be supplied with an air-fuel mixture for starting and then operated with vaporized liquid fuel from the fuel tank.
This document summarizes a patent for manufacturing oximes of cycloaliphatic ketones. It describes a process where salts of thiosulphuric acid or polythionic acids are used as reducing agents in aqueous solution to produce oximes from water-soluble salts of secondary nitro-compounds in the cycloaliphatic series. The ratio used is 1 mole of nitro-compound to 1-1.5 moles of reducing agent salt. Examples provided demonstrate producing cyclohexanone oxime from nitrocyclohexane using sodium thiosulphate or sodium trithionate as the reducing agent. Yields of up to 92% of the oxime product are achieved.
This document describes glyoxalidine corrosion inhibitors for use in hydrocarbon liquids like gasoline and diesel fuel. Specifically, it describes new chemical compounds that are salts of a glyoxalidine and an organic aliphatic dicarboxylic acid with at least 10 carbon atoms. These compounds are effective corrosion inhibitors for ferrous metals in contact with hydrocarbon liquids that contain small amounts of water. Test results show that reactions products of sebacic acid and certain glyoxalidines can inhibit corrosion in gasoline-water systems at low concentrations.
This document describes a patent for improvements in the production of the antibiotic griseofulvin under deep culture conditions. It finds that griseofulvin can be produced on a large scale through submerged aerobic culture of suitable organisms, such as Penicillium patulum, if the available nitrogen level in the culture medium is carefully controlled between 0.04-0.3% nitrogen. Optimum yields are obtained at nitrogen levels of 0.075-0.25%, with the specific optimum depending on factors like inoculum type and fermenter size.
The document describes new disazo dyes and copper complexes of those dyes. The dyes correspond to general formula 1, where R1 is the residue of an oxybenzene-ortho-carboxylic acid, R2 and R3 are benzene residues with the carbon atoms bound to the azo linkage and carboxamide group separated by at least one carbon atom, and R4 is a benzene residue containing a sulphonic acid, carboxylic acid, or carboxymethoxy group. The dyes can be prepared by coupling a diazo compound of an aminoazo dye with a phenylamino-8-oxynaphthalene compound. The resulting dyes and their copper complexes are
This document describes improvements to self-supporting containers made of carbon or graphite. It discusses how prior containers used ceramic linings that had poor thermal conductivity. The new containers described are built from interlocking carbon or graphite plates that form a self-supporting inner structure. This allows the container to be spaced within an outer metal or concrete vessel, improving heat transfer and accommodating different expansion rates of the materials. Diagrams show how the plates interlock at joints and are held together with cement.
The document describes improvements to the "oxo process" for producing oxygenated organic compounds from olefins using carbon monoxide, hydrogen, and a carbonylation catalyst. Specifically, it involves using a catalyst combination that is particularly effective for catalyzing the reaction. The oxo process typically involves three stages - an initial reaction of the olefin with carbon monoxide and hydrogen over a cobalt catalyst to produce aldehydes, removal of soluble metal compounds from the product, and then hydrogenation of the aldehydes to alcohols. The invention relates to improving the catalyst used in the first stage of the reaction.
1) The document describes improvements to packaging containers that provide reinforcement and strength.
2) The containers have a non-metallic shell and bottom each with a corrosion-resistant thin inner lining that is partly inside and partly outside the container.
3) The shell has an outer reinforcing metal covering that is folded together with the outer parts of the linings to seal the container while keeping the bottom and shell unfolded.
This document summarizes a patent for recovering cooking liquor from spent soda pulping liquors. It describes how traditional soda pulping processes are expensive and wasteful due to the loss of sodium hydroxide in washings and stack gases. The invention provides a practical method for regenerating the soda with minimal loss, eliminating hazards and allowing recovery of soda cooking liquor from waste liquors containing it.
This document describes a multi-tray clarifier system for clarifying liquids containing suspended solids. The system uses multiple compartments and a central feedwell system to evenly distribute incoming feed between compartments. This even distribution allows for simplification of the clarifier design by reducing the number of intermediate compartments needed compared to previous clarifier designs.
This document describes improvements to control means for electric current converters. It discusses providing control of discharge paths through respective control electrodes over a wide range, from rectifier to inverter operation. Each control electrode is connected to two inductive members (transformers or chokes) supplied with phase-displaced operating currents/voltages from AC busbars. There are means for imparting a commonly variable direct current premagnetization and means for imparting independently pre-settable direct current premagnetizations, allowing control of each electrode's feed to provide a control voltage during a portion of the converter's total control range.
The document describes improvements to a storage device for cylindrical objects like barrels. The storage device features an inclined rack with a gate at the lower end that retains the cylindrical objects. The gate has two angular portions - a first portion with an upstanding stop member, and a second portion that acts as a positive stop as long as an object is resting on the first portion. This allows objects to be released individually from the storage device when the gate is opened.
This document summarizes an invention for improvements in single-sideband radio transmission systems. It describes a system that uses band compression at the transmitter and band expansion at the receiver to transmit a single-sideband signal while reducing the required bandwidth. The system detects the signal envelope and uses it to amplitude modulate the compressed single-sideband signal before transmission. At the receiver, the system uses the detected envelope to reconstruct the original single-sideband signal from the received compressed signal. The document provides detailed descriptions and diagrams of transmitter and receiver embodiments.
This document summarizes a patent for an improved paper pattern that can be temporarily bonded to fabric. The pattern is made of thin, flexible paper with markings on top. The underside has a heat-sealable, lubricous resin that is non-adhesive at room temperature but becomes adhesive when heated. This allows the pattern to be temporarily bonded to fabric to facilitate needlework while maintaining lubricity for easy needle passage. The resin may be an ethylene polymer, vinyl chloride polymer, or other specified thermoplastic. Figures show applying multiple patterns to fabric with an iron, an enlarged cross-section, and joining cut fabric pieces with attached patterns.
This document describes improvements to gyroscope apparatus. It summarizes two different gyroscope designs that use air bearings to support a rotating gyroscope rotor. In the first design, the rotor is supported within a concentric casing on a spherical air bearing. The casing is driven by a tubular drive shaft connected to conventional bearings. In the second design, a wheel-shaped rotor is supported within a spherical casing on an air bearing. The casing is driven by electric motor integrated with the lower casing portion and supported by ball bearings. Both designs use pickoffs and electromagnetic means to apply torques to the rotor and counteract precession forces to keep the rotor axis aligned with the casing rotation axis.
This document describes improvements to telephone systems, specifically regarding private automatic branch exchanges (PABX) serving large numbers of subscribers across multiple locations. It details a system with a parent PABX connected via two-wire tie-lines to satellite automatic exchanges. The parent PABX operator can set up calls to subscribers on satellite exchanges and receive visual supervisory indications of call progress over the tie-lines. This is achieved through signals sent on a non-speaking conductor and distinctive signals involving potential reversals at the tie-line conductors.
This document describes a patent for improvements in reciprocating motors that are actuated by a fluid supplied at constant pressure. It involves a piston valve that moves alternately into two positions, connecting one side of the piston to the pressure fluid supply and the other side to exhaust. Plungers on each side of the piston can enter cylindrical spaces at the end of the piston's working stroke to build up pressure and cause the valve to switch positions for the return stroke. Optional features include non-return valves in ducts connecting the valve cavities to the spaces to control fluid flow. The invention is intended for hydraulic motors but not limited to that application or liquid as the working fluid.
This document provides details of GB784673 (A) and GB784674 (A), which are patent specifications for two inventions. GB784673 (A) describes a method of producing printed circuit master drawings by removing portions of a black layer on a board to define a circuit pattern. GB784674 (A) describes a mending plug for tubeless tires, specifically a hollow rubber cylindrical plug inserted into punctures using an insertion tool. The document outlines the techniques and provides figures to illustrate the methods.
This document summarizes a patent for a machine that applies rubber caps to containers. It describes a machine with fingers arranged in an annular form that can place a cap, and pistons that impart radial movement to the fingers. It also includes a rotary table to carry containers, a head carrying the fingers that can slide, and a piston to actuate the head. The machine applies caps by extending the fingers to stretch the cap over the container, then retracting the fingers to leave the cap in place.
This document describes a process for dyeing or printing textiles or foils made of cellulose esters or linear aromatic polyesters. Specifically, it involves using acid dyestuffs from the anthraquinone series that have a sulphonic acid group that can be split off by a reducing agent. This causes the dyestuff to become insoluble and bond to the textile or foil substrate. Examples are provided of dyeing various materials like polyester fibers, acetate rayon and cellulose triacetate fibers using different dyestuffs and reducing agents. The dyed materials exhibit good light and wash fastness according to the document.
Boudoir photography, a genre that captures intimate and sensual images of individuals, has experienced significant transformation over the years, particularly in New York City (NYC). Known for its diversity and vibrant arts scene, NYC has been a hub for the evolution of various art forms, including boudoir photography. This article delves into the historical background, cultural significance, technological advancements, and the contemporary landscape of boudoir photography in NYC.
KALYAN MATKA | MATKA RESULT | KALYAN MATKA TIPS | SATTA MATKA | MATKA.COM | MATKA PANA JODI TODAY | BATTA SATKA | MATKA PATTI JODI NUMBER | MATKA RESULTS | MATKA CHART | MATKA JODI | SATTA COM | FULL RATE GAME | MATKA GAME | MATKA WAPKA | ALL MATKA RESULT LIVE ONLINE | MATKA RESULT | KALYAN MATKA RESULT | DPBOSS MATKA 143 | MAIN MATKA
❼❷⓿❺❻❷❽❷❼❽ Dpboss Kalyan Satta Matka Guessing Matka Result Main Bazar chart Final Matka Satta Matta Matka 143 Kalyan Chart Satta fix Jodi Kalyan Final ank Matka Boss Satta 143 Matka 420 Golden Matka Final Satta Kalyan Penal Chart Dpboss 143 Guessing Kalyan Night Chart
The cherry: beauty, softness, its heart-shaped plastic has inspired artists since Antiquity. Cherries and strawberries were considered the fruits of paradise and thus represented the souls of men.
Fashionista Chic Couture Maze & Coloring Adventures is a coloring and activity book filled with many maze games and coloring activities designed to delight and engage young fashion enthusiasts. Each page offers a unique blend of fashion-themed mazes and stylish illustrations to color, inspiring creativity and problem-solving skills in children.
This tutorial offers a step-by-step guide on how to effectively use Pinterest. It covers the basics such as account creation and navigation, as well as advanced techniques including creating eye-catching pins and optimizing your profile. The tutorial also explores collaboration and networking on the platform. With visual illustrations and clear instructions, this tutorial will equip you with the skills to navigate Pinterest confidently and achieve your goals.
This document announces the winners of the 2024 Youth Poster Contest organized by MATFORCE. It lists the grand prize and age category winners for grades K-6, 7-12, and individual age groups from 5 years old to 18 years old.
Ealing London Independent Photography meeting - June 2024
4981 4985.output
1. * GB785388 (A)
Description: GB785388 (A) ? 1957-10-30
Improvements in or relating to pigment compositions
Description of GB785388 (A)
Translate this text into Tooltip
[75][(1)__Select language]
Translate this text into
The EPO does not accept any responsibility for the accuracy of data
and information originating from other authorities than the EPO; in
particular, the EPO does not guarantee that they are complete,
up-to-date or fit for specific purposes.
PATENT SPECIFICATION
7 f f i Date of Application and filing Complete Specification: Aug22,
1955.
No 24168155.
Application made in United States of America on Nov 16, 1954.
Complete Specification Published: Oct 30, 1957.
Index at acceptance:-Class 95, AS.
International Classification:-CO 9 d.
COMPLETE SPECIFICATION
Improvements in or relating to Pigment Compositions We, ARMOUR AND
COMPANY, a corporation organized under the laws of the State of
Illinois, United States of America, of Union Stock Yards, City of
Chicago, State of Illinois, United States of America, do hereby
declare the invention, for which we pray that a patent may be granted
to us, and the method by which it is to be performed, to be
particularly described and by the following statement:This invention
relates to an improved pigment composition and to a process for its
manufacture.
Pigments are finely divided insoluble solids which are used in many
various materials such as for example, coating compositions and
rubber, for many different purposes In coating compositions they are
mostly used to provide a colour or hue, but they may also be used to
2. perform an opacifying function In rubber, especially tyre rubber,
carbon black is used to impart strength and abrasion resistance as
well as colour It is hardly possible to look around and not see some
article which contains a pigment material.
In practically every application of pigmentary materials it is
necessary that they be dispersed, generally in a liquid medium Pigment
dispersion, as encountered in the field of coating compositions,
involves generally transferring a dry pigmentary material existing
really as a heterogeneous dispersion in air to a dispersion as uniform
as possible in a liquid.
The attainment of optimum dispersion usually results in the maximum
practical development of such desirable properties as tinctorial
strength, opacity, gloss and uniform pigment particle distribution.
Pigment particles can be pictured as irregularly shaped solids
surrounded by a bound envelope of air, gas or moisture which is to be
considered distinctly different in its physical relationship to the
pigment from the free air that separates the pigment particles.
Both the free air and the surface-bound air constitute the initial
obstacle to be overcome in converting the pigment from a dispersion
_,,1 in the air to a dispersion in a liquid Pigments in the dry form
are generally in the form of agglomerates which may be either in a
relatively loose or in a compacted condition.
In the dispersion process, a vehicle is added to the pigment mass in a
mixing operation which is extended further by a so-called grinding
operation The dispersion processes employed by the manufacturer of
coating compositions are not really true grinding operations, but the
tendency of the pigment to cluster or coalesce under the conditions of
packing, shipment and storage, as well as a natural tendency of many
pigments to agglomerate when initial wetting is attempted, are factors
which might lead one to believe that real grinding does occur in the
dispersion process Any attempt to truly grind the pigment, if actually
accomplished, would probably result in mill scoring, contamination by
abrasion, change in colour, quality and other possibly undesirable
effects.
As a result of the work done on a mixture of pigment and vehicle, a
pigmented composition is obtained which may be represented by two
extreme conditions, with, of course, the possibility of an actual
composition which combines some of the characteristics of both.
A poor dispersion is one in which the work done has failed to separate
the pigment particles with the result that much of the original air is
retained and the particles have become tightly packed into a hard
aggregate as a consequence of the forces exerted The ideal result is
one in which the pigment particles have been completely separated with
an envelope of adsorbed vehicle replacing the original air envelope,
3. and free vehicle displacing the original free air.
Wetting agents are well known in the field of dispersion, and are
employed in emulsification as well as in dispersing solids Since most
pigment manufacturing processes involve the formation of the pigment
at some stage as a precipitate in an aqueous dispersion, it is known
to coat the pigment with a wetting agent to render the pigment surface
more oil85,388 acceptable However, most of the pigment wetting agents
on the market today are potassium or sodium rosinates and petroleum
sulphonates, which rely solely on the partial adsorption of the
reagent upon the pigment in water, and are only 50 %' efficient These
types of compounds generally remain watersoluble, and a large portion
is washed away in the filtrate when filtering the pigment.
We have discovered that if an aqueous precipitate of pigmentary
material is treated in such a manner as to ultimately coat the pigment
particle with a water-insoluble diacid salt of a N-aliphatic alkylene
diamine, the coating will remain on the pigment during the filtration
step and will act as a spacer between the pigment particles and
prevent the formation of clusters of pigment particles or agglomerates
Further, the amount of time required for grinding or dispersing these
improved pigments into oil or resin-type vehicles is considerably
diminished, and there is no adverse effect upon the properties of the
resulting coating compositions.
It is, therefore, an object of the present invention to provide an
improved pigment composition.
It is a further object of this invention to provide an improved
process for the preparation of pigment materials.
Still another object of this invention is to provide an improved
process for transferring pigmentary material from an aqueous
dispersion to an oil or resin type dispersion.
This invention is applicable, generally, to hydrophilic or
water-wettable pigments and involves treating the pigment in an
aqueous system so as to ultimately coat the pigment particles with a
strongly-adsorbed waterinsoluble salt of an N-aliphatic alkylene
diamine According to a preferred modification of our invention, a
small amount of a water-soluble salt of an N-aliphatic alkylene
diamine is admixed with a slurry of water-wet pigment material,
preferably at a stage in its manufacture prior to drying, and agitated
for a time sufficient to adsorb the watersoluble salt on to the
surface of the pigment particles, generally about 10 to 15 minutes.
Next a stoichiometric quantity of a compound selected from the group
consisting of RCOOZ and R-NHI-A-COOZ wherein R is an aliphatic
hydrocarbon radical having from 12 to 22 carbon atoms, Z is an alkali
metal, and A is a divalent aliphatic hydrocarbon radical having from 2
to 3 carbon atoms, is added and the agitation continued, whereby the
4. surface of the pigment particles is coated with a water-insoluble,
oil-soluble diacid salt of the N-aliphatic alkylene diamine, which
diamine has the general formula R-NH-(CGH 2),;-NH 2 and which acid has
the general formula R'COOH or R'-NH A-COOH wherein R and RI are
aliphatic hydrocarbon radicals or a mixture of radicals having from 12
to 22 carbon atoms, x is an integer of from 2 to 10 and A is a
divalent aliphatic hydrocarbon radical having 2 to 3 carbon atoms in a
quantity ranging from -l to 4 weight per cent, and the alkali metal
salt reaction product is dissolved in the aqueous phase The coated
pigment can then be collected in a filter and dried in an oven at
about 95 to 110 ' C, while the clear filtrate containing the dissolved
alkali metal salt is discarded The coated pigment is now ready for
incorporation into an oil or oleoresinous vehicle and will disperse
with much less effort than an uncoated pigment.
It will be appreciated that the order of addition of the water-soluble
diamine salt and the alkali metal salt can be reversed That is, the
alkali metal salt or soap can first be admixed with the aqueous
pigment system followed by the addition of the water-soluble salt of
the diamine Our experience has been that the order of addition is not
critical However, it is preferred to add the water-soluble salt of the
diamine first because of the comparative ease and strength with which
it is adsorbed upon the surface of the pigment particles.
Among the diamine compounds which can be employed according to the
present invention are the water-soluble salts, for example the acetate
or hydrochloride, of an N-aliphatic alkylene diamine having the
formula R-NH-(CH 2),-NH 2 wherein x is an integer of from 2 to 10, and
R is an aliphatic hydrocarbon radical having from 12 to 22 carbon
atoms R can also 100 represent mixtures of radicals as obtained from
tallow, soybean oil, coconut oil, or other naturally-occurring oils
The preferred class of diamines are those in which x is 3, that is the
N-aliphatic trimethylene diamines The 105 preferred salts are the
acetates and the preferred compound is N-tallow trimethylene diamine
diacetate.
The alkali metal salts or soaps which can be used in accordance with
the present inven 110 tion are represented by the general formulae
RCOOZ and R-NH-A-COOZ wherein Z is an alkali metal, A is a divalent
aliphatic hydrocarbon radical having 2 or 3 carbon atoms, and R is an
aliphatic hydro 115 carbon radical having from 12 to 22 carbon atoms R
might also represent mixtures of radicals as obtained for example from
tallow, soybean oil, coconut oil, or the like The class of compounds
represented by the first general 120 formula are the soaps of long
chain fatty acids, examples of which include sodium oleate, sodium
stearate, sodium palmitate, potassium 785,388 our invention is
applicable to such dry pigments when they are brought into an aqueous
5. dispersion Also within the scope of our invention are the above
pigments as they are ultimately coated according to the process of
this invention.
By the term pigment is meant substances which are generally considered
insoluble in the vehicle as distinguished from dyestuffs, which are
generally considered soluble For example, pigments generally have the
property of light refractivity, tending to give opacity to the system,
whereas dyes generally only have the property of light absorption,
tending to retain the transparency of the system.
The following examples are intended to illustrate the underlying
principles of our invention and are not to be construed as limiting
the scope thereof.
The fineness of grind of pigments was determined on the Hegman Grind
Gauge The fundamental feature of the gauge is a wedgeshaped channel 42
inch wide and ranging in depth from zero to 0 005 inches, cut in a
hardened tool steel block A linear scale beginning with 0 where the
channel is 0 004 inches deep and ending with 8 where the channel is
zero inches deep, is etched along-side the channel and reading
expresses the "grind number " The method as described by Henry A.
Gardner and G C Eward in "Physical and Chemical Examination of Paints,
Varnishes, Lacquers, and Colors" was used to evaluate the fineness of
the grind The gauge was laid flat and the deep end filled to slight
overflowing with paint The scraper, held perpendicularly on the gauge,
was drawn with a firm pressure towards the shallow end of the channel
The drawdown at grazing incidence was viewed immediately and it was
noted where the coarse particles appeared on the surface of the film
The occasional particles in the deeper end were disregarded.
When this method is used for viscous pastes, they should be reduced to
flowing consistency.
oleate, and the like The preferred compound of this class is sodium
oleate The class of compounds represented by the second general
formula are the alkali metal salts of Naliphatic aminoaliphatic
carboxylic acids.
These compounds are formed by the reaction between a long chain amine
and an unsaturated acid or ester such as crotonic, acrylic,
methacrylic, etc The preferred compound of this class is sodium
N-Coco-fl-amino-butyrate, formed by the reaction between Coco amine
and crotonic acid For purposes of simplicity, this compound has been
designated as "A1300," and will be so referred to hereinafter.
As an illustration of the calculations involved in determining
quantities of reagents, the reaction between N-tallow trimethylene
diamine diacetate and sodium oleate yields approximately 80 % of
coating material and 20 % of sodium acetate as shown by the following
reaction.
6. o o Ri-NH 2 C 920 H 2 Nn 3 + 2 a-0 R 2+,C-R 2,-G-R 2 + 2 NPO-C-CI 5 l
RI-NR 2 C Hlell CIH 3 ll wherein R 1 represents a mixture of radicals
as found in tallow and R 2 CO represents an oleyl radical If it was
desired to coat 100 lbs of pigment with 3 0 weight per cent of
N-tallow trimethylene diamine dioleate, the amount of reagents added
to the pigment water slurry can be determined as follows:
The molecular weights of N-tallow trimethylene diamine diacetate and
N-tallow trimethylene dioleate are 440 and 884 respectively 3 % of 100
lbs requires 3 lbs of Ntallow trimethylene dioleate, which will
require 3 0 x 440/884 or 1 49 lbs of N-tallow trimethylene diamine
diacetate Since N-tallow trimethylene diamine diacetate is
approximately 83 % active the corrected quantity of diacetate will
amount to 1 79 lbs The molecular weight of sodium oleate is 304 Since
2 mols of oleate are required to replace the 2 mols of acetate, the
quantity of sodium oleate will be 1 x 3 0 x 304/884 or 2 03 lbs.
This invention includes the use of the above mentioned chemical agents
for treatment of aqueous dispersions containing all pigments,
preferably hydrophilic type pigments, including such materials well
known commercially as iron blue, chrome yellow, chrome orange, chrome
green, zinc chromate, red lead, azo type toners, aluminium hydrate,
lakes, carbon black, iron oxide, zinc oxide, titaniumcontaining
pigments, zinc sulphide-containing pigments, white lead and extenders
Although it is realized that certain of these pigments, such as carbon
black are not generally an aqueous mixture, it is to be understood
that Ex AMPLE I 105 An iron blue pigment, either as a dry stock or a
wet press cake, was coated with varying quantities of N-tallow
trimethylene diamine dioleate or N-tallow trimethylene diamine
di-A-1300, according to the preferred pro 110 cess of this invention
as hereinbefore described.
All of the coated pigments along with uncoated control samples were
made into fairly highly pigmented roller mill pastes and passed over a
laboratory roller mill A determination 115 was made of grinding time,
the number of passes required to produce an enamel grind, and yield
value These pastes were made into paints and checked further for rate
of dry as indicated by dust free time, tack free time 120 (with Zapon
(Registered Trade Mark) Tack tester), colour and gloss comparison, and
pencil 785,388 785,388 hardness If the drying time exceeded the normal
8-hour day, the samples were checked the following morning and were
found to be even It was found that the coating of the pigments did not
impair the final film hardness.
Table I summarizes some of the results of roller mill data obtained
while Table II shows the effect of N-tallow trimethylene diamine
dioleate and the corresponding di-A-1300 10 salt, on heat-cured and
air-dried paint panels.
7. TABLE I
Coating Material Wetting 1st Pass 2nd Pass Applied Aid Consis Total
Pigment % Wt from Added in tency Grind Sample % of Aqueous Vehicle of
Grind Time Grind Time Number Pigment Vehicle By Wt Vehicle Solution
Portion Paste No Sec No Time on Mill Iron Blue Castor 1217 Dry Stock
Oil 40 60 None None B 0 4.0 % 1218,, None D T D O S B 2 4.0 % 1219 D T
D O None F 8 Iron Blue 1230 Press Cake None None B 1 42 5 2 38 9 81 4
Iron Blue 3 0 % 1231 Dry Stock None D T D O S B 2 37 5 8 42 4 79 9
Iron Blue 3 0 % 1232 Press Cake D T D O None <F 8 29 2 29 2 Iron Blue
3 0 % 1233 Dry Stock D T D O None <F 6 38 0 8 48 4 86 4 3.0 % 1234,,
A-1300 None <F 1 37 7 7 52 2 89 9 Iron Blue 3 0 % 1235 Press Cake
A-1300 None <F 8 31 0 31 0 Iron Blue Long Oil 35 1236 Dry Stock Alkyd
52-R-13 65 None None S B 1 15 7 3 17 1 32 8 Iron Blue 1237 Press
Cake,, 35 65 None None S B 0 18 8 2 20 8 39 6 k^j TABLE I-continued.
Coating Material Wetting 1st Pass 2nd Pass Applied Aid Consis Total
Pigment % Wt from Added in tency Grind Sample % of Aqueous Vehicle of
Grind Time Grind Time Number Pigment Vehicle By Wt Vehicle Solution
Portion Paste No Sec No Time on Mill Iron Blue Long Oil 35 3 % 1238
Dry Stock Alkyd 52-R-13 65 D T D O None S B 2 16 6 6 28 0 34 1 Iron
Blue 3 0 % 1239 Press Cake,, 35 65 D T D O None S B 6 20 2 20 2 Iron
Blue 3 0 % 1241 Dry Stock,,,, ,, A-1300 None B 4 Slips on Rolls Iron
Blue 2 0 % 1243 Press Cake,, a) D T D O S B 5 22 4 8 30 0 52 4 3.0 %
1244,, ,, D T D O S B 8 259 25 9 4.0 % 1245,,,,,, ,, D T D 1 O,, <F 8
25 8 25 8 2.0 % 1246,,,,,, ,, A-1300,, <F 5 21 2 8 29 5 50 7 3.0 %
1247,,,,,, ,, A-1300,, <F 8 26 4 26 4 4.0 % 1248,,,,,, A-1300,, <F 8
24 5 24 5 B Bodied MILL SETTING Ca 005 Front Roll S.B = Slightly
Bodied 010 " Rear Roll F Fluid <F = Will Flow Slightly D.T D O _
N-tallow trimethylene diamine dioleate.
52-R-13 is a Federal Specification designation for an alkyd resin
modified with vegetable oils, where the product is supplied as a
liquid containing 68 to 72 % resin and 28 to 32 % petroleum solvent.
00 ui 785,388, TABLE II
Humidity-(High) Sample No.
7/28/53 No No.
1243 1244 No No.
1245 1246 No.
1247 No No.
1248 1236 % Coating 2 0 % 3 0 % 4 0 % 2 0 % 3 0 % 4 0 % None D.T D O D
T D O D T D O A 1300 A-1300 A-1300 Blank Starting Time 8:45 AM 8:49 AM
8:55 AM 8:58 AM 9:00 AM 9:01 AM 9:02 AM Dust Free 4:00 PM 4:00 PM 4:00
PM 4:00 PM 4:00 PM 4:00 PM 4:00 PM Time Tack Free OVER-NIGHT Time g /5
sec.
Tack Free OVER-NIGHT Time g /5 sec.
Tack Free BETWEEN18-24 HOURS > Time g /5 sec.
8. 24 Hour Pencil Hardness 48 Hour Pencil 3 B 3 B 3 B 3 B 3 B 3 B 3 B
Hardness Heat Cured Panels 1 hour 2750 F Gloss Good Good Good Good
Good Good Poor Pencil Hardness 2 B 2 B 2 B 2 B 2 B 2 B 2 B Settling
Test No Set No No No No No Yes Skinning Some Some Some None None None
Some The use of N-tallow trimethylene diamine dioleate in this
formulation of Iron Blue CB-50, and Long-Oil alkyd resin did not
prevent skinning, while the samples containing the Di-A 1300 salt of
N-tallow trimethylene diamine showed no signs of skinning.
Iron Blue CB-50 is an iron blue pigment supplied by the Standard
Ultramarine and Color Company Iron Blues are complex ferric
ferrocyanides containing an alkali metal or ammonia in the crystal
lattice.
"-g/5 secs " refers to the most weight in grams put on the Zapon Tack
Tester for 5 seconds which will allow the foil to pull free from the
film within 5 seconds.
We have found that a paste consisting of blue pigmented paints on
final pencil hardness, parts of iron blue and 60 parts castor oil,
dust free time, tack free time, colour, gloss, when passed over a
roller mill once will gel and hiding power Further, paints that conThe
addition of more castor oil to the formu tain either of the tvo coated
pigments showed lation can prevent this, but this is not desir no
signs of hard settling, or caking on standing, able because an excess
will overplasticize the while the pigments of the control samples
final lacquer film Samples 1217, 1218 and formed a hard cake at the
bottom of the 1219 in Table I are good examples of how container.
the coating of N-tallow trimethylene diamine EXAMPLE II dioleate can
correct this condition Referring Chrome green pigments are mixtures of
to the table, it will be seen that Sample 1217 iron blue with a very
fine particle size of 0 05 bodied so badly on one pass over the roller
microns, and chrome yellow with a relatively mill it could not be
passed over the mill again large particle size of 0 3 microns Upon
Sample 1218 was prepared with N-tallow tri application of chrome green
pigmented paints, methylene diamine dioleate added in the the heavy
chrome yellow particles settle in the vehicle portion of the paste as
a "wetting aid " paint film and the lighter and smaller iron This
sample made a slightly better dispersion, blue particles are pushed to
the surface of the but most important the paste consistency was film
This causes the green paint film to turn sufficiently fluid to pass
over -the mill a second blue upon drying We have found that floctime
Sample 1219 is a pigment coated with culation in chrome green
pigmented paints N-tallow trimethylene diamine dioleate from can be
controlled if the chrome green pigment an aqueous solution, which has
lowered inter is coated in accordance with the present facial tension
between pigment and oil to a invention The pigment particles so coated
9. minimum, leaving a very fluid paint which can no longer act
independently of one will disperse easily in one pass over the roller
another, and they will not migrate in the paint mill to an enamel
grind of 7-g to 8 (as per film to produce flooding and floating.
Hegmanf Gauge) A first sample of a chrome green pigment It will be
seen from Table I that pig was coated with N-tallow trimethylene
diamine ments coated according to the present inven dioleate according
to the process of the present tion will enable a paint manufacturer to
invention A second sample of a chrome green formulate fluid pastes
with high pigment pigment was coated with a petroleum sulratios, and
further to obtain a decrease in phonate according to the conventional
method.
grinding time, as well as to cut down the These two samples along with
a third control number of passes formerly required on the sample were
formulated into a pigment paste roller mill and subsequently into a
finished paint comThe data presented in Table II illustrates position
Table III lists the dispersion and that the coating of the pigments
according to roller mill data Table IV summarizes the the present
invention has no effects in iron results of film characteristics.
785,388 785,388 TABLE III
Roller Mill Data Sample No.
Pigment Vehicle Pigment: Percent by Wt.
Vehicle: Percent by Wt.
Coating Material Applied from Aqueous Solution Consistency of Paste No
1270 No 1273 No 1274 Chrome Chrome Chrome Green Green Green 52-R-13
52-R-13 52-R-13 Alkyd Alkyd Alleyd 65 65 35 35 None Med.
heavy 1st Pass on Mill: Grind No.
Grind Time, Sec.
2nd Pass on Mill: Grind No.
Grind Time, Sec.
3rd Pass on Mill: Grind No.
Grind Time, Sec.
Final Grind No.
Total Time Consumed Passes Required 3 7.8 10.0 53 L 11.6 5:1 29.4 Pet.
Sulph.
Heavy 3 7.6 31 9.0 N-tallow trimethylene diamin& dioleate Thin 782 8.2
6 10.0 6 26.6 271, 8.2 TABLE IV
Sample No.
Heat Cured Panels 1 hour at 2750 F.
Gloss Comparative Pencil Hardness Film Thickness No 1270 No 1273 No
1274 Poor 2 B 002 " Good 2 B 002 " Good 2 B 002 " Colour "Settling
Test" Separation of Yellow and Blue Pigments Even Yes 24 hrs.
Referring to Table III, the control sample No 1270 had a grind number
of 3 (as per Hegman Gauge) on the first pass over the mill; 5 on the
10. second, and 511 f on the third.
The total time consumed for all three passes was 294 seconds Sample No
1273 was Yes No 24 hrs Still Dispersed after 3 months treated with 3 0
% by weight of petroleum sulphonate from a water slurry, filtered and
10 dried This sample passed over the mill in the first pass to produce
a grind of 3, 3 on the second pass, and 6 on the third pass The total
grinding time for this sample was 266 seconds Sample No 1274 coated
with 3 0 % by weight of N-tallow trimethylene diamine dioleate,
reached a grind number of 7 T (enamel specifications) on the first
pass over the mill in 8 2 seconds.
Referring to Table IV, the data illustrates that coating chrome green
pigments with Ntallow trimethylene diamine dioleate does not impair
gloss, pencil hardness or colour and settling does not occur in chrome
green paint.
There is some indication in the literature that chrome yellow pigments
have a tendency to react with certain organic coating materials at
high temperatures, and thereby cause discolouration of the paint upon
baking Because of this heat cured panels were prepared of the paints
containing the coated pigments as well as the control It was found
that chrome green pigments coated in accordance with the invention and
made into a paint did not show any discolouration on heat curing
Further, the coated pigments according to the invention produced a
paint with a higher gloss, owing to a more uniform dispersion.
EXAMPLE III
Two samples of iron blue pigments in the form of a water slurry
containing 4 28 and 3.1 weight per cent solid, respectively, and
designated Iron Blue No 10 and Iron Blue No 10 A, were treated as
follows:
Four thousand ( 4000) parts by weight of Sample No 10 was divided into
two equal parts of 2000 parts by weight each The control was vacuum
filtered and dried at 110 C for 5 hours and 85 6 parts by weight of
dry uncoated iron blue pulverized control was obtained To the other
2000 parts by weight, 1.42 parts by weight of N-tallow trimethylene
diamine diacetate dissolved in hot water was added and mixed for 15
minutes To this 1.84 parts of sodium oleate dissolved in hot water was
added and agitated for about 15 minutes The resulting slurry was
vacuum filtered and dried at 1100 C for 5 hours.
85.6 parts by weight of pulverized 3 %' Ntallow trimethylene diamine
dioleate coated iron blue was obtained.
Sample No 10 A was treated exactly as Sample No 10.
The coated and uncoated pigments were mixed with a linseed varnish and
dispersed on a 3-roll mill The data obtained is recorded in Tables V
and VI.
TABLE V
11. Dispersion Data for Iron Blue No 10 3 Roll Mill Sample No.
Vehicle Used No 10 Control Linseed Varnish No 10 Coated Linseed
Varnish Vehicle by Wt.
Pigment by Wt.
Relative Viscosity 1st Grind No.
Pass Grind Time 2nd Grind No.
Pass Grind Time Roll Front Setting Back Oil Absorption Total Time
Consumed on Mill parts parts Lowest 0 1 ' 43 O " < 5 1 '15 9 " 001 "
51.0 2 ' 58 9 parts parts 2 1 ' 20 6 6 1 '17 7 m Unchanged 41.0 2 ' 38
4 " Relative Viscosity means that one sample, namely that marked
"lowest" was less viscous than the other sample.
so 785,388 785,388 TABLE VI
Roller Mill Data for Iron Blue No 10 A Sample No.
Vehicle Used No 10 A Control Linseed Varnish No 10 A Coated Linseed
Varnish Vehicle by Wt.
Pigment by Wt.
Relative Viscosity 1st Grind No.
Pass Grind Time 2nd Grind No.
Pass Grind Time 3rd Grind No.
Pass Roll Front Setting Back Total Time Consumed on Mill Oil
Absorption Results of iron blue samples No 10 and A coated pigment
show a better dispersion and a decrease in the time consumed on the
mill when compared to the uncoated controls.
The actual time saving is much more pronounced on a large production
basis Assuming that it is expected to obtain an enamel grind number of
6 with this blue pigment, it would be necessary to pass an uncoated
pigment paste twice over a 5 roll mill On the other hand, it would be
possible to obtain a grind number of 6 with one pass of a pigment
coated in accordance with the invention.
Therefore, the paint manufacturer can actually enjoy better than a 50
% saving of time.
* Sitemap
* Accessibility
* Legal notice
* Terms of use
* Last updated: 08.04.2015
* Worldwide Database
* 5.8.23.4; 93p
* GB785389 (A)
12. Description: GB785389 (A) ? 1957-10-30
Aralkyl carbinols and process for their preparation
Description of GB785389 (A)
Translate this text into Tooltip
[75][(1)__Select language]
Translate this text into
The EPO does not accept any responsibility for the accuracy of data
and information originating from other authorities than the EPO; in
particular, the EPO does not guarantee that they are complete,
up-to-date or fit for specific purposes.
COMPLETE SPECIFICATION
Aralkyl Carbinols and process for their preparation
We, UNION CARBIDE CORPORATION(formerly Union Carbide and Carbon
Corporation), of 30, East 42nd Street, New
York, State of New York, United States of
America, a Corporation organised under the laws of the State of New
York, United States of America, (Assignee of JOSEPHAUGUSTINE
LAMBRECH), do hereby declare the invention, for which we pray that a
patent may be granted to us, and the method by which it is to be
performed, to be particularly described in and by the following
statement :
This invention relates to an improved process for making aralkyl
carbinols.
The aralkyl carbinols obtained by the process of this invention have
the general formula: where R is either a carbonyl (-CO-) group or a
hydrogenated carbonyl group (-HCOH-). These compounds may be named
2-benzoyl-2,2-dichloroethanol and 3phenyl-2,2-dichloropropanediol 3
respectively. Such compounds are useful for forming resins by reaction
with formaldehyde. If desired, they may be esterified with acids to
form plasticizers for synthetic resins. They may also be used as dye
carriers for synthetic fibres such as polyethyleneterphthalate.
According to one modification of the invention,
2-benzoyl-2,2-dichloroethanol may be prepared by condensing
substantially equimolar amounts of formaldehyde and
alpha-alpha-dichloroacetophenone in the presence of an alkaline
catalyst and at a temperature between 0
C. and 40 C. The reaction may be represented as follows:
13. <img class="EMIRef" id="026445184-00010001" />
<img class="EMIRef" id="026445184-00010002" />
The condensation is conducted in the pre sence of an alkaline catalyst
preferably in an amount between 1 per cent and 3 per cent by weight of
the reactants. The alkaline catalyst may be an alkali metal hydroxide,
an alkaline earth metal hydroxide or a tertiary amine and the reaction
is carried out at a temperature of from 0 C. to 40 C. Preferably, the
reaction is conducted at 20 C. and for a period of from two hours to
twenty-four hours. After the reaction is complete, from one to three
volumes of water may be added to the reaction mixture, whereby oil and
water layers are formed. The oil layer is separated from the water
layer and distilled to yield 2-benzoyl-2,2-dichloroethanol as a
distillate.
If desired, 2-benzoyl-252-dichloroethanol may be reduced by reaction
with a low-boiling aliphatic secondary alcohol to form
3-phenyl2,2-dichloropropanediol- 1,3. Preferably the reduction
reaction is conducted by reacting the ketoalcohol with an excess of a
low-boiling aliphatic secondary alcohol, such as isopropanol, in the
presence of an aluminum alcoholate, such as aluminum isopropoxide, as
a catalyst at a temperature corresponding to the boiling point of the
low-boiling alcohol until the lowerboiling ketone by-product of the
reaction is no longer distilled from the reaction mixture. The
reduction reaction can be graphically represented by the equation:
<img class="EMIRef" id="026445184-00010003" />
wherein R is an alkyl group.
The invention is more partlcularlrt described in the following
examples:
EXAMPLE I.
2-benzoyl-2, 2-dichloroetbanol was prepared by slowly adding a
methanolic solution of sodium hydroxide (12 grams of sodium hydroxide
in 150 cc. water and 300 cc. methanol) to a mixture of 567 grams of
alpha-alpha-dichloro-acetophenone and 255 grams of 40 per cent
formalin at 20 C. The reaction mixture was maintained at 20 C. for 24
hours and then added to two liters of water. The oil layer which
formed was separated from the water and distilled. The fraction which
boiled at 134
C. at an absolute pressure of 5 mm Hg. was recovered as the distilIate
product. It had a specific gravity of 1.367 (20Q/20 C.). The yield was
90 per cent. This product is soluble in alcohols and ketones and is
2-benzoyl-2,3- dichloroethanol.
EXAMPLE II.
3 -Phenyl-2,2-dichloropropanediol-1,3 was prepared by adding 300 grams
of the product obtained in Example I to a mixture of 65 grams of
aluminum isopropoxide and 1000 cc. of isopropanol at its boiling
14. point(70" C. to 85" C.). Heating was continued until acetone no longer
distilled from the mixture. The isopropanol was removed by
distillation and the catalyst neutralized with dilute sulfuric acid.
The residue solidified. It was recrystallized from benzene in the form
of a white crystalline solid melting at 107 C. It is soluble in
alcohols and ketones and is 3-phenyl-2,2-dichloropropanediol.
What we claim is:
1. As a new chemical compound an aralkyl carbinol having the general
formula:
<img class="EMIRef" id="026445184-00020001" />
where R is either a carbonyl group (-CO-) or a hydrogenated carbonyl
group (-HCOH-).
2. A process for producing an aralkyl carbinol having the formula:
<img class="EMIRef" id="026445184-00020002" />
which comprises condensing substantially equimolar amounts of alpha,
alpha-dichloroacetophenone and formaldehyde in the presence of an
alkaline catalyst at a temperature between 0 C. and 40 C.
3. A process for producing an aralkyl carbinol having the formula:
<img class="EMIRef" id="026445184-00020003" />
* Sitemap
* Accessibility
* Legal notice
* Terms of use
* Last updated: 08.04.2015
* Worldwide Database
* 5.8.23.4; 93p
* GB785390 (A)
Description: GB785390 (A) ? 1957-10-30
Improvements in methods of preparing cement raw slurry
Description of GB785390 (A)
P A Et N X S P a E C I F, I ATN
PATENT SPE CIFICATION a 2 J,0 Inventor: JORGEN OLAF CLEEMAN 71
( O W N Date of Application and filing Complete Specification: Sept 5,
15. 1955.
No 254521/55.
Complete Specification Published: Oct 30, 1957.
Index at acceptance:-Class 22, A 1 X International Classification:-CO
4 b.
COMPLETE SPECIFICATION
Improvements in methods of preparing Cement Raw Slurry ERRATUM
SPECIFICATION N'O, 785,390
85,390 Page 4, line 50, fort "Centrlfugedn read ncentrifugal".
TFIE PATENT OFFICE, 28th A/wit, al 8 DB 04462/2 ( 8)3604 150 4/58 R
ferred method on account of its lower power requirements is
closed-circuit grinding; in this method the raw materials after
wet-grinding are passed to a separator which divides them into a fine
and a coarse fraction; the coarse fraction is fed back to; the mill to
be ground again and the fine fraction usually constitutes the raw
slurry.
The separator commonly used in closedcircuit grinding is a rake
classifier or other apparatus in which the separation takes place
under the action of gravity Now if separation is to take place at a
suitable particle size by sedimentation the water content of the S 1
lurry must be as high as 70 or 80 %/ Qor even more On the other hand
for efficient kiln operation the water content of the slurry should be
as low as possible However if the raw slurry is too dry it cannot be
pumped, and this obviously complicates its handling.
Therefore for efficient kiln operation the raw slurry should be as dry
as is consistent with pumping, and a water content of about 30 to 40/o
meets these conflicting requirements.
This water content is considerably lower than that required by the
rake-classifier or the like and it is therefore usual to remove some
of this water in a thickener, which is however costly to instal and
operate and complicates the plant In some closed-circuit grinding
plants gravity-action separators have somelPrice 3 s 6 d l able if
efficient kiln operation is to be achieved.
According to this invention a part of the raw materials is wvet-ground
in a closed circuit that includes a centrifugal separator, thus
removing from the circuit a fine fraction with a substantial water
content Relatively dry raw materials are then mixed with the finet
fraction to form a mixture which either as such or after further
grinding constitutes the raw slurry.
A centrifugal separator used in a cement works should be robust and
simple and sve have found that it is advantageous to use a
hydrocyclone.
The proportions in which the m aterials may be used can be calculated
in the manner set out below, these calculations being illustrated by
16. Figures 1 and 2 of the accompanying drawings.
In Figure 1, the area I represents raw material of low water content
(or containing no water at all, that is, the material is available as
a dry powder), the area II the closedcircuit-ground material of
comparatively high water content and the area III a slurry produced by
mixing materials I and II T and V denote the absolute amounts of dry
matter and water, respectively, contained in I, II and III.
Then obviously I PATENT SPECIFICATION
Inventor: JORGEN OLAF CLEEMAN 785,390 0 W t 3 Date of Application and
filing Complete Specification: Sept 5, 1955.
No 25452/55.
___ty Complete Specification Published: Oct 30, 1957.
Index at acceptance:-Class 22, A 1 X International Classification:-CO
4 b.
COMPLETE SPECI'F'ICATION Improvements, in methods of preparing Cement
Raw Slurry We, F L SMIDTH & Co A/S, a Danish Company, of 33,
Vestergade, Copenhagen K, Denmarki, do hereby declare the invention,
for which we pray that a patent may be granted to us, and the method
by which it is to be performed, to be particularly described in and by
the following statement: -
This invention relates to the production of cement raw slurry by
grinding the raw materials.
There are two methods of grinding in common use Straight grinding is
the older method, and in this the raw materials are finish ground by a
single passage through a grinding mill The newer and now the preferred
method on account of its lower power requirements is closed-circuit
grinding; in this method the raw materials after wet-grinding are
passed toa separator which divides them into a fine and a coarse
fraction; the coarse fraction is fed back to, the mill to be ground
again and the fine fraction usually constitutes the raw slurry.
The separator commonly used in closedcircuit grinding is a rake
classifier or other apparatus in which the separation takes place
under the action of gravity Now if separation is to take place at a
suitable particle size by sedimentation the water content of the
slurry must be as high as 70 or 80 % or even more On the other hand
for efficient kiln operation the water content of the slurry should be
as low as possible However if the raw slurry is too dry it cannot be
pumped, and this obviously complicates its handling.
Therefore for efficient kiln operation the raw slurry should be as dry
as is consistent with pumping, and a water content of about 30 to /%
meets these conflicting requirements.
This water content is considerably lower than that required by the
rake-classifier or the like and it is therefore usual to remove some
of this water in a thickener, which is however costly to instail and
17. operate and complicates the plant In some closed-circuit grinding
plants gravity-action separators have somelPrice 3 s 6 d l times of
late been replaced by centrifugal separators such as hydrocyclones;
the separation in the latter is effected by centrifugal force, which
may he several thousand times greater than the force of gravity A
snialeir water content in the closed-circuit can therefore be accepted
However effective separation by hydrocyclones requires that the raw
materials should have a water content slightly higher than that
required for efficient kiln operation Thus a hydrocyclone either works
inefficiently due to too low a water content or efficiently with the
correct water content, but then the fine fraction forming the raw
slurry has a water content larger than that desirable if effcient kiln
operation is to be achieved.
According to this invention a part of the raw materials is wet-ground
in a closed circuit that indludes a centrifugal separator, thus
removing from the circuit a fine fraction with a substantial water
content Relatively dry raw materials are then mixed with the fine
fraction to form a mixture which either as such or after further
grinding constitutes the raw slurry.
A centrifugal separator used in a cement works should be robust and
sinple and we have found that it is advantageous to use a
hydrocyclone.
The proportions in which the materials may be used can be calculated
in the manner set out below, these calculations being illustrated by
Figures 1 and 2 of the accompanying drawings.
In Figure 1, the area I represents raw material of 'low water content
(or containing no water at all, that is, the matzrial is available as
a dry powder), the area II the closedcircuit-ground material of
comparatively high water content 'and the area III a slurry produced
by mixing materials I and HI T and V denote the absolute amounts of
dry matter and water, respectively, contained in I, II and III.
Then obviously 785,390 T==T 1 +T 2 V.=V 1 +V 2 The percentages of
water II and III are V 1 X 100 vi = T, + V, V 2 x 100 V 2 = T+ V 2 V 3
X 100 T, + V.
From these the following V, and V, are obtained:
v, X T V, 100-v 1 v x T V = _ 100-v.
V 3 x T 3 V 3 = 100-v.
On substituting ( 6), ( 7) and ( 8, sult is:
v x T, v, x T v,,x _ = +__100-v 3 100-v, 100Assuming now T, to be= 1
tion ( 1) may be written:
=t 1 tn t, and te being the distributio cf lry matter contained in I
at t, = 100 t, On substituting from ( 10), -to ( 9) we have 100o v, (
100 62 -v 100 -v, cort ( 1) and This equation contains four variables,
viz.
18. v,, v 2, v, and t-.
( 2) If v, is fixed absolutely, for instance at ttained in I, 333-l,
while v, is given different values in turn, for instance, 0, 10 % and
20 %I, curves may be drawn, showing the variation of to in f 2
accordance with v,.
These curves are shown in Figure 2 at P, Q and R, the curve P
corresponding to a water content of 0 %l in the raw materials of ( 4)
and low water content, Q to a water content of % and R to a water
content of 20 %,.
Auxiliary lines show by way of example that, when manufacturing a
cement rawv ( 5) slurry (III) containing 3310,% water, about % of the
raw materials (II) mray be subjected to closed-circuit grinding at a
water values for V 1, content of about 5 % higher (that is, 38 t33.1)
than the water content in III if tha remaining 20 %Q of the raw
materials I is entirely witheut water If on the other hand, ( 6) the
water cont Lent of I is say 10 %, it is not possible to let more than
about 75 % of the dry material pass through the closed-circuit
grinding installation in order to obtain the ( 7) and desired 33-1 %
water in the sluiry mix JII so long as the difference in swater
content of III and II is to be maintained at 5 Under the same
conditions the amount of drv ( 8) materi Al passing throurh closed
circuit grindin R will be 68 % only if the water content in (), he e
of I is 20 % 1.
)mi ( 2), the re Figures 3 to 7 of the accompanying drawings are
diagrams of different ways in which T Ccthe invention may be carried
out.
2 ( 9) In the plant shown in Figure 3 raw v materials A and B are
used, and, as also in the other examples, rnay be of the same or 00 (
10), equa differ ent composition The material A is ground dry in a
mi'i M, to produce the material I of the calculations Water 1 is ( 111
added to the material B, which is wet-ground in a mill M,, in
closed-circuit with a hydron in p er cent cyclone H, more water being
added at 2 to the 7 d II, or material entering the hydrocvclone and
the coarse fraction from the hydrecyclone being ( 12) returned to the
mill as shown at 3 = The fine fraction is the material II of the
calculations, ( 11) and ( 12) and it is mixed with the ground material
I in a mixer G and then fcmis the final slurry III.
vt The compositions of suitable materials for ( 13) working by thi S
method are shown in the folv lowing table:
SO 785,390 TABLE 1
A = I B II III Parts of dry matter 22 78 78 100 Parts of water 0 0 to
52 52 52 % dry matter 100 100 to 60 60 66 % water 0 O to 40 40 34
Generally water is added at both 1 and 2 in Figure 3, but if the
material B has a high enough water content it may be unnecessary to
19. add water at 1, and if the water content of the ground material is
high enough for efficient separation in the hydrocyclone no water need
be added at 2.
The arrangement shown in Figure 4 nway be used when the material A is
not dry Here the fine fraction II from the hydrocyclone H is fed to a
mill M,p tin which the material A is wet-ground, and there is no need
for a special mixer G Suitable compositions for carrying out the
method shown in Figure 4 are given in Table 2.
TABLE 2
A = 1 B II III Parts of dry matter 50 50 50 100 Parts of 5 0 to 45 45
50 water % dry matter 91 100 to 53 53 67 % water 9 0 to 47 47 33 When
the raw materials contain both hard and soft particles they may be
subjected to an initial grinding and then separated finto fine and
coarse fractions, the coarse fraction constituting the part of the raw
material that is ground in the closed circuit The fine fraction from
the separation in the closed circuit is mixed either with the raw
material before the initial grinding or with the first fine fraction.
This method is illustrated by Figure 5.
In Figure 5, the raw material A is mixed in a mill M 11 with a fine
fraction II from a hydrocyclone H This mill grinds the mix selectively
whereby the soft particles aren'iore finely ground than the hard
particles; if the materials are of suitable composition they may be
reduced in size in a wash drum instead of being ground The mixture III
then passes to a screen S which divides the materials into a coarse
fraction and a fine fraction Water 1 and a coarse fraction 3 tare
added to the coarse fraction B before it passes into the closed
circuit containing the mill MA, and the hydrocyclone H; more water may
be added at 2 if required.
The fine fraction from the screen S is ground in a mill M,, and then
constitutes the finished cement raw slurry IV.
The fine fraction coming from the closedcircuit grinding may be passed
as II to the mill M,, as indicated by the dotted line, but usually the
method shown in solid lines is preferred.
Materials to be treated as shown in Figure may have the composition
given in Table 3.
785,390 TABLE 3
A = I B II III IV Parts of dry matter 100 60 60 160 100 Parts of water
19 10 45 64 54 % dry matter 84 86 57 71 65 % water 16 14 43 29 35
Figures 6 and 7 are suitable when the raw materials A and B are
different, A consisting of substantially dry materials whilst B
consists of materials having a substantial water content In the two
arrangements illustrated in these drawings only a fine fraction of the
relatively dry raw material is mixed swith the fine fraction from the
closed circuit to form the raw slurry, the remainder being fed into
20. the closed circuit.
In the arrangement shown in Figure 6 the material A is first passed
through a screen S, where they are divided into a fine fraction 5 and
a coarse fraction 6 The coarse fraction 6 is passed through a mill M,
to another screen 52 which divides this fraction into a fine fraction
9 and a coarse fraction 8 The materials B to which are added the fine
fraction 5, the coarse fraction 8, another coarse fraction 3 and water
1 are passed into a closed circuit comprising the mill M,, and a
hydrocyclone H; further water may be added to the materials at 2 if
required The coarse fraction 3 from the hydrocyclone is fed bach into
the circuit, whilst the fine fraction 1 I is fed to a mixer G The fine
fraction 9 is passed through the mill M 1 ' to the mixer G where it
combines with the fine fraction II to form the raw slurry III.
The arrangement shown in Figure 7 is very similar to that shown in
Figure 6 In it an air separator W replaces the screen 52, and as a
result it is not necessary to carry out any further grinding of the
fine fraction 9.
It will be clear from these Figures and Tables that by the invention
it is possible, to supply sufficient water to the rawv materials
undergoing closed-circuit grinding to enable the hydrocyclone to work
effectively, and at the same time without using a thickener to product
a cement raw slurry having a water content say, 35 %, suitable for
'efficient kiln operation.
* Sitemap
* Accessibility
* Legal notice
* Terms of use
* Last updated: 08.04.2015
* Worldwide Database
* 5.8.23.4; 93p
* GB785391 (A)
Description: GB785391 (A) ? 1957-10-30
Improvements in rotary thermal regenerators, particularly for gas turbines
Description of GB785391 (A)
21. PATENT SPECIFICATION
Date of Application and filing Complete Specification: Sept 12, 1955.
785,391 No 26008/55.
l v a g o DA Application made in Germany on Sept 10, 1954.
Complete Specification Published: Oct 30, 1957.
Index at acceptance:-Class 64 ( 1)5 L 4 (C:E).
International Classification:-P 25 h.
COMPLETE SPECIFICATION
Improvements in Rotary Thermal Regenerators, Particularly for Gas
Turbines We, HENSCHEL & SOHN GESELLSCHAFT MIT BESCHRANKTER HAFTUNG, of
2, Henschelstrasse, Kassel, Germany, a Joint-Stock Company organised
under the Laws of Germany, do hereby declare the invention, for which
we pray that a patent may be granted to us, and the method by which it
is to be performed, to be particularly described in and by the
following statement:-
This invention relates to rotary thermal regenerators.
Gas turbines for use as power units for driving lorries omnibuses and
the like vehicles must answer the following requirements: they must be
of low weight, inexpensive to manufacture, take up little room, and
have a low fuel consumption The last requirement can only be satisfied
by equipping the gas turbine with a heat exchanger For this purpose a
thermal regenerator, or regenerative heat exchanger, is particularly
suitable, that is to say a heat exchanger consisting of a plurality of
chambers filled with a heat-absorbing filling material of steel,
ceramic, or the like, which are traversed alternately by the hot waste
gases from the turbine and by the air to be heated coming from the
compressor in the opposite direction of flow.
According to the present invention there is provided a rotary thermal
regenerator having a plurality of chambers arranged in parallel with
the axis of rotation and containing heattransfer material,
characterised in that the individual chambers consist of cylindrical
tubes filled with the heat-transfer filling material which extends
wholly over the crosssection of the tube bore and through which the
gases flow axially in their passage along the tube.
The centres of the chambers are for preference arranged on a plurality
of concentric circles around the axis of rotation and on radii
extending from the axis of rotation, the number of chambers disposed
on the different concentric circles being equal.
lPrice 3/ 6 l As a further development of the invention, the diameters
of the chambers disposed on the different concentric circles are so
graduated that the tube-like chambers are tangent to the radii
directed to the tubes of the outer 50 concentric circle on both sides.
Shaped sheet metal strips are preferably used according to the
22. invention as filling material for the numerous tubular chambers, being
simple to produce and offering only 55 slight resistance to flow Sheet
metal strips of this kind can easily be inserted in a circular tube A
tube-shaped chamber has furthermore the great advantage that it can be
designed to have a lesser wall thickness than 60 chambers of any other
shape with the same internal pressure.
A preferred embodiment of the regenerator of the invention is shown
diagrammatically and by way of example in the accompanying 65
drawings, in which:Fig 1 is a partial cross-section through an end
chamber of the regenerator on the line I-I of Fig 2; Fig 2 is a
partial longitudinal section of 70 the same; and Fig 3 shows a sheet
metal strip forming the filling material.
In the embodiment shown in Figs 1 and 2 only two concentric rows of
tubular chambers 73 are provided The tubular chambers 1 are disposed
on an outer circle 2 and the tubular chambers 3 on an inner concentric
circle 4.
The tubular chambers 3 have a smaller diameter corresponding to the
smaller diameter 80 of the circle 4 All the tubular chambers disposed
on one circle are of equal area.
The diameters of the two rows of tubular chambers 1 and 3 are so
selected that radii extending from the axis of rotation and 83
tangential to both sides of an outer chamber 1 are also tangential to
both sides of the corresponding inner chamber 3 The tubular chambers 1
and 3 are filled with a filling material 5 and 6, indicated by
cross-hatching 90 785,391 in the drawing At their ends the tubular
chambers are secured in round ring-shaped chambers 7 and 8 by welding,
soldering or other means The chambers 7 and 8 each consist of an inner
circular bounding wall 9, an outer circular bounding wall 10, and each
has a cover plate 11 receiving the ends of the tubular chambers 1 and
3, and a cover plate 12 having as many openings 13 of segmental
cross-section as there are tubular chambers on a circle The chambers 7
and 8 are furthermore divided by radial ribs 14 into as many chambers
as there are tubular chambers on a circle.
The filling materials 5 and 6 consist of a continuous band composed of
a straight sheet metal strip 15 of slight thickness and a sheet metal
strip 16 likewise of slight thickness bent into semi-circular
undulations The two sheet metal strips 15 and 16 are placed loosely
upon one another and rolled up so that they can be easily inserted
into the tubular chambers 1 and 2.
* Sitemap
* Accessibility
* Legal notice
* Terms of use
23. * Last updated: 08.04.2015
* Worldwide Database
* 5.8.23.4; 93p
* GB785392 (A)
Description: GB785392 (A) ? 1957-10-30
Differential
Description of GB785392 (A)
A high quality text as facsimile in your desired language may be available
amongst the following family members:
DE1025279 (B) US2786367 (A)
DE1025279 (B) US2786367 (A) less
Translate this text into Tooltip
[81][(1)__Select language]
Translate this text into
The EPO does not accept any responsibility for the accuracy of data
and information originating from other authorities than the EPO; in
particular, the EPO does not guarantee that they are complete,
up-to-date or fit for specific purposes.
PATENT SPECIFICATION
78 f Date of Application and filing Complete If/ t Specification:
Sept14, 1955 No 2
Application made in United States of America on Sept 28, 1954.
Complete Specification Published: Oct 30, 1957.
Index at acceptance:-Class 80 ( 2), D 1 A.
International Classification:-F 06 h.
COMPLETE SPECIFICATION
Differential We, ALIAS-CHALMERS MANUFACTURING CO-m PANY, a Corporation
organised under the laws of the State of Delaware, United States of
America, of Post Box 512, Milwaukee 1, Wisconsin, United States of
America, do hereby declare the invention, for which we pray that a
patent may be granted to us, and the method by which it is to be
24. performed to be particularly described in and by the following
statement:-
This invention relates to power transmitting gearing and is concerned
more particularly with a bevel gear differential, that is, a
differential wherein a pair of bevel side gears and a set of planetary
bevel pinions in mesh with the side gears are rotatably mounted within
a rotary cage or housing structure.
Bevel gear differentials are widely -used in motor vehicles and it is
a primary object of the invention to provide an improved automotive
type of bevel gear differential which permits removal of the side
gears and planet pinions from the cage without the necessity of first
removinn' the cage from its supporting structure, so that a
substantial amount of time may be saved when component parts of the
differential such as gears, bearings and thrust washers are to be
inspected or replaced.
Although it is possible to remove the bevel side gears and bevel
planet pinions from some prior art differentials without removing the
differential cage from its support, these previously suggested
differential mechanisms are not entirely satisfactory, particularly
those which employ only two planet pinions In a two pinion bevel gear
differential it is difficult, for instance, to provide for even load
distribution on the teeth of the pinions and side gears and to obtain
satisfactory tooth life.
More specifically, therefore, it is an object of this invention to
provide an improved bevel gear differential of the type hereinbefore
set forth in which the planet pinions are rotatably mounted in 50
registering relation, respectively, with peripheral apertures of the
cage, and in which the peripheral cage apertures and the planet
pinions are relatively proportioned so that the pinions may be moved
55 into and out of the cage through their respective cage apertures.
It is a further object of this invention to provide an improved bevel
gear differential of the torque proportioning 60 type.
According to the invention, a bevel gear differential including a
rotary cage structure, a pair of bevel side gears mounted therein and
a plurality of bevel 65 planet pinions in mesh with the side gears, is
characterised in that the cage structure has a peripheral aperture so
proportioned and arranged with respect to the side gears as to
accommodate move 70 ment of the side gears into and out of the cage
structure through the aperture, and a releasably secured cover for
said aperture serving, when secured, as a structure for mounting one
75 of the planet pinions in its operative position.
The invention is illustrated by way of example in the accompanying
drawings, in which: 80 Fig 1 is a sectional view taken on line I-I of
Fig 2, of a differential gear installation for motor vehicles; Fig 2
25. is a plan view of the installation shown in Fig 1 with parts omitted
for 85 purposes of exposure; Fig 3 is an end view taken in section on
line III-III of Fig 1, the bevel ring gear at the right of Fig 1 being
omitted in Fig 3; 90 ,392 6345/55.
785,392 Fig 4 is a sectional view corresponding to the lupper part of
Fig 1, and showing a modification of the mounting structure for the
planet pinions; and Fig 5 is a sectional view similar to Fig 4 and
showing a further modification of the planet pinion mounting
structure.
Referring to Fig 1, a differential cage 11 is rotatably supported on
stationary walls 12 and 13 through supporting tubes 14 and 16 and
tapered roller bearings 17 and 18 A bevel ring gear 19 is secured to a
circular flange 21 formed on cage 11 by a plurality of cap screws 22
which are threaded into drilled and tapped holes in flange 21 The ring
gear 19 is driven by a driving pinion 23 formed on the end of a power
shaft 24 connected to a power source, not shown.
The cage 11 has a pair of inusardly extending hub portions 26 and 27
which present inwardly facing and radially' extending thrust
transmitting surfaces 28 and 29, respectively Aligned bores 31 and 32
are formed in cage 11 and provide interior openings in hub portions 26
and 27, respectively A pair of bevel side gears 33 and 34 are
positioned within the interior of the cage 11 and have their hubs 36
and 37 connected in splined, driving relation, respectively, to a pair
of differential half shafts 38 and 39 The shafts 38 and 39 may be
connected to vehicle traction wheels, not shown The splined
connections between shafts 38 and 39 and their associated hubs 36 and
37 are axially loose so as to allow the shafts to be withdrawn from
the side gears 33 and 34 Shaft 38 is withdrawable to the 401 eft and
shaft 39 is withdrawable to the right as viewed in Fig 1 A cylindrical
surface 41 is formed on the portion 42 of hub 36 which extends into
bore 31 The cylindrical surface 41 is in radially confronting relation
to bore 31 and the diameter of portion 42 of hub 36 is slightly less
than the diameter of bore 31 so that there is clearance between
surface 41 and bore 31 allowing gear 33 to float in bore 31 A similar
relation exists between a cylindrical surface 43 formed on a portion
44 of hub 37 of side gear 34 and bore 32 of the cage 11.
A thrust washer 46 surrounds hub portion 42 and is interposed between
surface 28 of cage 11 and back side of bevel gear 33 Thus the axially
outward thrust of gear 3-3 is transmitted to hub 26 of cage 11 through
thrust washer 46.
Similarly, a thrust washer 47 surrounds hub portion 44 and is
interposed between the back side of bevel gear 34 and surface 29 of
cage huh 27.
When the side gears 33 and 34 are in 65their installed condition
26. within the cage structure 11 as shown in Fig 1, the distance between
the axially innermost portions of their hubs 36 and 37 is greater than
the distance which either hub portion 42 or 43 extends axially into 70
bores 31 and 32 respectively.
Referring to Figs 1, 2 and:3, three cylindrical surfaces define three
peripheral apertures 51 which communicate with the interior of cage 11
These apertures are 75 equally spaced circumferentially about the axis
52 of the side gears:33 and 34 this axis 52 also being the axis of
shafts:3,8 and 39 and the axis of rotation of cage 11.
A bevel planet pinion 53 is positioned 80 within each of the three
apertures 51 and these pinions 53 are in mesh with the two side gears
In Figs 1, 2 and:3, the planet pinions 53 each have a frusto-conical
head portion 54 secured, as by welding, to an 85 outward extending
stub portion 56 The frusto-conical head portions 54 each present a
conical surface 57 which tapers radially outward, that is toward an
apex at the outside of cage 11 As shown in go Fio' 3, the axes 38, 59
and 61 of pinions a radiate at right angles from axis 52 and like the
axes of the conical surfaces 57 are spaced 120 degrees apart so as to
coincide with the latter 95 Three annular retainers 62 are releasably
secured to cage 11 by cap screws 63 wrhihel are threaded into tapped
holes 64 in underlyinoa annular portions of the cage 11 As shown in
Fig 1, each retainer 100 62 has a circular flange 66 extending
radially relative to the axis of the associated aperture 51, the
retainer 62 having drilled holes 67 through which cap screws 63 extend
Each of the retainers 105 62 also has an inward extending collar 68
which has a cylindrical surface in thrust transmitting contact with
the surrounding cylindrical surface of the associated aperture 51 Each
of the 110 retainers 62 further has a conical surface 69 at its inner
periphery and the retainers 62 are secured to the eage 11 in such
positions that the conical retainer surfaces 69, like the conical head
surfaces 57 taper 115 radially outward, that is, toward the ontside of
cage 11 The annular retainers 62 surround the frusto-conical head
portions 54, respectively, and the relatively contacting conical
surfaces 57 and 69 are 120 complementary to each other Preferably, the
same taper is used for all three heads 54 and for all three retainers
62 all having the same common taper The three planet pinions 53 which
are disposed 125 within the three apertures 51 in the cage 11 are
adjusted for coaction with the side gears 3, and 34 so as to radially
center the latter relative to the axis of rotation of cage 11 The
retainers 62 may be 130 785,392 radially adjusted relative to the cage
11 by a variable number of shims 71 which are interposed between each
retainer 62 and the underlying annular portion of the 3 cage 11.
From the forgoing description it is apparent that a mounting structure
is provided for each planet pinion 53 which bridges the associated
27. aperture 51 in cage 11 Each of the planet pinion mounting structures
includes a retainer element 62 releasably secured to the cage 11, and
a bearing or head portion 54 formed on the respective pinion 53.
Referring to Fig 2, the cap screws 63, retainer 62 and pinion 53 of
Fig 1 have been removed to reveal the relative size of the peripheral
cage apertures 31 and the side gears 33, 34 It is seen that the side
gears and aperture 51 are so proportioned and arranged as to
accommodate movement of the side gears 33 and 34 into and out of the
cage 11 through the aperture 51 Although each of the apertures 51 is
large enough to permit the side gears to be moved therethrouogh, it is
evident that only one of the apertures need be so formed for the
purposes of this invention.
Before the side gears:33 and 34 can be removed from the interior of
the cage 11, the cap screw 63 attaching the retainers 62 to the cage
are unscrewed from cage 11 and the retainers and associated pinions
are withdrawn outwardly from the cage.
Also the half shafts 38, 39 are withdrawn from the hubs of the bevel
gears 33 and 34 The dash dotted lines 72 in Fig 2 indicate, for
instance, the position to which shaft 39 may be withdrawn preparatory
to removal of side gear 34 from the cage 11 Before removing side gear
34 the shaft 38 must be withdrawn axially to the left in Figs 1 and 2
After the shafts have been properly withdrawn the gear 34 may be moved
axially inwardly to the position shown by dash dotted lines 73, and
thence the side gear 34 may be removed outwardly through the exposed
aperture 51 in the cage 11 Side gear 33 may be removed from cage 11 in
a like manner.
Referring to Fig 1, the conical surfaces 57 and 69 co-operate to
frictionally resist rotation of the planet pinions 53 and thus resist
differential rotation of the shafts 38 and 39 The radial outward
thrust transmitted in the direction of axis 58 from the side gears 33,
34 to the planet pinions 53 causes a wedging action to occur between
the co-operating conical surfaces 57 and 69, thereby producing the
desired friction to resist rotation of the planet pinions
Differentials ineorporating this invention may be used in motor
vehicles in which it is desirable to have differential action when the
vehicle is in nonlinear travel, however, unobstructed differential
action is not desired where slippage of one of the traction wheels
occurs The frictional resistant to 70 differentiation afforded by the
wedg-,ing, action between the conical surfaces is not so great as to
prevent differential action when the vehicle is steered in a nonlinear
course, yet it is great enough to propor 75 tion the torque between
the half shafts 3)9.
39 so as to insure driving power to the wheel having good traction
when the other driving wheel has little or no traction due to slippery
28. ground conditions, for instance 80 Fig 4 shows an alternative planet
pinion mounting structure for rotatabljournaling the planet pinions on
the eage 11 The planet member 76 shown in Fig.
4 corresponds to the planet pinion 53 in 85 Fig 1, and the means for
mounting planet member 76 includes a disk like head.
portion 77 of the pinion and an annular retainer or bearing member 78
The head portion 77 includes a disk 77 ' and a 90 removable ring 79
which is secured to the disk 77 ' by cap screws 81 extending through
drilled holes 82 in ring 79 and threaded into drilled and tapped holes
83 in disk 77 ' A pair of relatively converg 95 ing conical surfaces
84 and 86 are formed on the disk head 77 on an axis 87 coineident with
the axis on which the bevel teeth of pinion 76 are formed A pair of
coaxial and relatively converging conical surfaces 100 88 and 89 are
formed on retainer 78 in complementary thrust transmitting relation to
conical surfaces 84 and 86.
respectively The conical surfaces 84 and 86 are formed to converge
relative to one 105 another in a radially inward direction relative to
their common axis The removable ring 79 permits the pinion 76 together
with the disk 77 ' to be separated from the retainer 78 The double
conical 110 surface arrangement stablizes the pinion so-that its axis
87 will not deviate from a right angle relationship with the axis of
side gears 33 and 34.
A plurality of shims 90 are interposed 115 between ring 79 and disk 77
' and when the conical surfaces 84, 86, 88 and 89 become worn through
luse one or more ol the shims 90 may be removed to compensate for the
wear Thus the ring 79 is 120 adjustably secured to the pinion member
76 so as to permit the establishment and maintainence of a close fit
between the co-operating conical surfaces 84, 86, 98 and 89 125 In Fig
5 a further alternative planet pinion mounting structure is shown in
which there is provided a two piece retainer or bearing member 93 for
a planet member 92 Ring portions 94 and 130 785,392 96 of retainer 93
bear upon each other in the direction of pinion axis 91 and have
relatively Converging conical surfaces 97 and 9 S, respectively, in
coaxial relation to axis 91 The relative convergence of conical
surface 97 formed on ring portion 94 and of conical surface 98 formed
on ring poirtion 96 is radially outward relative to axis 91 The head
portion 99 secured to planet pinion 92 has a pair of relatively
converging coaxial conical surfaces 101 and 102 formed thereon in
complementary relation to conical surfaces 97 and 98, respectively
Thus, the planet pinion 92 is stabilized against movement relative to
cage 11 except for rotation on axis 91 which is at right angles to the
axis of rotation of cage 11.
A plurality of shims 103 are interposed betveen ring portions 94 and
96 and by varying the number of shims the proper fit between the
29. co-operating conical bearing surfaces 97, 98, 101 and 102 man be
provided For instance, if the conical surfaces become -worn in use one
or more shims may be removed to compensate therefor.
The co-operating conical surfaces of the pinion mountings shown in
Figs 4 and 5 serve to proportion the torque to the differential half
shafts in a manner similar to that previously described in regard to
the pinion mounting shown in Fig 1.
It will be noted that each of the herein disclosed planetary
differentials has a pair of bevel side gears 33 and 34, bevel planet
pinions in mesh with the side gears, a cage structure 11 and separable
mounting means associated with the side gears, bevel pinions and cage
structure 11 for operatively positioning the side gears and planet
pinions within the cage structure, these mounting means including a
head portion non-rotatably connected with one of the planet pinions,
and a retainer rotatably and releasably securing the head portion
within a peripheral aperture of the cage structure 11 In each of the
illustrated embodiments of the invention the side gears 33 and 34 and
a peripheral cage apertures are so proportioned and arranged as to
accommodate movement of the side gears 33 and 34 into and out of the
cage structure 11 through said aperture, the latter being bridged by
the planet pinion mounting structure.
The provision of a peripheral aperture ill the cage structure large
enough to pass side gears 33 and 34 therethrough permits <o the cage
11 to be formed in one piece as )v casting The use of three planet
pinions is desirable to balance the loads on the bevel teeth of the
side gears 33 and 34 and planet pinions; also the use of three planet
pinions is desirable to floatingly position the side oears 2, and 34
radially in relation to the axis of rotation of the cage 11.
The differentials hereinbefore described permit the bevel pinions side
gears and 70 thrust washers to be remox ed for repair or replacement
without removing the cage from its support and this feature results in
a saving of time and labour cost.
Also, by providing shimis 71 between the 75 retainers and cage
structure 11, it is possible to adjust the position of the pinions so
that they centre the side gears radiallv relative to the axis of
rotation of the cage By providing radial clearance 80 between the side
gear hub portions 42 and 44 and cage bores 31 and 32 respectivelv, the
loads on the teeth of the side gears and pinions will be substantially
balanced Further, the radial thrust from 85 the side gears to the
pinions will be equally distributed to the three pinions and this is
particularly desirable in torque proportioning differentials of the
type herein disclosed, in that the frictional resistances 90 afforded
by the three pinion mounting structures are permitted to be simul
taneously effective.
30. * Sitemap
* Accessibility
* Legal notice
* Terms of use
* Last updated: 08.04.2015
* Worldwide Database
* 5.8.23.4; 93p