Grade of powder.ppt
•Download as PPT, PDF•
0 likes•138 views
This document discusses the grading and size separation of powders. It separates powders into categories based on mesh size, from coarse to very fine, and explains that size separation is important for uniform dosage formulation, preparing granules of a required size, and removing undesirable particles. The objectives are to define powder grades and classify methods of size separation.
Report
Share
Report
Share
Recommended
Good Warehousing Practice.pptx-1.pdf
This document discusses good warehousing practices, including warehouse layout and design, safety and security measures, quality control and inspection, and environmental considerations. Proper inventory management, efficient warehouse layout, safety protocols, quality checks, and sustainability efforts are important for maintaining product quality, delivering goods efficiently, and reducing costs and environmental impact. Implementing good warehousing practices provides benefits like increased productivity, profitability, reputation, and customer satisfaction.
Complaints.pptx
1. The document outlines the standard operating procedure (SOP) for handling product complaints at a pharmaceutical company. It describes the process for receiving, investigating, taking corrective actions for complaints, and generating monthly reports.
2. Key aspects of the SOP include categorizing complaints, timelines for investigation, using a product complaint data sheet to document details, conducting documentation-based and laboratory investigations, and providing feedback and corrective actions to customers.
3. Monthly reports analyze complaint trends to assess quantities and types of complaints received. This allows the company to improve product quality and maintain good customer relationships.
ICH introduction.pptx
The International Conference on Harmonization (ICH) aims to harmonize technical requirements for pharmaceutical registration across regions to increase consistency, make more efficient use of resources, and help develop and make more medicines available while maintaining quality and efficacy. ICH seeks to standardize guidelines and requirements for drug registration to reduce costs and better meet public health needs. Its objectives include achieving greater consistency in technical guidelines, more economical use of human and material resources, and facilitating more drug development and availability with safeguards for quality and effectiveness.
Training.pptx
Training is essential for personnel at a pharma company. The manufacturer must provide training for all employees who work in production or quality control to ensure they can properly operate equipment and perform duties that affect product quality. Maintaining training records for every employee can improve quality performance by helping to ensure personnel have the necessary skills.
Responsibilities In Pharma Company
The document outlines the responsibilities of individuals in a pharma company's quality control and production departments. The head of quality control is responsible for approving or rejecting materials and finished products, validating analytical procedures and equipment calibration. The head of production is responsible for maintaining appropriate documentation to improve production instructions, and ensuring proper maintenance of departments, premises, and equipment.
Hygiene In Pharma Company
Personal hygiene is extremely important for those working in a pharmaceutical company. Workers must be healthy and have good hygiene habits like proper hand sanitization. They should avoid eating, drinking, smoking or storing food in the manufacturing unit. Anyone infected should not be permitted in the unit to prevent the spread of infection.
Elements and objectives of QBD.pptx
The document discusses the elements, objectives, benefits, and advantages of Quality by Design (QBD). QBD aims to ensure robust manufacturing processes, demonstrate understanding to regulators, and encourage sufficient product understanding. Benefits include reduced validation costs, improved product design, fewer manufacturing problems, enabling continuous improvement, and lower costs. The objectives are to have robust processes, demonstrate enhanced understanding to agencies, and develop sufficient product knowledge.
QBD.pptx
Quality by Design (QBD) is a systematic approach to pharmaceutical development that begins with predefined objectives and emphasizes product and process understanding and control based on sound science and quality risk management. It provides benefits like less validation burden, better product design, fewer manufacturing problems, enabling continuous improvement, and lower costs. The key elements of QBD include its definition, benefits, and components like defining objectives, understanding variability, and setting in-process controls.
Recommended
Good Warehousing Practice.pptx-1.pdf
This document discusses good warehousing practices, including warehouse layout and design, safety and security measures, quality control and inspection, and environmental considerations. Proper inventory management, efficient warehouse layout, safety protocols, quality checks, and sustainability efforts are important for maintaining product quality, delivering goods efficiently, and reducing costs and environmental impact. Implementing good warehousing practices provides benefits like increased productivity, profitability, reputation, and customer satisfaction.
Complaints.pptx
1. The document outlines the standard operating procedure (SOP) for handling product complaints at a pharmaceutical company. It describes the process for receiving, investigating, taking corrective actions for complaints, and generating monthly reports.
2. Key aspects of the SOP include categorizing complaints, timelines for investigation, using a product complaint data sheet to document details, conducting documentation-based and laboratory investigations, and providing feedback and corrective actions to customers.
3. Monthly reports analyze complaint trends to assess quantities and types of complaints received. This allows the company to improve product quality and maintain good customer relationships.
ICH introduction.pptx
The International Conference on Harmonization (ICH) aims to harmonize technical requirements for pharmaceutical registration across regions to increase consistency, make more efficient use of resources, and help develop and make more medicines available while maintaining quality and efficacy. ICH seeks to standardize guidelines and requirements for drug registration to reduce costs and better meet public health needs. Its objectives include achieving greater consistency in technical guidelines, more economical use of human and material resources, and facilitating more drug development and availability with safeguards for quality and effectiveness.
Training.pptx
Training is essential for personnel at a pharma company. The manufacturer must provide training for all employees who work in production or quality control to ensure they can properly operate equipment and perform duties that affect product quality. Maintaining training records for every employee can improve quality performance by helping to ensure personnel have the necessary skills.
Responsibilities In Pharma Company
The document outlines the responsibilities of individuals in a pharma company's quality control and production departments. The head of quality control is responsible for approving or rejecting materials and finished products, validating analytical procedures and equipment calibration. The head of production is responsible for maintaining appropriate documentation to improve production instructions, and ensuring proper maintenance of departments, premises, and equipment.
Hygiene In Pharma Company
Personal hygiene is extremely important for those working in a pharmaceutical company. Workers must be healthy and have good hygiene habits like proper hand sanitization. They should avoid eating, drinking, smoking or storing food in the manufacturing unit. Anyone infected should not be permitted in the unit to prevent the spread of infection.
Elements and objectives of QBD.pptx
The document discusses the elements, objectives, benefits, and advantages of Quality by Design (QBD). QBD aims to ensure robust manufacturing processes, demonstrate understanding to regulators, and encourage sufficient product understanding. Benefits include reduced validation costs, improved product design, fewer manufacturing problems, enabling continuous improvement, and lower costs. The objectives are to have robust processes, demonstrate enhanced understanding to agencies, and develop sufficient product knowledge.
QBD.pptx
Quality by Design (QBD) is a systematic approach to pharmaceutical development that begins with predefined objectives and emphasizes product and process understanding and control based on sound science and quality risk management. It provides benefits like less validation burden, better product design, fewer manufacturing problems, enabling continuous improvement, and lower costs. The key elements of QBD include its definition, benefits, and components like defining objectives, understanding variability, and setting in-process controls.
Total quality management
Total quality management (TQM) is defined as an integrated organizational effort to improve quality at every level based on key principles: focusing on customers, continuous improvement, teamwork and mutual respect, and producing quality work the first time. TQM is characterized by process improvements, measuring processes, flexible production, and an open organization. Benefits of TQM include improved teamwork, quality, productivity, and profitability. Seven gurus contributed to the development of TQM, including Deming who proposed the PDCA cycle and Juran who developed the concept of quality trilogy.
TQM Benefits and Gurus.pptx
Total quality management (TQM) aims to improve quality at all levels through an integrated organizational effort. The main TQM principles are focusing on customers, continuous improvement, teamwork, and producing quality work. TQM is characterized by process improvements, measuring processes, flexible production, and an open organization. Benefits of TQM include improved teamwork, quality, productivity, and profitability. The seven gurus of TQM who developed key concepts include Walter Shewhart, W. Edwards Deming, Joseph Juran, Armand Feigenbaum, Philip Crosby, Genichi Taguchi, and Kaoru Ishikawa.
TQM Advantages & disadvantages.pptx
Total quality management (TQM) aims to improve quality at all levels through an integrated organizational effort focused on customer satisfaction. Key elements of TQM include focusing on the customer, employee involvement, and continuous improvement. Some advantages of TQM are improved quality, employee participation, teamwork, and better working relationships, while disadvantages can include initial introduction costs and worker resistance to change. TQM is important in the pharmaceutical industry for ensuring quality in areas like handling, storage, packaging, facilities, equipment, and sterile areas.
ICH goals and process.pptx
The document discusses the goals and process of the International Conference on Harmonization (ICH). The ICH aims to harmonize technical requirements for pharmaceutical registration across regions to increase efficiency and access to new medicines while maintaining quality and safety. The ICH process involves developing guidelines through formal procedures, answering questions, revising existing guidelines, and maintaining established standards.
Introduction to ICH.pptx
The document introduces the International Conference on Harmonization (ICH), which aims to harmonize technical requirements for pharmaceutical registration across regions to increase consistency, make more efficient use of resources, and help develop new medicines while maintaining safety and effectiveness. ICH seeks to standardize guidelines and registration processes for drugs to reduce costs and better meet public health needs.
Mixing.pptx
The document discusses mixing in the context of pharmaceutical production. It outlines that the main objective of mixing is to produce a bulk mixture that, when divided into doses, ensures each dose contains the correct proportions. It notes mixing is a critical intermediate step for tablets and capsules. The document also lists factors that affect mixing and different mechanisms for solid, liquid, and semisolid mixing. Specifically, it explains solid mixing involves convective, shear, and diffusive mechanisms while liquid mixing uses bulk transport, turbulent flow, laminar flow, and molecular diffusion.
Freeze dryer.pptx
Freeze drying, or lyophilisation, is a process that converts solutions or suspensions into solids for storage and distribution. It works by sublimating a material, changing it directly from a solid to a gas, below the triple point. Key components of a freeze dryer include a drying chamber, heating elements, a vapor condensing system, and a vacuum pump. Freeze drying has advantages like preserving heat-sensitive materials and proteins without denaturation. However, it is an expensive and slow process limited to specific valuable products.
Vacuum dryer
The document describes a vacuum dryer used to dry heat sensitive and hygroscopic materials. It works by reducing chamber pressure below water vapor pressure through a vacuum pump, allowing water to boil and evaporate faster. Trays inside the hollow oven increase surface area for heat conduction. Materials are dried at 25-30°C as water vapor is evaporated under vacuum and condenses before being collected.
FLUIDIZED BED DRYER
The document summarizes a fluidized bed dryer. It works by fluidizing wet solid particles using hot air forced through a perforated bed from the bottom. The dryer is made of stainless steel or plastic with a detachable bowl for charging and discharging materials. Hot air is circulated through the bed to dry particles completely before exiting through bag filters. It allows for continuous, rapid drying at a constant rate with high efficiency and capacity compared to other dryers. Pharmaceutical uses include drying granules for tablet production and granule coating.
SPRAY DRYER
Spray drying is an industrial process that transforms a liquid feed containing dissolved or dispersed solids into a spray of small droplets that are exposed to hot air to be dried. It allows for effective control of product quality and properties during continuous high-tonnage production. While spray dryers are bulky and expensive, they permit thermolabile pharmaceuticals to be dried at low temperature and are used to dry products like penicillin, enzymes, and vaccines.
Drum Dryer
The document describes a drum dryer, which consists of one or two horizontally mounted hollow cylinders or drums that are heated internally by steam and rotated. Liquid or slurry is spread as a film onto the heated, rotating drum surface where it dries rapidly via conduction and steam heating. The dried material is then scraped off and collected while the drum continues rotating. Drum drying allows for rapid drying of thermosensitive materials in a compact system, though it requires careful control of processing parameters and has high maintenance costs.
tray drayer.pptx
The tray dryer uses forced hot air convection to remove moisture from solids placed on stainless steel trays. It has double-walled insulation and doors with gaskets. Hot air is blown through the chamber at 2-5 meters per second to evaporate water from the surface of the solids on each tray, which are loaded and unloaded batch-wise. Tray dryers are efficient, require little labor, and are available with capacities from 6 to 192 trays.
Mechanism f drying
The document discusses the mechanisms and principles of drying, including that drying involves the removal of moisture through evaporation and transport using heat, and describes key terms used in drying systems like bound water, free moisture content, equilibrium moisture content, and critical moisture content. It also provides a classification of different types of dryers based on their mode of operation and heating method.
Drying.pptx
Drying involves the removal of water or other solvents from solids, semi-solids, or liquids through the application of heat to produce a liquid-free solid product. The main objectives of drying are to preserve foods by reducing water content and activity to increase shelf life without refrigeration, reduce storage and transport costs, and improve stability of pharmaceutical products by removing moisture. Drying techniques include thermal methods using heat as well as non-thermal methods like squeezing, adsorption, or extraction. Water is the solvent most commonly removed through drying of bioproducts like foods and pharmaceuticals like vaccines.
DRYING.pptx
This document discusses drying and its objectives and applications in pharmaceutical technology. It begins by defining drying as the removal of water or other solvents from a solid, semi-solid, or liquid material through the application of heat. The main objectives of drying are to preserve foods and drugs by reducing water content and avoiding the need for refrigeration during storage and transport. In pharmaceuticals specifically, drying is used to avoid moisture that can degrade drugs, improve material properties, reduce volume for transportation and handling, and serve as the final step in various processes like evaporation and crystallization. The document provides examples of how drying is used in preparing bulk drugs and preserving drug products and materials.
Heat transfer Mechanism.pptx
Heat transfer is a form of energy associated with the motion of atoms or molecules that is transferred from higher temperature objects to lower temperature objects. Precise temperature control through heat transfer is important for pharmaceutical manufacturing processes like purification where applying heat causes crystallization. Various industries like oil and gas processing utilize heat transfer mechanisms like conduction, convection, and radiation using heat transfer fluids to control temperatures in heating and cooling phases. Heat transfer can be classified based on the process of heat flowing from higher to lower temperature objects through conduction, convection, or radiation.
evaporation.pptx
Evaporation is the process by which a liquid is vaporized from a solution, leaving behind a more concentrated residue. It is commonly used to prepare liquid, soft, and dry extracts from solutions by removing the solvent through heating. Evaporation is also employed to concentrate blood plasma, serum, enzymes, hormones, antibiotics, and other agents. The rate of evaporation is influenced by factors like temperature, time, moisture content, the type of desired product, and concentration of the solution.
VACCUM DISTILLATION.pptx
Vacuum distillation is a distillation technique where the pressure above the liquid mixture is reduced below the vapor pressure of the mixture. This allows distillation to occur at lower temperatures than normal distillation, making it suitable for heat-sensitive materials. Vacuum distillation works by causing boiling when the vapor pressure exceeds the reduced ambient pressure. The document provides an introduction to distillation and vacuum distillation, explaining that distillation separates mixtures based on differences in boiling points under reduced pressure.
STEAM DISTILLATION.pptx
Steam distillation is a process that uses steam to separate high boiling substances from non-volatile impurities. It works by introducing steam into a mixture, which causes volatile components to evaporate more readily than they otherwise would. This allows for the separation of volatile oils and other compounds from immiscible liquids and water. Steam distillation is useful for extracting volatile oils from plants like clove and eucalyptus because it can separate these oils at lower temperatures than simple distillation, avoiding potential degradation of heat-sensitive compounds.
Simple distillation.pptx
Distillation is a process that separates mixtures into their component parts based on differences in boiling points. Simple distillation involves a single stage of vaporization and condensation to separate components with large boiling point differences of 25-35°C, such as separating volatile liquids from nonvolatile liquids. It is used to purify seawater but only provides an impure product. The document discusses the basic principles and six types of distillation processes including simple, flash, fractional, reduced pressure, steam, and molecular distillation.
Butterfly Valves Manufacturer (LBF Series).pdf
We have designed & manufacture the Lubi Valves LBF series type of Butterfly Valves for General Utility Water applications as well as for HVAC applications.
Impartiality as per ISO /IEC 17025:2017 Standard
This document provides basic guidelines for imparitallity requirement of ISO 17025. It defines in detial how it is met and wiudhwdih jdhsjdhwudjwkdbjwkdddddddddddkkkkkkkkkkkkkkkkkkkkkkkwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwioiiiiiiiiiiiii uwwwwwwwwwwwwwwwwhe wiqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq gbbbbbbbbbbbbb owdjjjjjjjjjjjjjjjjjjjj widhi owqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq uwdhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhwqiiiiiiiiiiiiiiiiiiiiiiiiiiiiw0pooooojjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjj whhhhhhhhhhh wheeeeeeee wihieiiiiii wihe
e qqqqqqqqqqeuwiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiqw dddddddddd cccccccccccccccv s w c r
cdf cb bicbsad ishd d qwkbdwiur e wetwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwww w
dddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddfffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffw
uuuuhhhhhhhhhhhhhhhhhhhhhhhhe qiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiii iqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq eeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee qqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqccccccccccccccccccccccccccccccccccccccccccccccccccccccccccccc ccccccccccccccccccccccccccccccccccc bbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbu uuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuum
m
m mmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmm m i
g i dijsd sjdnsjd ndjajsdnnsa adjdnawddddddddddddd uw
More Related Content
More from KashishWilson1
Total quality management
Total quality management (TQM) is defined as an integrated organizational effort to improve quality at every level based on key principles: focusing on customers, continuous improvement, teamwork and mutual respect, and producing quality work the first time. TQM is characterized by process improvements, measuring processes, flexible production, and an open organization. Benefits of TQM include improved teamwork, quality, productivity, and profitability. Seven gurus contributed to the development of TQM, including Deming who proposed the PDCA cycle and Juran who developed the concept of quality trilogy.
TQM Benefits and Gurus.pptx
Total quality management (TQM) aims to improve quality at all levels through an integrated organizational effort. The main TQM principles are focusing on customers, continuous improvement, teamwork, and producing quality work. TQM is characterized by process improvements, measuring processes, flexible production, and an open organization. Benefits of TQM include improved teamwork, quality, productivity, and profitability. The seven gurus of TQM who developed key concepts include Walter Shewhart, W. Edwards Deming, Joseph Juran, Armand Feigenbaum, Philip Crosby, Genichi Taguchi, and Kaoru Ishikawa.
TQM Advantages & disadvantages.pptx
Total quality management (TQM) aims to improve quality at all levels through an integrated organizational effort focused on customer satisfaction. Key elements of TQM include focusing on the customer, employee involvement, and continuous improvement. Some advantages of TQM are improved quality, employee participation, teamwork, and better working relationships, while disadvantages can include initial introduction costs and worker resistance to change. TQM is important in the pharmaceutical industry for ensuring quality in areas like handling, storage, packaging, facilities, equipment, and sterile areas.
ICH goals and process.pptx
The document discusses the goals and process of the International Conference on Harmonization (ICH). The ICH aims to harmonize technical requirements for pharmaceutical registration across regions to increase efficiency and access to new medicines while maintaining quality and safety. The ICH process involves developing guidelines through formal procedures, answering questions, revising existing guidelines, and maintaining established standards.
Introduction to ICH.pptx
The document introduces the International Conference on Harmonization (ICH), which aims to harmonize technical requirements for pharmaceutical registration across regions to increase consistency, make more efficient use of resources, and help develop new medicines while maintaining safety and effectiveness. ICH seeks to standardize guidelines and registration processes for drugs to reduce costs and better meet public health needs.
Mixing.pptx
The document discusses mixing in the context of pharmaceutical production. It outlines that the main objective of mixing is to produce a bulk mixture that, when divided into doses, ensures each dose contains the correct proportions. It notes mixing is a critical intermediate step for tablets and capsules. The document also lists factors that affect mixing and different mechanisms for solid, liquid, and semisolid mixing. Specifically, it explains solid mixing involves convective, shear, and diffusive mechanisms while liquid mixing uses bulk transport, turbulent flow, laminar flow, and molecular diffusion.
Freeze dryer.pptx
Freeze drying, or lyophilisation, is a process that converts solutions or suspensions into solids for storage and distribution. It works by sublimating a material, changing it directly from a solid to a gas, below the triple point. Key components of a freeze dryer include a drying chamber, heating elements, a vapor condensing system, and a vacuum pump. Freeze drying has advantages like preserving heat-sensitive materials and proteins without denaturation. However, it is an expensive and slow process limited to specific valuable products.
Vacuum dryer
The document describes a vacuum dryer used to dry heat sensitive and hygroscopic materials. It works by reducing chamber pressure below water vapor pressure through a vacuum pump, allowing water to boil and evaporate faster. Trays inside the hollow oven increase surface area for heat conduction. Materials are dried at 25-30°C as water vapor is evaporated under vacuum and condenses before being collected.
FLUIDIZED BED DRYER
The document summarizes a fluidized bed dryer. It works by fluidizing wet solid particles using hot air forced through a perforated bed from the bottom. The dryer is made of stainless steel or plastic with a detachable bowl for charging and discharging materials. Hot air is circulated through the bed to dry particles completely before exiting through bag filters. It allows for continuous, rapid drying at a constant rate with high efficiency and capacity compared to other dryers. Pharmaceutical uses include drying granules for tablet production and granule coating.
SPRAY DRYER
Spray drying is an industrial process that transforms a liquid feed containing dissolved or dispersed solids into a spray of small droplets that are exposed to hot air to be dried. It allows for effective control of product quality and properties during continuous high-tonnage production. While spray dryers are bulky and expensive, they permit thermolabile pharmaceuticals to be dried at low temperature and are used to dry products like penicillin, enzymes, and vaccines.
Drum Dryer
The document describes a drum dryer, which consists of one or two horizontally mounted hollow cylinders or drums that are heated internally by steam and rotated. Liquid or slurry is spread as a film onto the heated, rotating drum surface where it dries rapidly via conduction and steam heating. The dried material is then scraped off and collected while the drum continues rotating. Drum drying allows for rapid drying of thermosensitive materials in a compact system, though it requires careful control of processing parameters and has high maintenance costs.
tray drayer.pptx
The tray dryer uses forced hot air convection to remove moisture from solids placed on stainless steel trays. It has double-walled insulation and doors with gaskets. Hot air is blown through the chamber at 2-5 meters per second to evaporate water from the surface of the solids on each tray, which are loaded and unloaded batch-wise. Tray dryers are efficient, require little labor, and are available with capacities from 6 to 192 trays.
Mechanism f drying
The document discusses the mechanisms and principles of drying, including that drying involves the removal of moisture through evaporation and transport using heat, and describes key terms used in drying systems like bound water, free moisture content, equilibrium moisture content, and critical moisture content. It also provides a classification of different types of dryers based on their mode of operation and heating method.
Drying.pptx
Drying involves the removal of water or other solvents from solids, semi-solids, or liquids through the application of heat to produce a liquid-free solid product. The main objectives of drying are to preserve foods by reducing water content and activity to increase shelf life without refrigeration, reduce storage and transport costs, and improve stability of pharmaceutical products by removing moisture. Drying techniques include thermal methods using heat as well as non-thermal methods like squeezing, adsorption, or extraction. Water is the solvent most commonly removed through drying of bioproducts like foods and pharmaceuticals like vaccines.
DRYING.pptx
This document discusses drying and its objectives and applications in pharmaceutical technology. It begins by defining drying as the removal of water or other solvents from a solid, semi-solid, or liquid material through the application of heat. The main objectives of drying are to preserve foods and drugs by reducing water content and avoiding the need for refrigeration during storage and transport. In pharmaceuticals specifically, drying is used to avoid moisture that can degrade drugs, improve material properties, reduce volume for transportation and handling, and serve as the final step in various processes like evaporation and crystallization. The document provides examples of how drying is used in preparing bulk drugs and preserving drug products and materials.
Heat transfer Mechanism.pptx
Heat transfer is a form of energy associated with the motion of atoms or molecules that is transferred from higher temperature objects to lower temperature objects. Precise temperature control through heat transfer is important for pharmaceutical manufacturing processes like purification where applying heat causes crystallization. Various industries like oil and gas processing utilize heat transfer mechanisms like conduction, convection, and radiation using heat transfer fluids to control temperatures in heating and cooling phases. Heat transfer can be classified based on the process of heat flowing from higher to lower temperature objects through conduction, convection, or radiation.
evaporation.pptx
Evaporation is the process by which a liquid is vaporized from a solution, leaving behind a more concentrated residue. It is commonly used to prepare liquid, soft, and dry extracts from solutions by removing the solvent through heating. Evaporation is also employed to concentrate blood plasma, serum, enzymes, hormones, antibiotics, and other agents. The rate of evaporation is influenced by factors like temperature, time, moisture content, the type of desired product, and concentration of the solution.
VACCUM DISTILLATION.pptx
Vacuum distillation is a distillation technique where the pressure above the liquid mixture is reduced below the vapor pressure of the mixture. This allows distillation to occur at lower temperatures than normal distillation, making it suitable for heat-sensitive materials. Vacuum distillation works by causing boiling when the vapor pressure exceeds the reduced ambient pressure. The document provides an introduction to distillation and vacuum distillation, explaining that distillation separates mixtures based on differences in boiling points under reduced pressure.
STEAM DISTILLATION.pptx
Steam distillation is a process that uses steam to separate high boiling substances from non-volatile impurities. It works by introducing steam into a mixture, which causes volatile components to evaporate more readily than they otherwise would. This allows for the separation of volatile oils and other compounds from immiscible liquids and water. Steam distillation is useful for extracting volatile oils from plants like clove and eucalyptus because it can separate these oils at lower temperatures than simple distillation, avoiding potential degradation of heat-sensitive compounds.
Simple distillation.pptx
Distillation is a process that separates mixtures into their component parts based on differences in boiling points. Simple distillation involves a single stage of vaporization and condensation to separate components with large boiling point differences of 25-35°C, such as separating volatile liquids from nonvolatile liquids. It is used to purify seawater but only provides an impure product. The document discusses the basic principles and six types of distillation processes including simple, flash, fractional, reduced pressure, steam, and molecular distillation.
More from KashishWilson1 (20)
Recently uploaded
Butterfly Valves Manufacturer (LBF Series).pdf
We have designed & manufacture the Lubi Valves LBF series type of Butterfly Valves for General Utility Water applications as well as for HVAC applications.
Impartiality as per ISO /IEC 17025:2017 Standard
This document provides basic guidelines for imparitallity requirement of ISO 17025. It defines in detial how it is met and wiudhwdih jdhsjdhwudjwkdbjwkdddddddddddkkkkkkkkkkkkkkkkkkkkkkkwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwioiiiiiiiiiiiii uwwwwwwwwwwwwwwwwhe wiqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq gbbbbbbbbbbbbb owdjjjjjjjjjjjjjjjjjjjj widhi owqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq uwdhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhwqiiiiiiiiiiiiiiiiiiiiiiiiiiiiw0pooooojjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjjj whhhhhhhhhhh wheeeeeeee wihieiiiiii wihe
e qqqqqqqqqqeuwiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiqw dddddddddd cccccccccccccccv s w c r
cdf cb bicbsad ishd d qwkbdwiur e wetwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwwww w
dddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddddfffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffffw
uuuuhhhhhhhhhhhhhhhhhhhhhhhhe qiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiii iqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq eeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee qqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqccccccccccccccccccccccccccccccccccccccccccccccccccccccccccccc ccccccccccccccccccccccccccccccccccc bbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbu uuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuum
m
m mmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmm m i
g i dijsd sjdnsjd ndjajsdnnsa adjdnawddddddddddddd uw
Digital Twins Computer Networking Paper Presentation.pptx
A Digital Twin in computer networking is a virtual representation of a physical network, used to simulate, analyze, and optimize network performance and reliability. It leverages real-time data to enhance network management, predict issues, and improve decision-making processes.
A high-Speed Communication System is based on the Design of a Bi-NoC Router, ...
The Network on Chip (NoC) has emerged as an effective
solution for intercommunication infrastructure within System on
Chip (SoC) designs, overcoming the limitations of traditional
methods that face significant bottlenecks. However, the complexity
of NoC design presents numerous challenges related to
performance metrics such as scalability, latency, power
consumption, and signal integrity. This project addresses the
issues within the router's memory unit and proposes an enhanced
memory structure. To achieve efficient data transfer, FIFO buffers
are implemented in distributed RAM and virtual channels for
FPGA-based NoC. The project introduces advanced FIFO-based
memory units within the NoC router, assessing their performance
in a Bi-directional NoC (Bi-NoC) configuration. The primary
objective is to reduce the router's workload while enhancing the
FIFO internal structure. To further improve data transfer speed,
a Bi-NoC with a self-configurable intercommunication channel is
suggested. Simulation and synthesis results demonstrate
guaranteed throughput, predictable latency, and equitable
network access, showing significant improvement over previous
designs
AI + Data Community Tour - Build the Next Generation of Apps with the Einstei...
AI + Data Community Tour - Build the Next Generation of Apps with the Einstei...Paris Salesforce Developer Group
Build the Next Generation of Apps with the Einstein 1 Platform.
Rejoignez Philippe Ozil pour une session de workshops qui vous guidera à travers les détails de la plateforme Einstein 1, l'importance des données pour la création d'applications d'intelligence artificielle et les différents outils et technologies que Salesforce propose pour vous apporter tous les bénéfices de l'IA.FUNDAMENTALS OF MECHANICAL ENGINEERING.pdf
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
EMERSON EDUARDO RODRIGUES
3rd International Conference on Artificial Intelligence Advances (AIAD 2024)
3rd International Conference on Artificial Intelligence Advances (AIAD 2024) will act as a major forum for the presentation of innovative ideas, approaches, developments, and research projects in the area advanced Artificial Intelligence. It will also serve to facilitate the exchange of information between researchers and industry professionals to discuss the latest issues and advancement in the research area. Core areas of AI and advanced multi-disciplinary and its applications will be covered during the conferences.
Tools & Techniques for Commissioning and Maintaining PV Systems W-Animations ...
Join us for this solutions-based webinar on the tools and techniques for commissioning and maintaining PV Systems. In this session, we'll review the process of building and maintaining a solar array, starting with installation and commissioning, then reviewing operations and maintenance of the system. This course will review insulation resistance testing, I-V curve testing, earth-bond continuity, ground resistance testing, performance tests, visual inspections, ground and arc fault testing procedures, and power quality analysis.
Fluke Solar Application Specialist Will White is presenting on this engaging topic:
Will has worked in the renewable energy industry since 2005, first as an installer for a small east coast solar integrator before adding sales, design, and project management to his skillset. In 2022, Will joined Fluke as a solar application specialist, where he supports their renewable energy testing equipment like IV-curve tracers, electrical meters, and thermal imaging cameras. Experienced in wind power, solar thermal, energy storage, and all scales of PV, Will has primarily focused on residential and small commercial systems. He is passionate about implementing high-quality, code-compliant installation techniques.
DESIGN AND MANUFACTURE OF CEILING BOARD USING SAWDUST AND WASTE CARTON MATERI...
The need for ecofriendly materials as building materials in this century cannot be overemphasized
一比一原版(爱大毕业证书)爱荷华大学毕业证如何办理
原版一模一样【微信：741003700 】【(爱大毕业证书)爱荷华大学毕业证成绩单】【微信：741003700 】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问Q/微741003700
【主营项目】
一.毕业证【q微741003700】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【q/微741003700】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
办理(爱大毕业证书)爱荷华大学毕业证【微信：741003700 】外观非常简单，由纸质材料制成，上面印有校徽、校名、毕业生姓名、专业等信息。
办理(爱大毕业证书)爱荷华大学毕业证【微信：741003700 】格式相对统一，各专业都有相应的模板。通常包括以下部分：
校徽：象征着学校的荣誉和传承。
校名:学校英文全称
授予学位：本部分将注明获得的具体学位名称。
毕业生姓名：这是最重要的信息之一，标志着该证书是由特定人员获得的。
颁发日期：这是毕业正式生效的时间，也代表着毕业生学业的结束。
其他信息：根据不同的专业和学位，可能会有一些特定的信息或章节。
办理(爱大毕业证书)爱荷华大学毕业证【微信：741003700 】价值很高，需要妥善保管。一般来说，应放置在安全、干燥、防潮的地方，避免长时间暴露在阳光下。如需使用，最好使用复印件而不是原件，以免丢失。
综上所述，办理(爱大毕业证书)爱荷华大学毕业证【微信：741003700 】是证明身份和学历的高价值文件。外观简单庄重，格式统一，包括重要的个人信息和发布日期。对持有人来说，妥善保管是非常重要的。
Open Channel Flow: fluid flow with a free surface
Open Channel Flow: This topic focuses on fluid flow with a free surface, such as in rivers, canals, and drainage ditches. Key concepts include the classification of flow types (steady vs. unsteady, uniform vs. non-uniform), hydraulic radius, flow resistance, Manning's equation, critical flow conditions, and energy and momentum principles. It also covers flow measurement techniques, gradually varied flow analysis, and the design of open channels. Understanding these principles is vital for effective water resource management and engineering applications.
Determination of Equivalent Circuit parameters and performance characteristic...
Includes the testing of induction motor to draw the circle diagram of induction motor with step wise procedure and calculation for the same. Also explains the working and application of Induction generator
一比一原版(uoft毕业证书)加拿大多伦多大学毕业证如何办理
原版一模一样【微信：741003700 】【(uoft毕业证书)加拿大多伦多大学毕业证成绩单】【微信：741003700 】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问Q/微741003700
【主营项目】
一.毕业证【q微741003700】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【q/微741003700】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
办理(uoft毕业证书)加拿大多伦多大学毕业证【微信：741003700 】外观非常简单，由纸质材料制成，上面印有校徽、校名、毕业生姓名、专业等信息。
办理(uoft毕业证书)加拿大多伦多大学毕业证【微信：741003700 】格式相对统一，各专业都有相应的模板。通常包括以下部分：
校徽：象征着学校的荣誉和传承。
校名:学校英文全称
授予学位：本部分将注明获得的具体学位名称。
毕业生姓名：这是最重要的信息之一，标志着该证书是由特定人员获得的。
颁发日期：这是毕业正式生效的时间，也代表着毕业生学业的结束。
其他信息：根据不同的专业和学位，可能会有一些特定的信息或章节。
办理(uoft毕业证书)加拿大多伦多大学毕业证【微信：741003700 】价值很高，需要妥善保管。一般来说，应放置在安全、干燥、防潮的地方，避免长时间暴露在阳光下。如需使用，最好使用复印件而不是原件，以免丢失。
综上所述，办理(uoft毕业证书)加拿大多伦多大学毕业证【微信：741003700 】是证明身份和学历的高价值文件。外观简单庄重，格式统一，包括重要的个人信息和发布日期。对持有人来说，妥善保管是非常重要的。
ELS: 2.4.1 POWER ELECTRONICS Course objectives: This course will enable stude...
Introduction - Applications of Power Electronics, Power Semiconductor Devices, Control Characteristics of Power Devices, types of Power Electronic Circuits. Power Transistors: Power BJTs: Steady state characteristics. Power MOSFETs: device operation, switching characteristics, IGBTs: device operation, output and transfer characteristics.
Thyristors - Introduction, Principle of Operation of SCR, Static Anode- Cathode Characteristics of SCR, Two transistor model of SCR, Gate Characteristics of SCR, Turn-ON Methods, Turn-OFF Mechanism, Turn-OFF Methods: Natural and Forced Commutation – Class A and Class B types, Gate Trigger Circuit: Resistance Firing Circuit, Resistance capacitance firing circuit.
Beckhoff Programmable Logic Control Overview Presentation
This presentation is to describe the overview of PLC Beckhoff for beginners
Recently uploaded (20)
Digital Twins Computer Networking Paper Presentation.pptx
Digital Twins Computer Networking Paper Presentation.pptx
A high-Speed Communication System is based on the Design of a Bi-NoC Router, ...
A high-Speed Communication System is based on the Design of a Bi-NoC Router, ...
AI + Data Community Tour - Build the Next Generation of Apps with the Einstei...
AI + Data Community Tour - Build the Next Generation of Apps with the Einstei...
3rd International Conference on Artificial Intelligence Advances (AIAD 2024)
3rd International Conference on Artificial Intelligence Advances (AIAD 2024)
Tools & Techniques for Commissioning and Maintaining PV Systems W-Animations ...
Tools & Techniques for Commissioning and Maintaining PV Systems W-Animations ...
DESIGN AND MANUFACTURE OF CEILING BOARD USING SAWDUST AND WASTE CARTON MATERI...
DESIGN AND MANUFACTURE OF CEILING BOARD USING SAWDUST AND WASTE CARTON MATERI...
Determination of Equivalent Circuit parameters and performance characteristic...
Determination of Equivalent Circuit parameters and performance characteristic...
SENTIMENT ANALYSIS ON PPT AND Project template_.pptx
SENTIMENT ANALYSIS ON PPT AND Project template_.pptx
ELS: 2.4.1 POWER ELECTRONICS Course objectives: This course will enable stude...
ELS: 2.4.1 POWER ELECTRONICS Course objectives: This course will enable stude...
Beckhoff Programmable Logic Control Overview Presentation
Beckhoff Programmable Logic Control Overview Presentation
Grade of powder.ppt
- 1. KASHISH WILSON Grade of Powders and size seperation 1
- 2. 2 Size separation: • Separation of the particles according to their sizes Importance: • To formulate a uniform dosage form • To prepare granules of required size • To separate undesirable particles
- 3. 3 Objectives •Grades of powders • Classification of size separation
- 4. 4 Grading of powders Coarse powder : 10/44 Moderately coarse powder : 22/60 Moderately fine powder : 44/85 Fine powder : 85 Very fine powder : 120