Lanthanide and actinide chemistry, inorganic chemistry. inner transistion ser...RAHUL SINWER
This document discusses lanthanide and actinide chemistry. It begins by outlining the session objectives, which include an introduction to lanthanides and actinides, their oxidation states, lanthanide contraction, and a comparison of actinides and lanthanides. The document then discusses the electronic configuration, atomic and ionic sizes, ionization energies, magnetic properties, oxidation states, and chemical reactivity of lanthanides. It also covers the similar topics for actinides, and compares the similarities and differences between lanthanides and actinides.
This document discusses electronic spectroscopy of transition metal complexes. It begins by explaining the different types of electronic transitions that can occur, including transitions involving p, s, n, d and f electrons. It then discusses absorption spectroscopy of species containing p, s and n electrons, as well as n→π* and π→π* transitions which are most common in organic compounds. The document also covers topics like orbital spin states, ligand field theory, effects of metal oxidation state and ligand identity on color, and how distortion of the octahedral geometry affects the d-orbital energies.
Photolysis is a chemical process where molecules are broken down by light absorption. Flash photolysis is commonly used to study short-lived intermediates in photochemical reactions, employing a photolysis flash to initiate reactions followed by a monitoring flash to measure absorption spectra. To study processes in the nanosecond time range, lasers can be used to generate photolysis pulses less than 20 nanoseconds, allowing observation of excited singlet state lifetimes and other fast reactions. Laser flash photolysis systems employ a laser pulse to synchronize a photolysis spark and provide pulses to initiate reactions and monitor absorption on nanosecond timescales, enabling identification of transient intermediates and insight into fast reaction mechanisms.
The document discusses charge transfer complexes and the different types of charge transfer that can cause color in transition metal complexes. It explains that ligand to metal charge transfer and metal to ligand charge transfer can produce color when pi donor or accepting ligands are present with metals lacking or having low oxidation state d-electrons, respectively. As an example, it describes the metal to ligand charge transfer observed in the spectra of the tris(bipyridine)ruthenium(II) dichloride complex.
Photoelectric Effect and Photochemical Reactions. Photons of Light and Chemical Reactions. photodissociation of O2. It was found that Stopping voltage is proportional to the frequency of the incident light but independent of the light intensity
A carbene is any neutral carbon species which contains a non-bonding valance pair of electrons.
Contributed by Alison Brown & Nathan Buehler, Undergraduates, University of Utah
The document discusses the lability and inertness of coordination complexes. It defines labile complexes as those where ligand exchange occurs rapidly, while inert complexes have slow ligand exchange. Lability is determined by factors like the metal ion size, charge, and d-electron configuration, not thermodynamic stability. Smaller or higher charged metal ions and complexes with less than 3 d-electrons tend to be more labile. The rate of ligand substitution depends on both the leaving and entering ligands. Steric effects and solvent also influence the rate. Complexes may undergo dissociative or associative substitution based on their structure.
The document discusses various factors that affect the stability of metal complexes. It explains that complexes formed with ligands having higher charge and smaller size are generally more stable. It also discusses the Irving-Williams order of stability and the factors of charge to radius ratio, electronegativity, and basicity of ligands. The chelate effect is described as an important ligand effect where multidentate ligands form more stable complexes due to entropy gains. Kinetic and thermodynamic stability are distinguished from reactivity concepts of labile and inert complexes.
Lanthanide and actinide chemistry, inorganic chemistry. inner transistion ser...RAHUL SINWER
This document discusses lanthanide and actinide chemistry. It begins by outlining the session objectives, which include an introduction to lanthanides and actinides, their oxidation states, lanthanide contraction, and a comparison of actinides and lanthanides. The document then discusses the electronic configuration, atomic and ionic sizes, ionization energies, magnetic properties, oxidation states, and chemical reactivity of lanthanides. It also covers the similar topics for actinides, and compares the similarities and differences between lanthanides and actinides.
This document discusses electronic spectroscopy of transition metal complexes. It begins by explaining the different types of electronic transitions that can occur, including transitions involving p, s, n, d and f electrons. It then discusses absorption spectroscopy of species containing p, s and n electrons, as well as n→π* and π→π* transitions which are most common in organic compounds. The document also covers topics like orbital spin states, ligand field theory, effects of metal oxidation state and ligand identity on color, and how distortion of the octahedral geometry affects the d-orbital energies.
Photolysis is a chemical process where molecules are broken down by light absorption. Flash photolysis is commonly used to study short-lived intermediates in photochemical reactions, employing a photolysis flash to initiate reactions followed by a monitoring flash to measure absorption spectra. To study processes in the nanosecond time range, lasers can be used to generate photolysis pulses less than 20 nanoseconds, allowing observation of excited singlet state lifetimes and other fast reactions. Laser flash photolysis systems employ a laser pulse to synchronize a photolysis spark and provide pulses to initiate reactions and monitor absorption on nanosecond timescales, enabling identification of transient intermediates and insight into fast reaction mechanisms.
The document discusses charge transfer complexes and the different types of charge transfer that can cause color in transition metal complexes. It explains that ligand to metal charge transfer and metal to ligand charge transfer can produce color when pi donor or accepting ligands are present with metals lacking or having low oxidation state d-electrons, respectively. As an example, it describes the metal to ligand charge transfer observed in the spectra of the tris(bipyridine)ruthenium(II) dichloride complex.
Photoelectric Effect and Photochemical Reactions. Photons of Light and Chemical Reactions. photodissociation of O2. It was found that Stopping voltage is proportional to the frequency of the incident light but independent of the light intensity
A carbene is any neutral carbon species which contains a non-bonding valance pair of electrons.
Contributed by Alison Brown & Nathan Buehler, Undergraduates, University of Utah
The document discusses the lability and inertness of coordination complexes. It defines labile complexes as those where ligand exchange occurs rapidly, while inert complexes have slow ligand exchange. Lability is determined by factors like the metal ion size, charge, and d-electron configuration, not thermodynamic stability. Smaller or higher charged metal ions and complexes with less than 3 d-electrons tend to be more labile. The rate of ligand substitution depends on both the leaving and entering ligands. Steric effects and solvent also influence the rate. Complexes may undergo dissociative or associative substitution based on their structure.
The document discusses various factors that affect the stability of metal complexes. It explains that complexes formed with ligands having higher charge and smaller size are generally more stable. It also discusses the Irving-Williams order of stability and the factors of charge to radius ratio, electronegativity, and basicity of ligands. The chelate effect is described as an important ligand effect where multidentate ligands form more stable complexes due to entropy gains. Kinetic and thermodynamic stability are distinguished from reactivity concepts of labile and inert complexes.
Reference,
https://en.wikipedia.org/wiki/Term_symbol
James E. Huheey, Ellen A. Keiter, Richard L.Keiter and Okhil K. Medhi, Inorganic Chemistry, Principles of Structure and Reactivity. 4th Edn. Pearsons
The document summarizes key aspects of SN2 reactions including reaction mechanism, kinetics, stereochemistry, and factors that affect the rate of the reaction. It describes the SN2 reaction as a bimolecular nucleophilic substitution where the nucleophile attacks the substrate simultaneously as the leaving group departs, resulting in an inversion of configuration. Rate depends on both the nucleophile and substrate concentrations. The stability of the transition state is affected by substrate structure, nucleophilicity, leaving group ability, solvent properties, and conjugation effects in allylic and benzylic systems. Cyclic substrates and those without available orbital overlap do not undergo SN2 reactions as easily.
Classification Of Mechanisms, Ligand Substitution In Octahedral Complexes Without Breaking Metal-ligand Bond, Substitution Reaction In Square Planar Complexes, Factors Which Affect The Rate Of Substitution, Trans Effect (Labilizing Effect), Theories and applications Of Trans Effect
This document provides an overview of interfacial electrochemistry. It discusses how interfaces form boundaries between different phases of matter and influence interactions with the environment due to changed atomic structures. Most electrochemical events occur at interfaces, making interfacial electrochemistry important. When two dissimilar materials contact, charge separation occurs across the interface, creating an interfacial potential difference. The document also describes models of the electrical double layer that forms at electrode-electrolyte interfaces, such as the Helmholtz-Perrin and Gouy-Chapman models.
This document discusses electrolytic solutions and electrochemistry. It begins by defining electrochemistry as the study of chemical reactions involving electron transfer between an electrode and electrolyte. It then discusses different types of solutions, distinguishing between electrolytic and non-electrolytic solutions. Electrolytic solutions contain ions and are electrically conductive. The document also discusses the differences between electronic and electrolytic conductors, and how conductivity is affected by various factors like temperature, concentration, and ion size. It introduces concepts like equivalent conductance, molar conductance, activity, and activity coefficients. In summary, the document provides an overview of key concepts relating to electrolytic solutions and electrochemistry.
Photochemistry is the study of chemical reactions caused by light. Key points include:
- Photochemistry involves light interacting with matter, causing physical or chemical changes.
- Photolysis is the process of carrying out a photochemical reaction using light, usually infrared, visible, or ultraviolet light.
- Important natural photochemical reactions include photosynthesis, photography, ozone formation, and solar energy conversion.
- The photochemical process involves light absorption promoting an electron to a higher energy state, followed by primary processes like isomerization, dissociation, or secondary processes like chain reactions.
Pawan Homogeneous catalyst for CO2 reductionPawan Kumar
This document provides an overview of homogenous photocatalytic reduction of CO2. It discusses key topics such as what photocatalysis is, problems with CO2 reduction, classifications of photocatalysts including homogeneous and heterogeneous examples, and mechanisms of type I and type II catalysts. Molecular complexes like rhenium and ruthenium are described as promising homogeneous photocatalysts. The effects of catalyst structure, reaction conditions, and anchoring to surfaces are reviewed. Future areas of improvement include increasing turnover numbers and standardizing test conditions for fair catalyst comparisons.
An element is identified by its symbol, atomic number, and mass number. Isotopes are atoms of the same element with the same number of protons but different numbers of neutrons. Kinetic isotope effects occur when isotopically substituted molecules react at different rates. The kinetic isotope effect is expressed as a ratio of rate constants for reactions involving different isotopes. Primary kinetic isotope effects occur when a bond to the isotopically labeled atom is broken or formed. Secondary kinetic isotope effects occur when rehybridization is involved or the isotope is remote from the changing bond. Differences in vibrational frequencies between bonds lead to different zero-point energies and measurable kinetic isotope effects.
Chromium, molybdenum, and tungsten are transition metals that share several properties. They have high melting points and are relatively inert. Chromium forms protective oxide coatings and is used to make stainless steel. Molybdenum and tungsten can form a variety of oxidation states and complexes, including clusters. Notable compounds include chromates, molybdates, tungstates, and heteropolyacids containing combinations of these elements. The metals have various industrial uses related to their hardness and corrosion resistance.
This document discusses substitution reactions and their mechanisms in coordination complexes. There are two main types of substitution reactions: electrophilic and nucleophilic. Nucleophilic substitution can occur through acid hydrolysis, base hydrolysis, and ligand exchange reactions. The main mechanisms of substitution are associative, dissociative, and interchange mechanisms. Lability and inertness of complexes depends on both kinetic and thermodynamic factors. According to valence bond theory, the electronic configuration of the metal center determines if a complex is labile or inert. Crystal field theory also aims to explain lability and inertness based on crystal field stabilization energies. Square planar complexes can exhibit substitution governed by trans influence effects.
The document discusses pericyclic reactions and the Woodward-Hoffmann rules for predicting their stereochemistry. It begins by defining pericyclic reactions as concerted reactions where bonds are formed or broken in a cyclic transition state. It then provides examples of different types of pericyclic reactions, including electrocyclizations, cycloadditions, and sigmatropic rearrangements. The Woodward-Hoffmann theory is explained, showing how it can be used to predict whether a reaction will proceed with antarafacial conrotation or suprafacial disrotation based on whether the reaction is thermally or photochemically induced. Specific examples like cyclobutene formation and the Diels-Alder reaction are analyzed in
This document discusses how activity coefficients can explain the effect of inert salts on solubility and acid dissociation constants. It provides examples showing that a precipitate is more soluble and a weak acid dissociates more when the ionic strength is increased by adding an inert salt. This is because the activity coefficients of the ions are less than 1 and decrease with increasing ionic strength, making the activities higher than concentrations. The Debye-Huckel equation can be used to calculate activity coefficients based on ionic charge and strength.
REACTION MECHANISM OF TRANSITION METAL COMPLEXES-I (UNIT-1).pptxKNagaraj7
The document discusses the concepts of lability and inertness in transition metal complexes, noting that labile complexes rapidly exchange ligands while inert complexes exchange ligands slowly. It explains that lability is determined by factors like the size and charge of the central metal ion, with smaller, higher charged ions forming more inert complexes due to stronger metal-ligand bonds. Examples are provided of both labile and inert complexes to illustrate these concepts.
Part 2, Substitution reactions in square planar complexes, Factors.pptxGeeta Tewari
Dr. Geeta Tewari discusses factors that affect the rates of substitution reactions in square planar complexes.
(1) The nature of the entering and leaving ligands impacts the rate, with more polarizable and soft ligands being better nucleophiles for Pt(II) complexes, and the leaving group bond strength determining the rate.
(2) Steric effects of non-leaving ligands can slow the rate, as bulky ligands create hindrance.
(3) For associative mechanisms common in square planar complexes, the charge on the metal center does not impact the rate.
This document discusses electronic spectra and transitions between energy levels in atoms and molecules. It begins by introducing emission spectra and term symbols used to describe atomic energy levels. It then discusses how to determine total angular momentum quantum numbers like spin (S) and orbital angular momentum (L) for different electronic configurations. The document also covers energy level diagrams, selection rules for transitions, and spectra of transition metal complexes. Key topics include naming electronic states, determining allowed d-d transitions, and explaining the relative intensities of bands based on Laporte and spin selection rules.
The Nuclear Overhauser Effect (NOE) describes a change in the NMR signal intensity of one nuclear spin when a nearby spin is saturated. There are two main relaxation mechanisms, W0 and W2, that determine whether the NOE will be positive or negative. W0 typically leads to a negative NOE for macromolecules or in viscous solutions, while W2 usually gives a positive NOE for small molecules in non-viscous solutions. The magnitude of the NOE depends on factors like molecular weight, temperature, and solvent and can provide information about internuclear distances that is useful for assigning protein NMR spectra.
This document discusses electronic spectra of metal complexes. It begins by defining quantum numbers related to electron configuration, such as L (total orbital angular momentum) and l (secondary quantum number). It then describes two main types of electronic transitions in coordination compounds: d-d transitions specific to metals, and charge-transfer transitions. The remainder of the document discusses charge-transfer transitions in more detail, defining ligand-to-metal and metal-to-ligand charge transfer, and how solvent polarity affects these transitions.
Reference,
https://en.wikipedia.org/wiki/Term_symbol
James E. Huheey, Ellen A. Keiter, Richard L.Keiter and Okhil K. Medhi, Inorganic Chemistry, Principles of Structure and Reactivity. 4th Edn. Pearsons
The document summarizes key aspects of SN2 reactions including reaction mechanism, kinetics, stereochemistry, and factors that affect the rate of the reaction. It describes the SN2 reaction as a bimolecular nucleophilic substitution where the nucleophile attacks the substrate simultaneously as the leaving group departs, resulting in an inversion of configuration. Rate depends on both the nucleophile and substrate concentrations. The stability of the transition state is affected by substrate structure, nucleophilicity, leaving group ability, solvent properties, and conjugation effects in allylic and benzylic systems. Cyclic substrates and those without available orbital overlap do not undergo SN2 reactions as easily.
Classification Of Mechanisms, Ligand Substitution In Octahedral Complexes Without Breaking Metal-ligand Bond, Substitution Reaction In Square Planar Complexes, Factors Which Affect The Rate Of Substitution, Trans Effect (Labilizing Effect), Theories and applications Of Trans Effect
This document provides an overview of interfacial electrochemistry. It discusses how interfaces form boundaries between different phases of matter and influence interactions with the environment due to changed atomic structures. Most electrochemical events occur at interfaces, making interfacial electrochemistry important. When two dissimilar materials contact, charge separation occurs across the interface, creating an interfacial potential difference. The document also describes models of the electrical double layer that forms at electrode-electrolyte interfaces, such as the Helmholtz-Perrin and Gouy-Chapman models.
This document discusses electrolytic solutions and electrochemistry. It begins by defining electrochemistry as the study of chemical reactions involving electron transfer between an electrode and electrolyte. It then discusses different types of solutions, distinguishing between electrolytic and non-electrolytic solutions. Electrolytic solutions contain ions and are electrically conductive. The document also discusses the differences between electronic and electrolytic conductors, and how conductivity is affected by various factors like temperature, concentration, and ion size. It introduces concepts like equivalent conductance, molar conductance, activity, and activity coefficients. In summary, the document provides an overview of key concepts relating to electrolytic solutions and electrochemistry.
Photochemistry is the study of chemical reactions caused by light. Key points include:
- Photochemistry involves light interacting with matter, causing physical or chemical changes.
- Photolysis is the process of carrying out a photochemical reaction using light, usually infrared, visible, or ultraviolet light.
- Important natural photochemical reactions include photosynthesis, photography, ozone formation, and solar energy conversion.
- The photochemical process involves light absorption promoting an electron to a higher energy state, followed by primary processes like isomerization, dissociation, or secondary processes like chain reactions.
Pawan Homogeneous catalyst for CO2 reductionPawan Kumar
This document provides an overview of homogenous photocatalytic reduction of CO2. It discusses key topics such as what photocatalysis is, problems with CO2 reduction, classifications of photocatalysts including homogeneous and heterogeneous examples, and mechanisms of type I and type II catalysts. Molecular complexes like rhenium and ruthenium are described as promising homogeneous photocatalysts. The effects of catalyst structure, reaction conditions, and anchoring to surfaces are reviewed. Future areas of improvement include increasing turnover numbers and standardizing test conditions for fair catalyst comparisons.
An element is identified by its symbol, atomic number, and mass number. Isotopes are atoms of the same element with the same number of protons but different numbers of neutrons. Kinetic isotope effects occur when isotopically substituted molecules react at different rates. The kinetic isotope effect is expressed as a ratio of rate constants for reactions involving different isotopes. Primary kinetic isotope effects occur when a bond to the isotopically labeled atom is broken or formed. Secondary kinetic isotope effects occur when rehybridization is involved or the isotope is remote from the changing bond. Differences in vibrational frequencies between bonds lead to different zero-point energies and measurable kinetic isotope effects.
Chromium, molybdenum, and tungsten are transition metals that share several properties. They have high melting points and are relatively inert. Chromium forms protective oxide coatings and is used to make stainless steel. Molybdenum and tungsten can form a variety of oxidation states and complexes, including clusters. Notable compounds include chromates, molybdates, tungstates, and heteropolyacids containing combinations of these elements. The metals have various industrial uses related to their hardness and corrosion resistance.
This document discusses substitution reactions and their mechanisms in coordination complexes. There are two main types of substitution reactions: electrophilic and nucleophilic. Nucleophilic substitution can occur through acid hydrolysis, base hydrolysis, and ligand exchange reactions. The main mechanisms of substitution are associative, dissociative, and interchange mechanisms. Lability and inertness of complexes depends on both kinetic and thermodynamic factors. According to valence bond theory, the electronic configuration of the metal center determines if a complex is labile or inert. Crystal field theory also aims to explain lability and inertness based on crystal field stabilization energies. Square planar complexes can exhibit substitution governed by trans influence effects.
The document discusses pericyclic reactions and the Woodward-Hoffmann rules for predicting their stereochemistry. It begins by defining pericyclic reactions as concerted reactions where bonds are formed or broken in a cyclic transition state. It then provides examples of different types of pericyclic reactions, including electrocyclizations, cycloadditions, and sigmatropic rearrangements. The Woodward-Hoffmann theory is explained, showing how it can be used to predict whether a reaction will proceed with antarafacial conrotation or suprafacial disrotation based on whether the reaction is thermally or photochemically induced. Specific examples like cyclobutene formation and the Diels-Alder reaction are analyzed in
This document discusses how activity coefficients can explain the effect of inert salts on solubility and acid dissociation constants. It provides examples showing that a precipitate is more soluble and a weak acid dissociates more when the ionic strength is increased by adding an inert salt. This is because the activity coefficients of the ions are less than 1 and decrease with increasing ionic strength, making the activities higher than concentrations. The Debye-Huckel equation can be used to calculate activity coefficients based on ionic charge and strength.
REACTION MECHANISM OF TRANSITION METAL COMPLEXES-I (UNIT-1).pptxKNagaraj7
The document discusses the concepts of lability and inertness in transition metal complexes, noting that labile complexes rapidly exchange ligands while inert complexes exchange ligands slowly. It explains that lability is determined by factors like the size and charge of the central metal ion, with smaller, higher charged ions forming more inert complexes due to stronger metal-ligand bonds. Examples are provided of both labile and inert complexes to illustrate these concepts.
Part 2, Substitution reactions in square planar complexes, Factors.pptxGeeta Tewari
Dr. Geeta Tewari discusses factors that affect the rates of substitution reactions in square planar complexes.
(1) The nature of the entering and leaving ligands impacts the rate, with more polarizable and soft ligands being better nucleophiles for Pt(II) complexes, and the leaving group bond strength determining the rate.
(2) Steric effects of non-leaving ligands can slow the rate, as bulky ligands create hindrance.
(3) For associative mechanisms common in square planar complexes, the charge on the metal center does not impact the rate.
This document discusses electronic spectra and transitions between energy levels in atoms and molecules. It begins by introducing emission spectra and term symbols used to describe atomic energy levels. It then discusses how to determine total angular momentum quantum numbers like spin (S) and orbital angular momentum (L) for different electronic configurations. The document also covers energy level diagrams, selection rules for transitions, and spectra of transition metal complexes. Key topics include naming electronic states, determining allowed d-d transitions, and explaining the relative intensities of bands based on Laporte and spin selection rules.
The Nuclear Overhauser Effect (NOE) describes a change in the NMR signal intensity of one nuclear spin when a nearby spin is saturated. There are two main relaxation mechanisms, W0 and W2, that determine whether the NOE will be positive or negative. W0 typically leads to a negative NOE for macromolecules or in viscous solutions, while W2 usually gives a positive NOE for small molecules in non-viscous solutions. The magnitude of the NOE depends on factors like molecular weight, temperature, and solvent and can provide information about internuclear distances that is useful for assigning protein NMR spectra.
This document discusses electronic spectra of metal complexes. It begins by defining quantum numbers related to electron configuration, such as L (total orbital angular momentum) and l (secondary quantum number). It then describes two main types of electronic transitions in coordination compounds: d-d transitions specific to metals, and charge-transfer transitions. The remainder of the document discusses charge-transfer transitions in more detail, defining ligand-to-metal and metal-to-ligand charge transfer, and how solvent polarity affects these transitions.
The document discusses reactions of haloalkanes and haloarenes. It describes various nucleophilic substitution, elimination, and electrophilic substitution reactions of haloalkanes. For haloarenes, it discusses that nucleophilic substitution is less favorable due to resonance effects. It also outlines electrophilic substitution reactions like halogenation, nitration, sulfonation, and Friedel-Crafts reactions that are possible for haloarenes. Reaction of haloarenes with metals like Wurtz-Fittig and Fittig reactions are additionally summarized.
The document discusses basic concepts of chemistry including atoms, molecules, mixtures, elements, compounds, laws of chemical combinations, Dalton's atomic theory, the mole concept, percentage composition, empirical and molecular formulas, stoichiometry, mass percent, mole fraction, molarity, and molality. It is presented by Studyduniya, an educational social network, to provide an overview of fundamental topics in physical chemistry.
Photosynthesis, process by which green plants and certain other organisms use the energy of light to convert carbon dioxide and water into the simple sugar glucose. In so doing, photosynthesis provides the basic energy source for virtually all organisms.
The document discusses different types of hydrocarbons including alkanes, alkenes, and alkynes. It describes their general formulas, properties, reactions, and methods of preparation. Alkanes contain single bonds between carbons and do not react easily. Alkenes contain double bonds and participate in reactions like halogenation and oxidation. Alkynes contain triple bonds and undergo addition reactions with dihydrogen, halogens, and hydrogen halides. The document is from an educational social network providing chemistry content for IIT JEE preparation.
SY - PP II - Colloidal dipsersionyuyhujbjj.pdfparmarkeval1610
This document provides an overview of colloidal dispersions. It defines colloids as dispersed systems with particle sizes between 1 nm and 1000 nm. Colloids are classified based on particle size, shape, and interaction with the dispersion medium. The key properties of colloids discussed include optical properties like Tyndall effect, kinetic properties like Brownian motion and diffusion, electric properties like electric double layer and zeta potential, and concepts like Donnan membrane equilibrium and coacervation. Coacervation refers to the separation of a colloidal system into two liquid phases driven by differences in ionic forces.
The word colloid, is derived from the Greek word “kolla” meaning “glue” and is defined as a system containing particles of size from one millimicron to 0.1 micron (10-6 to 10-4 mm).
This document discusses the differences between liquids, solids, and gases in terms of molecular behavior and intermolecular forces. It explains that in liquids and solids, molecules are close together with little empty space between them due to attractive intermolecular forces. Molecules in liquids can move past one another but are constrained by these forces, while molecules in solids are held rigidly in position with almost no freedom of movement. Gases, in contrast, have greater distances between molecules and no attractive forces constraining their movement. The document then covers different types of intermolecular forces including London dispersion forces, dipole-dipole interactions, hydrogen bonding, and ion-dipole forces.
Soft matter or soft condensed matter is a subfield of condensed matter comprising a variety of physical systems that are deformed or structurally altered by thermal or mechanical stress of the magnitude of thermal fluctuations. They include liquids, colloids, polymers, foams, gels, granular materials, liquid crystals, and a number of biological materials. These materials share an important common feature in that predominant physical behaviors occur at an energy scale comparable with room temperature thermal energy. At these temperatures, quantum aspects are generally unimportant. Pierre-Gilles de Gennes, who has been called the "founding father of soft matter,"[1] received the Nobel Prize in physics in 1991 for discovering that methods developed for studying order phenomena in simple systems can be generalized to the more complex cases found in soft matter, in particular, to the behaviors of liquid crystals and polymers.[2]
Contents
1 Distinctive physics
2 Applications
3 Research
4 Related
5 See also
6 References
7 External links
This document provides an overview of colloidal dispersions, including their classification. It discusses 5 ways that colloids can be classified: 1) based on the physical state of the dispersed and continuous phases, 2) based on the electrical charge of the dispersed phase, 3) based on their appearance, 4) based on the size of dispersed particles, and 5) based on the interaction between the dispersed and continuous phases. Key colloid types discussed include sols, gels, lyophilic colloids, and lyophobic colloids. The purpose is to develop student understanding of the core concepts and characteristics of colloidal dispersions.
The document discusses colloids and their classification. It defines colloids as substances that are microscopically dispersed through another substance, with particle sizes between 10-10000 Angstroms. Colloids are classified in several ways, including by particle size (molecular dispersion, colloidal dispersion, coarse dispersion), physical state of phases, type of dispersed particles (multimolecular, macromolecular), appearance (sols, gels), and electrical charge on particles (positive, negative). Common colloidal systems include sols, emulsions, foams and aerosols. Micelle formation in colloids and the critical micelle concentration are also explained.
This document provides information about colloidal dispersions. It defines a colloid as a substance microscopically dispersed throughout another substance, with particle sizes between 1-1000nm. Colloids can be classified based on their physical state, nature of interactions, size, appearance, or electric charge. Key properties of colloids include Brownian motion, diffusion, sedimentation, viscosity, light scattering, and electrical behaviors like electrophoresis and electrosmosis. Colloids find applications in areas like therapy, absorption, solubility, stability, and drug targeting.
6. Colloidal properties of any colloidal substanceManteeKumari
This document discusses colloidal systems and their properties. It begins by defining colloids as mixtures where one substance is divided into minute particles dispersed throughout a second substance. The particles in a colloid are larger than atoms or molecules in solutions, but smaller than particles in suspensions.
It then discusses some key properties of colloids, including that colloidal particles do not diffuse through membranes, they scatter light and exhibit the Tyndall effect, and they undergo constant random motion called Brownian movement. Colloidal particles also acquire and maintain a net electric charge via preferential adsorption of ions from the dispersion medium. This charge prevents the particles from aggregating due to electrical repulsions between them.
In
The document discusses various topics related to the solid state including classification of solids, crystalline and amorphous structures, unit cells, point defects, magnetic properties, and more. Solids are classified as molecular, ionic, metallic, covalent and further divided based on their crystalline structure. Crystalline solids have definite geometric arrangements while amorphous solids have irregular particle shapes. Unit cells are the basic repeating units that make up crystal lattices. There are various types of unit cells including primitive, body-centered, and face-centered cells. Point defects refer to irregularities in the positions of atoms in crystalline solids. Magnetic properties of materials include paramagnetism, diamagnetism, ferromag
The document discusses the classification and properties of different types of polymers. Polymers are classified based on their mode of polymerization into addition polymers and condensation polymers. They are also classified based on molecular forces into elastomers, fibers, thermoplastic polymers, thermosetting polymers, and natural rubber. Examples of various polymers are provided along with their common uses such as nylon 6 for tire cords and fabrics and nylon 6,6 for textiles. Teflon is noted for its chemical inertness and use in non-stick coatings.
General Principle and Process of Isolation (Metallurgy)Shivani Jadhav
An In-Depth Concept of General Principle and Process of Isolation (Metallurgy) For IIT JEE (CHEMISTRY) Exams.
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This presentation includes basic of PCOS their pathology and treatment and also Ayurveda correlation of PCOS and Ayurvedic line of treatment mentioned in classics.
Thinking of getting a dog? Be aware that breeds like Pit Bulls, Rottweilers, and German Shepherds can be loyal and dangerous. Proper training and socialization are crucial to preventing aggressive behaviors. Ensure safety by understanding their needs and always supervising interactions. Stay safe, and enjoy your furry friends!
A Strategic Approach: GenAI in EducationPeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
MATATAG CURRICULUM: ASSESSING THE READINESS OF ELEM. PUBLIC SCHOOL TEACHERS I...NelTorrente
In this research, it concludes that while the readiness of teachers in Caloocan City to implement the MATATAG Curriculum is generally positive, targeted efforts in professional development, resource distribution, support networks, and comprehensive preparation can address the existing gaps and ensure successful curriculum implementation.
Executive Directors Chat Leveraging AI for Diversity, Equity, and InclusionTechSoup
Let’s explore the intersection of technology and equity in the final session of our DEI series. Discover how AI tools, like ChatGPT, can be used to support and enhance your nonprofit's DEI initiatives. Participants will gain insights into practical AI applications and get tips for leveraging technology to advance their DEI goals.
A workshop hosted by the South African Journal of Science aimed at postgraduate students and early career researchers with little or no experience in writing and publishing journal articles.
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
Main Java[All of the Base Concepts}.docxadhitya5119
This is part 1 of my Java Learning Journey. This Contains Custom methods, classes, constructors, packages, multithreading , try- catch block, finally block and more.
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The accumulation of molecular species at
the surface rather than in the bulk of a solid
or liquid is termed as Adsorption.
The molecular species or substance, which
concentrates or accumulates at the surface
is termed Adsorbate & the material on
the surface of which the adsorption takes
place is called Adsorbent.
ADSORPTION
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Adsorption- The substance is concentrated
only at the surface & does not penetrate
through the surface to the bulk of the solid.
Absorption- The substance is uniformly
distributed throughout the bulk of the solid.
Both adsorption and absorption can take
place simultaneously also, & termed
as Sorption
DIFFERENCE BETWEEN
ADSOPTION & ABSORPTION
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A kind of adsorption in which the
accumulation of adsorbate on the surface of a
solid occurs on account of weak van der
Waals’ forces, is termed as physical
adsorption or physisorption.
A kind of adsorption in which the molecules
or atoms are held to the solid surface by
chemical bonds, is termed as chemical
adsorption or chemisorption.
TYPES OF ADSORPTION
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TYPES OF ADSORPTION
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The variation in the amount of adsorbate
adsorbed by the adsorbent with pressure at
const. temperature is expressed by a curve
termed as adsorption isotherm.
ADSORPTION ISOTHERMS
FREUNDLICH ADSORPTION ISOTHERM:
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To adsorb poisonous gases in Gas masks.
To remove colours from solutions
For producing high vacuum.
To control humidity.
As a heterogeneous catalyst.
For separating inert gases.
In chromatographic analysis.
APPLICATIONS OF ADSORPTION
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Colloids is a heterogeneous mixture in which
one substance is dispersed (called dispersed
phase) as very fine particles in another
substance called dispersion medium.
range of diameters is in between 1 and 1000
nm
COLLOIDS
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CLASSIFICATION OF COLLOIDS
Based on Physical State of dispersed Phase
and Dispersion Medium
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CLASSIFICATION OF COLLOIDS
Based on Nature of Interaction between
Dispersed Phase and Dispersion Medium
Lyophilic colloids: liquid-loving, formed by
mixing substances like gum, gelatine, starch,
rubber, etc., with a dispersion medium.
Lyophobic colloids: liquid-hating, Substances
like metals, their sulphides, etc., with the
dispersion medium can be prepared only by
special methods.
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CLASSIFICATION OF COLLOIDS
Based on Type of Particles of the Dispersed
Phase
Multimolecular: A gold sol may contain
particles of various sizes having many atoms.
Macromolecular: starch, cellulose, proteins &
enzymes; and polythene, nylon, polystyrene,
synthetic rubber, etc, in suitable solvents.
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CLASSIFICATION OF COLLOIDS
Based on Type of Particles of the Dispersed
Phase
Associated Colloids: Some substances which
at low concentrations behave as normal
strong electrolytes, but at higher
concentrations exhibit colloidal behaviour
due to the formation of aggregates. The
aggregated particles thus formed are called
micelles.
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PREPARATION OF COLLOIDS
Chemical methods
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PREPARATION OF COLLOIDS
Electrical disintegration or Bredig’s Arc method
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PREPARATION OF COLLOIDS
Peptization
Peptization may be defined as the process
in which a precipitate is converted into
colloidal sol by shaking it with dispersion
medium in the presence of a small amount
of electrolyte. The electrolyte used for this
purpose is called peptizing agent.
It is used to convert a freshly prepared
precipitate into a colloidal sol
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PROPERTIES OF COLLOIDAL
SOLUTIONS
Colligative properties: The number of particles
in a colloidal solution is comparatively small
as compared to a true solution.
Colour: The colour of colloidal solution
depends on the wavelength of light scattered
by the dispersed particles which on further
depends on the size and nature of the
particles.
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PROPERTIES OF COLLOIDAL
SOLUTIONS
Tyndall effect:
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PROPERTIES OF COLLOIDAL
SOLUTIONS
Brownian movement:
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PROPERTIES OF COLLOIDAL
SOLUTIONS
Charge on colloidal particles:
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PROPERTIES OF COLLOIDAL
SOLUTIONS
Electrophoresis:
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EMULSIONS
An emulsion is a special type of mixture
made by combining two liquids that
normally don't mix.
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SURFACTANT
Surfactant is a substance, such as a detergent,
that can reduce the surface tension of a liquid
and thus allow it to foam or penetrate solids; a
wetting agent.