The Colloidal Domain: Where Physics, Chemistry, Biology, and Technology MeetThis new edition provides students and professionals with a comprehensive and up-to-date treatment of colloid science theory, methods, and applications. Emphasizing the molecular interactions that determine the properties of colloidal systems, the authors provide an authoritative account of critical developments in colloid science that have occurred over the past several decades. Combining all of the best features of a professional reference and a student text, the Second Edition features: * Concept maps preceding each chapter that put subject matter into perspective. * Numerous worked examples - many new to this edition - illustrating key concepts. * More than 250 high-quality illustrations that help clarify processes described. * A new chapter that integrates the development of colloid science and technology in the twentieth century with challenges facing the field today. The Colloidal Domain, Second Edition is an indispensable professional resource for chemists and chemical engineers working in an array of industries, including petrochemicals, food, agricultural, ceramic, coatings, forestry, and paper products. It is also a superb educational tool for advanced undergraduate and graduate-level students of physical chemistry and chemical engineering. |
From inside the book
Results 1-3 of 81
Page 255
... effect can totally overpower the double - layer repulsion . For highly charged systems and mono- valent ions , this effect can contribute a substantial correlation correction to the repulsive double - layer force . In colloidal systems ...
... effect can totally overpower the double - layer repulsion . For highly charged systems and mono- valent ions , this effect can contribute a substantial correlation correction to the repulsive double - layer force . In colloidal systems ...
Page 289
... effect occurs when the particles move relative to one another . We can distinguish between two kinds of dynamical effect . The most obvious is that if particles move rapidly enough , there is not enough time for equilibrating the ...
... effect occurs when the particles move relative to one another . We can distinguish between two kinds of dynamical effect . The most obvious is that if particles move rapidly enough , there is not enough time for equilibrating the ...
Page 588
... effect , but destabilization can very well occur if instead ionic surfactants are used as stabilizers . For cooling the situation is the reverse . Adding electrolyte will have a moderate , but measurable , effect on the stability of the ...
... effect , but destabilization can very well occur if instead ionic surfactants are used as stabilizers . For cooling the situation is the reverse . Adding electrolyte will have a moderate , but measurable , effect on the stability of the ...
Contents
Solutes and Solvents SelfAssembly | 1 |
Surface Chemistry and Monolayers | 45 |
3Electrostatic Interactions in Colloidal | 99 |
Copyright | |
14 other sections not shown
Common terms and phrases
acid adsorbed adsorption aggregation number amphiphilic aqueous attractive behavior bilayer bulk calculate CHAPTER charge density charged surface chemical potential coagulation coefficient coil colloidal colloidal particles colloidal systems component concentration counterions curvature curve decreases depends determine diffusion dipole dispersion distance distribution DLVO theory double layer droplets effect electrolyte electrostatic electrostatic interactions emulsion entropy equation equilibrium example force free energy head group hydrocarbon hydrophobic illustrated increases interac interface ionic kJ/mol lamellar latex lipid measured membrane micellar micelles microemulsion molecular molecules monolayer monomer nucleation obtain occurs osmotic osmotic pressure parameter phase diagram Poisson-Boltzmann equation polar polymer pressure properties protein R₁ radius range regular solution repulsive result Section shown in Figure shows solid solubility solvent spherical stability structure surface charge surface potential surface tension surfactant surfactant film temperature term thermodynamic tion transition vesicles Waals zeta potential