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 86
Page 280
... decreases , the solubility of alkylbenzenes in water initially decreases but then becomes almost constant . For many substances , like the rare gases , the solubility displays a minimum around 20 ° C and then actually increases with ...
... decreases , the solubility of alkylbenzenes in water initially decreases but then becomes almost constant . For many substances , like the rare gases , the solubility displays a minimum around 20 ° C and then actually increases with ...
Page 421
... decrease in total number of particles is linear in time , while for long times , t > t , the decrease is inversely propor- tional to t . The characteristic time t separating the two regimes decreases with increasing total particle ...
... decrease in total number of particles is linear in time , while for long times , t > t , the decrease is inversely propor- tional to t . The characteristic time t separating the two regimes decreases with increasing total particle ...
Page 563
... decreases for all the oils except tetradecane as we move from the AB line towards the water corner of the phase diagram along constant surfactant / oil ( S / O ) ratio , as shown in Figure 11.14 , and we can observe a transition to a ...
... decreases for all the oils except tetradecane as we move from the AB line towards the water corner of the phase diagram along constant surfactant / oil ( S / O ) ratio , as shown in Figure 11.14 , and we can observe a transition to a ...
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