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About: Wetting is a(n) research topic. Over the lifetime, 32297 publication(s) have been published within this topic receiving 804678 citation(s). more


Open accessBook
01 Jan 1960-
Abstract: Capillarity. The Nature and Thermodynamics of Liquid Interfaces. Surface Films on Liquid Substrates. Electrical Aspects of Surface Chemistry. Long--Range Forces. Surfaces of Solids. Surfaces of Solids: Microscopy and Spectroscopy. The Formation of a New Phase--Nucleation and Crystal Growth. The Solid--Liquid Interface--Contact Angle. The Solid--Liquid Interface--Adsorption from Solution. Frication, Lubrication, and Adhesion. Wetting, Flotation, and Detergency. Emulsions, Foams, and Aerosols. Macromolecular Surface Films, Charged Films, and Langmuir--Blodgett Layers. The Solid--Gas Interface--General Considerations. Adsorption of Gases and Vapors on Solids. Chemisorption and Catalysis. Index. more

Topics: Wetting (57%), Adsorption (54%), Chemisorption (52%)

10,786 Citations

Open accessBook
01 Jan 1978-
Abstract: Preface. 1 Characteristic Features of Surfactants. A Conditions Under Which Interfacial Phenomena and Surfactants Become Significant. B General Structural Features and Behavior of Surfactants. 1 General Use of Charge Types. 2 General Effects of the Nature of the Hydrophobic Group. I Characteristic Features and Uses of Commercially Available Surfactants. I.A Anionics. 1 Carboxylic Acid Salts. 2 Sulfonic Acid Salts. 3 Sulfuric Acid Ester Salts. 4 Phosphoric and Polyphosphoric Acid Esters. 5 Fluorinated Anionics. I.B Cationics. 1 Long-Chain Amines and Their Salts. 2 Acylated Diamines and Polyamines and Their Salts. 3 Quaternary Ammonium Salts. 4 Polyoxyethylenated (POE) Long-Chain Amines. 5 Quaternized POE Long-Chain Amines. 6 Amine Oxides. I.C Nonionics. 1 POE Alkylphenols, Alkylphenol "Ethoxylates". 2 POE Straight-Chain Alcohols, Alcohol "Ethoxylates". 3 POE Polyoxypropylene glycols. 4 POE Mercaptans. 5 Long-Chain Carboxylic Acid Esters. 6 Alkanolamine "Condensates," Alkanolamides. 7 Tertiary Acetylenic Glycols and Their "Ethoxylates". 8 POE Silicones. 9 N-Alkylpyrrolidones. 10 Alkylpolyglycosides. I.D Zwitterionics. 1 pH-Sensitive Zwitterionics. 2 pH-Insensitive Zwitterionics. I.E Newer Surfactants Based Upon Renewable Raw Materials. 1 a-Sulfofatty Acid Methyl Esters (SME). 2 Acylated Aminoacids. 3 N-Acyl L-Glutamates (AG). 4 N-Acyl Glycinates. 5 N-Acyl DL-Alaninates. 6 Other Acylated Aminoacids. 7 Nopol Alkoxylates. II Environmental Effects of Surfactants. II.A Surfactant Biodegradability. II.B Surfactant Toxicity To and Bioconcentration in Marine Organisms. III Some Useful Generalizations. References. Problems. 2 Adsorption of Surface-Active Agents at Interfaces: The Electrical Double Layer. I The Electrical Double Layer. II Adsorption at the Solid-Liquid Interface. II.A Mechanisms of Adsorption and Aggregation. II.B Adsorption Isotherms. 1 The Langmuir Adsorption Isotherm. II.C Adsorption from Aqueous Solution Onto Adsorbents with Strongly Charged Sites. 1 Ionic Surfactants. 2 Nonionic Surfactants. 3 pH Change. 4 Ionic Strength. 5 Temperature. II.D Adsorption from Aqueous Solution Onto Nonpolar, Hydrophobic Adsorbents. II.E Adsorption from Aqueous Solution Onto Polar Adsorbents without Strongly Charged Sites. II.F Effects of Adsorption from Aqueous Solution on the Surface Properties of the Solid Adsorbent. 1 Substrates with Strongly Charged Sites. 2 Nonpolar Adsorbents. II.G Adsorption from Nonaqueous Solution. II.H Determination of the Specific Surface Areas of Solids. III Adsorption at the Liquid-Gas (L/G) and Liquid-Liquid (L/L) Interfaces. III.A The Gibbs Adsorption Equation 60 III.B Calculation of Surface Concentrations and Area per Molecule at the Interface By Use of the Gibbs Equation. III.C Effectiveness of Adsorption at the L/G and L/L Interfaces. III.D The Szyszkowski, Langmuir, and Frumkin Equations. III.E Efficiency of Adsorption at the L/G and L/L Interfaces. III.F Calculation of Thermodynamic Parameters of Adsorption at the L/G and L/L Interfaces. III.G Adsorption from Mixtures of Two Surfactants. References. Problems. 3 Micelle Formation by Surfactants. I The Critical Micelle Concentration (CMC). II Micellar Structure and Shape. II.A The Packing Parameter. II.B Surfactant Structure and Micellar Shape. II.C Liquid Crystals. III Micellar Aggregation Numbers. IV Factors Affecting the Value of the CMC in Aqueous Media. IV.A Structure of the Surfactant. 1 The Hydrophobic Group. 2 The Hydrophobic Group. 3 The Counterion in Ionic Surfactants: Degree of Binding to the Micelle 139 4 Empirical Equations. IV.B Electrolyte. IV.C Organic Additives. 1 Class I Materials. 2 Class II Materials. IV.D The Presence of a Second Liquid Phase. IV.E Temperature. V Micellization in Aqueous Solution and Adsorption at the Aqueous Solution-Air or Aqueous Solution-Hydrocarbon Interface. V.A. The CMC/C20 ratio. VI CMCs in Nonaqueous Media. VII Equations for the CMC Based on Theoretical Considerations. VIII Thermodynamic Parameters of Micellization. IX Mixed Micelle Formation in Mixtures of Two Surfactants. References. Problems. 4 Solubilization by Solutions of Surfactants: Micellar Catalysis. I Solubilization in Aqueous Media. I.A Locus of Solubilization. I.B Factors Determining the Extent of Solubilization. 1 Structure of the Surfactant. 2 Structure of the Solubilizate. 3 Effect of Electrolyte. 4 Effect of Monomeric Organic Additives. 5 Effect of Polymeric Organic Additives. 6 Mixed Anionic-Nonionic Micelles. 7 Effect of Temperature. 8 Hydrotropy. I.C Rate of Solubilization. II Solubilization in Nonaqueous Solvents. II.A Secondary Solubilization. III Some Effects of Solubilization. III.A Effect of Solubilization on Micellar Structure. III.B Change in the Cloud Points of Aqueous Solutions of Nonionic Surfactants. III.C Reduction of the CMC. III.D Miscellaneous Effects of Solubilization. IV Micellar Catalysis. References. Problems. 5 Reduction of Surface and Interfacial Tension by Surfactants. I Efficiency in Surface Tension Reduction. II Effectiveness in Surface Tension Reduction. II.A The Krafft Point. II.B Interfacial Parameter and Chemical Structural Effects. III Liquid-Liquid Interfacial Tension Reduction. III.A Ultralow Interfacial Tension. IV Dynamic Surface Tension Reduction. IV.A Dynamic Regions. IV.B Apparent Diffusion Coefficients of Surfactants. References. Problems. 6 Wetting and Its Modification by Surfactants. I Wetting Equilibria. I.A Spreading Wetting. 1 The Contact Angle. 2 Measurement of the Contact Angle. I.B Adhesional Wetting. I.C Immersional Wetting. I.D Adsorption and Wetting. II Modification of Wetting by Surfactants. II.A General Considerations. II.B Hard Surface (Equilibrium) Wetting. II.C Textile (Nonequilibrium) Wetting. II.D Effect of Additives. III Synergy in Wetting by Mixtures of Surfactants. IV Superspreading (Superwetting). References. Problems. 7 Foaming and Antifoaming by Aqueous Solutions of Surfactants. I Theories of Film Elasticity. II Factors Determining Foam Persistence. II.A Drainage of Liquid in the Lamellae. II.B Diffusion of Gas Through the Lamellae. II.C Surface Viscosity. II.D The Existence and Thickness of the Electrical Double Layer. III The Relation of Surfactant Chemical Structure to Foaming in Aqueous Solution. III.A Efficiency as a Foaming Agent. III.B Effectiveness as a Foaming Agent. III.C Low-Foaming Surfactants. IV Foam-Stabilizing Organic Additives. V Antifoaming. VI Foaming of Aqueous Dispersions of Finely Divided Solids. References. Problems. 8 Emulsification by Surfactants. I Macroemulsions. I.A Formation. I.B Factors Determining Stability. 1 Physical Nature of the Interfacial Film. 2 Existence of an Electrical or Steric Barrier to Coalescence on the Dispersed Droplets. 3 Viscosity of the Continuous Phase. 4 Size Distribution of Droplets. 5 Phase Volume Ratio. 6 Temperature. I.C Inversion. I.D Multiple Emulsions. I.E Theories of Emulsion Type. 1 Qualitative Theories. 2 Kinetic Theory of Macroemulsion Type. II Microemulsions. III Nanoemulsions. IV Selection of Surfactants as Emulsifying Agents. IV.A The HLB Method. IV.B The PIT Method. IV.C The HLD Method. V Demulsification. References. Problems. 9 Dispersion and Aggregation of Solids in Liquid Media by Surfactants. I Interparticle Forces. I.A Soft (electrostatic) and van der Waals Forces: DLVO Theory. 1 Limitations of the DLVO Theory. I.B Steric Forces. II Role of the Surfactant in the Dispersion Process. II.A Wetting of the Powder. II.B Deaggregation or Fragmentation of Particle Clusters. II.C Prevention of Reaggregation. III Coagulation or Flocculation of Dispersed Solids by Surfactants. III.A Neutralization or Reduction of the Potential at the Stern Layer of the Dispersed Particles. III.B Bridging. III.C Reversible Flocculation. IV The Relation of Surfactant Chemical Structure to Dispersing Properties. IV.A Aqueous Dispersions. IV.B Nonaqueous Dispersions. References. Problems. 10 Detergency and Its Modification by Surfactants. I Mechanisms of the Cleaning Process. I.A Removal of Soil from Substrate. 1 Removal of Liquid Soil. 2 Removal of Solid Soil. I.B Suspension of the Soil in the Bath and Prevention of Redeposition. 1 Solid Particulate Soils: Formation of Electrical and Steric Barriers Soil Release Agents. 2 Liquid Oily Soil. I.C Skin Irritation. I.D Dry Cleaning. II Effect of Water Hardness. II.A Builders. II.B Lime Soap Dispersing Agents. III Fabric Softeners. IV The Relation of the Chemical Structure of the Surfactant to Its Detergency. IV.A Effect of Soil and Substrate. 1 Oily Soil. 2 Particulate Soil. 3 Mixed Soil. IV.B Effect of the Hydrophobic Group of the Surfactant. IV.C Effect of the Hydrophilic Group of the Surfactant. IV.D Dry Cleaning. References. Problems. 11 Molecular Interactions and Synergism in Mixtures of Two Surfactants. I Evaluation of Molecular Interaction Parameters. I.A Notes on the Use of Equations 11.1-11.4. II Effect of Chemical Structure and Molecular Environment on Molecular Interaction Parameters. III Conditions for the Existence of Synergism. III.A Synergism or Antagonism (Negative Synergism) in Surface or Interfacial Tension Reduction Efficiency. III.B Synergism or Antagonism (Negative Synergism) in Mixed Micelle Formation in Aqueous Medium. III.C Synergism or Antagonism (Negative Synergism) in Surface or Interfacial Tension Reduction Effectiveness. III.D Selection of Surfactants Pairs for Optimal Interfacial Properties. IV The Relation between Synergism in Fundamental Surface Properties and Synergism in Surfactant Applications. References. Problems. 12 Gemini Surfactants. I Fundamental Properties. II Interaction with Other Surfactant. III Performance Properties. References. Problems. Answers to Problems. Index. more

6,069 Citations

Journal ArticleDOI: 10.1103/REVMODPHYS.57.827
P. G. de Gennes1Institutions (1)
Abstract: The wetting of solids by liquids is connected to physical chemistry (wettability), to statistical physics (pinning of the contact line, wetting transitions, etc.), to long-range forces (van der Waals, double layers), and to fluid dynamics. The present review represents an attempt towards a unified picture with special emphasis on certain features of "dry spreading": (a) the final state of a spreading droplet need not be a monomolecular film; (b) the spreading drop is surrounded by a precursor film, where most of the available free energy is spent; and (c) polymer melts may slip on the solid and belong to a separate dynamical class, conceptually related to the spreading of superfluids. more

Topics: Wetting transition (64%), Wetting (56%), van der Waals force (52%)

5,699 Citations

Journal ArticleDOI: 10.1021/JA00183A049
Colin D. Bain1, E. Barry Troughton1, Yu-Tai Tao1, Joseph Evall1  +2 moreInstitutions (2)
Abstract: : Long-chain alkanethiols, HS(CH2)nX, adsorb from solution onto gold surfaces and form ordered, oriented monolayer films. The properties of the interfaces between the films and liquids are largely independent of chain length when n > 10; in particular, wetting is not directly influenced by the proximity of the underlying gold substrate. The specific interaction of gold with sulfur and other soft nucleophiles and its low reactivity toward most hard acids and bases make it possible to vary the structure of the terminal group, X, widely and thus permit the introduction of a great range of functional groups into a surface. Studies of wettability of these monolayers, and of their composition using X-ray photoelectron spectroscopy (XPS), indicate that the monolayers are oriented with the tail group, X, exposed at the monolayer-air or monolayer- liquid interface. The adsorption of simple n-alkanethiols generates hydrophobic surfaces whose free energy (19 mJ/sq. m) is the lowest of any hydrocarbon surface studied to date. Measurement of contact angles is a useful tool for studying the structure and chemistry of the outermost few angstroms of a surface. This work used contact angles and optical ellipsometry to study the kinetics of adsorption of monolayer films and to examine the experimental conditions necessary for the formation of high-quality films. more

Topics: Monolayer (61%), Wetting (53%), Contact angle (53%) more

3,116 Citations

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Lei Jiang

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