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Organic coatings : science and technology / Frank N. Jones, Mark E. Nichols, S. Peter Pappas.
- Format:
- Book
- Author/Creator:
- Jones, Frank N., 1936- author.
- Nichols, Mark E., author.
- Pappas, S. Peter, author.
- Language:
- English
- Subjects (All):
- Plastic coatings.
- Physical Description:
- 1 online resource (515 pages) : illustrations
- Edition:
- Fourth edition.
- Place of Publication:
- Hoboken, New Jersey : Wiley, 2017.
- Summary:
- The definitive guide to organic coatings, thoroughly revised and updated-now with coverage of a range of topics not covered in previous editions Organic Coatings: Science and Technology, Fourth Edition offers unparalleled coverageof organic coatings technology and its many applications. Written by three leading industry experts (including a new, internationally-recognized coatings scientist) it presents a systematic survey of the field, revises and updates the material from the previous edition, and features new or additional treatment of such topics as superhydrophobic, ice-phobic, antimicrobial, and self-healing coatings; sustainability, artist paints, and exterior architectural primers. making it even more relevant and useful for scientists and engineers in the field, as well as for students in coatings courses. The book incorporates up-to-date coverage of recent developments in the field with detailed discussions of the principles underlying the technology and their applications in the development, production, and uses of organic coatings. All chapters in this new edition have been updated to assure consistency and to enable extensive cross-referencing. The material presented is also applicable to the related areas of printing inks and adhesives, as well as areas within the plastics industry. This new edition * Completely revises outdated chapters to ensure consistency and to enable extensive cross-referencing * Correlates the empirical technology of coatings with the underlying science throughout * Provides expert troubleshooting guidance for coatings scientists and technologists * Features hundreds of illustrative figures and extensive references to the literature * A new, internationally-recognized coatings scientist brings fresh perspective to the content. Providing a broad overview for beginners in the field of organic coatings and a handy reference for seasoned professionals, Organic Coatings: Science and Technology, Fourth Edition, gives you the information and answers you need, when you need them.
- Contents:
- Intro
- Title Page
- Copyright Page
- Contents
- Preface
- Chapter 1 Introduction to Coatings
- 1.1 Definitions and Scope
- 1.2 Types of Coatings
- 1.3 Composition of Coatings
- 1.4 Coating History
- 1.5 Commercial Considerations
- References
- Chapter 2 Polymerization and Film Formation
- 2.1 Polymers
- 2.1.1 Molecular Weight (MW)
- 2.1.2 Morphology and Glass Transition Temperature, Tg
- 2.2 Polymerization
- 2.2.1 Chain-Growth Polymerization
- 2.2.2 Step-Growth Polymerization
- 2.3 Film Formation
- 2.3.1 Film Formation by Solvent Evaporation from Solutions of Thermoplastic Binders
- 2.3.2 Film Formation from Solutions of Thermosetting Resins
- 2.3.3 Film Formation by Coalescence of Polymer Particles
- General References
- Chapter 3 Flow
- 3.1 Shear Flow
- 3.2 Types of Shear Flow
- 3.3 Determination of Shear Viscosity
- 3.3.1 Capillary Viscometers
- 3.3.2 Rheometers
- 3.3.3 Rotating Disk Viscometers
- 3.3.4 Bubble Viscometers
- 3.3.5 Efflux Cups
- 3.3.6 Paddle Viscometers
- 3.4 Shear Viscosity of Resin Solutions
- 3.4.1 Temperature Dependence of Viscosity
- 3.4.2 Dilute Polymer Solution Viscosity
- 3.4.3 Concentrated Polymer Solution Viscosity
- 3.5 Viscosity of Liquids With Dispersed Phases
- 3.5.1 Thickeners for Latex Coatings
- 3.6 Other Modes of Flow
- 3.6.1 Turbulent Flow
- 3.6.2 Normal Force Flow
- 3.6.3 Extensional Flow
- Chapter 4 Mechanical Properties
- 4.1 Introduction
- 4.2 Basic Mechanical Properties
- 4.2.1 Glass Transition Temperature (Tg)
- 4.2.2 Viscoelasticity
- 4.2.3 Dynamic Mechanical Behavior
- 4.3 Fracture Mechanics
- 4.4 Abrasion, Scratch, and Mar Resistance
- 4.4.1 Abrasion Resistance
- 4.4.2 Scratch and Mar Resistance
- 4.5 Measurement of Mechanical Properties
- 4.6 Tests of Coatings on Substrates.
- 4.6.1 Field Exposure Tests
- 4.6.2 Laboratory Simulation Tests
- 4.6.3 Empirical Tests
- Chapter 5 Exterior Durability
- 5.1 Photoinitiated Oxidative Degradation
- 5.2 Photostabilization
- 5.2.1 UV Absorbers and Excited State Quenchers
- 5.2.2 Antioxidants
- 5.2.3 Hindered Amine Light Stabilizers
- 5.2.4 Pigmentation Effects
- 5.3 Degradation of Chlorinated Resins
- 5.4 Hydrolytic Degradation
- 5.5 Other Modes of Failure on Exterior Exposure
- 5.6 Testing For Exterior Durability
- 5.6.1 Natural Weathering
- 5.6.2 Accelerated Outdoor Exposure
- 5.6.3 Accelerated Laboratory Weathering Devices
- 5.6.4 Analysis of Coating Changes during Weathering
- 5.7 Service Life Prediction
- Chapter 6 Adhesion
- 6.1 Mechanisms of Adhesion
- 6.1.1 Surface Mechanical Effects on Adhesion
- 6.1.2 Relationships between Wetting and Adhesion
- 6.1.3 Chemical Interactions between Coatings and Surfaces
- 6.2 Mechanical Stresses and Adhesion
- 6.3 Adhesion to Metal Surfaces
- 6.3.1 Conversion Coating and Pretreatment of Metal Substrates
- 6.4 Characterization of Surfaces
- 6.5 Organic Chemical Treatment of Substrates to Enhance Adhesion
- 6.6 Covalent Bonding To Glass and Metal Substrates
- 6.7 Adhesion to Plastics and to Coatings
- 6.8 Testing for Adhesion
- Chapter 7 Corrosion Protection by Coatings
- 7.1 Corrosion Basics
- 7.2 Corrosion of Uncoated Steel
- 7.3 Corrosion Protection of Metals
- 7.3.1 Passivation: Anodic Protection
- 7.3.2 Cathodic Protection
- 7.3.3 Barrier Protection and Inhibition
- 7.4 Corrosion Protection by Intact Coatings
- 7.4.1 Critical Factors
- 7.4.2 Adhesion for Corrosion Protection
- 7.4.3 Factors Affecting Oxygen and Water Permeability
- 7.5 Corrosion Protection by Nonintact Films.
- 7.5.1 Minimizing Growth of Imperfections: Cathodic Delamination
- 7.5.2 Primers with Passivating Pigments
- 7.5.3 Cathodic Protection by Zinc-Rich Primers
- 7.5.4 Smart Corrosion Control Coatings
- 7.6 Evaluation and Testing
- Chapter 8 Acrylic Resins
- 8.1 Thermoplastic Acrylic Resins
- 8.2 Thermosetting Acrylic Resins
- 8.2.1 Hydroxy-Functional Acrylic Resins
- 8.2.2 Acrylics Having Other Functional Groups
- 8.3 Water-Reducible Thermosetting Acrylic Resins
- Chapter 9 Latexes
- 9.1 Emulsion Polymerization
- 9.1.1 Raw Materials for Emulsion Polymerization
- 9.1.2 Emulsion Polymerization Variables
- 9.1.3 Sequential Polymerization
- 9.2 Acrylic Latexes
- 9.3 Vinyl Ester Latexes
- 9.4 Thermosetting Latexes
- 9.4.1 One-Package Thermosetting Latex Coatings That Require Baking for Cure
- 9.4.2 Two-Package (2 K) Thermosetting Latex Coatings That Do Not Require Baking
- 9.4.3 One-Package Thermosetting Latex Coatings That Do Not Require Baking
- Chapter 10 Polyester Resins
- 10.1 Hydroxy-Terminated Polyester Resins for Conventional Solids Coatings
- 10.1.1 Selection of Polyols
- 10.1.2 Selection of Polyacids
- 10.2 Polyester Resins for High Solids Coatings
- 10.3 Carboxylic Acid-Terminated Polyester Resins
- 10.4 Carbamate-Functional Polyester Resins
- 10.5 Water-Reducible Polyester Resins
- 10.6 Polyester Resins for Powder Coatings
- Chapter 11 Amino Resins
- 11.1 Synthesis Of Melamine-Formaldehyde Resins
- 11.1.1 The Methylolation Reaction
- 11.1.2 The Etherification Reaction
- 11.1.3 Self-Condensation Reactions
- 11.2 Types of Mf Resins
- 11.3 Mf-Polyol Reactions in Coatings
- 11.3.1 Catalysis of MF-Polyol Reactions
- 11.3.2 Kinetics and Mechanism of MF-Polyol Co-condensation
- 11.3.3 Package Stability Considerations.
- 11.3.4 MF Resin Reactions with Carboxylic Acids, Urethanes, Carbamates, and Malonate-Blocked Isocyanates
- 11.4 Other Amino Resins
- 11.4.1 Urea-Formaldehyde Resins
- 11.4.2 Benzoguanamine-Formaldehyde Resins
- 11.4.3 Glycoluril-Formaldehyde Resins
- 11.4.4 Poly(meth)acrylamide- Formaldehyde Resins
- Chapter 12 Polyurethanes and Polyisocyanates
- 12.1 Reactions of Isocyanates
- 12.2 Kinetics of Reactions of Isocyanates with Alcohols
- 12.2.1 Noncatalyzed Reactions
- 12.2.2 Catalysts
- 12.2.3 Interrelationships in Catalysis
- 12.3 Isocyanates Used in Coatings
- 12.3.1 Aromatic Isocyanates
- 12.3.2 Aliphatic Isocyanates
- 12.4 Two-Package (2K) Solventborne Urethane Coatings
- 12.4.1 2K Polyurea Coatings
- 12.5 Blocked Isocyanates
- 12.5.1 Principles of Blocking and Deblocking
- 12.5.2 Blocking Groups
- 12.5.3 Catalysis of Blocked Isocyanate Coatings
- 12.6 Moisture-Curable Urethane Coatings
- 12.7 Waterborne Polyurethane Coatings
- 12.7.1 Polyurethane Dispersions
- 12.7.2 Acrylic/Polyurethane Blends and Hybrid Dispersions
- 12.7.3 2K Waterborne Urethanes
- 12.8 Hydroxy-Terminated Polyurethanes
- Chapter 13 Epoxy and Phenolic Resins
- 13.1 Epoxy Resins
- 13.1.1 Bisphenol A Epoxy Resins
- 13.1.2 Other Epoxy Resins
- 13.2 Amine Cross-Linked Epoxy Resins
- 13.2.1 Pot Life and Cure Time Considerations
- 13.2.2 Toxicity and Stoichiometric Considerations
- 13.2.3 Graininess and Blushing
- 13.2.4 Tg Considerations
- 13.2.5 Other Formulating Considerations
- 13.2.6 Waterborne Epoxy-Amine Systems
- 13.3 Other Cross-Linking Agents for Epoxy Resins
- 13.3.1 Phenols
- 13.3.2 Carboxylic Acids and Anhydrides
- 13.3.3 Hydroxyl Groups
- 13.3.4 Mercaptans
- 13.3.5 Homopolymerization
- 13.4 Water-Reducible Epoxy/Acrylic Graft Copolymers: Epoxy/Acrylic Hybrids
- 13.5 Epoxy Resin Phosphate Esters.
- 13.6 Phenolic Resins
- 13.6.1 Resole Phenolic Resins
- 13.6.2 Novolac Phenolic Resins
- 13.6.3 Ether Derivatives of Phenolic Resins
- Chapter 14 Drying Oils
- 14.1 Compositions of Natural Oils
- 14.2 Autoxidation and Cross-Linking
- 14.2.1 Nonconjugated Drying Oils
- 14.2.2 Catalysis of Autoxidation and Cross-Linking
- 14.2.3 Conjugated Drying Oils
- 14.3 Synthetic and Modified Drying Oils
- 14.3.1 Heat Bodied Oils, Blown Oils, and Dimer Acids
- 14.3.2 Varnishes
- 14.3.3 Synthetic Conjugated Oils
- 14.3.4 Esters of Higher Functionality Polyols
- 14.3.5 Maleated Oils
- 14.3.6 Vinyl-Modified Oils
- Chapter 15 Alkyd Resins
- 15.1 Oxidizing Alkyds
- 15.1.1 Monobasic Acid Selection
- 15.1.2 Polyol Selection
- 15.1.3 Dibasic Acid Selection
- 15.2 High Solids Oxidizing Alkyds
- 15.3 Waterborne Oxidizing Alkyds
- 15.3.1 Water-Reducible Alkyds
- 15.3.2 Alkyd Emulsions
- 15.4 Nonoxidizing Alkyds
- 15.5 Synthetic Procedures for Alkyd Resins
- 15.5.1 Synthesis from Oils or Fatty Acids
- 15.5.2 Process Variations
- 15.6 Modified Alkyds
- 15.7 Uralkyds and Other Autoxidizable Urethanes
- 15.7.1 Uralkyds
- 15.7.2 Autoxidizable Polyurethane Dispersions
- 15.8 Epoxy Esters
- Chapter 16 Silicon Derivatives
- 16.1 Silicones
- 16.1.1 Silicone Rubbers and Resins
- 16.1.2 Modified Silicone Resins
- 16.1.3 Silicone-Modified Resins
- 16.2 Reactive Silanes
- 16.3 Orthosilicates
- 16.3.1 Sol-Gel Coatings
- Chapter 17 Other Resins and Cross-Linkers
- 17.1 Halogenated Polymers
- 17.1.1 Solution-Grade Thermoplastic Vinyl Chloride Copolymers
- 17.1.2 Vinyl Chloride Dispersion Copolymers
- 17.1.3 Chlorinated Rubber, Chlorinated Ethylene/Vinyl Acetate Copolymers, and Chlorinated Polyolefins.
- 17.1.4 Fluorinated Polymers.
- Notes:
- Includes bibliographical references at the end of each chapters and index.
- Description based on print version record.
- ISBN:
- 9781523123711
- 1523123710
- 9781119337157
- 1119337151
- 9781119337218
- 1119337216
- 9781119337201
- 1119337208
- OCLC:
- 975176535
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