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High performance polymers /
Annotation
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Norwich, NY :
William Andrew,
2014.
|
| Edición: | Second edition. |
| Colección: | Plastic design library.
|
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Half Title; PDL Series; Title Page; Copyright; Contents; Preface; Preface; Acknowledgments; 1 Carbazole Polymers; 1.1 Monomers; 1.1.1 N-Vinylcarbazole; 1.1.2 Nonlinear Optical Side Chain Monomers; 1.1.3 Molecular Glasses; 1.2 Polymerization and Fabrication; 1.2.1 Polymerization; 1.2.1.1 Poly(N-vinylcarbazole); 1.2.1.2 NVK/Pyrrol Composites; 1.2.2 Other Vinylcarbazole Compounds; 1.2.2.1 Grignard Coupling; 1.2.2.2 Anionic Polymerization; 1.2.2.3 Heck Cross Coupling; 1.2.2.4 Copolymers; 1.2.2.5 Solution Processing; 1.3 Properties; 1.3.1 Liquid Crystalline Phases.
- 1.3.1.1 Charge Transporting Materials1.3.1.2 Principle of Xerography; 1.3.2 Optical Properties; 1.3.2.1 Polarization Rotators; 1.3.2.2 Enhanced Photorefractive Performance; 1.3.2.3 Hologram Images; 1.3.2.4 Holographic Recording Medium; 1.3.2.5 Effect of Molecular Weight of PVK on Photorefractive Performance; 1.3.2.6 Fluorescence Quenching; 1.4 Applications; 1.4.1 Electrophotographic Films; 1.4.1.1 Photoconductivity; 1.4.1.2 TNF-PVK Complexes; 1.4.1.3 Photoconductive Copolymers; 1.4.1.4 Copolymers; 1.4.2 Polymeric Light-Emitting Diodes; 1.4.2.1 F�orster Energy Transfer; 1.4.2.2 Service Time.
- 1.4.2.3 Methods of Fabrication of LEDs1.4.2.4 Poly(fluorene)s; 1.4.2.5 NVK/PBD; 1.4.2.6 Functionalized Polymers; 1.4.2.7 Metal Complexes; 1.4.2.8 Mixed Dyes; 1.4.2.9 Multilayer Light-Emitting Diode; 1.4.2.10 Other Chromophores; 1.4.3 Organic Photorefractive Materials; 1.4.3.1 Photorefractive Formulations; 1.4.3.2 Holograms; 1.4.4 Photovoltaic Devices; 1.4.5 Amplified Spontaneous Emission; 1.4.6 Optical Elements; 1.4.7 Antistatic Polymer; 1.4.8 Other Applications; 1.4.8.1 Microscopic Imaging; 1.4.9 Analytical Applications; 1.4.10 Nanocomposites; 1.4.10.1 Poly(pyrrole)-Modified Nanocomposites.
- 1.4.10.2 Poly(aniline)-Modified Nanocomposites1.4.10.3 Carbon Nanotubes; 1.4.10.4 Clay Nanohybrids; 1.4.11 Fuel Cells; 1.4.12 Coatings; 1.4.13 Fibers; 1.5 Suppliers and Commercial Grades; 1.6 Safety; References; 2 Poly(p-xylylene)s; 2.1 Monomers; 2.1.1 Chlorine-Substituted Monomers; 2.2 Sulfide Modified Polymers; 2.3 Polymerization and Fabrication; 2.3.1 Chemical Vapor Deposition; 2.3.1.1 Fluor Containing Parylenes; 2.3.1.2 Copolymers; 2.3.1.3 Organic Transistors; 2.3.1.4 CMOS Devices; 2.3.1.5 Siloxane-Substituted Poly(p-Xylylene)s; 2.3.1.6 Soft Magnetic Composites.
- 2.3.2 Solution Polymerization2.3.3 Self-Assembly Polymerization; 2.4 Properties; 2.4.1 Mechanical Properties; 2.4.2 Electrical Properties; 2.5 Applications; 2.5.1 Coatings; 2.5.1.1 Coatings for Solder Powders; 2.5.1.2 Waveguide Coatings; 2.5.1.3 Reinforcement Layers; 2.5.1.4 Printed Circuit Boards; 2.5.2 Medical Applications; 2.5.2.1 Surface Modification; 2.5.2.2 Drug Release; 2.5.2.3 Modification of Poly(dimethylsiloxane) for Biomedical Applications; 2.5.2.4 Parylene Coating for Cardiac Pacemaker Electrodes; 2.5.2.5 Implants; 2.5.3 Microelectrode Arrays; 2.5.4 Nanocomposites.