Chain Mobility and Progress in Medicine, Pharmaceuticals, and Polymer Science and Technology 1st edition by George Wypych – Ebook PDF Instant Download/DeliveryISBN: 1927885663, 9781927885666
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ISBN-10 : 1927885663
ISBN-13 : 9781927885666
Author: George Wypych
Chain Mobility and Progress in Medicine, Pharmaceuticals, and Polymer Science and Technology covers the core fundamentals and applications of chain movement, chain mobility, segmental mobility, segmental dynamics, and chain orientation in polymer science, medicine, pharmaceuticals, and other disciplines. The book starts by defining principal terms, then looks at the work of Pierre-Gilles de Gennes and his 1991 Nobel Prize in Physics for his work on polymer-chain motion. From there the book discusses the different mechanisms of chain motion of macromolecular substances, the conditions under which chains move, and the effects of these movements on properties of materials, such as chain alignment, chain orientation, creation of free volume, dimensional stability, and more. The final chapters provide insight on analytical methods of chain movement, chain movement phenomena in different polymers, and various fields of application. All concepts, findings, and applications are discussed in easy-to-understand language stripped of disciplinary slang, making the book accessible to researchers and practitioners across a variety of scientific fields.
Chain Mobility and Progress in Medicine, Pharmaceuticals, and Polymer Science and Technology 1st Table of contents:
Chapter 1: INTRODUCTION. NOBEL PRIZE JUSTIFICATION FOR PIERRE-GILLES DE GENNES
Chapter 2: ANALYSIS OF EXISTING PUBLICATIONS
Chapter 3: MECHANISMS OF CHAIN MOTION OF MACROMOLECULAR SUBSTANCES
3.1 BEAD-CHAIN
3.2 BOND FLUCTUATION MODEL
3.3 BRILL TRANSITION
3.4 CHAIN DIFFUSION
3.5 CHAIN ORIENTATION
3.6 CHEMO-RESPONSIVE
3.7 COARSE-GRAINED
3.8 FLUORESCENCE BLOB
3.9 INTRA- VS. INTER-CHAIN
3.10 LIGHT-ACTIVATED
3.11 MAGNETIC-ACTIVATED
3.12 MICROWAVE
3.13 ROD CHAIN
3.14 ROUSE
3.15 SHAPE MEMORY
3.16 SLIP-LINK
3.17 STRAIN-INDUCED
3.18 TUBE MODELS
3.19 SUMMARY
Chapter 4: PARAMETERS (CONDITIONS) OF CHAIN MOVEMENT
4.1 ACTIVATION ENERGY
4.2 ANNEALING
4.3 CHAIN ADSORPTION
4.4 CHAIN SCISSION
4.5 COMPACTION PRESSURE
4.6 CONFIGURATION
4.7 CONFINEMENT DIMENSIONS
4.8 CROSSLINKS
4.9 CRYSTALLIZATION
4.10 DYNAMIC RATIO
4.11 ELECTROSTATIC INTERACTION
4.12 ENTANGLEMENTS
4.13 FREE SURFACE
4.14 FREE VOLUME
4.15 GLASS TRANSITION TEMPERATURE
4.16 HYDROPHILICITY
4.17 INTERACTION LENGTH
4.18 INTERFACE LAYER
4.19 LAYER THICKNESS
4.20 MICROSTRUCTURE
4.21 MISCIBLE AND IMMISCIBLE BLENDS
4.22 MOLECULAR WEIGHT
4.23 NANOPARTICLES
4.24 PACKING DENSITY
4.25 PRESENCE OF LOW MOLECULAR COMPOUNDS
4.26 PRESSURE
4.27 RELAXATION TIME
4.28 ROTATIONAL MOTION
4.29 SEGMENTAL DYNAMICS
4.30 SIDE CHAINS
4.31 TEMPERATURE
4.32 TIME OF CHAIN MOVEMENT
4.33 SUMMARY
Chapter 5: THE EFFECT OF CHAIN MOVEMENT ON THE PROPERTIES OF MATERIALS
5.1 CHAIN ALIGNMENT
5.2 CHAIN ORIENTATION
5.3 CREATION OF FREE VOLUME
5.4 CRYSTALLIZATION
5.5 DIMENSIONAL STABILITY
5.6 FORMATION OF POROUS STRUCTURES
5.7 IONIC TRANSPORT
5.8 MECHANICAL PROPERTIES
5.9 POLAR GROUPS
5.10 POLYMER BLENDS
5.11 POLYMER REDISTRIBUTION
5.12 PROTON TRANSFER
5.13 RELEASE RATE OF LOW MOLECULAR COMPOUNDS
5.14 REINFORCEMENT
5.15 SELF-HEALING
5.16 SOUND ATTENUATION
5.17 STERIC HINDRANCE
5.18 STORAGE MODULUS
5.19 SWELLING
5.20 THERMAL EXPANSION
5.21 THERMAL STABILITY
5.22 WEAR
5.25 SUMMARY
Chapter 6: SIGNIFICANT ANALYTICAL METHODS OF STUDY
6.1 ATOMIC FORCE MICROSCOPY
6.2 IN SITU SYNCHROTRON X-RAY
6.3 NMR IMAGING
6.4 NMR MOUSE
6.5 NMR SOLID-STATE
6.6 POSITRON ANNIHILATION SPECTROSCOPY
6.7 WAXD AND SAXS
Chapter 7: CHAIN MOBILITY IN DIFFERENT POLYMERS
7.1 ACRYLONITRILE-BUTADIENE-STYRENE
7.2 CELLULOSE
7.3 CELLULOSE ACETATE
7.4 CARRAGEENAN
7.5 CHITOSAN
7.6 ETHYL CELLULOSE
7.7 EPOXY
7.8 ETHYLENE-PROPYLENE DIENE TERPOLYMER
7.9 ETHYLENE-CO-TETRAFLUOROETHYLENE
7.10 ETHYLENE-VINYL ACETATE COPOLYMER
7.11 ETHYLENE-VINYL ALCOHOL COPOLYMER
7.12 GELATIN
7.13 HIGH-DENSITY POLYETHYLENE
7.14 LOW-DENSITY POLYETHYLENE
7.15 POLYAMIDE
7.16 POLY(ACRYLIC ACID)
7.17 POLYACRYLAMIDE
7.18 POLYACRYLONITRILE
7.19 POLYARYLATE
7.20 POLYBUTADIENE
7.21 POLY(BUTYLENE TEREPHTHALATE)
7.22 POLYCARBONATE
7.23 POLY( -CAPROLACTONE)
7.24 POLYDIMETHYLSILOXANE
7.25 POLY(ESTER CARBONATE)
7.26 POLYETHERETHERKETONE
7.27 POLY(ETHYLENE OXIDE)
7.28 POLY(ETHYLENE TEREPHTHALATE)
7.29 POLYETHYLENE, SILANE-CROSSLINKABLE
7.30 POLY(3-HYDROXYBUTYRATE)
7.31 POLYIMIDE
7.32 POLY(LACTIC ACID)
7.33 POLYMETHYLMETHACRYLATE
7.34 POLYPROPYLENE
7.35 POLY(P-PHENYLENE SULFIDE)
7.36 POLY(PROPYLENE TEREPHTHALATE)
7.37 POLY(1,4-PHENYLENE VINYLENE)
7.38 POLYSTYRENE
7.39 POLYSULFONE
7.40 POLYTETRAFLUOROETHYLENE
7.41 POLY(TRIMETHYLENE TEREPHTHALATE)
7.42 POLYURETHANE
7.43 POLY(VINYL ALCOHOL)
7.44 POLY(VINYL CHLORIDE)
7.45 POLY(VINYLIDENE FLUORIDE)
7.46 POLY(VINYL METHYL ETHER)
7.47 POLY(STYRENE-CO-BUTADIENE)
7.48 STYRENE-ETHYLENE-BUTYLENE-STYRENE TRIBLOCK COPOLYMER
7.49 STARCH
7.50 ULTRAHIGH MOLECULAR WEIGHT POLYETHYLENE
7.51 SUMMARY
Chapter 8: COMPARISON OF JUSTIFICATION OF NOBEL PRIZE BY THE SELECTION COMMITTEE WITH AC
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