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Polymer Dynamics and Relaxation [Kõva köide]

(University of Utah), (University of Utah)
  • Formaat: Hardback, 266 pages, kõrgus x laius x paksus: 244x170x16 mm, kaal: 630 g
  • Ilmumisaeg: 13-Sep-2007
  • Kirjastus: Cambridge University Press
  • ISBN-10: 0521814197
  • ISBN-13: 9780521814195
Teised raamatud teemal:
  • Formaat: Hardback, 266 pages, kõrgus x laius x paksus: 244x170x16 mm, kaal: 630 g
  • Ilmumisaeg: 13-Sep-2007
  • Kirjastus: Cambridge University Press
  • ISBN-10: 0521814197
  • ISBN-13: 9780521814195
Teised raamatud teemal:
Boyd and Smith (both at the U. of Utah) have written an authoritative text describing the relaxation processes of polymers and the many methods used for their study that will be essential reading for researchers and graduate students of materials science, physics, and chemistry. The initial 5 chapters are devoted to methodology, with descriptions of mechanical and dielectric relaxation, NMR spectroscopy, dynamic neutron scattering, and molecular dynamics simulations of amorphous polymers. The three stages from primary transition region, secondary (subglass) relaxations, and the transition from melt to glass of amorphous polymers are described in separate chapters, with discussion of the molecular basis of the transition from melt to glass. The volume concludes with discussion of semi-crystalline polymers and miscible polymer blends, including the models for miscible blend dynamics. Two appendices describe the Rouse model and site models for localized relaxation. Annotation ©2008 Book News, Inc., Portland, OR (booknews.com)

A detailed discussion on the different types of relaxation processes and the experimental methods used to study them.

Polymers exhibit a range of physical characteristics, from rubber-like elasticity to the glassy state. These particular properties are controlled at the molecular level by the mobility of the structural constituents. Remarkable changes in mobility can be witnessed with temperature, over narrow, well defined regions, termed relaxation processes. This is an important, unique phenomenon controlling polymer transition behaviour and is described here at an introductory level. The important types of relaxation processes from amorphous to crystalline polymers and polymeric miscible blends are covered, in conjunction with the broad spectrum of experimental methods used to study them. In-depth discussion of molecular level interpretation, including recent advances in atomistic level computer simulations and applications to molecular mechanism elucidation, are discussed. The result is a self-contained, up-to-date approach to polymeric interpretation suitable for researchers in materials science, physics and chemistry interested in the relaxation processes of polymeric systems.

Arvustused

Review of the hardback: 'The authors have a real gift for conveying the gist of an idea intelligently and effectively the book is consistently accessible and clear-headed in a way that can engage many an undergraduate's interest warmly recommended. Boyd and Smith have done a good job of explaining the problems and will certainly get you thinking.' Current Engineering Practice

Muu info

A detailed discussion on the different types of relaxation processes and the experimental methods used to study them.
Preface ix
Part I Methodology
1(80)
Mechanical relaxation
3(24)
Regimes of behavior
3(2)
Superposition principle
5(1)
Relaxation modulus
5(1)
Simple stress relaxation
6(1)
Dynamic modulus
7(2)
Interconversion of stress relaxation and dynamic modulus
9(2)
Representation of the relaxation function: single relaxation time (SRT)
11(2)
Relaxations in polymeric materials tend to be ``broad''
13(1)
Distribution of relaxation times
14(1)
Relaxation spectrum from ER(t)
15(3)
Creep compliance
18(1)
Dynamic compliance
19(2)
Representation of the retardation function
21(1)
Summary of the data transformations illustrated
22(5)
Appendix A1 A brief summary of elasticity
23(3)
References
26(1)
Dielectric relaxation
27(17)
Dielectric permittivity
27(3)
Measurement of dielectric permittivity
30(1)
Time dependence of polarization: reorientation of permanent dipoles
31(2)
Polarization and permittivity in time dependent electric fields
33(2)
Empirical representations of the dielectric permittivity
35(9)
References
43(1)
NMR spectroscopy
44(13)
NMR basics
45(2)
The pulsed NMR method
47(2)
NMR relaxation measurements
49(5)
NMR exchange spectroscopy
54(3)
References
56(1)
Dynamic neutron scattering
57(13)
Neutron scattering basics
57(6)
Time-of-flight (TOF) and backscattering QENS
63(3)
Neutron spin echo (NSE) spectroscopy
66(4)
References
69(1)
Molecular dynamics (MD) simulations of amorphous polymers
70(11)
A brief history of atomistic MD simulations of amorphous polymers
70(1)
The mechanics of MD simulations
71(4)
Studying relaxation processes using atomistic MD simulations
75(1)
Classical atomistic force fields
76(5)
References
79(2)
Part II Amorphous polymers
81(116)
The primary transition region
83(37)
Mechanical relaxation
83(7)
Dielectric relaxation
90(6)
Mechanical vs. dielectric relaxation
96(8)
NMR relaxation
104(6)
Neutron scattering
110(10)
References
118(2)
Secondary (subglass) relaxations
120(22)
Occurrence of mechanical and dielectric secondary processes
120(1)
Complexity and multiplicity of secondary processes
121(8)
Flexible side group motion as a source of secondary relaxation
129(9)
NMR spectroscopy studies of flexible side group motion
138(4)
References
140(2)
The transition from melt to glass and its molecular basis
142(55)
Experimental description
142(15)
Molecular basis
157(40)
References
194(3)
Part III Complex systems
197(47)
Semi-crystalline polymers
199(28)
Phase assignment
200(9)
Effect of crystal phase presence on amorphous fraction relaxation
209(5)
Relaxations in semi-crystalline polymers with a crystal phase relaxation
214(9)
NMR insights
223(4)
References
226(1)
Miscible polymer blends
227(17)
Poly(isoprene)/poly(vinyl ethylene) (PI/PVE) blends
228(1)
Models for miscible blend dynamics
229(4)
MD simulations of model miscible blends
233(6)
PI/PVE blends revisited
239(5)
References
243(1)
Appendix AI The Rouse model
244(4)
Formulation and normal modes
244(1)
Establishment of Rouse parameters for a real polymer
245(1)
The viscoelastic response of a Rouse chain
245(1)
Bead displacements and the coherent single-chain structure factor
246(2)
References
247(1)
Appendix AII Site models for localized relaxation
248(5)
Dipolar relaxation in terms of site models
248(3)
Mechanical relaxation in terms of site models
251(2)
References
252(1)
Index 253


Richard H. Boyd is a Distinguished Professor Emeritus of Materials Science and Engineering and of Chemical Engineering at the University of Utah. He was awarded the Polymer Physics Prize from the American Physical Society and is the author of over 150 technical papers and book chapters. Grant D. Smith is a Professor at the University of Utah. He has been awarded the NSF Career Award and the Outstanding Research Contribution award from the Eloret Insititute. He is also the author or co-author of over 170 papers.