Neutron Spin Echo Spectroscopy Viscoelasticity Rheology (Advances in Polymer Science, 134, Band 134)

Ewen, B., M. Mours D. Richter u. a.:

ISBN 10: 3540627138 / ISBN 13: 9783540627135

Published by Springer, 1997

About this Item

255 p. Very good condition, nearly like new! Unread book. Retired library exemplar with library markings. Minimal traces of storage. Otherwise very good exemplar. 9783540627135 Sprache: Englisch Gewicht in Gramm: 508 Hardcover: 16.5 x 1.9 x 24.8 cm.

Seller Inventory # 227257

Bibliographic Details

• Title: Neutron Spin Echo Spectroscopy Viscoelasticity Rheology (Advances in Polymer Science, 134, Band 134)
• Publisher: Springer
• Publication Date: 1997
• Language: English
• ISBN 10: 3540627138
• ISBN 13: 9783540627135
• Binding: Hardcover
• Edition: 1.
• Seller catalogs:
  • Kunststofftechnik

About this title

Synopsis

Viscoelasticandtransportpropertiesofpolymersintheliquid(solution,melt)or liquid-like (rubber) state determine their processing and application to a large extent and are of basic physical interest [1―3]. An understanding of these dynamic properties at a molecular level, therefore, is of great importance. However,thisunderstandingiscomplicatedbythefactsthatdi?erentmotional processes may occur on di?erent length scales and that the dynamics are governed by universal chain properties as well as by the special chemical structure of the monomer units [4,5]. The earliest and simplest approach in this direction starts from Langevin equations with solutions comprising a spectrum of relaxation modes [1―4]. Special features are the incorporation of entropic forces (Rouse model, [6]) which relax uctuations of reduced entropy, and of hydrodynamic interactions (Zimm model, [7]) which couple segmental motions via long-range back ow elds in polymer solutions, and the inclusion of topological constraints or entanglements (reptation or tube model, [8―10]) which are mutually imposed within a dense ensemble of chains. Another approach, neglecting the details of the chemical structure and concentratingontheuniversalelementsofchainrelaxation,isbasedondynamic scalingconsiderations[4,11].Inparticularinpolymersolutions,thisapproach o?ers an elegant tool to specify the general trends of polymer dynamics, although it su?ers from the lack of a molecular interpretation. A real test of these theoretical approaches requires microscopic methods, which simultaneously give direct access to the space and time evolution of the segmental di?usion. Here, quasi-elastic scattering methods play a crucial role sincetheyallowthemeasurementofthecorrespondingcorrelationfunctions.Inparticular,thehigh-resolutionneutronspinecho(NSE)spectroscopy[12―15]is very suitable for such investigations since this method covers an appropriate range in time (0.005)t/ns)40) and space (r/nm [15). Furthermore, the possibilityoflabellingbyhydrogen-deuteriumexchangeallowstheobservation of single-chain behavior even in the melt.