Neutron spin echo spectroscopy, viscoelasticity, rheology

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 importa...

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Muut tekijät: Ewen, B. (Toimittaja), Mours, Marian (Toimittaja), Richter, Dieter, 1947-...., physicien (Toimittaja)
Aineistotyyppi: Livre numérique
Kieli:Anglais
Julkaistu: Berlin ; Paris [etc.] : Springer-Verlag Berlin Heidelberg : Springer e-books [20..].
Cham : Springer Nature
Sarja:Advances in polymer science 134
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Huomautus: Archives Springer e-books (Licence nationale)
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Edition sous un autre format:• Neutron spin echo spectroscopy. Viscoelasticity. Rheology, with contributions by B. Ewen, M. Mours, D. Richter. T. Shiga, H.H. Winter, Berlin, Springer, 1997, 1 vol. (248 p.), Advances in polymer science, 3-540-62713-8
• Neutron Spin Echo Spectroscopy Viscoelasticity Rheology, Texte imprimé, 9783662148020
• Neutron Spin Echo Spectroscopy Viscoelasticity Rheology, Texte imprimé, 9783662148037
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Yhteenveto: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.
Huomautukset:Archives Springer e-books (Licence nationale)
Archives Springer e-books (Licence nationale)
ISBN:9783540684497 (PDF)
ISSN:1436-5030
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