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Synthesis and degradation of model network polymers

Theoretical expressions essentially based on the Flory-Stockmayer statistics of gelation were experimentally examined for their applicability beyond the gel point. By studying the crosslinking process of a polyester network formed from 1,3,5-benzenetriacetic acid and 1,10-decamethylene glycol beyond the gel point, the validity of the expressions was quantitatively confirmed, and their limitations were delineated. / On stepwise degradation of a similar network, increasingly large soluble fractions were obtained at each step, and their weight-average molecular weights increased as the degelation point was approached. The molecular weights and distributions of these fractions were in close quantitative agreement with theory, i.e., they represented a near-mirror image of the molecular weights of sol fractions obtained on crosslinking beyond the gel point. Similar results were obtained by degrading a network prepared by the random crosslinking of monodisperse primary chains of polystyrene. / Experimental support was thus obtained for treating random network degradation by reversing the statistics of the Flory-Stockmayer theory of gelation.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:QMM.72032
Date January 1985
CreatorsArgyropoulos, Dimitris S.
PublisherMcGill University
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Formatapplication/pdf
CoverageDoctor of Philosophy (Department of Chemistry.)
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
Relationalephsysno: 000227267, proquestno: AAINL24029, Theses scanned by UMI/ProQuest.

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