Rheological changes during a urethane network polymerization

Stephen D. Lipshitz, Christopher W. Macosko

Research output: Contribution to journalArticlepeer-review

117 Scopus citations

Abstract

Trifunctional poly‐ε‐caprolactone polyol was polymerized with a chain‐extended 1,6‐hexane diisocyanate, and the rheology followed by cone and plate flow. Viscosity was found to be independent of shear rate up to at least 102 N.s/m2 (103 poise) and 30s−1. Extent of reaction was monitored by a periodic titration for isocyanate groups. Using branching theory, viscosity was related to extent of reaction and temperature. Such relations should be useful for process models. Normal force data for the curing system are also reported.

Original languageEnglish (US)
Pages (from-to)803-810
Number of pages8
JournalPolymer Engineering & Science
Volume16
Issue number12
DOIs
StatePublished - Dec 1976

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