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Transition diagrams for a liquid crystalline thermoset containing a rigid-rod epoxy
by
Douglas, Elliot P.
, Lee, Jun Young
, Cho, Seunghyun
in
Applied sciences
/ Chemical properties
/ Diagrams
/ Epoxy compounds
/ Epoxy resins
/ Exact sciences and technology
/ Liquid crystal polymers
/ Polymer industry, paints, wood
/ Polymer processing
/ Properties and testing
/ Structure
/ Technology of polymers
/ Thermosetting composites
/ Transitions
2006
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Transition diagrams for a liquid crystalline thermoset containing a rigid-rod epoxy
by
Douglas, Elliot P.
, Lee, Jun Young
, Cho, Seunghyun
in
Applied sciences
/ Chemical properties
/ Diagrams
/ Epoxy compounds
/ Epoxy resins
/ Exact sciences and technology
/ Liquid crystal polymers
/ Polymer industry, paints, wood
/ Polymer processing
/ Properties and testing
/ Structure
/ Technology of polymers
/ Thermosetting composites
/ Transitions
2006
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Do you wish to request the book?
Transition diagrams for a liquid crystalline thermoset containing a rigid-rod epoxy
by
Douglas, Elliot P.
, Lee, Jun Young
, Cho, Seunghyun
in
Applied sciences
/ Chemical properties
/ Diagrams
/ Epoxy compounds
/ Epoxy resins
/ Exact sciences and technology
/ Liquid crystal polymers
/ Polymer industry, paints, wood
/ Polymer processing
/ Properties and testing
/ Structure
/ Technology of polymers
/ Thermosetting composites
/ Transitions
2006
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Transition diagrams for a liquid crystalline thermoset containing a rigid-rod epoxy
Journal Article
Transition diagrams for a liquid crystalline thermoset containing a rigid-rod epoxy
2006
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Overview
The liquid crystalline thermoset monomers 4,4′‐diglycidyloxy‐α‐methylstilbene (DOMS) and D2A1 that resulted from the reaction between DOMS and aniline were synthesized. DOMS was cured with sulfanilamide and D2A1 was cured with catalytic curing agent 1‐methyl imidazole. Transition diagrams have been constructed and the percent conversion data were determined from dynamic differential scanning calorimetry scan to examine the applicability of Flory's gelation theory. The results reveal that even though the amount of reaction that occurs in the liquid crystalline phase is different at different cure temperatures, the isoconversion theory of gelation fits quite well. POLYM. ENG. SCI. 46:623–629, 2006. © 2006 Society of Plastics Engineers
Publisher
Wiley Subscription Services, Inc., A Wiley Company,Wiley Subscription Services,Society of Plastics Engineers, Inc,Blackwell Publishing Ltd
Subject
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