Preparation of copolyestercarbonates by the bischloroformate process
A process for preparing a polyestercarbonate copolymer which is nearly devoid of diarylcarbonates and that exhibits a glass transition temperature lower than bisphenol-A carbonate homopolymer, and that shows improved processability is herein described. The desired lower Tg and improved flow can be a...
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creator | FONTANA, LUCA PIETRO BUCKLEY, PAUL WILLIAM BODEN, EUGENE PAULING |
description | A process for preparing a polyestercarbonate copolymer which is nearly devoid of diarylcarbonates and that exhibits a glass transition temperature lower than bisphenol-A carbonate homopolymer, and that shows improved processability is herein described. The desired lower Tg and improved flow can be achieved by the polycondensation of a dihydric phenol an aliphatic dicarboxylic acid and a carbonate forming reagent. In the claimed process a dihydric phenol is phosgenated to form chloroformate end-capped oligomers which are then polycondensed after the addition of a chain stopper and a carbonate forming reagent. The aliphatic dicarboxylic acid may be introduced in the beginning or after the formation of the chloroformates. |
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The desired lower Tg and improved flow can be achieved by the polycondensation of a dihydric phenol an aliphatic dicarboxylic acid and a carbonate forming reagent. In the claimed process a dihydric phenol is phosgenated to form chloroformate end-capped oligomers which are then polycondensed after the addition of a chain stopper and a carbonate forming reagent. 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The desired lower Tg and improved flow can be achieved by the polycondensation of a dihydric phenol an aliphatic dicarboxylic acid and a carbonate forming reagent. In the claimed process a dihydric phenol is phosgenated to form chloroformate end-capped oligomers which are then polycondensed after the addition of a chain stopper and a carbonate forming reagent. 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The desired lower Tg and improved flow can be achieved by the polycondensation of a dihydric phenol an aliphatic dicarboxylic acid and a carbonate forming reagent. In the claimed process a dihydric phenol is phosgenated to form chloroformate end-capped oligomers which are then polycondensed after the addition of a chain stopper and a carbonate forming reagent. The aliphatic dicarboxylic acid may be introduced in the beginning or after the formation of the chloroformates.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | Preparation of copolyestercarbonates by the bischloroformate process |
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