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New polymer systems: Chain extension by dianhydridesThe results are presented for a systematic investigation on the use of anhydrides to prepare stable elastomeric materials for space use, under mild reaction conditions. The three anhydrides investigated were found to provide effective chain extension of hydroxy-terminated poly(alkylene oxides) and poly(butadienes). These were tetrahydrofuran tetracarboxylic dianhydride, pyromellitic dianhydride, and benzophenone tetracarboxylic diahydride. The most effective catalyst investigated was ferric acetylacetonate, which resulted in chain extension at 333 K (60 C). One feature of these anhydride reactants is that they are difunctional as anhydrides, but tetrafunctional if conditions are selected that lead to reaction of all carboxyl groups. Therefore, chain extension can be effected and then followed by crosslinking via the residual carboxyl groups.
Document ID
19720010249
Acquisition Source
Legacy CDMS
Document Type
Reprint (Version printed in journal)
Authors
Rhein, R. A.
(Jet Propulsion Lab., California Inst. of Tech. Pasadena, CA, United States)
Ingham, J. D.
(Jet Propulsion Lab., California Inst. of Tech. Pasadena, CA, United States)
Date Acquired
August 6, 2013
Publication Date
January 1, 1972
Publication Information
Publication: JPL Quart. Tech. Rev., Vol. 1, No. 4
Subject Category
Chemistry
Accession Number
72N17899
Distribution Limits
Public
Copyright
Public Use Permitted.
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