Mikroyannidis, 1993 - Google Patents
Synthesis and curing of heat-resistant homopolyamide and copolyamides containing enamino nitrile segmentsMikroyannidis, 1993
- Document ID
- 9280015535714844970
- Author
- Mikroyannidis J
- Publication year
- Publication venue
- European polymer journal
External Links
Snippet
A new aminocarboxylic acid bearing an enamino nitrile segment was used as starting material for the preparation of modified homopolyamide and various copolyamides. The polycondensations were carried out by the phosphorylation method. Poly (benzamide) was …
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 C=1C=CC=CC=1C/C=C(/C#N)NC1=CC=CC=C1 0 title abstract description 18
Classifications
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- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
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- C—CHEMISTRY; METALLURGY
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- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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