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Journal of Polymer Science Part A: Polymer Chemistry
Article

FT–IR spectroscopic study on the thermal and thermal oxidative degradation of nylons

C. H. Do

Polymer Research Institute and Department of Chemistry, Polytechnic University, 333 Jay St., Brooklyn, New York 11201

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E. M. Pearce

Corresponding Author

Polymer Research Institute and Department of Chemistry, Polytechnic University, 333 Jay St., Brooklyn, New York 11201

Polymer Research Institute and Department of Chemistry, Polytechnic University, 333 Jay St., Brooklyn, New York 11201
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B. J. Bulkin

Polymer Research Institute and Department of Chemistry, Polytechnic University, 333 Jay St., Brooklyn, New York 11201

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H. K. Reimschuessel

Corporate Research Center, Allied Corporation, Morristown, New Jersey 07960

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First published: September 1987
Cited by: 39

Abstract

The effects of heat and oxygen on nylon films were studied by FT–IR spectroscopy. Nylons 6, 66 and nylons containing carbonyl groups in either the diamine or the diacid moiety were prepared. Nylon films cast on aluminum were studied in an environmental chamber under controlled conditions. The progress of chemical and physical changes was monitored by FT–IR spectroscopy. Thermal energy caused largely an increase in crystallinity due to annealing and also an increase of nonhydrogen‐bonded amide groups, which seemed to entail mainly amide groups from the amorphous region. The intensities of IR absorption bands related to the folded structure reduced as soon as heating began. The IR spectra of the carbonyl groups formed by thermal oxidation showed band shapes that indicated that the formed carbonyl groups were of many different origins. The presence of keto groups purposely inserted into the backbone chains increased the rate of oxidation. Pyrolysis of the nylons was also studied to supplement data obtained at lower temperatures.

Number of times cited: 39

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