{"title":"尼龙66降解与稳定研究进展","authors":"P. Thanki, R. Singh","doi":"10.1080/15583729808546033","DOIUrl":null,"url":null,"abstract":"1. INTRODUCTION The two principal commercial polyamides are poly(hexamethylene adipamide) (nylon 66) and polycaprolactam (nylon 6). They are produced by direct amidation of a diacid with a diamine and ring-opening polymerization of ɛ-caprolactam, respectively. Poly(hexamethylene adipamide) is synthesized by hexamethylene diamine and adipic acid [1]. A stoichiometric balance of amine carboxylic group is readily obtained by the preliminary formation of a 1:1 ammonium salt:","PeriodicalId":16139,"journal":{"name":"Journal of Macromolecular Science-reviews in Macromolecular Chemistry and Physics","volume":"211 1","pages":"595-614"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"19","resultStr":"{\"title\":\"Progress in the Area of Degradation and Stabilization of Nylon 66\",\"authors\":\"P. Thanki, R. Singh\",\"doi\":\"10.1080/15583729808546033\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"1. INTRODUCTION The two principal commercial polyamides are poly(hexamethylene adipamide) (nylon 66) and polycaprolactam (nylon 6). They are produced by direct amidation of a diacid with a diamine and ring-opening polymerization of ɛ-caprolactam, respectively. Poly(hexamethylene adipamide) is synthesized by hexamethylene diamine and adipic acid [1]. A stoichiometric balance of amine carboxylic group is readily obtained by the preliminary formation of a 1:1 ammonium salt:\",\"PeriodicalId\":16139,\"journal\":{\"name\":\"Journal of Macromolecular Science-reviews in Macromolecular Chemistry and Physics\",\"volume\":\"211 1\",\"pages\":\"595-614\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"19\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Macromolecular Science-reviews in Macromolecular Chemistry and Physics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/15583729808546033\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Macromolecular Science-reviews in Macromolecular Chemistry and Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/15583729808546033","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Progress in the Area of Degradation and Stabilization of Nylon 66
1. INTRODUCTION The two principal commercial polyamides are poly(hexamethylene adipamide) (nylon 66) and polycaprolactam (nylon 6). They are produced by direct amidation of a diacid with a diamine and ring-opening polymerization of ɛ-caprolactam, respectively. Poly(hexamethylene adipamide) is synthesized by hexamethylene diamine and adipic acid [1]. A stoichiometric balance of amine carboxylic group is readily obtained by the preliminary formation of a 1:1 ammonium salt: