Yu Feng , Doudou Li , Weiwei He , Lifen Zhang , Zhenping Cheng
{"title":"环氧树脂用高效聚磷腈共价三嗪阻燃剂:苯环的双面作用及阻燃机理","authors":"Yu Feng , Doudou Li , Weiwei He , Lifen Zhang , Zhenping Cheng","doi":"10.1016/j.polymdegradstab.2025.111530","DOIUrl":null,"url":null,"abstract":"<div><div>Despite significant progress has been made, fabricating organic flame retardants with excellent fire resistance at low level addition remains a challenging task. In this work, four polyphosphazene covalent triazine (PCT) flame retardants which are named as MTP, B-MTP, CTP and B-CTP respectively, are synthesized through simple precipitation polymerization, and introduced into epoxy resin (EP) to investigate the anti-flammability. An addition of 3 wt% B-MTP significantly improves the char residue at 800 °C and enhances the thermal stability of EP. In addition, the peak heat release rate (p-HRR), fire growth index (FGI), total smoke production (TSP), and total heat release (THR) decrease by 40.2 %, 64.9 %, 32.3 %, and 28.8 %, respectively. Subsequently, the flame-ratardant mechanisms of PCT with different structures are studied in detail using thermogravimetric analysis-Fourier transform infrared, X-ray photoelectron, and Raman spectroscopy. Interestingly, for the first time the double-faced role of benzene ring in the flame-ratardant performance of the prepared PCT flame retardants is discovered, probably due to the delayed noncombustible gas generation mechanism. This work provides theoretical support for future construction of efficient PCT based flame retardants.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"241 ","pages":"Article 111530"},"PeriodicalIF":6.3000,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient polyphosphazene covalent triazine flame retardants for epoxy resin: Double-faced role of benzene ring and flame-ratardant mechanism\",\"authors\":\"Yu Feng , Doudou Li , Weiwei He , Lifen Zhang , Zhenping Cheng\",\"doi\":\"10.1016/j.polymdegradstab.2025.111530\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Despite significant progress has been made, fabricating organic flame retardants with excellent fire resistance at low level addition remains a challenging task. In this work, four polyphosphazene covalent triazine (PCT) flame retardants which are named as MTP, B-MTP, CTP and B-CTP respectively, are synthesized through simple precipitation polymerization, and introduced into epoxy resin (EP) to investigate the anti-flammability. An addition of 3 wt% B-MTP significantly improves the char residue at 800 °C and enhances the thermal stability of EP. In addition, the peak heat release rate (p-HRR), fire growth index (FGI), total smoke production (TSP), and total heat release (THR) decrease by 40.2 %, 64.9 %, 32.3 %, and 28.8 %, respectively. Subsequently, the flame-ratardant mechanisms of PCT with different structures are studied in detail using thermogravimetric analysis-Fourier transform infrared, X-ray photoelectron, and Raman spectroscopy. Interestingly, for the first time the double-faced role of benzene ring in the flame-ratardant performance of the prepared PCT flame retardants is discovered, probably due to the delayed noncombustible gas generation mechanism. This work provides theoretical support for future construction of efficient PCT based flame retardants.</div></div>\",\"PeriodicalId\":406,\"journal\":{\"name\":\"Polymer Degradation and Stability\",\"volume\":\"241 \",\"pages\":\"Article 111530\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-07-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Degradation and Stability\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0141391025003593\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141391025003593","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Efficient polyphosphazene covalent triazine flame retardants for epoxy resin: Double-faced role of benzene ring and flame-ratardant mechanism
Despite significant progress has been made, fabricating organic flame retardants with excellent fire resistance at low level addition remains a challenging task. In this work, four polyphosphazene covalent triazine (PCT) flame retardants which are named as MTP, B-MTP, CTP and B-CTP respectively, are synthesized through simple precipitation polymerization, and introduced into epoxy resin (EP) to investigate the anti-flammability. An addition of 3 wt% B-MTP significantly improves the char residue at 800 °C and enhances the thermal stability of EP. In addition, the peak heat release rate (p-HRR), fire growth index (FGI), total smoke production (TSP), and total heat release (THR) decrease by 40.2 %, 64.9 %, 32.3 %, and 28.8 %, respectively. Subsequently, the flame-ratardant mechanisms of PCT with different structures are studied in detail using thermogravimetric analysis-Fourier transform infrared, X-ray photoelectron, and Raman spectroscopy. Interestingly, for the first time the double-faced role of benzene ring in the flame-ratardant performance of the prepared PCT flame retardants is discovered, probably due to the delayed noncombustible gas generation mechanism. This work provides theoretical support for future construction of efficient PCT based flame retardants.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.