Jingjing Zhao, Wenhui Wang, Chenguang Liu, Aihua He
{"title":"结晶反式-1,4聚丁二烯-共异戊二烯嵌段共聚物(tir)改性天然橡胶阻燃复合材料的研究","authors":"Jingjing Zhao, Wenhui Wang, Chenguang Liu, Aihua He","doi":"10.1016/j.polymdegradstab.2025.111409","DOIUrl":null,"url":null,"abstract":"<div><div>The flame retardancy of simple mechanical blending of trans-1,4-poly (butadiene-co-isoprene) block copolymer rubber (TBIR) with natural rubber (NR) and intumescent flame retardant (IFR) was investigated in this work. Compared with NR@IFR composite materials, the mechanical properties of NR/TBIR@IFR composite materials had been significantly improved. Especially, as the addition amount of TBIR increased, the 100 % tensile fatigue life was enhanced by 129.3 %, resolving the issue of mechanical property deterioration caused by additive flame retardants. The limit oxygen index (LOI) value of NR/TBIR@IFR was slightly improved and passed the UL-94 Vertical Burning test, fulfilling the requirement of self-extinguishing when removed from the fire. After the addition of TBIR, the peak heat release rate (PHRR) of the NR/TBIR@IFR system decreased from 295 kW/m<sup>2</sup> to 228.8 kW/m<sup>2</sup>, and the total heat release rate (THR) dropped from 118.11 MJ/m<sup>2</sup> to 99.32 MJ/m<sup>2</sup>. The flame retardant mechanism of the material after adding TBIR was analyzed by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and Raman spectroscopy. The research results showed that TBIR, by synergistically constructing a network structure with uniformly dispersed flame retardants, promoted the rapid formation of a continuous and dense carbon layer, effectively suppressing the combustion behavior of NR composites in both condensed and gas phases. The addition of TBIR not only improved the dispersion of flame retardants in the rubber matrix but also enhanced the flame retardant and mechanical properties of NR composite materials through interfacial synergistic effects. It provided a new environmentally friendly strategy for the preparation of flame retardant rubber materials for high-fatigue service environments.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"239 ","pages":"Article 111409"},"PeriodicalIF":6.3000,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigation into the flame retardant composite of natural rubber modified by crystalline trans-1,4-poly(butadiene-co-isoprene) block copolymer (TBIR)\",\"authors\":\"Jingjing Zhao, Wenhui Wang, Chenguang Liu, Aihua He\",\"doi\":\"10.1016/j.polymdegradstab.2025.111409\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The flame retardancy of simple mechanical blending of trans-1,4-poly (butadiene-co-isoprene) block copolymer rubber (TBIR) with natural rubber (NR) and intumescent flame retardant (IFR) was investigated in this work. Compared with NR@IFR composite materials, the mechanical properties of NR/TBIR@IFR composite materials had been significantly improved. Especially, as the addition amount of TBIR increased, the 100 % tensile fatigue life was enhanced by 129.3 %, resolving the issue of mechanical property deterioration caused by additive flame retardants. The limit oxygen index (LOI) value of NR/TBIR@IFR was slightly improved and passed the UL-94 Vertical Burning test, fulfilling the requirement of self-extinguishing when removed from the fire. After the addition of TBIR, the peak heat release rate (PHRR) of the NR/TBIR@IFR system decreased from 295 kW/m<sup>2</sup> to 228.8 kW/m<sup>2</sup>, and the total heat release rate (THR) dropped from 118.11 MJ/m<sup>2</sup> to 99.32 MJ/m<sup>2</sup>. The flame retardant mechanism of the material after adding TBIR was analyzed by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and Raman spectroscopy. The research results showed that TBIR, by synergistically constructing a network structure with uniformly dispersed flame retardants, promoted the rapid formation of a continuous and dense carbon layer, effectively suppressing the combustion behavior of NR composites in both condensed and gas phases. The addition of TBIR not only improved the dispersion of flame retardants in the rubber matrix but also enhanced the flame retardant and mechanical properties of NR composite materials through interfacial synergistic effects. It provided a new environmentally friendly strategy for the preparation of flame retardant rubber materials for high-fatigue service environments.</div></div>\",\"PeriodicalId\":406,\"journal\":{\"name\":\"Polymer Degradation and Stability\",\"volume\":\"239 \",\"pages\":\"Article 111409\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-05-03\",\"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/S0141391025002381\",\"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/S0141391025002381","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Investigation into the flame retardant composite of natural rubber modified by crystalline trans-1,4-poly(butadiene-co-isoprene) block copolymer (TBIR)
The flame retardancy of simple mechanical blending of trans-1,4-poly (butadiene-co-isoprene) block copolymer rubber (TBIR) with natural rubber (NR) and intumescent flame retardant (IFR) was investigated in this work. Compared with NR@IFR composite materials, the mechanical properties of NR/TBIR@IFR composite materials had been significantly improved. Especially, as the addition amount of TBIR increased, the 100 % tensile fatigue life was enhanced by 129.3 %, resolving the issue of mechanical property deterioration caused by additive flame retardants. The limit oxygen index (LOI) value of NR/TBIR@IFR was slightly improved and passed the UL-94 Vertical Burning test, fulfilling the requirement of self-extinguishing when removed from the fire. After the addition of TBIR, the peak heat release rate (PHRR) of the NR/TBIR@IFR system decreased from 295 kW/m2 to 228.8 kW/m2, and the total heat release rate (THR) dropped from 118.11 MJ/m2 to 99.32 MJ/m2. The flame retardant mechanism of the material after adding TBIR was analyzed by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), and Raman spectroscopy. The research results showed that TBIR, by synergistically constructing a network structure with uniformly dispersed flame retardants, promoted the rapid formation of a continuous and dense carbon layer, effectively suppressing the combustion behavior of NR composites in both condensed and gas phases. The addition of TBIR not only improved the dispersion of flame retardants in the rubber matrix but also enhanced the flame retardant and mechanical properties of NR composite materials through interfacial synergistic effects. It provided a new environmentally friendly strategy for the preparation of flame retardant rubber materials for high-fatigue service environments.
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.