{"title":"硅基烯基交联分子高性能阻燃热塑性硫化胶的性能及机理","authors":"Siqi Chen , Yihuimeng Xiong , Lijun Qian , Lijie Qu , Jingyu Wang , Wei Tang","doi":"10.1016/j.polymdegradstab.2025.111627","DOIUrl":null,"url":null,"abstract":"<div><div>A novel flame retardant was synthesized by introducing tetramethyl tetravinyl cyclotetrasiloxane (MVC) into the alkenyl-crosslinking structure formed by anhydrous piperazine and vinyl phosphoric acid, resulting in a silicon-based alkenyl-crosslinking molecule GMA-nMVC. The GMA-15 %MVC, with an optimal component ratio, enhanced the flame retardancy and mechanical properties of thermoplastic vulcanizate (TPV) composites. At 20 wt.% loading, the limiting oxygen index of the GMA-15 %MVC/MPP/TPV system reached 30.2 %, and both 3.2 mm and 1.6 mm samples passed UL 94 V-0. Compared to GMA/MPP/TPV and pure TPV, GMA-15 %MVC significantly reduced the peak heat release rate, total heat release, smoke release, and effective combustion heat, while increasing residual char yield and promoting a denser char layer. The tensile strength of GMA-15 %MVC/MPP/TPV system reached 17.2 MPa, with an increase of 48.3 % and 23.7 % compared to GMA/MPP/TPV and pure TPV, respectively. The corresponding elongation at break reached 987.7 %, surpassing GMA/MPP/TPV and pure TPV. Siloxane’s flexible chain segments and strong char-forming ability led to excellent synergistic effects, offering a new approach for developing TPV materials with high flame retardancy and superior mechanical properties.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"242 ","pages":"Article 111627"},"PeriodicalIF":7.4000,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Properties and mechanism of high-performance flame retardant thermoplastic vulcanizate with silicon-based alkenyl-crosslinking molecule\",\"authors\":\"Siqi Chen , Yihuimeng Xiong , Lijun Qian , Lijie Qu , Jingyu Wang , Wei Tang\",\"doi\":\"10.1016/j.polymdegradstab.2025.111627\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A novel flame retardant was synthesized by introducing tetramethyl tetravinyl cyclotetrasiloxane (MVC) into the alkenyl-crosslinking structure formed by anhydrous piperazine and vinyl phosphoric acid, resulting in a silicon-based alkenyl-crosslinking molecule GMA-nMVC. The GMA-15 %MVC, with an optimal component ratio, enhanced the flame retardancy and mechanical properties of thermoplastic vulcanizate (TPV) composites. At 20 wt.% loading, the limiting oxygen index of the GMA-15 %MVC/MPP/TPV system reached 30.2 %, and both 3.2 mm and 1.6 mm samples passed UL 94 V-0. Compared to GMA/MPP/TPV and pure TPV, GMA-15 %MVC significantly reduced the peak heat release rate, total heat release, smoke release, and effective combustion heat, while increasing residual char yield and promoting a denser char layer. The tensile strength of GMA-15 %MVC/MPP/TPV system reached 17.2 MPa, with an increase of 48.3 % and 23.7 % compared to GMA/MPP/TPV and pure TPV, respectively. The corresponding elongation at break reached 987.7 %, surpassing GMA/MPP/TPV and pure TPV. Siloxane’s flexible chain segments and strong char-forming ability led to excellent synergistic effects, offering a new approach for developing TPV materials with high flame retardancy and superior mechanical properties.</div></div>\",\"PeriodicalId\":406,\"journal\":{\"name\":\"Polymer Degradation and Stability\",\"volume\":\"242 \",\"pages\":\"Article 111627\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-08-25\",\"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/S0141391025004562\",\"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/S0141391025004562","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Properties and mechanism of high-performance flame retardant thermoplastic vulcanizate with silicon-based alkenyl-crosslinking molecule
A novel flame retardant was synthesized by introducing tetramethyl tetravinyl cyclotetrasiloxane (MVC) into the alkenyl-crosslinking structure formed by anhydrous piperazine and vinyl phosphoric acid, resulting in a silicon-based alkenyl-crosslinking molecule GMA-nMVC. The GMA-15 %MVC, with an optimal component ratio, enhanced the flame retardancy and mechanical properties of thermoplastic vulcanizate (TPV) composites. At 20 wt.% loading, the limiting oxygen index of the GMA-15 %MVC/MPP/TPV system reached 30.2 %, and both 3.2 mm and 1.6 mm samples passed UL 94 V-0. Compared to GMA/MPP/TPV and pure TPV, GMA-15 %MVC significantly reduced the peak heat release rate, total heat release, smoke release, and effective combustion heat, while increasing residual char yield and promoting a denser char layer. The tensile strength of GMA-15 %MVC/MPP/TPV system reached 17.2 MPa, with an increase of 48.3 % and 23.7 % compared to GMA/MPP/TPV and pure TPV, respectively. The corresponding elongation at break reached 987.7 %, surpassing GMA/MPP/TPV and pure TPV. Siloxane’s flexible chain segments and strong char-forming ability led to excellent synergistic effects, offering a new approach for developing TPV materials with high flame retardancy and superior mechanical properties.
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.