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首页> 外文期刊>Polymer Degradation and Stability >Inherently flame retardant vinyl bearing hyperbranched polysiloxanes having improved thermal stability-Ceramization and analysis of associated thermal properties
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Inherently flame retardant vinyl bearing hyperbranched polysiloxanes having improved thermal stability-Ceramization and analysis of associated thermal properties

机译:具有改善的热稳定性的固有阻燃性乙烯基乙烯基超支化聚硅氧烷-陶瓷化和相关的热性能分析

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AbstractThis study describes the synthesis and characterization of novel hyperbranched silicone polymers having high thermal stability and inherent flame retardancy achieved purely by molecular architecture, without the incorporation of any specific additive or filler. A series of hyper-branched terpolymers (MeDPhDViT) containing vinyl, phenyl and methyl moieties were synthesized by the acid catalysed copolymerization of vinyltriethoxysilane (VTES), diphenyldimethoxysilane (DPDMS) and dimethyldiethoxysilane (DMDES). Curing of these polymers is effected through condensation of the hydroxyl groups triggered by dibutyltindiluarate (DBTDL) catalyst. Glass to rubber transition temperature (Tg)of the cured polymers vary systematically from −110 °C to +50 °C with the increase in the content of vinyl T (ViT) units in the polymer backbone. The terpolymer with maximumViT-unit content shows an onset of thermal decomposition above 540 °C and leaves 86% char residue at 900 °C, attributed to the retardation of depolymerisation byViT unit. The limiting oxygen index (LOI) of the terpolymers increases from 26 to 37% with increase inViT unit content alone, from 13.4 to 53.3 mol% and the terpolymer with 53.3 mol %ViT unit rates as V-0, the best in the UL-94 flame test. The ceramic residue from the cured elastomer comprises of free carbon and silica/Si-O-C ceramics. A probable mechanism has been proposed for the rearrangement of vinyl groups to carbonaceous ceramics under high temperature environment. The vinyl groups promote the formation of a carbonized, in particular graphitized, layer and SiOC phases during pyrolysis, as evidenced by TG-MS, pyrolysis GC-MS, Raman spectroscopy and FESEM analysis. Comparative study with a non-phenylated silicone elastomer confirms the mechanism of formation of carbon rich residue by the thermal rearrangement of vinyl groups.HighlightsNovel hyperbranched polysiloxanes having inherent flame retardancy syntheisized.Flame retardancy and thermal stability achieved without any additives.Detailed thermal decomposition studies carried out and probable mechanism proposed.These are promising pre-ceramic polymers for Si-O-C type ceramics.
机译: 摘要 此研究描述了具有高热稳定性和固有阻燃性的新型超支化有机硅聚合物的合成和表征,这些聚合物仅通过分子结构即可实现,而无需掺入任何特定的添加剂或填料。一系列超支化三元共聚物( Me D Ph D g )从-110°C到+50°C有系统地变化。聚合物骨架中的( Vi T)单元。具有最大 Vi T单元含量的三元共聚物在540°C以上会发生热分解,在900°C时会留下86%的残炭,这归因于阻滞作用通过 Vi T单元解聚。随着 Vi T单元含量的增加,三元共聚物的极限氧指数(LOI)从26%增至37%,而三元共聚物的极限氧指数从13.4%增至53.3mol%其53.3 mol% Vi T单位速率为V-0,是UL-94火焰测试中最好的。来自固化的弹性体的陶瓷残余物包括游离碳和二氧化硅/ Si-O-C陶瓷。已经提出了在高温环境下乙烯基重新排列为碳质陶瓷的可能机理。 TG-MS,热解GC-MS,拉曼光谱和FESEM分析证明,乙烯基基团促进了热解过程中碳化,特别是石墨化的层和SiOC相的形成。与非苯基化有机硅弹性体的比较研究证实了乙烯基热重排形成富碳残基的机理。 突出显示 •• 已合成具有固有阻燃性的新型超支化聚硅氧烷。 不添加任何添加剂即可实现阻燃性和热稳定性。 < / ce:list-item> 详细信息d进行了热分解研究,并提出了可能的机理。 < ce:para id =“ p0025” view =“ all”>这些是很有希望的用于Si-OC型陶瓷的陶瓷前聚合物。

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