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Synthesis and decomposition performance of a polymeric foaming agent containing a sulfonyl hydrazide moiety

机译:含磺酰肼部分的聚合物发泡剂的合成和分解性能

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摘要

A new monomer, methacryloyloxybis(benzenesulfonyI hydrazide) (MAOBSH) containing a foamable sulfonyl hydrazide functional group after decomposition by heating, was synthesized from 4,4'-oxybis(benzenesulfonyl hydrazide) (OBSH) with methacryloyl chloride, and used to obtain poly(MAOBSH) as a polymeric foaming agent (PFA) in dry tetrahydrofuran at 70 °C using azobisisobutyronitrile as an initiator. The structures of the synthesized MAOBSH and poly(MAOBSH) were identified using Fourier transform infrared and1 H NMR spectroscopies. The decomposition temperature of poly(MAOBSH) was determined to be 245 °C and this temperature was decreased to around 160 °C by adding an activator such as surface-treated urea to the polymer. The exothermic temperature and heat determined by the decomposition of the polymer were 256 °C and 287 J g~(-1). The amount of gas evolution for poly(MAOBSH) measured at the decomposition temperature was 74 mL g~(-1). Furthermore, polymers incorporating the PFA showed better skin and finer cell structure as well as better mechanical properties such as elongation and compression set than polymers with added OBSH due to the better compatibility of the developed PFA with polymers.
机译:由4,4'-氧双(苯磺酰肼)(OBSH)与甲基丙烯酰氯合成,合成了一种新的单体,该单体在加热分解后含有可发泡的磺酰肼官能团,即甲基丙烯酰氧基双(苯磺酰肼)(MAOBSH),并用于获得聚(MAOBSH)作为聚合发泡剂(PFA),在70°C的干燥四氢呋喃中,使用偶氮二异丁腈作为引发剂。合成的MAOBSH和聚(MAOBSH)的结构使用傅立叶变换红外光谱和1 H NMR光谱进行了鉴定。聚(MAOBSH)的分解温度确定为245℃,并且通过向聚合物中添加活化剂例如经表面处理的尿素将该温度降低至约160℃。由聚合物分解确定的放热温度和热为256℃和287J g〜(-1)。在分解温度下测得的聚(MAOBSH)的气体逸出量为74 mL g〜(-1)。此外,由于已开发的PFA与聚合物的相容性更好,因此与掺有OBSH的聚合物相比,掺入PFA的聚合物表现出更好的表皮和细密的细胞结构,以及更好的机械性能,例如伸长率和压缩永久变形。

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