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Stability and Degradation of Polymethacrylates with Controlled Structure

机译:结构可控聚甲基丙烯酸酯的稳定性与降解

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Thermal degradation behaviors for homo- and copolymers of methacrylates prepared by stereospecific living polymerizations as well as radical polymerization were studied. Thermal stability of radically prepared PMMAs can be improved by careful control of end groups and by incorporation of methyl acrylate into the chain. The mechanism of the stabilization was elucidated. Tacticity dependence of thermal stability of PMMAs was examined using isotactic and syndiotactic PMMAs with molecular weights (Mn) of 2,500–500,000 under nitrogen. Syndiotactic PMMAs showed higher degradation temperatures than the isotactic PMMAs of the sameMnwhen theMnwas lower than 25,000, andvice versafor the higherMn. A similarMnand tacticity dependence was observed in degradation in air, and the criticalMnwas found to be about 10,000. These phenomena are discussed in terms of zip length of degradation and the difference in flexibility between isotactic and syndiotactic PMMA chains. Thermal degradation behavior of polymethacrylates were examined and classified as single-step and two-step degradations. This was related with the structures of the ester group. The glass transition temperatures of stereoregular homo- and copolymers of methacrylates are also discussed in some detail.
机译:研究了立体特异性活聚合和自由基聚合制备的甲基丙烯酸酯均聚物和共聚物的热降解行为。通过仔细控制端基和将丙烯酸甲酯掺入链中,可以提高自由制备的PMMA的热稳定性。阐明了稳定的机制。使用分子量 (Mn) 为 2,500–500,000 的同规和同规 PMMA 在氮气下检验了 PMMA 热稳定性的定向依赖性。当Mn低于25,000时,同规PMMA的降解温度高于同规PMMA,反之亦然。在空气降解中观察到类似的Mnand战术依赖性,临界Mn被发现约为10,000。这些现象从降解的拉链长度以及同规PMMA链和同规PMMA链之间的柔韧性差异的角度进行了讨论。研究了聚甲基丙烯酸酯的热降解行为,并将其分为一步降解和两步降解。这与酯基团的结构有关。还详细讨论了甲基丙烯酸酯的立体规则均聚物和共聚物的玻璃化转变温度。

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