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Effect of stabilizer on scission and crosslinking rate changes during photo-oxidation of polypropylene

机译:稳定剂对聚丙烯光氧化过程中断裂和交联速率变化的影响

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Chain scission and crosslinking rates have been derived from molecular mass distributions obtained by gel permeation chromatography at different stages during photodegradation of polypropylene samples exposed to ultraviolet irradiation (UV). Results for rubber-toughened polypropylene (PP) containing no photostabilizer are compared with those for the same polymer stabilized using a commercial photostabilizing package (PPS). The samples were in the form of 3 mm thick bars and measurements were obtained at various depths from the exposed surface after different exposure times. The depth profiles for PP and PPS were very different. Reaction rates in the interior of PP showed oxygen diffusion limited behaviour and after prolonged exposure, the rates in the interior of PPS were higher than those in PP. The ratio of scission rate/crosslink rate fell when reaction rate increased. Crosslinking became relatively more likely when reaction rates were low. The low degradation rates obtained with stabilized polymer coupled with the sensitivity of the method of analysis enabled detection of inhibition of photodegradation attributed to residual moulding stresses in the samples.
机译:断链和交联速率已经从通过凝胶渗透色谱法在暴露于紫外线(UV)的聚丙烯样品光降解过程中的不同阶段获得的分子量分布中得出。将不含光稳定剂的橡胶增韧聚丙烯(PP)的结果与使用市售光稳定剂包装(PPS)稳定的相同聚合物的结果进行比较。样品为3 mm厚的条形,在不同的暴露时间后,从暴露的表面以不同的深度获得测量值。 PP和PPS的深度轮廓非常不同。 PP内部的反应速率显示出氧扩散受限的行为,长时间暴露后,PPS内部的反应速率高于PP中的速率。当反应速率增加时,断裂速率/交联速率之比下降。当反应速率低时,交联变得相对更有可能。用稳定的聚合物获得的低降解率与分析方法的灵敏度相结合,使得能够检测到归因于样品中残余成型应力的光降解抑制作用。

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