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Macromolecular scission and crosslinking rate changes during polyolefin photo-oxidation

机译:聚烯烃光氧化过程中的大分子断裂和交联速率变化

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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 various thermoplastics exposed to ultraviolet irradiation (UV). Results are given for a high density polyethylene (HDPE); a low density polyethylene (LDPE); a linear low density polyethylene (LLDPE); a polypropylene homopolymer (PPHO); and a polypropylene copolymer (PPCO). As the oxidation progressed, it was observed that the scission rate for HDPE, LLDPE, PPHO and PPCO increased near to the exposed surface whereas for LDPE the rate remained almost unchanged. The crosslink rate fell near to the surface with HDPE and LDPE but increased with PPHO and PPCO. The reaction rates near to the bar centre (~ 1.5 mm from the exposed surface) were low for HDPE, PPHO and PPCO; this is attributed to oxygen starvation, caused by consumption of oxygen by rapid reaction near the surface. Reaction was observed in the interior with LDPE and LLDPE, presumably because of a combination of a higher oxygen diffusion rate than for HDPE and a lower rate of consumption of oxygen near the surface than with the polypropylenes.
机译:断链和交联速率已经从通过凝胶渗透色谱在暴露于紫外线(UV)的各种热塑性塑料的光降解过程中的不同阶段获得的分子量分布中得出。给出了高密度聚乙烯(HDPE)的结果;低密度聚乙烯(LDPE);线性低密度聚乙烯(LLDPE);聚丙烯均聚物(PPHO);和聚丙烯共聚物(PPCO)。随着氧化的进行,观察到HDPE,LLDPE,PPHO和PPCO的断裂速率在裸露表面附近增加,而LDPE的断裂速率几乎保持不变。 HDPE和LDPE的交联速率接近表面,而PPHO和PPCO则提高。对于HDPE,PPHO和PPCO,靠近棒材中心(距暴露表面约1.5 mm)的反应速率较低;这归因于氧气饥饿,这是由于表面附近的快速反应消耗了氧气造成的。在室内发现与LDPE和LLDPE发生了反应,这可能是由于与HDPE相比,氧气的扩散速率更高,而与聚丙烯相比,其表面附近的氧气消耗速率更低。

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