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A chemiluminescence study on thermal and photostability of ethylene/alpha-olefin copolymers synthesized with rac-Et(Ind)(2)ZrCl2/MAO catalyst system

机译:用rac-Et(Ind)(2)ZrCl2 / MAO催化剂体系合成的乙烯/α-烯烃共聚物的热稳定性和光稳定性的化学发光研究

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Copolymers of ethylene and alpha-hexene or alpha-octadecene were synthesised, and the relationship between their degradation and the type and content of comonomer was investigated by chemiluminescence, FTIR and thermogravimetric analysis. A clear effect of the length of branches on the thermal behaviour of copolymers was found. The insertion of octadecene caused the formation of a higher content of oxidised species in those copolymers. It may be related to the increase of length of branching which favoured the scission of the carbon-carbon bonds to form alkyl radicals in the earlier stages. It was observed that thermal stability decreased as the comonomer was incorporated. The isothermal CL curves under oxygen exhibited double stage, oxygen independent and oxygen diffusion controlled reactions. The intensity of CL of second stage, decreased and shifted to longer time as the comonomer content increased. This effect was attributed to crosslinking processes which are favoured with the increase of branching degree. Otherwise, for copolymers with high comonomer content, the chemiluminescence intensity enhanced and shifted to shorter time. It was associated to the decrease of the molecular weight, and as consequence, more reactive terminal groups which drives to the promotion of the initiation of thermal oxidation. Copolymers were UV-exposured and CL measured at different irradiation period of times. From the beginning, CL intensity slightly increased with time, followed by a drastically enhancement of emission intensity, and enhancement of chemiluminescence decay rate values, as result of degradation of samples and the higher mobility of peroxides to recombine. The results were supported by FTIR and TGA analysis, which revealed the higher degree of degradation for the copolymers as the comonomer content increased.
机译:合成了乙烯与α-己烯或α-十八烯的共聚物,并通过化学发光,FTIR和热重分析研究了它们的降解与共聚单体的类型和含量之间的关系。发现支链的长度对共聚物的热行为有明显影响。十八碳烯的插入导致在那些共聚物中形成更高含量的氧化物质。这可能与支链长度的增加有关,支链长度的增加有利于在早期阶段切断碳-碳键以形成烷基。观察到随着掺入共聚单体,热稳定性降低。氧气下的等温CL曲线表现出双阶段,不依赖氧和受氧扩散控制的反应。随着共聚单体含量的增加,第二阶段的CL强度降低,并转移到更长的时间。该效果归因于交联过程,该过程有利于支化度的增加。否则,对于具有高共聚单体含量的共聚物,化学发光强度增强并转移到更短的时间。这与分子量的降低有关,并且因此与更多的反应性端基相关,这驱动了热氧化引发的促进。将共聚物暴露于紫外线下并在不同的照射时间段测量CL。从一开始,CL强度就随时间而略有增加,随后是发射强度的急剧增加以及化学发光衰减率值的增加,这是样品降解和过氧化物重新结合的更高迁移率的结果。 FTIR和TGA分析支持了该结果,结果表明,随着共聚单体含量的增加,共聚物的降解程度更高。

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