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Functionalization and cross-linking of high-density polyethylene in the presence of dicumyl peroxide - An FTIR study

机译:高密度聚乙烯在过氧化二异丙苯存在下的功能化和交联 - FTIR 研究

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摘要

High-density polyethylene was thermolysed with short-chain organic compounds (additives) with an ester functional group in the presence of free radical initiator such as dicumyl peroxide at 160 degrees C. The experimental results inferred that an additive with a hydrogen donor containing a thiol group showed better efficiency toward functionalization and an additive with a methylene bridged group showed better efficiency toward cross-linking. The FTIR spectral results indicated that the area of the carbonyl peak at 1730 cm(-1) increased with the increase in percentage grafting of additives with simultaneous increase of cross-linking. The ester grafting was further confirmed by saponification reaction. The possibility of acid functionalization via intramolecular hydrogen transfer was also checked through acid hydrolysis of the saponified products. A suitable reaction mechanism was proposed in order to explain the experimental and spectral data obtained. (c) 2005 Wiley Periodicals, Inc.
机译:在自由基引发剂(如过氧化二异丙苯)存在下,用具有酯官能团的短链有机化合物(添加剂)在160°C下热解高密度聚乙烯。实验结果推断,含有硫醇基团的氢供体的添加剂对官能团化表现出更好的效率,而具有亚甲基桥基的添加剂对交联表现出更好的效率。傅里叶变换红外光谱结果表明,1730 cm(-1)处羰基峰面积随添加剂接枝百分比的增加而增加,交联率同时增加。通过皂化反应进一步证实了酯接枝。还通过皂化产物的酸水解检查了通过分子内氢转移进行酸官能团化的可能性。提出了一种合适的反应机理,以解释所获得的实验和光谱数据。(c) 2005 Wiley Periodicals, Inc.

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