镍(II)二(1-苯基-3-甲基-4-癸醇-5-吡唑酸酯)在聚丙烯基体中的光稳定作用

Norman S. Allen , Alfonso Chirinos-Padron , John H. Appleyard
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引用次数: 3

摘要

采用常规和二阶导数紫外、红外和磷光光谱技术和过氧化氢分析研究了金属螯合物镍(II)双(1-苯基-3-甲基-4-癸醇-5-吡唑酸酯)在聚丙烯中的光稳定作用。虽然螯合剂猝灭了强致敏剂二苯甲酮的磷光发射,但当含有螯合剂和致敏剂的样品辐照时,没有光保护作用。在蒽醌的情况下,没有淬火和光保护。加工历史对螯合物的光稳定性能起着重要的控制作用。研究了365 nm光致敏氧化的效果。虽然初始过氧化氢浓度似乎控制了聚合物中羰基生长的开始,但螯合物的光分解速率并不依赖于过氧化氢浓度。此外,多色照射下的光氧化速率与单色照射下的光氧化速率具有相同的趋势。结果可以从加工过程中的过氧化氢抑制、光氧化过程中的稳定剂消耗和大烷基自由基(P·)清除等方面进行解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photostabilising action of Ni(II) bis(1-phenyl-3-methyl-4-decanoyl-5-pyrazolate), sanduvor NPU, in a polypropylene matrix

The photostabilising action of the metal chelate nickel(II) bis(1-phenyl-3-methyl-4-decanoyl-5-pyrazolate) in polypropylene is examined using normal and second-order derivative ultraviolet, infrared and phosphorescence spectroscopic techniques and hydroperoxide analysis. Although the chelate quenched the phosphorescence emission of a powerful sensitiser, benzophenone, there was no photoprotective action when the samples containing the chelate and the sensitiser were irradiated. In the case of anthraquinone there was no quenching and no photoprotection. Processing history plays a major role in controlling the photostabilising performance of the chelate. The effect of photosensitised oxidation with 365 nm light is examined. While the initial hydroperoxide concentration appears to control the onset of carbonyl growth in the polymer, the rate of photodecomposition of the chelate shows no dependence on hydroperoxide concentration. Furthermore, the rates of photooxidation under polychromatic irradiation follow the same trends as those obtained under monochromatic irradiation. The results are explained in terms of hydroperoxide inhibition during processing, stabiliser consumption during photooxidation and macroalkyl radical (P·) scavenging.

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