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Catalytic hydrodechlorination of p-chloro-m-cresol and 2,4,6-trichlorophenol with Pd and Rh supported on Al-pillared clays

机译:al柱撑粘土负载pd和Rh催化加氢脱氯对氯间甲酚和2,4,6-三氯苯酚

摘要

Hydrodechlorination (HDC) of p-chloro-. m-cresol (PCMC) and 2,4,6-trichlorophenol (246TCP) under ambient-like conditions (25. °C, 1. atm) with Pd and Rh supported on Al-pillared clays (Al-PILC) has been studied. The two target pollutants were completely converted into biodegradable products with both catalysts in short reaction time. The Pd catalyst was selective towards m-cresol and 3-methyl-cyclohexanone in the HDC of PCMC and to phenol and cyclohexanone in the case of 246TCP. The Rh catalyst showed a high hydrogenating activity leading to the formation of 3-methyl-cyclohexanol and cyclohexanol as final products of the HDC of PCMC and 246TCP, respectively. This led to a dramatic decrease of ecotoxicity. The dechlorination of PCMC at short reaction times allowed a high improvement of the biodegradability whereas increasing the reaction time favors the formation of highly hydrogenated byproducts, like 3-methyl-cyclohexanone and 3-methyl-cyclohexanol, which showed a lower biodegradability. A kinetic study of the HDC of PCMC and 246-TCP with the two mentioned catalysts is also presented
机译:对氯-的加氢脱氯(HDC)。研究了在类似环境条件下(25.°C,1. atm),Pd和Rh负载在铝柱状粘土(Al-PILC)上的间甲酚(PCMC)和2,4,6-三氯苯酚(246TCP) 。在较短的反应时间内,两种催化剂都将两种目标污染物完全转化为可生物降解的产物。在246TCP的情况下,Pd催化剂对PCMC的HDC中的间甲酚和3-甲基-环己酮具有选择性,对苯酚和环己酮具有选择性。 Rh催化剂显示出高的氢化活性,导致形成了3-甲基-环己醇和环己醇,分别作为PCMC和246TCP的HDC的最终产物。这导致了生态毒性的急剧下降。 PCMC在较短的反应时间下进行脱氯可以大大提高生物降解性,而增加反应时间则有利于形成高度氢化的副产物,例如3-甲基-环己酮和3-甲基-环己醇,它们显示出较低的生物降解性。还介绍了PCMC和246-TCP的HDC与上述两种催化剂的动力学研究。

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