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Influence of Pd Precursor and Method of Preparation on Hydrodechlorination Activity of Alumina Supported Palladium Catalysts

机译:钯前驱体和制备方法对氧化铝负载钯催化剂加氢脱氯活性的影响

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摘要

A series of alumina supported Pd catalysts were prepared by the novel deposition-precipitation method adopting the chloride precursor(DP-C1)of Pd and varying the metal content from 0.25 to 1.0 wt%.The catalytic properties of prepared catalysts were studied by various characterization techniques such as N2 adsorption,CO chemisorption,TPR,XRD,XPS,and TEM techniques.The activity and stability of the catalysts were evaluated for the gas phase hydrodechlorination(HDC)of chlorobenzene operating at atmospheric pressure.At 1 wt% of Pd the catalyst showed higher chlorobenzene conversion with good stability when tested for a period of 25 h,whereas the other catalysts exhibited a loss in activity with time.In order to elucidate the exceptional activity and stability of this catalyst,a few more catalysts with 1 wt% Pd were prepared by impregnation technique and also using a non-chloride precursor,palladium nitrate.The 1 wt% DP-C1 catalyst again was found to be the best among the others.The activity and stability of the DP-C1 catalyst was also found to be superior to two low-dispersed catalysts,each with 10 wt% Pd,prepared by conventional impregnation method using the chloride and nitrate as the precursors.The characterization results reveal that the high activity and stability of the DP-C1 catalyst is related to the formation of electron deficient Pd species and its stabilization in the octahedral vacancies of alumina.
机译:采用新型沉积-沉淀法,采用钯的氯化物前驱物(DP-C1),金属含量从0.25wt%改变为1.0wt%,制备了一系列氧化铝负载的Pd催化剂。通过各种表征研究了制备的催化剂的催化性能。 N2吸附,CO化学吸附,TPR,XRD,XPS和TEM技术。在常压下,以1wt%的Pd浓度对催化剂的活性和稳定性进行了评估,以评估氯苯的气相加氢脱氯(HDC)。在25 h的测试中,该催化剂显示出较高的氯苯转化率并具有良好的稳定性,而其他催化剂随时间显示活性下降。为阐明该催化剂的出色活性和稳定性,另一些催化剂的重量百分比为1%钯是通过浸渍技术制备的,也使用非氯化物前体硝酸钯制备。再次发现1wt%的DP-C1催化剂是其他催化剂中最好的。还发现DP-C1催化剂的y和稳定性优于两种低分散的催化剂,每种催化剂均以传统的浸渍方法(以氯化物和硝酸盐为前体)制备,每种钯的Pd含量均为10 wt%。 DP-C1催化剂的活性和稳定性与缺电子的Pd物种的形成及其在氧化铝八面体空位中的稳定性有关。

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