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Synthesis, characterisation and catalytic performance of nanocrystalline Co_3O_4 for gas-phase chlorinated VOC abatement

机译:纳米晶Co_3O_4的合成,表征及催化气相气化VOC的催化性能

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摘要

Several nanocrystalline Co_3O_4 catalysts were investigated for their activity and selectivity during the oxidation of 1,2-dichloroethane, which was selected as a model chlorinated volatile organic compound. A wide number of synthesis routes starting from cobalt(II) nitrate were examined, namely calcination of the precursor salt, solid-state reaction, precipitation and sol-gel. The catalysts prepared by precipitation decomposed the chlorinated feed at the lowest temperatures. Activity was observed to be chiefly governed by a small crystallite size which may give rise to more easily accessible active sites (oxygen -O~- or O~(2-)- species), which were not present on the more highly crystalline Co_3O _4 catalysts. Additionally, surface Lewis acidity played a relevant catalytic role. Interestingly, the behaviour of some of the nanocrystalline oxides was superior to that of supported noble metal catalysts and other bulk oxide catalysts. Conversion to deep oxidation products was complete (CO _2, HCl and Cl_2), and no appreciable deactivation with time on stream was noticed.
机译:研究了几种纳米晶Co_3O_4催化剂在1,2-二氯乙烷氧化过程中的活性和选择性,该催化剂被选作典型的氯化挥发性有机化合物。研究了从硝酸钴(II)开始的多种合成路线,即前体盐的煅烧,固态反应,沉淀和溶胶-凝胶。通过沉淀制备的催化剂在最低温度下分解氯化进料。观察到活性主要受较小的微晶尺寸支配,这可能会导致更容易接近的活性位点(氧-O〜-或O〜(2-)-种类),而更高的结晶Co_3O _4上不存在催化剂。另外,表面路易斯酸度起到了相关的催化作用。有趣的是,某些纳米晶氧化物的行为优于负载型贵金属催化剂和其他本体氧化物催化剂的行为。完全转化为深度氧化产物(CO _2,HCl和Cl_2),并且未观察到随着运行时间的明显减活化。

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