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Study of Te and V as counter-cations in Keggin type phosphomolybdic polyoxometalate catalysts for isobutane oxidation

机译:Keggin型磷钼多金属氧酸盐催化异丁烷氧化中Te和V作为抗衡阳离子的研究

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Keggin-type phosphomolybdic acid and cesium salts with protons partially substituted by tellurium and by both tellurium and vanadium have been prepared, characterized using several techniques and tested as catalysts in the partial oxidation of isobutane into methacrylic acid (MAA). The results showed that tellurium when introduced as counter-cation was present as Te4+ capping the Keggin anion and was randomly distributed in the acid or in the cesium salt. This cation induced a positive effect on the selectivity to MAA and methacrolein (MA) without significant effect on the activity except in the acid at low loading where it also increased the activity. The co-substitution of protons by vanadyl cations had a slight effect on the selectivity but increased the activity especially at low level of substitution, which led to a very efficient catalyst. Selectivity to MAA and MA and isobutane conversion rate of 65 and 17% respectively were reached at 350 degrees C and were both very constant with time on stream. The catalytic results obtained in both stationary and transient conditions allowed to propose a reaction mechanism very close to one already proposed with four intermediates amongst which one is common to both MAA and MA. These results were used to understand the catalytic effect of tellurium and vanadium. (C) 2008 Elsevier Inc. All rights reserved.
机译:制备了质子被碲以及碲和钒均取代的质子化的Keggin型磷钼酸和铯盐,使用多种技术进行了表征,并在异丁烷部分氧化为甲基丙烯酸(MAA)中作为催化剂进行了测试。结果表明,碲作为反阳离子引入时,会以Te4 +的形式覆盖Keggin阴离子,并随机分布在酸或铯盐中。该阳离子对MAA和甲基丙烯醛(MA)的选择性产生积极影响,而对活性没有明显影响,但在低负荷的酸中也会增加活性。钒基阳离子对质子的共取代对选择性的影响很小,但特别是在低取代水平下增加了活性,这导致了非常有效的催化剂。在350℃下,对MAA和MA的选择性分别达到65%和17%的异丁烷转化率,并且都随着生产时间的变化非常恒定。在固定和过渡条件下获得的催化结果使得提出的反应机理非常接近已经提出的具有四种中间体的反应机理,其中一种对于MAA和MA都是共同的。这些结果用于了解碲和钒的催化作用。 (C)2008 Elsevier Inc.保留所有权利。

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