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NiO-polyoxometalate nanocomposites as efficient catalysts for the oxidative dehydrogenation of propane and isobutane

机译:NiO-多金属氧酸盐纳米复合材料,是丙烷和异丁烷氧化脱氢的有效催化剂

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摘要

Novel nanocomposites of NiO and polyoxometalate (Cs_(2.5)H_(0.5)PMo_(12)O_(40)) with particle sizes in the range of 5-10 nm showed exceptional oxygen and ammonia adsorption capabilities, and the nanocomposites catalyzed the oxidative dehydrogenation of propane and isobutane efficiently under mild conditions.rnSelective oxidation of light alkanes into olefins and organic oxygenates is an attractive route for the utilization of abundant light alkane resources. Although intensive efforts have been made in this field, selective oxidation of C_1-C_4 alkanes still remains an unsolved challenge, except for the conversion of n-butane to maleic anhydride. The main reason is that the alkane activation generally requires severe conditions, under which the consecutive oxidation of reactive target products to CO and CO_2 can easily occur, leading to low selectivities to target products at reasonably high conversions. Therefore, the development of efficient catalysts which are capable of working under mild conditions would be a promising route.
机译:NiO和多金属氧酸盐的新型纳米复合材料(Cs_(2.5)H_(0.5)PMo_(12)O_(40))的粒径在5-10 nm之间,具有出色的氧和氨吸附能力,并且该纳米复合材料催化了氧化脱氢在温和的条件下有效地丙烷和异丁烷。轻质烷烃选择性氧化为烯烃和有机含氧化合物是利用丰富的轻质烷烃资源的诱人途径。尽管在该领域已经做出了巨大努力,但是除了将正丁烷转化为马来酸酐以外,C_1-C_4烷烃的选择性氧化仍然是一个尚未解决的挑战。主要原因是烷烃活化通常需要严格的条件,在此条件下,很容易发生反应性目标产物向CO和CO_2的连续氧化,导致目标产物在较高转化率下的选择性较低。因此,开发能够在温和条件下工作的高效催化剂将是一个有前途的途径。

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  • 来源
    《Chemical Communications》 |2009年第17期|2376-2378|共3页
  • 作者单位

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

    State Key Laboratory of Physical Chemistry of Solid Surfaces, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China;

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