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Ammonia decomposition over Ru and Ni catalysts supported on fumed SiO_2,MCM-41,and SBA-15

机译:气相法SiO_2,MCM-41和SBA-15负载的Ru和Ni催化剂上的氨分解

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The effects of using fumed SiO_2,MCM-41,and SBA-15 as supports for Ru and Ni catalysts on ammonia decomposition were investigated.It was found that the supported catalysts on these siliceous materials are more active than those supported on ordinary silica.In general,the supported Ru catalysts are more active than the Ni catalysts,and MCM-41 is the best support material for Ru and Ni.Significant enhancement in activity was observed when the supported Ru catalysts were modified by KOH,but such effect was minimal in the cases of supported Ni catalysts.The results of N_2 adsorption and transmission electron microscopy studies revealed that the Ni particles of Ni/MCM-41 (TIE) prepared by template-ion exchange (TIE) method are largely located inside the pores of MCM-41.Compared with the Ni/MCM-41 (IMP) catalyst prepared by impregnation method,the Ni/MCM-41 (TIE) catalyst exhibited appropriate Ni dispersion and weaker Ni/support interaction,and consequently higher catalytic activity.In terms of the remarkable changes in turnover frequency (TOF) with Ni dispersion on different catalysts,it was demonstrated that NH_3 decomposition over Ni is significantly structure sensitive.Some unique metal clusters similar to B5 active sites should be responsible for the catalytic activities.Preparation methodology has a substantial influence on metal dispersion.For the supported Ni catalysts prepared by the TIE method,the generated metal particles are very small and the constitution of unique active sites becomes unfavorable,which accounts for the apparently lower TOF values.
机译:研究了气相SiO_2,MCM-41和SBA-15作为Ru和Ni催化剂的载体对氨分解的影响。发现这些硅质材料上的负载型催化剂比普通二氧化硅上的负载型活性高。通常,负载型Ru催化剂比Ni催化剂更具活性,MCM-41是Ru和Ni的最佳载体材料。当负载型Ru催化剂用KOH改性时,其活性显着提高,但在KOH中这种作用很小。 N_2吸附和透射电子显微镜研究的结果表明,通过模板离子交换(TIE)方法制备的Ni / MCM-41(TIE)的Ni颗粒主要位于MCM-孔的内部41.与浸渍法制备的Ni / MCM-41(IMP)催化剂相比,Ni / MCM-41(TIE)催化剂表现出适当的Ni分散性和较弱的Ni /载体相互作用,因此具有较高的催化活性。 Ni分散在不同催化剂上周转频率(TOF)的显着变化的结果表明,NH_3在Ni上的分解对结构非常敏感。一些类似于B5活性位点的独特金属簇应负责催化活性。对于用TIE方法制备的负载型Ni催化剂,生成的金属颗粒非常小,独特的活性位点的组成变得不利,这说明TOF值明显降低。

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