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CHARACTERIZATION OF CO/SILICA CATALYSTS PREPARED BY A NOVEL NO CALCINATION METHOD

机译:新型NO煅烧法制备的CO /二氧化硅催化剂的表征

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摘要

A novel conversion of cobalt nitrate to cobalt oxide using NO (J.R. A. Sietsma et al., patent applications WO 2008029177 and WO 2007071899) was utilized to prepare silica-supported cobalt research catalysts, in order to test the materials for their sensitivity to Fischer-Tropsch synthesis process parameters. In the current contribution, extensive characterization of air calcined and nitric oxide calcined 15% and 25% cobalt-loaded silica catalysts by TPR, hydrogen chemisorption/pulse reoxidation, EXAFS, and XANES is described. For catalysts activated at a standard condition of 350oC for 10 h in H2, despite a lower percentage of reduction observed with the nitric oxide calcined catalysts, the smaller average metal Co crystallite size more than compensates for this effect, leading to a higher Co surface metal active site density on a per gram catalyst basis. The NO calcined catalysts were found to result in higher CO conversion rates on a per g catalyst basis relative to their air calcined counterparts.
机译:利用NO(JRA Sietsma等人,专利申请WO 2008029177和WO 2007071899)将硝酸钴新转化为氧化钴用于制备二氧化硅负载的钴研究催化剂,以测试该材料对费-托反应的敏感性。合成工艺参数。在当前的贡献中,描述了通过TPR,氢化学吸附/脉冲再氧化,EXAFS和XANES对煅烧的空气和一氧化氮煅烧的15%和25%钴负载的二氧化硅催化剂的广泛表征。对于在350°C的标准条件下在H2中活化10h的催化剂,尽管在一氧化氮煅烧的催化剂中观察到的还原百分率较低,但较小的平均金属Co晶粒尺寸可以弥补这一影响,从而导致较高的Co表面金属活性位密度(以每克催化剂计)。发现相对于其空气煅烧的对应物,以每克催化剂计,NO煅烧的催化剂导致更高的CO转化率。

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