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

机译:新颖的NO煅烧方法制备的CO /二氧化硅催化剂的表征

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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 350°C 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:使用NO(JRA Sietsma等,专利申请WO 2008029177和WO 2007071899)的新型硝酸钴转化为氧化钴氧化物,以制备二氧化硅支持的钴研究催化剂,以便对其对Fischer-Tropsch的敏感性来测试材料合成过程参数。在目前的贡献中,描述了通过TPR,氢气化学/脉冲再氧化,外爆和Xanes煅烧的空气煅烧和一氧化氮煅烧的空气煅烧和一氧化氮煅烧的二氧化硅催化剂。对于在H 2中以350℃的标准条件激活的催化剂,尽管用一氧化氮煅烧催化剂观察到较低的减少百分比,但较小的平均金属CO微晶尺寸比补偿这种效果,导致更高的CO表面金属活性位点密度为克催化剂基础。发现NO煅烧的催化剂相对于其空气煅烧的对应物导致每G催化剂的催化剂较高。

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