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Comparison of Ethylene Glycol Steam Reforming Over Pt and NiPt Catalysts on Various Supports

机译:各种载体上Pt和NiPt催化剂上乙二醇蒸汽重整的比较

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摘要

Steam reforming of ethylene glycol (EG) was studied on Pt and NiPt catalysts supported on γ-Al2O3, TiO2, and carbon. On all supports bimetallic NiPt catalysts show higher activity for H2 production than the corresponding Pt catalysts as predicted from model surface science studies. The kinetic trends are similar for all catalysts (Pt and NiPt) with the H2 production rate being zero-order and fractional order with respect to water and ethylene glycol, respectively. Slight differences in selectivity to minor products are observed depending both on active metal and support. On y-Al2O3, NiPt shows higher H2 and less alkane formation than Pt. TiO2 supported catalysts show increased water-gas shift activity but also increased selectivity to alkane precursors. NiPt/C is identified as an active and selective catalyst for EG reforming.
机译:在负载于γ-Al2O3,TiO2和碳的Pt和NiPt催化剂上研究了乙二醇(EG)的蒸汽重整。在所有载体上,双金属NiPt催化剂显示的H2生成活性均高于模型表面科学研究所预测的相应Pt催化剂。对于所有催化剂(Pt和NiPt),动力学趋势相似,H 2的生成速率相对于水和乙二醇分别为零级和分数级。观察到对次要产物的选择性略有不同,这取决于活性金属和载体。在y-Al2O3上,NiPt比Pt显示更高的H2和更少的烷烃形成。 TiO2负载的催化剂显示出增加的水煤气变换活性,但也增加了对烷烃前体的选择性。 NiPt / C被确定为EG重整的活性和选择性催化剂。

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