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A Highly Stable and Efficient Co-Mg-Sr Mixed Oxide Catalysts for Hydrogen Production from Glycerol Steam Reforming

机译:一种高稳态高效的Co-Mg-Sr混合氧化氧化物催化剂,用于甘油蒸汽重整的氢气产生

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The production of hydrogen from glycerol steam reforming (GSR) was studied over a series of Co-Mg-Sr (CMS) mixed oxide catalysts. Co-precipitation method was adopted to prepare catalysts by varying the molar ratios of MgO-SrO and keeping Co3O4 content constant. The physico-chemical properties of the samples were investigated by BET surface area, X-ray diffraction, hydrogen chemisorption, temperature programmed reduction, temperature programmed desorption of CO2, Raman spectroscopy and CHNS analysis. The reforming activity depended on the composition of the metal oxides. The catalyst with Co-Mg-Sr molar ratio of 3:1:1 exhibited the highest catalytic activity at 700 degrees C. Glycerol was completely converted to gaseous products and showed 72% hydrogen yield. Catalytic activity of the catalysts was explained on the basis of cobalt particle size, basicity and metal oxides interaction. The catalysts basicity originating from MgO-SrO is also playing an important role in GSR. The present catalyst activity was unaltered even after 100 h of time on stream analysis.
机译:研究了来自甘油蒸汽重整(GSR)的氢的产生在一系列CO-Mg-Sr(CMS)混合氧化物催化剂上进行了研究。采用共沉淀法通过改变MgO-SRO和保持CO3O4含量常数的摩尔比来制备催化剂。通过BET表面积,X射线衍射,氢化学吸附,温度编程,CO2,RAMAN光谱和CHN分析的X射线衍射,氢化学吸附,温度编程解吸来研究样品的物理化学性质。重整活性依赖于金属氧化物的组成。具有3:1:1的CO-Mg-SR摩尔比的催化剂在700℃下表现出最高的催化活性。甘油完全转化为气态产物并显示出72%的氢屈服。基于钴粒径,碱度和金属氧化物相互作用来解释催化剂的催化活性。源自MgO-SRO的催化剂碱度也在GSR中发挥着重要作用。即使在流分析100小时后,即使在流分析100小时后,本发明的催化剂活性也是未嵌入的。

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