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Enrichment of Hydrogen Production from Biomass-Gasification-Derived Syngas over Spinel-Type Aluminate-Supported Nickel Catalysts

机译:通过尖晶石型铝酸铝基镍催化剂从生物量气化衍生合成气中富集氢气

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摘要

Synthesis gas produced through biomass gasification can be converted into H-2-rich gas by catalytic methane decomposition or reforming reactions. In this study, we investigate the promotion of hydrogen production by the catalytic reforming of a model biomass-gasification-derived syngas over Ni/MAl2O4 (M = Mg, Ni, and Ca) catalysts. Three mesoporous spinel supports were synthesized by solution combustion. Ni/NiAl2O4 and Ni/CaAl2O4 exhibited better catalytic activities and stabilities for syngas reforming than the other catalysts. These results are ascribable to interactions between the metallic catalyst and spinel supports, and stronger interactions lead to smaller catalyst particles. The formation of coke deposits is associated with CH4 decomposition during the syngas reforming reaction. Clearly, H-2 production is lower at 900 degrees C because of increased competition from the reverse water-gas shift reaction that shifts the reaction between CO2 and H-2 toward the generation of CO and H2O.
机译:通过生物质气化产生的合成气可以通过催化甲烷分解或重整反应转化为富含H-2的气体。在这项研究中,我们通过Ni / Mal2O4(M = Mg,Ni和Ca)催化剂的模型生物质 - 气化衍生的合成气的催化重整促进氢气产生。通过溶液燃烧合成了三种介孔尖晶石载体。 Ni / Nial2O4和Ni / CaAL2O4表现出比其他催化剂更好的催化活性和合成气重整的稳定性。这些结果可归因于金属催化剂和尖晶石载体之间的相互作用,并且较强的相互作用导致较小的催化剂颗粒。焦炭沉积物的形成与合成气重整反应过程中的CH 4分解相关。显然,由于逆水 - 气体变换反应的竞争增加,H-2生产较低,从反向水气体变换反应转变CO 2和H-2之间的反应朝向CO和H2O的产生。

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