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Renewable hydrogen from glycerol reforming over nickel aluminate-based catalysts

机译:来自甘油重整镍铝铝酸铝催化剂的可再生氢

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Nickel aluminate (NiAl2O4) was synthesized by citrate method and used as a precursor for supported Ni catalysts. This bulk sample as well as an alumina-supported NiAl2O4 and a dual catalytic system obtained by its simple and straightforward physical mixture with alumina were investigated on glycerol reforming at different water:glycerol molar ratio conditions. All catalyst precursors and the reduced catalysts made thereof were characterized by XRF, porosity, H-2-TPR, powder XRD and temperature-resolved XRD. Spent catalysts were complementarily analyzed by TPO/TGA-MS and FE-SEM in order to infer on deactivation process. NiAl2O4 precursor structure rendered highly active systems accomplishing a level of glycerol conversion to gaseous products roughly equivalent to glycerol global conversion. Therefore, hydrogen and CO2 were the main products obtained, reaching hydrogen yields usually higher than 80% with respect to the theoretical maximum production. The way NiAl2O4 phase is settled in catalyst formulation (bulk, supported or physically mixed) revealed an important influence on catalyst deactivation. Deactivation was associated with the formation of carbon filaments as no other type of carbon species, more or less reactive, could be identified. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过柠檬酸盐法合成镍铝(NiAl 2 O 4)并用作负载Ni催化剂的前体。在不同水处的甘油重整上研究了该块状样品以及通过其简单和直接的物理混合物获得的氧化铝样品及其通过与氧化铝的简单和直接的物理混合物获得的双催化系统进行研究:甘油摩尔比条件。所有催化剂前体和其制备的还原催化剂的特征在于XRF,孔隙率,H-2-TPR,粉末XRD和温度分辨XRD。通过TPO / TGA-MS和Fe-SEM互补地分析废催化剂以推断出停用过程。 NiAl2O4前体结构使得高活性系统完成甘油转化水平,对气态产物大致相当于甘油全局转化。因此,氢和二氧化碳是获得的主要产物,相对于理论最大产量,达到氢气产率通常高于80%。 Nial 2O4相溶解在催化剂制剂中的方式(体积,负载或物理混合)揭示了对催化剂失活的重要影响。如果不能鉴定任何其他类型的碳素,则碳丝的形成与形成有关的碳丝,或多或少反应。 (c)2016年Elsevier B.v.保留所有权利。

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