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Production of hydrogen by ethanol steam reforming over catalysts from reverse microemulsion-derived nanocompounds

机译:由逆微乳液衍生的纳米化合物在催化剂上进行乙醇蒸汽重整制氢

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In the present work, hydrotalcite-like compound precursor for preparing mixed oxide catalyst was successfully synthesized by a novel method, which was a combination of the reverse microemulsion and coprecipitation methods. It was observed that the precursor obtained from the above method possessed superior characteristics for preparing mixed oxide catalyst used in ethanol steam reforming (ESR). Furthermore, for comparison, catalysts prepared from conventional coprecipitation and impregnation methods had been characterized together with the catalyst prepared from the new method. Besides ICP, BET, X-ray diffraction (XRD), temperature-programmed reduction (TPR), H_2-TPD, TG, and TEM analytic techniques, catalytic performance for ESR was also investigated. The results of XRD and TPR indicated that a solid solution phase existed in the catalysts obtained from reverse microemulsion and coprecipitation methods, while spinel phase together with solid solution were observed in the catalyst obtained from the impregnation method. The high BET surface area of the catalyst obtained from the reverse microemulsion method enhanced the dispersion and the surface area of nickel, which improved the catalyst performance. From TEM images, the aggregated Ni could be found in the catalyst obtained from the impregnation method, while the hydrotalcite-like compound precursors prepared from reverse microemulsion and coprecipitation methods produced homogeneously distributed active Ni metal species. The catalyst obtained from reverse microemulsion exhibited the best activity, stability, and least carbon deposition because of the formation of hydrotalcite-like compound precursor, uniform dispersion of active Ni metal species, and much more surface area supporting the active Ni metal sites.
机译:在本工作中,通过反向微乳液法和共沉淀法相结合的新方法成功合成了制备复合氧化物催化剂的类水滑石化合物前体。观察到,通过上述方法获得的前体具有优异的特性,用于制备用于乙醇蒸汽重整(ESR)的混合氧化物催化剂。此外,为了进行比较,已经表征了由常规共沉淀和浸渍方法制备的催化剂以及由新方法制备的催化剂。除了ICP,BET,X射线衍射(XRD),程序升温还原(TPR),H_2-TPD,TG和TEM分析技术外,还研究了ESR的催化性能。 XRD和TPR的结果表明,在反向微乳液和共沉淀法制得的催化剂中存在固溶相,而在浸渍法制得的催化剂中观察到尖晶石相和固溶体。通过反向微乳液法获得的催化剂的高BET表面积提高了镍的分散性和表面积,从而改善了催化剂性能。从TEM图像可以看出,在浸渍法制得的催化剂中发现了聚集的Ni,而由反向微乳液和共沉淀法制得的类水滑石化合物前体则产生了均匀分布的活性Ni金属。由于形成了类似水滑石的化合物前体,活性镍金属种类均匀分散以及支持活性镍金属位点的表面积大得多,所以由反向微乳液制得的催化剂表现出最佳的活性,稳定性和最少的碳沉积。

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