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Performance comparison of mesoporous alumina supported Cu & Ni based catalysts in acetic acid reforming

机译:介孔氧化铝负载的Cu和Ni基催化剂在乙酸重整中的性能比较

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Steam reforming of acetic acid (AcOH) was investigated over mesoporous alumina supported mono- and bi-metallic Ni and/or Cu based catalysts. Results obtained with mesoporous alumina supported catalysts were compared with another set of experiments performed using a commercial Cu Zn based HifuelR-120 catalyst and Ni impregnated HifuelR-120. Comparison of catalytic performances of Cu and Ni based catalysts showed that Cu activated the decomposition of AcOH giving mainly CH4 and CO2, while Ni was highly active for steam reforming reaction, yielding quite high H-2 selectivities, reaching to 70%. This H-2 selectivity was quite close to the equilibrium limit. Very low CO selectivity observed with HifuelR-120 and low CO/CO2 ratios observed especially with the Cu based catalysts clearly indicated that CO was not an intermediate of AcOH reforming reaction, but formed mainly as a result of reverse water gas shift reaction. Ni containing catalysts were shown to have high activity also for the reverse water gas shift reaction. Comparison of the performances of mono-metallic Ni and bi-metallic Ni Cu containing MA catalysts showed that the performance of the bi-metallic catalyst was better, yielding less CH4. Although the activities of nickel containing catalysts were quite high in steam reforming of AcOH, they yield more coke as compared to Cu based materials. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在介孔氧化铝负载的单金属和双金属Ni和/或Cu基催化剂上研究了乙酸(AcOH)的蒸汽重整。将使用介孔氧化铝负载的催化剂获得的结果与使用市售Cu Zn基HifuelR-120催化剂和Ni浸渍的HifuelR-120进行的另一组实验进行了比较。 Cu和Ni基催化剂的催化性能比较表明,Cu激活了AcOH的分解,主要生成CH4和CO2,而Ni对水蒸气重整反应具有很高的活性,产生了很高的H-2选择性,达到70%。 H-2的选择性非常接近平衡极限。用HifuelR-120观察到的非常低的CO选择性和特别是用Cu基催化剂观察到的低CO / CO2比值清楚地表明,CO不是AcOH重整反应的中间体,而是主要由逆水煤气变换反应形成的。含镍催化剂对逆水煤气变换反应也显示出高活性。比较含单金属Ni和双金属Ni Cu的MA催化剂的性能表明,双金属催化剂的性能更好,生成的CH4更少。尽管在AcOH的蒸汽重整中含镍催化剂的活性很高,但与基于Cu的材料相比,它们产生的焦炭更多。 (C)2017氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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