首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Oxidative and non-oxidative steam reforming of crude bio-ethanol for hydrogen production over Rh promoted Ni/CeO2-ZrO2 catalyst
【24h】

Oxidative and non-oxidative steam reforming of crude bio-ethanol for hydrogen production over Rh promoted Ni/CeO2-ZrO2 catalyst

机译:Rh促进的Ni / CeO2-ZrO2催化剂对粗制生物乙醇的氧化和非氧化蒸汽重整以制氢

获取原文
获取原文并翻译 | 示例
           

摘要

The catalytic oxidative and non-oxidative steam reforming of crude bio-ethanol for hydrogen production was studied in a tubular fixed bed reaction system over 30 wt.%Ni/CeO2-ZrO2 and 1 wt.%Rh30 wt.%Ni/CeO2-ZrO2 catalysts. The catalysts were prepared by impregnation-co-precipitation method and characterized by BET, XRD, TPR, TGA, XPS, XANES and EXAFS techniques. Characterization results revealed that the addition of Rh promotes reducibility of NiO at lower temperature for the bimetallic catalysts. Extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) analysis depicted that NiO with 6-fold local co-ordination is present in all the samples. Ethanol conversion, hydrogen yield and product selectivity were investigated at 600 C and space time of 9.17 kgcat h/kgmol[EtOH]) at atmospheric pressure. In steam reforming of crude bio-ethanol, 81% ethanol conversion was achieved with 59% hydrogen selectivity on Ni/CeO2-ZrO2 catalyst, whereas, higher ethanol conversion (86%) with 73% hydrogen selectivity was achieved using Rh-Ni/CeO2-ZrO2 catalysts. In oxidative steam reforming of crude bio-ethanol, hydrogen yield and selectivity reduced due to the partial oxidation of oxygenate compounds present in the feed. The used catalysts were also analysed by BET, TGA/DTA, TPR, TPO, Raman spectroscopy, SEM, and TEM techniques to identify the cause of catalyst deactivation. The results indicate that the catalyst deactivation occurred mainly due to amorphous and filamentous carbon deposition on the catalysts surface, due to the presence of the impurities in the feed. (C) 2015 Elsevier B.V. All rights reserved.
机译:在管式固定床反应系统中研究了在30 wt。%Ni / CeO2-ZrO2和1 wt。%Rh30 wt。%Ni / CeO2-ZrO2上的粗制生物乙醇的催化氧化和非氧化蒸汽重整以生产氢气。催化剂。催化剂采用浸渍共沉淀法制备,并通过BET,XRD,TPR,TGA,XPS,XANES和EXAFS技术表征。表征结果表明,Rh的添加促进了双金属催化剂在较低温度下的NiO还原性。扩展的X射线吸收精细结构(EXAFS)和X射线吸收近边缘结构(XANES)分析表明,所有样品中均存在具有6倍局部配位的NiO。在大气压下于600℃和9.17 kgcat h / kgmol [EtOH])的时空下研究了乙醇转化率,氢产率和产物选择性。在粗制生物乙醇的蒸汽重整中,在Ni / CeO2-ZrO2催化剂上实现了81%的乙醇转化率和59%的氢选择性,而使用Rh-Ni / CeO2达到了73%的氢选择性的更高的乙醇转化率(86%) -ZrO2催化剂。在粗制生物乙醇的氧化蒸汽重整中,由于进料中存在的含氧化合物部分氧化,氢的产率和选择性降低。还通过BET,TGA / DTA,TPR,TPO,拉曼光谱,SEM和TEM技术对用过的催化剂进行了分析,以确定催化剂失活的原因。结果表明,由于进料中存在杂质,催化剂失活主要是由于无定形和丝状碳沉积在催化剂表面上。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号