文献类型：期刊文献

英文题名：Sorption-enhanced steam methane reforming by in situ CO2 capture on a CaO-Ca9Al6O18 sorbent

作者：Xie, Miaomiao[1]; Zhou, Zhiming[1]; Qi, Yang[1]; Cheng, Zhenmin[1]; Yuan, Weikang[1]

机构：[1] State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China

年份：2012

卷号：207-208

起止页码：142

外文期刊名：Chemical Engineering Journal

收录：EI(收录号：20124015499052)

语种：英文

外文关键词：Steam - Carbon dioxide - Mass transfer - Methane - Sorbents - Temperature - Catalysts - Hydrogen production - Aluminum compounds - Chemical reactors - Sorption

摘要：Sorption-enhanced steam methane reforming (SESMR) that combines steam methane reforming (SMR) with simultaneous CO2 capture is a promising route for hydrogen production. In this paper, a Ni0.50/Mg2.50Al catalyst and a CaO-Ca9Al6O18 sorbent were prepared by a co-precipitation technique and by a wet mixing method, respectively, and applied to the SESMR process. The experiments conducted in both a thermogravimetric analyzer and a fixed bed reactor demonstrated excellent CO2 capture capacity and long-term stability of CaO-Ca9Al6O18, about 83% of its initial sorption capacity being retained after 50 consecutive carbonation/calcination cycles at 650°C. The effects of operation conditions on the SESMR process were investigated, and the results showed that low temperature, high H2O/CH4 ratio and low space velocity were favorable for high purity H2, but the sorbent/catalyst ratio has almost no effect on the H2 purity. The impacts of the usage patterns of catalyst and sorbent were also studied. Large catalyst/sorbent particles exhibited lower conversion of CH4 than small particles for the whole time period, but the integration of catalyst and sorbent into one particle (combined catalyst) can offset the loss of conversion of CH4 during the prebreakthrough period. In view of the excellent reactivity and stability as well as the improved mass transfer, the combined catalyst composed of Ni0.50/Mg2.50Al and CaO-Ca9Al6O18 is expected to be a potential candidate for the SESMR process. ? 2012 Elsevier B.V.