In-situ metal doping to boost the reactivity of layered double hydroxide derived Mg-Fe-Al-O oxygen carriers for chemical looping CH4 reforming with CO2 reduction
编号:65 稿件编号:104 访问权限:仅限参会人 更新:2023-03-22 12:02:58 浏览:459次 口头报告

报告开始:2021年08月10日 08:00 (Asia/Shanghai)

报告时间:15min

所在会议:[P] 大会报告 » [2] 分会场一:反应器设计及系统优化

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摘要
Layered double hydroxide (LDH) is a powerful self-template to synthesize high performance oxygen carriers for chemical looping processes. Since active and support species can be easily combined from the M2+ and M3+ metal layers in LDH structure, in this work, doping M2+ metal (M = Ni, Cu, Mn, Ca) was applied to improve the redox reactivity of the Mg-Fe-Al-O oxygen carriers. From XRD patterns, M doped LDH derived Mg-Fe-Al-O oxygen carriers mainly formed spinel phase and MgO phase (except for Ca2+, formed CaFe2O5 instead). SEM images showed that the Ni and Cu doped oxygen carriers form clear layered and classic flower-grain morphologies, respectively, while the Mn and Ca doped oxygen carriers are both appeared a granular morphology. Ni doped oxygen carriers exhibited an oxygen storage capacity of 20 mol[O]·kgFe+Ni-1 while that of other M doped oxygen carriers were around 10 mol[O]·kgFe+Ni-1. After 20 CH4-CO2 cycles, Ni doped oxygen carriers performed with 7 mol[CO]·kgFe+Ni-1·min-1 CO space time yield during CO2 oxidation half-cycle. This might be ascribed to that: (i) Ni catalyzes methane to decompose into carbon, (ii) CO2 eliminates the carbon deposition formed during CH4 reforming half-cycle.
关键字
化学链重整,化学链二氧化碳还原,LDH衍生氧载体,原位掺杂
报告人
金波
湖南大学

稿件作者
樊伊晗 湖南大学
金波 湖南大学
梁志武 湖南大学
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