Mg-promoted Ni-CaO microsphere as bi-functional catalyst for hydrogen production from sorption-enhanced steam reforming of glycerol

被引:64
|
作者
Dang, Chengxiong [1 ]
Liu, Liqiang [1 ]
Yang, Guangxing [2 ]
Cai, Weiquan [1 ]
Long, Juan [1 ]
Yu, Hao [2 ]
机构
[1] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Guangdong Prov Key Lab Green Chem Prod Technol, Guangzhou 510640, Guangdong, Peoples R China
关键词
SESR; Porous structure; Stability; MgO; Bi-functional catalyst; TEMPERATURE CO2 SORBENTS; HIGH-PURITY HYDROGEN; ACETIC-ACID; ETHANOL; BIOMASS; CAPTURE; GASIFICATION; PERFORMANCE; CONVERSION; REDUCTION;
D O I
10.1016/j.cej.2019.123204
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The sorption-enhanced steam reforming (SESR) process provides a simple way to produce high-purity hydrogen. And a key requirement for SESR is the availability of high cyclic stability of sorbent due to the rapid decline of sorption capacity caused by the sorbent sintering. Herein, we report a facile one-pot hydrothermal synthesis method by using in situ generated carbon microspheres as templates to prepare porous Ni-CaO-MgO bi-functional catalyst. The catalyst possessed MgO-stabilized, Ni and CaO microspheres featuring highly porous structure, which provided sufficient void space for volume variations and reduced the contact between CaO particles which was beneficial to improving the stability. Meanwhile, the uniformly distributed MgO had been found to reduce the particle size of CaO and stabilize the structure of bi-functional catalyst to ensure a stable CO2 uptake. 10Ni-CM7 as the best performing material only required 8.1 wt% MgO, showing 40% loss in sorption-enhanced effect after 10 cycles of repeated SESRG-desorption, where CaO utilization kept 59.1% exceeding the commercial CaO by similar to 109%.
引用
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页数:9
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