Thermo-catalytic conversion of greenhouse gases (CO2 and CH4) to CO-rich hydrogen by CeO2 modified calcium iron oxide supported nickel catalyst

被引:12
作者
Hossain, Mohammed Anwar [1 ]
Ayodele, Bamidele, V [2 ,3 ]
Ong, Huei R. [4 ]
Mustapa, Siti, I [3 ]
Cheng, Chin K. [1 ,2 ]
Khan, Maksudur R. [1 ,2 ]
机构
[1] Univ Malaysia Pahang, Fac Chem & Proc Engn Technol, Gambang Kuantan 26300, Pahang, Malaysia
[2] Univ Malaysia Pahang, Ctr Excellence Adv Res Fluid Flow, Lebuhraya Tun Razak 26300, Gambang, Malaysia
[3] Univ Tenaga Nas, Inst Energy Policy & Res, Jalan IKRAM UNITEN Kajang, Kajang, Selangor, Malaysia
[4] DRB HICOM Univ Automot Malaysia, Fac Engn & Technol, Pekan, Malaysia
关键词
calcium iron oxide; ceria promoter; hydrogen; methane dry reforming; syngas; SYNGAS PRODUCTION; CARBON DEPOSITION; COMBINED STEAM; METHANE; NI; DEACTIVATION; ADSORPTION; DESIGN; CERIA; LA;
D O I
10.1002/er.5346
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In this study, the thermo-catalytic conversion of two principal greenhouse gases (methane and carbon dioxide) to carbon monoxide (CO)-rich hydrogen (H-2) is investigated over cerium oxide (CeO2) promoted calcium ferrite supported nickel (Ni/CaFe2O4) catalyst. The CeO2 promoted Ni/CaFe2O4 catalyst was prepared using wet-impregnation technique. To ascertain the physicochemical properties, the as-prepared catalyst was characterized using various instrument techniques. The characterization of the catalysts reveals that CeO2-Ni/CaFe2O4 possesses suitable physicochemical properties for the conversion of methane (CH4) and carbon dioxide (CO2) to CO-rich H-2. The thermo-catalytic reaction revealed that the CeO2 promoted Ni/CaFe2O4 catalyst displayed a higher CH4 and CO2 conversions of 90.04% and 91.2%, respectively, at a temperature of 1073 K compared to the unpromoted catalyst. The highest H-2 and CO yields of 78% and 76%, respectively, were obtained over the CeO2-Ni/CaFe2O4 at 1073 K and CH4/CO2 ratio of 1. The CeO2 promoted Ni/CaFe2O4 catalyst remained stable throughout the 30 hours time on stream (TOS) while that of the unpromoted Ni/CaFe2O4 catalyst sharply decreased after 22 hours TOS. The characterization of the used catalysts confirms the evidence of carbon depositions on the unpromoted Ni/CaFe2O4 which is solely responsible for its deactivation. Whereas, there was a slightly gasifiable carbon deposited on the CeO2 promoted Ni/CaFe2O4 catalyst which could be ascribed to the interaction effect of the CeO2 promoter on the Ni/CaFe2O4 catalyst.
引用
收藏
页码:6325 / 6337
页数:13
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