Catalytic reforming of biomass pyrolysis gas over Ni catalysts: Alumina, spent fluid catalytic cracking catalyst and char as supports

被引:3
|
作者
Low, Ching Wei [1 ]
Veksha, Andrei [1 ]
Aryal, Rupendra [1 ]
Chan, Wei Ping [1 ]
Lisak, Grzegorz [1 ,2 ]
机构
[1] Nanyang Technol Univ, Residues & Resource Reclamat Ctr R3C, Nanyang Environm & Water Res Inst, Singapore 637141, Singapore
[2] Nanyang Technol Univ, Sch Civil & Environm Engn, 50 Nanyang Ave, Singapore 639798, Singapore
基金
新加坡国家研究基金会;
关键词
Alumina; Catalytic steam reforming; Biomass pyrolysis gas; Char; Spent FCC catalyst; RAW BIO-OIL; HYDROGEN-PRODUCTION; DEACTIVATION PATHWAYS; STEAM; TAR; CARBON; METHANE; GASIFICATION; PERFORMANCE; COKING;
D O I
10.1016/j.apcata.2024.120074
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The potential replaceability of a Ni catalyst supported on commercial alpha-Al2O3 (Ni/Al2O3) by Ni on biomassderived char (Ni/Char), and Ni on spent fluid catalytic cracking catalyst (Ni/FCC) for steam reforming of biomass pyrolysis gas was investigated (14 h at 850 degrees C, steam/carbon ratio = 5). The catalysts reformed 60-80 % of C2-C5 hydrocarbons, producing 2.7-4.1 mg min-1 of H2. The reforming activity of Ni/Al2O3 and Ni/FCC was higher compared to Ni/Char, indicating the beneficial role of metal oxide supports. The use of Al2O3 and FCC resulted in a lower thermo-oxidative stability of coke formed on Ni/Al2O3 and Ni/FCC compared to Ni/Char. Furthermore, the deposited Ni showed higher stability towards oxidation by steam into NiO in case of Al2O3 and FCC compared to char. According to reforming activity, H2 production rate, coking, and Ni oxidation of the catalysts, FCC has better prospects as an alternative support in a reforming catalyst than char.
引用
收藏
页数:13
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