脱氢
催化作用
选择性
镧
化学
乙烯
分解
纳米颗粒
钙钛矿(结构)
氢
锰酸镧
无机化学
程序升温还原
材料科学
物理化学
纳米技术
结晶学
有机化学
电极
电解质
作者
Xiaofeng Yang,Tong Wei,Bo Chi,Jian Pu,Jian Li
标识
DOI:10.1016/j.jcat.2019.08.008
摘要
An A-site deficient and Ni-doped LaMnO3 perovskite (LMN) is prepared and reduced in 5% H2-N2 at 800 °C for 1 (R-LMN) and 6 (ER-LMN) h for evaluation as catalysts for C2H6 dehydrogenation to co-produce C2H4 and H2. The 1 h reduction causes the formation of Ni nanoparticles embedded in a perovskite substrate similar to LMN, but the excessive reduction for 6 h causes LMN decomposition to La2O3, MnO and Ni nanoparticles. The performance of the catalysts increases with increasing temperature. R-LMN demonstrates the highest performance among the catalysts studied, with 41.6% C2H6 conversion and 98.0% C2H4 selectivity at 750 °C; ER-LMN exhibits the lowest catalytic performance because of LMN decomposition. The performance of R-LMN is essentially stable during a 50 h test; and the slow growth of Ni nanoparticles slightly increases C2H6 conversion and decreases C2H4 selectivity due to the increase of the surface area of the Ni nanoparticles.
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