催化作用
二氧化碳重整
材料科学
化学工程
化学
合成气
有机化学
工程类
作者
Anastasios I. Tsiotsias,Nikolaos D. Charisiou,Víctor Sebastián,Safa Gaber,Steven J. Hinder,Mark Baker,Kyriaki Polychronopoulou,Maria A. Goula
标识
DOI:10.1016/j.ijhydene.2021.11.194
摘要
CO 2 utilization through the activation of ethane, the second largest component of natural and shale gas, to produce syngas, has garnered significant attention in recent years. This work provides a comparative study of Ni catalysts supported on alumina, alumina modified with CaO and MgO, as well as alumina modified with La 2 O 3 for the reaction of dry ethane reforming. The calcined, reduced and spent catalysts were characterized employing XRD, N 2 physisorption, H 2 -TPR, CO 2 -TPD, TEM, XPS and TPO. The modification of the alumina support with alkaline earth oxides (MgO and CaO) and lanthanide oxides (La 2 O 3 ), as promoters, is found to improve the dispersion of Ni, enhance the catalyst's basicity and metal-support interaction, as well as influence the nature of carbon deposition . The Ni catalyst supported on modified alumina with La 2 O 3 exhibits a relatively stable syngas yield during 8 h of operation, while H 2 and CO yields decrease substantially for Ni/Al 2 O 3 . • Ni catalysts on Al 2 O 3 modified with MgO/CaO and La 2 O 3 for the DER reaction. • Modification of Al 2 O 3 improves the catalyst basicity and metal-support interaction. • Extensive ethane cracking into CH 4 takes place during the first 3–4 h. • Ni/La–Al 2 O 3 is the most active and stable with H 2 and CO yields remaining constant. • Modification of Al 2 O 3 aids the coke gasification and reduces catalyst degradation.
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