Ni catalysts for dry methane reforming prepared by A-site exsolution on mesoporous defect spinel magnesium aluminate

被引:41
作者
Cho, Eunkyung [1 ]
Lee, Young-Hee [2 ]
Kim, Hyunjoung [2 ]
Jang, Eun Jeong [3 ]
Kwak, Ja Hun [3 ]
Lee, Kyubock [2 ]
Ko, Chang Hyun [1 ]
Yoon, Wang Lai [4 ]
机构
[1] Chonnam Natl Univ, Sch Chem Engn, Gwangju 61186, South Korea
[2] Chungnam Natl Univ, Grad Sch Energy Sci & Technol, Daejeon 34134, South Korea
[3] Ulsan Natl Inst Sci & Technol UNIST, Sch Energy & Chem Engn, Ulsan 44919, South Korea
[4] Korea Inst Energy Res, Hydrogen Energy Res Ctr, Daejeon 34129, South Korea
基金
新加坡国家研究基金会;
关键词
Mesoporous magnesium aluminate; Defect spinel structure; Dry methane reforming; Ni catalyst; A-site exsolution; NANOCRYSTALLINE MGAL2O4 SPINEL; CO2; NICKEL; PERFORMANCE; PEROVSKITE; REDUCTION; PARTICLES; STABILITY; ZEOLITES; SUPPORT;
D O I
10.1016/j.apcata.2020.117694
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
In dry methane reforming, the selection of a suitable support is critical due to coke formation and metal particle sintering. We prepared two types of mesoporous defect spinel magnesium aluminate support, namely DS09, with a Mg/Al molar ratio (Mg/Al) of 0.1, and DS19 with Mg/Al = 0.24. Each support has a high surface area, large mesopore volume, and a phase between its defect spinel (Mg0.388Al2.408O4) and spinel (MgAl2O4) structures. Magnesium aluminate with a Mg/Al of 0.5 (MG30), which has a low surface area and is devoid of mesopores, was used as the reference support. Ni was supported on DS09 (Ni-DS09) and DS19 (Ni-DS19) by A-site ex-solution. These catalysts display significant advantages over Ni-supported MG30 (Ni-MG30); Ni-DS19 exhibited a higher coke resistance than Ni-DS09, due to its lower acidity, while DS19, which contains a defect spinel structure, optimized acidity, and well-developed mesopores, was the best support for the DMR.
引用
收藏
页数:9
相关论文
共 39 条
[31]   TEMPERATURE-PROGRAMMED REDUCTION STUDY OF NIO-MGO INTERACTIONS IN MAGNESIA-SUPPORTED NI CATALYSTS AND NIO-MGO PHYSICAL MIXTURE [J].
PARMALIANA, A ;
ARENA, F ;
FRUSTERI, F ;
GIORDANO, N .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1990, 86 (14) :2663-2669
[32]   Effect of composition and thermal pretreatment on properties of Ni-Mg-Al catalysts for CO2 reforming of methane [J].
Perez-Lopez, OW ;
Senger, A ;
Marcilio, NR ;
Lansarin, MA .
APPLIED CATALYSIS A-GENERAL, 2006, 303 (02) :234-244
[33]   A-site deficient perovskite: the parent for in situ exsolution of highly active, regenerable nano-particles as SOFC anodes [J].
Sun, Yifei ;
Li, Jianhui ;
Zeng, Yimin ;
Amirkhiz, Babak Shalchi ;
Wang, Mengni ;
Behnamian, Yashar ;
Luo, Jingli .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (20) :11048-11056
[34]  
Szanyi J, 2014, PHYS CHEM CHEM PHYS, V16, P15117, DOI 10.1039/c4cp00616j
[35]   Correlation between activity and acidity on zeolites: a high temperature infrared study of adsorbed acetonitrile [J].
Thibault-Starzyk, F ;
Travert, A ;
Saussey, J ;
Lavalley, JC .
TOPICS IN CATALYSIS, 1998, 6 (1-4) :111-118
[36]   Step-change in high temperature steam electrolysis performance of perovskite oxide cathodes with exsolution of B-site dopants [J].
Tsekouras, George ;
Neagu, Dragos ;
Irvine, John T. S. .
ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (01) :256-266
[37]   Significant roles of mesostructure and basic modifier for ordered mesoporous Ni/CaO-Al2O3 catalyst towards CO2 reforming of CH4 [J].
Xu, Leilei ;
Miao, Zhichao ;
Song, Huanling ;
Chen, Wei ;
Chou, Lingjun .
CATALYSIS SCIENCE & TECHNOLOGY, 2014, 4 (06) :1759-1770
[38]   A review of CH4-CO2 reforming to synthesis gas over Ni-based catalysts in recent years (2010-2017) [J].
Zhang, Guojie ;
Liu, Jiwei ;
Xu, Ying ;
Sun, Yinghui .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2018, 43 (32) :15030-15054
[39]   Exsolution of Re-alloy catalysts with enhanced stability for methane dry reforming [J].
Zubenko, Daria ;
Singh, Sarika ;
Rosen, Brian A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2017, 209 :711-719