High entropy oxide catalysts with SO2 resistance in RWGS reaction

被引:4
|
作者
Zhang, Mengyuan [1 ,2 ]
Lu, Xiaoyan [1 ]
Luo, Kongliang [1 ]
Ye, Jian [1 ]
Dong, Jia li [1 ]
Lu, Nana [1 ]
Wang, Xiaopeng [1 ]
Niu, Qiang [3 ]
Zhang, Pengfei [1 ,2 ]
Dai, Sheng [4 ]
机构
[1] Ningxia Univ, Coll Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[3] Inner Mongolia Erdos Elect Power & Met Grp Co Ltd, Natl Enterprise Technol Ctr, Ordos 016064, Inner Mongolia, Peoples R China
[4] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37830 USA
关键词
High entropy oxide; SO; 2; resistance; Entropy engineering; In situ FTIR; In situ XPS; RWGS reaction; REDUCTION; MECHANISM; NOX;
D O I
10.1016/j.apcatb.2024.123845
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
Ubiquitous presence of SO2 usually shows adverse effects on industrial catalysis. Herein, a concept of engineering entropy to design SO2 resistance oxide catalysts is proposed. (Ni0.2Mg0.2Cu0.2Zn0.2Co0.2)Fe2O4 showed excellent performance (the CO2 conv. = 41.4%, CO selec. = 99.6% at 400 degrees C) compared to the control samples in the reverse water-gas shift (RWGS). In addition, (Ni0.2Mg0.2Cu0.2Zn0.2Co0.2)Fe2O4 had the SO2-tolerant ability (the CO2 conv. = 38.5%, CO selec. = 99.2% at 400 degrees C) after being poisoned with 1000 ppm SO2 at 400 degrees C for 1 h. In sharp contrast, the control samples NiFe2O4, MgFe2O4, CuFe2O4 and CoFe2O4 lost their activity. O-1S XPS indicated that (Ni0.2Mg0.2Cu0.2Zn0.2Co0.2)Fe2O4 had higher oxygen vacancy concentrations. SO2 resistance mechanism was studied by infrared spectroscopy, SO2-TPD, in situ S 2p XPS and the DFT results, confirming that the low SO2 adsorption energy of (Ni0.2Mg0.2Cu0.2Zn0.2Co0.2)Fe2O4, which was attributed to the lower Gibbs free energy. This work may inspire the rational design of SO2-resistant catalysts.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] REACTION OF SO2 AND NO2 WITH POLYMERS
    JELLINEK, HH
    FLAJSMAN, F
    KRYMAN, FJ
    JOURNAL OF APPLIED POLYMER SCIENCE, 1969, 13 (01) : 107 - &
  • [32] Significant Enhanced SO2 Resistance of Pt/SiO2 Catalysts by Building the Ultrathin Metal Oxide Shell for Benzene Catalytic Combustion
    Yang, Dan
    Dong, Fang
    Han, Weigao
    Zhang, Jiyi
    Tang, Zhicheng
    ACS APPLIED MATERIALS & INTERFACES, 2023, 15 (36) : 42541 - 42556
  • [33] SO RADICAL DETECTION IN REACTION OF SO2 CATALYTIC REDUCTION
    MINASYAN, VT
    NALBANDY.AB
    DOKLADY AKADEMII NAUK SSSR, 1974, 218 (02): : 393 - 395
  • [34] High Entropy Spinel Oxide (AlCrCoNiFe2)O as Highly Active Oxygen Evolution Reaction Catalysts
    Dadvari, Pouria
    Hung, Wei-Hsuan
    Wang, Kuan-Wen
    ACS OMEGA, 2024, 9 (25): : 27692 - 27698
  • [35] Activation of Au nanoparticles on oxide surfaces:: reaction of SO2 with Au/MgO(100)
    Rodriguez, JA
    Pérez, M
    Jirsak, T
    Evans, J
    Hrbek, J
    González, L
    CHEMICAL PHYSICS LETTERS, 2003, 378 (5-6) : 526 - 532
  • [36] Influence of different doped metal cations on the activity and SO2 resistance of Mn based catalysts for NH3-SCR reaction
    掺杂元素对Mn基催化剂SCR性能及抗硫性能的影响
    Sun, Hong (sunhonglzg@163.com), 1600, Materials China (39): : 2440 - 2446
  • [37] The reaction and poisoning mechanism of SO2 and perovskite LaCoO3 film model catalysts
    Zhu, YF
    Tan, RQ
    Feng, J
    Ji, SS
    Cao, LL
    APPLIED CATALYSIS A-GENERAL, 2001, 209 (1-2) : 71 - 77
  • [38] Properties of platinum-containing glass-fiber catalysts in the SO2 oxidation reaction
    S. V. Vanag
    E. A. Paukshtis
    A. N. Zagoruiko
    Reaction Kinetics, Mechanisms and Catalysis, 2015, 116 : 147 - 158
  • [39] NEW DATA ON KINETICS AND REACTION-MECHANISM FOR SO2 OXIDATION OVER VANADIUM CATALYSTS
    IVANOV, AA
    BALZHINIMAEV, BS
    REACTION KINETICS AND CATALYSIS LETTERS, 1987, 35 (1-2): : 413 - 424
  • [40] Properties of platinum-containing glass-fiber catalysts in the SO2 oxidation reaction
    Vanag, S. V.
    Paukshtis, E. A.
    Zagoruiko, A. N.
    REACTION KINETICS MECHANISMS AND CATALYSIS, 2015, 116 (01) : 147 - 158