EFFECT OF SULFIDING TEMPERATURES ON THE FORMATION OF SULFIDES OF MO/AL2O3 AND COMO/AL2O3

被引:0
作者
SEO, IK [1 ]
SEONG, IW [1 ]
机构
[1] KOREA ADV INST SCI & TECHNOL, DEPT CHEM ENGN, POB 150, CHEONG RYANG, SEOUL 131, SOUTH KOREA
来源
APPLIED CATALYSIS | 1991年 / 74卷 / 01期
关键词
ALUMINA; CATALYST CHARACTERIZATION (ESR; XRD; TPR); COBALT; MOLYBDENUM; SULFIDING TEMPERATURE;
D O I
暂无
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 structures and activities of Mo/Al2O3 and CoMo/Al2O3 sulfided with hydrogen sulfide/hydrogen at various temperatures were studied in the range of temperatures between 573 and 1073 K. The sulfide structures were characterized by electron spin resonance, oxygen chemisorption, sulfur content analysis, temperature-programmed reduction and X-ray diffraction. The thiophene hydrodesulfurization reaction and the ethene hydrogenation reaction were used as probe reactions. As the sulfiding temperature increased, oxo-Mo5+ interacting with alumina in Mo/Al2O3 and CoMo/Al2O3 decreased and finally disappeared at 1073 K. The decrease in oxo-Mo5+ facilitates the formation of crystalline molybdenum sulfide. Cobalt facilitates the formation of molybdenum sulfide weakly interacting with alumina. Cobalt also retarded the aggregation and crystallization of molybdenum sulfide. Cobalt sulfide [spectroscopic splitting factor, g = 2.16, H(PP) (peak-to-peak width) = 200 Gs] was formed when sulfided at 1073 K in CoMo/Al2O3. The rapid decrease in the ratio of activity of CoMo/Al2O3 to Mo/Al2O3 in the thiophene hydrodesulfurization reaction when CoMo/Al2O3 and Mo/Al2O3 was sulfided above 873 K can be explained by the transformation of the sulfide structure.
引用
收藏
页码:109 / 123
页数:15
相关论文
共 50 条
  • [21] Recovery and regeneration of Al2O3 with a high specific surface area from spent hydrodesulfurization catalyst CoMo/Al2O3
    Liu, Qi
    Wang, Wen-Qiang
    Yang, Yue
    Liu, Xue-Gang
    Xu, Sheng-Ming
    RARE METALS, 2019, 38 (01) : 1 - 13
  • [22] Effect of support modifications for CoMo/γ-Al2O3 and CoMo/ASA catalysts in the hydrodeoxygenation of guaiacol
    Mora, Ivan D.
    Mendez, Edna
    Duarte, Liseth J.
    Giraldo, Sonia A.
    APPLIED CATALYSIS A-GENERAL, 2014, 474 : 59 - 68
  • [23] Effect of phosphorus on Mo/Al2O3 catalysts for Maya crude improvement
    Garcia-Vila, Antonio
    Cuevas-Garcia, Rogelio
    Ramirez, Jorge
    Puente-Lee, Ivan
    CATALYSIS TODAY, 2014, 220 : 310 - 317
  • [24] Reaction kinetics of propane catalytic combustion on Cr/γ-Al2O3, Co/Cr/γ-Al2O3, and Au/Cr/γ-Al2O3
    Lin, JN
    Wan, BZ
    JOURNAL OF THE CHINESE INSTITUTE OF CHEMICAL ENGINEERS, 2004, 35 (02): : 149 - 159
  • [25] Kinetic study of glycerol hydrodeoxygenation on Al2O3 and NiMo2C/Al2O3 catalysts
    Duarte, Rafael Belo
    Corazza, Marcos Lucio
    Pimenta, Joao Lourenco Castagnari Willimann
    Jorge, Luiz Mario de Matos
    FUEL, 2023, 354
  • [26] Effect of nanocrystalline χ-Al2O3 structure on the catalytic behavior of Co/Al2O3 in CO hydrogenation
    Chaitree, Wasu
    Jiemsirilers, Sirithan
    Mekasuwandumrong, Okorn
    Jongsomjit, Bunjerd
    Shotipruk, Artiwan
    Panpranot, Joongjai
    CATALYSIS TODAY, 2011, 164 (01) : 302 - 307
  • [27] Role of Al2O3 in Al2O3–Bi2O3–P2O5 glasses
    Yasser B. Saddeek
    A. El-Denglawey
    H. Doweidar
    Applied Physics A, 2021, 127
  • [28] Effect of CeO2 and Al2O3 contents on Ce-ZrO2/Al2O3 composites
    Guo, Wei-Ming
    Zeng, Ling-Yong
    Wu, Li-Xiang
    Wang, Hong-Jian
    Sun, Shi-Kuan
    Lin, Hua-Tay
    Wu, Shang-Hua
    Wang, Cheng-Yong
    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2018, 101 (05) : 2066 - 2073
  • [29] Ionized physical vapor deposited Al2O3 films: Does subplantation favor formation of α-Al2O3?
    Sarakinos, K.
    Music, D.
    Nahif, F.
    Jiang, K.
    Braun, A.
    Zilkens, C.
    Schneider, J. M.
    PHYSICA STATUS SOLIDI-RAPID RESEARCH LETTERS, 2010, 4 (07): : 154 - 156
  • [30] Room-temperature synthesis of χ-Al2O3 and ruby (α-Cr:Al2O3)
    Cortes-Vega, Fernando D.
    Yang, Wenli
    Zarate-Medina, J.
    Brankovic, Stanko R.
    Herrera Ramirez, Jose M.
    Hernandez, Francisco C. Robles
    CRYSTENGCOMM, 2018, 20 (25): : 3505 - 3511