Thermodynamics of Sulfur in Carbon Saturated Ni-Mo Alloys

被引:1
作者
Kim, Do-Hyeong [1 ]
Won, Seung-Yeon [2 ]
Paek, Min-Kyu [3 ]
Son, Hae-Sol [1 ]
Pak, Jong-Jin [1 ]
机构
[1] Hanyang Univ ERICA, Dept Mat Engn, Ansan 15588, South Korea
[2] Hyundai Steel Co, Dangjin 31719, South Korea
[3] Aalto Univ, Dept Chem & Met Engn, Espoo 02150, Finland
关键词
spent catalysts; nickel; molybdenum; carbon; sulfur; interaction parameters; SOLUBILITY; ALUMINATE; FE;
D O I
10.2355/isijinternational.ISIJINT-2019-064
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Nickel-molybdenum alloys can be produced by the carbothermic reduction of spent catalysts containing nickel and molybdenum discarded from the petroleum refinery operations for desulfurization. However, sulfur can be picked up into alloy melts from the sulfur bearing spent catalysts during the smelting process. Thermodynamics of sulfur in this alloy melt is very important for producing low sulfur Ni-Mo alloys to be used in steel industry. In the present study, thermodynamic interaction coefficients of carbon and molybdenum on sulfur in carbon saturated liquid Ni-Mo alloys were measured using the slag/metal equilibration technique at 1 773 and 1 873 K. The equilibrium sulfur distribution was measured between a slag with a known sulfide capacity and carbon saturated liquid Ni-Mo-S alloys of various compositions. The carbon solubility in liquid Ni-Mo alloy was significantly changed with molybdenum content, and the specific effects of carbon and molybdenum on sulfur was determined using Wagner's formalism as the first- and second-order interaction parameters.
引用
收藏
页码:1801 / 1805
页数:5
相关论文
共 50 条
  • [21] Ni and Ni-Mo hydrogen evolution electrocatalysts electrodeposited in a polyaniline matrix
    Damian, Alexis
    Omanovic, Sasha
    [J]. JOURNAL OF POWER SOURCES, 2006, 158 (01) : 464 - 476
  • [22] Ni-Mo Nanopowders for Efficient Electrochemical Hydrogen Evolution
    McKone, James R.
    Sadtler, Bryce F.
    Werlang, Caroline A.
    Lewis, Nathan S.
    Gray, Harry B.
    [J]. ACS CATALYSIS, 2013, 3 (02): : 166 - 169
  • [23] Some reactions of Ni-Mo and Ni-W propargylic cations with nucleophiles
    Chetcuti, MJ
    McDonald, SR
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2004, 689 (11) : 1882 - 1889
  • [24] Investigation of Ni-Mo and Co-Mo alloys electrodeposition involving choline chloride based ionic liquids
    Costovici, Stefania
    Manea, Adrian-Cristian
    Visan, Teodor
    Anicai, Liana
    [J]. ELECTROCHIMICA ACTA, 2016, 207 : 97 - 111
  • [25] Kinetic study of carbon monoxide methanation over mesoporous Ni-Mo catalyst prepared by a hydrothermal method
    Zhang Jiaying
    [J]. PROGRESS IN REACTION KINETICS AND MECHANISM, 2019, 44 (01) : 3 - 17
  • [26] Selective extraction of Mo from a Ni-Mo ore using pressure alkaline leaching
    Wang, Mingshuang
    Wei, Chang
    Fan, Gang
    Li, Minting
    Deng, Zhigan
    Wang, Sifu
    [J]. HYDROMETALLURGY, 2015, 153 : 6 - 11
  • [27] Preparation and Microstructure of Nanocrystalline Ni-Mo Films
    Du, Jingjing
    Sun, Xiaotong
    Tang, Zengmin
    Xu, Lijian
    Wu, Ruomei
    Chen, Baizhen
    [J]. JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2013, 13 (08) : 5844 - 5848
  • [28] X-RAY-ELECTRON AND ELECTRON DIFFRACTION STUDY OF ORDERING ALLOYS OF THE Ni-Mo SYSTEM
    Ustinovshchikov, Yu. I.
    Shabanova, I. N.
    Terebova, N. S.
    [J]. METAL SCIENCE AND HEAT TREATMENT, 2011, 53 (7-8) : 338 - 343
  • [29] Establishing relationships between bath composition and the properties of amorphous Ni-Mo alloys obtained by electrodeposition
    de Almeida, Arthur Filgueira
    de Souto, Joyce Ingrid Venceslau
    dos Santos, Mathews Lima
    de Santana, Renato Alexandre Costa
    Alves, Jose Jailson Nicacio
    Campos, Ana Regina Nascimento
    Prasad, Shiva
    [J]. JOURNAL OF ALLOYS AND COMPOUNDS, 2021, 888
  • [30] Comparison of the Catalytic Performance of Ni, Mo, and Ni-Mo Impregnated on Acid Halloysite Nanotubes in the n-Decane Hydroconversion
    Torres-Luna, J. A.
    Moreno, S.
    Molina, R.
    Carriazo, J. G.
    [J]. ENERGY & FUELS, 2019, 33 (12) : 12647 - 12655