• Title of article

    Activity of alumina-silica-supported NiMoS prepared by controlled mixing of alumina into SiO2 hydrogels for HDS of gas oil

  • Author/Authors

    Nakano، نويسنده , , Koji and Pang، نويسنده , , Weiwei and Lee، نويسنده , , Jihn-Koo and Park، نويسنده , , Joo-Il and ، نويسنده , , Yoon، نويسنده , , Seong-Ho and Mochida، نويسنده , , Isao، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2011
  • Pages
    7
  • From page
    1012
  • To page
    1018
  • Abstract
    Alumina-silica-supported NiMoS composites were examined in single- and dual-layer catalyst beds in a high-pressure (5 MPa) flow reactor to achieve ultra low sulfur (10 ppm) diesel fuels. Three types of alumina-silica composite supports were prepared by co-precipitation to control the particle size and arrangement of alumina and silica. The SiO2 content was found to be influential on catalytic performance, being best by around 27% regardless of preparation conditions. Alumina crystal size controlled the acidity and surface area of the support, key factors influencing catalytic performance. NiMoASA-2(27), prepared by procedure 2, achieved 4.5 and 3 ppm S at 345 and 360 °C, respectively, in the single bed reactor at a liquid hourly space velocity (LHSV) of 1 h− 1. NiMoASA-2(27) achieved the best performance of the supports examined in this study. The double-layer catalyst bed contained commercial CoMoS (LX6) and NiMoASA-2(27) in the first and the second beds at 345 and 360 °C, respectively, and achieved 5 and 2 ppm S, indicating better performance at higher temperatures. The reaction order for the hydrodesulfurization (HDS) of refractory sulfur species was close to unity over NiMoASA-2(27), which was significantly higher than that of the commercial CoMoS catalyst. Alumina-silica-supported NiMoS in the second bed of the dual-layer catalyst bed achieved less than 10 ppm S for refractory sulfur species with around 500 ppm S.
  • Keywords
    activity , Preparation , Alumina-silica , Particle size , SiO2 content
  • Journal title
    Fuel Processing Technology
  • Serial Year
    2011
  • Journal title
    Fuel Processing Technology
  • Record number

    1509771