Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Chung Shan Medical University
  3. Pure學術人才庫轉入
  4. Catalytic activity of mesoporous Ni/CNT, Ni/SBA-15 and (Cu, Ca, Mg, Mn, Co)-Ni/SBA-15 catalysts for CO2 reforming of CH4
 
  • Details
Options

Catalytic activity of mesoporous Ni/CNT, Ni/SBA-15 and (Cu, Ca, Mg, Mn, Co)-Ni/SBA-15 catalysts for CO2 reforming of CH4

Journal
RSC Advances
Date Issued
2016-01-01
Author(s)
CHI-YUAN LU  
DOI
10.1039/c6ra07635a
URI
https://www.scopus.com/pages/publications/84981484535
https://scholars.csmu.edu.tw/handle/123456789/27455
Abstract
The CO2 reforming of CH4 to H2 over a catalyst is an effective method for renewable energy generation. In this study, SBA-15 and CNT were chosen as supports for the Ni-based catalysts prepared by the impregnation method. The FESEM images demonstrated that NiO particles were rhombic and well distributed on the SBA-15 surface. The XRD patterns showed that the chemical state of Ni changed after the reforming reaction; the main crystals on the fresh and spent Ni/SBA-15 were found to be NiO and Ni0. The catalytic performance of Ni/SBA-15 in CO2/CH4 reforming was found to be superior to that of Ni/CNT. The results of the TGA and BET analysis demonstrated that spent Ni/SBA-15 (at 600 °C) showed no catalytic decay as an insignificant amount of coke was deposited on the catalyst supports. Moreover, Ni-based bimetallic catalysts were studied for the reforming reaction, and the activity of the catalysts with respect to metals was observed to follow a particular order: Cu-Ni > Mg-Ni > Co-Ni > Ca-Ni > Mn-Ni. The Cu-Ni/SBA-15 catalyst exhibited higher catalytic activity at a reaction temperature of 650 °C as compared to the others; the H2 yield (40%) was not decreased as the reaction time increased, and the conversion of CO2 and CH4 is 77% and 75%, respectively.
Type
journal article
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your Institution's web identity.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback