MISC

2009年10月

Effects of HCl and SO2 Concentration on Mercury Removal by Activated Carbon Sorbents in Coal-Derived Flue Gas

ENERGY & FUELS
  • Ryota Ochiai
  • ,
  • Md Azhar Uddin
  • ,
  • Eiji Sasaoka
  • ,
  • Shengji Wu

23
10
開始ページ
4734
終了ページ
4739
記述言語
英語
掲載種別
DOI
10.1021/ef900057e
出版者・発行元
AMER CHEMICAL SOC

The effect of the presence of HCl and SO2 in the simulated coal combustion flue gas on the Hg-0 removal by a commercial activated carbon (coconut shell AC) was investigated in a laboratory-scale fixed-bed reactor in a temperature range of 80-200 degrees C. The characteristics (thermal stability) of the mercury species formed on the sorbents under various adsorption conditions were investigated by the temperature-programmed decomposition desorption (TPDD) technique. It was found that the presence of HCl and SO2 in the flue gas affected the mercury removal efficiency of the sorbents as well as the characteristics of the mercury adsorption species. The mercury removal rate of AC increased with the HCl concentration in the flue gas. In the presence of HCl and the absence of SO2 during Hg-0 adsorption by AC, a single Hg-0 desorption peak at around 300 degrees C was observed in the TPDD spectra and intensity of this peak increased with the HCl concentration during mercury adsorption. The peak at around 300 degrees C may be derived from the decomposition and desorption of mercury chloride species. The presence of SO2 during mercury adsorption had an adverse effect on the mercury removal by AC in the presence of HCl. In the presence of both HCl and SO2 during Hg-0 adsorption by AC, the major TPDD peak temperatures changed drastically depending upon the concentration of HCl and SO2 in flue gas during Hg-0 adsorption.

リンク情報
DOI
https://doi.org/10.1021/ef900057e
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000270671800005&DestApp=WOS_CPL
ID情報
  • DOI : 10.1021/ef900057e
  • ISSN : 0887-0624
  • eISSN : 1520-5029
  • Web of Science ID : WOS:000270671800005

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