期刊论文详细信息
Sustainability
Biochars as Potential Adsorbers of CH4, CO2 and H2S
Yong Sik Ok1  Sang Ryong Lee2  Ming Zhang3  Sumathi Sethupathi4  Anushka Upamali Rajapaksha5  Norhusna Mohamad Nor6  Abdul Rahman Mohamed7  Mohammad Al-Wabel7  Sang Soo Lee8 
[1] Agricultural Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Saudi Arabia;School of Natural Resources and Environmental Science, Kangwon National University, Chuncheon 24341, Korea;Department of Environmental Engineering, China Jiliang University, Hangzhou 310018, China;Faculty of Engineering and Green Technology, Universiti Tunku Abdul Rahman, 31900 Kampar, Perak, Malaysia;;Korea Biochar Research Center &National Institute of Animal Science, RDA, Wanju55365, Korea;School of Chemical Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Pulau Pinang, Malaysia;;Soil Science Department, College of Food &
关键词: adsorption;    biochar;    carbon dioxide;    hydrogen sulphide;   
DOI  :  10.3390/su9010121
来源: DOAJ
【 摘 要 】

Methane gas, as one of the major biogases, is a potential source of renewable energy for power production. Biochar can be readily used to purify biogas contaminants such as H2S and CO2. This study assessed the adsorption of CH4, H2S, and CO2 onto four different types of biochars. The adsorption dynamics of biochars were investigated in a fixed-bed column, by determining the breakthrough curves and adsorption capacities of biochars. The physicochemical properties of biochars were considered to justify the adsorption performance. The results showed that CH4 was not adsorbed well by the subjected biochars whereas CO2 and H2S were successfully captured. The H2S and CO2 breakthrough capacity were related to both the surface adsorption and chemical reaction. The adsorption capacity was in the following order: perilla > soybean stover > Korean oak > Japanese oak biochars. The simultaneous adsorption also leads to a competition of sorption sites. Biochars are a promising material for the biogas purification industry.

【 授权许可】

Unknown   

  文献评价指标  
  下载次数:0次 浏览次数:0次