期刊文献+

Electromotive Force for Solid Oxide Fuel Cells Using Biomass Produced Gas as Fuel 被引量:2

Electromotive Force for Solid Oxide Fuel Cells Using Biomass Produced Gas as Fuel
下载PDF
导出
摘要 当燃料用一个内部计算机节目在 700-1,200 K 被计算,用生物资源的稳固的氧化物燃料房间的起电的力量(e.m.f ) 生产了气体(BPG ) ,基于热力学的平衡分析。旅游节目也在燃料房间以及象 H <SUB>2</SUB>, 公司,公司 <SUB>2</SUB> 和 CH <SUB>4</SUB> 那样的平衡种类的集中预言氧的集中。与把氢用作燃料相比,为把 BPG 用作燃料的房间的 e.m.f 是由碳免职低、强烈影响的亲戚。移开碳免职, H <SUB>2</SUB 的最佳数量 > 增加的 O 在各种各样的操作温度被决定。进一步,为房间的 e.m.f 基于氧化钇稳定了氧化锆并且当电解质被比较,做了 ceria。因为电解质是相对小的,当与那相比使用氧化钇稳定了氧化锆时,学习表明当把 BPG 用作燃料时,为使用的 SOFC 的 e.m.f 的消沉做了 ceria。 The electromotive force (e.m.f.) of solid oxide fuel cells using biomass produced gas (BPG) as the fuels is calculated at 700-1,200 K using an in-house computer program, based on thermodynamic equilibrium analysis. Tour program also predicts the concentration of oxygen in the fuel chamber as well as the concentration of equilibrium species such as H2, CO, CO2 and CH4. Compared with using hydrogen as a fuel, the e.m.f. for cells using BPG as the fuels is relative low and strongly influenced by carbon deposition. To remove carbon deposition, the optimum amount of H2O to add is determined at various operating temperatures. Further the e.m.f, for cells based on yttria stabilized zirconia and doped ceria as electrolytes are compared. The study reveals that when using BPG as fuel, the depression of e.m.f, for a SOFC using doped ceria as electrolyte is relatively small when compared with that using Yttria stabilized zirconia.
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2006年第4期325-328,共4页 化学物理学报(英文)
基金 V. ACKN0WLEDGMENT This work was supported by the National Natural Science Foundation of China (No.50372066 and No.50332040).
关键词 生物质气 电动势 固体氧化物燃料电池 热力学平衡 Biomass produced gas, Electromotive force, Solid oxide fuel cells, Thermodynamic equilibrium
分类号 O [理学]
  • 相关文献

参考文献13

  • 1E.P.Murray,T.Tsai and S.A.Barnett,Nature 400,649 (1999).
  • 2S.Park,J.M.Vohs and R.J.Gorte,Nature 404,265 (2000).
  • 3E.P.Murray,S.J.Harris and H.W.Jen,J.Electrochem.Soc.149,A1127 (2002).
  • 4Y.Jiang and A.V.Virkar,J.Electrochem.Soc.148,A706 (2001).
  • 5M.Zhou,L.F.Yan,Q.X.Guo and Q.S.Zhu,Chin.J.Chem.Phys.16,350 (2003).
  • 6T.Ishihara,T.Yamada,T.Akbay and Y.Takita,Chem.Eng.Sci.54,1535 (1999).
  • 7J.Staniforth and R.M.Ormerod,Cata.Lett.81,19 (2002).
  • 8D.S.Tannhauser,J.Electrochem.Soc.125,1277 (1978).
  • 9S.W.Zha,C.R.Xia and G.Y.Meng,J.Appl.Electrochem.31,93 (2001).
  • 10H.Jiang,X.F.Zhu,Q.X.Guo and Q.S.Zhu,Ind.Eng.Chem.Res.42,5745 (2003).

同被引文献6

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部