期刊文献+

Production of Light Olefins from Biosyngas by Two-stage Catalytic Conversion Process via Dimethyl Ether 被引量:1

生物质气经由二甲醚两步法制备低碳烯烃
下载PDF
导出
摘要 NiSAPO-34 and NiSAPO-34/HZSM-5 were prepared and evaluated for the performance of dimethyl ether (DME) conversion to light olefins (DTO). The processes of two-stage light olefin production, DME synthesis and the following DTO, were also investigated using biosyngas as feed gas over Cu/Zn/A1/HZSM-5 and the optimized 2%NiSAPO-34/HZSM- 5. The results indicated that adding 2%Ni to SAPO-34 did not change its topology structure, but resulted in the forming of the moderately strong acidity with decreasing acid amounts, which slightly enhanced DME conversion activity and C2=-C3= selectiw ity. Mechanically mixing 2%NiSAPO-34 with HZSM-5 at the weight ratio of 3.0 further prolonged DME conversion activity to be more than 3 h, which was due to the stable acid sites from HZSM-5. The highest selectivity to light olefins of 90.8% was achieved at 2 h time on stream. The application of the optimized 2%NiSAPO-34/HZSM-5 in the second-stage reactor for DTO reaction showed that the catalytic activity was steady for more than 5 h and light olefin yield was as high as 84.6 g/m3syngas when the biosyngas (H2/CO/CO2/N2/CH4=41.5/26.9/14.2/14.6/2.89, vol%) with low H/C ratio of 1.0 was used as feed gas.
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2014年第2期227-232,I0004,共7页 化学物理学报(英文)
基金 ACKNOWLEDGM ENTS This work was supported by the National Natural Science Foundation of China (No.51006110, No.51276183, and No.51036006), the National Natural Research Foundation of China/Japan Science and Technology Agency (No.51161140331), and National Key Basic Research Program 973 Project Founded by MOST of China (No.2013CB228105).
关键词 Light olefins Two-stage conversion Dimethyl ether Biosyngas NiSAPO-34/HZSM-5 低碳烯烃 二甲醚 两步转化 NiSAPO-34 HZSM-5 生物质气
  • 相关文献

参考文献31

  • 1S.N.Khadzhiev,N.V.Kolesnichenko,and N.N.Ezhova,Pet.Chem.48,325(2008).
  • 2B.Vora,J.Q.Chen,A.Bozzano,B.Glover,and P.Barger,Catal.Today 141,77(2009).
  • 3Y.P.Li,T.J.Wang,X.L.Yin,C.Z.Wu,L.L.Ma,H.B.Li,and L.Sun,Fuel 88,2181(2009).
  • 4D.S.Mao,J.C.Xia,B.Zhang,and G.Z.Lu,Energy Convers.Manage.51,1134(2010).
  • 5S.Soundararajan,A.K.Dalai,and F.Berruti,Fuel 80,1187(2001).
  • 6V.Yangali-Quintanilla,A.Verliefde,T.U.Kim,A.Sadmani,M.Kennedy,and G.Amy,J.Membr.Sei.342,251(2009).
  • 7S.C.Baek,Y.J.Lee,K.W.Jun,and S.B.Hong,Energy Fuels 23,593(2009).
  • 8F.J.Keil,Mieroporous Mesoporous Mater.29,49(1999).
  • 9X.Zhang,R.J.Wang,X.X.Yang,and F.B.Zhang,Mieroporous Mesoporous Mater.i16,210(2008).
  • 10A.G.Gayubo,A.T.Aguayo,M.Olazar,R.Vivaneo,and J.Bilbao,Chem.Eng.Sci.58,5239(2003).

同被引文献7

引证文献1

二级引证文献12

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