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纯四方相硫化氧化锆催化剂的制备及其生物柴油合成应用研究(英文) 被引量:7

Synthesis of tetragonal sulfated zirconia via a novel route for biodiesel production
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摘要 将过硫酸铵浸渍于直接合成的纳米氧化锆晶体表面,经300-500℃高温焙烧处理获得硫化氧化锆催化剂。采用X射线衍射(XRD)、氮气吸附-脱附、氨气程序升温脱附(NH_3-TPD)、傅里叶红外光谱(FT-IR)、扫描电镜(SEM)和能谱仪(EDS)等分析手段对催化剂的结构性能进行了表征。结果表明,所有的催化剂均展现出纯四方相结构和高的结晶度。其中,经500℃热处理获得的催化剂拥有最高的硫含量和酸性位,将其应用于大豆油与甲醇酯交换反应合成生物柴油,获得了脂肪酸甲酯收率高达84.6%的催化效果,进一步表明该催化剂表面存在优越的超强酸位。 The sulfated zirconia was prepared by directly impregnating ammonium persulphate on the crystalline zirconia and followed by the calcination temperatures of 300-500℃.The structural properties of the catalysts were characterized by X-ray diffraction (XRD), N2 adsorption-desorption, ammonia temperature programmed desorption (NH3-TPD), Fourier transform infrared spectroscopy (FT-IR) and a scanning electron microscope (SEM) equipped with an energy dispersive spectroscope (EDS).The experiment results demonstrated that the catalysts presented the tetragonal structure of zirconia and high crystallinity.The catalyst calcined at 500℃ possessed the highest sulfur content and acidic sites in the catalysts.The catalyst exhibited high catalytic activity in transesterification of soybean oil with methanol.The yield of biodiesel achieved 84.6% because of the preferable super-acid sites on the surface of the catalyst.
出处 《燃料化学学报》 EI CAS CSCD 北大核心 2017年第3期311-316,共6页 Journal of Fuel Chemistry and Technology
基金 supported by the National Natural Science Foundation of China(21376157,21406153) Shanxi Province Science Foundation for Youths(2013021008-3) Research Fund for the Doctoral candidate of Taiyuan University of Science and Technology(20162017)~~
关键词 四方相硫化锆 浸渍 晶体氧化锆 酯交换反应 生物柴油 tetragonal sulfated zirconia impregnating crystalline zirconia transesterification biodiesel
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  • 1J.Zhu,H.Bienayme,Multicomponent Reactions,Wiley-VCH,Weinheim,2005.
  • 2I.Devi,P.J.Bhuyan,Tetrahedron Lett.45(2004) 8625.
  • 3S.H.Mashraqui,M.B.Patil,H.D.Mistry,et al.Chem.Lett.33(2004) 1058.
  • 4A.Chetia,C.J.Saikia,K.C.Lekhok,et al.Tetrahedron Lett.45(2004) 2649.
  • 5A.K.Bose,S.Pednekar,S.N.Ganguly,et al.Tetrahedron Lett.45(2004) 8351.
  • 6D.Prajapati,J.S.Sandhu,Synlett(2004) 235.
  • 7A.Domling,I.Ugi,Angew.Chem.Int.Ed.39(2000) 3168.
  • 8G.F.Ross,E.Herdtweck,I.Ugi,Tetrahedron 58(2002) 6127.
  • 9T.A.Keating,R.W.Armstrong,J.Am.Chem.Soc.117(1995) 7842.
  • 10H.Groger,M.Hatam,J.Martens,Tetrahedron 51(1995) 7173.

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