期刊文献+

大比表面层柱磷酸锡的制备和催化性能 被引量:3

Preparation and Catalytic Behaviour of Cr_2O_3-Pillared Tin Phosphate with High Surface Area
下载PDF
导出
摘要 详细研究了氧化铬层柱磷酸锡的制备规律,革新了文献中丙胺加大量季铵盐的两步胶体化法,用有机胺使层板一步胶体化成功地制备了高比表面积的层柱磷酸锡,其最高比表面积达445m2/g。样品经400℃焙烧后仍具有良好的层柱结构,可形成规整的平行板型中孔,孔径集中在1.7~5nm范围内.丙醇脱水和异丙苯裂解反应表明氧化锆层柱磷酸锡具有弱酸催化活性;环己烷脱氢反应表明,氧化铬层柱磷酸锡比负载型氧化铬催化剂有更高的脱氢活性. The preparation of Cr2O3-pillared tin phosphate was studied in detail. The previ-ous method with two-step colloidization by propylamine and a great amount of NMe4Cl was innovated, and Cr2O3-pillared tin phosphate samples with a high surface area were prepared successfully through one-step colloidization by various ammes. The surface area of the sam-ples prepared reached 445m2/g, which was much higher than the value 380m2/g reported in literatures. After calcination at 400℃ the samples possess a prefect pillared structure and uniform slit-shaped mesopores with diameters between 1.7~5.0nm.The Cr2O3-pillared tin phosphate samples are weakly acidic, and are catalytically active for dehydration of iso-propanol and n-propanol. The cyclohexane dehydrogenation activity of the samples are high-er than that of a conventional Cr2O3 supported catalyst, showing that Cr2O3 in the pillared catalysts is in highly dispensed state.
机构地区 复旦大学化学系
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1997年第8期1337-1342,共6页 Chemical Journal of Chinese Universities
基金 国家自然科学基金
关键词 氧化铬 层柱 磷酸锡 制备 催化活性 Pillared layered tin phosphate,Pore structure, Acid catalytic reaction,Dehydrogenation reaction
  • 相关文献

参考文献2

  • 1徐金锁,高等学校化学学报,1997年,18卷,88页
  • 2徐金锁,高等学校化学学报,1987年,18卷,93页

同被引文献29

  • 1谢有畅 杨乃芳 等.某些催化剂活性组分在载体表面分散的自发倾向[J].中国科学:B辑,1982,8:673-682.
  • 2Das D.P.,Parida K.M..Catal.Surv.Asia.[J] ,2008.12:203-213.
  • 3Roziere J.,Jones D.J.,Cassagneau T..J.Mater.Chem.[J] ,1991,1(6):1081-1082.
  • 4Jim(e)nez-Jim(e)nez J.,Rubio-Alonao M.,Quesada D.E.,Rodriguez-Castellon E.,Jim(e)nez-Lopez A..J.Mater.Chem.[J] ,2005,15:3466-3472.
  • 5Jim(e)nez-Jim(e)nez J.,Maireles-Torres P.,Olivera-Pastor P.,Rodriguez-Castellon E.,Jim(e)nez-Lopez A..Langmuir[J] ,1997,13.2857-2862.
  • 6Moreno-Tost R.,Oliveira M.L,Eliehe-Quesada D.,Jim(e)nez-Jim(e)ez J.,Jim(e)nez-Lopez A.,Rodriguez-Castellon E..Chemosphere[J] ,2008,72:608-615.
  • 7Eliche-Quesada D.,Macias-Ortiz M.I.,Jim(e)nez-Jim(e)nez J.,Rodriguez-Castenon E.,Jim(e)nez-Lopez A..J.Mol.Catal.A:Chem.[J] ,2006,255(1/2):41-48.
  • 8Li Y.,WangC.,Chen H.,Hua W.M.,Yue Y.H.,Gao Z..Catal.Lett.[J] ,2009,131:560-565.
  • 9Cranston R.W.,Inkley F.A..Adv.Catal.[J] ,1957,9:143.
  • 10Yang C.Y.,Clearfield A..Reactive Polymers,Ion Exchangers,Sorbents[J] ,1987,5(1):13-21.

引证文献3

二级引证文献6

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