期刊文献+

氮化MCM-22分子筛的程序升温制备 被引量:1

THE PREPERATION OF NITROGEN-INCORPORATED MCM-22 THROUGH TEMPERATURE-PROGRAMMED ROUTE
下载PDF
导出
摘要 利用程序升温的方法分别在700、800、900℃对除去和未除去模板剂的MCM-22分子筛进行高温氮化。结果表明,以2℃/min的升温速率进行氮化后的分子筛的N含量高于以5℃/min进行氮化的分子筛的N含量,含模板剂的分子筛氮化后的N含量要高于不含模板剂的分子筛氮化后的N含量。通过对比氮化前后分子筛的骨架红外谱图,在-1400cm^-1处发现1个随着N含量变化而变化的新峰,将其归属为-NH4特征峰。将氮化后的分子筛用于甲苯甲醇烷基化制对二甲苯的反应,发现甲苯的转化率明显提高。 The nitrogen-incorporated MCM-22 molecular sieves were respectively synthesized at 700, 800, 900℃ through temperature-programmed route. The nitrogen contents of samples nitrided at 2;C/min were higher than those of the samples nitrided at 5℃/min, and the nitrogen contents of samples with template before nitridation were also higher than that of the samples without template. Compared with the pure MCM-22, a new peak at -1400 cm^-1 changed with the nitrogen content was found in the FT-IR spectrum of nitrogen-incorporated sample, which were attributed to the -NHx. The sample nitrided at 800℃ was used in the alkylation of toluene and methanol and the reactive activity was found to be obviously improved.
出处 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2006年第B10期193-195,共3页 Acta Petrolei Sinica(Petroleum Processing Section)
基金 国家自然科学基金(20233030,20573059)和973计划(2003CB615801)资助项目
关键词 MCM-22 分子筛 氮化 程序升温 N含量 MCM-22; molecular sieve; nitridation; temperature-programmed nitrogen content
  • 相关文献

参考文献13

  • 1Ernst S,Hartmann M,Sauerbeck S,et al.Appl Catal A,2000,200:117-123.
  • 2Xiong J,Ding Y,Zhu H,et al.J Phys Chem B,2003,107:1366-1369.
  • 3Zhang C,Xu Z,Wan K,et al.Appl Catalysis A,2004,258:55-56.
  • 4Narasimharao K,Hartmann M,Thiel H H,et al.Micropor Mesopor Mater,2006,90:377-383.
  • 5Xia Y,Mokaya R.J Mater Chem,2004,14:2507-2515.
  • 6Wan K,Liu Q,Zhang C.Chem Lett,2003,32:362-363.
  • 7Xia Y,Mokaya R.Angew Chem Int Ed,2003,42:2639-2644.
  • 8Rubin M K,Chu P.USP4 954 325.1990.
  • 9Lawton S,Leonowicz M,Partridge R,et al.Micropor Mesopor Mater,1998,23:109-117.
  • 10Wu P,Komatsu T,Yashima T.Micropor Mesopor Mater,1998,22:343-356.

二级参考文献11

  • 1Chen N Y, Kaeding W W, Dwyer F G. J Am Chem Soc,1979, 101(22) : 6783.
  • 2Kaeding W W, Chu C, Young L B, Weinstein B, Butter S A. J Catal, 1981, 67(1): 159.
  • 3Young L B, Butter S A, Kaeding W W. J Catal, 1982,76(2) : 418.
  • 4KimJ H, Namba S, Yashima T. Zeolites, 1991, 11(1):59.
  • 5Grange P, Bastians P, Conanec R, Marchand R, Laurent Y. Appl Catal A, 1994, 114(2): L191.
  • 6Climent M J, Corma A, Fornes V, Frau A, Gull-Lopez R,Iborra S, Primo J. J Catal, 1996, 163(2) : 392.
  • 7Blasco T, Corma A, Fernandez L, Fornes V, Guil-Lopez R. Phys Chem Chem Phys, 1999, 1(18): 4493.
  • 8Ernst S, Hartmann M, Sauerbeck S, Bongers T. Appl Catal A, 2000, 200(1-2): 117.
  • 9Ding Y J, Xiong J M, Lu Y, He X S, Lin L W. Cuihua Xuebao ( Chin J Catal ), 2001, 22(3) : 227.
  • 10Xiong J M, Ding Y J, Zhu H J, Yan L, Liu X M, Lin L W. J Phys Chem B, 2003, 107(6) : 1366.

共引文献6

同被引文献7

引证文献1

二级引证文献1

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