期刊文献+

钛钨改性HMS的合成及催化氧化苯甲醇合成苯甲醛 被引量:7

Catalytic Oxidation of Benzyl Alcohol to Benzyl Aldehyde with Ti/W-HMS
下载PDF
导出
摘要 通过改变硅钛摩尔比和硅钨摩尔比合成了Ti-HMS和Ti/W-HMS型分子筛,并进行了NH3-TPD测试分析。结果表明,当n(Si)∶n(Ti)=30∶1、n(Si)∶n(W)=400∶1时,分子筛的酸量最大。利用上述不同HMS为催化剂,ω(H2O2)=30%的H2O2水溶液为氧化剂,在无有机溶剂及相转移催化剂条件下,氧化苯甲醇制备苯甲醛。结果表明,Ti/W-HMS可选择性氧化苯甲醇制备苯甲醛;催化剂的酸量和酸强度越大,越有利于提高催化活性和选择性。利用Ti(30)/W(400)-HMS为催化剂,当n(醇)∶n(H2O2)=1∶2、ω(催化剂)=4%、反应时间为5 h时,苯甲醇的转化率和苯甲醛的选择性分别为72.6%、96.9%。催化剂重复使用4次后,苯甲醇的转化率和苯甲醛的选择性分别为63.2%、89.1%。 Ti-HMS and Ti/W-HMS molecular sieves were synthesized by varying the ratio of n (Si)/n (Ti) and n( Si)/n( W), and were used for the NH3-TPD analysis. The acidity of the molecular sieve is the largest when n ( Si ) : n ( Ti ) = 30: 1, n ( Si ) : n (W) = 400: 1. Different HMS were used for the oxidation of benzyl alcohol to benzyl aldehyde with 30% hydrogen peroxide solution as the oxidizing agent without any organic solvent and phase transfer catalyst. The results show that benzyl alcohol can be selectivity oxidized to benzyl aldehyde by Ti/W-HMS molecular sieves. The activity and selectivity of catalyst can be improved with increasing the acidity and acid strength. With Ti (30)/W (400) -HMS as catalyst, at n (alcohol) : n ( hydrogen peroxide) = 1:2, to(catalyst) = 4%, and the reaction time 5 h, the conversion of benzyl alcohol and the selectivity of benzyl aldehyde reached to 72.6% and 96.9%, respectively. The conversion of benzyl alcohol and the selectivity of benzyl aldehyde reached to 63.2% and 89. 1%, respectively, after catalyst was used for four times.
出处 《应用化学》 CAS CSCD 北大核心 2009年第2期168-172,共5页 Chinese Journal of Applied Chemistry
基金 黑龙江省自然科学基金资助项目(B200608)
关键词 HMS 苯甲醇 苯甲醛 HMS, benzyl alcohol, benzyl aldehyde
  • 相关文献

参考文献9

二级参考文献74

  • 1纪红兵,钱宇,何笃贵,王乐夫.一步法催化氧化正辛醇生成正辛酸[J].化工学报,2005,56(9):1673-1678. 被引量:4
  • 2[1]Taramasso M,Perego G,Notari B.US 4 410 501.1983
  • 3[2]Corma A,Navarro M T,Perez-Pariente J.J Chem Soc,Chem Commun,1994,(1):147
  • 4[3]Koyano K A,Tatsumi T.Chem Commun,1996,(2):145
  • 5[4]Tanev P T,Chibwe M,Pinnavaia T J.Nature,1994,368(6469):321
  • 6[6]Gontier S,Tuel A.Zeolites,1995,15(7):601
  • 7[7]Blasco T,Camblor M A,Corma A,Perez-Pariente J.J Am Chem Soc,1993,115(25):11806
  • 8Sato K,Aoki M,Hashimoto T,et al. J Org Chem[J],1996,61:8 310
  • 9Sato K,Aoki M,Ogawa M,et al. Bull Chem Soc Jpn[J],1997,70:905
  • 10Venturello C,D′Aloisio R,Banrt J,et al. J Mol Catal[J],1985,32:107

共引文献50

同被引文献74

引证文献7

二级引证文献21

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