高等学校化学学报 ›› 2017, Vol. 38 ›› Issue (12): 2248.doi: 10.7503/cjcu20170355

• 物理化学 • 上一篇    下一篇

磷钨杂多酸类离子液体催化环戊烯选择性氧化制备戊二醛

张金帅1, 于凤丽1, 陶仁清1, 解从霞1(), 袁冰1, 于世涛2   

  1. 1. 青岛科技大学生态化工国家重点实验室培育基地
    2. 化工学院, 青岛 266042
  • 收稿日期:2017-06-07 出版日期:2017-12-10 发布日期:2017-11-20
  • 作者简介:联系人简介: 解从霞, 女, 博士, 教授, 博士生导师, 主要从事精细化学品的合成及性能研究. E-mail: xiecongxia@126.com
  • 基金资助:
    国家自然科学基金(批准号: 21476120)资助

Selective Oxidation of Cyclopentene to Glutaraldehyde Catalyzed by Heteropolyphosphatotungstate Ionic Liquids

ZHANG Jinshuai1, YU Fengli1, TAO Renqing1, XIE Congxia1,*(), YUAN Bing1, YU Shitao2   

  1. 1. State Key Laboratory Base of Eco-chemical Engineering, Qingdao 266042, China
    2. College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China
  • Received:2017-06-07 Online:2017-12-10 Published:2017-11-20
  • Contact: XIE Congxia E-mail:xiecongxia@126.com
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21476120)

摘要:

以H2O2为氧化剂, 将一系列磷钨杂多酸类离子液体用于催化环戊烯(CPE)选择性氧化制备戊二醛(GA)反应, 筛选出催化活性最高的催化剂为[π-C5H5NC16H33]3PW4O16. 分别探讨了溶剂种类、 用量、 催化剂用量、 H2O2用量、 反应温度和反应时间等因素对反应的影响. 确定了优化的反应条件: 5 mL乙酸乙酯, n(Cat.)∶n(H2O2)∶n(CPE)=0.03∶50∶33, 35 ℃, 18 h, 环戊烯的转化率达100%, 戊二醛的选择性达87%. 催化剂[π-C5H5NC16H33]3PW4O16循环使用7次后, 戊二醛的选择性仍保持在80%以上.

关键词: 杂多酸离子液体, 环戊烯, 催化氧化, 戊二醛, 过氧化氢

Abstract:

With H2O2 as oxidant, a series of heteropolyphosphatotungstate ionic liquids was used to catalyze the selective oxidation of cyclopentene(CPE) to prepare glutaraldehyde(GA). Among these catalysts, [π-C5H5NC16H33]3PW4O16 exhibited the best catalytic activity. PW4O163- easily combined with H2O2 to form W—O—O—W. Using [π-C5H5NC16H33]3PW4O16 as catalyst, the effects of the amount of catalyst, molar ratio of H2O2 to CPE, type and dosage of solvent, reaction temperature and reaction time on the catalytic behavior were investigated and discussed, respectively. The results show the best reaction conditions as follows: 5 mL of ethyl acetate, n(Cat.)∶n(H2O2)∶n(CPE)=0.03∶50∶33, 35 ℃, 18 h. The conversion of cyclopentene could reach 100%, and the yield of glutaraldehyde was 87%. After the reaction, the catalyst could automatically precipitate from the reaction liquid. After the upper liquid was poured out, the remaining catalyst could be directly reused by the addition of fresh reactants. Under the optimal reaction conditions, the recycling efficiency of the catalyst [π-C5H5NC16H33]3PW4O16 was investigated. Because the structure of the catalyst didn’t change before and after reaction by the analysis of FTIR spectra, [π-C5H5NC16H33]3PW4O16 has exhibited a good recyclability. After 7 recycles, the yield of glutaraldehyde was still above 80%.

Key words: Heteropolyacid ionic liquid, Cyclopentene, Catalytic oxidation, Glutaraldehyde, Hydrogen peroxide

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