Immobilization of copper(II)-poly(N-vinylimidazole) complex on magnetic nanoparticles and its catalysis of oxidative polymerization of 2,6-dimethylphenol in water

被引:21
|
作者
Wang, Huan [1 ]
Zhang, Wenli [1 ]
Shentu, Baoqing [1 ]
Gu, Cheng [1 ]
Weng, Zhixue [1 ]
机构
[1] Zhejiang Univ, State Key Lab Chem Engn, Dept Chem & Biol Engn, Hangzhou 310027, Zhejiang, Peoples R China
关键词
immobilized Cu(II)-PVI complex catalyst; 2; 6-dimethylphenol; oxidative polymerization; water; OXIDE;
D O I
10.1002/app.36484
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(N-vinylimidazole) (PVI) was grafted onto magnetic Fe3O4 nanoparticles through siloxane bonds to produce PVI-grafted Fe3O4 nanoparticles (shortened as Fe3O4-g-PVI). The amount of imidazolyl groups in Fe3O4-g-PVI was estimated to be 1.16 mmol/g by elemental analysis and thermal gravimetric analysis. The Fe3O4-g-PVI coordinated with Cu(II) to form the immobilized Cu(II)-PVI complex. The stoichiometric ratio between imidazolyl groups in Fe3O4-g-PVI and Cu(II) was found to be 4 and the complex formation constant (K) was calculated to be 5.6 x 10(14) mol-4 L4. The immobilized Cu(II)-PVI complex was employed to catalyze the oxidative polymerization of 2,6-dimethylphenol (DMP) in water and showed excellent C?O/C?C selectivity to form PPO. After polymerization, the immobilized Cu(II)-PVI complex catalyst was collected by an external magnetic field and reused in the next run with additional immobilized catalyst and copper ions. After three runs of oxidative polymerization of DMP, the recovery rate of the immobilized Cu(II)-PVI catalyst was above 95% and the yield of PPO maintained as high as 79.2% with the addition of supplementary catalysts. (C) 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
引用
收藏
页码:3730 / 3736
页数:7
相关论文
共 50 条
  • [1] Aerobic Oxidative Polymerization of 2,6-Dimethylphenol in Water with a Highly Efficient Copper(II)-Poly(N-vinylimidazole) Complex Catalyst
    Zhang, Wenli
    Wang, Huan
    Shentu, Baoqing
    Gu, Cheng
    Weng, Zhixue
    JOURNAL OF APPLIED POLYMER SCIENCE, 2011, 120 (01) : 109 - 115
  • [2] Oxidative polymerization of 2,6-dimethylphenol in water by copper catalyst
    Kuwashiro, N. (naekuwa@suou.waseda.jp), 1600, (Society of Polymer Science):
  • [3] KINETICS OF OXIDATIVE POLYMERIZATION OF 2,6-DIMETHYLPHENOL WITH COPPER-AMINE COMPLEX
    KANEKO, M
    NISHIDE, H
    TSUCHIDA, E
    KOG KAGAKU ZASSHI, 1971, 74 (06): : 1194 - &
  • [4] Application of the copper(II)-aminosilane catalysts in the oxidative polymerization of 2,6-dimethylphenol
    Firlik, Sebastian
    Skupinski, Wincenty
    Wielgosz, Zbigniew
    Stasinski, Janusz
    POLIMERY, 2015, 60 (06) : 372 - 376
  • [5] INVESTIGATION AND IMMOBILIZATION OF THE COPPER COMPLEX OF POLY[N-(2-ETHOXYCARBONYLETHYL)IMINOTRIMETHYLENE] AS A CATALYST FOR THE OXIDATIVE COUPLING OF 2,6-DIMETHYLPHENOL
    KONING, CE
    HIEMSTRA, BL
    CHALLA, G
    VANDEVELDE, M
    GOETHALS, EJ
    JOURNAL OF MOLECULAR CATALYSIS, 1985, 32 (03): : 309 - 324
  • [6] A Heterogeneous Kinetic Model of the Oxidative Polymerization of 2,6-Dimethylphenol with a Copper-EDTA Complex in Water
    Liu, Qun
    Shentu, Baoqing
    Gu, Cheng
    Zhu, Jinhua
    Weng, Zhixue
    AICHE JOURNAL, 2009, 55 (10) : 2716 - 2724
  • [7] OXIDATIVE COUPLING POLYMERIZATION OF 2,6-DIMETHYLPHENOL CATALYZED BY COPPER(II) COMPLEXES OF N-METHYLIMIDAZOLE
    CHEN, W
    CHALLA, G
    EUROPEAN POLYMER JOURNAL, 1990, 26 (11) : 1211 - 1216
  • [8] COPPER(II)-CATALYZED OXIDATIVE COUPLING OF 2,6-DIMETHYLPHENOL
    TSURUYA, S
    KISHIKAWA, Y
    TANAKA, R
    KUSE, T
    JOURNAL OF CATALYSIS, 1977, 49 (03) : 254 - 264
  • [9] POLYMERIZATION BY OXIDATIVE COUPLING . FUNCTION OF COPPER IN OXIDATION OF 2,6-DIMETHYLPHENOL
    FINKBEIN.H
    HAY, AS
    BLANCHAR.HS
    ENDRES, GF
    JOURNAL OF ORGANIC CHEMISTRY, 1966, 31 (02): : 549 - &
  • [10] Oxidative Polymerization of 2,6-Dimethylphenol in Water Using bis-Triazacyclononane Copper Catalyst
    Saito, Kei
    Pant, Sweta
    Hearn, Milton T. W.
    JOURNAL OF APPLIED POLYMER SCIENCE, 2011, 122 (04) : 2174 - 2180