Improved syntheses of poly(oxy-1,3-phenylenecarbonyl-1,4-phenylene) and related poly(ether-ketones) using polyphosphoric acid/P2O5 as polymerization medium

被引:51
作者
Baek, JB
Tan, LS
机构
[1] USAF, Res Lab, MLBP, Mat & Mfg Directorate,Polymer Branch, Wright Patterson AFB, OH 45433 USA
[2] Univ Dayton, Res Inst, Dayton, OH 45469 USA
关键词
poly(phosphoric acid); poly(ether-ketones); AB monomer;
D O I
10.1016/S0032-3861(03)00374-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P2O5 mixture as an effective catalytic/dehydrative medium for the preparation of poly(ether-ketones) was optimized. Thus, with the optimal weight ratio of 4:1 (PPA:P2O5), the electrophilic substitution polycondensation of 3-phenoxybenzoic acid and related AB monomers was substantially promoted at 130 degreesC to yield the subject polymer abbreviated as mPEK and related poly(ether-ketones) with significantly higher molecular weights. In the cases where the polymerization systems were completely homogeneous, the ensuing polycondensation was rapid and yielded high molecular weight polymers (e.g. mPEK [eta] = 2.10 dl/g) at 130 degreesC within 30 min., as compared to PPMA (phosphorus pentoxide/methanesulfonic acid) method which gave only moderate molecular weight polymers, e.g. mPEK ([eta] = 0.64 dl/g). In some cases, where the monomers and PPA/P2O5 were not fully compatible, polycondensation did proceed and reasonable molecular weight range ([eta] = 0.69-0.76 dl/g) could be achieved. However, the complete incompatibility between the poly(ether-sulfone) and PPA/P2O5 medium precluded the successful polymerization of 4-phenoxybenzenesulfonic acid. Published by Elsevier Science Ltd.
引用
收藏
页码:4135 / 4147
页数:13
相关论文
共 27 条
  • [1] [Anonymous], [No title captured]
  • [2] [Anonymous], ENCY POLYM SCI ENG
  • [3] SYNTHESIS AND PROPERTIES OF POLYARYLETHERKETONES
    ATTWOOD, TE
    DAWSON, PC
    FREEMAN, JL
    HOY, LRJ
    ROSE, JB
    STANILAND, PA
    [J]. POLYMER, 1981, 22 (08) : 1096 - 1103
  • [4] Baek J. B., 2002, POLYM PREPR, V43, P1130
  • [5] Baek J-B, 2003, POLYM PREPR, V44, P825
  • [6] CHARACTERIZATION, PROCESSING, AND PROPERTIES OF AN AROMATIC POLY(ETHER KETONE)
    BAI, SJ
    DOTRONG, M
    SOLOSKI, EJ
    EVERS, RC
    [J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1991, 29 (01) : 119 - 128
  • [7] SYNTHESIS OF AROMATIC POLYETHERKETONES IN TRIFLUOROMETHANESULPHONIC ACID
    COLQUHOUN, HM
    LEWIS, DF
    [J]. POLYMER, 1988, 29 (10) : 1902 - 1908
  • [8] Dahl K. J, 1976, U. S. Patent, Patent No. [3,953,400 (A), 3953400]
  • [9] FRIED JR, 1999, POLYM DATA HDB, P479
  • [10] XANTHONES - CYCLISATION OF 3'-SUBSTITUTED 2-CARBOXYDIPHENYL ETHERS
    GOLDBERG, AA
    WRAGG, AH
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1958, (DEC): : 4227 - 4234