Improved syntheses of poly(oxy-1,3-phenylenecarbonyl-1,4-phenylene) and related poly(ether–ketones) using polyphosphoric acid/P 2O 5 as polymerization medium
Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P 2O 5 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:P 2O 5), the electrophilic substitution polycondensa...
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Published in | Polymer (Guilford) Vol. 44; no. 15; pp. 4135 - 4147 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.07.2003
|
Subjects | |
Online Access | Get full text |
ISSN | 0032-3861 1873-2291 |
DOI | 10.1016/S0032-3861(03)00374-4 |
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Abstract | Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P
2O
5 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:P
2O
5), the electrophilic substitution polycondensation of 3-phenoxybenzoic acid and related AB monomers was substantially promoted at 130 °C 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
[η]=2.10
dl/
g
) at 130 °C within 30 min., as compared to PPMA (phosphorus pentoxide/methanesulfonic acid) method which gave only moderate molecular weight polymers, e.g.
mPEK
([η]=0.64
dl/
g).
In some cases, where the monomers and PPA/P
2O
5 were not fully compatible, polycondensation did proceed and reasonable molecular weight range
([η]=0.69–0.76
dl/
g)
could be achieved. However, the complete incompatibility between the poly(ether–sulfone) and PPA/P
2O
5 medium precluded the successful polymerization of 4-phenoxybenzenesulfonic acid. |
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AbstractList | Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P
2O
5 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:P
2O
5), the electrophilic substitution polycondensation of 3-phenoxybenzoic acid and related AB monomers was substantially promoted at 130 °C 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
[η]=2.10
dl/
g
) at 130 °C within 30 min., as compared to PPMA (phosphorus pentoxide/methanesulfonic acid) method which gave only moderate molecular weight polymers, e.g.
mPEK
([η]=0.64
dl/
g).
In some cases, where the monomers and PPA/P
2O
5 were not fully compatible, polycondensation did proceed and reasonable molecular weight range
([η]=0.69–0.76
dl/
g)
could be achieved. However, the complete incompatibility between the poly(ether–sulfone) and PPA/P
2O
5 medium precluded the successful polymerization of 4-phenoxybenzenesulfonic acid. Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P[2O[5 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: P[2O[5), the electrophilic substitution polycondensation of 3-phenoxybenzoic acid and related AB monomers was substantially promoted at 130DGC 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 [*h] = 2.10 dl/g) at 130DGC within 30 min., as compared to PPMA (phosphorus pentoxide /methanesulfonic acid) method which gave only moderate molecular weight polymers, e.g. mPEK ([*h] = 0.64 dl/g). In some cases, where the monomers and PPA/P[2O[5 were not fully compatible, polycondensation did proceed and reasonable molecular weight range ([*h] = 0.69-0.76 dl/g) could be achieved. However, the complete incompatibility between the poly(ether-sulfone) and PPA/P[2O[S medium precluded the successful polymerization of 4-phenoxybenzenesulfonic acid. |
Author | Baek, Jong-Beom Tan, Loon-Seng |
Author_xml | – sequence: 1 givenname: Jong-Beom surname: Baek fullname: Baek, Jong-Beom organization: University of Dayton Research Institute, 300 College Park, Dayton, OH 45469, USA – sequence: 2 givenname: Loon-Seng surname: Tan fullname: Tan, Loon-Seng email: loon-seng.tan@wpafb.af.mil organization: Polymer Branch, Materials and Manufacturing Directorate, AFRL/MLBP, Air Force Research Laboratory, 2941 P Street, Room 136 Wright-Patterson Air Force Base, Dayton, OH 45433-7750, USA |
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References_xml | – reference: Bonner WH. US Patent 3 065 205; 1962. – volume: 130 start-page: 45 year: 1969 ident: BIB4 publication-title: Makromol Chem – volume: 29 start-page: 119 year: 1991 ident: BIB17 publication-title: J Polym Sci B: Polym Phys – reference: Marks BM. US Patent 3 441 538; 1969. – volume: 29 start-page: 479 year: 1999 end-page: 6441 ident: BIB1 publication-title: Polymer data handbook – volume: 20 start-page: 1965 year: 1982 ident: BIB12 publication-title: J Polym Sci A: Polym Chem – volume: 34 start-page: 753 year: 2001 end-page: 758 ident: BIB14 publication-title: Acc Chem Res – ident: BIB20 – reference: Dahl K. US Patent 3 953 400; 1976. – volume: 29 start-page: 1902 year: 1988 ident: BIB9 publication-title: Polymer – volume: 29 start-page: 6432 year: 1996 end-page: 6441 ident: BIB15 publication-title: Macromolecules – volume: 43 start-page: 1130 year: 2002 ident: BIB19 publication-title: Polym Prepr – reference: Goodman I, McIntyre JE, Russell W. Br Patent Appl 971227; 1964. – volume: 5 start-page: 2375 year: 1967 ident: BIB3 publication-title: J Polym Sci A1 – volume: 6 start-page: 323 year: 1984 ident: BIB10 publication-title: Synthesis – start-page: 4227 year: 1958 ident: BIB18 publication-title: J Chem Soc – volume: 39 start-page: 321 year: 1958 end-page: 414 ident: BIB13 article-title: Polyphosphoric acid publication-title: Chem Rev – volume: 22 start-page: 1096 year: 1981 ident: BIB5 publication-title: Polymer – volume: 20 start-page: 2675 year: 1987 ident: BIB11 publication-title: Macromolecules – start-page: 283 year: 1984 ident: BIB16 publication-title: Synthesis |
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Snippet | Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P
2O
5 mixture as an effective catalytic/dehydrative medium for the... Based on the model-compound studies, the composition of polyphosphoric acid (PPA)/P[2O[5 mixture as an effective catalytic/dehydrative medium for the... |
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StartPage | 4135 |
SubjectTerms | AB monomer Poly(ether–ketones) Poly(phosphoric acid) |
Title | Improved syntheses of poly(oxy-1,3-phenylenecarbonyl-1,4-phenylene) and related poly(ether–ketones) using polyphosphoric acid/P 2O 5 as polymerization medium |
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