## Abstract The mechanisms of thermal degradation of poly(ether‐ketone) (PEK) and four poly(ether‐ketone)/poly(ether‐sulfone) copolymers (PEK/PES) have been investigated by direct pyrolysis‐mass spectrometry (DPMS). Several families of pyrolysis compounds with H, OH and CHO end‐groups have been ide
Sequence distribution of poly(ether-sulfone)/poly(ether-ketone) copolymers by mass spectrometry and 13C NMR
✍ Scribed by Giorgio Montaudo; Maurizio S. Montaudo; Concetto Puglisi; Filippo Samperi
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 551 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The sequence distributions of four poly(ether‐sulfone)/poly(ether‐ketone) (PES/PEK) copolymer samples were determined by means of fast atom bombardment mass spectrometry (FAB‐MS) and by ^13^C NMR spectroscopy. The controlled partial degradation of the copolymer chains to produce oligomers suitable of FAB‐MS analysis was performed with sodium methoxide in dimethyl sulfoxide solution at 130°C, and the experimental conditions were optimized. The sequential arrangements of ether‐sulfone/ether‐ketone units present in these materials were estimated by a best‐fit minimization method using the MACO4 computer program which compares the experimental FAB‐MS spectral intensities with theoretical intensities. Random PES/PEK copolymer samples showed quite the same sequence arrangements as expected from monomer feed‐ratios used in the syntheses. Instead, a PES/PEK copolymer sample expected to be exactly alternating (from the synthesis procedure) showed 44% of random sequences owing to the transetherification reaction which occurred in the synthesis. The results of sequential analysis obtained from ^13^C NMR data compare well with the data obtained by the FAB‐MS analysis.
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Republic of China ## SYNOPSIS Poly(ether ether ketone ketone)-poly(ether sulfone) (PEEKK/PES) block copolymers were prepared from the corresponding oligomers via a nucleophilic aromatic substitution reaction, and the A?" of the PEEKK segment was fixed a t 12,000, while the M,,'s of the PES segmen
Poly(ether sulfone) and poly(ether sulfone ketone) copolymers (I-V) were synthesized by the nucleophilic substitution reaction of 4,4Ј-dihydroxy diphenyl sulfone (DHDPS, A) with various mole proportions 4,4Ј-difluoro benzophenone (DFBP, B) and 4,4Ј-difluoro diphenyl sulfone (DFDPS, C) using sulfolan
## Abstract Poly(ether ether ketone) (PEEK)/poly(ether sulfone) (PES) block copolymers were synthesized via condensation reaction between fluorine‐terminated PEEK oligomers and hydroxyl‐terminated PES oligomers. The dynamic mechanical behavior of a composite sample prepared by compression molding o
Microstructure of poly(ether ketone sulfone) copolymers I-V, derived from varying mol proportions of dihydroxy diphenyl sulfone (DHDPS, A) and dihydroxybenzophenone (DHBP, C) with stochiometric amounts of difluorobenzophenone (DFBP, B) was studied by 13 C nuclear magnetic resonance spectroscopy. The