## Abstract Hydroxy‐terminated polysulfones (PSs) of number‐average molecular weights from 3000 to 26,000 g/mol were converted to the corresponding 4‐ethynylbenzoate–terminated PS through a three‐step synthesis. The initial step involved the reaction of the hydroxy precursor with 4‐bromobenzoyl chl
Synthesis and characterization of carboxylated polysulfones
✍ Scribed by Guiver, Michael D. ;Croteau, S. ;Hazlett, John D. ;Kutowy, O.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1990
- Tongue
- English
- Weight
- 829 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0007-1641
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✦ Synopsis
Abstract
Polysulfone has been carboxylated, via a metalated intermediate, by reaction of a THF solution of polymer with n‐butyllithium and then treatment with carbon dioxide. The polymer reactions with n‐butyllithium were close to quantitative and did not require the use of a tertiary amine catalyst. A series of polymers ranging from 0.2 to 1.9 carboxyl groups per repeat unit was prepared by this method in the salt, acid and ester form. The structures of these polymer derivatives were characterized by ^1^H‐NMR, ^13^C‐NMR and IR. The glass transition temperatures and thermal stabilities were characterized by differential scanning calorimetry (DSC) and thermogravimetry (TG).
📜 SIMILAR VOLUMES
## Abstract Phase behavior in polysulfone‐carboxylated polysulfone (PSf‐CPSf) blends was studied by glass transition observations in conjunction with enthalpy relaxation technique. Miscibility in all proportions was detected in blends where CPSf has a degree of carboxylation (DC, i.e. number of car
High molecular weight carboxylated polybutadienes (cPBDs) with numberaverage molecular weight (M n ) from 98,000 to 200,000 and carboxylic acid (COOH) contents of 0.5-10 mol % were successfully synthesized through hydrocarboxylation of polybutadienes (PBDs) at temperatures of 140 -150°C using PdCl 2