Synthesis of polycarbonate from dimethyl carbonate and bisphenol-a through a non-phosgene process
โ Scribed by Osamu Haba; Isao Itakura; Mitsuru Ueda; Shigeki Kuze
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 141 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
A novel nonphosgene process for producing bisphenol-A polycarbonate (PC) was developed through a transesterification between bisphenol-A (BPA) and dimethyl carbonate (DMC) and a melt-polycondensation of the resulting bisphenol-A bismethylcarbonate (1). The transesterification was carried out by heating bisphenol A in dimethylcarbonate in the presence of Lewis acid catalysts, removing the by-producing methanol using molecular shieves 4A. Among various catalysts, a combination of (Bu 2 SnCl) 2 O and dimethylaminopyridine gave the best results to produce 1 in 22% yield for 48 h. Using a larger amount of the molecular sieves further improved the yield to 80% in 120 h. The resulting 1 was heated under reduced pressure in the presence of titanium catalysts to produce PC in good yields. The resulting PC had high weight average molecular weight (M w ) of 75,000.
๐ SIMILAR VOLUMES
An o,oะ-methylene-bridged bisphenol A (BPA) dimer 2 was synthesized by a one-step reaction between formalin and excess BPA in the presence of a cation exchange resin in a polar aprotic solvent. Novel oligomeric polycyclic structures were synthesized by the reaction of reactive difunctional halides,