This study utilizes different types of bisphenol monomers instead of bisphenol-A to synthesize phenol terminated polydimethylsiloxane-polycarbonate block copolymers. The copolymers were synthesized by interfacial phosgenation of โฃ, -phenol-organofunctional polydimethylsiloxane oligomer with various
Synthesis and characterization of phenoxy resins prepared from diglycidyl ether of bisphenol a and various aromatic dihydroxyl monomers
โ Scribed by Wen-Chang Shih; Chen-Chi M. Ma
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 434 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
This work describes the synthesis of various phenoxy resins by in situ fusion reaction of aromatic dihydroxyl and low molecular weight liquid diglycidyl ether of bisphenol A (DGEBA) with an aryl phosphonium salt catalyst. FTIR and 1 H-NMR spectra and GPC analyses were performed to characterize the resins. Analyses results indicated that resins have an adequate high molecular weight and physical properties when the reaction occurred after 5-10 min at 225-230ยฐC. In addition, DSC and TGA analyses were performed to investigate the thermal properties of these phenoxy resins. According to these results, the lack of steric hindrance of the molecular structure in these phenoxy resins depressed the changes of T g and weight loss. A series of phenoxy modified epoxy networks containing narrower polydisperity and higher M n will exhibit the most significant effect on impact toughness. Moreover, the FTIR spectrum of the phenoxy resin as a function of temperature correlates well with the glass transition temperature. Furthermore, results presented herein demonstrate effective miscibility with thermoplastic polyurethane elastomer (TPU).
๐ SIMILAR VOLUMES
## Abstract The surface of the blend films of poly(ethylene glycol) diglycidyl ether (PEGโE) and bisphenol A diglycidyl ether (BPAโE) cured with 5โ(2,5โdioxotetrahydrofuryl)โ3โmethylโ3โcyclohexeneโ1,2โdicarboxylic acid anhydride at 200ยฐC for 5 h was metallized by the reduction of polymerโincorporat