Thermal cure behavior and pyrolysis of methyl-tri(phenylethynyl)silane resin
β Scribed by Quan Zhou; Lizhong Ni
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 414 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A polyfunctional organicβinorganic hybrid monomer, methylβtri(phenylethynyl)silane (MTPES) could be thermally polymerized by a free radical mechanism to a highly crosslinked structure of interest as a high temperature composite matrix resin. The structural changes during thermal cure process were characterized by fourier transform infrared spectrum and ^13^CβCPβMASβNMR spectrum. The disappearance of secondary acetylene stretching band at 2166 cm^β1^ was used successfully to monitor cure reaction accompanied with the formation of cisβpolyene structure at 1600 and 754 cm^β1^. The possible cure mechanism of MTPES was also proposed. The pyrolysis of cured MTPES under a stream of argon to 1450Β°C gave a ceramic in high yield (81%). Thermal conversion of polymer to ceramic was studied by means of Xβray diffraction, Raman spectrum, and energy dispersive spectrometer analysis. The results showed that pyrolytic products were made up of Ξ²βSiC, graphite, and glassy carbon. Β© 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
π SIMILAR VOLUMES
The cure reactions of tetraglycidyl methylene diamine (TGMDA) epoxy cured with tetrasubstituted aromatic diamine on one hand and diglycidyl ether of bisphenol A and diglycicyl ether tetrabromobisphenol A epoxies cured with methylene bis (phenyl-4-cyanate) on the other hand are reported. Systematic F
The curing reaction of bisphenol-A epoxy resin (BPAER) with boron-containing phenol-formaldehyde resin (BPFR) was studied by isothermal and dynamic differential scanning calorimetry (DSC). The kinetic reaction mechanism in the isothermal reaction of BPAER-BPFR was shown to follow autocatalytic kinet