Synthesis of bisphenol a novolac epoxy resins for coating applications
β Scribed by Ayman M. Atta; Nevin O. Shaker; Notaila E. Nasser
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 128 KB
- Volume
- 107
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Bisphenol A novolacs were synthesized in both melting and solution processes using pβformaldehyde and formalin solution in presence of oxalic acid catalyst, respectively. Hydrogen nuclear magnetic resonance, ^1^H NMR, investigations show a high methylene bridge contents in the novolacs synthesized in a melting process. These novolacs were analyzed by gel permation chromatography (GPC) and fourier transform infrared spectroscopy (FTIR). The bisphenol A novolac was cured with 1β(2βamino ethyl) piprazine (AEP) as a curing agent for epoxy resins. The cured resins were evaluated as organic coating for steel. The mechanical properties of the cured epoxy resins were evaluated. The chemical resistances of the cured resins were evaluated through salt spray resistance, hot water, solvents, acid and alkali resistance measurements. The data indicate that the cured epoxy resins have excellent chemical resistances as organic coatings among other cured resins. Β© 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
π SIMILAR VOLUMES
A series of trifunctional epoxy resins were successfully synthesized by the condensation of 2,6-dimethylol-4-methylphenol with phenol , cresol, 2,6-dimethylphenol or 2-naphthol, respectively, followed by epoxidation with a halohydrin. The structures of the synthesized triphenols were characterized b
A series of phenol-based and naphthol-based aralkyl epoxy resins were synthesized by the condensation of p-xylylene glycol with phenol, o-cresol, p-cresol, or 2-naphthol, respectively, followed by the epoxidation of the resulting aralkyl novolacs with epichlorohydrin. The incorporation of stable dis