The curing reaction of two kinds of epoxy resins, (bisphenol A epoxy DER331, and novolac epoxy DEN438) with aryl phosphinate anhydride (9,10dihydro-9-oxa-10-phosphaphenanthrene-10-oxide)-methyl succinic anhydride (DMSA), and benzyldimethylamine (BDMA) as the catalyst, was investigated by di β erentia
Aryl phosphinate anhydride curing for flame retardant epoxy networks
β Scribed by Cho, Ching-Sheng; Fu, Shih-Chi; Chen, Leo-Wang; Wu, Tseng-Rong
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 253 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
An aryl phosphinate anhydride (9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide)-methyl succinic anhydride (DMSA), with a pendent phosphorus group was synthesized and used as a reactive type Γame retardant. The structure of DMSA was conΓrmed by FTIR, mass, elemental analysis, 1H and 31P NMR spectroscopies. The aryl phosphinate anhydride was successfully used to cure some commercial epoxides, such as bisphenol A diglycidyl ether (DGEBA) and epoxy-novolac. The epoxy networks obtained were characterized by dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), and the limiting oxygen index (LOI) test. Epoxy resins cured with DMSA exhibit higher LOI values and char yields compared with those cured by commercial anhydrides, such as phthalic anhydride (PA) and hexahydrophthalic anhydride (HHPA). Furthermore, the LOI value and the char yield of the epoxy-resin composites increase with increasing phosphorus content. The Γame retardancies of the epoxy-resin composites were signiΓcantly improved by using aryl phosphinate anhydride.
Society of Chemical Industry.
π SIMILAR VOLUMES
Two phosphorus-containing diamine compounds, bis(4-aminophenoxy)phenyl phosphine oxide and bis(3-aminophenyl)phenyl phosphine oxide, were synthesized for use as curing agents of epoxy resins. Phosphorylated epoxy resins were obtained by curing Epon 828 and Eponex 1510 with these two diamine agents.
The curing reaction of a phosphorus containing epoxide, bis-(3-glycidyloxy) phenylphosphine oxide (BGPPO), was studied by differential scanning calorimeter (DSC) using dynamic and isothermal methods. Kinetic parameters and activation energy of the BGPPO cured with diamine or dianhydride curing agent