Epoxy/anhydride networks modified by epoxy/anhydride oligomers containing SiOH groups
✍ Scribed by Adriana N. Mauri; Carmen C. Riccardi; Roberto J. J. Williams
- Book ID
- 101255411
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 151 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Epoxy/anhydride oligomers containing variable amounts of trialkoxysilane groups were synthesized from phenyl glycidyl ether (PGE), 3-glycidoxypropyl trimethoxysilane (GPMS), and methyl tetrahydrophthalic anhydride (MTHPA), using benzyldimethylamine (BDMA) as an initiator. They were hydrolyzed and partially condensed using diluted formic as a catalyst, with the last step carried out in a solution of diglycidyl ether of bisphenol A (DGEBA). By curing with a stoichiometric amount of MTHPA, in the presence of BDMA, plasticized epoxy/anhydride networks were obtained without any evidence of phase separation. These materials showed a better abrasion resistance than that of the neat matrix. The presence of free SiOH groups can be used to improve the adhesion to glass surfaces.
📜 SIMILAR VOLUMES
The reaction-induced phase separation in a blend of a commercial polysulfone (PSu) with diepoxide-cyclic anhydride monomers, was studied. The diepoxide was based on diglycidylether of bisphenol A (DGEBA) and the hardener was methyl tetrahydrophthalic anhydride (MTHPA), used in stoichiometric proport
## Abstract **Summary:** Phenolic alkylimidazolineamides were prepared and applied as modifiers in order to render layered silicates organophilic and to prepare polymeric nanocomposites. The imidazolineamine, 2‐{2‐[heptadec‐8‐enyl]‐4,5‐dihydro‐1‐imidazol‐1‐yl}‐1‐ethaneamine (IA), was reacted in bul