The modification of the poly (ethylene-co-vinyl acetate) (EVA) by direct esterification of its ethylene-vinyl alcohol copolymer with mercaptoacetic acid was carried out. The amount of the mercaptan group was controlled to avoid gel formation during the graft polymerization with styrene by chain tran
Poly(ethylene-co-vinyl acetate)-graft-poly(methyl methacrylate) (EVA-graft-PMMA) as a modifier of epoxy resins
✍ Scribed by Filiberto González García; Bluma G Soares; Roberto J J Williams
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 272 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0959-8103
- DOI
- 10.1002/pi.1020
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Conventional approaches to toughen thermosets are: (1) the polymerization‐induced phase separation of a rubber or a thermoplastic, or (2) the use of a dispersion of preformed particles in the initial formulation. In the present study it is shown that it is possible to combine both techniques by using graft copolymers with one of the blocks being initially immiscible and the other that phase separates during polymerization. This is illustrated by the use of poly(ethylene‐co‐vinyl acetate)‐graft‐poly(methyl methacrylate) (EVA‐graft‐PMMA) as modifier of an epoxy resin. EVA is initially immiscible and PMMA phase separates during polymerization. Blends of an epoxy monomer based on diglycidylether of bisphenol A (DGEBA, 100 parts by weight), piperidine (5 parts by weight), and PMMA (5 parts by weight), showed the typical polymerization‐induced phase separation of PMMA‐rich domains before gelation of the epoxy network. Replacing PMMA by EVA‐graft‐PMMA (5 parts by weight), yielded stable dispersions of EVA blocks, favoured by the initial solubility of PMMA blocks. Phase separation of PMMA blocks in the course of polymerization led to a dispersion of in situ generated biphasic particles (plausibly composed of EVA cores surrounded by PMMA shells), with average diameters varying from 0.3 to 0.6 µm with the cure temperature. This procedure may be used to generate stable dispersions of biphasic particles for toughening purposes.
© 2002 Society of Chemical Industry
📜 SIMILAR VOLUMES
## Abstract Polystyrene‐grafted poly[ethylene‐__co__‐(vinyl acetate)] (EVA‐g‐PS) has been synthesized from functionalized polystyrene containing acyl chloride end group (PS‐COCl) and partly (5%) hydrolyzed poly[ethylene‐__co__‐(vinyl acetate)] (EVALVA‐5%). The graft efficiency is ca. 100% when low‐
Functionalization of poly(ethylene-co-vinyl acetate) (EVA) with vinyltriethoxysilane (VTEOS) has been carried out by a free-radical melt-grafting procedure in the presence of added comonomers. The influence of comonomers on silane graft yield and crosslink density has been assessed. Experiments were