This paper describes the radical graft polymerization of vinyl monomers from glass fiber surface initiated by alkylazo groups introduced onto the fiber surface. The introduction of azo groups onto the glass fiber surface was achieved by reaction of isocyanate groups which were previously attached on
Plasma-graft polymerization of vinyl monomers with reactive groups onto a surface of poly(p-phenylene terephthalamide) fiber
โ Scribed by Kenji Yamada; Toshihide Haraguchi; Tisato Kajiyama
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 864 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
The mechanical properties of a fiber-reinforced plastic are influenced by the adhesion between a reinforcing fiber and a matrix resin. In this work we tried to obtain strong adhesion between Kevlar 4gTM yarn and a matrix resin through the formation of covalent bonds. Reactive groups were introduced onto a surface of the yarn by means of plasmagraft polymerization and then reacted with an epoxy resin/curing agent mixture as a matrix resin to form covalent bonds. Glycidyl methacrylate and acrylamide were used as monomers for plasma-graft polymerization. The degree of grafting was increased with increasing polymerization time. The grafted yarns enclosed with diglycidal ether of bisphenol-A/triethylenetetramine 2.2 : 1 mixture were pulled out to obtain pull-out force after curing.
The pull-out force increased with increasing degrees of grafting. The covalent bonds formed between the graft polymer and the matrix resin result in an increment of pull-out force.
๐ SIMILAR VOLUMES
The mechanical properties of a fiber-reinforced plastic are influenced by the adhesion between a reinforced fiber and a matrix resin. In this work it is shown how to obtain strong adhesion between a carbon yarn and an epoxy resin through the formation of covalent bonds. Acid amide groups reactive wi
Surface modified poly(ethy1ene terephthalate) (PET) films with 2-(methacryloyloxy)ethylphosphorylcholine (MPC) and 2-(glucosy1oxy)ethyl methacrylate (GEMA) moieties, PMPC-g-PET and PGEMAg-PET, were prepared by graft copolymerization using an Ar plasma-post polymerization technique. The degrees of po