Abstract
A novel vapor-phase process has been developed for grafting relatively volatile acrylic monomers onto various polymeric substrates, using photo-initiation by near ultraviolet irradiation in the presence of biacetyl vapors. With it, very even graft polymerizations on the substrates, with minimum amounts of homopolymerization, were found. Furthermore, there were essentially no changes in the tensile or aesthetic properties of the treated surfaces. The degree of photografting is dependent upon the chemical composition and porosity of the substrate, the volatility and reactivity of the monomers, prewetting of the substrate with a suitable wetting agent, and the conditions of irradiation used. The effects of various reaction parameters on the photo-induced grafting of methyl acrylate, methyl methacrylate, and acrylonitrile on wool keratin are studied in detail. Increasing biacetyl and monomer flow rates and flow times, irradiation times, and moisture content of the wool all caused progressive increases in the amount of polymer grafted to the wool, up to limiting values dependent on the reaction parameters involved and monomer used. In all instances, the amount of homopolymer found on the fiber was limited and remained essentially constant over the range of conditions studied. A series of acrylic monomers of different volatilities and reactivities including methyl acrylate, methyl methacrylate, butyl acrylate, acrylic acid, acrylamide, acrylonitrile, N,N-dimethylaminoethyl methacrylate, and 2,2,2-trifluoroethyl methacrylate was successfully grafted onto several hydrophilic and hydrophobic textile fibers (wool, cotton, rayon, nylon, acrylics, polyester, and polypropylene) and other polymeric surfaces such as filter paper, cellophane, and acetate film by this process. The wetting agents used included water, methyl and n-propyl alcohol, N,N-dimethylformamide, dimethylsulfoxide, benzene, and chlorinated hydrocarbon solvents.
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