1968
DOI: 10.1002/app.1968.070121202
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Infrared spectroscopy of graft polymers separated from graft copolymers of wool and silk with methyl methacrylate

Abstract: SynopsisThe IIC1-or papain-decomposition residues obtained from rednced wool fibers grafted wit,h 1 .5-3.0yo methyl methacrylate were extractively fractionated successively wit,h cold acetone, hot acetone, and benzene. Each fraction was examined by infrared spectroscopy. Generally, the 715 cm-' spectral band considered to he due to YC-S-C was found iri the hot acetone-soluble fraction. It was concluded that the thiol groups on wool keratin provide the main sites of grafting, as might he expected. A similar res… Show more

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Cited by 27 publications
(8 citation statements)
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“…Graft copolymerization of vinyl monomers onto natural fibers have been studied using peroxydisulfate. [12][13][14][15] Agarwal and Sreenivasan 16,17 have studied graft copolymerization of methyl methacrylate (MMA), acrylonitrile (AN), vinyl acetate (VA) and styrene onto jute fibers by gamma radiation. Mishra et al 18 grafted MMA onto chemically modified jute fibers.…”
Section: Introductionmentioning
confidence: 99%
“…Graft copolymerization of vinyl monomers onto natural fibers have been studied using peroxydisulfate. [12][13][14][15] Agarwal and Sreenivasan 16,17 have studied graft copolymerization of methyl methacrylate (MMA), acrylonitrile (AN), vinyl acetate (VA) and styrene onto jute fibers by gamma radiation. Mishra et al 18 grafted MMA onto chemically modified jute fibers.…”
Section: Introductionmentioning
confidence: 99%
“…Arai and coworkers [6][7][8][9][10][11][12][13][14][15] have made extensive work on the graft copolymerization of vinyl monoThe chemical modification of wool through graft mers onto wool fibers. Grafting, i.e., in situ formacopolymerization of vinyl monomers can be effection of vinyl polymers, can be accomplished by tive in improving some fiber properties and endmeans of the free radical initiation mechanism.…”
Section: Introductionmentioning
confidence: 99%
“…In all the initiating systems containing thiourea (I) the redox component is isothiourea18 (11), a thiol (existing in a tautomeric equilibrium with thiourea in an aqueous solution) is the reductant. The generation of a free radical in this system takes place by the abstraction of the reactive hydrogen atom attached to the sulfur atom in isothiourea generating the amidinosulfenyl radical (111) ,NH, NH…”
Section: Reaction Mechanismmentioning
confidence: 99%