Graft copolymers of acrylonitrilc, methyl metliacrylate and vinyl acetate on blcached holocellulose were obtained by the use of ceric ions. The ceric ion concentration, a t which maximum graft levels were attained, depends on the type of monomer. The dependence of the extent of graft copolytncr form
Graft copolymerization of methyl methacrylate on holocellulose
โ Scribed by E. F. Okieimen; K. I. Idehen; H. Ahiedu
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 291 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
Graft copolymerization of methyl methacrylate initiated by ceric ion in aqueous medium on bleached holocellulose was studied at 29OC. It was found that an increase in the concentration of ceric ion and oxidation of the holocellulase with aqueous potassium &chromate solution resulted in increased levels of incorporation of poly(methy1 methacrylate) graft copolymer, but were associated with reductions in the efficiency of grafting. Thiol groups were introduced on the holocellulose by treatment with dilute thioglycollic acid solutions at 29ยฐC. The influence on the level of grafting and on the molecular weight of the grafted polymer by the incorporated thiol groups on the substrate was examined.
Methods
Commercial methyl methacrylate monomer was extracted with dilute NaOH solution to remove the hydroquinone stabilizer. The monomer was then distilled under reduced pressure. Ceric ammonium nitrate was used without further purification. Holocellulose from Gosweilerodenron balsamiferum was obtained as described previously.16 The holocellulose was steeped in sodium hypochlorite solution for 45 min at 29ยฐC. The bleached holocellulose was then rinsed in a large volume of distilled water and then air-dried. A portion of the *To whom correspondence should be addressed.
๐ SIMILAR VOLUMES
Graft copolymers of acrylonitrile (ACN), methyl methacrylate (MMA), and their mixtures on carboxy methyl cellulose (d.S 0.4-0.5) were prepared by the use of ceric ion initiator in aqueous medium. The graft copolymers were characterized by IR spectroscopy. The extent of graft copolymerization of ACN