Graft copolymers (polystyrene-graft-polyoxyethylene) (PS-graft-PEO) were prepared by the dispersion copolymerization of methacryloyl-terminated polyoxyethylene macromonomer and styrene initiated by an oil-soluble initiator (dibenzoyl peroxide, DBP). The apparent molecular weights of graft copolymers
Dispersion copolymerization of polyoxyethylene macronomer and styrene 4. Solution properties of polystyrene-graft-polyoxyethylene copolymers
✍ Scribed by Ignác Capek; Renata Murgas̆ová; Diether Lath; Elena Lathová; Viera Juranic̆ová; Jaroslav Barton̆
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 163 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
The graft copolymers (polystyrene-graft-polyoxyethylene) (PSt-graft-PEO) were prepared by the radical dispersion copolymerization of methacryloyl (MA)-terminated PEO macromonomer and styrene. By means of size-exclusion chromatography, liquid chromatography at the critical adsorption point, and light scattering, the molecular weight parameters and the solution properties of PSt-graft-PEO were investigated. The apparent average molecular weight and the molecular weight distribution (MWD) of graft copolymers were found to decrease with increasing molecular weight of PEO-MA macromonomer. This decreased molecular weight was attributed to the chain transfer to PEO unit and increased contribution of the solution polymerization. The broad MWD varied with the ratio of the polymerization in the continuous phase and the polymer particles. The number of PEO grafts per PSt backbone decreased with increasing molecular weight of the PSt-graft-PEO copolymer, which was attributed to the intramolecular association of PEO segments. The intrinsic viscosity or the coil size of graft copolymer molecules varied with temperature as a result of the dehydration of PEO segments.
📜 SIMILAR VOLUMES
The unsaturated polyoxyethylene (PEO) was synthesized by copolymerization of ethylene oxide with allyl glycidyl ether in toluene using bimetallic-oxo-alkoxide as a catalyst. The effects of polymerization conditions on conversion and intrinsic viscosity of the copolymer were studied. The unsaturated