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
Synthesis and properties of unsaturated polyoxyethylene and its graft copolymers with styrene
✍ Scribed by Hong-Quan Xie; Dong Xie; Yong Liu
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 218 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
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 copolymer was characterized with infrared spectra, 1 H NMR, and wide-angle X-ray diffraction. The relationship between crystallinity of the copolymers and conductivity of their LiClO 4 complexes were investigated. The copolymer with ϳ 65 wt % PEO content exhibits a room temperature conductivity of 1 ϫ 10 Ϫ4 S cm Ϫ1 at a molar ratio of EO/Li ϭ 20. The unsaturated PEO was graft-copolymerized with styrene using 2,2Ј-azobis(isobutyronitrile) as initiator in toluene, with grafting efficiency ϳ 50%. The purified graft copolymer was characterized with infrared spectra, 1 H NMR, and wide-angle X-ray diffraction, and was shown to have good emulsifying properties and a phase-transfer catalytic property. LiClO 4 complex of the graft copolymer with 70 wt % PEO content exhibits a room temperature conductivity approaching 1 ϫ 10 Ϫ4 S cm Ϫ1 at molar ratio of EO/Li ϭ 20/1.
📜 SIMILAR VOLUMES
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
A monomer, diethyl a,a-dimethyl-m-isopropenylbenzyl carbamoylphosphonate, has been prepared by the base-catalyzed reaction of the isocyanate m-TMI ( a,adimethyl-m-isopropenylbenzylisocyanate) with diethyl phosphite. The structure of the carbamoylphosphonate monomer and its styrene copolymer was conf
The graft copolymerizations of vinyltrimethoxysilane (VTMO) and styrene (St) onto ethylene-propylene-diene terpolymer (EPDM) were carried out with benzoyl peroxide (BPO) as an initiator in toluene. The effects of EPDM concentration, mole ratio of VTMO to St, reaction time, reaction temperature, and