## Abstract Well defined graft copolymers have been synthesized by a nitroxide‐mediated “living” free radical process using pre‐formed macromonomers. Analysis of the graft systems revealed that the macromonomer was efficiently incorporated into the polymeric backbone to give block copolymers of con
‘Living’ Free Radical Graft Copolymers, II: Structure
✍ Scribed by Huskić, M.; Roha, Max; Harwood, H. James; Šebenik, Anton
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 506 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0959-8103
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✦ Synopsis
Poly(viny1 chloride)-n-propyl xanthate (PVC-nPX) macroinitiators with 3 to 14 bonded xanthate groups per molecule were synthesized using PVC and potassium n-propyl xanthate. The reaction took place rapidly between 30 and 45°C. Ultraviolet (UV) and nuclear magnetic resonance studies confirmed the presence of xanthyl groups on these macroinitiators. The PVC-nPX macroinitiators were grafted by methyl methacrylate under UV irradiation of 254, 302 and 336 nm producing graft copolymers and homopolymers. The molecular weights increased with increasing conversion, which is consistent with a 'living' polymerization process. The active species in these polymerizations are believed to be macroradicals and xanthyl radicals.
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## Abstract A tubular reactor model for “living” free‐radical polymerization is developed in this study. The model may be used as a tool to design efficient processes for tailored polymers from “living” free‐radical polymerization. Examples presented include preparing bimodal polymers and copolymer