Synthesis of poly(butadiene-b-sulphone) has been carried out by two methods. Reaction of ~t,~o-di(sodium phenolate) oligosulphone with ct,¢o-di(chlorocarbonyl)oligobutadiene or reaction of ct,~odiphenol oligosulphone with cq~o-di(chlorocarbonyl)oligobutadiene in the presence of magnesium. For both m
Synthesis and characterization of poly(butadiene-b-sulphone) by block-copolycondensation—II. Synthesis from α,ω-dicarboxylic oligobutadienes and α,ω-diepoxy oligosulphones
✍ Scribed by A. Pourdjavadi; P.J. Madec; E. Maréchal
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 526 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The synthesis of poly(butadiene-b-sulphone) by two methods was described in part I (Eur. Polym. J. 20, 305 [1]). The results obtained by reaction of ~,c0-dicarboxylic oligobutadiene with ct,co-diepoxy oligosulphones are reported here. The kinetics of the reaction are studied on models; reaction orders, rate constants, activation parameters are determined. Their values fit Madec's kinetic pattern and are close to those obtained by Cr6peau [6] for the grafting of hydroxybenzoic acid onto a copolymer bearing epoxy side-groups. Contribution of the side-reaction [2] is quantified. Block-copolycondensation of the reactive oligomers are carried out both in solution and in the melt. Contribution of the side-reaction is higher in the melt than in solution, but in both cases block-copolymers are obtained and characterized by GPC.
📜 SIMILAR VOLUMES
Using the results obtained in part I, we studied the polycondensation of ¢x,to-diphenol oligosulphones with c¢,to-diepoxy oligosiloxanes. Structural study of the resulting copolymers by ~Hand I~C-NMR and by GPC showed that poly(sulphone-b-siloxane)s were formed. The reactions were carried out either