Modification of styrene-isoprene copolymers—1. End-terminated products
✍ Scribed by Z.G. Mitov; R.S. Velichkova
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 381 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
A~tract--Functionalization of various types of mono-and a, to-bifunctional copolymers was achieved by termination with carbon dioxide, the potassium salt of chloracetic acid, maleic anhydride, carbon disulphide or ethylene oxide. The functionality was determined on the basis of -g/'n (GPC and VPO) and the concentration of the end-groups obtained from ~H-NMR and i.r. spectra. The experimental conditions for quantitative carbonation and hydroxylation without side reactions were established.
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Al~tract--Chain extension of styrene-isoprene hydroxyl-terminated prepolymers was used to obtain polymers having different sequences and lengths of styrene, isoprene, ethylene oxide and 1,3,6-trioxacyclooctane blocks. The structures and the chemical and composition homogeneities of the copolymers we
Al~tract--The mechanism and site of addition of maleic anhydride to styrene-isoprene block copolymers have been investigated. Conditions have been found for modification of the olefinic unsaturation up to 15-20% without crosslinking. ~H-NMR and ~C-NMR and i.r. spectra showed that the modification co
AIWI"~'t--A kinetic study of the addition of maleic anhydride to styrene--isoprene block copolymers at 60, 70 and 80 ° in the presence of Gt,a'-azoisobutyronitdle has been made using i.r. spectroscopy. The reaction is first order with respect to maleic anhydride. The order with respect to at,~t'-azo