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Head-to-head polymers—I. The preparation and some properties of head-to-head polypropylene

✍ Scribed by S. Arichi; M.Y. Pedram; J.M.G. Cowie


Book ID
107753639
Publisher
Elsevier Science
Year
1979
Tongue
English
Weight
439 KB
Volume
15
Category
Article
ISSN
0014-3057

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📜 SIMILAR VOLUMES


Head-to-head polymers—II. Dilute solutio
✍ S. Arichi; M.Y. Pedram; J.M.G. Cowie 📂 Article 📅 1979 🏛 Elsevier Science 🌐 English ⚖ 423 KB

The behaviour in dilute solution of head-to-head (H-HI polypropylenes, covering the range M,, = 0.22 to 4.19 × 104, has been studied in cyclohexane as solvent at 303 K. The data could be represented by two distinct Mark-Houwink equations describing the low and the high molecular weight regions. The

Head-to-head vinyl polymers. VI. Prepara
✍ Quach, Loc ;Otsu, Takayuki 📂 Article 📅 1982 🏛 John Wiley and Sons ⚖ 530 KB

## Abstract Head‐to‐head (H–H) poly(allyl alcohol) (PAA) was prepared by the LiAlH~4~ reduction of H–H poly(methyl acrylate) obtained from the methylation of alternating copolymer of ethylene with maleic anhydride. H–H poly(allyl acetate) (PAAc) and H–H poly(allyl benzoate) (PABz) were further deri

Head-to-head vinyl polymers. VII. Hydrol
✍ Quach, Loc ;Otsu, Takayuki 📂 Article 📅 1982 🏛 John Wiley and Sons ⚖ 647 KB

## Abstract Head‐to‐head (H–H) and head‐to‐tail (H–T) poly(methyl acrylate)s (PMAs) were hydrolyzed in a mixture of acetone and water (4:1 by volume) at 30°C by using various alkali hydroxides as catalysts. For comparison, the H–T copolymer with 26% H–H units, dimethyl succinate (DMS), dimethyl glu