## Abstract 2‐Phenyl‐1,3‐oxazoline was injected into poly(ethene‐__co__‐methacrylic acid), containing 4,25 mol‐% methacrylic acid units, at 225°C. In the first stage, 2‐phenyl‐1,3‐oxazoline reacted with carboxylic acid groups to form esteramide side chains via grafting reaction. In the second stage
1,3-Oxazoline intermediates in reactive processing applications, 1. Melt grafting of poly(ethene-co-methacrylic acid) with 2-substituted 1,3-oxazolines
✍ Scribed by Philipp Müller; Christof Wörner; Rolf Mülhaupt
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 533 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A novel family of functional ethene copolymers with various side chains were prepared by melt grafting of poly(ethene‐co‐methacrylic acid), containing 3,00 and 4,25 mol‐% of methacrylic acid, with 2‐substituted 1,3‐oxazolines such as 2‐phenyl‐1,3‐oxazoline, 2‐undecyl‐1,3‐oxazoline, 2‐heptadecyl‐1,3‐oxazoline, and 4‐(1,3‐oxazolin‐2‐yl)phenyl 4‐methoxybenzoate. ^1^H NMR and FTIR studies of the polymer microstructures revealed that carboxylic acid groups reacted with 1,3‐oxazolines within few minutes to form esteramide‐coupled side chains in very high yields. Torque of the reaction mixture, mechanical and thermal properties of the graft copolymers were measured. In the case of 2‐heptadecyl‐esteramide‐substituted polyethenes, the side‐chain cocrystallization accounted for higher crystallinity of the resulting graft copolymers.
📜 SIMILAR VOLUMES
Various copolyesteramides were prepared by melt compounding at 220 °C involving reaction of poly(styrene-co-maleic anhydride), SMA, with 6, 17, and 28 wt % maleic anhydride content, and 1-dodecanol, C12OH, in the presence of 2-undecyl-1,3oxazoline, C11OXA. Copolymer architectures were examined by me