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Complexation of sequence-ordered methacrylic acid copolymers with poly(4-vinylpyridine)

โœ Scribed by Yoshihito Inai; Shin-Ichiro Kato; Tadamichi Hirabayashi; Kenji Yokota


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
634 KB
Volume
34
Category
Article
ISSN
0887-624X

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โœฆ Synopsis


The complexation of three kinds of sequence-ordered acid (co)polymers with a base homopolymer was studied. The acid polymers used are poly(methacry1ic acid) 1, alternating (1 : 1) ethylene-methacrylic acid copolymer 2, and periodic (2 : 1) ethylene-methacrylic acid copolymer 3, and the base polymer is poly(4-vinylpyridine) 4. When mixing a methanol solution of 1,2, or 3 with that of 4 (0.1M of each functional group), precipitate was formed immediately for all polymer pairs. All the precipitates contained carboxyl and pyridyl groups in ca. 1 : 1 molar ratio and showed IR spectra indicating the hydrogen bonding between carboxyl and pyridyl groups. When mixing dilute methanol solutions ( w 4 M ) of the above polymer pairs, no precipitation was observed, but the extinction coefficient (cB) a t 255 nm of pyridyl groups in 4 was found to increase with an increasing acid polymer concentration. This is ascribed to hydrogen bonding between carboxyl and pyridyl groups in methanol. Based on the cB variation, the order of complexation constants for acid/base polymer pairs was estimated as follows: 114 pair -214 pair % 314 pair.


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Moisture sorption of polyelectrolyte com
โœ Yoshiyuki Hirai; Toshinari Nakajima ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 418 KB ๐Ÿ‘ 2 views

Successive differential sorptions have been measured for the system polyelectrolyte complex of poly(acrylic acid)/poly(4-vinylpyridine) + water vapor. The sorption data revealed that the sorption process of water vapor in the complex is controlled not only by diffusion mechanism but also by relaxati