A novel thermosensitive poly( N-vinylisobutyramide)(polyNVIBA) hydrogel was prepared by the copolymerization of N-vinylisobutyramide (NVIBA) with butylene-bis-NVA(B-BNVA) as a crosslinker in a high yield. The swelling transition behavior was examined in comparison with poly(N-isopropylacrylamide)(po
Synthesis and functionalities of poly(N-vinylalkylamide). V. Control of a lower critical solution temperature of poly(N-vinylalkylamide)
β Scribed by Kazuo Suwa; Keitaro Morishita; Akio Kishida; Mitsuru Akashi
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 160 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
N-vinyl-n-butyramide (NVBA)
, N-vinylisovaleramide (NVIVA), and N-vinyl-n-valeramide (NVVA), which are N-vinylalkylamides with different alkyl groups were synthesized and their solution behavior in a polymeric form was examined. Copolymers of N-vinylisobutyramide (NVIBA) with N-vinylacetamide (NVA), NVIBA with NVVA, and NVVA with NVA were prepared by the solution polymerization to control the LCSTs. The resultant polyNVBA showed a lower critical solution temperature (LCST) sharply at 32ΠC, but polyN-vinylisovaleramide (polyNVIVA) and poly N-vinyln-valeramide(polyNVVA) that have n-butyl and isobutyl groups, respectively, on their side chains were insoluble even in cold water. The water solubility of the resulting polymers was found to vary, depending on the molecular shapes as well as the side chain length of the alkyl groups in question. The copolymers consisting of NVVA, NVIBA, and NVA in water showed LCSTs sharply between 10 and 90ΠC, depending on changes in their comonomer content. It was found that the changes in LCST that are caused by the incorporation of comonomers are due to changes in the overall hydrophilicity of the polymer.
π SIMILAR VOLUMES
## Abstract The molecular weights of poly(__N__βvinylformamide) [poly(NVF)] obtained by freeβradical polymerization were expanded from being in the range of thousands to hundreds of thousands. Primary amino groups were introduced by the hydrolysis of poly(NVF) under both acidic and basic conditions
The differences in the polymerization abilities of N-vinylformamide (NVF) and N-vinylisobutyramide (NVIBA) and the synthesis of their copolymers were studied. The polymerization abilities were fairly good and quite similar to those of N-vinylacetamide (NVA), a monomer in the same class as N-vinylalk
It was found that a poly( N-vinylacetamide) (polyNVA) -dextran system formed two phases. The top was polyNVA-rich and the bottom phase was dextran-rich, which is the same as the poly(ethylene glycol) (PEG) -dextran system, and the phase separation occurred at a lower concentration than the PEG-dextr
Pyrolysis of ( N-a-isopropoxyethyl)isobutyramide, which was obtained by the reaction of isobutyramide, 2-propanol, and acetaldehyde in the presence of conc. sulfuric acid, produced N-vinylisobutyramide (NVIBA). The free radical polymerization of NVIBA was carried out in various solvents in the prese