To enhance the physical properties of syndiotacticity-rich (syndiotactic diad content 63ร4%) ultra-high molecular weight (UHMW) (number-average degree of polymerization 12 300) poly(vinyl alcohol) (PVA) รlm, it was solution blended with rigid-rod imogolite in dimethyl sulphoxide. In addition, the bl
Preparation of syndiotacticity-rich high molecular weight poly(vinyl alcohol) microfibrillar fiber by photoinitiated bulk polymerization and saponification
โ Scribed by Won Seok Lyoo; Wan Shik Ha
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 375 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
โฆ Synopsis
Vinyl pivalate (VPi) was polymerized in bulk by ultraviolet-ray initiation at low temperatures using 2,2-azobis(2,4-dimethylvaleronitrile) (ADMVN) and 2,2'-azobis(isobutyronitrile) (AIBN) as photoinitiators. High molecular weight (HMW) poly(vinyl pivalate) (PVPi), having a number-average degree of polymerization (P n ) of 13,000-28,000, was obtained at conversions below 30% and converted by saponification to a syndiotacticityrich HMW poly(vinyl alcohol) (PVA) microfibrillar fiber with P n of 7300-18,300, syndiotactic diad (S-diad) and triad contents of ร 64% and ร 39%, respectively, and crystal melting temperature (T m ) of ร 249ะC. ADMVN gave higher P n than AIBN. On the other hand, conversion was smaller with the former than with the latter, and it was found that the initiation rate of ADMVN was lower than that of AIBN. P n of PVA was constant while P n of the precursor PVPi increased with increasing conversion. The syndiotacticity, T m and thermal stability of PVA obtained from PVPi were much superior to those of PVA derived from poly(vinyl acetate) prepared under the same polymerization conditions. Polymerization of VPi at lower temperatures gave PVA with higher syndiotacticity.
๐ SIMILAR VOLUMES
A new method using a simple zone-drawing technique has been suggested for determining the optimum initial concentration of a polymer solution that has suitable macromolecular entanglements. This method was developed to replace the incorrect inherent viscosity-measuring method for syndiotacticity-ric