“Radical-controlled” oxidative polymerization of phenols. Substituent effect of phenol monomers on the reaction rate
✍ Scribed by Hideyuki Higashimura; Kiyoshi Fujisawa; Yoshihiko Moro-oka; Shuhei Namekawa; Masaaki Kubota; Akinobu Shiga; Hiroshi Uyama; Shiro Kobayashi
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 131 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1042-7147
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The crosslinked spherical phenolic beads (PB) were prepared with phenol and formaldehyde in alkaline medium by suspension polymerization technique. Poly(vinyl alcohol) (PVA) hexamethylenetetramine (HMTA), and triethylamine (TEA) were used as stabilizer, crosslinking agent, and basic cat
Rate constant ratios, k d /k c , for the disproportionation/combination reaction at a temperature of 295 Ϯ 2 K, have been measured as 0.034 Ϯ 0.009 for the collision between CF 3 CH 2 CF 2 ϩ CF 3 radicals and as 0.075 Ϯ 0.019 for CF 3 CH 2 CF 2 ϩ CF 3 CH 2 CF 2 radicals. The effect of the two fluori
Disproportionationkombination rate constant ratios, kd/&[, for the reactive collision between CF3CH2CHX + CF, radicals and between CF3CH2CHX + CF3CH2CHX radicals have been measured for X = CF, The kd/k, = 0.066 -t 0 01 3 when H is transferred to the CF3 radical and 0 I25 ? 0.025 for H transfer to th