Kinetics of radical polymerization LVII. Investigation of the effect of molecule inhibitors on the radical polymerization of p-methyl styrene (pMS). Aromatic nitro compounds
✍ Scribed by I Gyöngyhalmi; T Földes-Berezsnich; F Tüdös
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 409 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The effect of aromatic nitro compounds (s-trinitrobenzene, o-and p-dinitrobenzene) was studied on the polymerization of p-methyl styrene by dilatometric method, using AIBN initiator at 50°C. The value of the stoichiometric coefficient 01) and of the relative reactivity (kJ&) was determined. In bulk polymerization, s-TNB exerted a medium strong and p-DNB a weak inhibiting effect, while o-DNB was a typical retarder.
For p-DNB, the value of p was determined in an inert solvent (benzene) at various concentrations, a systematic increase of p was found with the dilution, i.e. with the decrease of the monomer mole fraction. The change can quantitatively be described in terms of the hot radical theory.
📜 SIMILAR VOLUMES
## Abstract The grafting through method was employed to study the effect of nanoclay confinement on the atom transfer radical polymerization (ATRP) of styrene. An ammonium salt containing a double bond on its structure was used as a clay modifier. Employing ATRP to polymerize styrene in the presenc