1955•Proceedings of the Royal Society of London A Mathematical and Physical SciencesRequires access

Studies in chain transfer V. Acrylonitrile

Suryya Kumar Das, S. R. Chatterjee, Santi Ranjan Palit

Open publisher page 35 citations

Abstract

Abstract Chain-transfer coefficients (Cs) with twenty-six different solvents at 60° C for acrylonitrile (M) have been measured by catalyzed polymerization studies using azobisisobutyronitrile (I) as catalyst ([l]/[M] = 6.1 x 10-4 mol/l.). For non-halogenated solvents the Cs values are found to be generally higher by an order than those of styrene, but the relative trend is more or less similar in both cases. The transfer characteristics of acrylonitrile with halogenated solvents are, however, in striking contrast with those of all other monomers so far studied. The halogenated solvents such as CCl4 which are usually extremely high chain-transferring agents are found to be devoid of any special susceptibility to an attack by the free radical of acrylonitrile. It is suggested that the inherent instability of compounds containing the group of >C(Cl)CN is responsible for the above unusual behaviour. The CM and 8 (= k1/2t/kv) for acrylonitrile (60° C) have also been determined and are 2.6 x 10-5 and 2.8 respectively.

About this research paper

What this paper is about

Abstract Chain-transfer coefficients (Cs) with twenty-six different solvents at 60° C for acrylonitrile (M) have been measured by catalyzed polymerization studies using azobisisobutyronitrile (I) as catalyst ([l]/[M] = 6.1 x 10-4 mol/l.). For non-halogenated solvents the Cs values are found to be generally higher by an order than those of styrene, but the relative trend is more or less similar in both cases. The transfer characteristics of acrylonitrile with halogenated solvents are, however, in striking contrast with those of all other monomers so far studied. The halogenated solvents such as CCl4 which are usually extremely high chain-transferring agents are found to be devoid of any special susceptibility to an attack by the free radical of acrylonitrile. It is suggested that the inherent instability of compounds containing the group of >C(Cl)CN is responsible for the above unusual behaviour. The CM and 8 (= k1/2t/kv) for acrylonitrile (60° C) have also been determined and are 2.6 x 10-5 and 2.8 respectively.

Why it matters

OpenAlex reports 35 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Chain-transfer coefficients (Cs) with twenty-six different solvents at 60° C for acrylonitrile (M) have been measured by catalyzed polymerization studies using azobisisobutyronitrile (I) as catalyst ([l]/[M] = 6.1 x 10-4 mol/l.). For non-halogenated solvents the Cs values are found to be generally higher by an order than those of styrene, but the relative trend is more or less similar in both cases. The transfer characteristics of acrylonitrile with halogenated solvents are, however, in striking contrast with those of all other monomers so far studied. The halogenated solvents such as CCl4 which are usually extremely high chain-transferring agents are found to be devoid of any special susceptibility to an attack by the free radical of acrylonitrile. It is suggested that the inherent instability of compounds containing the group of >C(Cl)CN is responsible for the above unusual behaviour. The CM and 8 (= k1/2t/kv) for acrylonitrile (60° C) have also been determined and are 2.6 x 10-5 and 2.8 respectively.

Key concepts: Acrylonitrile, Azobisisobutyronitrile, Chemistry, Monomer, Chain transfer, Polymerization, Polymer chemistry, Catalysis

Related papers

Back to paper searchBrowse research topicsOriginal source
Studies in chain transfer V. Acrylonitrile — Research Paper | ScholarLens