Radical polymerization of methyl mcthacrylate (MMA) initiated with various diacyl peroxideamine systems was studied. Benzoyl peroxide (BPO) and lauroyl peroxide (LPO) were used as diacyl peroxide component
N
N-dimethyl aniline (DMA) and its para substituted derivatives
i.e.
N
N-dimethyl-p-toluidine (DMT)
p-hydroxymethyl-N
N-dimethyl aniline (HDMA)
p-nitro-N
N-dimethyl aniline (NDMA) and p-dimethylamino benzaldehyde (DMAB) were used as amine components. It was found that the peroxide-DMT systems give higher rates of bulk polymerization RP of MMA than the organic hydroperoxide-DMT systems with the following descending order BPO-DMT>LPO-DMT>CHP(cumene hydroperoxide)-DMT>TBH(tert-butyl hydroperoxide)-DMT.The aromatic tertiary amines possess obvious structural effect on the Rp values in the diacyl peroxideamine system.The overall activation energy of MMA polymerization was determined and the kinetics of polymerization of MMA initiated with BPO-DMT system was investigated.
Abstract
Radical polymerization of methyl mcthacrylate (MMA) initiated with various diacyl peroxideamine systems was studied. Benzoyl peroxide (BPO) and lauroyl peroxide (LPO) were used as diacyl peroxide component
N
N-dimethyl aniline (DMA) and its para substituted derivatives
i.e.
N
N-dimethyl-p-toluidine (DMT)
p-hydroxymethyl-N
N-dimethyl aniline (HDMA)
p-nitro-N
N-dimethyl aniline (NDMA) and p-dimethylamino benzaldehyde (DMAB) were used as amine components. It was found that the peroxide-DMT systems give higher rates of bulk polymerization RP of MMA than the organic hydroperoxide-DMT systems with the following descending order BPO-DMT>LPO-DMT>CHP(cumene hydroperoxide)-DMT>TBH(tert-butyl hydroperoxide)-DMT.The aromatic tertiary amines possess obvious structural effect on the Rp values in the diacyl peroxideamine system.The overall activation energy of MMA polymerization was determined and the kinetics of polymerization of MMA initiated with BPO-DMT system was investigated.
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