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有机过氧化物-芳叔胺体系引发甲基丙烯酸甲酯聚合的研究 总被引:1,自引:2,他引:1
以过氧化二酰(BPO、LPO)或有机过氧化氢物(TBH、CHP)和芳叔胺如DMA或对位具有不同取代基的衍生物组成的引发体系进行MMA聚合,研究过氧化物与胺的结构对聚合的影响。结果表明,过氧化二酰的活性要比有机过氧化氢物大,其顺序为BPO>LPO>CHP>TBH。对于BPO-芳叔胺或LPO-芳叔胺体系,芳叔胺中给电子取代基能提高聚合速度,而吸电子取代基能降低聚合速度。测定了MMA聚合的总活化能E_α,BPO-芳叔胺体系时E_α=36-54kJ/mole,LPO-芳叔胺体系时E_α=56-71kJ/mole;还研究聚合动力学。 相似文献
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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 R_p 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 R_p values in the diacyl peroxideamine system. The overall activation energy of MMA polymerization was determined and thekinetics of polymerization of MMA initiated with BPO-DMT system was investigated. 相似文献
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