首页> 外文期刊>Indian Journal of Chemical Technology >Free radical cross-linking copolymerization of acrylamide and N,N' methylene-bis-acrylamide by using Fe(III)/thiourea and Ce(IV)/thiourea redox initiator systems
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Free radical cross-linking copolymerization of acrylamide and N,N' methylene-bis-acrylamide by using Fe(III)/thiourea and Ce(IV)/thiourea redox initiator systems

机译:Fe(III)/硫脲和Ce(IV)/硫脲氧化还原引发剂体系的丙烯酰胺和N,N'亚甲基双丙烯酰胺的自由基交联共聚

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摘要

Acrylamide (AM) and N,N'methylene-bis-acrylamide (Bis) copolymerization in water has been investigated at a total monomer concentration (AM + Bis) of 0.4 M. Extent of conversion of monomer into polymer was measured as a function of the reaction time upto the onset of macrogelation (gelation observed visually). The critical conversion at the gel point shows a minimum at ~5.7 mol% Bis concentration for Fe(III)/thiourea (TU) redox system whereas for Ce(IV)/TU redox system it occurs at ~2.6 mol% Bis concentration. It was found that polymer formed after gel points with different Bis% were not soluble in water, acetic acid, toluene or chloroform. In the copolymerization reaction involving Fe(III)/TU redox initiator system, no induction period is observed at 50°C. In the case of Ce(IV)/TU redox initiator system, however, a significant induction period is observed at 40°C, which depends upon the Bis% in the monomer mixture. Unlike Fe(III)/TU, the reaction, takes only a few minutes to complete for Ce(IV)/TU redox initiator system after the induction period is over.
机译:在总单体浓度(AM + Bis)为0.4 M的条件下,研究了丙烯酰胺(AM)和N,N'亚甲基-双丙烯酰胺(Bis)在水中的共聚反应。直至大胶凝现象开始的反应时间(肉眼观察到胶凝现象)。 Fe(III)/硫脲(TU)氧化还原体系在胶凝点的临界转化率在Bis浓度约为5.7 mol%处最小,而Ce(IV)/ TU氧化还原体系的Bis浓度则在Bis浓度约2.6 mol%处发生。发现在具有不同Bis%的凝胶点之后形成的聚合物不溶于水,乙酸,甲苯或氯仿。在涉及Fe(III)/ TU氧化还原引发剂体系的共聚反应中,在50℃下没有观察到诱导期。但是,在Ce(IV)/ TU氧化还原引发剂体系的情况下,在40°C观察到明显的诱导期,这取决于单体混合物中的Bis%。与Fe(III)/ TU不同,诱导期结束后,对于Ce(IV)/ TU氧化还原引发剂体系,反应仅需几分钟即可完成。

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