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Reaction Kinetics of Nanoconfined Linear Epoxy Polymerization: a DSC Study

机译:纳米胺线性环氧聚合的反应动力学:DSC研究

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The reaction kinetics of a linear epoxy/amine polymerization in bulk and 55 nm native controlled pore glass (CPG) nanopores have been investigated using dynamic differential scanning calorimetry (DSC). The polymerization reaction was found to be accelerated in the nanopores, as indicated by a 90 C decrease in the onset temperature of the nanoconfined reaction. A second order autocatalytic reaction model describes both bulk and nanoconfined data well, but the autocatalytic behavior is considerably weaker in the nanopores. In fact, a non-autocatalytic second order model can describe the nanoconfined reaction kinetics. The initial reaction rate in CPG nanopores is 240-fold faster than in the bulk, presumably due to silanol groups on the CPG nanopores surface.
机译:使用动态差分扫描量热法(DSC)研究了大块和55nm天然控制的孔玻璃(CPG)纳米孔的线性环氧/胺聚合的反应动力学。发现聚合反应在纳米孔中加速,如90℃的起始温度下降的90℃下降。二阶和催化反应模型描述了批量和纳米醌的数据,但纳米孔的自催化行为显着较弱。实际上,非自动催化的二阶模型可以描述纳米醌反应动力学。 CpG纳米孔中的初始反应速率比体积更快240倍,可能是由于CPG纳米孔表面上的硅烷醇基团。

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