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Reaction Kinetics of Nanoconfined Linear Epoxy Polymerization: a DSC Study

机译:纳米约束线性环氧聚合反应动力学: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:使用动态差示扫描量热法(DSC)研究了本体和55 nm天然可控孔玻璃(CPG)纳米孔中线性环氧/胺聚合的反应动力学。如纳米限制反应的起始温度降低90℃所表明的,发现聚合反应在纳米孔中被加速。二阶自动催化反应模型可以很好地描述大量数据和纳米限制的数据,但是纳米孔中的自动催化行为相当弱。实际上,非自催化的二阶模型可以描述纳米约束的反应动力学。 CPG纳米孔的初始反应速率比本体反应速率快240倍,这大概是由于CPG纳米孔表面的硅烷醇基。

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