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层状和反向六方相软纳米受限中的聚合反应。

Polymerization in soft nanoconfinement of lamellar and reverse hexagonal mesophases.

机构信息

Department of Chemical and Materials Engineering, New Mexico State University, Las Cruces, NM 88003, USA.

出版信息

Soft Matter. 2019 Oct 23;15(41):8238-8250. doi: 10.1039/c9sm01565e.

Abstract

This work describes the kinetics of thermal polymerization in nanoconfined domains of lyotropic liquid crystal (LLC) templates by using chemorheological studies at different temperatures. We investigate lamellar and reverse hexagonal LLC phases with the same concentration of the monomeric phase. Results show that the mesophase structures remain intact during thermal polymerization with very slight changes in the domain size. The polymerization rate decreases in the nanoconfined structure compared to the bulk state due to the segregation effect, which increases the local monomer concentration and enhances the termination rate. Additionally, the polymerization rate is faster in the studied reverse hexagonal systems compared to the lamellar ones due to their lower degree of confinement. A higher degree of confinement also induces a lower monomer conversion. Differential scanning calorimetry confirms the obtained results from chemorheology.

摘要

这项工作通过在不同温度下进行化学流变学研究,描述了溶致液晶(LLC)模板纳米受限域内热聚合反应动力学。我们研究了具有相同单体相浓度的层状和反六方 LLC 相。结果表明,在热聚合过程中,中间相结构保持完整,只有非常小的相畴尺寸变化。由于隔离效应,聚合速率在纳米受限结构中比在本体状态下降低,这会增加局部单体浓度并提高终止速率。此外,由于受限程度较低,研究的反六方体系的聚合速率比层状体系更快。较高的受限程度也会导致单体转化率降低。差示扫描量热法证实了化学流变学得到的结果。

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