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Two routes towards photoinitiator-free photopolymerization in miniemulsion: Acrylate self-initiation and photoactive surfactant

机译:细乳液中实现无光引发剂光聚合的两条途径:丙烯酸酯自引发和光活性表面活性剂

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摘要

Two novel photoinitiator-free approaches to photopolymerize acrylic monomers with a conventional Hg lamp starting from an acrylates monomer miniemulsion are investigated. In one system the acrylate nanodroplet reaction is self-initiated and in the other the use of a photoactive diphenyl ether surfactant yields phenyl and phenoxyl initiating radicals upon UV irradiation. Photopolymerization kinetics are monitored in situ by real-time Fourier transform near infrared spectroscopy (RT-FTNIR) and the colloidal properties are systematically investigated by dynamic light scattering (DLS). The up-scaling of these PI-free miniemulsion photopolymerizations is carried out in an annular photoreactor. Acrylate miniemulsion polymerization is conducted under UV-C irradiation without the assistance of any radical photoinitiator. The uses of monomer self-initiation and a photoINISURF as two separate routes to yield polymer latexes are investigated and both achieve 100% conversion. The former route also gives full conversion when it is scaled up to a 400 mL photoreactor.
机译:研究了两种新颖的无光引发剂的方法,它们是从丙烯酸酯单体细乳液开始,用常规的Hg灯使丙烯酸单体光聚合。在一种体系中,丙烯酸酯纳米滴反应是自引发的,而在另一种体系中,使用光活性二苯醚表面活性剂在紫外线照射下会产生苯基和苯氧基引发自由基。通过实时傅里叶变换近红外光谱(RT-FTNIR)原位监测光聚合动力学,并通过动态光散射(DLS)系统研究胶体性质。这些无PI的细乳液光聚合的放大反应是在环形光反应器中进行的。丙烯酸酯微乳液聚合是在UV-C辐射下进行的,无需任何自由基光引发剂的帮助。研究了单体自引发和光INISURF作为产生聚合物胶乳的两种独立途径的用途,两者均实现了100%的转化率。当放大到400 mL光反应器时,前一种方法也可以实现完全转化。

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