Confocal Raman microscopy study of several factors known to influence the oxygen inhibition of acrylate photopolymerization under LED

被引:32
作者
Courtecuisse, Francois [1 ]
Karasu, Feyza [1 ]
Allonas, Xavier [1 ]
Croutxe-Barghorn, Celine [1 ]
van der Ven, Leendert [2 ]
机构
[1] Univ Haute Alsace, Lab Macromol Photochem & Engn Macromol, 3 Rue Alfred Werner, F-68093 Mulhouse, France
[2] AkzoNobel, Automot & Aerosp Coatings, NL-2171 AJ Sassenheim, Netherlands
关键词
Free-radical photopolymerization; Oxygen inhibition; Confocal Raman spectroscopy; Depth profiling; DEPTH RESOLUTION; COATINGS; KINETICS;
D O I
10.1016/j.porgcoat.2015.11.020
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
The free-radical photopolymerization (FRP) suffers from inhibition by atmospheric oxygen which reacts with excited species and radicals leading to inhibition period, longer irradiation time, incomplete conversion of the coating and heterogeneity in depth conversion with a possibly tacky surface. A study of the influence of several factors that affect oxygen inhibition on the depth conversion was performed by Confocal Raman Microscopy (CRM). Increasing the photoinitiator content is shown to increase the surface conversion and decrease the oxygen affected layer thickness. Interestingly, increasing the irradiance mostly affects the oxygen affected layer. The viscosity of the resin was also found to be important to reduce the depth heterogeneities in conversion. Finally, triphenylphosphine was used to highlight the decrease of the oxygen inhibition by using an oxygen scavenger. By selection of the reactive diluent, a tack-free sample surface was obtained under visible light in open-air atmosphere. This study clearly evidences the potential of CRM to assess oxygen inhibition in FRP bringing additional information oxygen affected layer, conversion profile which cannot be determined by commonly used experimental techniques such as real time Fourier transform infrared spectroscopy or even by attenuated total reflection spectroscopy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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