Xanthene dyes/amine as photoinitiators of radical polymerization: A comparative and photochemical study in aqueous medium

被引:115
作者
Encinas, M. V. [1 ]
Rufs, A. M. [1 ]
Bertolotti, S. G. [2 ]
Previtali, C. M. [2 ]
机构
[1] Univ Santiago Chile, Fac Quim & Biol, Santiago, Chile
[2] Univ Nacl Rio Cuarto, Dept Quim, Rio Cuarto, Argentina
关键词
Xanthene dye photoinitiators; Aqueous photopolymerization; Relation between photochemistry and photoinitiation; LASER FLASH-PHOTOLYSIS; VISIBLE-LIGHT POLYMERIZATION; ELECTRON-TRANSFER PROCESS; ROSE-BENGAL; VINYL POLYMERIZATION; ABSORPTION-SPECTRA; QUANTUM YIELDS; TRIPLET-STATE; EOSIN-Y; PHOTOPOLYMERIZATION;
D O I
10.1016/j.polymer.2009.04.024
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
The efficiency of several xanthene dyes as photoinitiators of the free radical polymerization in aqueous medium was evaluated. These results show that dyes with triplet quantum yield higher than 0.1 present similar efficiencies, independently of their different chemical structure. A detailed study of the photophysics of the dyes under the polymerization conditions was carried out using laser time-resolved spectroscopies. These studies show that the active radicals are those which formed in the interaction of excited triplet state of the dye with the amine through an electron transfer process. In spite of this, the photoinitiation efficiency is not correlated with the triplet quantum yield. Also, the photophysics studies show that the quantum yield of the different pathways of the decomposition of the charge transfer intermediate is an important parameter to predict the efficiency of these photoinitiator systems. The experimentally measured active radical formation is well correlated with that calculated from the polymerization rate. The presence of heavy atoms in the xanthene ring increases the triplet quantum yield, but decreases the active radical yield, and then the polymerization rate. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2762 / 2767
页数:6
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