Kabatc Janina, Iwińska Katarzyna, Balcerak Alicja, Kwiatkowska Dominika, Skotnicka Agnieszka, Czech Zbigniew, Bartkowiak Marcin
University of Science and Technology, Faculty of Chemical Technology and Engineering Seminaryjna 3 85-326 Bydgoszcz Poland
West Pomeranian University of Technology, Institute of Chemical Organic Technology Pułaskiego 10 70-322 Szczecin Poland.
RSC Adv. 2020 Jul 1;10(42):24817-24829. doi: 10.1039/d0ra03818k. eCollection 2020 Jun 29.
The aim was study the influence of onium salts on the kinetics of photopolymerization in the visible light region. Trimethylolpropane triacrylate TMPTA was selected as a monomer, and activated by 1,3-bis(phenylamino)squaraine (SQ) used as a photosensitizer in addition to tetramethylammonium -butyltriphenylborate (B2). The iodonium salt [A-I-B]X functioned as a second radical initiator, bearing a different substitution pattern for the cation. The ternary system was formulated with different concentrations of both borate and diphenyliodonium salts. Differential scanning calorimetry was used to investigate the polymerization reaction over the photoactivation time carried out at 300 nm < < 500 nm irradiation. When the squaraine dye/borate salt was used as photoinitiator, a slow polymerization reaction was observed and a lower monomer conversion. The addition of a third component (onium salt) increased the polymerization rate and conversion. Ternary photoinitiator systems showed improvement in the polymerization rate of triacrylate leading to high conversion in a short photoactivation time. The photoinitiating ability of bi- and tri-component photoinitiators acting in the UV-Vis region for initiation polymerization of triacrylate was compared with those of some commercially used photoinitiating systems. It was also found, that, the parallel electron transfer from an excited state of the sensitizer to [A-I-B]X, and an electron transfer from a ground state of R(Ph)BN(CH) to an excited state of the sensitizer results in two types of initiating radical.
目的是研究鎓盐对可见光区域光聚合动力学的影响。选用三羟甲基丙烷三丙烯酸酯(TMPTA)作为单体,并除了四甲基铵丁基三苯基硼酸盐(B2)外,还使用1,3-双(苯基氨基)方酸菁(SQ)作为光敏剂对其进行活化。碘鎓盐[A-I-B]X用作第二自由基引发剂,阳离子具有不同的取代模式。三元体系由不同浓度的硼酸盐和二苯基碘鎓盐配制而成。使用差示扫描量热法研究在300 nm<λ<500 nm照射下光活化时间内的聚合反应。当使用方酸菁染料/硼酸盐作为光引发剂时,观察到聚合反应缓慢且单体转化率较低。添加第三种组分(鎓盐)提高了聚合速率和转化率。三元光引发剂体系显示出三丙烯酸酯聚合速率的提高,从而在短时间的光活化时间内实现了高转化率。将在紫外-可见光区域起作用的二元和三元光引发剂引发三丙烯酸酯聚合的光引发能力与一些商业使用的光引发体系进行了比较。还发现,从敏化剂的激发态到[A-I-B]X的平行电子转移,以及从R(Ph)BN(CH)的基态到敏化剂的激发态的电子转移会产生两种引发自由基。