Visible light and water-soluble photoinitiating system based on the charge transfer complex for free radical photopolymerization

Author(s):  
Jingfang Li ◽  
Xin Zhang ◽  
Jun Nie ◽  
Xiaoqun Zhu
Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3195
Author(s):  
Hong Chen ◽  
Mehdi Vahdati ◽  
Pu Xiao ◽  
Frédéric Dumur ◽  
Jacques Lalevée

The development of visible-light 3D printing technology by using water-soluble initiating systems has attracted widespread attention due to their potential applications in the manufacture of hydrogels. Besides, at present, the preparation of water-soluble photoinitiators suitable for visible light irradiation (such as LEDs) still remains a challenge. Therefore, this work is devoted to developing water-soluble photoinitiators (PI)/photoinitiating systems (PIS) upon irradiation with a LED @ 405 nm. In detail, a new water-slightly-soluble chalcone derivative dye [(E)-3-(4-(dimethylamino) phenyl)-1-(4-(2-(2-(2-methoxyethoxy) ethoxy) ethoxy) phenyl) prop-2-en-1-one] was synthesized here and used as a PI with a water-soluble coinitiator, i.e., triethanolamine (TEA) which was also used as an electron donor. When combined together, a charge transfer complex (CTC) formed immediately which exhibited excellent initiating ability for the free radical photopolymerization of poly(ethyleneglycol)diacrylate (PEG-DA). In light of the powerful CTC effect, the [dye-TEA] CTC could not only exhibit enhanced water solubility and mechanical properties but could also be effectively applied for 3D printing. This CTC system is environmentally friendly and cost-saving which demonstrates a great potential to prepare hydrogels via photopolymerization.


Author(s):  
Jacques Lalevée ◽  
Fatima Hammoud ◽  
Nicolas giacoletto ◽  
Guillaume Noirbent ◽  
Bernadette Graff ◽  
...  

In this paper, a series of coumarin chromophore-based oxime-esters was designed and synthesized as visible light photoinitiators (PIs). Interestingly, upon exposure to irradiation of a LED at 405 nm, the...


Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1463
Author(s):  
Lucas A. Almeida ◽  
Margarita Habran ◽  
Rafael dos Santos Carvalho ◽  
Marcelo E. H. Maia da Costa ◽  
Marco Cremona ◽  
...  

The improvement of photocatalytic activity of TiO2-based nanomaterials is widely investigated due to the tentative of their industrialization as environmental photocatalysts and their inherently low solar spectrum sensitivity and rapid recombination of charge carriers. Coupling of oxygen-based bidentate diketone to nanocrystalline TiO2 represents a potential alternative for improving the holdbacks. Formation of TiO2-acetylacetone charge transfer complex (CTC) by sol-gel route results in a hybrid semiconductor material with photodegradation activity against toxic NOx gas. In this research, the influence of the chelating agent acetylacetone (ACAC) content on the CTC photocatalytic efficiency under visible light was evaluated. A high content of ACAC in the CTC is not a decisive factor for efficiency of photocatalytic reactions. In fact, the highest efficiency for NOx degradation (close to 100%, during 1 h of visible light exposure) was reported for the material calcined in air at 300 °C with the content of strongly bonded acetylacetone not higher than 3 wt.%. Higher calcination temperature (400 °C) left TiO2 almost completely depleted in ACAC, while at the highest applied temperature (550 °C) a portion of anatase was transformed into rutile and the sample is free of ACAC. The analyses pointed out that superoxide anion radical (O2−) plays an active role in photo-oxidation of NOx. Our findings indicate that this CTC has both high visible light spectral sensitivity and photocatalytic efficiency.


2015 ◽  
Vol 7 (36) ◽  
pp. 20280-20284 ◽  
Author(s):  
Tsz-Wai Ng ◽  
Hrisheekesh Thachoth Chandran ◽  
Chiu-Yee Chan ◽  
Ming-Fai Lo ◽  
Chun-Sing Lee

2009 ◽  
Vol 121 (47) ◽  
pp. 9124-9127 ◽  
Author(s):  
Chao Wang ◽  
Yinsheng Guo ◽  
Yapei Wang ◽  
Huaping Xu ◽  
Ruji Wang ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document