Photoinitiating Behavior of Bifunctional Photoinitiator Containing a-Hydroxyalkylphenone Group on Free-Radical Polymerization Guodong Ye,1,2 Jianwen Yang,1 Tianyi Zhao,1 Rui Rao,1 Zhaohua Zeng,1 Yonglie Chen1 1School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, People’s Republic of China 2Department of Chemistry, Guangzhou Medical College, Guangzhou 510182, People’s Republic of China Received 26 April 2006; accepted 26 April 2006 DOI 10.1002/app.24822 Published online in Wiley InterScience (www.interscience.wiley.com). ABSTRACT: Photoinitiating behaviors of bis[4-(2-hydroxy- at the beginning of polymerization, suggesting that the photo- isopropionyl)]ether photoinitiator on free-radical polymeriza- polymerization initiated by bis[4-(2-hydroxy-isopropionyl)] tion have been investigated. The kinetics of photopolymeriza- ether followed biradical termination mechanism. Photosensi- tion initiated by the photoinitiator was studied by means of tizer triethylamine improves the initiating efficiency while ox- differential photocalorimetry. The bifunctional photoinitiator ygen is shown to restrict polymerization in this system. Ó 2006 showed comparative performance with those commercial pho- Wiley Periodicals, Inc. J Appl Polym Sci 102: 5297–5302, 2006 toinitiators with monofunctional chromophoric group. The effect of UV intensity on the polymerization rate was investi- Key words: photochemistry; coatings; radical polymeriza- gated, and the value of exponential factor was found to be 0.5 tion; differential scanning calorimetry INTRODUCTION molecular weight, thereby lowering migration tendency comparing with low molecular weight photoinitiators. The UV-induced crosslinking or polymerization of A great effort has been made.5 One successful example acrylates and other monomers has become a widely is Esacure KIP 150, which was developed and commer- used curing technology. Generally, photoinitiator plays cialized by Lamberti, but the cured film based on it is a crucial role in the UV-curing system.1–3 It absorbs UV often rigid and brickle because of the a-methyl styrene radiation and then generates free radicals, which initi- backbone in KIP 150. Another disadvantage of this ate polymerization reaction. Good compatibility and approach is that for most of photoinitiators the photo- high reactivity have always been major requirement for initiating activity will descend in some degree as they a photoinitiator. Properties such as low migration tend- are immobilized to the macromolecular backbone. ency are gaining increasing importance for certain Recently, we have developed a novel bifunctio- applications. However, as the conventional photoinitia- nal photoinitiator bis[4-(2-hydroxy-isopropionyl)]ether tors do not all participate in the actual photopolymeri- (BHPE), which contains two a-hydroxyalkylphenone zation, their excess, unreacted residues, as well as their chromophoric groups. Very low migration tendency degradation products formed during the photochemical was found for this photoinitiator.6 It was synthesized reaction remain in the finished product. Initiator resi- from diphenyl ether and a-chloroisobutyryl chloride dues and/or degradation products may cause unpleas- through the procedures of acylation, bromination, ant odor, which should be avoided in some applications and hydrolyzation. The illustrated diagram of syn- such as food packaging and cosmetic bottle. Their diffu- thesis is shown in Scheme 1, and more details are sion out of the coating and into surrounding media reported elsewhere.6 In this article, the photoinitiat- may also create problems.4 Conventional monofunc- ing behaviors of the concerned bifunctional photo- tional photoinitiators suffer from VOC problem due to initiator on free-radical polymerization have been their low molecular weight. One approach to overcome investigated by differential photocalorimetry (DPC; the problem is to synthesize photoinitiators with higher also named photo-DSC). Correspondence to: Zhaohua Zeng ([email protected]). EXPERIMENTAL Contract grant sponsor: National Natural Science Foun- dation of China; contract grant number: 60378029. Materials Journal of Applied Polymer Science, Vol. 102, 5297–5302 (2006) BHPE was synthesized by procedure described in VC 2006 Wiley Periodicals, Inc. another paper.6 1-Hydroxycyclohexylphenyl ketone 5298 YE ET AL. Scheme 1 Synthetic route of BHPE. À (HCPK, Irgacure 184), 2-hydroxy-2-methyl-1- phenyl- polymerization (80.0 kJ mol 1 for the acrylate ester À propanone (HMPP, Irgacure 1173) were chosen as pho- double bond calculation, 57 kJ mol 1 for methylacry- toinitiators for comparison and purchased from Ciba late ester double bond calculation7), and m the mole (Shanghai, China). Hydroxyethyl methyacrylate (HEMA) number of carbon double bond in the system. Conver- and trimethyolpropane triacrylate (TMPTA) were sion curve (a t) can be obtained by integrating the selected as monomers and provided by Cognis. polymerization rate curve (da=dt t). The conversion curve for photopolymerization of TMPTA initiated by BHPE is shown in Figure 1. To Measurements evaluate the initiation efficiency of BHPE, two com- UV/vis spectra were detected by a VARIAN CARY100 mercial photoinitiators with low molecular weight, instrument. DPC tests were carried out on a modified HMPP and HCPK, which can be regarded as the mono- CDR-4 DSC (from Shanghai Balance Instrument Plant) functional photoinitiator homologue, were chosen for with a middle pressure mercury lamp as radiation the comparison. It is well established that the photode- source. The light intensity was measured by a UV-radi- compositions of HMPP and HCPK follow Norrish ometer (type UV-A, from Photoeletric Instrument Fac- type I mechanism. By comparing the three conversion tory, Beijing Normal University, China) that is sensi- curves, it can be found that the BHPE has the competi- tive in the wavelength range of 320–400 nm. The sam- tive performance with those monofunctional photoini- ples containing 1–5 wt % of the initiator were sonicated tiators. The induction period for BHPE is similar to for 30 min to ensure complete dissolving, and then the those for monofunctional photoinitiator HMPP and sample weighed 2–4 mg was placed in an open clear HCPK, and the final conversion is almost the same. aluminum sample pan. Each sample was held in iso- The photoactive chromophore in BHPE has a weak thermal conditions at 358C in nitrogen prior to irradia- CÀÀC bond, with dissociation energy lower than the tion. The photopolymerization reaction as carried out until no heat was evolved. Data reported for each com- position are an average of separate photopolymeriza- tions. The baseline is subtracted to ensure the result is unaffected by the radiation enthalpy of background. RESULTS AND DISCUSSION Photoinitiation behavior of BHPE For the free-radical polymerization reaction is exother- mic, the polymerization progress can be monitored by means of DPC, by which the heat flow (dH/dt) from the sample during irradiation is measured as the func- tion of reaction time (t). The reaction rate is calculated from the reaction enthalpy by the following equation: a ð = Þ = ¼ d ¼ d H H1 ¼ dH dt Rp  (1) dt dt H0 m Figure 1 Polymerization rate and conversion versus ¼ reaction time for the photopolymerization of TMPTA initi- where Rp is the polymerization rate, H!( H0m) the ated by various photoinitiators at room temperature, nitro- ¼¼ À2 total enthalpy, H0 the molar enthalpy of C C bonds in gen atmosphere, light intensity: 2.0 mW cm . PHOTOINITIATING BEHAVIOR OF BIFUNCTIONAL PHOTOINITIATOR 5299 Scheme 2 Proposed mechanism of photochemical decomposition of the bifunctional photoinitiator BHPE. excitation energy of its reactive excited state. a-cleav- and shorter induction period than does monofunc- age will take place when the sample is irradiated by tional monomer HEMA in the early stage of polymer- UV light. The proposed photodecomposition process ization. In the case of multifunctional monomer, the is shown in Scheme 2. chain radicals are embedded by more rapid onset of Because there are two weak CÀÀC bonds within a gelation and vitrification caused by higher density of molecule, the biradical intermediates will appear crosslinks, and the chain radical was diffusion con- in the photodecomposition fragments. It can increase trolled even at early stage of the curing reaction.8 As a the initiating efficiency or the probability of fragment result of higher reaction rates due to higher concentra- bonded to the backbone of formed polymer chain. tions of functional groups, more dense networks Figure 2 shows the photoinitiation behavior of BHPE reduce the extent of double bond conversion, leaving a in initiating the polymerization of two types of mono- large portion of them unreacted (40–50% for TMPTA). mers, HEMA and TMPTA. These monomers exhibit similar polymerization profiles to those initiated with Kinetics monofunctional photoinitiators. The sharp rise at the beginning of polymerization indicates autoaccelera- The plots of conversion versus exposure time for tion of the bulk polymerization reaction. After reach- TMPTA with various light intensity are shown in Fig- ing the maximum polymerization rate, the reaction ure 3. It is found that increasing light intensity can slows down as the polymer gels. Trifunctional mono- increase the polymerization rate and the final mono- mer TMPTA shows much higher polymerization rate mer conversion. Figure 2 Conversion versus reaction time for the photo- Figure 3 Conversion versus reaction