Photocurable composition for PCB containing alkenyl ether and/or oxetane compounds and free radical polymeric compounds
A polymeric compound and light-curable technology, applied in applications, household utensils, inks, etc., can solve the problems of short light source life, poor performance of light-cured film, ozone pollution and other problems, and achieve steep imaging side walls and good curing performance Excellent, improve the effect of surface polymerization
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[0138]According to one embodiment of the present invention, the photocurable composition includes at least one other cationically polymerizable compound different from component (a2).
[0139]The other cationic polymer compound may be in the form of monomers or resins (such as oligomers or prepolymers). According to an embodiment of the present invention, the other cationic polymerizable compound may be selected from ethylene oxide-based compounds and aziridine-based compounds.
[0140]The ethylene oxide compound may be selected from, for example, glycidyl ether epoxy compounds, glycidyl ester epoxy compounds, glycidylamine epoxy compounds, aliphatic epoxy compounds, alicyclic epoxy compounds, and the like. The ethylene oxide compounds may be in the form of monomers or resins (such as oligomers or prepolymers). Mention may also be made of compounds having both an oxirane group and a radical polymerizable group (such as an acrylate group), such as epoxy (meth)acrylate resins. Preference is...
Example
[0240]Example 1-77 and Comparative Example 1-3
[0241]Infrared light-curable inkjet printing inks were prepared according to the above-mentioned preparation method, according to the components and proportions in Table 1 to Table 8 below, to prepare the inkjet printing inks of Examples 1-77 and Comparative Examples 1-3, respectively.
[0242]Table 1 Formulation of infrared light-curable inkjet printing ink
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[0244]Table 2 Formulation of infrared light-curable inkjet printing ink
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[0247]Table 3 Formulation of infrared curing inkjet printing ink
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[0250]Table 4 Formulation of infrared light-curable inkjet printing ink
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[0253]Table 5 Formulation of infrared curing inkjet printing ink
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[0256]Table 6 Formulation of infrared light curing inkjet printing ink
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[0259]Table 7 Formulation of infrared light-curable inkjet printing ink
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[0262]Table 8 Formulations of infrared light-curable inkjet printing inks and light-curable inks of compa...
Example Embodiment
[0368]Example 78: Reaction of vinyl ether monomers and methacrylate monomers in the presence of free radical photoinitiators
[0369]Using high-efficiency free radical photoinitiator bis(2,4,6-trimethylbenzoyl)phenyl phosphine oxide (trade name 819) as free radical photoinitiator, using 395nm UV-LED light source (light intensity 100mW / cm2), using the Photo-DSC test method to test the initiation effect of 819 on the acrylic ester radical polymerizable monomer TPGDA and 4-hydroxybutyl vinyl ether monomer (HBVE). The experimental results are attachedfigure 1 (The relationship between sample heat flow and exposure time). The experimental results show that the light intensity is 100mW / cm2When 819 was used to initiate TPGDA polymerization under the 395nm UV-LED light source, the heat flow curve of the sample changed significantly. This was caused by the cross-linking reaction of the double bond of TPGDA and the release of heat. When 819 had HBVE polymerization, There was almost no change in ...
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