2009
DOI: 10.1016/j.ijadhadh.2009.02.001
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UV- and thermal-curing behaviors of dual-curable adhesives based on epoxy acrylate oligomers

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Cited by 187 publications
(71 citation statements)
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“…After UV-curing, the peaks at 1636 and 809 cm -1 attributed to C=C bonds disappeared or decreased (for CF formulation in Figure 2b). It means that C=C bonds in the reactive monomers took part was the cross-linking reaction by photopolymerization 27,28 . Adding AgNPs into the formulations, no difference was observed on the FTIR spectrum apart from a decreasing of peak intensity (Figure 2c).…”
Section: Ft-ir Characteristicsmentioning
confidence: 99%
“…After UV-curing, the peaks at 1636 and 809 cm -1 attributed to C=C bonds disappeared or decreased (for CF formulation in Figure 2b). It means that C=C bonds in the reactive monomers took part was the cross-linking reaction by photopolymerization 27,28 . Adding AgNPs into the formulations, no difference was observed on the FTIR spectrum apart from a decreasing of peak intensity (Figure 2c).…”
Section: Ft-ir Characteristicsmentioning
confidence: 99%
“…Photoinitiator, Irgacure 184, was kindly provided by Ciba. An epoxy acrylate oligomer was synthesized as adapted in the literature [17]. Photoresist lift-off layer, LOL-2000, was purchased from MicroChem Corp. (Marlboro, MA).…”
Section: Methodsmentioning
confidence: 99%
“…For these reasons, the other curing mechanisms, such as dual curing technology, typically UV/thermal [12], UV/moisture [13] or only thermal curing [14] system have been developed. The thermal cationic curing process of epoxy resin is one of the most suitable industrial technologies.…”
Section: Introductionmentioning
confidence: 99%