2003
DOI: 10.1016/s0014-3057(02)00367-1
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UV photo curing of N,N′-bismaleimido-4, 4′-diphenylmethane

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Cited by 17 publications
(10 citation statements)
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“…The degree of conversion obtained then reaches a maximum and starts to decrease thereafter. This is in accordance with the effect seen in the photopolymerization of other systems [141,142] and has been attributed to excess initiator molecules at higher concentrations absorbing most of the light intensity in the surface layer, preventing it from penetrating the entire depth of the sample. The optimum amount of photoinitiator is one that minimizes this absorption, as well as gives a high degree of monomer conversion.…”
Section: Figure 3 Typical Dpc Curve From Photopolymerization Of Dialsupporting
confidence: 88%
“…The degree of conversion obtained then reaches a maximum and starts to decrease thereafter. This is in accordance with the effect seen in the photopolymerization of other systems [141,142] and has been attributed to excess initiator molecules at higher concentrations absorbing most of the light intensity in the surface layer, preventing it from penetrating the entire depth of the sample. The optimum amount of photoinitiator is one that minimizes this absorption, as well as gives a high degree of monomer conversion.…”
Section: Figure 3 Typical Dpc Curve From Photopolymerization Of Dialsupporting
confidence: 88%
“…UV-induced curing of thermosetting systems involving maleimides have been investigated with regard to the resulting structures, 6,7 kinetics and mechanism, 7-10 bulk and surface properties 11 reactivity, 8,9 effect of the UV dosage, 10 effect of the photoinitiators, and curing temperature. 12 None of these studies, however, have proposed a generally valid kinetic rate equation, with the sole exception of the Decker's study, 9 in which a kinetic rate equation was introduced for a special system. Decker investigated the influence of the light intensity on the cure kinetic of a DVE-3/Qbond system, where DVE-3 refers to divinyl ether of triethyleneglycol, and Q-bond is a liquid bismaleimide with a 36-carbon-atom cycloaliphatic branched structure from Quantum Materials; Decker proposed the following kinetic rate equation:…”
Section: Introductionmentioning
confidence: 99%
“…UV‐induced curing of polymer coatings has until recently been dominated by photoinitiated radical polymerization processes, partly because of their curing efficiency. UV‐induced curing of thermosetting systems involving maleimides have been investigated with regard to the resulting structures,6, 7 kinetics and mechanism,7–10 bulk and surface properties11 reactivity,8, 9 effect of the UV dosage,10 effect of the photoinitiators, and curing temperature 12. None of these studies, however, have proposed a generally valid kinetic rate equation, with the sole exception of the Decker's study,9 in which a kinetic rate equation was introduced for a special system.…”
Section: Introductionmentioning
confidence: 99%
“…Photo-initiated curing reactions are powerful processes to quickly create highly cross-linked polymer networks by supplying an appropriate form of energy, generally ultraviolet (UV) light, to a thermosetting material like epoxy, unsaturated polyester, acrylic resins etc., containing photo initiating species [1][2][3][4][5] In recent years, epoxy acrylate prepolymer suitable for use in ultraviolet (UV) curing systems, command the largest use in the market and are typically used in applications ranging from paper and card over-print varnishes, wood coatings, screen and lithographic inks and solder resist inks for printed circuit boards 6-9. Other areas such as vacuum metallizing base coatings, adhesive laminates, release coatings and video disc coatings are also becoming more important 10. Epoxy acrylates are noted for adhesive properties, flexibility, nonyellowing, hardness, and chemical resistance 11-13. The epoxy backbone promotes tough-ness and flexibility to cured films whilst the carbon-carbon and ether bonds of the same improve the chemical resistance. The epoxy acrylate resins have the merits of: (a) high reactivity (b) possibility of structural variation in backbone (e.g.…”
Section: Introductionmentioning
confidence: 99%