2000
DOI: 10.1007/bf02733784
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Cationic, thermally cured coatings using epoxidized soybean oil

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Cited by 36 publications
(28 citation statements)
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“…[4,5] Especially, its derivatives epoxidized soybean oil (ESO) and acrylated epoxidized soybean oil (AESO) have been widely applied in the UV curable coatings. [6,7] However, due to the flexible long aliphatic chain of soybean oil, as much as 50% or more petroleum-based rigid compounds, such as styrene [8,9], acrylate acid [10] and divinylbenzene [11,12], are necessary to make its mechanical or thermal properties acceptable for end use. Recently, with the rapid progress on bio-based materials, the exploration of bio-based compounds to strengthen the polymers derived from soybean oil so as to ensure a higher bio-based content has been frequently reported [5,[13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%
“…[4,5] Especially, its derivatives epoxidized soybean oil (ESO) and acrylated epoxidized soybean oil (AESO) have been widely applied in the UV curable coatings. [6,7] However, due to the flexible long aliphatic chain of soybean oil, as much as 50% or more petroleum-based rigid compounds, such as styrene [8,9], acrylate acid [10] and divinylbenzene [11,12], are necessary to make its mechanical or thermal properties acceptable for end use. Recently, with the rapid progress on bio-based materials, the exploration of bio-based compounds to strengthen the polymers derived from soybean oil so as to ensure a higher bio-based content has been frequently reported [5,[13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%
“…[24][25][26] However,s everals econdary reactions could theoretically occur:a )the catalyzed/uncatalyzed homopolymerization of ELO;b )the transesterification of glycerol moieties by FA ; c) epoxy ring openingw ith the water released by FA polycondensation;d )ELO inter-cross-linking etherification from the hydroxyl derived from an ELO openedr ing that reacts with another oxiran ring. [24][25][26] However,s everals econdary reactions could theoretically occur:a )the catalyzed/uncatalyzed homopolymerization of ELO;b )the transesterification of glycerol moieties by FA ; c) epoxy ring openingw ith the water released by FA polycondensation;d )ELO inter-cross-linking etherification from the hydroxyl derived from an ELO openedr ing that reacts with another oxiran ring.…”
Section: Introductionmentioning
confidence: 99%
“…Poorer thermal and mechanical properties result from both partially unreacted ESO and saturated fatty acid (FA) chains that reduce reactivity and self-plasticize. Most ESO industrial uses are thus limited to nonstructural, additive applications such as plasticizers or stabilizers for poly (vinyl chloride) [13], oil-base coatings [14] with low strength requirements [15]. Though the mechanical strength of cured ESO can be improved with the addition of nano-reinforcements [16], or fiber reinforcement [17], an inherently low T g inevitably limits practical applications because T g for a polymer must be appropriately higher than the temperature of its intended work environment to serve as a useful plastic [18].…”
Section: Introductionmentioning
confidence: 99%