2013
DOI: 10.1166/asl.2013.4811
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Bioplastic Nanocomposite Prepared from Acrylated Epoxidized Soybean Oil-PMMA Copolymer and Nano-Titanium Dioxide

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Cited by 5 publications
(5 citation statements)
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“…In Figure 3 A, the signal at 5.3 ppm (peak g) corresponds to the unsaturated double bond (C=C) that is present in MO. According to Sathai et al, [ 31 ], an unsaturated double bond signal can be seen at 5.2–5.41 ppm whereas signals for the long chain aliphatic (CH 2 ) and terminal CH 3 would appear at 1.2–1.4 (peak b) and 0.8–0.9 ppm (peak a), respectively. During the epoxidation process, the double bond (C=C) in MO was converted to an epoxide ring (C-O-C) in EMO.…”
Section: Resultsmentioning
confidence: 99%
“…In Figure 3 A, the signal at 5.3 ppm (peak g) corresponds to the unsaturated double bond (C=C) that is present in MO. According to Sathai et al, [ 31 ], an unsaturated double bond signal can be seen at 5.2–5.41 ppm whereas signals for the long chain aliphatic (CH 2 ) and terminal CH 3 would appear at 1.2–1.4 (peak b) and 0.8–0.9 ppm (peak a), respectively. During the epoxidation process, the double bond (C=C) in MO was converted to an epoxide ring (C-O-C) in EMO.…”
Section: Resultsmentioning
confidence: 99%
“…oil (AESO) AESO was prepared from a reaction between ESO and acrylic acid in a similar way to previous reports [39,40]. About 50 g of ESO were placed in a 250 mL round-bottom flask equipped with a magnetic stirrer and a reflux condenser.…”
Section: Synthesis Of Acrylated Epoxidized Soybeanmentioning
confidence: 99%
“…It has been established that AESO shows higher mechanical properties than ESO [22,39]. AESO has been used for copolymerization with other materials such as a vinyl ester resin containing styrene [8][9][10] and with poly(methyl methacrylate) [38][39][40]. It was found that the mechanical properties of an AESO-co-PMMA copolymer were higher than those of AESO.…”
mentioning
confidence: 99%
“…With respect to the radical polymerization, since the double bonds in most of the oils are nonconjugated which are inactive for radical polymerization, their reactivity can be chemically improved by conjugating the double bonds or converting double bonds into more active groups, such as epoxy [8,9]. The epoxidized plant oils can be chemically produced from plant oil by in-situ epoxidation with hydrogen peroxide and acetic acid in the presence of sulfuric acid as catalyst [10][11][12]. The conversion of double bonds into epoxide groups increases the reactivity of oils due to the ring strain in the epoxy group.…”
Section: Introductionmentioning
confidence: 99%