1997
DOI: 10.1002/(sici)1097-4628(19970725)65:4<705::aid-app9>3.0.co;2-o
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Properties of fatty-acid esters of starch and their blends with LDPE

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Cited by 148 publications
(84 citation statements)
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“…This increase in thermal stability with increasing DS was attributed to the low amount of remaining hydroxyl groups in starch molecules after modification. The decomposition of starch occurs as a result of the inter-or intramolecular dehydration reactions having water as a main product of decomposition [7]. The opportunity for this condensation reaction was reduced with substitution of hydroxyl group by fatty acid ester group and higher DS contribute to its thermal stability.…”
Section: Thermogravimetric Analysissupporting
confidence: 56%
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“…This increase in thermal stability with increasing DS was attributed to the low amount of remaining hydroxyl groups in starch molecules after modification. The decomposition of starch occurs as a result of the inter-or intramolecular dehydration reactions having water as a main product of decomposition [7]. The opportunity for this condensation reaction was reduced with substitution of hydroxyl group by fatty acid ester group and higher DS contribute to its thermal stability.…”
Section: Thermogravimetric Analysissupporting
confidence: 56%
“…The initial degradation of native starch began at 280°C with a weight loss of 30%. Further heating, to 600°C, resulted in carbonisation and ash formation as reported [7]. The TGA has shown that the esterification of starch increases its thermal stability.…”
Section: Thermogravimetric Analysismentioning
confidence: 99%
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“…In general, the preparation of long-chain fatty acid esters of starch is carried out by converting the polymer with the acid chloride in a slurry medium like dioxan (Teng and Rha 1970), N,N-dimethyl formamide (DMF, Peltonen and Harju 1994), toluene (Lower 1996;Bader et al 1997), and pyridine (Aburto et al , 1999aThiebaud et al 1997;Bikiaris et al 1999). In addition, n-hexane (Bader et al 1997) and mixtures of carbon tetrachloride/ ethanol (Whistler 1988) and dioxan/toluene (Gros and Feuge 1962) have been applied.…”
Section: Introductionsupporting
confidence: 53%
“…Although they show a variety of promising properties, e.g. thermoplasticity (Aburto et al , 1999aThiebaud et al 1997;Bikiaris et al 1999;Sagar and Merrill 1995;Frigant et al 1998) and they are of interest as dipcoatings both in food and non-food area (Gros and Feuge 1962;Rooney 1976), no commercial application was realized up to now. Moreover, various patents claim the use as binders in coating, adhesive and ink compositions (Jonker 1991), as chewing gum base (Teng and Rha 1970), as thermoplastic, hydrophobic coating material (Bader et al 1997) and applications for hot-melt adhesives and in controlled release (Peltonen and Harju 1994).…”
Section: Introductionmentioning
confidence: 99%