2010
DOI: 10.1002/star.201000021
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Process‐product studies on starch acetylation reactions in pressurised carbon dioxide

Abstract: An in-depth study on the effect of process conditions (pressure, temperature and type of catalyst) on the acetylation of starch with acetic anhydride in pressurised carbon dioxide is described. A total of 22 experiments were performed and the experimental data were analysed using non-linear multivariable regression. The highest degree of substitution (DS) value (0.46) was obtained using K 2 CO 3 as the catalyst at 908C, 15 MPa pressure, and a catalyst to starch ratio of 0.5 mol/mol anhydroglucose units (AGUs).… Show more

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Cited by 21 publications
(21 citation statements)
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“…The acetylation reactions are typically carried out in water, though organic solvents also have been shown to be effective . Ac starch is a starch ester that has been extensively studied over the last two decades . Introduction of acetyl groups reduces the bond strength between starch molecules causing an increase in the swelling power and solubility of the modified starch.…”
Section: Chemical Modificationmentioning
confidence: 99%
“…The acetylation reactions are typically carried out in water, though organic solvents also have been shown to be effective . Ac starch is a starch ester that has been extensively studied over the last two decades . Introduction of acetyl groups reduces the bond strength between starch molecules causing an increase in the swelling power and solubility of the modified starch.…”
Section: Chemical Modificationmentioning
confidence: 99%
“…27% at 420°C, which is more than cassava starch with a residue of only 13 % at 420°C. This is an indication of an overall higher thermal stability for starch vernolate [33,34]. The thermogram also shows difference in degradation products between the starch and starch vernolate, which could be another signal for the modification of starch i.e., esterification.…”
Section: Differential Scanning Calorimetric (Dsc) Analysismentioning
confidence: 83%
“…The K 2 CO 3 content of 0.27 mmol resulted in degree of substitution that significantly differed from what obtained by the beginning of the content of K 2 CO 3 ( p < 0.05). This reaction was achieved through base‐catalyzed transesterification reaction in which the deprotonation of hydroxyl group of starch was activated by base catalyst; then the resultant intermediate starch alkoxide was later reacted with ester to produce starch acetate 5, 24, 26, 29–31.…”
Section: Resultsmentioning
confidence: 99%
“…Acetylation of starch with vinyl esters is an alternative approach that does not produce acid as by‐product 8, also it is cheaper than acetic anhydride and the acetaldehyde as a by‐product can be easily removed from the reaction medium due to its low boiling point (bp = 21°C) 22. Preparation of starch acetates with K 2 CO 3 as activator and different esterefying agent in different conditions were studied 8, 23, 24. It was reported that when comparing the catalytic activity of K 2 CO 3 with other catalyst, the degree of substitution directly dependent upon the basicity of the catalyst 24–26.…”
Section: Introductionmentioning
confidence: 99%
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