Esters starch

Starch Esters. As with the starch ethers, a large number of starch esters have been prepared and patented, but only a few are manufactured and used commercially. Both inorganic and organic acid esters can, and have been, made. The latter are prepared by the same general procedure used to make starch ethers. 

Throughout the 1990s a large portion of the research and development effort for hot melt adhesives focused on developing adhesives that are either environmentally friendly or functional [69,81,82]. Environmentally friendly attributes include biodegradability, water dispersibility (repulpability), renewability, and water releasability. Biodegradable adhesives have been developed based on starch esters [83-86] and polyesters such as poly (hydroxy butyrate/hydroxy valerate) [87], poly(lactide) [88-91], and poly(hydroxy ether esters) [92-94]. All but the... 

Starch esters have been obtained by reactions of starch and carboxylic or sulfonic acid imidazolides in aqueous NaOH or nonaqueous solutions, as described in reference [226]. The esterification of dextran with butyric or palmitic acid using CDI in DMSO or formamide is discussed in reference [174]. 

Hydroxypropyl starch Starch esters Carboxymethyl starch... 

This group (sometimes called water-soluble resins) includes such chemically treated natural polymers as carboxymcthylcclluosc, mcthylccllulosc, and other cellulose esters, as well as various kinds of modified starches (esters and acetates). 

Starches may be used directly as feedstocks, or in more technical uses in modified form (typically as starch esters and ethers), or simply converted to glucose syrups for use in industrial fermentation processes or for onward conversion to isoglucose (fructose). After use of unmodified starches in ethanol production, the largest industrial user of both unmodified and modified starches is the papermaking... 

Starch esters are thermoplastic materials with properties that are somewhat similar to that of cellulose esters. In particular, starch acetate (DS < 0.2) is used as a coating agent for paper and as a food or detergent additive. 

Benzimidazole derivatives, III, 161 Benzimidazole rule of rotation, I, 21 1,3-Benzodioxan, 8,8 -methyIenebis(6- nitro-), III, xvii Benzoic acid, cellulose esters, I, 320 labelled with isotopic C, III, 231 starch esters, I, 302, 303 —, 2,4-dihydroxy-, effect on conductivity of boric acid, IV, 195 —, 2,4,5-trihydroxy-, effect on conductivity of boric acid, IV, 195 —, 3,4,5-trihydroxy-. See Gallic acid. 

Cinnamic acid, starch ester, I, 303 Cinnamaldehyde, phytochemical reduction of, IV, 79, 91 Cinnamyl alcohol, IV, 91 phytochemical reduction of, IV, 92 Citraconic acid, IV, 327 Citral, phytochemical reduction of, IV, 79... 

Formic acid, cellulose ester, I, 310 from inositol oxidation, III, 52 labelled with C1, III, 237 labelled with isotopic C, III, 231, 232 starch ester, I, 300 from sucrose, IV, 309 Formose, IV, 27... 

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