Method for biological catalysis for preparing konjak glucomannan esters in mixed solvent
The technology of konjac glucomannan and glucomannan ester is applied in the field of preparation of functional polymer materials, and can solve the problems of easy generation of by-products, poor reaction selectivity, complicated reaction system, etc., and achieves simple and easily controllable reaction process, The effect of mild reaction conditions and high degree of reaction
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Embodiment 1
[0020] The water activity is 0.5g konjac glucomannan of 0.11, 100U is derived from the lipase of Candida antarctica, 5.0ml vinyl acetate, 5.0ml mixed solvent (wherein mixed solvent, main solvent isooctane and cosolvent N, N-dimethylacetamide (volume ratio: 9:1) was put into a stoppered Erlenmeyer flask, the bottle mouth was strictly sealed with polytetrafluoroethylene sealing tape, and then placed in a water bath constant temperature oscillator at 30°C and 100rpm to oscillate, and reacted for 6 hours. , take out the reactor, add absolute ethanol to stop the reaction, remove the precipitate obtained by suction filtration to remove the mixed solvent, wash thoroughly with absolute ethanol, and dry to constant weight. The lipase is removed through an 80-mesh sieve to obtain konjac glucomannan acetate with a degree of substitution of 0.13.
Embodiment 2
[0022] The water activity is 0.5g konjac glucomannan of 0.53, 1000U is derived from the lipase of Candida antarctica and 0.9ml vinyl acetate, 20.0ml mixed solvent (wherein mixed solvent, main solvent carbon tetrachloride and auxiliary solvent N , the volume ratio of N dimethylacetamide is 9:1) into a stoppered Erlenmeyer flask, tightly sealed with polytetrafluoroethylene sealing tape, and then placed in a water bath constant temperature oscillator at 70°C and 200rpm to vibrate, and the reaction After 48 hours, the reactor was taken out, and anhydrous ethanol was added to stop the reaction. The precipitate obtained by removing the mixed solvent was suction-filtered, washed thoroughly with anhydrous ethanol, and dried to constant weight. The lipase is removed through a 200-mesh sieve to obtain konjac glucomannan acetate with a degree of substitution of 0.15.
Embodiment 3
[0024] The water activity is 0.5g konjac glucomannan of 0.23, 1000U lipase derived from Candida antarctica and 5.0ml vinyl acetate, 50.0ml mixed solvent (wherein mixed solvent, main solvent isooctane and cosolvent N, The volume ratio of N-dimethylacetamide is 9:1) into a stoppered Erlenmeyer flask, the bottle mouth is strictly sealed with a polytetrafluoroethylene sealing tape, and then placed in a water bath constant temperature oscillator at 50°C and 200rpm to oscillate and react for 24 hours Finally, the reactor was taken out, and absolute ethanol was added to stop the reaction, the precipitate obtained by removing the mixed solvent by suction filtration was fully washed with absolute ethanol, and then dried to constant weight. Remove the lipase through a 200-mesh sieve to obtain konjac glucomannan acetate with a degree of substitution of 0.28.
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