Method for enzymatic degumming of high-acid-value rice bran oil
A high-acid value rice bran oil and degumming technology, which is applied in the direction of oil/fat refining, fat production, etc., can solve the problems of low efficiency and slow degumming rate of high-acid value rice bran oil by enzymatic method, so as to achieve slow solution speed and increase contact probability. , the effect of improving the reaction rate and efficiency
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Embodiment 1
[0030] Accurately weigh 200g high-acid value rice bran crude oil (acid value 50.92mg KOH / g) and place it in a 500mL conical flask with a stopper; heat the rice bran crude oil to 40°C in a glycerin bath constant temperature magnetic stirrer, then add 10mL to remove Ionized water and 60U / g (U / w, relative to the quality of the substrate oil) Lipase G "Amano" 50; continue to stir and react at 500rpm and 40°C for 30min; Centrifuge at 12,000rpm for 2min, collect the upper oil layer and remove water by rotary evaporation at 0.09Mpa, 70°C; the lower aqueous phase is collected for the next batch of reactions. Accurately weigh 100g of Lipase G "Amano" 50 pretreated high-acid rice bran crude oil and place it in a 500mL conical flask with a stopper; heat the pretreated high-acid value rice bran crude oil to 70°C, add 120 μL of citric acid solution with a mass concentration of 45% and homogenize with a high-speed homogenizer at a speed of 10,000 rpm for 1 min; then continue to stir and rea...
Embodiment 2
[0032]Accurately weigh 200g high-acid value rice bran crude oil (acid value 50.92mg KOH / g) and place it in a 500mL conical flask with a stopper; heat the rice bran crude oil to 35°C in a glycerin bath constant temperature magnetic stirrer, then add 10mL to remove Ionized water and 100U / g (U / w, relative to the quality of the substrate oil) Lipase G "Amano" 50; continue to stir the reaction at 350rpm and 35°C for 15min; after the reaction, the above mixture is quickly centrifuged Centrifuge at 12,000rpm for 2min, collect the upper oil layer and remove water by rotary evaporation at 0.09Mpa, 70°C; the lower aqueous phase is collected for the next batch of reactions. Accurately weigh 100g of Lipase G "Amano" 50 pretreated high-acid rice bran crude oil and place it in a 500mL conical flask with a stopper; heat the pretreated high-acid value rice bran crude oil to 70°C, add 120 μL of citric acid solution with a mass concentration of 45% and homogenize with a high-speed homogenizer a...
Embodiment 3
[0034] Accurately weigh 200g high-acid value rice bran crude oil (acid value 50.92mg KOH / g) and place it in a 500mL conical flask with a stopper; heat the rice bran crude oil to 25°C in a glycerin bath constant temperature magnetic stirrer, then add 10mL to remove Ionized water and 40U / g (U / w, relative to the quality of the substrate oil) Lipase SMG1 (refer to the preparation method described in the document J.Mol.Catal.B-Enzym., 2012,77:87-91 to prepare Lipase Freeze-dried enzyme powder of SMG1); continue to stir the reaction at 400rpm and 25°C for 1h; after the reaction, quickly centrifuge the above mixture with a centrifuge at 12,000rpm for 2min, collect the upper oil layer and store it at 0.09Mpa at 70°C The water was removed by rotary evaporation under certain conditions; the lower aqueous phase was collected for the next batch of reactions. Accurately weigh 100g of high acid value crude rice bran oil pretreated by Lipase SMG1, and place it in a 500mL conical flask with a...
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