Clean productive process for extracting citric acid from citric acid fermentation liquid
A citric acid fermentation broth and citric acid technology, applied in the separation/purification of carboxylic acid compounds, organic chemistry, etc., to achieve the effects of reducing operators, shortening the production process, and saving production sites
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example 1
[0040] Example 1 Oil Phase A
[0041] Styrene 40 g; Acrylic acid 50 g; Divinylbenzene 15 g (82%);
[0042] Isoheptane 45g; Benzoyl peroxide 1g Water Phase B
[0043] 180 grams of water; 40 grams of sodium chloride; 0.3 grams of sodium carboxymethylcellulose; 15 drops of 1% methylene blue
[0044] Slowly add the oil phase A into the water phase B under stirring, and adjust the stirring speed until the oil phase forms droplets of the desired size in the water phase. Then slowly raise the temperature to 75-80°C, and react under heat preservation. After 5 hours, the product was filtered and washed thoroughly, and dried in vacuum at 100° C. to obtain 98 g of the product, with a yield of 93.3%.
[0045] The product obtained was in the form of beige round particles with an anion exchange capacity of 3.8 meq / g dry resin.
example 2
[0047] Quaternization of the resin obtained in Example 1: add 10 grams of the product to a mixed solution of 8 milliliters of dichloroethane and 10 milliliters of methyl chloride ether, soak at 30°C for 3 hours; cool down to about 25°C, add 8 grams of chlorine Zinc, heat up to 45°C and keep it warm; after 8 hours, cool down to room temperature, filter out the mother liquor, wash with water until pH = 2-3, and then air-dry for several hours; add 15 ml of acetone, then control the temperature below 40°C, and add 20 Milliliter trimethylamine aqueous solution was adjusted to pH = 11, and kept at 30°C for 6 hours; after the reaction was completed, it was filtered and washed with water until neutral to obtain 122 g of the product.
[0048] The product obtained was in the form of dark brown round particles with an anion exchange capacity of 4.9 meq / g dry resin.
example 3
[0049] Example 3 Oil Phase A
[0050] Styrene 40 g; Vinyl acetate 50 g; Divinylbenzene 15 g (82%);
[0051] Benzoyl Peroxide 1 g Water Phase B
[0052] 150 grams of water; 30 grams of sodium chloride; 0.25 grams of sodium carboxymethylcellulose; 10 drops of 1% methylene blue
[0053] The synthesis conditions are as in Example 1, and the product yield is 95.3%.
[0054] The product obtained was in the form of off-white round particles with an anion exchange capacity of 4.3 meq / g dry resin.
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