Low methoxyi pectin preparation technique using orange peel
A low-methoxyl pectin and citrus peel technology, which is applied in the field of food engineering, can solve the problems of citrus peel waste, pollution, environmental pollution, etc., achieve good decolorization effect, solve environmental pollution problems, and have stable process performance Effect
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example 1
[0019] Take 5kg of citrus skin dregs from the juice factory, cut it into 0.5×0.5cm 2 block, immersed in boiling water for 10 minutes to inactivate the enzyme. Add 15 kg of water, then add 1 g of pectin esterase, mix well, adjust the pH to 7, and deesterify at a temperature of 55° C. for 1 hour. Heat the deesterified pectin extract to 95°C for 10 minutes to inactivate the enzyme. Add 35 kg of water to the sterilized extract, adjust the pH to 1.5 with a 50% hydrochloric acid solution, stir at 80°C for 1 hour for hydrolysis, then filter the hydrolyzate with a filter cloth, take the filtrate, and carry out the above-mentioned process again on the filter residue hydrolysis. Concentrate the filtrate after two times of hydrolysis in vacuum, the temperature of the water bath is between 65°C, and the concentrated solution is reduced to 1 / 4 of the extract before concentration. Quickly cool the concentrated solution, add 90ml of 30% concentration of hydrogen peroxide to the cooled con...
example 2
[0021] Cut the waste residue from citrus juice from the juice factory into 0.3×0.5cm 2 In block form, immerse in boiling water for 9 minutes to inactivate the enzyme, and dry at 65°C. Get 5kg of dried citrus peels, soak the raw material in 25kg of water to soften, drain the citrus peels after softening, weigh, add water 5 times the weight of the softened peels, then add 5g of pectin esterase, mix well, Adjust the pH value to 7.5, and deesterify at a temperature of 55° C. for 1 hour. Heat the deesterified pectin extract to 95°C for 10 minutes to inactivate the enzyme. Add water 10 times the weight of the skin dregs after softening to the sterilized extract, adjust the pH to 2.0 with a 50% hydrochloric acid solution, stir at 80°C for 1.5 hours, and filter the hydrolyzed solution with a filter cloth after hydrolysis. Take the filtrate, and carry out the above-mentioned hydrolysis on the filter residue again. Concentrate the filtrate after two times of hydrolysis in vacuum, the...
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