Method for separating hydroquinone from alpha-arbutin fermentation solution
A technology of hydroquinone and arbutin, which is applied in the field of separation of hydroquinone, can solve the problems of low efficiency, high cost, and needs to be improved, and achieve the effect of reducing energy consumption and moderate price
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2014-01-01
Abstract
Description
technical field
[0001] The invention relates to the field of biochemical industry, more specifically, the invention relates to a method for separating hydroquinone from α-arbutin fermentation liquid. Background technique
[0002] α-Arbutin belongs to hydroquinone glycosides, its chemical name is 4-hydroxyphenyl-D-glucopyranoside, and its whitening activity is ten times that of β-arbutin. Researchers found that arbutin, as an inhibitor of tyrosinase, can block the synthesis of dopa and dopaquinone, thereby effectively inhibiting the production of melanin, has whitening effect, and is not irritating to the skin, with little side effects. It has the effect of significantly inhibiting the activity of tyrosinase. It is an emerging non-irritating, non-allergic and compatible natural whitening active substance. The recommended dosage of arbutin in cosmetics is 1%~5%, which has a high economical effect. value.
[0003] Hydroquinone (hydroquinone) chemical name hydroquinone, its mo...
Examples
Embodiment 1
[0031] In this example, tributyl phosphate is selected as the extractant, and α-arbutin fermentation liquid is used as raw material, wherein α-arbutin 20g / L, sodium chloride 64 g / L, pH5.5, hydroquinone 5.0g / L, the specific extraction recovery method is carried out according to the following steps.
[0032] (1) The α-arbutin fermentation broth and tributyl phosphate were subjected to three-stage countercurrent liquid-liquid extraction at 25°C at a volume ratio of 1:1, and the extraction phase and raffinate phase were collected after the extraction was completed.
[0033] (2) Add the extract phase and sodium hydroxide solution obtained in step (1) into the extraction tower at a volume ratio of 1:0.05. The operating temperature of the extraction tower is 35°C and the operating pressure is -0.1 Mpa. The top effluent is cooled and stratified. The upper organic phase can be reused as the extraction agent, and the lower aqueous phase can be recovered.
[0034] (3) The hydroquinone s...
Embodiment 2
[0040]In this example, tributyl phosphate was selected as the extractant, and α-arbutin fermentation liquid was used as raw material, wherein α-arbutin 30g / L, ammonium sulfate 20g / L, pH 5.0, hydroquinone 5.0g / L, the specific extraction recovery method is carried out according to the following steps.
[0041] (1) The α-arbutin fermentation broth and tributyl phosphate were subjected to liquid-liquid extraction at a volume ratio of 1:2 at 30°C. After the extraction was completed, it was left to stand until the two phases were separated. The two phases were separated, and the upper extract phase and the lower raffinate phase were collected.
[0042] (2) Add the extract phase obtained in step (1) and sodium hydroxide solution into the extraction tower at a volume ratio of 1:0.1. The operating temperature of the extraction tower is 30°C and the operating pressure is -0.1 Mpa. The top effluent is cooled and stratified. The upper organic phase can be reused as the extraction agent,...
Embodiment 3
[0048] In this example, propyl formate is selected as the extractant, and α-arbutin fermentation liquid is used as raw material, wherein α-arbutin is 24 g / L, magnesium sulfate is 40 g / L, pH5.5, and hydroquinone is 5.2 g / L, the specific extraction recovery method is carried out according to the following steps.
[0049] (1) The α-arbutin fermentation broth and tributyl phosphate were subjected to liquid-liquid extraction at a volume ratio of 1:2 at 35°C. After the extraction was completed, it was left to stand until the two phases were separated. The two phases were separated, and the upper extract phase and the lower raffinate phase were collected.
[0050] (2) Add the extract phase obtained in step (1) and sodium hydroxide solution into the extraction tower at a volume ratio of 1:0.04. The operating temperature of the extraction tower is 30°C and the operating pressure is -0.5 Mpa. The top effluent is cooled and stratified. The upper organic phase can be reused as the extrac...