Bacteria cellulose pervaporation membrane and uses thereof
A technology of pervaporation membrane and bacterial cellulose, which is applied in the field of bacterial cellulose pervaporation membrane and separation of organic matter aqueous solution, can solve the problems of complex process and difficult control of membrane uniformity, achieve high separation selectivity, solve chemical stability, Cost-effective preparation
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Embodiment 1
[0018] Example 1. A bacterial cellulose pervaporation membrane, the preparation method of which is as follows: take the activated Acetobacter xylinum DT4.2 strain and insert it into a seed culture solution, and after 8 hours of shaking culture on a constant temperature shaker at 25°C, insert the seed solution into a fermentation culture In the liquid, shake well, transfer the fermentation liquid to a container, cultivate at a constant temperature of 25°C for 7 days, form a film on the surface of the fermentation liquid, take out the film and treat it with lye with a mass concentration of 1%, and rinse the film with deionized water. The remaining lye in the medium becomes neutral, and it is dried to form a film.
Embodiment 2
[0019] Example 2. A bacterial cellulose pervaporation membrane, the preparation method of which is as follows: take the activated Acetobacter xylinum DT4.2 strain and insert it into a seed culture solution, and after 32° C. constant temperature shaker shaking culture for 24 hours, insert the seed solution into the fermentation culture In the liquid, shake well, transfer the fermentation liquid to a container, cultivate at a constant temperature of 32 °C for 15 days, form a film on the surface of the fermentation liquid, take out the film and treat it with lye solution with a mass concentration of 20%, rinse the film with deionized water The remaining lye in the medium becomes neutral, and it is dried to form a film.
Embodiment 3
[0020] Example 3. A bacterial cellulose pervaporation membrane, the preparation method of which is as follows: take the activated Acetobacter xylinum DT4.2 strain and insert it into a seed culture solution, and after 28° C. constant temperature shaker shaking culture for 10 hours, insert the seed solution into the fermentation culture In the liquid, shake well, transfer the fermentation liquid to a container, cultivate at a constant temperature of 28°C for 9 days, form a film on the surface of the fermentation liquid, take out the film and treat it with lye with a mass concentration of 3%, and rinse the film with deionized water. The remaining lye in the medium becomes neutral, and it is dried to form a film.
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