Method for preparing cellulose ether by using bast fiber crops, straws and other herbaceous plants as raw materials
A technology of herbal plants and cellulose ethers, applied in the use of microorganisms/enzyme cellulose treatment, non-woody plants/crop pulp, fiber raw material treatment, etc., can solve the problem of low function of degumming strains, imperfect degumming process, and insufficient enzyme activity Advanced problems, to achieve the effect of complete removal of gum, complete enzyme system and high enzyme activity
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Embodiment 1
[0042] This embodiment provides a kind of hemp bast ethyl cellulose ether, its preparation flow chart is as follows figure 1 As shown, the preparation method is as follows:
[0043] (1) Raw hemp grinding and crushing
[0044] Sun-dry the mildew-free cannabis bast until the water content is lower than 10%, fluff and remove impurities. Grind it into a fine loose crumb powder with a length of about 2 mm with a plant pulverizer.
[0045] (2) Bacteria culture
[0046] Plant spoilage bacteria PW (Pectobacterium wasabiae IBFC 2016) and Bacillus subtilis BSE (Bacillus subtilis BSE) were mixed and cultured to prepare a bacterial suspension; culture conditions: broth culture solution, pH 7, temperature 34°C, ventilation 0.2~ 0.3m 3 / (m 3 • h) with stirring at 120 rpm.
[0047] (3) Diluted solution
[0048] Pour tap water into the fermenter with heating, stirring and ventilation functions, and adjust to pH 7, temperature 34°C ± 1°C; add 2% of the bacterial suspension obtained in s...
Embodiment 2
[0058] This embodiment provides a kind of sisal leaf carboxymethyl cellulose ether, the preparation method is as follows:
[0059] (1) Raw hemp grinding and crushing
[0060] Dry the mildew-free sisal leaves until the water content is lower than 10%, fluff them and remove impurities. Grind it into a small loose crumb powder of about 2 mm with a plant pulverizer.
[0061] (2) Bacteria culture
[0062] Plant spoilage bacteria PW and Bacillus subtilis BSE were cultured together to prepare a bacterial suspension. Culture conditions: Broth culture medium, pH7, temperature 35°C, ventilation volume 0.2~0.3m 3 / (m 3 • h) with stirring at 120 rpm.
[0063] (3) Diluted solution
[0064] Pour tap water into the fermenter with heating, stirring and ventilation functions, and adjust to pH 7, temperature 34°C ± 1°C; add 2% of the bacterial suspension obtained in step (2) to it, mix and dilute to obtain the total activity Bacterial content of at least 1×10 7 cfu / mL dilution.
[0065...
Embodiment 3
[0074] This example provides a rice straw hydroxyethyl cellulose film ether, the preparation method is as follows:
[0075] (1) Raw hemp grinding and crushing
[0076] Dry the mildew-free rice straw to a moisture content of 8%, fluff it up and remove impurities. Use grinding equipment such as a plant pulverizer to grind it into a fine, loose crumb-like powder of about 2 mm.
[0077] (2) Bacteria culture
[0078] Plant spoilage bacteria PW and Bacillus subtilis BSE were cultured together to prepare a bacterial suspension. Culture conditions: Broth culture medium, pH7, temperature 33°C, ventilation volume 0.2~0.3m 3 / (m 3 • h) with stirring at 130 rpm.
[0079] (3) Diluted solution
[0080] Pour tap water into the fermenter with heating, stirring and ventilation functions, and adjust to pH 7, temperature 34°C ± 1°C; add 2% of the bacterial suspension obtained in step (2) to it, mix and dilute to obtain the total activity Bacterial content of at least 1×10 7 cfu / mL diluti...
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