Preparation method of compound bacterium microcapsule for treating salinization and promoting growth of cotton
A technology of microcapsules and composite bacteria, applied in the direction of microcapsule preparations, methods based on microorganisms, biochemical equipment and methods, etc., can solve problems such as interference with normal plant metabolism, water balance breakdown, plant cell toxicity, etc., to protect viability , Conditioning soil alkalinity, good slow-release effect
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Embodiment 1
[0051] The present embodiment controls the preparation method of the compound bacteria microcapsules that salinization promotes the growth of cotton, comprises following main steps:
[0052] (1) Preparation of the main material of the microcapsule skeleton
[0053] 1.1 The cotton stalks are pulverized, deashed, dewaxed and dried to obtain cotton stalk powder; the cotton stalks in this embodiment are agricultural waste cotton stalks;
[0054] in,
[0055] 1.11 After the cotton stalks are pulverized by a pulverizer, the obtained waste cotton stalks are crushed into powder and sent to the deashing device for deashing;
[0056] 1.12 Cook with absolute ethanol for 2 hours for dewaxing, and rinse with deionized water;
[0057] 1.13 Place the material obtained in step 1.12 in an oven and dry at 105°C for 12 hours;
[0058] 1.2 Feed 60% sulfuric acid, cotton stalk powder and γ-valerolactone at a ratio of 1:10:100, mix evenly, stir at 80°C for 1 hour, then filter at the same tempera...
Embodiment 2
[0083] The difference between this embodiment and embodiment 1 is that
[0084] Step 1.13, drying at 100°C for 10 hours;
[0085] Step 1.2, 150g of cotton stalk powder, stirred at 90°C for 1.5h;
[0086] Step 1.3, the filter residue of step 1.2 was boiled with deionized water for 2.5 hours, added with sodium hydroxide solution and boiled for 2.5 hours;
[0087] Step 1.4, mix the slurry with sodium hypochlorite and hydrogen peroxide, stir at 45°C for 40 minutes, and acidify for 12 minutes;
[0088] Step 1.5, after mixing the filter residue and sodium hydroxide solution, stir and react at 30°C for 40 minutes. The temperature of the autoclave is 230°C;
[0089] Step 2.2, the culture substrate includes 30g glucose, 30g hemicellulose and 150g sodium alginate;
[0090] Step 2.3, Rs-198 strain 10g, Pseudomonas chloropinus R5 strain 10g, Bacillus subtilis GB03 strain 10g;
[0091] Steps 2.31 to 2.33, pH control is 7.0;
[0092] Step 3.1, the temperature of the water bath is kept ...
Embodiment 3
[0098]The difference between this embodiment and embodiment 1 is that
[0099] Step 1.13, drying at 110°C for 12 hours;
[0100] Step 1.2, 200g of cotton stalk powder, stirred at 100°C for 1h;
[0101] Step 1.3, the filter residue of step 1.2 was boiled with deionized water for 1.5h, added with sodium hydroxide solution and boiled for 1.5h;
[0102] Step 1.4, mixing the slurry with sodium hypochlorite and hydrogen peroxide and stirring at 35°C for 60 minutes;
[0103] Step 1.5, the temperature of the autoclave is 225°C;
[0104] Step 2.2, the culture substrate includes 40g glucose, 40g hemicellulose and 200g sodium alginate;
[0105] Step 2.3, Rs-198 strain 15g, Pseudomonas chloropinus R5 strain 15g, Bacillus subtilis GB03 strain 15g;
[0106] Steps 2.31 to 2.33, pH control is 7.5;
[0107] Step 3.1, keep the temperature of the water bath at 80°C;
[0108] Step 3.2, constant temperature ultrasonic dispersion at 55°C for 45 minutes. After centrifugal washing, dry at 90°C...
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