Preparation method and application of efficient antibacterial bactericide for melons, fruits and vegetables
A fungicide and vegetable technology, applied in the field of preparation and application of agricultural and sideline products, can solve the problems of delayed effect, high price, and less application of natural antibacterial agents, and achieve the effects of strong inhibition, low production cost, and low residual rate
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Embodiment 1
[0020] Add 10 grams of polyvinylamine into the reaction kettle at normal temperature, then add 1000 milliliters of water, mix well, add 10 grams of difluorobenzoic acid and continue stirring. After 50 minutes, raise the temperature to 40°C, add 0.1M dilute hydrochloric acid to adjust the pH value of the solution to 6.0 and slowly add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride under nitrogen protection 10 grams, after stirring for 3 hours, cooling and discharging. The reaction solution was separated and purified through a dialysis membrane for 3 days. After drying, 0.2 g of lanthanum trichloride was added to the product and stirred evenly to obtain the final product 1.
Embodiment 2
[0022] Add 10 grams of polyvinylamine into the reaction kettle at normal temperature, then add 1000 milliliters of water and 100 milliliters of ethanol, mix well, add 5 grams of difluorobenzoic acid and continue stirring. After 90 minutes, the temperature was raised to 65°C, acetic acid was added to adjust the pH value of the solution to 4.0 and 18 grams of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was slowly added under nitrogen protection, After stirring for 4 hours, cool down and discharge. The reaction solution was separated and purified through a 2-day dialysis membrane. After drying, 0.4 g of neodymium chloride was added to the product and stirred evenly to obtain the final product 2.
Embodiment 3
[0024] Add 10 grams of polyvinylamine in reactor at normal temperature, then add 800 milliliters of water and 25 milliliters of methanol, add 4 grams of difluorobenzoic acid after mixing and continue to stir. After 60 minutes, the temperature was raised to 35°C, 0.1M oxalic acid was added to adjust the pH value of the solution to 5.0, and 5 g of diisopropylcarbodiimide was slowly added under the protection of nitrogen, and after stirring for 2 hours, the temperature was lowered and discharged. The reaction solution was separated and purified by the dialysis membrane of 4 days time, after drying, 0.6g cerium tetrachloride was added in the product and stirred evenly and final product 3 could be obtained.
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