Preparation method and application of evodia rutaecarpa serving as agricultural fungicide
A technology of Evodia and fungicides, applied in the field of Evodia fungicides and its preparation, can solve the problems of long research and development cycle and huge cost, and achieve the effects of low equipment requirements, long application history and simple processing.
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Embodiment 1
[0030] Evodia rutaecarpa fruit, stalk, and shell 5kg were extracted with 75% ethanol at 60°C for 3 times to obtain the total extract, which was adsorbed with A8 macroporous resin and eluted with water, 30%, 50%, and 75% ethanol respectively , collect 30%, 50% and 75% elution parts of the macroporous resin, concentrate the eluate to 1.5kg liquid extract, and obtain the total alkaloid extract of Evodia rutaecarpa. Put 0.5kg of surfactant (such as polysorbate-80) and 1.5kg of the total alkaloid extract of Evodia rutaecarpa into the homogenizer, heat to 30°C, and add 1kg of water into the homogenizer while stirring , stirred for 30 minutes, fully mixed, cooled to normal temperature, and formed water emulsion to obtain fungicide Evodia rutaecarpa.
Embodiment 2
[0032] 50kg of Evodia rutaecarpa leaves were extracted three times with 95% ethanol at 60°C to obtain the total extract, which was adsorbed with D101 macroporous resin, eluted with water, 30%, 50%, and 80% ethanol respectively, and the macroporous resin was collected for 30 %, 50% and 80% of the eluted parts, the eluate was concentrated to 1.5kg liquid extract to obtain the total alkaloid extract of Evodia rutaecarpa. Put 0.5kg of surfactant (such as polyethylene oxide non-ionic surfactant: OP-10) and 1.5kg of liquid extract of Evodia rutaecarpa total alkaloid extract into a homogenizer, heat to 50°C, and stir Add 1 kg of water into the homogenizer, stir for 30 minutes, fully mix, cool to normal temperature, form water emulsion, and obtain the bactericide of Evodia rutaecarpa.
Embodiment 3
[0034] Indoor toxicity measurement of the fungicide Evodia rutaecarpa prepared in Example 1:
[0035] Indoor virulence assay The tested plant pathogens include Sclerotinias clerotiorum, Fusarium graminearum, Botrytiscinerea, Colletotrichumgloeosporioides, Rhizoctoniasolani, corn Helminthosporium maydis, Botrytiscinerea, Fusarium moniliforme, Rhizoctoniacerealis, Alternariasolani, Verticilliumdahliae and rice blast 12 common plant pathogens including Magnaportheoryzae. All the tested pathogenic bacteria were isolated strains collected in the field.
[0036] The virulence of 12 kinds of plant pathogenic bacteria was determined by mycelial growth rate method. Each bacterial strain was activated and cultured on a PDA plate, and then a 5mm caliber punch was used to punch out a bacterial disk at the edge of the colony. The tested bactericide was made into a mother solution with sterile water, and then five drug-containing plates of PDA with concentration gradients were prepared b...
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