Plant volatile oil slow-release core agent and application thereof
A plant volatile oil and slow-release core agent technology, applied in the field of pesticide research and development, can solve the problems of high humidity, fast prevalence of plant diseases, and unsatisfactory spray control effects of fungicides, etc., and achieve the effect of simple preparation method and prolonged effective period
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Embodiment 1
[0023] Example 1 : the preparation of volatile oil slow-release core agent (by weight)
[0024] Weigh 8 parts of L-carvone, 2 parts of D-limonene, 0.05 parts of 2,6-di-tert-butyl-p-cresol, and 0.05 parts of 2-hydroxy-4-methoxybenzophenone, mix well, and weigh Add 10 mg of the mixture dropwise to the desulfurized rubber sheet, and then add 100 μL of n-hexane dropwise to each desulfurized rubber sheet, and wait for the n-hexane to volatilize to obtain it.
Embodiment 2
[0025] Example 2 : the preparation of volatile oil slow-release core agent (by weight)
[0026] Weigh 7 parts of L-carvone, 3 parts of D-limonene, 0.03 parts of 2,6-di-tert-butyl-p-cresol, 0.03 parts of 2-hydroxy-4-methoxybenzophenone, mix well, and weigh Add 10 mg of the mixture dropwise to the desulfurized rubber sheet, and then add 100 μL of n-hexane dropwise to each desulfurized rubber sheet, and wait for the n-hexane to volatilize to obtain it.
Embodiment 3
[0027] Example 3 : Inhibitory effect of two kinds of volatile oil monomer compound on tomato gray mold (Botrytis cinerea)
[0028] Determination method: Mycelia growth rate method.
[0029] Add the melted PDA culture medium in the 90mm petri dish to make a plate with uniform thickness, and inoculate the plant pathogenic fungus cake with a diameter of 5mm for the test in the center of the plate. Place a sterilized circular filter paper piece on the lid of the dish, and add the volatile oil monomer mixture dropwise on the filter paper piece, 2 μL / dish. After the bottom of the dish was buckled, it was sealed with Parafilm, and cultured upside down. After 72 hours, the growth of the fungus was observed, and the diameter of the colony was measured by the cross method, and the antibacterial rate was calculated. Each experiment was repeated three times.
[0030] Bacterial inhibition rate=(average colony diameter of control group-average colony diameter of test group) / average colon...
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