Sterilizing composition containing pyraclostrobin and zoxamide
A technology of pyraclostrobin and benzamid, applied in the directions of fungicides, biocides, biocides, etc., can solve the problems of insufficient virulence, short duration of effect, single control effect, etc., and reduce environmental pollution. , The effect of increasing the action site and improving the bactericidal effect
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Embodiment 1
[0037] Example 1: 50% pyraclostrobin·benzamid water dispersible granules (active ingredient ratio 1:1)
[0038] Weigh 25% pyraclostrobin original drug, 25% benzamid original drug, 4% NNO (alkyl naphthalene sulfonate formaldehyde condensate), 2% pull open powder BX (sodium dibutyl naphthalene sulfonate ), 2% K-12 (sodium lauryl sulfate), 15% ammonium sulfate, starch added to 100%. According to the proportion of the formula, the original drug, additives, fillers, etc. are mixed evenly, and the powder is obtained after jet crushing, mixed with a certain amount of water, granulated in a granulator, and then dried and sieved to obtain a granular product.
Embodiment 2
[0039] Example 2: 50% pyraclostrobin·benzamid water dispersible granules (active ingredient ratio 1:4)
[0040] Weigh 10% pyraclostrobin original drug, 40% benzamidr original drug, 3.5% NNO (alkyl naphthalene sulfonate formaldehyde condensate), 2.5% pull open powder BX (sodium dibutylnaphthalene sulfonate ), 3% K-12 (sodium lauryl sulfate), 15% ammonium sulfate, starch added to 100%. According to the proportion of the formula, the original drug, additives, fillers, etc. are mixed evenly, and the powder is obtained after jet crushing, mixed with a certain amount of water, granulated in a granulator, and then dried and sieved to obtain a granular product.
Embodiment 3
[0041] Example 3: 55% pyraclostrobin·benzamid water dispersible granules (active ingredient ratio 1:10)
[0042] Weigh 5% pyraclostrobin original drug, 50% benzamid original drug, 3.5% NNO (alkyl naphthalene sulfonate formaldehyde condensate), 2.5% pull open powder BX (sodium dibutyl naphthalene sulfonate ), 3% K-12 (sodium lauryl sulfate), 15% ammonium sulfate, starch added to 100%. According to the proportion of the formula, the original drug, additives, fillers, etc. are mixed evenly, and the powder is obtained after jet crushing, mixed with a certain amount of water, granulated in a granulator, and then dried and sieved to obtain a granular product.
[0043] 2. Preparation of suspending agent
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