Missible oil preparation taking secbutyl acetate as solvent and preparation method thereof
The technology of sec-butyl acetate and solvent is applied in the field of emulsifiable concentrate preparation and preparation thereof, and achieves the effects of easy biodegradation, high production efficiency, and meeting the needs of pollution-free prevention and control.
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Embodiment 1
[0026] Example 1: 30% cyhalofop-ethyl EC
[0027] 1. Preparation method:
[0028] (1) Accurately weigh 31.2 grams of active ingredient 96.3% cyhalofop-ethyl, add 3 grams of isooctyl alcohol, and set aside.
[0029] (2) When stirring in step 1, add 2 grams of emulsifier castor oil polyoxyethylene ether and 4.5 grams of polyol fatty acid ester for later use.
[0030] (3) While stirring in step 2, make up to 100 grams with sec-butyl acetate.
[0031] (4) Stir for 15 minutes with a magnetic stirrer.
[0032] (5) cooling at normal temperature to obtain the finished product.
[0033] 2. Stability observation experiment.
[0034] The 30% cyhalofop-ethyl EC preparation was prepared according to the above-mentioned experimental operation steps. Under the conditions of cold storage (0±1°C) for 7 days, hot storage (54±2°C) for 14 days, and normal temperature ultraviolet light irradiation for 24 hours, the cyanofluoride The decomposition rates of grass ester were 0.09%, 0.23%, 0.19%....
Embodiment 2
[0035] Example 2: 25% Thiazophosphonate EC
[0036] 1. Preparation method:
[0037] (1) Accurately weigh 29.4 grams of the active ingredient 85% thiazophosphine, add 5 grams of N-methylpyrrolidone, and set aside.
[0038] (2) While stirring in step 1, add 2.4 grams of emulsifier dioctyl maleate sulfonate sodium and 2.6 grams of styrylphenol polyoxyethylene ether, and set aside.
[0039] (3) While stirring in step 2, make up to 100 grams with sec-butyl acetate.
[0040] (4) Stir for 10 minutes with a magnetic stirrer.
[0041] (5) cooling at normal temperature to obtain the finished product.
[0042] 2. Stability observation experiment:
[0043] The 25% thiazophosphine emulsifiable concentrate preparation was prepared according to the above-mentioned experimental operation steps. The decomposition rates were 0.30%, 0.68%, and 1.17%, respectively.
Embodiment 3
[0044] Embodiment 3: 5% bifenthrin emulsifiable concentrate
[0045] 1. Preparation method:
[0046] (1) Accurately weigh 5.1 grams of active ingredient 98% bifenthrin, add 5 grams of n-octanol, and set aside.
[0047] (2) While stirring in step 1, add 2.9 grams of emulsifier alkylphenol polyoxyethylene ether and 3.6 grams of sodium alkylphenol polyoxyethylene phosphate, and set aside.
[0048] (3) While stirring in step 2, make up to 100 grams with sec-butyl acetate.
[0049] (4) Stir for 20 minutes with a magnetic stirrer.
[0050] (5) cooling at normal temperature to obtain the finished product.
[0051] 2. Stability observation experiment:
[0052] The 5% bifenthrin emulsifiable concentrate preparation was prepared according to the above-mentioned experimental operation steps. After cold storage (0±1°C) for 7 days, hot storage (54±2°C) for 14 days, and normal temperature ultraviolet light irradiation for 24 hours, the bifenthrin The decomposition rates of permethrin wer...
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