Triazole Pesticide Molecularly Imprinted Polymer Microspheres, Solid Phase Extraction Column and Its Application
A molecular imprinting and triazole technology, applied in the directions of alkali metal compounds, separation methods, other chemical processes, etc., can solve the problem of poor hydrophilic properties and inability to extract vegetable and fruit matrices with high water content, weak class-specific recognition ability, and polymers. Problems such as poor adsorption uniformity, to achieve the effects of excellent adsorption performance, simple steps, and good particle size distribution
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Embodiment 1
[0063] A), 0.0145g triadimefon template molecule (0.05mmol) and 0.07mL methacrylic acid (0.35mmol) were dissolved in 20mL acetonitrile, and oscillated in a shaker for 25min;
[0064] B), after pre-polymerization of the template molecule and methacrylic acid, add 0.1824mL TRIM (final concentration 0.6mmol) and 30.0mg AIBN to the mixture in A) and mix thoroughly. Sealed after filling with nitrogen to remove oxygen;
[0065] C), heating in a constant temperature water bath at 55°C for 26 hours, cooling, centrifuging, sieving, discarding the supernatant to obtain a precipitate, and then drying the precipitate naturally;
[0066] D), elution with a mixed solution of acetic acid and methanol with a volume ratio of 1:9 to remove residual monomers and crosslinking agents, and then wash with methanol for 5 hours to remove acetic acid until no triadimefon is detected by high performance liquid chromatography ;
[0067] Drying the powder from which template molecules have been eluted a...
Embodiment 2
[0070] A), 0.0435g triadimefon template molecule (0.15mmol) and 0.15mL methacrylic acid (0.75mmol) were dissolved in 20mL acetonitrile, and oscillated in a shaker for 35min;
[0071] B), after pre-polymerization of template molecules and methacrylic acid, add 0.4256mL TRIM (final concentration 1.4mmol) and 30.0mg AIBN to the mixture in A) and mix thoroughly. Sealed after filling with nitrogen to remove oxygen;
[0072] C), heating in a constant temperature water bath at 65°C for 22 hours, cooling, centrifuging, sieving, discarding the supernatant to obtain a precipitate, and then drying the precipitate naturally;
[0073] D), elution with a mixed solution of acetic acid and methanol with a volume ratio of 1:9 to remove residual monomers and crosslinking agents, and then wash with methanol for 5 hours to remove acetic acid until no triadimefon is detected by high performance liquid chromatography ;
[0074] Drying the powder from which template molecules have been eluted and ...
Embodiment 3
[0077] A), 0.029g triadimefon template molecule (0.1mmol) and 0.12mL methacrylic acid (0.6mmol) were dissolved in 20mL acetonitrile, and oscillated in a shaker for 30min;
[0078] B), after pre-polymerization of the template molecule and methacrylic acid, add 0.304 mL TRIM (final concentration 1.0 mmol) and 30.0 mg AIBN to the mixture in A) and mix thoroughly. Sealed after filling with nitrogen to remove oxygen;
[0079] C), heating in a constant temperature water bath at 60°C for 24 hours, cooling, centrifuging, sieving, discarding the supernatant to obtain a precipitate, and then drying the precipitate naturally;
[0080] D), elution with a mixed solution of acetic acid and methanol with a volume ratio of 1:9 to remove residual monomers and crosslinking agents, and then wash with methanol for 5 hours to remove acetic acid until no triadimefon is detected by high performance liquid chromatography ;
[0081] Drying the powder from which template molecules have been eluted an...
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