Preparation method of pirimicarb microcapsules

A technology of pirimicarb and microcapsules, which is applied in the field of preparation of pirimicarb microcapsules, can solve problems such as high cost, complex process, and environmental pollution, and achieve the effects of less organic solvent, simple preparation process, and environmental friendliness

Inactive Publication Date: 2016-05-04
周德志
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since then, the research and development of microcapsules has carried out a lot of basic research in agriculture, and has made some progress. At present, more than 200 agrochemical companies are conducting research on the development and application of microcapsules. It has a history of more than 40 years, but compared with the field of pharmaceutical microcapsules, its development is relatively slow. At present, there are few commercialized pesticide microcapsules.
[0006] The methods of pesticide microencapsulation mainly include interfacial polymerization method, condensed phase separation method, in-situ polymerization method, solvent evaporation method, etc., and these methods are not only complicated in process and high in cost, but also use a large amount of organic solvents, polluting the environment

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] (1) Preparation of carrier: put succinic acid, butanediol, lactic acid and 0.1wt% catalyst tetraisoendoxytitanium and phosphoric acid with a molar ratio of 1:1:0.2 into an electric booster stirrer, condense In the two-necked flask of the reflux tube, heat the oil bath to 240°C under the protection of nitrogen, dehydrate for 1 hour, then vacuumize, control the pressure to a vacuum degree lower than 50Pa, and carry out the degreasing reaction, stop the reaction after 3 hours, and then stop the reaction under the protection of nitrogen After cooling, a white solid polymer copolymer PBS-co-PLA was obtained, and the obtained product was vacuum-dried at 60°C.

[0026] (2) Preparation of oil phase: Accurately weigh 3.5 mg of PBS-co-PLA and dissolve in 10 mL of dichloromethane. After it is completely dissolved, add 1 mg of pirimicarb original drug, stir well and accelerate the dissolution with an ultrasonic cleaner to obtain the oil phase .

[0027] (3) Water phase preparation...

Embodiment 2

[0030] (1) Preparation of carrier: put succinic acid, butanediol, lactic acid and 0.12wt% catalyst tetraisoendoxytitanium and phosphoric acid with a molar ratio of 1:1:0.3 into an electric booster stirrer, condense In the two-neck flask of the reflux tube, heat the oil bath to 240°C under the protection of nitrogen, dehydrate for 1 hour, then vacuumize, control the pressure to a vacuum degree lower than 80Pa, and carry out the degreasing reaction, stop the reaction after 4 hours, and then stop the reaction under the protection of nitrogen After cooling, a white solid polymer copolymer PBS-co-PLA was obtained, and the obtained product was vacuum-dried at 60°C.

[0031] (2) Preparation of oil phase: Accurately weigh 4.5mg of PBS-co-PLA and dissolve it in 10mL of dichloromethane. After it is completely dissolved, add 1mg of pirimicarb original drug, stir well and accelerate the dissolution with an ultrasonic cleaner to obtain the oil phase .

[0032] (3) Water phase preparation:...

Embodiment 3

[0035] (1) Carrier preparation: Put succinic acid, butanediol, lactic acid and 0.115wt% catalyst tetraisoendoxytitanium and phosphoric acid with a molar ratio of 1:1:0.25 into an electric booster stirrer, condensing In the two-neck flask of the reflux tube, heat the oil bath to 240°C under the protection of nitrogen, dehydrate for 1 hour, then vacuumize, control the pressure to a vacuum degree lower than 67Pa, and carry out the degreasing reaction. After 3.5 hours, stop the reaction. Under protection, after cooling, a white solid polymer copolymer PBS-co-PLA was obtained, and the obtained product was vacuum-dried at 60°C.

[0036] (2) Preparation of oil phase: Accurately weigh 4 mg of PBS-co-PLA and dissolve in 10 mL of dichloromethane. After complete dissolution, add 1 mg of pirimicarb original drug, stir well and accelerate dissolution with an ultrasonic cleaner to obtain an oil phase.

[0037] (3) Preparation of water phase: Measure 98 mL of deionized water, add 3wt% PVA-17...

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PUM

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Abstract

The invention discloses a preparation method of pirimicarb microcapsules. The preparation method comprises the following steps: (1) carrier preparation: performing a polymerization reaction of succinic acid, butanediol and lactic acid in a molar ratio of 1:1:(0.2-0.3) to obtain a carrier PBS-co-PLA; (2) oil phase preparation: weighing the components PBS-co-PLA, pirimicarb and dichloromethane in a mass ratio of (3.5-4.5):1:10; dissolving the carrier PBS-co-PLA in dichloromethane; and after complete dissolution, adding pirimicarb raw medicine and dissolving to obtain an oil phase; (3) water phase preparation: weighing deionized water in a mass ratio of a water phase to the oil phase being (5-7):1, adding an emulsifier and a dispersing agent and dissolving to obtain the water phase; and (4) microcapsule preparation: adding the oil phase into the water phase to obtain an oil-water mixed emulsion; adding an antifoaming agent and curing to obtain a microcapsule suspension; and washing and removing the supernate and drying to obtain a finished product. The method is simple in technology and environmentally friendly. The obtained pirimicarb microcapsules have relatively good form, the encapsulation efficiency reaches 78%, the pesticide loading capacity is up to 50%, the effective release period is 30 days, the pesticide release amount is 94%, and thus the pirimicarb microcapsules are an ideal pesticide slow-release agent.

Description

technical field [0001] The invention belongs to the technical field of pesticide preparation, and in particular relates to a preparation method of pirimicarb microcapsules. Background technique [0002] Pirimicarb is a moderately toxic insecticide. No irritation to eyes and skin, no chronic toxicity, low toxicity to fish, bees and birds, safe to natural enemies of aphids. It has contact killing, fumigation and foliar penetration effects. It is a highly selective aphidicide, which can effectively control all aphids except cotton aphid, and is also effective for aphids resistant to organophosphate. Rapid insecticide, but short residual period. It is safe for crops and does not harm natural enemies. It is an ideal agent for comprehensive control. It is suitable for controlling aphids on vegetables, tobacco and food crops. [0003] Microcapsules (Microcapsules, MC) are a kind of active substances (in pesticides, original drugs) that use natural or synthetic polymers or some...

Claims

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Application Information

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IPC IPC(8): A01N47/18A01N25/28A01P7/04
CPCA01N47/18A01N25/28
Inventor 周德志
Owner 周德志
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