Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method for methoprene microcapsules

A technology of methoprene and microcapsules, applied in the field of preparation of methoprene microcapsules, can solve problems such as high cost, complex process, pollute the environment, etc., and achieve the effects of less organic solvent, simple preparation process and environmental friendliness

Inactive Publication Date: 2016-03-23
周德志
View PDF0 Cites 0 Cited by
  • 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

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

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 it in 10 mL of dichloromethane. After it is completely dissolved, add 1 mg of methoprene technical material, stir well and accelerate the dissolution with an ultrasonic cleaner to obtain the oil phase .

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

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 methoprene 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 methoprene technical material, 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% P...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a preparation method for methoprene microcapsules. The preparation method comprises the following steps: firstly, carrier preparation is carried out, namely, a polymerization reaction with a mol ratio of succinic acid, butylene glycol and lactic acid being 1:1:0.2-0.3 is carried out, and a carrier PBS-co-PLA is obtained; secondly, oil phase preparation is carried out, namely, PBS-co-PLA, methoprene and dichloromethane are weighed with a mass ratio of PBS-co-PLA, methoprene and dichloromethane being 3.5-4.5:1:10, the PBS-co-PLA carrier is dissolved in dichloromethane, after the PBS-co-PLA is dissolved in dichloromethane fully, the methoprene active compound is added and dissolved and an oil phase is obtained; thirdly, water phase preparation is carried out, deionized water is measured and taken with a mass ratio of the oil phase to the water phase being 1:5-7, an emulsifier dispersant is added in water and dissolved and a water phase is obtained; fourthly, microcapsule preparation is carried out, namely, the oil phase is added in the water phase, an oil and water mixed emulsion is obtained, an antifoaming agent is added, microcapsule suspension is prepared after curing, water washing is carried out, the supernatant is removed, and a finished product is obtained after drying. The method is simple in technology and is environmentally friendly. The obtained methoprene microcapsules have a good form, the encapsulation efficiency is 78%, the drug loading capacity is 50%, the effective release period is 30 days, the drug release amount is 94%, and the methoprene microcapsule is an ideal pesticide sustained release agent.

Description

technical field [0001] The invention belongs to the technical field of pesticide preparation, and in particular relates to a method for preparing methoprene microcapsules. Background technique [0002] The original drug of methoprene is a light yellow liquid with a density of 0.9261g / mL (ZO°C), a boiling point of 100°C, a melting point of -20°C, a solubility of 1.4mg / L in water, and is miscible with organic solvents. The appearance of the preparation is a transparent blue liquid with a density of o. 79~0.80g / mL (240C~25℃). The toxicity is low toxicity, which interferes with the molting process of insects. It is effective for various insects of Lepidoptera, Diptera, Coleoptera and Homoptera, and it is used to control sanitary pests such as mosquitoes and flies, and pests such as tobacco borer moths during storage. [0003] Microcapsules (Microcapsules, MC) are a kind of active substances (in pesticides, original drugs) that use natural or synthetic polymers or some suitabl...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A01N37/36A01N25/28A01P7/04
CPCA01N37/36A01N25/28
Inventor 周德志
Owner 周德志
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products