CN103053513A - Pyraclostrobin nano-preparation and preparation method thereof - Google Patents

Pyraclostrobin nano-preparation and preparation method thereof Download PDF

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Publication number
CN103053513A
CN103053513A CN2012105828989A CN201210582898A CN103053513A CN 103053513 A CN103053513 A CN 103053513A CN 2012105828989 A CN2012105828989 A CN 2012105828989A CN 201210582898 A CN201210582898 A CN 201210582898A CN 103053513 A CN103053513 A CN 103053513A
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China
Prior art keywords
pyraclostrobin
preparation
solution
distilled water
nanometer formulation
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Pending
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CN2012105828989A
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Chinese (zh)
Inventor
吕建洲
李建宇
郑伟光
刘照斌
姜国盛
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Liaoning Normal University
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Liaoning Normal University
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Priority to CN2012105828989A priority Critical patent/CN103053513A/en
Publication of CN103053513A publication Critical patent/CN103053513A/en
Pending legal-status Critical Current

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  • Pretreatment Of Seeds And Plants (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The present invention discloses a pyraclostrobin nano-preparation which can improve the application effect of the pyraclostrobin, decrease pyraclostrobin usage amount, and reduce the cost of production of crops, and a preparation method thereof. The preparation method comprises the following steps: dissolving the pyraclostrobin powder in distilled water, and magnetic stirring at 900r/min for 20min, wherein the usage ratio of the pyraclostrobin powder to distilled water is 10mg: 100ml; adding sodium dodecyl sulfate into the pyraclostrobin solution and magnetic stirring at a rotational speed of 900r/min for 20min, wherein the usage ratio of the sodium dodecyl sulfate to the pyraclostrobin solution is 5mg: 100ml; and treating the obtained solution with ultrasonic vibration of a frequency of 40KHz for 2 hours.

Description

Pyraclostrobin nanometer formulation and preparation method
Technical field
The present invention relates to inhale in a kind of broad spectrum activity the low toxicity bactericide, especially a kind of effect that improves pyraclostrobin, reduce the pyraclostrobin usage amount, reduce the crops production cost pyraclostrobin nanometer formulation and preparation and purposes.
Background technology
Pyraclostrobin has another name called pyraclostrobin, chemical name: methyl (N)-[[[1-(4-chlorobenzene) pyrazoles-3 base)-oxygen]-the 0-methoxyl group]-the N-methoxymethyl carbamate, molecular formula: C19H18ClN3O4.
Pyraclostrobin is wide-spectrum bactericide, has permeability and local systemic activity, and the lasting period is long, and the resistance of rainwater washing against characteristics reach protection, treatment, blade infiltration conduction.Be widely used in preventing and treating wheat, paddy rice, peanut, grape, vegetables, potato, banana, lemon, coffee, fruit tree, walnut, tea tree, tobacco and ornamental plants etc.For the large stigma of control of maize, powdery mildew of cucumber, downy mildew and banana freckle, leaf spot etc. better effects is arranged.
Nanometer technology is in the mechanism of 1 ~ 100nm yardstick research material and the cutting edge technology of character, its final goal is the product that has specific function with the characteristic manufacturing on nanoscale of molecule, atom and material, but up to now, also less than the relevant report about the pyraclostrobin nanometer formulation.
Summary of the invention
The present invention is in order to solve the existing above-mentioned technical problem of prior art, a kind of effect that improves pyraclostrobin to be provided, reducing pyraclostrobin nanometer formulation and the preparation method of the production costs such as pyraclostrobin usage amount, reduction crops.
Technical solution of the present invention is: a kind of preparation method of pyraclostrobin nanometer formulation is characterized in that carrying out according to the following steps successively:
A. the pyraclostrobin pulvis is mixed with distilled water, 900r/min magnetic agitation 20min makes pyraclostrobin solution, and the amount ratio of pyraclostrobin pulvis and distilled water is 10mg:100ml;
B. dodecyl sodium sulfate is added in the pyraclostrobin solution with rotating speed 900r/min magnetic agitation 20min, the amount ratio of dodecyl sodium sulfate and pyraclostrobin solution is 5mg:100ml;
C. be the ultrasonic oscillation 2 hours of 40KHz with gained solution frequency.
The pyraclostrobin nanometer formulation a kind of as preparation method above-mentioned pyraclostrobin nanometer formulation prepares.
Preparation method of the present invention is simple, and prepared pyraclostrobin nanometer formulation granularity is comparatively even, good dispersion.Pyraclostrobin is played a role at nanometer level, not only kept the bactericidal action of pyraclostrobin, and strengthen its action effect, reduce the pyraclostrobin usage amount, reduced the production cost of crops.
Description of drawings
Fig. 1 is 100k times of SEM figure of pyraclostrobin nanometer formulation of the embodiment of the invention.
Fig. 2 is 1k times of SEM figure of pyraclostrobin solvent.
Embodiment
Embodiment 1:
Carry out according to the following steps successively:
A. weigh and be purchased from Shandong sea and pyraclostrobin pulvis that three sharp biochemical industry Co., Ltds produce is dissolved in the distilled water, with constant temperature blender with magnetic force with 900r/min magnetic agitation 20min, the pyraclostrobin solution of making;
B. dodecyl sodium sulfate is added in the pyraclostrobin solution, with rotating speed 900r/min magnetic agitation 20min, the amount ratio of dodecyl sodium sulfate and pyraclostrobin solution is 5mg:100ml with constant temperature blender with magnetic force again;
C. be the ultrasonic oscillation 2 hours of 40KHz again with gained solution frequency, namely make the pyraclostrobin nanometer formulation.
The type of used supersonic wave cleaning machine is JCP-1004.
Pyraclostrobin nanometer formulation and former pyraclostrobin solvent that the present invention makes are observed such as Fig. 1,2 under SU8010 type SEM.As can be seen from the figure nano particle diameter is to dwindle 1000 times than original reagent particle size between 50 ~ 100nm, and can find out that phase is pure, and free from admixture exists.
Can with gained pyraclostrobin nanometer formulation distilled water constant volume, obtain the pyraclostrobin nanometer formulation of variable concentrations, such as 0.1g/L, 0.4g/L, 1g/L.
Under light microscope, can observe, concentration is that 1g/L pyraclostrobin distribution of particles is the most even in three kinds of concentration, the highest effect of particle nanorize degree is best, and concentration is that the pyraclostrobin effect of 0.4g/L is taken second place, and concentration is that pyraclostrobin effect in three kinds of concentration of 0.1g/L is the poorest.

Claims (2)

1. the preparation method of a pyraclostrobin nanometer formulation is characterized in that carrying out according to the following steps successively:
A. the pyraclostrobin pulvis is mixed with distilled water, 900r/min magnetic agitation 20min makes pyraclostrobin solution, and the amount ratio of pyraclostrobin pulvis and distilled water is 10mg:100ml;
B. dodecyl sodium sulfate is added in the pyraclostrobin solution with rotating speed 900r/min magnetic agitation 20min, the amount ratio of dodecyl sodium sulfate and pyraclostrobin solution is 5mg:100ml;
C. be the ultrasonic oscillation 2 hours of 40KHz with gained solution frequency.
2. pyraclostrobin nanometer formulation of the preparation method preparation of pyraclostrobin nanometer formulation as claimed in claim 1.
CN2012105828989A 2012-12-28 2012-12-28 Pyraclostrobin nano-preparation and preparation method thereof Pending CN103053513A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012105828989A CN103053513A (en) 2012-12-28 2012-12-28 Pyraclostrobin nano-preparation and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012105828989A CN103053513A (en) 2012-12-28 2012-12-28 Pyraclostrobin nano-preparation and preparation method thereof

Publications (1)

Publication Number Publication Date
CN103053513A true CN103053513A (en) 2013-04-24

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0275790A1 (en) * 1986-12-30 1988-07-27 SAT Société Anonyme de Télécommunications Terminal for data transmission over an analogous bidirectional line with echo cancellation coupled to the reception clock
CN101692808A (en) * 2009-09-30 2010-04-14 深圳诺普信农化股份有限公司 Emamectin benzoate solid lipid nanoparticle and preparation method and application thereof in pesticide formulation
CN101946776A (en) * 2009-12-15 2011-01-19 辽宁师范大学 Uniconazol nano-preparation serving as plant growth regulation and control agent and preparation method thereof
CN102017952A (en) * 2010-11-29 2011-04-20 辽宁师范大学 Diniconazole nano preparation as well as preparation method and application thereof
CN102090424A (en) * 2009-12-11 2011-06-15 胥建中 Method for producing nano water-soluble neem oil preparation
CN102450269A (en) * 2011-12-27 2012-05-16 辽宁师范大学 Triazolone nanometer colloid suspending agent and preparation method thereof
CN102524261A (en) * 2011-12-16 2012-07-04 辽宁师范大学 Nanometer preparation of strong rooting agent, preparation method and application thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0275790A1 (en) * 1986-12-30 1988-07-27 SAT Société Anonyme de Télécommunications Terminal for data transmission over an analogous bidirectional line with echo cancellation coupled to the reception clock
CN101692808A (en) * 2009-09-30 2010-04-14 深圳诺普信农化股份有限公司 Emamectin benzoate solid lipid nanoparticle and preparation method and application thereof in pesticide formulation
CN102090424A (en) * 2009-12-11 2011-06-15 胥建中 Method for producing nano water-soluble neem oil preparation
CN101946776A (en) * 2009-12-15 2011-01-19 辽宁师范大学 Uniconazol nano-preparation serving as plant growth regulation and control agent and preparation method thereof
CN102017952A (en) * 2010-11-29 2011-04-20 辽宁师范大学 Diniconazole nano preparation as well as preparation method and application thereof
CN102524261A (en) * 2011-12-16 2012-07-04 辽宁师范大学 Nanometer preparation of strong rooting agent, preparation method and application thereof
CN102450269A (en) * 2011-12-27 2012-05-16 辽宁师范大学 Triazolone nanometer colloid suspending agent and preparation method thereof

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Application publication date: 20130424