WO2007139217A1 - マイクロカプセル剤 - Google Patents
マイクロカプセル剤 Download PDFInfo
- Publication number
- WO2007139217A1 WO2007139217A1 PCT/JP2007/061235 JP2007061235W WO2007139217A1 WO 2007139217 A1 WO2007139217 A1 WO 2007139217A1 JP 2007061235 W JP2007061235 W JP 2007061235W WO 2007139217 A1 WO2007139217 A1 WO 2007139217A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- imidacloprid
- microcapsule
- water
- slurry
- polymer
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
Definitions
- the present invention relates to a micro turnip ij encapsulating imidacloprid as a component in an unpleasant manner, its i * method, and pest control i using the same. Longan
- ⁇ , termites? ⁇ ⁇ Insects, cockroaches, etc. 3 ⁇ 4 Internal pests, Côteum plantations 3 ⁇ 4 Various slaughterers have been craned to prevent mansions by insects such as 3 ⁇ 4 insects. As a game of insecticidal thread to prevent these pests, initially aw-based bandits were often deceived, but toxicity and residual toxicity became a problem, and more High organophosphorus and carbamate killing IJs were developed. Since then, pyrethroid-type killing and control agents have been developed and are widely used.
- Imidacloprid non-specific «3 ⁇ 41
- Imidacloprid is a typical neonicotinoid insecticide, and is used as an insecticide for the control of Coleoptera insects such as aphids, whiteflies, hunka's, etc. It has been highly painful in the world. In Japan, it is widely regarded as the above-mentioned pests, as well as through termites. For example, oils, $ agents, emulsions, m-powder, etc. have been used as examples.
- the present invention seeks to provide a micro turnip for imidacloprid in high boats and a pest control i ⁇ y using it.
- the present inventor has developed the above-mentioned problem, that is, outside the microcapsule, by wetting a slurry in which imidacloprid is suspended in water-immiscible organic solvent ij and then wetting the urethane polymer. 3 ⁇ 4: It has been found that the problem of the imidaclopridoca is improved. That is, the present invention provides the following [1] to [4].
- the water-immiscible organic iJ used in the present invention is not particularly used, and usually does not dissolve imidacloprid very much.
- Aromatics such as dimethylylennaphthalene and dodecylbenzene, diethyl phthalate, dibutyle adipate, dinonyl adipate, esters of adipic acid adipic acid, kerosene, wisteria kerosene, etc.
- Vegetable oil such as oil, hard oil, cotton, castor oil, oil and corn oil can be used. These Samurai J can be used in battles, and two or more can be used in combination.
- a powder crusher that converts the imidaku mouth pride in the water-soluble organic debris can be used when the floor plate is generally ⁇ . Specifically, a bead mill, a sand mill, an Ateli evening “ ⁇ 3 ⁇ 4 (powder using a book, a homomixer, a dishno, etc.). M3 ⁇ 4) If the slurry becomes W "during crushing, the agent may be 3 ⁇ 43 ⁇ 4bn. As such a dispersant, we can shelve water for paint water ⁇ W. It can be used in the form of acrylic copolymer copolymer, high-powder ester-based agent, imidazoline-based agent, etc. These fractions can be used alone or in combination. By adding a urethane polymer to the imidacloprid slurry obtained as a result of the frame, it is possible to obtain microcapsules encapsulating imidacloprid at a high level.
- a polyester toluyl disiloxane modified polyurethan system is high: ⁇ polymerized # ⁇ ⁇ preferably: 3 ⁇ 43 ⁇ 4 ⁇ , 0 0 0 ⁇ : l o o, 0 0 0 polyester! ⁇ r Toludi diisocyanate-modified polyurethane polymer: ⁇ ? S is more preferable, polyester of 3 ⁇ 4 2, 0 0 0 to 6 0, 0 0 0!
- ⁇ Toludi di isocyanate modified polyurethane Highly preferred polymer-based polymer ⁇ 3 ⁇ 4 is more preferred, and polyester-containing tol diisocyanate-modified polyurethane polymer having a molecular weight of 2,000 to 30,000 is particularly preferred, specifically, , D isperby k- 1 6 3 Sung f Raw Polyurethane High Polymerization # Quantity 5 0, 0 0 0, Big Chemi-Japan 3 ⁇ 4 ⁇ 3 ⁇ 4 $ 3 ⁇ 4), D isperby k- 1 6 4 Polyurethane High Polymerization # ⁇ H3 ⁇ 42, 0 0 0- 1 0, 0 0 0, Big Chemi--Japan Conference etc.
- the microcube ij encapsulating the imidacloprid of the present invention as an example can be difficult in accordance with the conventional interfacial polymerization method. By using these methods, quality quantity, boats and average particle size can be controlled.
- As the quality of the microphone mouth capsule of the present invention polyurethane, polyurea, polyamide, polyester, polycarbonate and the like are usable, but polyurea and polyurethane are preferred.
- the microcapsule slurry obtained in this way is pest control!
- ⁇ lj can also be used, but for the purpose of making crane ij, it is necessary to add 3 ⁇ 43 ⁇ 43 ⁇ 4Q, anti-oxidant, ⁇ i anti-oxidation, chelating agent, anti-foaming agent, antifoaming agent, pH regulator, etc. Also good. It can also be used in combination with organophosphorus lj, pyrethroid-type killers, other neonicotinoid-type killers, cocoon length control agents, acaricides, mosquito killers, and the like. To measure the average particle size of the microphone mouth capsule, for example, laser diffraction 3 ⁇ 4 ⁇ 3 ⁇ 4 ⁇ ⁇ »SAL D
- the average vertical diameter of the microcapsules of the present thread cord is usually 5 zm or more and 10 0 or less, preferably 10 or more 5 0 If the average particle size of the microcapsules is smaller than 5 m, the insects will not be easily destroyed when they are trapped, so that it will not be sufficiently effective. It becomes difficult to prepare the microcapsule, and the microphone mouth capsule is easily heated by the operation of dilution and stirring of the micro force, resulting in sustained efficacy as the microphone mouth capsule. There is a risk that it cannot be voluntarily performed.
- the M3 ⁇ 4 of the present invention is effective for controlling a large number of pests such as insects, indoor pests, agricultural and horticultural pests, and TO is particularly preferred for fields requiring fertility.
- W3 ⁇ 4 powerful pests include mosquito reeds, white ants, American power i termites, etc .; Coganem, ⁇ Coleoptera insects, Gotoum, Aomushi, Roh, Scarlet moth, Otapacoga, etc. Diptera, other insects, insects of insects such as rubber bugs, warabimushi, etc. are particularly suitable for moths of dwarf pests.
- various pests can be controlled effectively and for a long time. »Example
- Example 1 the difficult examples of the present invention and!: Will be described, but the present invention is not limited to these. All the blending ratios shown below are% by weight. Example 1
- Pinicai 4 0 (Diisoptyl adipate, Kao ⁇ ; Kai 2 5 0 g, soft alkyl benzene ( ⁇ Xie ⁇ 3 kai) to the difficulty obtained by uniformly mixing so-called 50 g, added imidacloprid 80 g Wet with glass peas for 30 minutes (03 ⁇ 4). Disperse k-1 6 4 (tff) 5 g in this slurry and mix uniformly. 7 5 W., Polyisocyanate, main piezourethane group 3 ⁇ 4
- An aqueous phase was prepared by dissolving 3 g in ion-equilibrated J ⁇ 97 7 g.
- the oil phase was spouted while the aqueous phase was mixed with TK homomic mix ⁇ (special mist at m «3 5 0 0 r pm ⁇ t.
- the resulting solution was stirred at 3 ⁇ 4 5 0 0 pm , Mixed with ethylenediamine 0.5 g and ion exchange K 10 g uniformly, then transferred to a 60 ° C water bath with stirring at 1 «5 0 00 rpm
- a micro force Pseed dispersion was obtained for 10 hours, to which was added 0.2% solution of Kelzan S (xanthan gum, Tricrystal Co. 3 ⁇ 4S) so that imidacloprid was 8%.
- Kelzan S xanthan gum, Tricrystal Co. 3 ⁇ 4S
- J, 3 ⁇ 4» 3 ⁇ 4 ⁇ 3 ⁇ 43 ⁇ 4) obtained by uniformly mixing lg Imidacloprid 1 20 g was added and moistened with glass beads for 30 minutes. byk-164 (previously mixed with 5 g and mixed uniformly. The resulting slurry was mixed with 96 g of Sumidur L-75 (4 g of 3 ⁇ 43 ⁇ 41 and mixed uniformly to form an oil phase.
- the aqueous phase was prepared by dissolving 3 g in 33 ⁇ 4 97 g of ions, and the aqueous phase was dispersed at Hj3 ⁇ 43 ⁇ 43500 rpm using a TK homomic mixer.
- the reaction was carried out for 10 hours while winning the solution, and a micro Kabuse ⁇ "spray was obtained.
- 0.2% solution of Kelzan S previously described was added so that imidacloprid ⁇ was 10%.
- Pinicizer 40 (previous 3 ⁇ 4!) 250 g, soft alkylbenzene 50 g, homogenol L 95 (add 1 g of the previous mixture to 120 ml of imidacloprid and mix with glass beads for 30 minutes.
- the slurry was 96 g of Sumidur L-75 (previously described) 4 g3 ⁇ 43 ⁇ 43 ⁇ 4 and mixed uniformly to form an oil phase Gohsenol GL—05 3 g dissolved in 97 g of ion age was used as the aqueous phase.
- the aqueous phase was spun using a TK homomic mixer and the oil phase was sprinkled while being dispersed at 3500 rpm, while the resulting dispersion was won at H «500 rpm and 0.5 ml of ethylenediamine.
- a mixture of 10 g of ion and 10 g of ion ion was uniformly mixed, then transferred to a hot water bath at 60 ° C. and reacted for 10 hours with ⁇ : 500 rpm 7 to obtain a microcapsule dispersion.
- Vinicisa's 40 front 150 g, soft recycle! ⁇ Sen 150 g, homogenole L 95 (previously) 1 g of the mixture was added to 120 ml of imidacloprid and moistened with glass beads for 30 minutes. To this slurry was added 5 g of D is per r byk-109 (1-hydroxyethyl-2-alkenylimidazoline, Big Chemi. Japan Association »), and mixed uniformly. In addition, 4 g of Sumijoule L—75 &) was excited and mixed uniformly to make the oil phase. Gohsenol GL— 05 (M 3 g dissolved in ion-concentration _ 97 g was used as the aqueous phase.
- the aqueous phase was removed at 113 ⁇ 43500 rpm and the oil phase was removed.
- the obtained ⁇ ir solution was beaten at 113 ⁇ 4500 rpm, and the mixture of ethylenediamine 0.5 g and ion 0 g was mixed, and then transferred to a hot water bath at 60 1 «500 r
- the result was 10 hours while winning at pm, and the result was obtained by adding Gelzan S (0.2% of the previous 5% solution) so that the concentration of imidacloprid was 10%.
- the average insulator diameter was measured and found to be 25 m.
- microcapsule imidacloprid according to the present invention exhibits high anti-5 effects and fertility against many pests including termites and can be used for pest control.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/302,754 US20090182015A1 (en) | 2006-06-01 | 2007-05-28 | Microcapsule formulations |
AU2007268494A AU2007268494B2 (en) | 2006-06-01 | 2007-05-28 | Microcapsule |
EP07767016A EP2025229A4 (en) | 2006-06-01 | 2007-05-28 | MICRO CAPSULE |
CN2007800199418A CN101453896B (zh) | 2006-06-01 | 2007-05-28 | 微胶囊剂 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006-153745 | 2006-06-01 | ||
JP2006153745A JP4965899B2 (ja) | 2006-06-01 | 2006-06-01 | マイクロカプセル剤 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007139217A1 true WO2007139217A1 (ja) | 2007-12-06 |
Family
ID=38778731
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/061235 WO2007139217A1 (ja) | 2006-06-01 | 2007-05-28 | マイクロカプセル剤 |
Country Status (6)
Country | Link |
---|---|
US (1) | US20090182015A1 (ja) |
EP (1) | EP2025229A4 (ja) |
JP (1) | JP4965899B2 (ja) |
CN (1) | CN101453896B (ja) |
AU (1) | AU2007268494B2 (ja) |
WO (1) | WO2007139217A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104938483A (zh) * | 2015-06-26 | 2015-09-30 | 青岛农业大学 | 一种环境友好型二氧化碳基聚合物载吡虫啉微胶囊及其制备方法 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5682905B2 (ja) * | 2010-08-31 | 2015-03-11 | 住化エンバイロメンタルサイエンス株式会社 | マイクロカプセル剤 |
JP5659695B2 (ja) * | 2010-10-28 | 2015-01-28 | 住友化学株式会社 | マイクロカプセル製剤の製造方法およびその製造方法で製造されるマイクロカプセル製剤 |
CN106577739A (zh) * | 2016-11-04 | 2017-04-26 | 东莞市联洲知识产权运营管理有限公司 | 一种触破式微胶囊剂及其制备方法 |
MX2021001044A (es) * | 2018-07-27 | 2021-04-12 | Bayer Ag | Formulaciones de liberacion controlada para agroquimicos. |
CN112741101A (zh) * | 2021-02-09 | 2021-05-04 | 中国科学技术大学 | 一种防治对拟除虫菊酯类杀虫剂有抗药性的烟草甲的方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5538325B2 (ja) | 1977-10-07 | 1980-10-03 | ||
JPH0692282B2 (ja) | 1986-01-07 | 1994-11-16 | 住友化学工業株式会社 | 有機リン系殺虫組成物 |
JP2000247821A (ja) * | 1999-02-26 | 2000-09-12 | Takeda Chem Ind Ltd | シロアリ防除剤 |
JP2004535276A (ja) * | 2001-04-10 | 2004-11-25 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | マイクロカプセル |
JP2005170956A (ja) | 2005-02-14 | 2005-06-30 | Sumitomo Chemical Co Ltd | マイクロカプセル化農薬の製造方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61249904A (ja) * | 1985-04-25 | 1986-11-07 | Nippon Kayaku Co Ltd | シロアリ防除剤 |
JP2002294890A (ja) * | 2001-04-02 | 2002-10-09 | Takeda Chem Ind Ltd | 床下用断熱材 |
JP4334984B2 (ja) * | 2002-11-29 | 2009-09-30 | 日本エンバイロケミカルズ株式会社 | 防蟻剤 |
JP4328264B2 (ja) * | 2004-06-18 | 2009-09-09 | 日本エンバイロケミカルズ株式会社 | 木材保存剤 |
JP4485417B2 (ja) * | 2005-06-14 | 2010-06-23 | 日本エンバイロケミカルズ株式会社 | 木材保存剤 |
JP2007056245A (ja) * | 2005-07-26 | 2007-03-08 | Japan Enviro Chemicals Ltd | 防蟻性樹脂成形体およびその製造方法 |
-
2006
- 2006-06-01 JP JP2006153745A patent/JP4965899B2/ja active Active
-
2007
- 2007-05-28 AU AU2007268494A patent/AU2007268494B2/en not_active Ceased
- 2007-05-28 WO PCT/JP2007/061235 patent/WO2007139217A1/ja active Application Filing
- 2007-05-28 CN CN2007800199418A patent/CN101453896B/zh not_active Expired - Fee Related
- 2007-05-28 EP EP07767016A patent/EP2025229A4/en not_active Withdrawn
- 2007-05-28 US US12/302,754 patent/US20090182015A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5538325B2 (ja) | 1977-10-07 | 1980-10-03 | ||
JPH0692282B2 (ja) | 1986-01-07 | 1994-11-16 | 住友化学工業株式会社 | 有機リン系殺虫組成物 |
JP2000247821A (ja) * | 1999-02-26 | 2000-09-12 | Takeda Chem Ind Ltd | シロアリ防除剤 |
JP2004535276A (ja) * | 2001-04-10 | 2004-11-25 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | マイクロカプセル |
JP2005170956A (ja) | 2005-02-14 | 2005-06-30 | Sumitomo Chemical Co Ltd | マイクロカプセル化農薬の製造方法 |
Non-Patent Citations (2)
Title |
---|
"Zoku Iyakuhin no Kaihatsu vol. 18, Noyaku no Kaihatsu III", vol. 18, HIROKAWA SHOTEN, pages: 629 - 648 |
See also references of EP2025229A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104938483A (zh) * | 2015-06-26 | 2015-09-30 | 青岛农业大学 | 一种环境友好型二氧化碳基聚合物载吡虫啉微胶囊及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
JP2007320914A (ja) | 2007-12-13 |
EP2025229A4 (en) | 2011-11-23 |
AU2007268494B2 (en) | 2012-08-23 |
JP4965899B2 (ja) | 2012-07-04 |
CN101453896B (zh) | 2012-09-26 |
AU2007268494A1 (en) | 2007-12-06 |
US20090182015A1 (en) | 2009-07-16 |
EP2025229A1 (en) | 2009-02-18 |
CN101453896A (zh) | 2009-06-10 |
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