PT95429A - PROCESS FOR THE PREPARATION OF MICROENCAPSULATED AGROCHEMICAL COMPOSITIONS - Google Patents

PROCESS FOR THE PREPARATION OF MICROENCAPSULATED AGROCHEMICAL COMPOSITIONS Download PDF

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Publication number
PT95429A
PT95429A PT95429A PT9542990A PT95429A PT 95429 A PT95429 A PT 95429A PT 95429 A PT95429 A PT 95429A PT 9542990 A PT9542990 A PT 9542990A PT 95429 A PT95429 A PT 95429A
Authority
PT
Portugal
Prior art keywords
process according
prepolymer
agrochemical
compound
microcapsules
Prior art date
Application number
PT95429A
Other languages
Portuguese (pt)
Inventor
David Cavanaugh Creech
Ralston Curtis
Original Assignee
Sandoz Sa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sandoz Sa filed Critical Sandoz Sa
Publication of PT95429A publication Critical patent/PT95429A/en

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons
    • B01J13/06Making microcapsules or microballoons by phase separation
    • B01J13/14Polymerisation; cross-linking
    • B01J13/18In situ polymerisation with all reactants being present in the same phase
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • A01N25/28Microcapsules or nanocapsules

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Agronomy & Crop Science (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Manufacturing Of Micro-Capsules (AREA)

Claims (1)

controlo era o seguinte:— PERCENTAGEM DE CONTROLO Exemplos Cânhamo chinês Quenopódio 81 84 85 84 96 98 Banvel Este ensaio comprova a excelente persistência, na zona das ervas daninhas em questão, das microcápsulas de acordo com a presente invenção, em comparação com o mesmo ingrediente activo na forma convencional. REIVINDICAÇÕES lã - Processo para a preparação microencapsuladas de lixiviação to de compreender as operações a) se adicionar a uma suspensão líquido, pré-polímero de ureia, de composições agoquímicas rápida, caracterizado pelo fao-que consistem em do composto agroquímico num tio-ureia ou melamina formal- 2 5control was as follows: - CONTROL PERCENTAGE Examples Chinese Hemp Hound Kopopod 81 84 85 84 96 98 Banvel This test demonstrates the excellent persistence in the weed zone in question of the microcapsules according to the present invention compared to the same ingredient active in the conventional way. Process for the microencapsulated leaching preparation to comprise the steps a) is added to a liquid suspension, urea prepolymer, of fast tacky compositions, characterized in that the compound consists of the agrochemical compound in a thiourea or melamine formaldehyde deído ou suas misturas, sendo o referido pré-polímero ou mistura miscivel com o citado liquido, e b) se curar o citado pré-polímero para se obter um polímero reticulado que encerra o agente agroquímico. 2- - Processo de acordo com a reivindicação 1, caracteriza-do pelo facto de o agente agroquímico estar sob a forma cristalina. 3â - Processo de acordo com as reivindicações 1 ou 2, carac-terizado pelo facto de se suspender o composto agroquímico a ser encapsulado numa forma pouco solúvel a um valor de pH superior a 4. 4§ _ Processo de acordo com as reivindicações la 3, carac-terizado pelo facto de o pré-polímero ser um pré-polímero de melamina formaldeído ou uma mistura de um pré-polímero de me-lamina formaldeído com um pré-polímero de ureia formaldeído. 5ã - Processo de acordo com as reivindicações 1 a 4, caracte-rizado pelo afeto de a operação de microencapsulagem se realizar em fases sucessivas pela repetição das operações a) e b).or mixtures thereof, said prepolymer or mixture being miscible with said liquid, and b) curing said prepolymer to provide a crosslinked polymer enclosing the agrochemical. 2. A process according to claim 1, wherein the agrochemical is in crystalline form. 3. A process according to claim 1 or 2, wherein the agrochemical compound to be encapsulated in a poorly soluble form is suspended at a pH value of more than 4. The process according to claim 1, , characterized in that the prepolymer is a melamine formaldehyde prepolymer or a mixture of a metallamine formaldehyde prepolymer with a urea formaldehyde prepolymer. 5. A process according to any one of claims 1 to 4, characterized in that the microencapsulation step takes place in successive steps by repeating steps a) and b). 6- - Processo de acordo com as reivindicações 1 a 5, caracte-rizado pelo facto de o tamanho médio das partículas do composto agroquímico estar compreendido no intervalo entre 1 e Γ 7- - Processo de acordo com as reivindicações 1 a 6, caracte-rizado pelo facto de o tamanho das partículas do produto em microcápsulas estar compreendido entre 10 e 50 Mm. 8- - Processo de acordo com as reivindicações 1 a 7, caracte-rizado pelo facto de o composto agroquímico ser escolhido do grupo formado por 2-cloro-N-(2,6-dietilfenil)-N-(metoximetil)--acetamida (alaclor); 2-cloro-21-etil-61-metil-N-(etoximetil)--acetamida (acetoclor), 2-cloro-N-(2-etil-6-metilfenil)-N-(2--metoxi-l-metiletil)-acetamida (metolaclor) e 2-cloro-N-£ 1--metil-2-metoxij| -N-(2,4-dimetil-tien-3-il)-acetamida e pela forma de sal de ferro ou de alumínio de ácido 3,6-dicloro-2--metoxibenzóico (dicamba), ácido (4-cloro-2-metil fenoxi)--acético (MCPA)- ou ácido (2,4-diclorofenoxi)-acético (2,4-D). 9- - Processo de acordo com a reivindicação 8, caracterizado pelo facto de o composto agroquímico ser dicamba. 10- - Processo de acordo com qualquer das reivindicações anteriores, caracterizado pelo facto de se obter microcápsulas corn tendo um composto agroquímico de lixiviação rápida encerrado um pré-polímero de ureia formaldeído ou melamina formaldeído, ou um pré-polímero misto reticulado. 11- - Processo de acordo com a reivindicação 10, caracterizado pelo facto de o polímero reticulado ser um polímero de melamina formaldeído ou uma mistura de um polímero de lemamina formaldeído com um polímero de ureia formaldeído. 1Ζ- - Processo de acordo com as reivindicações 10 ou 11, ca-racterizado pelo facto de se adicionar ao composto agroquími-co encerrado nas microcápsulas um agente veicular agricolamen— to aceitável. 13â - Processo de acordo com a reivindicação 12, caracteriza-do pelo facto de se adicionar ainda um composto agroquímico que não fica encerrado nas microcápsulas. 14§ _ Processo para controlar a presença de pestes ou o desenvolvimento de plantas indesejáveis, caracterizado pelo facto de se aplicar ao local onde se encontram essas pestes ou plarv-tas indesejáveis ou antecipadamente uma quantidade efectiva de microcápsulas de acordo com os processos 1 a 13, de preferência, compreendida entre cerca de 0,11 a 1,1 Kg de substância activa por hectare. Lisboa,26 de Setembro de 1990 0 Agente ~J“n "--------' ’ 1 Industrial6. A process as claimed in any one of claims 1 to 5, wherein the average particle size of the agrochemical compound is in the range of 1 to 7. A process according to claims 1 to 6, characterized in that the particle size of the microcapsule product is between 10 and 50 μm. 8. A process according to any one of claims 1 to 7, wherein the agrochemical is selected from the group consisting of 2-chloro-N- (2,6-diethylphenyl) -N- (methoxymethyl) acetamide (alachlor); 2-chloro-N- (2-ethyl-6-methylphenyl) -N- (2-methoxy-1-methyl-N- (ethoxymethyl) acetamide (acetochlor) methylethyl) -acetamide (metolachlor) and 2-chloro-N-1-methyl-2-methoxy- Dimethyl-thien-3-yl) -acetamide and the iron or aluminum salt form of 3,6-dichloro-2-methoxybenzoic acid (dicamba), (4-chloro- 2-methylphenoxy) acetic acid (MCPA) - or (2,4-dichlorophenoxy) acetic acid (2,4-D). 9. A process according to claim 8, wherein the agrochemical compound is dicamba. 10. A process as claimed in any one of the preceding claims, wherein microcapsules having a fast leaching agrochemical compound are made of a preformed urea formaldehyde or melamine formaldehyde or a cross-linked mixed prepolymer. 11. A process according to claim 10, wherein the crosslinked polymer is a melamine formaldehyde polymer or a mixture of a lemamine formaldehyde polymer with a urea formaldehyde polymer. 11. A process as claimed in claim 10 or 11, characterized in that an agriculturally acceptable carrier is added to the agrochemical compound contained in the microcapsules. 13. A process according to claim 12, characterized in that an agrochemical compound which is not enclosed in the microcapsules is further added. 14. A process for controlling the presence of pests or the development of undesirable plants, characterized in that an effective amount of microcapsules according to processes 1 to 13 are applied to the place where such pests or pests are present or in advance. , preferably from about 0.11 to 1.1 kg of active substance per hectare. Lisbon, September 26, 1990 Agent "J" n " -------- "1 Industrial Ag»nfo Oficial du P, j.U ti I*· raí.-i-.l fi. Castilho, 201-3. £.-1000 LiòuOA Telefs. Ó51339-654613The present invention relates to a process for the preparation of a compound of the formula (I). Castilho, 201-3. £.-1000 LiòuOA Telefs. Ó51339-654613
PT95429A 1989-09-28 1990-09-26 PROCESS FOR THE PREPARATION OF MICROENCAPSULATED AGROCHEMICAL COMPOSITIONS PT95429A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41379589A 1989-09-28 1989-09-28

Publications (1)

Publication Number Publication Date
PT95429A true PT95429A (en) 1991-05-22

Family

ID=23638669

Family Applications (1)

Application Number Title Priority Date Filing Date
PT95429A PT95429A (en) 1989-09-28 1990-09-26 PROCESS FOR THE PREPARATION OF MICROENCAPSULATED AGROCHEMICAL COMPOSITIONS

Country Status (16)

Country Link
EP (1) EP0445266A1 (en)
JP (1) JPH04502016A (en)
KR (1) KR920700535A (en)
CN (1) CN1050483A (en)
AU (1) AU641694B2 (en)
BR (1) BR9006932A (en)
CA (1) CA2040418A1 (en)
HU (1) HUT56998A (en)
IE (1) IE903470A1 (en)
IL (1) IL95801A0 (en)
MY (1) MY106614A (en)
PL (1) PL287075A1 (en)
PT (1) PT95429A (en)
WO (1) WO1991004661A2 (en)
YU (1) YU182890A (en)
ZA (1) ZA907807B (en)

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ATE149095T1 (en) * 1991-09-11 1997-03-15 Ciba Geigy Ag PESTICIDE FORMULATIONS
GB9306852D0 (en) * 1993-04-01 1993-05-26 Ciba Geigy Ag Multiply-coated particles
GB9306808D0 (en) * 1993-04-01 1993-05-26 Ciba Geigy Ag Coated microparticle agglomerates
WO1999033341A1 (en) * 1997-12-24 1999-07-08 Kiwitech Limited Substantially water-insoluble matrix containing bioactive substances for slow release
ES2205908T3 (en) * 1998-11-12 2004-05-01 Fmc Corporation PROCEDURE TO PREPARE MICROENCAPSULATED FORMULATIONS.
JP2000342956A (en) * 1999-04-01 2000-12-12 Dai Ichi Kogyo Seiyaku Co Ltd Microcapsule production method and microcapsule obtained thereby
JP2000302606A (en) 1999-04-15 2000-10-31 Novartis Ag Microcapsule of solid agrochemical, its production and application thereof
JP4121380B2 (en) * 2001-05-09 2008-07-23 トッパン・フォームズ株式会社 Microencapsulated antibacterial agent
CN100428886C (en) * 2005-12-30 2008-10-29 山东农业大学 High performance cypermethrin micro-capsule emulsion
US8530385B2 (en) 2007-12-13 2013-09-10 Donaghys Industries Limited Herbicidal formulations for combinations of dimethylamine and potassium salts of glyphosate
UA108623C2 (en) * 2009-09-30 2015-05-25 LOWER-CELL AMIN ANTI-PESTICIDE SALTS
CA2806388C (en) 2010-08-18 2019-04-02 Monsanto Technology Llc Early applications of encapsulated acetamides for reduced injury in crops
EP2460404A1 (en) 2010-12-01 2012-06-06 Basf Se Compositions containing identical polyamine salts of mixed anionic pesticides
US20130045869A1 (en) * 2011-08-16 2013-02-21 Dow Agrosciences Llc Complexes of herbicidal carboxylic acids and amine-containing polymers or oligomers
AU2012298627A1 (en) * 2011-08-25 2014-03-13 Dow Agrosciences Llc Pesticidal compositions with enhanced active ingredient retention in pest control zones
GB201115564D0 (en) * 2011-09-08 2011-10-26 Syngenta Ltd Herbicidal composition
BR112015020882B1 (en) 2013-03-26 2020-10-06 Basf Se MICROCAPULES, METHODS OF PREPARING MICROCAPULES AND CONTROLING VEGETABLE GROWTH AND COMPOSITION
BR102016019512B8 (en) 2015-08-26 2022-10-11 Dow Agrosciences Llc COMPOSITION INCLUDING PROTECTIVE COMPLEX INCLUDING CLOQUINTOCET AND POLYMERS OR OLIGOMERS CONTAINING AMINE, ITS PREPARATION METHOD, AND METHOD FOR CONTROL OF UNDESIRABLE VEGETATION
US11109591B2 (en) 2017-04-24 2021-09-07 Taminco Bvba Single phase liquids of alkanolamine salts of dicamba

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US3074845A (en) * 1959-10-14 1963-01-22 Plant Products Corp Particulate pesticidal composition coated with an amido-aldehyde resin polymerized in situ
US3516941A (en) * 1966-07-25 1970-06-23 Minnesota Mining & Mfg Microcapsules and process of making
GB1507739A (en) * 1975-11-26 1978-04-19 Wiggins Teape Ltd Capsules
JPS58124705A (en) * 1982-01-18 1983-07-25 Kureha Chem Ind Co Ltd Micro-capsule of agricultural chemical and its preparation
US4534783A (en) * 1984-01-03 1985-08-13 Monsanto Co. High concentration encapsulation of water soluble-materials
DE3560861D1 (en) * 1984-03-30 1987-12-10 Stauffer Chemical Co Microcapsules and microencapsulation process
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JPS62149607A (en) * 1985-12-25 1987-07-03 Kureha Chem Ind Co Ltd Capsule preparation of ethoprophos
DE3789078T2 (en) * 1986-07-09 1994-08-11 Monsanto Co Formulations of water-dispersible granules and processes for their production.
JPS63178840A (en) * 1987-01-19 1988-07-22 Toppan Moore Co Ltd Slowly-releasable microcapsule

Also Published As

Publication number Publication date
IE903470A1 (en) 1991-04-10
YU182890A (en) 1993-10-20
AU641694B2 (en) 1993-09-30
HUT56998A (en) 1991-11-28
WO1991004661A2 (en) 1991-04-18
EP0445266A1 (en) 1991-09-11
BR9006932A (en) 1991-10-08
ZA907807B (en) 1992-05-27
CN1050483A (en) 1991-04-10
JPH04502016A (en) 1992-04-09
MY106614A (en) 1995-06-30
IL95801A0 (en) 1991-06-30
WO1991004661A3 (en) 1991-05-16
PL287075A1 (en) 1991-09-09
CA2040418A1 (en) 1991-03-29
KR920700535A (en) 1992-08-10
AU6420790A (en) 1991-04-28

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Effective date: 19901217

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Effective date: 19970217