EP1012129A1 - Umhüllte düngemittelgranulate - Google Patents

Umhüllte düngemittelgranulate

Info

Publication number
EP1012129A1
EP1012129A1 EP98932486A EP98932486A EP1012129A1 EP 1012129 A1 EP1012129 A1 EP 1012129A1 EP 98932486 A EP98932486 A EP 98932486A EP 98932486 A EP98932486 A EP 98932486A EP 1012129 A1 EP1012129 A1 EP 1012129A1
Authority
EP
European Patent Office
Prior art keywords
controlled
indole
fertilizer according
acid
acetic acid
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP98932486A
Other languages
English (en)
French (fr)
Inventor
Arie Markus
Zeev Wiesman
David Wolf
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ben Gurion University of the Negev Research and Development Authority Ltd
Original Assignee
Ben Gurion University of the Negev Research and Development Authority Ltd
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 Ben Gurion University of the Negev Research and Development Authority Ltd filed Critical Ben Gurion University of the Negev Research and Development Authority Ltd
Publication of EP1012129A1 publication Critical patent/EP1012129A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05FORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
    • C05F11/00Other organic fertilisers
    • C05F11/10Fertilisers containing plant vitamins or hormones
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G5/00Fertilisers characterised by their form
    • C05G5/30Layered or coated, e.g. dust-preventing coatings
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G5/00Fertilisers characterised by their form
    • C05G5/30Layered or coated, e.g. dust-preventing coatings
    • C05G5/37Layered or coated, e.g. dust-preventing coatings layered or coated with a polymer

Definitions

  • the present invention relates to controlled-release encapsulated fertilizer. More particularly, the present invention relates to a controlled-release encapsulated fertilizer comprising a core containing at least one fertilizer and a polymeric envelope containing at least one hormone encapsulating said fertilizer Background Art
  • aqueous dispersions of pesticide and herbicide micro-capsules are particularly useful in controlled release pesticidal and herbicidal formulations because they can be diluted with water or liquid fertilizer and sprayed using conventional equipment, thereby producing uniform field coverage of the pesticide or herbicide/additives such as film forming agents can be added directly to the finished formulation to improve the adhesion of micro-capsules to foliage. In some cases, reduced toxicity and extended activity of encapsulated herbicides and pesticides have been noted.
  • a polymer separates from a solvent solution of the polymer by the action of a precipitating agent that reduces the solubility of the polymer in the solvent (e.g., a salt or a non-solvent for the polymer).
  • a precipitating agent that reduces the solubility of the polymer in the solvent (e.g., a salt or a non-solvent for the polymer).
  • Patents describing such processes and their shell wall material includes U. S. Patent Nos. 2,800,458 (hydrophilic colloids); 3,069,370 and 3,116,216 (polymers); 3,137,631 (denatured proteins); 3,418,250 (hydrophobic thermoplastic resins); and others.
  • British Patent No. 1 ,371 ,179 discloses a process which consists of dispersing an organic pesticide phase containing a poiymethyiene polyphenylisocyanate or toluylene diisocyanate monomer into an aqueous phase.
  • the wall forming reaction is initiated by heating the batch to an elevated temperature at which point the isocyanate monomers are hydrolyzed at the interface to form amines, which in turn react with unhydrolyzed isocyanate is the possibility of continued reaction of monomer after packaging. Unless all monomer is reacted during the preparation, there will be continued hydrolysis of the isocyanate monomer with evolution of CO 2 , resulting in the development of pressure when the formulation is packaged.
  • U. S. Patent No. 3,577,515 describes a continuous or batch method which requires a first reactant and a second reactant complimentary to the first reactant, with each reactant in separate phases, such that the first and second reactants react at the interface between the droplets to form encapsulated droplets.
  • the process is applicable to a large variety of polycondensation reactions, i.e., to many different pairs of reactants capable of interfacial condensation from respective carrier liquids to yield solid film at the liquid interface.
  • the resulting capsule skin may be produced as a polyamide, polysulfonamide, polyester, polycarbonate, polyurethane, polyurea or mixtures of reactants in one or both phases so as to yield corresponding condensation copolymers.
  • the reference describes the formation of a polyurea skin when diamines or polyamines (e.g. ethylene diamine, phenylene diamine, toluylene diamine, hexamethylene diamine and the like) are present in the water phase and di-isocyanates or polyisocyanates (e.g., toluene diisocyanate, hexamethylene diisocyanate and poiymethyiene polyphenylisocyanate) are present in the organic/oil phase.
  • diamines or polyamines e.g. ethylene diamine, phenylene diamine, toluylene diamine, hexamethylene diamine and the like
  • di-isocyanates or polyisocyanates e.g., toluene diisocyanate, hexamethylene diisocyanate and poiymethyiene polyphenylisocyanate
  • the world's nursery industry utilizes numerous products and techniques in order to maintain and produce millions of ornamental plants and fruit trees.
  • the nursery industry uses sophisticated agrotechnologies and consumes large quantities of rooting stimulators.
  • novel products that could increase rooting percentages of difficult-to-root (mainly woody or semi-woody plant species) plants.
  • a common procedure in a nursery entails the sporadic addition of fertilizers and hormones to the roots of new cuttings.
  • the present inventors have found that the addition of a controlled-release encapsulated fertilizer can maintain the presence of the necessary compounds for the entire period of rooting and development of rooted plants. Disclosure of the Invention
  • a controlled-release encapsulated fertilizer comprising a core containing at least one fertilizer and a polymeric envelope containing at least one hormone encapsulating said fertilizer.
  • said envelope contains at least one hormone selected from the group consisting of Auxin; indole alkyl acid; indole acetic acid(IAA); indole propionic acid(IPA); indole butyric acid(IBA); 2,4 dichlorophenoxy acetic acid; 2,4 chlorophenoxy propionic acid; 2,4 dichloro phenoxyacetic acid propyl ester; and, Naphthalene acetic acid.
  • a process for encapsulating a fertilizer comprising: a) coating a fertilizer with a mixture of a first monomer and a hormone; b) adding a mixture of a second monomer and additional a hormone; and, c) heating said mixtures to induce the polymerization of said first and second monomers to form a polymeric envelope incorporating said hormone and encapsulating said fertilizer.
  • said envelope contains at least one hormone selected from the group consisting of Auxin; indole alkyl acid; indole acetic acid(IAA); indole propionic acid(IPA); indole butyric acid(IBA); 2,4 dichlorophenoxy acetic acid; 2,4 chlorophenoxy propionic acid; 2,4 dichloro phenoxyacetic acid propyl ester; and, Naphthalene acetic acid.
  • said polymeric envelope is formed by a polymer selected from the group consisting of polyurethane; polyurea; and, polyolefins.
  • a series of formulations were prepared according to the present invention.
  • the fertilizer is the core of the formulation and the hormone is incorporated in the envelope.
  • the hormones that were incorporated in the slow release formulations were from the following families: • Auxin- Indole alkyl acid IAA (Indole alkyl acid) ,
  • IPA Indole Propionic Acid
  • IBA Indole Butynic Acid
  • NAA Naphthalene acetic acid
  • Triazole - Paclobutrazole growth retardant that has an anti- gibberllin-enhanching effect on stimulation of root formation and increasing survival of rooted pland grown in stress conditions.
  • the coating consists of the following families of polymers:
  • Carbohydrates such as sucrose, starch, etc. that are enhancing auxin effect on stimulation of root regeneration and development are added to the envelope.
  • Other materials that are added to the formulation are to increase the nutritional content (micro elements such as: Fe, B, Mg, Zn, Mn, Ca, Mo, etc.), to increase biotic tolerance (Benedate), Falpane, Merpan, Prochloraz, propionazol, diazinone, nephorex, etc), and to increase a biotic togruace of the plants (triazole compounds such as majic that increase drought resistance by stimulation of wax cover of the leaves).
  • the above mentioned hormones increase the rate of cell division and differentiation and the result of said increased rate is a stimulation of root regeneration and development.
  • Growth retardants such as Triazole e.g. paclobutrazole can also be added. Said retardant has an anti-gibberllin-enhancing auxin effect on stimulation of root formation.
  • Other materials that are added to the formulation are to increase biotic (pathogens) and abiotic (drought) tolerance of plants.
  • Hormones can also be added to the core if desired. Procedure:
  • the granules of fertilizer were put in a coating pan and one monomer with- part of the hormone was added.
  • the coating pan rotated until the granules were covered with one monomer containing part of the hormones, then a second monomer with the rest of the hormones and catalyst were added.
  • the coating pan rotated and the mixture was heated up to 50 °C. When the condensation polymerization ended, and when the granules are not sticky, talcum was added followed by melted wax.
  • the coating pan was rotated continuously. The formulation is then put in bags.
  • Type Amount type aiiHHint Talc, g Wax, g reitilizer % Polyethylene %
  • Each cutting was put in a vessel with special earth and with 3 granules, the cuttings were put in green houses. The amount of roots and the length of the roots were measured.
  • the plants utilized included were Phelargonium: roses, melloloica, olives from different clutivars, eucalyptus of different kinds and many others.
  • Root svstem development ladder
  • the release rate was determined by the following method, one gram of the granules were placed in a dissolution system. Samples were taken from the vessels and the amount released was determined in the following way: the amount of the fertilizer by conductometeric method and the amount of the hormone by HPLC.
  • the formulations were found to be most effective in: accelerating root formation, increasing rooting percentage, improving the quality of root system, and stimulation of young plant (vegetative and reproductive) development in comparison to untreated control and IBA talc powder (the common substance used at present for rooting in all nurseries).

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Botany (AREA)
  • Fertilizers (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP98932486A 1997-08-07 1998-07-09 Umhüllte düngemittelgranulate Withdrawn EP1012129A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IL12149697 1997-08-07
IL12149697A IL121496A (en) 1997-08-07 1997-08-07 Fertilizers wrapped for controlled release
PCT/IL1998/000322 WO1999007654A1 (en) 1997-08-07 1998-07-09 Encapsulated fertilizers

Publications (1)

Publication Number Publication Date
EP1012129A1 true EP1012129A1 (de) 2000-06-28

Family

ID=11070478

Family Applications (1)

Application Number Title Priority Date Filing Date
EP98932486A Withdrawn EP1012129A1 (de) 1997-08-07 1998-07-09 Umhüllte düngemittelgranulate

Country Status (6)

Country Link
EP (1) EP1012129A1 (de)
AU (1) AU741233B2 (de)
CA (1) CA2299334A1 (de)
IL (1) IL121496A (de)
NZ (1) NZ502497A (de)
WO (1) WO1999007654A1 (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3030877A (en) * 1957-07-18 1962-04-24 Sperry Rand Corp Hay balers
ATE402915T1 (de) 2000-09-12 2008-08-15 Don Wiley Smith Verfahren und zusammensetzungen zum behandeln belasteter bäume
EP1247436A1 (de) 2001-04-02 2002-10-09 Incotec International B.V. Polymerbeschichtungen für Saaten oder Embryos
US20070072775A1 (en) 2005-09-29 2007-03-29 Oms Investments, Inc. Granular controlled release agrochemical compositions and process for the preparation thereof
GB201106761D0 (en) * 2011-04-20 2011-06-01 Exosect Ltd Compositions for growth and vigour in ornamentals
GB201106763D0 (en) * 2011-04-20 2011-06-01 Exosect Ltd Compositions for growth and vigour in cotton
GB201106762D0 (en) * 2011-04-20 2011-06-01 Exosect Ltd Compositions for growth and vigour from oilseeds
GB201106759D0 (en) 2011-04-20 2011-06-01 Exosect Ltd Compositions for growth and vigour in soybean
GB201106764D0 (en) * 2011-04-20 2011-06-01 Exosect Ltd Composition for seed growth and vigour in monocots
GB201106758D0 (en) * 2011-04-20 2011-06-01 Exosect Ltd Compositions for growth and vigour in vegetables
AU2014351424A1 (en) * 2013-11-21 2016-07-07 Ballance Agri-Nutrients Limited Fertiliser composition
WO2016186526A1 (en) * 2015-05-20 2016-11-24 Ballance Agri-Nutrients Limited Fertiliser composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3323898A (en) * 1961-12-12 1967-06-06 Pierce Harold Ladd Controlled solubility micronutrient-containing soil amendment material comprising expanded perlite
US4704160A (en) * 1984-04-02 1987-11-03 The O. M. Scott & Sons Company Combination fertilizer composition
US5413856A (en) * 1993-08-17 1995-05-09 Exxon Research And Engineering Co. Sustained release agricultural substrate coated with a blend of EPDM and asphalt
US5874165A (en) * 1996-06-03 1999-02-23 Gore Enterprise Holdings, Inc. Materials and method for the immobilization of bioactive species onto polymeric subtrates

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9907654A1 *

Also Published As

Publication number Publication date
AU741233B2 (en) 2001-11-29
CA2299334A1 (en) 1999-02-18
IL121496A (en) 2001-06-14
WO1999007654A1 (en) 1999-02-18
IL121496A0 (en) 1998-02-08
NZ502497A (en) 2001-12-21
AU8239098A (en) 1999-03-01

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