WO1996023408A1 - Pesticidal granules containing fertilizer and surfactant - Google Patents
Pesticidal granules containing fertilizer and surfactant Download PDFInfo
- Publication number
- WO1996023408A1 WO1996023408A1 PCT/US1996/001233 US9601233W WO9623408A1 WO 1996023408 A1 WO1996023408 A1 WO 1996023408A1 US 9601233 W US9601233 W US 9601233W WO 9623408 A1 WO9623408 A1 WO 9623408A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formula
- fertilizer
- pesticide
- weight percent
- composition
- Prior art date
Links
- VVDIZWFSGJERMA-UHFFFAOYSA-N CC(C1O)OCC1O Chemical compound CC(C1O)OCC1O VVDIZWFSGJERMA-UHFFFAOYSA-N 0.000 description 1
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
- A01N25/00—Biocides, 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
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/006—Coating of the granules without description of the process or the device by which the granules are obtained
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C3/00—Fertilisers containing other salts of ammonia or ammonia itself, e.g. gas liquor
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES 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
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/60—Biocides or preservatives, e.g. disinfectants, pesticides or herbicides; Pest repellants or attractants
Definitions
- the present invention relates to pesticidal granules containing rapidly dissolutioning or dispersing fertilizer and surfactant compositions. More particularly, the fertilizers are water-soluble nitrogen-containing and the surfactant compositions comprise solid, nonionic surfactants.
- active pesticides as water dissolutioning or dispersible compositions which can be easily mixed with water and applied by means of a spraying apparatus to a locus to be protected.
- the art has also recognized the particular importance of two of the adjuvant properties. They are first, the hydrophilic - hydrophobic balance (HLB) and secondly, the physical form of the initial surface deposit, ideally a moist gel. It has been theorized that with surfactants in the appropriate HLB range, the surfactant is hydrophilic enough to solubilize the herbicide in water and lipophilic enough to penetrate the cuticle of a leaf. In moist gels, the surfactants are hypothesized to form monolayers on the leaf surfaces with the lipophilic portion along the waxes and the hydrophilic portion forming "hydrophilic channels" through surface imperfections such as cracks, punctures, and pores. These channels absorb water and slightly swell to allow herbicides to diffuse through the cuticle into the cell walls.
- HLB hydrophilic - hydrophobic balance
- the surfactants preferred by the art and which can realize the above-described properties when admixed with pesticides in aqueous medium, are the nonionics.
- the solid, nonionic surfactants are desired by the end-user, usually a farmer, for ease of handling such as when preparing a pesticidal spray tank mix.
- the solid nonionics are also preferred to eliminate the need for triple rinsing of the liquid surfactant containers, e.g., the 2.5 gallon jugs, usually used to deliver liquid surfactant concentrates to farmers and to avoid the attendant jug disposal problem.
- dry water-soluble nitrogen fertilizers such as urea, ethylurea, mono and diammonium phosphate; mono and diammonium sulfate, and mixtures thereof can enhance the efficacy of pesticides, especially the herbicides.
- This significant increase in herbicide phytotoxicity in the presence of nitrogen fertilizers has been especially observed with the use of diammonium sulfate adjuvant.
- Large increases in herbicidal efficacy have been reported (Adjuvants and Agrochemicals, Vol. II, Chapter 34) when diammonium sulfate was used as an adjuvant in combination with methylated seed oil, a known cuticle "softener".
- Glyphosate one of the most frequently used herbicides worldwide, usually has diammonium sulfate added to its spray tank solution to enhance its herbicidal efficacy.
- diammonium sulfate appears to have at least two modes of action when coupled to glyphosates : firstly, by directly increasing the glyphosates phytotoxicity and secondly, by overcoming antagonism from certain cations. It has been theorized that the sulfate ions precipitate calcium and sodium ions by forming calcium and sodium sulfates which have low water solubility. The ammonium ions form the more toxic glyphosate-ammonium complex and prevent formation of the less phytotoxic glyphosate - sodium complex during droplet drying.
- Extrusion processing to prepare melt-admixed granules such as is taught in EP 501,798A1, wherein pesticides, binders and diluents are extruded together, has the disadvantage of always intimately admixing all of the components thus inherently placing a restriction on the individual components that can be utilized in such a process. For example, in many situations, the individual components sought to be used are incompatible in intimate contact. Furthermore, in extruded granules, all of the material components will be exposed to the aqueous medium simultaneously, i.e., one cannot program for differing dissolution rates.
- granule-type products i.e., multi-component particles are desirable in many end-use applications such as when they are to be used in pesticidal tank mixes for they are more stable during storage and transport than mere physical mixtures of the dry individual components and provide ease of handling.
- It is an object of the present invention to realize a process for preparing pesticidal granules comprising a dry water-soluble nitrogen fertilizer coated by solid nonionic surfactant compositions and granulated with pesticide adhered to the granule, and the resulting granule.
- This is accomplished by spray-coating the molten surfactant composition onto from about 1 to about 99 weight percent dry water-soluble, nitrogen-containing fertilizer, preferably diammonium sulfate crystals, said percent based on the final weight of the dry bonded adjuvant granule, and granulating the composition in the presence of pesticide to incorporate same into the granule.
- dry water-soluble nitrogen- containing fertilizers preferably diammonium sulfate can provide excellent substrates for certain solid nonionic surfactants when the surfactant composition is dry bonded onto from about 1 to about 99 weight percent (based on the total dry bonded particle weight) of the fertilizer by spray-coating the fertilizer with the molten surfactant and these particles provide excellent carrier systems for pesticides.
- the time for complete dissolution in water of the solid, nonionic surfactant compositions can ofttimes be significantly reduced.
- the instant pesticide-fertilizer carrier systems are exceptionally stable and relatively unaffected by attrition during storage and shipping. These unique delivery systems permit components, normally incompatible with the pesticide and/or nitrogen-containing fertilizer to be physically incorporated in the granule. For example, if an adjuvant is incompatible with the fertilizer, it can be adhered to the granule; if incompatible with the pesticide, it can be added prior to the spray coating, i.e., made part of the substrate.
- adjuvants that require a longer exposure time to a given aqueous medium for optimum efficiency as an inherent part of the granule, for example, guar particles that require additional hydration time; pH buffers, etc., they can be preferentially or sequentially released by not having the adjuvant incorporated uniformly throughout the particle as would occur using the processing of the prior art, but rather having the adjuvant adhered to the outer surfactant coating of the granule.
- spray-coated is meant that the solid surfactant is melted and coated upon a substrate comprising the fertilizer while still in the molten state. This is done by spraying the molten surfactant onto the substrate, most preferably the diammonium sulfate particles in a coating blender. Complete coating of the substrate particles is not always necessary but, rather, the degree of completeness of the coating is often determined by specific requirements such as the need to isolate the fertilizer from other added incompatible adjuvants. The sprayed material, while still-in a sticky state is then continuously tumbled to partially agglomerate or granulate the individual particles while preferably the pesticide is added and bonded so as to yield dry bonded flowable granules.
- the solid, nonionic surfactants that can be used in the process of this invention are those known in the art which are solid or of a hard, nontacky wax consistency at room temperature.
- nonionics are the following:
- R' and R" each can be -H, -CH 2 CH 2 OH, or
- esters such as: i) fatty acid esters of the formula -
- Ethoxylates such as: i) alkylphenol ethoxylates of the formula - ii) alcohol ethoxylates of the formula - R - O - (CH 2 CH 2 O) n H; iii) tristyrylphenol ethoxylates of the formula -
- R is a fatty alkyl group, preferably a C 6 - C 22 fatty alkyl group, most preferably a C 8 - C 18 fatty alkyl group;
- R 1 is -H or a fatty alkyl group, preferably -H or a C 6 - C 22 fatty alkyl group, most preferably -
- x, ⁇ ', y, y' and n are each independently moles of ethylene oxide preferably 1 to 300; most preferably 1 to 150; and
- n, m', l and l' are each independently moles of propylene oxide, preferably 1 to 300; most preferably 1 to 150;
- the surfactant composition is a solid at room temperature (24oC), preferably a solid at 50oC.
- Mixtures of the above surfactants are acceptable and, in fact, mixtures of the above surfactants with other nonionics that alone are liquid even at room temperature may be acceptable provided that the amount or nature of the liquid surfactant is such that the final particulate product does not exhibit tackiness at room temperature. Preferably, tackiness is not exhibited even at 50oC.
- the more preferred solid nonionic surfactants are the aforedescribed alkyl alcohol ethoxylates and alkylphenol ethoxylates.
- the solid, nonionic surfactant composition of the instant granules should be from about 1 to about 99 weight percent, preferably from about 3 to about 95 weight percent based on the total granule formulation weight.
- the most preferred solid nonionic surfactant is dinonylphenol ethoxylate ( ⁇ 100 EO) for it has been discovered that this compound possesses the ability to provide excellent wetting characteristics together with a high melting point. Furthermore, the material exhibits an ability to dissolve in aqueous medium without formation of a gel phase.
- the amount of the dry water-soluble nitrogen-containing fertilizer to be spray-coated by the solid nonionic composition can be from about 1 to about 99 weight percent, preferably from about 1 to about 95 weight percent based on the total weight of the final spray-coated composition.
- the pesticides contemplated for use in the granules of this invention are those active ingredients well known to be of value to agriculture and are normally distributed to loci via aqueous spray means such as herbicides, fungicides, bactericides, insecticides, insect antifeedants, acaricides, miticides, nematocides, and plant growth regulants.
- Preferred pesticides are the herbicides selected from the group consisting of the herbicidal sulfonyl ureas, imidazolines, and glyphosates.
- the active ingredients should be present in the granules in pesticidally effective amounts, preferably from about 0.01 to about 90 weight percent, most preferably from about 0.03 to about 80 weight percent based on the total granule formulation weight.
- the essence of the preferred embodiment of the instant invention lies in the discovery that if solid nonionic surfactant compositions are spray-coated upon dry, water-soluble nitrogen-containing fertilizers such as diammonium sulfate, the dissolution rate of the dry surfactant particulate composition in aqueous solution can be greatly enhanced. It is also hypothesized that in addition to the action of the fertilizer per se upon the dissolution rate of the solid, nonionic surfactant composition, the coating/granulation process tends to entrap air within the coated granules thereby increasing the surface area ultimately exposed to the aqueous medium which increases the dissolution rate (as opposed to compaction and extrusion processes which tend to compress air out of the particles). Also, the pockets of entrapped air function as flotation aids which assist in keeping the coated granules from settling.
- the preferred process of the instant spray-coating invention comprises the steps of:
- the fertilizer particles are initially blended for at least 10 minutes before the spraying step to ensure that the initial crystal or particle sizes are uniformly distributed throughout the batch.
- the preferred spray blender-mixers are those of the Mark VI design manufactured by Continental Rollo or an equivalent.
- the mixture should continue to be blended for at least three additional minutes after the spraying has ceased. If it is desired to have any additional components adhere to the surface of the coated granules, e.g., if an additional additive is a fine powder and one desires to reduce dusting in the final product, the material can also be added while the coated granules are still tacky to obtain adherence, i.e., the material can be added before the granules are completely cooled.
- optional additional components include anti-foam agents, flow agents, anti-caking agents, stabilizers, inert fillers, gas-generating agents, dyes, and/or any adjuvants particular to the specific end-use application of the resulting product.
- Optional adjuvants can be added from about 0 to about 20 weight percent of the granular composition.
- Inert ingredients can be added up to about 80 weight percent.
- one of the distinct advantages of the instant spray-coated, i.e., multi-layered particle is that it frees the preparer from many of the restrictions normally imposed upon multi-component systems manufacturers.
- additional adjuvant components which normally would be incompatible with the fertilizer, specifically the diammonium sulfate can be made a part of the coated granule by introducing the component after the pesticide granulation process is essentially completed, but while the multi-layered material is still tacky so that the adjuvant can be adhered to the outer surface, i.e., the component would only be in contact with the pesticide and the nonionic composition layer.
- Another advantage realized by this adherence contact procedure is that in addition to the pesticide, it allows other material to be placed on the outside of the spray-coated granule, thus giving the adhered material preferential or advanced exposure to the aqueous media. Thus, one can also selectively sequence the exposure times of certain components of the granule.
- the fertilizer of the instant process preferably should be of a coarse grade; most preferably 95 weight percent of the material should have an average particle size diameter of from about 200 to about 600 microns, i.e., 95 weight percent should pass through a 30 mesh (U. S. Standard) screen and not pass through a 70 mesh (U. S. Standard) screen. Elimination of fines is preferred to minimize compaction or agglomeration of the fertilizer particles during the coating process.
- the granules may be used as is or, if preferred, screened to a desired particle size.
- a flaked dinonylphenol ethoxylate ( ⁇ 100 EO) (sold under the Rhone-Poulenc trademark Igepal DM- 970 FLK) is blended with a sufficient amount of a liquid isodecyl alcohol ethoxylate (4 EO) (sold under the Rhone-Poulenc trademark Rhodasurf DA-530) to produce a non-tacky, solid mixture with a 85:15 respectively weight ratio surfactant Composition A (said blend also sold by Rhone-Poulenc under the trademark AgRHô DS 420).
- isodecyl alcohol ethoxylate has an adverse effect on the melting point of the solid dinonylphenol ethoxylated surfactant, its presence is useful for the improved wetting characteristic it provides, i.e., the lower surface tension realized in the final aqueous solution as a result of its incorporation.
- dry diammonium sulfate is added to the dry Composition A prepared above in a Sigma Blade Mixer in a weight ratio of approximately 85:15 weight percent sulfate to surfactant. Blending is unable to be accomplished because the materials compress together and cake.
- the test is run again utilizing solely the flaked dinonylphenol ethoxylate ( ⁇ 100 EO) , i.e., Igepal DM-970 FLK in lieu of Composition A. Again, the blending is unsuccessful because, even at room temperature, the surfactant and diammonium sulfate compact to form cakes.
- Diammonium sulfate is charged into a Continental Rollo mixer Mark VI blender. The sulfate is rotationally blended for about 10 minutes.
- a solid nonionic surfactant composition comprising an 85:15 weight ratio of dinonylphenol ethoxylate
- the resulting dissolution time of the solid nonionic surfactant composition indicates the significantly enhanced dissolution rates that can be unexpectedly realized by this invention, i.e., by the spray-coating of diammonium sulfate with the molten nonionic surfactant composition.
- 84.05 weight percent diammonium sulfate is charged into a Continental Rollo mixer Mark VI blender. The sulfate is rotationally blended for about 10 minutes. 15 weight percent of a solid nonionic surfactant composition comprising a 85:15 weight ratio of dinonylphenol ethoxylate ( ⁇ 100 EO) (Igepal DM 970) to isodecyl alcohol ethoxylate (4 EO) (Igepal DA 530) respectively, (said nonionic surfactant composition blend sold under the Rhone-Poulenc trademark AgRHô DS 420) is heated at a temperature of about 85o C until the surfactant composition is melted.
- a solid nonionic surfactant composition comprising a 85:15 weight ratio of dinonylphenol ethoxylate ( ⁇ 100 EO) (Igepal DM 970) to isodecyl alcohol ethoxylate (4 EO) (Igepal DA 530) respectively, (said nonionic sur
- the molten surfactant is then sprayed onto the rotating ammonium sulfate through five sized 8008E spray tips.
- the mixture is blended continuously for three additional minutes to ensure uniform granulation.
- the mixture is then cooled to about 45o C at which time 0.2 weight percent of antifoam Rhodorsil Silicone EP 6703 is blended into the mixture for three minutes.
- 0.75 weight percent of an anti-caking or free flow aid (Tixosil 38AB) is blended in for a few minutes.
- the coated granular product is collected through a #8 mesh sieve.
- the dissolution times of the resulting coated granules are less than half that of the solid nonionic surfactant composition alone.
- Example IV The process of Example IV is followed utilizing the following weight percentages: ammonium sulfate - 93.15%; AgRHô DS 420 - 6.0%; Rhodorsil EP 6703 - 0.1%; and Tixosil 38 AB - 0.75%.
- Example IV the dissolution times of the resulting coated granules are again less than half that of the solid nonionic surfactant compositions alone.
- the spray-admixed compositions of this invention do not suffer from particle separation that can occur with simple solid blends of the same materials.
- the coated products of this invention also realize a very uniform granule size together with excellent attrition resistance. Serendipitously, the process is significantly less energy intensive and more capital cost effective than other melt-admixing processes, e.g., the extrusion processes of the prior art.
- Adjuvant A Twenty five pounds of Adjuvant A is prepared by charging 93.15 weight percent diammonium sulfate into a Continental Rollo Mixer Mark VI Blender. The sulfate is rotationally blended for about 10 minutes. 6.0 weight percent of a solid nonionic surfactant composition comprising an 85:15 weight ratio of dinonylphenol ethoxylate ( ⁇ 100 EO) (Igepal DM 970) to isodecyl alcohol ethoxylate (4 EO) (Igepal DA 530) respectively, (said nonionic surfactant composition blend sold under the Rhone-Poulenc trademark AgRHô DS 420) is heated at a temperature of about 85o C until the surfactant composition is melted.
- a solid nonionic surfactant composition comprising an 85:15 weight ratio of dinonylphenol ethoxylate ( ⁇ 100 EO) (Igepal DM 970) to isodecyl alcohol ethoxylate (4 EO) (Ige
- the molten surfactant is then sprayed onto the rotating diammonium sulfate through five sized 8008E spray tips.
- the mixture is blended continuously for two additional minutes to ensure uniform granulating, at which time herbicides are identified and, in the amounts listed below, are added.
- the material is tumble blended an additional three minutes to adhere the particulate pesticide to and incorporate them in the granules.
- the mixture is then cooled to about 45oC, at which time 0.8 oz. of antifoam Rhodorsil Silicone EP 6703 is blended into the mixture for three minutes.
- 6.0 oz. of an anti-caking or free flow aid (Tixosil 38 AB) is blended in for a few minutes.
- the pesticide-adhered granules are cooled and collected through a sieve.
- the following table illustrates the enhanced phytotoxicity realized by the use of the dry bonded pesticidal-adjuvant systems of the instant invention prepared as above described compared to that realized by standard liquid adjuvant-pesticide blends.
- the carrier for the compositions listed in Table II is water at ten gallons per acre.
- Kinetic is a proprietary liquid surfactant adjuvant system comprising a polyorganosilicone and an ethyleneoxide/propyleneoxide block copolymer.
- Dynamic is a proprietary liquid adjuvant system comprising methylated seed oil (MSO) and a polyorganosilicone.
- MSO methylated seed oil
- C.O.C. is a crop oil concentrate usually about 83 weight percent paraffinic crop oil and 17 weight percent emulsifier.
- the following examples illustrate the enhanced phytotoxicity realized by the use of a glyphosate herbicide incorporated into the granulated products of the surfactant-fertilizer carrier systems of this invention prepared as described in Examples VI - XV with the following changes to the pesticidal granular composition: 84.05 weight percent diammonium sulfate; 15.0 weight percent AgRHô DS 420; 1.6 oz. Rhodorsil Silicone EP 6703; and 6.0 oz. of Tixosil 38 AB.
- the herbicide used is Roundup which is a trademark of Monsanto for a glyphosate herbicidal formulation. Quest is a proprietary ammonia-based water conditioner of Helena Chemical Co.
- the carrier for the compositions is again ten gallons of water per acre.
- the final granular product is such that it produces very little foam; low dust levels and odor; is non-compacting; and spills are easily swept up.
- the dry bonded granular pesticide delivery systems of this invention enable a rapidly dispersing, completely optimized and balanced pesticidal-adjuvant-fertilizer composition to be prepared and, therefore, combines performance, convenience, and safety to the end-user in one granular product - - an ideal situation.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fertilizers (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU47728/96A AU4772896A (en) | 1995-01-31 | 1996-01-31 | Pesticidal granules containing fertilizer and surfactant |
BR9607573-2A BR9607573A (en) | 1995-01-31 | 1996-01-31 | Granular pesticide systems |
JP8523671A JPH10513148A (en) | 1995-01-31 | 1996-01-31 | Granular pesticide system |
EP96903745A EP0806893A1 (en) | 1995-01-31 | 1996-01-31 | Pesticidal granules containing fertilizer and surfactant |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US38159995A | 1995-01-31 | 1995-01-31 | |
US08/381,599 | 1995-01-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996023408A1 true WO1996023408A1 (en) | 1996-08-08 |
Family
ID=23505646
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/001233 WO1996023408A1 (en) | 1995-01-31 | 1996-01-31 | Pesticidal granules containing fertilizer and surfactant |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0806893A1 (en) |
JP (1) | JPH10513148A (en) |
AU (1) | AU4772896A (en) |
BR (1) | BR9607573A (en) |
CA (1) | CA2211996A1 (en) |
WO (1) | WO1996023408A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998039273A1 (en) * | 1997-03-07 | 1998-09-11 | Aquatrols Corporation Of America Inc. | Fully compatible surfactant-impregnated water-soluble fertilizer; concentrate; and use |
EP0900786A1 (en) * | 1997-09-03 | 1999-03-10 | Monsanto Europe S.A./N.V. | New surface active compounds, method for their preparation, and their use |
EP0753256B1 (en) * | 1995-07-13 | 2002-09-25 | Cfpi Nufarm | New solid storage and selling form for pesticidal compositions and means for its preparation |
US6460290B1 (en) | 1997-03-07 | 2002-10-08 | Robert A. Moore | Fully compatible surfactant-impregnated water-soluble fertilizer; concentrate; and use |
EP2000027A1 (en) * | 2007-06-06 | 2008-12-10 | Bayer CropScience AG | Insecticide compounds with improved effect |
EP2840074A1 (en) | 2013-08-23 | 2015-02-25 | Biotensidon GmbH | Composition for stimulating the cultivation of plants, use of same and method of production |
EP3177143A2 (en) * | 2014-04-17 | 2017-06-14 | Basf Se | Combination of novel nitrification inhibitors and herbicides as well as combination of (thio)phosphoric acid triamides and herbicides |
EP3191430A4 (en) * | 2014-09-12 | 2018-05-23 | South Star Fertilizers Limited | Fertilizer coated with linear alcohol ethoxylate and optionally raw plant oil |
WO2021091400A1 (en) * | 2019-11-08 | 2021-05-14 | Donaghys Limited | A composition and related methods of manufacture and use |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000313685A (en) * | 1999-04-26 | 2000-11-14 | Nissan Chem Ind Ltd | Production of agrochemical-containing granular fertilizer |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3274052A (en) * | 1963-06-19 | 1966-09-20 | Fmc Corp | Preparation of pesticide granules |
EP0206537A1 (en) * | 1985-05-29 | 1986-12-30 | Stauffer Chemical Company | Solid, phytoactive compositions, methods of use and methods of preparation |
-
1996
- 1996-01-31 EP EP96903745A patent/EP0806893A1/en not_active Ceased
- 1996-01-31 CA CA002211996A patent/CA2211996A1/en not_active Abandoned
- 1996-01-31 BR BR9607573-2A patent/BR9607573A/en not_active Application Discontinuation
- 1996-01-31 AU AU47728/96A patent/AU4772896A/en not_active Abandoned
- 1996-01-31 WO PCT/US1996/001233 patent/WO1996023408A1/en not_active Application Discontinuation
- 1996-01-31 JP JP8523671A patent/JPH10513148A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3274052A (en) * | 1963-06-19 | 1966-09-20 | Fmc Corp | Preparation of pesticide granules |
EP0206537A1 (en) * | 1985-05-29 | 1986-12-30 | Stauffer Chemical Company | Solid, phytoactive compositions, methods of use and methods of preparation |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0753256B1 (en) * | 1995-07-13 | 2002-09-25 | Cfpi Nufarm | New solid storage and selling form for pesticidal compositions and means for its preparation |
WO1998039273A1 (en) * | 1997-03-07 | 1998-09-11 | Aquatrols Corporation Of America Inc. | Fully compatible surfactant-impregnated water-soluble fertilizer; concentrate; and use |
US6460290B1 (en) | 1997-03-07 | 2002-10-08 | Robert A. Moore | Fully compatible surfactant-impregnated water-soluble fertilizer; concentrate; and use |
EP0900786A1 (en) * | 1997-09-03 | 1999-03-10 | Monsanto Europe S.A./N.V. | New surface active compounds, method for their preparation, and their use |
EP2000027A1 (en) * | 2007-06-06 | 2008-12-10 | Bayer CropScience AG | Insecticide compounds with improved effect |
WO2008148483A1 (en) * | 2007-06-06 | 2008-12-11 | Bayer Cropscience Ag | Insecticide compositions having an improved effect |
EP2840074A1 (en) | 2013-08-23 | 2015-02-25 | Biotensidon GmbH | Composition for stimulating the cultivation of plants, use of same and method of production |
EP3177143A2 (en) * | 2014-04-17 | 2017-06-14 | Basf Se | Combination of novel nitrification inhibitors and herbicides as well as combination of (thio)phosphoric acid triamides and herbicides |
EP3191430A4 (en) * | 2014-09-12 | 2018-05-23 | South Star Fertilizers Limited | Fertilizer coated with linear alcohol ethoxylate and optionally raw plant oil |
WO2021091400A1 (en) * | 2019-11-08 | 2021-05-14 | Donaghys Limited | A composition and related methods of manufacture and use |
US11432544B2 (en) | 2019-11-08 | 2022-09-06 | Donaghys Limited | Composition and related methods of manufacture and use |
US11737456B2 (en) | 2019-11-08 | 2023-08-29 | Donaghys Limited | Composition and related methods of manufacture and use |
US20230354804A1 (en) * | 2019-11-08 | 2023-11-09 | Donaghys Limited | Composition and related methods of manufacture and use |
Also Published As
Publication number | Publication date |
---|---|
EP0806893A1 (en) | 1997-11-19 |
CA2211996A1 (en) | 1996-08-08 |
JPH10513148A (en) | 1998-12-15 |
BR9607573A (en) | 2000-10-31 |
AU4772896A (en) | 1996-08-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0807094B1 (en) | Dry-bonded nonionic adjuvants | |
AU651335B2 (en) | Water-dispersible or water-soluble pesticide granules from heat-activated binders | |
EP0465635B1 (en) | Pelletizing phosphoroamidothioate derivatives with fertilizers and other pesticides | |
US6749659B1 (en) | Controlled release rate fertilizers and methods of making same | |
NZ248289A (en) | Free-flowing water-soluble granular herbicidal composition comprising n-phosphonomethylglycine | |
US6878180B2 (en) | Combination ammonium sulfate/drift reducing adjuvant and wet bond process for making the same | |
WO1996023408A1 (en) | Pesticidal granules containing fertilizer and surfactant | |
JP2511431B2 (en) | Novel water dispersible granules and their uses | |
US4183740A (en) | Solid compositions of a liquid surfactant and a pyrazolium herbicide | |
JP2014037443A (en) | Granular agrochemical composition and production method of the same | |
US5100667A (en) | Process for pelletizing insecticidal N-hydrocarboyl phosphoroamidothioates and phosphoroamidodithioates | |
JP2770400B2 (en) | Pesticide solid formulation | |
EP0638235B1 (en) | Solid formulation | |
EP0807162B1 (en) | Nonionic surfactants with enhanced aqueous dissolution rates | |
TW202044993A (en) | Insecticidal compositions resistant to active ingredient degradation and process for preparation thereof | |
JPH11255609A (en) | Herbicidal composition, its production and use | |
JPH07291804A (en) | Water-soluble granular agrochemical | |
JP2001517207A (en) | Process for producing spontaneous water-dispersible carriers for pesticides and their use | |
WO1997024423A1 (en) | Processes for producing solid surfactant compositions with enhanced dissolution rates |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AM AT AU BB BG BR BY CA CH CN CZ DE DK EE ES FI GB GE HU IS JP KE KG KP KR KZ LK LR LT LU LV MD MG MN MW MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TT UA UG UZ VN |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): KE LS MW SD SZ UG AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
ENP | Entry into the national phase |
Ref document number: 2211996 Country of ref document: CA Ref country code: CA Ref document number: 2211996 Kind code of ref document: A Format of ref document f/p: F |
|
ENP | Entry into the national phase |
Ref country code: JP Ref document number: 1996 523671 Kind code of ref document: A Format of ref document f/p: F |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1996903745 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 1996903745 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWR | Wipo information: refused in national office |
Ref document number: 1996903745 Country of ref document: EP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 1996903745 Country of ref document: EP |