GB2104780A - Plant-protection compositions in the form of granules - Google Patents

Plant-protection compositions in the form of granules Download PDF

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Publication number
GB2104780A
GB2104780A GB08219949A GB8219949A GB2104780A GB 2104780 A GB2104780 A GB 2104780A GB 08219949 A GB08219949 A GB 08219949A GB 8219949 A GB8219949 A GB 8219949A GB 2104780 A GB2104780 A GB 2104780A
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GB
United Kingdom
Prior art keywords
composition according
granules
acid
weight
herbicide
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Withdrawn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
GB08219949A
Inventor
Robert J Hardy
David A Pearce
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.)
Bayer CropScience SA
Original Assignee
Rhone Poulenc Agrochimie 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 Rhone Poulenc Agrochimie SA filed Critical Rhone Poulenc Agrochimie SA
Publication of GB2104780A publication Critical patent/GB2104780A/en
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • A01N25/12Powders or granules
    • 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

Abstract

Effervescent bioactive compositions comprise an acid herbicide or plant growth regulator and an alkali metal carbonate or bicarbonate

Description

SPECIFICATION Plant-protection compositions in the form of granules The present invention relates to bioactive compositions consisting of effervescent granules containing an acid herbicide or growth regulator, an alkali metal carbonate or bicarbonate and, if appropriate, additives such as mould-release agents, binders and/or fillers.
The herbicide acifluorfen sodium salt, marketed under the trademarks Tackle and Blazer and consisting of sodium 5-[2-chloro-4 (trifluoromethyl)-phenoxy]-2-nitro-benzoate, is known; acifluorfen is itself 5-[2-chloro-4 (trifluoromethyl)-phenoxy]-2-nitrobenzoic acid.
The marketed formulations of acifluorfen sodium salt are compositions comprising water (76%) and only about 24% of herbicide as the main constituents.
One object of the present invention is to produce dry herbicidal compositions which are readily dispersible in water and which contain a relatively high concentration of herbicidal active ingredient.
On this point, it must be noted that, being hygroscopic, acifluorfen sodium salt is not in itself a suitable herbicidal concentrate in commercial terms.
Another object of the present invention is to provide herbicidal compositions which are not in powder form. In fact, the people who apply pesticidal products are increasingly dissatisfied with compositions in powder form, because of the harmful effects and the inconvenience of handling powders (the need for a mask, staining, and the like).
Furthermore, various kinds of water-dispersible pesticidal granules are well known, especially those called "dry flowables". In particular, effervescent granules have been proposed (French Patent 2,290,844 and British Patent 847,370), these granules comprising at least three essential constituents: the active ingredient, a carbonate and an acid capable of reacting with the carbonate.
Another object of the present invention is to provide herbicidal compositions which are as simple as possible and contain a high proportion of active ingredient.
Another object of the present invention is to provide dry herbicidal compositions which can easily be used to apply active ingredients such as acifluorfen sodium salt.
It has now been found that these various objects can be achieved by virtue of the compositions according to the present invention.
The present invention thus relates to bioactive pesticidal compositions, and more particularly herbicidal compositions, in the form of watersoluble granules, the said granules comprising 50 to 90% by weight of an acid herbicide or plant growth regulator, preferably an acid herbicide and about 10 to 40% by weight of an alkali metal carbonate or bicarbonate, the alkali metal being in particular potassium or, preferably, sodium, the said compositions containing also 0 to 10% by weight of impurities of the acid herbicide (such as isomers or manufacture by-products). The amount of acid active ingredient is preferably between 60 and 75% by weight.
It must be clearly understood that the term "granules" is not to be taken in a restricted sense, and that it includes any other similar form such as grains, pellets or briquettes.
In general, these granules have a minimum size of between 0.1 and 50 mm, preferably of between 0.3 and 3 mm.
The amount of herbicidal active ingredient, relative to the carbonate, is such that the molar ratio carbonate or bicarbonate/acid active ingredient is between 1 and 3, preferably between 1.3 and 2.
The compositions according to the present invention can contain minor amounts (e.g. 0.1 to 10% by weight) of other additives, such as lubricants or mould-release agents (e.g. 0.05 to 1% or less of aluminium stearate), stabilisers, binders, agents promoting cohesion of the granules (e.g. urea or cellulose derivatives) and agents promoting disintegration of the granules, or inert fillers, including water-insoluble inert fillers.
The compositions according to the invention can also contain other additives which are useful for the application of the pesticide in question.
Thus, it may be necessary to add surface-active agents or wetting or dispersing agents or any other product capable of promoting the penetration of the active ingredient into the plant.
These surface-active agents can be emulsifying, dispersing or wetting agents of ionic or non-ionic type, or a mixture of such surface-active agents.
Examples which may be mentioned are salts of polyacrylic acids, salts of lignosulphonic acids, polycondensates of ethylene oxide with fatty alcohols, fatty acids or fatty amines, substituted phenols (in particular alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (in particular aikyltaurates), phosphoric acid esters of condensates of ethylene oxide with alcohols or phenols, fatty acid esters of polyols, and derivatives of the above compounds containing sulphate, sulphonate or phosphate groups.
Preferably, in the compositions according to the present invention, the grains are separate from one another and they can flow in bulk when poured.
According to an advantageous variant, the compositions of the present invention do not contain any inert filler, in particular any waterinsoluble inert filler.
Acifluorfen is the active ingredient which is particularly appropriate to the invention, but it is also possible to use 5-[2-chloro-4 (trifluoromethyl)-phenoxy]-2-nitro-Nmethanesulphonylbenzamide, 2,4-dichlorophenoxyacetic acid, 2-methyl-4-chlorophenoxyacetic acid, naphthalene-1-acetic acid (as a plant growth regulator) and methyl paraaminophenyl suiphonylcarbamate.
The granules according to the present invention can be made by mixing and compressing the constituents (e.g. with the aid of a press or a compacter) so as to give a briquette, and then by granulating the compact material obtained.
A spraying mixture (solution or suspension) which is ready for use can be obtained from the granules according to the invention simply by placing the said granules in water, in an amount corresponding to the desired concentration of the active ingredient.
The CO2 released during effervescence causes rapid agitation of the solution and facilitates salification of the acid; this agitation accelerates the dissolution of the ingredients in the water; furthermore, the use of an acid in the formulation makes it possible to incorporate a higher proportion of active ingredient into the composition than in the case where the salt is added separately: this is a particularly valuable advantage in the field of plant protection, where it is desirable to handle the smallest possible amount of products.
The following non-limitative examples illustrate the present invention and the manner in which it can be carried out.
EXAMPLE 1 The following are mixed: 96% pure acifluorfen (7.23 g) anhydrous sodium carbonate (1.12 g) aluminium stearate (0.01 g).
The mixture is ground in a mill with glass beads, the mill containing the same weight of glass beads of diameter 5 mm. The mixture is then sieved and compressed. The pellets obtained are lightly crushed in a mortar and then pounded and sieved, and the fraction of 20 to 60 mesh (U.S.
standard specification for sieves, 0.25-0.84 mm) is retained.
On adding these granules to water, effervescence and dissolution take place and a solution of the sodium salt of acifluorfen ready for spraying is obtained, which is clear except that it comprises particles of aluminium stearate in suspension.
The mixture contains 83% of herbicidal acid, which is equivalent to 88% of the sodium salt.
EXAMPLE 2 The following are mixed: acifluorfen (96% pure) (7.22 g) sodium bicarbonate (1.85 g) aluminium stearate (0.01 g).
The mixture is treated as in Example 1. When the granules are added to water, the results obtained are equivalent to those of Example 1.
The mixture contains 76.4% of herbicidal acid, which is equivalent to 81% of the sodium salt.
EXAMPLE 3 The following are mixed: 80% pure acifluorfen (74.9 g) anhydrous sodium carbonate (25 g) aluminium stearate (0.1 g).
The mixture is finely ground in a mechanical mill so as to give 3 to 50 micron particles.
The mixture thus obtained is compressed under a pressure of 20 bars by a pelletising machine. The pellets obtained are crushed and then sieved so that the grains having a size of 20 to 60 mesh (0.25 to 0.84 mm) are retained. These grains contain about 60% of acifluorfen, which is equivalent to 63.6% of its sodium salt.
When added to water, these granules disaggregate with the release of carbon dioxide and the formation of the sodium salt of acifluorfen, as in the previous Examples 1 and 2.
EXAMPLE 4 The following are mixed: 80% pure acifluorfen (63 g) anhydrous sodium carbonate (25 g) aluminium stearate (0.1 g).
The mixture is ground as in Example 3.
The mixture obtained is compressed under a pressure of 5 bars by a pelletising machine. The pellets obtained are crushed and then sieved so that the particles having a size of 1 5 to 30 mesh (0.5 to 1.2 mm) are retained. These grains contain 57.2% of acifluorfen, which is equivalent to 60% of its sodium salt; when they are placed in water, they disintegrate perfectly and give an aqueous solution of the herbicide acifluorfen sodium salt.
EXAMPLE 5 The procedure of Example 3 is followed, but the anhydrous sodium carbonate (25 g) is replaced by anhydrous sodium carbonate (18 g) and urea (7 g).
This gives granules having a similar size, which are perfectly satisfactory as regards their disintegration in water.
EXAMPLE 6 Example 3 is repeated but replacing the acifluorfen by 5-[2-chloro-4-trifluoromethyl)phenoxy]-2-nitro-N-methanesulphonyl benzamide, 2,4-dichlorophenoxyacetic acid, 2methyl-4-chlorophenoxyacetic acid or naphthalene-1-acetic acid.
Satisfactory granules which disintegrate well in water are obtained in the same manner.

Claims (11)

1. A bioactive composition in the form of watersoluble granules, the said granules comprising 50 to 90% by weight of an acid herbicide or plant growth regulator and from 10 to 40% by weight of an alkali metal carbonate or bicarbonate, the said composition containing also 0 to 10% by weight of impurities of the acid herbicide.
2. A composition according to claim 1, wherein the active ingredient is an acid herbicide.
3. A composition according to claim 1 or 2, wherein the alkali metal carbonate or bicarbonate is sodium carbonate or bicarbonate.
4. A composition according to any one of claims 1 to 3, which contains 60 to 75% by weight of acid herbicide.
5. A composition according to any one of claims 1 to 4, wherein the molar ratio of carbonate or bicarbonate/acid herbicide or plant growth regulator is between 1 and 3, preferably between 1.3 and 2.
6. A composition according to any one of claims 1 to 5, wherein the granules are separate from one another, are capable of flowing in bulk and do not contain a water-insoluble inert filler.
7. A composition according to any one of claims 1 to 6, which contains 0.1 to 10% by weight of an additive such as a lubricant, mouldrelease agent, stabiliser, binder, agents promoting cohesion of the granules, agents promoting disintegration of the granules or a surface-active agent.
8. A composition according to any one of claims 1 to 7, which contains 0.05 to 1% of aluminium stearate.
9. A composition according to any one of claims 1 to 8, which contains urea.
10. A composition according to any one of claims 1 to 10, wherein the herbicide is acifluorfen.
11. A composition according to any one of claims 1 to 10 wherein the acid active ingredient is chosen from the group comprising 5-[2-chloro 4-(trifl uoromethyl )-phenoxy]-2-nitro-N-methane- sulphonylbenzamide, 2,4-dichlorophenoxyacetic acid, naphthalene-1-acetic acid, 2-methyl-4chlorophenoxyacetic acid or methyl para aminobenzenesulphonylcarbamate.
GB08219949A 1981-07-17 1982-07-09 Plant-protection compositions in the form of granules Withdrawn GB2104780A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US28427481A 1981-07-17 1981-07-17

Publications (1)

Publication Number Publication Date
GB2104780A true GB2104780A (en) 1983-03-16

Family

ID=23089557

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08219949A Withdrawn GB2104780A (en) 1981-07-17 1982-07-09 Plant-protection compositions in the form of granules

Country Status (21)

Country Link
JP (1) JPS5824501A (en)
KR (1) KR840000174A (en)
AU (1) AU8603082A (en)
BE (1) BE893863A (en)
BR (1) BR8204156A (en)
DD (1) DD202231A5 (en)
DE (1) DE3226534A1 (en)
DK (1) DK321582A (en)
ES (1) ES8308200A1 (en)
GB (1) GB2104780A (en)
GR (1) GR77225B (en)
IL (1) IL66268A0 (en)
IT (1) IT1156309B (en)
LU (1) LU84274A1 (en)
MA (1) MA19537A1 (en)
NL (1) NL8202814A (en)
OA (1) OA07150A (en)
PL (1) PL237496A1 (en)
PT (1) PT75263B (en)
SE (1) SE8204345L (en)
ZA (1) ZA825064B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2139893A (en) * 1983-05-03 1984-11-21 Wellcome Found Pesticidal composition
GB2184946A (en) * 1986-01-06 1987-07-08 Novo Industri As Effervescent pesticidal composition for water treatment
US4933000A (en) * 1987-10-05 1990-06-12 Ciba-Geigy Corporation Herbicidal compound concentrate
EP0985347A1 (en) * 1996-05-07 2000-03-15 Hiroshi Kawai Effervescent preparation for plants
US20140106973A1 (en) * 2012-01-19 2014-04-17 Shandong Weifang Rainbow Chemical Co., Ltd. Water-Soluble Granule Formulation of 2,4-D Salt and Preparation Method Thereof
WO2022210001A1 (en) 2021-04-01 2022-10-06 Nec Corporation Method for reporting a timing advance, user equipment, and network node

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61183219A (en) * 1985-02-07 1986-08-15 Takeda Chem Ind Ltd Production of foamable composition
ATA136687A (en) * 1987-05-27 1993-09-15 Technica Entwicklung METHOD AND DEVICE FOR ELIMINATING STRESSES ON CULTIVATED PLANTS DUE TO EXCESS OF NUTRIENTS
EP0391851B1 (en) * 1989-04-07 1994-06-22 Ciba-Geigy Ag Concentrates of pesticidal active agents and their preparation
EP0641161B1 (en) * 1991-08-16 1996-10-09 Pbi/Gordon Corporation Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicides and method of preparing same
BR9408403A (en) * 1993-12-22 1997-08-05 Zeneca Ltd Herbicidal composition and process to control undesirable vegetation
JP5415042B2 (en) * 2008-08-19 2014-02-12 株式会社エス・ディー・エス バイオテック Herbicidal composition and herbicidal method
CN111466374A (en) * 2020-05-11 2020-07-31 赵邦斌 Pesticide soluble granule and preparation method thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2139893A (en) * 1983-05-03 1984-11-21 Wellcome Found Pesticidal composition
GB2184946A (en) * 1986-01-06 1987-07-08 Novo Industri As Effervescent pesticidal composition for water treatment
US4933000A (en) * 1987-10-05 1990-06-12 Ciba-Geigy Corporation Herbicidal compound concentrate
EP0985347A1 (en) * 1996-05-07 2000-03-15 Hiroshi Kawai Effervescent preparation for plants
EP0985347A4 (en) * 1996-05-07 2002-10-09 Hiroshi Kawai Effervescent preparation for plants
US20140106973A1 (en) * 2012-01-19 2014-04-17 Shandong Weifang Rainbow Chemical Co., Ltd. Water-Soluble Granule Formulation of 2,4-D Salt and Preparation Method Thereof
US9854798B2 (en) * 2012-01-19 2018-01-02 Shangdong Weifang Rainbow Chemical Co., Ltd. Water-soluble granule formulation of 2,4-D salt and preparation method thereof
WO2022210001A1 (en) 2021-04-01 2022-10-06 Nec Corporation Method for reporting a timing advance, user equipment, and network node

Also Published As

Publication number Publication date
AU8603082A (en) 1983-01-20
BE893863A (en) 1983-01-17
MA19537A1 (en) 1983-04-01
ZA825064B (en) 1983-04-27
NL8202814A (en) 1983-02-16
IL66268A0 (en) 1982-11-30
PT75263A (en) 1982-08-01
DE3226534A1 (en) 1983-02-03
ES513922A0 (en) 1983-08-16
JPS5824501A (en) 1983-02-14
SE8204345L (en) 1983-01-18
DD202231A5 (en) 1983-09-07
ES8308200A1 (en) 1983-08-16
IT1156309B (en) 1987-02-04
DK321582A (en) 1983-01-18
KR840000174A (en) 1984-02-18
PT75263B (en) 1985-10-04
PL237496A1 (en) 1983-05-23
GR77225B (en) 1984-09-11
BR8204156A (en) 1983-07-12
SE8204345D0 (en) 1982-07-15
IT8222407A0 (en) 1982-07-15
LU84274A1 (en) 1984-03-22
OA07150A (en) 1984-03-31

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