AU648038B2 - Water-dispersible granules - Google Patents
Water-dispersible granules Download PDFInfo
- Publication number
- AU648038B2 AU648038B2 AU60925/90A AU6092590A AU648038B2 AU 648038 B2 AU648038 B2 AU 648038B2 AU 60925/90 A AU60925/90 A AU 60925/90A AU 6092590 A AU6092590 A AU 6092590A AU 648038 B2 AU648038 B2 AU 648038B2
- Authority
- AU
- Australia
- Prior art keywords
- weight
- granules
- water
- agents
- ammonium
- 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.)
- Ceased
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
- 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
-
- 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
Abstract
Novel water-dispersible granules of crop protection agents, in particular herbicides and growth regulators, are obtained when an aqueous dispersion or solution of 10 to 90% by weight of active substance is prepared with 10 to 90% by weight of solid wetting agents selected from the group comprising alkanesulphonates, alkylsulphonates, alkylnaphthalenesulphonates, alkylbenzenesulphonates, long-chain olefin sulphonates, alkyl polyol ether sulphonates, alkyl ether sulphates, alkyl ether phosphates, alkylsulphosuccinic monoesters, fatty acid isaethionates and fatty acid N-methyltaurides, or of an ammonium salt or a mixture of an ammonium salt and one or more of the above solid wetting agents, and 0 to 50% by weight of customary formulation auxiliaries, and granulating the mixture by the countercurrent or cocurrent method.
Description
Form COMMONWEALTH OF AUSTR 8 3 8 PATENTS ACT 1952-69 COMPLETE SPECIFICATION
(ORIGINAL)
Class Int. Class Application Number: Lodged: 9 0rr Complete Specification Lodged: Accepted: Published: Priority Related Art SName of Applicant: HOECHST AKTIENGESELLSCHAFT S 0* Address of Applicant: Actual Inventor Address for Service 50 Bruningstrasse, D-6230 Frankfurt/Main Republic of Germany 80, Federal HANS ROCHLING, JEAN KOCUR and KONRAD ALBRECHT WATERMARK PATENT TRADEMARK ATTORNEYS.
LOCKED BAG NO. 5, HAWTHORN, VICTORIA 3122, AUSTRALIA Complete Specification for the invention entitled: WATER-DISPERSIBLE GRANULES .The following statement is a full description of this invention, including the best method of performing it known to Us HOECHST AKTIENGESELLSCHAFT HOE 89/F 262 Dr. WE/AP Description Water-dispersible granules The present invention relates to novel water-dispersible granules for use in plant protection.
Plant protection agents are commercially available, mainly in the form of wettable powders, emulsifiable concentrates or aqueous dispersions. To prepare spray liquors, the agents are stirred into water.
Handling these presentation forms is not without problems. For example, the preparation and use of formulations of wettable powders often involve the occurrence of troublesome dust.
0*S@ 9 Emulsifiable concentrates contain solvents which may be readily inflammable, may irritate the skin or may cause troublesome odors.
Dispersions may form sediments upon long storage which can be difficult to shake up. Moreover, there are often problems in this type of formulation as regards the disposal of the packaging materials.
The water-dispersible granules (abbreviated do not have these disadvantages since they are free-flowing, low in dust and can be readily metered out. They can be packaged without problems in polyethylene containers, gusseted bags made of laminated film (paper/aluminum/ plastic) or cardboard boxes, all of which can be disposed of readily.
A large number of processes are available for the industrial preparation of dispersible granules (of. H.B. Ries "Granuliertechnik und Granuliergerate [Granulation Technology and Granulation Apparatuses]" in Aufbereitungstechnik No. 3, 1970, p. 147 and M. Rosch and 2 R. Probst in Verfahrenstechnik 9 (1975) p. 59 to 64).
In particular, it is known to prepare water-dispersible granules using the fluidized-bed process which can be carried out in countercurrent and in cocurrent.
US-A 3,920,442 and GB-A 1,401,304 as well as M. Rosch and R. Probst in Verfahrenstechnik 9 (1975) p. 59 describe the countercurrent process, while the cocurrent process is described in EP-A 0,026,918, EP-A-0,141,436 and EP-A 0,141,437 and also in Verfahrenstechnik 9 (1975), p. 61/62.
To guarantee perfect use, it is necessary for the water- *dispersible granules to be thoroughly wetted when they are introduced into water, to disintegrate as spontaneously as possible, and to form a suspension with good suspendibility.
However, the most important prerequisite for the usability of water-dispersible granules in practice is sufficiently high biological activity. There is a series of active substances which require the addition of wetting ,,20 agents to achieve their optimum biological action. Most of these wetting agents are liquid. If substantial amounts of these liquid wetting agents are used in liquid preparations such as, for example, emulsifiable concentrates, there are usually no problems. However, if this *25 formulation type is to be replaced by a WG formulation for the abovementioned reasons which are relevant to the S environment, there result considerable technical difficulties: the substantial amounts of liquid wetting agents, which are required in most cases, cannot be incorporated into the solid formulation mentioned.
Surprisingly, it has now been found that when certain solid wetting agents and/or ammonium salts are used, it is possible to prepare water-dispersible granules whose technical properties in use are perfect and whose 3 biological actions are not reduced compared with emulsifiable concentrates and often even improved.
The invention relates to water-dispersible granules which contain a) 10 to 90 by weight, preferably 20 to 80 by weight, of one or more plant protection agents, b) 10 to 90 by weight, preferably 20 to 85 by weight, of one or more solid wetting agents from the group containing alkanesulfonates, alkyl sulfates, alkylnaphthalenesulfonates, alkylbenzenesulfonates, long-chain olefinsulfonates, alkyl polyglycol ether sulfonates, alkyl ether sulfates, alkyl ether phosphates, alkylsulfosuccinic monoesters, fatty o acid isethionates and fatty acid N-methyltaurides, or of an ammonium salt, or of a mixture of an ammonium salt and one or more of the above solid wetting agents, and c) 0 to 50 by weight, preferably 0 to 15 by weight, of customary formulation agents, in particular from the group of the inert substances, fillers, dispersants, binders, wetting agents, penetrants, tackifiers, adhesives and antifoam agents.
Examples of active substances in which larger amounts of wetting agents in the formulations may be advantageous to increase their biological activity include the group of the herbicides and growth regulators, such as, for example, glufosinate-ammonium(D,L-phosphinothricin-ammonium), L-phosphinothricin-ammonium, D,L- and D-fenoxaprop-ethyl and diclofop-,methyl, as well as mixtures of racemic fenoxaprop-ethyl or D-fenoxaprop-ethyl with safeners such as, for example, from the series of the 1phenyltriazolecarboxylic esters (cf. EP-A-0,174,562, for example Examples 3 to 172 described therein, in particular fenchlorazole, ISO Document No. TC 81 N 896 of the Briti,:2 Standard Institution), from the series of the 1arylpyrazolecarboxylic acid derivatives (cf. European Patent Application No. 89,104,500.7, in particular 4 Examples 1 to 1236 therein), or from the series of the pyridazinone derivatives (cf. European Patent Application No. 89,109,649, Examples 1 to 222); furthermore mixtures of D,L- or D-fenoxaprop-ethyl with sulfonylureas such as the N-alkoxy- and N-alkylsulfonylaminosulfonylureas disclosed in EP-A 013,258, for example Hoe 75032 or other sulfonylureas such as DPX T 6376 (Ally(R), GropperR)), DPX-L 5300 (Granstar"R)) and DPX M 6316 (Harmony(R)) and the like, and also mixtures of D,L- or D-fenoxaprop-ethyl with the abovementioned safeners and the sulfonylureas mentioned; mixtures of D,L- or L-glufosinate-ammonium with other herbicides such as, for example, diuron, linuron, monolinuron, aminotriazole, imazapyr, oxyfluorfen, simazine, diuron simazine, and with sulfonylureas such as, for example, Hoe 75032, DPX T 6376 (Ally(R)), 0* GropperR), DPX L 5300 (Granstar")) and DPX M 6316 (Harmonya)), are also included.
e. The active substances mentioned are known and described in the publications mentioned or, most often, in "The Pesticide Manual", 8th edition, British Crop Protection Council, 1987. DPX-T 6376, DPX-L 5300 and DPX-M 6319 are commercially available herbicides manufactured by DuPont oe and described in "Farm Chemicals Handbook '89" (Meister Publishing Company, Willoughby, Ohio, 1989).
a* "425 Examples of suitable solid wetting agents in the waterdispersible granules according to the invention are: .sodium lauryl sulfate (for example (R)Texapon K12 or STexapon
Z),
sodium alkylnaphthalenesulfonates (for example (R)Supragil WP), alkylnaphthalenesulfonates (for example (R)Sellogen DFL), sodium oleoylmethyltauride (for example (R)Hostapon T), sodium dibutylnaphthalenesulfonate (for example (R)Leonil DB), sodium dodecylbenzenesulfonate (for example (R)Phenylsulfonate HS 90, R)Ufaryl DL 85 or "(Nansa HS di-sodium salt of iso-decylsulfosuccinic monoester (for 5 example Netzer IS), sodium lauryl ether phosphate (for example "(RForlanit P), sodium C 14
-C
19 -olefinsulfonate (for example (R)Hostapur OS), secondary n-alkanesulfonate (for example R'"Hostapur SAS), sodium alkyldiglycol ether sulfate (for example (R)Genapol LRO). The wetting agents mentioned are commercially availble.
The invention also relates to a process for preparing the water-dispersible granules according to the invention, which process comprises preparing a dispersion or solution of the, or of some of the, components b) and c), or of part of the components, in water, and granulating the dispersion or solution using the countercurrent or S* cocurrent process, if appropriate with the addition or 15 initial introduction of further customary granulation auxiliaries and of the remaining components. The waterdispersible granules according to the invention can be obtained analogously to the general processes for preparing granules mentioned at the outset. It is preferred to prepare the water-dispersible granules from solutions or dispersions by fluidized-bed granulation as described in EP-A 0,224,845 and German Patent 3,909,455.3.
As regards the use of combinations of wetting agents and ammonium salts, it has been disclosed that the biological activity of D,L- or L-glufosinate-ammonium can be enhanced by adding inorganic or organic ammonium salts such as, for example, ammonium sulfate, but also by urea (cf.
EP 0,036,106); however, only a limited addition of ammonium salts is possible in the case of liquid formulations of the active substances mentioned, because of the solubility properties of glufosinate-ammonium and ammonium sulfate. In the case of the granules according to the invention, in particular those with D,L- and L-glufosinate-ammonium as well as the mixtures of the two active substances with diuron, linuron, monolinuron, aminotriazole, oxyfluorfen, simazine, diuron simazine and the sulfonylureas Hoe 75032, DPX T 6376, DPX L 5300 and 6 DPX M 6316, it is possible, surprisingly, to replace the solid wetting agents completely or partially by ammonium salts such as, in particular, by ammonium sulfate, i.e., it is possible to prepare granules with good technical properties in use, in particular also granules having high salt contents. As component the water-dispersible granules according to the invention preferably contain one or more of the solid wetting agents or a mixture of an ammonium salt with one or more of the solid wetting agents, the ratio by weight of ammonium salt: wetting agent being up to 1.5:1, in particular up to 1:1.
It is surprising that by partially replacing the solid wetting agents by ammonium salts such as, for example, •inorganic ammonium salts, in particular ammonium sulfate, the same biological activity can be obtained, as is achieved in the corresponding formulation without ammounium salts. Such a replacement of solid wetting agent by ammonium salts can have considerable price advantages since ammonium salts such as, for example, ammonium sulfate, are considerably more inexpensive than solid wetting agents.
The invention also relates to the use of the water-dispersible granules according to the invention as plant protection agents, in particular as herbicidal agents.
"'25 The application rate depends on the particular active substance employed and can vary within broad limits; for o I example, in the case of herbicides, generally between 0.005 and 10 kg/ha of active ingredient.
V 0 When used, the granules according to the invention are processed with water (diluted) to give a spray liquor, analogously to wettable powders and liquid formulations, and they are applied to the plants or the areas under cultivation in this form. Apart from being metered out more easily and having better storability and other technical properties in use such as, for example, a better possibility for packaging, the active substances
SI
7 formulated in this manner have a very good biological activity which generally corresponds to the biological activity of liquid formulations or even surpasses the latter.
A. Preparation Examples General information on assessment and preparation The spontaneous dispersibility of the granule formulation is assessed using a scale from 1 to 4. For this purpose, 1 g of the granules is first transferred into a 1 1 measuring cylinder which is filled with standardized water (30 0 C, 342 ppm water hardness). After 1 minute, the measuring cylinder is slowly turned by 180"C and then returned to the initial position. This procedure is repeated three times. For the assessment, the scheme below is used.
o* Scale 1 All individual granules are dispersed.
6 If there are any undispersed granule particles, the cylinder is shaken another three times as described 2 minutes after commencement of the test and assessed as follows: 2 The granules are now completely dispersed.
S* 3 Residual granules are not dispersed.
4 Most of the granules are not dispersed.
The suspendibility was indicated as the amount of the preparation by weight) which is located in the upper nine tenths parts by volume of a suspension after a sedimentation time of 30 minutes has elapsed (see CIPAC- Handbook Vol. 1 (1970), p. 861).
8 The wet-screening residue is understood as meaning the amount of substance which remains on a screen of 250 pm or 71 pm after rinsing for 10 minutes with a defined amount of water. A description of the method can be found in "Specification for pesticides used in public health", WHO Geneva, p. 281 (1973).
A laboratory spray dryer (Bichi 190 (Bichi Laboratoriumstechnik GmbH, PO Box 11 54, 7332 Eislingen/Fils) is used for spray-drying smallish amounts, and a laboratory fluidized-bed granulator Buchi 710 is employed for fluidized-bed granulation.
For atches of up to 400 g of product, a laboratory fluidized-bed "Combi Coater" manufactured by Niro-Atomizer was used. Larger batches of up to 15 kg of product were carried ":15 out on a fluidized bed manufactured by Glatt (GPCG *e e Example 1 a) Dispersion for preparing the granules o. 111 g of a dispersion of the following composition are prepared: OB6r .20 9.30 by weight of D,L-fenoxaprop-ethyl, technical grade, 96.8 33.45 by weight of Na C 14
-C
1 ,-olefinsulfonate ((R)Hostapur OS) S* 0.90 by weight of defoamer SE 2 (defoamer based on silicone) 1.35 by weight of a cresol/formaldehyde condensation product (dispersant Hoe S 1494) 55.00 by weight of drinking water For this purpose, the components are mixed and the mixture is ground with the aid of a bead mill until of the particles have a size of 2 3 pm.
9 b) Preparation of the granules Approximately one third of the dispersion prepared under a) is spray-dried. The resulting fine powder is initially placed in a laboratory fluidized-bed granulator and granulated by spraying on the remainder of the dispersion.
Dry gas temperature: 50 In this manner, water-dispersible granules of the following composition are obtained: 20.66 by weight of D,L-fenoxaprop-ethyl, technical grade, 96.8 74.34 by weight of Na C 14
-C,
1 -olefinsulfonate ("(RHostapur OS) 2.00 by weight of defoamer SE 2 3.00 by weight of dispersant based on a cresol/ formaldehyde condensation product (dispersant Hoe S 1494) Yield: 90.5 Particle size 0.8 to 1.2 mm (granules): Spontaneous dispersibility: 1 Suspendibility: 88 *4 Example 2 a S a) Dispersion S *i 210 g of a dispersion of the following composition are prepared: 4.96 by weight of D,L-fenoxaprop-ethyl, technical grade, 96.8 10.80 by weight of Na alkyl diglycol ether sulfate ((R)Genapol LRO) 10 0.24 by weight of defoamer on silicone base (defoamer SE 2) 0.72 by weight of dispersant based on a cresol/ formaldehyde condensation product (dispersant Hoe S 1494) 7.28 by weight of aluminum silicate (Perlite 1-206, ground obsidian rock) 76.00 by weight of drinking water The components are mixed and the mixture is ground with the aid of a bead mill until 50 of the particles have a size of 2 3 pm.
b) Granules Approximately one third of the dispersion prepared under a) is spray-dried. The resulting fine powder 0S 15 is initially placed in a laboratory fluidized-bed granulator and granulated by spraying on the remainder of the dispersion at a dry gas temperature of 65 0
C.
Granules of the following composition are obtained: 20 20.66 by weight of D,L-fenoxaprop-ethyl, technical grade, 96.8 45.00 by weight of "(RGenapol LRO 1.00 by weight of defoamer SE 2 a. 3.00 by weight of dispersant Hoe S 1494 30.34 by weight of "(RPerlite 1-206 Yield: 73.3 Particle size 0.8 to 1.3 mm (granules): Spontaneous dispersibility: 1 Suspendibility: 85 11 Example 3 Analogously to Examples 1 and 2, granules of the following composition are prepared: 10.31 by weight of D-fenoxaprop-ethyl, 97 45.00 by weight of Genapol LRO 1.00 by weight of defoamer SE 2 3.00 by weight of dispersant Hoe S 1494 40.69 by weight of 'R'Perlite 1-206
SI
0
I
S
'S
SI
S~
I.
Yield: Particle size (granules): Spontaneous dispersibility: Suspendibility: 73.2 0.7 to 1.2 mm 1 86 Example 4 Analogously to Examples 1 and 2, granules of the following composition are prepared: ease a 5555 0e*5 SBa S. 10.31 by weight of D-fenoxaprop-ethyl, 97 46.00 by weight of (R"Hostapur OS 1.00 by weight of defoamer SE 2 4.00 by weight of dispersant Hoe S 1494 38.69 by weight of "(RPerlite 1-206 20 as u~ S.
Yield: Particle size (granules): Spontaneous dispersibility: Suspendibility: 87.2 0.4 to 1.5 mm 1 92 Example Granules of the following composition are prepared as described in Examples 1 and 2: 12 10.31 by weight of D-fenoxaprop-ethyl, 97% 1.00 by weight of (R)Hostapur OS 45.00 ght of secondary alkanesulfonate ((R)Hostapur SAS) 1.00 by weight of defoamer SE 2 4.00 by weight of dispersant Hoe S 1494 38.69 by weight of (Rperlite 1-206 Yield: Particle size (granuales): Spontaneous dispersibility: Suspendibility: 81.4 0.5 to 1.1 mm 2 82 Example 6 Granules of the following composition are prepared analogously to Examples 1 and 2: 0 0050 .20 00 0
S.
0 0@ *0 S.
@0 0 0 25 .00.00 0 10.31 1.00 45.00 1.00 4.00 38.69 by weight of D-fenoxaprop-ethyl, 97 by weight of (R)ostapur OS by weight of (R)Uf aryl DL-85 (sodium dodecylsulfonate) by weight of defoaxner SE 2 by weight of Hoe S 1494 by weight of (R)Perlite 1-206 Yield: Particle size (granules): Spontaneous dispersibility: Suspendibility: 74.2 0.4 to 009 mmn 1 79 Example 7 Granules of the following composition are prepared analogously to Examples 1 and 2: 10.31 by weight of D-fenoxaprop-ethyl, 97 13 5.06 by weight of safener fenchiorazole, 98.9 46.00 by weight of MRHostapur OS 1.00 by weight of defoamer SE 2 4.00 by weight of dispersant Hoe S 1494 33.63 by weight of Perlite 1-206 Yield: Particle size (granules): Spontaneous dispers ibility: Suspendibility: 78.8 0.05 to 1. 2 mm 1 88% go** ::1 0:.90 Example 8 Granules of the following composition are prepared analogously to Examples 1 and 2: .31 5.06 1.00 45.00 1.00 4.00 33.63 by weight of D-fenoxaprop-ethyl, 97 by weight of safener fenchlorazole, 98.8 by weight of (R)Hostapur OS by weight of (R)Hostapur SAS by weight of defoainer SE 2 by weight of Hoe S 1494 by weight of Perlite 1-206 see* .::20 1. 0 0*
S
*5 Yield: Particle size (granules): Spontaneous dispers ibility: Suspendibility: 81.7 0. 3 to 0. 8 mm 1 91%
S.
S S
S
IS
S S Example 9 Granules of the following compositL.)n are prepared analogously to Examples 1 and 2: 10.31 by weight of D-fenoxaprop-ethyl, 97 5.06 by weight of safener fenchlorazole, 98.9 1.00 by weight of (R)Hostapur OS 14 45.00 by weight of (R)Genapol IJRO 1.00 by weight of defoamer SE 2 4.00 by weight of dispersant Hoe S 1494 33.63 by weight of (R)Perlite 1-206 Yield: Particle size (granules): Spontaneous dispersibility; Suspendibility: 87.4 0. 4 to 1. 1 mm 1 89 *460 0 0 6 00S 0 to Example Granules of the following composition are prepared analogously to Examples 1 and 2: 10.31 by weight of D-fenoxaprop-ethyl, 97 *5.06 by weight of safener fenchiorazole, 98.83 615 1.00 by weight of (R)Hostapur OS 45.00 by weight of ")Ufaryl 1.00 by weight of defoamer SE 2 4.00 by weight of Hoe S 1494 *33.63 by weight of (R)Perlite 1-206 Yield: Particle size (granules): Spontaneous dispersibility: Suspendibility: 85.2 0.4 'to 0. 9 mm 2 83 44 44 4 4
S
4 0*454 S S S Example 11 Granules of the following composition are prepared analogously to Examples 1 and 2: 12.90 by weight of D-fenoxaprop-ethyl, 93 6.30 by weight of safener fenchlorazole, 96 54.00 by weight of (R)Hostapur OS 10.00 by weight of dispersant, based on a 15 sulfonated cresol/formaldehyde condensation product, Na salt (")Rapidamin Reserve C) 0.50 by weight of defoamer SE 2 15.30 by weight of kaolin 1777 (finely divided clay) 1.00 by weight of residual moisture Suspendibility: 97 Wet-screening residue on 250 Am screen: trace Example 2 Granules of the following composition are prepared analogously to Examples 1 and 2: 12.90 by weight of D-fenoxaprop-ethyl, 93 6.30 by weight of safener fenchlorazole, 96 15 4.90 by weight of sulfonylurea herbicide DPXL 5300 ('"Granstar) 54.00 by weight of "(Hostapur OS 10.00 by weight of (RRapidamin Reserve C 0.50 by weight of defoamer SE 2 :20 10.40 by weight of kaolin 1777 1.00 by weight of residual moisture Suspendibility: 100 no wet-screening residue on 250 Am screen Yield: 87 Spontaneous dispersibility: 2 Suspendibility: 99.6 Particle size: 0.3 1.1 mm Example 13 21.05 by weight of glufosinate-ammonium, 95 30.00 by weight of R)Genapol LRO, dry matter 11.97 by weight of kaolin 7a (divided clay) 16 11.98 by weight of attacote (magnesium aluminum silicate) 5.00 by weight of dispersant Hoe S 1494 10.00 by weight of calcium acetate, dried (inert substance) 10.00 by weight of (R)Sipernat 50 S (precipitated silica) Glufosinate-ammonium, kaolin, attacote, calcium acetate and (R)Sipernat are mixed and the mixture is ground in a hammer bar mill. The resulting pulverulent mixture is initially introduced into a fluidized-bed granulator and granulated by spraying on an aqueous solution of S. R)Genapol LRO and dispersant Hoe S 1494.
S" Yield: 99
**O
15 Spontaneous dispersibility: 3 goes Suspendibility: 99.3 Particle size: 0.5 1.8 nmi Example 14 20.14 by weight of glufosinate-ammonium, 99.3 73.86 by weight of (R)Hostapur OS 4.00 by weight of (R)Luviskol K 30 (binder polyvinylpyrrolidone) 2.00 by weight of defoamer SE 2 Glufosinate-ammonium, R)Hostapur OS and (R)Luviskol K are mixed and the mixture is ground in a hammer bar mill.
The resulting pulverulent mixture is initially introduced into a fluidized-bed granulator and granulated by spraying on an aqueous solution of the defoamer.
Yield: 84.8 Spontaneous dispersibility: 1 Suspendibility: 99.5 Particle size: 0.4 1.3 mm 17 Example 30.21 by weight of glufosinate-ammonium, 99.3 68.00 by weight of Hostapur OS 2.00 by weight of defoamer SE 2 The pulverulent wetting agent is initially introduced.
The granules are prepared by spraying on a 50 strength solution of active substance.
Examples 16 In each of Examples 16 20 below, a mixture of pulver- 0 ized Na C 14
-C
1 g-olefinsulfonate ((R)Hostapur OS) or a mixture thereof with ammonium sulfate is initially introduced and the aqueous solution of glufosinateammonium is sprayed on to form granules.
0 f ee 6400
S.
S
1 Example No.
Glufosinateammonium (R)Hostapur
OS
20 20 20 20 20 78 58 40 20 40 20 S 0
S*
Ammonium sulfate 60 80 Defoamer SE 2 *0
S
2 2 The yields are between 86 and 91 the spontaneous dispersibility is 2, and the examples is more than 99 suspendibility in all Example 21 Granules of the following composition are prepared analogously to Examples 1 and 2: 18 12.00 by weight of glufosinate-ammonium 18.20 by weight of diuron, 99 16.00 by weight of ")Hostapur OS 12.00 by weight of R)Genapol LRO 0.50 by weight of defoamer SE 2 5.00 by weight of sodium ligninsulfonate, degree of sulfonation 0.17 ((RVanisperse CB) 35.30 by weight of kaolin 1777 1.00 by weight of residual moisture; Suspendibility: 99 no wet-screening residue on 250 pm screen Example 22 Granules of the following composition are prepared Sanalogously to Examples 1 and 2: 12.00 by weight of glufosinate-ammonium 18.20 by weight of diuron, 99 28.00 by weight of (R)Hostapur OS 5.00 by weight of (R)Rapidamin Reserve C 0.50 by weight of defoamer SE 2 *20 35.30 by weight of kaolin 1777 1.00 by weight of water *1 e Suspendibility: 95 no wet-screening residue on 250 pm screen
*B
Example 23 Granules of the following composition are obtained analogously to Examples 1 and 2: 10.00 by weight of glufosinate-ammonium 16.70 by weight of linuron, 95.8 25.00 by weight of CR)Hostapur OS 5.00 by weight of (R)Rapidamin Reserve C 0.50 by weight of defoamer SE 2 19 41.80 by weight of kaolin 1777 1.00 by weight of residual moisture Suspendibility: 97 no wet-screening residue on 250 Am screen B. Biological Examples Seeds or rhizome pieces of monocotyledon and dicotyledon weeds, or seeds of crop plants, are placed in sandy loam soil in plastic pots, covered with soil and grown in the greenhouse under good growth conditions. Three weeks after sowing, the test plants are treated in the threeleaf stage.
o The water-dispersible granules, wettable powders or aqueous solutions are sprayed onto the green parts of the plants at various dosage rates at an application rate of water of 200 to 800 1/ha (converted) and, after the test plants have stood in the greenhouse under optimum growth conditions for the period indicated, the effect of the preparations was scored visually in comparison with 060* O* untreated controls.
0* 1. Comparison between a liquid formulation of glufo- 0 sinate-ammonium (SL) with two water-dispersible granules (WG) of glufosinate-ammonium as claimed in the present invention.
*0
S
S S 20 Product Application rate Effect on Commelina conimunis 11 14 21 days after application Glufosinateammonium SL WG as in Example 13 WG as in 01, Example 14 2 1/ha 3 1/ha 2 kg/ha 3 kg/ha 2 kg/h~a 3 kg/ha e.g 9 US C 9* *0 @606 6O 9* 0 4 *0 99 6 9069 SL aqueous solution 2. Comparison of tank mixes of a liquid formulation of glufosinate-ammonium. (SL) and formulations of linuron and diuron, respectively, as wettable powders, with the corresponding WG formulations.
0* 0S S 09 60 00 C C 0 0 *00600 0 r 21 Product Application rate 1 or kg/ha.
Effect 18 days application VF LOM af ter
HV
Tank mix Glufosimateaimoniumn SL (20 Linuron WP (48.5 0.156 0.3125 0.11 0.21 0.625 0.42 1.25 G,.84 5.0 1.68 3.37 C S 0e* S S. S S S
S.
e.g.
4* *4 0 OSSG 1~
V.-
85 0 C WG as in Example 23 0.312 0.625 1.25 2.5 10.0 42 83 99 100 100 40 62 85 96 99 100 33 48 90 100 100 100 100 100 100 63 82 1 C 1 100 100 100 100 100 13 77 99 100 100 0 20
S
S. S
C*
C S
S.
Tank mix Glufosimateammonium SL (20 Diuron WP 0.156 0.31 0.0586 0.117 0.625 0.235 1.25 0.469 100 25 0.938 1.875 WG as in Example 22 0.26 0.52 1.04 2.08 4.17 8.33 100 100 45 77 100 100 100 100 100 100 32 68 100 100 100 22 (Example 2, continuation) Product Application rate 1 or kg/ha Effect 18 days after application VF LOM MV go*** WG as in 0.26 43 33 28 Example 21 0.52 65 88 1.04 85 98 2.08 96 100 100 4.17 99 100 100 8.33 100 100 100 1 or kg/ha 1/ha in the case of SL and kg/ha in the case of WG WP wettable powder SL aqueous solution VF Vicia faba (broad bean) LOM Loli-J um multiflorum (ray grass) NV Hordeum vulgare (barley) 3. Comparison of glufosinate-amnmonium WG formulations in which increasing am~ounts of wetting agent were replaced by ammonium sulfate.
Preparation Example No. 16 17 18 19 Glufosinate- 20 20 20 20 20 1 amnmonium Hostapur OS 78 58 40 20 Ammonium 20 40 60 80 sulfate Herbicidal action in barley
SB
*B B .0 05 55 SO B S B
B
501GB 0 a S I I 23 The symbols denote: same action as glufosinate-ammonium SL (20 slightly less action than glufosinate-ammonium SL markedly less action than glufosinate-ammonium SL 4. Comparison of a liquid formulation (EW) of D-fenoxaprop-ethyl and a tank mix of this liquid formulation with herbicide DPX L 5300 ('(RGranstar) with corresponding water-dispersible granules according to the invention (WG formulations).
The formulations are applied in the post-emergence method as described above, and, after 19 days, the plants are scored in comparison with untreated plants. The results 15 are compiled in Table 4.
The abbreviations in Table 4 denote: EW-1 Liquid formulation with 75 g/kg D-fenoxapropethyl and 37.5 g/kg fenchlorazole WG-11 WG according to Preparation Example 11 WG-12 WG according to Preparation Example 12 HV Hordeum vulgare (barley) ALM Alopecurus myosuroides (blackgrass) SIA Sinapis arvensis (wild mustard) VIA Viola arvensis (field violet) not tested S e 4 6 24 Table 4 Product Application rate kg/ha Action after 19 days in ALM S IA VIA EW,-1 WG-11 S S 6*S SS S S A *5tS a.
4* i5 0*S~* i 0S*e 0.20 0.40 0 .8 1.20 0. 125 0.2 0.50 0.75 0.2 0.4 0.8 1.2 0. 125 0.25 0.50 0.75 EW- 1 DPX L 5300 0.008 0.016 0.032 0.048 WG-)12 *too :*%20
I
as S.
a S
S
4 045.5 a
S
24a C: COMPARISON OF DUST GENERATION To prove the efficacy of water dispersible granules of the invention over those of prior art references, and, in particular, over AU-A-74984/87, the following tests were performed.
1. A defined by weight amnunt of the granule is allowed to fall down through a tube.
2. The amount of dust is quantified optically by the decrease of a ray of light.
Results show that water dispersible granules according to the instant application have a "dust-number" of 0.4, whilst those of AU-A-74984/87 have a "dust-number" of 6.7.
0*
B
*ol *00 *oo *o* aoo
Claims (6)
1. Water-dispersible granules which contain 10 to 90 by weight of one or more plant protection agents selected from the group consisting of D, L- and D-fenoxa-prop-ethyl and diclofop methyl; 10 to 90 by weight of one or more solid wetting agents from the group containing alkanesulfonates, alkyl culfates, alkylnaphthalenesulfonates, alkylbenzenesulfonates, long-chain olefinsulfonates, alkyl polyglycol ether sulfonates, alkyl ether sulfates, alkyl ether phosphates, alkylsulfosuccinic monoesters, fatty acid isethionates and fatty acid N- methyltaurides, or of an ammonium salt, or of a mixture of an ammonium salt and one or more of the above solid wetting agents; and 0 to 50 by weight of customary formulation agents, in particular from the group of the inert substances, fillers, dispersants, binders, wetting agents, penetrants, tackifiers, adhesives and antifoam agents and wherein said granules have a particle size of 0.3 to 1.8 mm.
2. Water-dispersible granules as claimed in claim 1 which contain 20 to 80 by weight of plant protection agents; S 20 to 85 of solid wetting agents and/or ammonium salts; and V 0 to 15 by weight of customary formulation agents.
3. The granules as claimed in claim 1 or 2, which contain solid wetting agent and ammonium salt in the ratio by weight of wetting agent:ammonium salt of up to 1.5:1. S 4. The granules as claimed in claim 3, wherein the ratio by weight is up to 9*•oo* S, 26 The granules as claimed in one or more of claims 1 to 4 wherein the plant protection agents contain herbi- cides from the group comprising D,L- and L-glufosinate- ammonium and D,L- and D-fenoxaprop-ethyl.
6. A process for preparing the water-dispersible granules defined in claim 1, which comprises preparing a disper- sion or solution of the, or of some of the, components b) and or of part of the components, in water, and granulating the dispersion or solution using the countercurrent or cocurrent process, if appropriate with the addition or initial introduction of further customary granulation auxiliaries and of the remaining components.
7. The use of the water-dispersible granules as defined in one or more of claims 1 to 5 as plant protection q' i agents. OeeS
8. A method of controlling undesired plant growth, which comprises dispersing the granules as defined in one or more of claims 1 to 5 in water to give a spray liquor and applying an effective amount of the spray liquor to the plants or the areas under cultivation. 0 I* S DATED this 10th day of August 1990. HOECHST AKTIENGESELLSCHAFT WATERMARK PATENT TRADEMARK ATTORNEYS "THE ATRIUM" 290 BURWOOD ROAD HAWTHORN. VIC. 3122. fV T l
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3926800 | 1989-08-14 | ||
| DE3926800A DE3926800A1 (en) | 1989-08-14 | 1989-08-14 | WATER-DISPERSIBLE GRANULES FOR USE IN PLANT PROTECTION |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU6092590A AU6092590A (en) | 1991-02-14 |
| AU648038B2 true AU648038B2 (en) | 1994-04-14 |
Family
ID=6387076
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU60925/90A Ceased AU648038B2 (en) | 1989-08-14 | 1990-08-13 | Water-dispersible granules |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0413267B1 (en) |
| JP (1) | JP2677702B2 (en) |
| KR (1) | KR0179457B1 (en) |
| AT (1) | ATE160071T1 (en) |
| AU (1) | AU648038B2 (en) |
| DE (2) | DE3926800A1 (en) |
| DK (1) | DK0413267T3 (en) |
| ES (1) | ES2110954T3 (en) |
| GR (1) | GR3025609T3 (en) |
| MX (1) | MX173277B (en) |
| ZA (1) | ZA906382B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU656735B2 (en) * | 1990-09-15 | 1995-02-16 | Bayer Cropscience Ag | Synergistic herbicidal agents |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5679618A (en) * | 1990-07-06 | 1997-10-21 | Hoechst Aktiengesellschaft | Antifoams for solid crop protection agents |
| FI93416C (en) * | 1991-09-27 | 1995-04-10 | Kemira Oy | Process for the preparation of a herbicide product in granular or tablet form |
| US5651975A (en) * | 1991-09-27 | 1997-07-29 | Harju-Jeanty; Pontus | Method for the preparation of herbicidal granular products comprising two separate phases |
| US5224428A (en) * | 1991-10-31 | 1993-07-06 | Wronkiewicz Robert D | Strengthened structure for a steering arm assembly having a compound radial fillet at juncture |
| DE59206550D1 (en) | 1991-11-08 | 1996-07-18 | Hoechst Schering Agrevo Gmbh | Water-dispersible granules from suspo emulsions |
| ZA93400B (en) * | 1992-01-24 | 1993-08-05 | Ici Australia Operations | Water dispersible granules of liquid pesticides. |
| ATE139908T1 (en) * | 1992-03-17 | 1996-07-15 | Hoechst Schering Agrevo Gmbh | DEFOAMERS FOR SOLID PLANT PROTECTIVE PRODUCTS |
| DK169734B1 (en) * | 1993-03-09 | 1995-01-30 | Kvk Agro As | Herbicide preparation, method of preparation thereof and activating additive for admixture with herbicide preparations |
| JP3339907B2 (en) * | 1993-03-15 | 2002-10-28 | 竹本油脂株式会社 | Collapse type pesticide granule composition |
| TR28994A (en) * | 1993-03-19 | 1997-07-21 | Kemira Oy | A method for obtaining herbicide (herbicide) granular products. |
| DE19633271A1 (en) | 1996-08-19 | 1998-02-26 | Basf Ag | Liquid formulation of ethyl (Z) -2-chloro-3- [2-chloro-5- (4,5,6,7-tetrahydro-1,3-dioxoisoindoldion-2-yl) phenyl] acrylate |
| DE59804135D1 (en) | 1997-02-05 | 2002-06-20 | Basf Ag | SOLID MIXTURES BASED ON SULFONYL UREAS AND ADJUVANTS |
| BR9807175A (en) | 1997-02-10 | 2000-04-25 | Takeda Chemical Industries Ltd | Granular agrochemical composition humectable or soluble in water, and processes to produce the same and to control a pest. |
| FR2782243B1 (en) * | 1998-08-14 | 2001-08-17 | Rhodia Chimie Sa | PREPARATION OF A SOLID PHYTOSANITARY COMPOSITION BY ATOMIZATION IN THE PRESENCE OF AN ANTI-FOAM AGENT |
| JP2003171214A (en) * | 2001-07-17 | 2003-06-17 | Yashima Chemical Ind Co Ltd | Granular herbicide |
| DE102004026937A1 (en) * | 2004-06-01 | 2005-12-22 | Bayer Cropscience Gmbh | Concentrated aqueous formulations for crop protection |
| DE102004026938A1 (en) * | 2004-06-01 | 2005-12-22 | Bayer Cropscience Gmbh | Low-foam aqueous formulations for crop protection |
| UA90171C2 (en) | 2005-09-09 | 2010-04-12 | Байер Кропсайенс Акциенгезельшафт | Fungicidal composition and process for the preparation thereof |
| LT1928232T (en) | 2005-09-16 | 2016-09-26 | Bayer Intellectual Property Gmbh | Solid formulation |
| EP1882414A1 (en) * | 2006-07-29 | 2008-01-30 | Bayer CropScience AG | Melt granules |
| WO2018095083A1 (en) | 2016-11-22 | 2018-05-31 | 浙江脉联医疗设备有限公司 | Pulse wave propagation time correction method |
| WO2019030092A1 (en) * | 2017-08-09 | 2019-02-14 | Basf Se | Herbicidal mixtures comprising l-glufosinate or its salt and at least one photosynthesis inhibitor |
| BR122024002212A2 (en) * | 2017-08-09 | 2024-03-12 | Basf Se | SYNERGISTIC PESTICIDE MIXTURE |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0036106A2 (en) * | 1980-03-04 | 1981-09-23 | Hoechst Aktiengesellschaft | Synergistic mixtures of phosphinothricine |
| AU7498487A (en) * | 1986-07-02 | 1988-01-07 | Kao Corp. | A process for the production of a granule-shaped composition comprising agricultural chemical compound |
| AU611593B2 (en) * | 1988-09-23 | 1991-06-13 | Rhone-Poulenc Chimie | Granules for spreading and process for their preparation |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE638296A (en) * | 1963-10-07 | |||
| US3737551A (en) * | 1969-08-20 | 1973-06-05 | Vanderbilt Co R T | Wettable and dispersible powders |
| GB1399005A (en) * | 1972-03-08 | 1975-06-25 | Ciba Geigy Ag | Herbicidal compositions |
| JPS609687B2 (en) * | 1976-12-24 | 1985-03-12 | 三共株式会社 | Methomyl wettable powder composition with suppressed dust generation |
| DE3333872A1 (en) * | 1983-09-20 | 1985-03-28 | Norddeutsche Affinerie AG, 2000 Hamburg | GRANULATED COMPOSITION OF AQUEOUS OR INSOLUBLE IN WATER DISPERSABLE IN AQUEOUS MEDIA |
| JPH0676284B2 (en) * | 1984-05-24 | 1994-09-28 | アメリカン・サイアナミド・カンパニー | Water-dispersible granular pest control composition and method for producing the same |
| JPH0678204B2 (en) * | 1986-01-23 | 1994-10-05 | ヘキスト アクチエンゲゼルシヤフト | Herbicide microgranule and method for producing the same |
| BR8600462A (en) * | 1986-02-04 | 1987-09-01 | Monsanto Brasil | HERBICIDE FORMULATION |
| NZ231897A (en) * | 1988-12-30 | 1992-09-25 | Monsanto Co | Dry water-soluble granular composition comprising glyphosate and a liquid surfactant |
-
1989
- 1989-08-14 DE DE3926800A patent/DE3926800A1/en not_active Withdrawn
-
1990
- 1990-08-10 EP EP90115360A patent/EP0413267B1/en not_active Expired - Lifetime
- 1990-08-10 ES ES90115360T patent/ES2110954T3/en not_active Expired - Lifetime
- 1990-08-10 DE DE59010773T patent/DE59010773D1/en not_active Expired - Fee Related
- 1990-08-10 AT AT90115360T patent/ATE160071T1/en not_active IP Right Cessation
- 1990-08-10 DK DK90115360T patent/DK0413267T3/en active
- 1990-08-13 KR KR1019900012434A patent/KR0179457B1/en not_active IP Right Cessation
- 1990-08-13 ZA ZA906382A patent/ZA906382B/en unknown
- 1990-08-13 AU AU60925/90A patent/AU648038B2/en not_active Ceased
- 1990-08-13 JP JP2211760A patent/JP2677702B2/en not_active Expired - Lifetime
- 1990-08-14 MX MX021975A patent/MX173277B/en unknown
-
1997
- 1997-12-05 GR GR970403254T patent/GR3025609T3/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0036106A2 (en) * | 1980-03-04 | 1981-09-23 | Hoechst Aktiengesellschaft | Synergistic mixtures of phosphinothricine |
| AU7498487A (en) * | 1986-07-02 | 1988-01-07 | Kao Corp. | A process for the production of a granule-shaped composition comprising agricultural chemical compound |
| AU611593B2 (en) * | 1988-09-23 | 1991-06-13 | Rhone-Poulenc Chimie | Granules for spreading and process for their preparation |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU656735B2 (en) * | 1990-09-15 | 1995-02-16 | Bayer Cropscience Ag | Synergistic herbicidal agents |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0413267A1 (en) | 1991-02-20 |
| EP0413267B1 (en) | 1997-11-12 |
| ATE160071T1 (en) | 1997-11-15 |
| DE59010773D1 (en) | 1997-12-18 |
| JPH03193702A (en) | 1991-08-23 |
| KR0179457B1 (en) | 1999-04-01 |
| DE3926800A1 (en) | 1991-02-21 |
| KR910004093A (en) | 1991-03-28 |
| MX173277B (en) | 1994-02-14 |
| ES2110954T3 (en) | 1998-03-01 |
| DK0413267T3 (en) | 1998-07-27 |
| GR3025609T3 (en) | 1998-03-31 |
| AU6092590A (en) | 1991-02-14 |
| JP2677702B2 (en) | 1997-11-17 |
| ZA906382B (en) | 1991-05-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU648038B2 (en) | Water-dispersible granules | |
| KR920011035B1 (en) | Improved glyphosate formulations | |
| US5543385A (en) | Water-dispersible glufosinate granules | |
| JP2511431B2 (en) | Novel water dispersible granules and their uses | |
| JP3032545B2 (en) | Method for producing water-dispersible granules | |
| EP0638235B1 (en) | Solid formulation | |
| EP0141509A2 (en) | An easily water-dispersible procymidone-containing granular preparation | |
| AU637458B2 (en) | Water-dispersible granules of neophanes and azaneophanes for use in plant protection | |
| KR20050102662A (en) | Method for producing water-dispersible granules | |
| KR0142564B1 (en) | Paddyweed tablets or capsules | |
| EP0503869B1 (en) | Oxyfluorfen dispersible granule formulations | |
| JPH0640805A (en) | Water dispersible granular material of suspo-emulsion, preparation thereof and use thereof | |
| DD297055A5 (en) | WATER DISPERSIBLE GRANULES | |
| WO2002102152A1 (en) | Granulated wettable powder | |
| US20230309557A1 (en) | A solid agrochemical composition and process of preparation thereof | |
| CN110178847A (en) | Composition, preparation and its application | |
| PL140497B1 (en) | Liquid herbicide | |
| JPH0616502A (en) | Solid agricultural chemical composition for paddy field | |
| JPH05117102A (en) | Solid pesticide composition for paddy field | |
| JP2001192303A (en) | Method for using solid agrochemical preparation to be applied to flooded paddy field |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |