AU725067B3 - Herbicidal composition and adjuvants - Google Patents
Herbicidal composition and adjuvants Download PDFInfo
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- AU725067B3 AU725067B3 AU19472/00A AU1947200A AU725067B3 AU 725067 B3 AU725067 B3 AU 725067B3 AU 19472/00 A AU19472/00 A AU 19472/00A AU 1947200 A AU1947200 A AU 1947200A AU 725067 B3 AU725067 B3 AU 725067B3
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- glyphosate
- composition
- salt
- ammonium salt
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Description
P/00/012 Regulation 3.2
AUSTRALIA
Patents Act 1990
ORIGINAL
COMPLETE SPECIFICATION PETTY PATENT Invention Title: HERBICIDAL COMPOSITION AND ADJUVANT The following statement is a full description of this invention, including the best method of performing it known to me: 1 Oocument9 2 Herbicidal Composition and Adjuvant The present invention relates to a herbicidal composition and in particular a composition containing the herbicide glyphosate.
N-phosphonomethylglycine, known by its common name glyphosate, is a well known broad spectrum herbicide which is widely used in domestic and broadacre weed control. Glyphosate is a water insoluble acid and is therefore formulated as a water soluble salt, generally the isopropylamine salt.
Glyphosate is sold and used in a range of formulation types. The manufacturers of glyphosate generally prepare it for transport and shipping as an aqueous concentrate from which commercial products can readily be prepared by dilution and in some cases the addition of additives.
Glyphosate may be formulated for sale as an aqueous concentrate which is diluted by the end user prior to application. Concentrates may be packaged with surfactants and may be used with adjuvants which are mixed with the herbicide in a spray tank before use. Glyphosate is also sold to domestic markets as a dilute solution packaged with a spray applicator ready for direct application to weeds.
Water soluble granules or powders are also available which contain a glyphosate salt and generally also a surfactant. These dry formulations are dissolved in water by the end user before application.
Despite the versatility of glyphosate it tends to be less stable in solution particularly concentrated solutions at low temperature and the high viscosity of concentrated solutions makes them difficult to pump and handle. There is a need for a glyphosate composition which is stable and easy to handle in a wide range of formulations.
We have now found that by mixing the isopropylamine salt of glyphosate with the ammonium salt of glyphosate, particularly in certain ratios, compositions are stable at a wide range of concentrations. For example, the viscosity of aqueous JD W:Veannie\5pcces60985 .DOC 3 solutions is reduced allowing the composition to be more easily dispensed or allowing the concentration to be significantly increased while remaining stable.
This finding was surprising as the ammonium salt of glyphosate is much less soluble than the isopropylamine salt.
In accordance with the invention we provide a glyphosate composition including the monoisopropylamine salt of glyphosate and the ammonium salt of glyphosate.
The ratio of said monoisopropylamine salt to said ammonium salt is typically in the range of from 80:20 to 97:3 based on the weight of glyphosate in the acid form. In this ratio of salt the composition is surprisingly versatile allowing extremely high concentrations to be handled -more easily and with enhanced stability.
In a particularly preferred embodiment of the invention the weight ratio of said monoisopropylamine salt to said ammonium salt is in the range of 85:15 to 95:5 based on the weight of glyphosate in the acid form.
The glyphosate composition of the invention may use glyphosate at a wide range of concentrations. For example the composition may have a high concentration of 600g/litre or more such as may be used for transport and shipping, it may be a concentrate of the type to be diluted prior to use or it may be a dilute composition prepared from the concentrate or of the type sold in spray packs for domestic use.
It is desirable to sell and transport glyphosate as a high concentration aqueous solution however the useful concentration of conventional compositions is limited by viscosity of the formulation and its solution stability. Conventional glyphosate compositions become increasingly viscous in aqueous solution at concentrations above 300g/L (based on the acid form) and particularly from about 360g/L with the result that at high concentrations they cannot as readily be dispensed by the end user. The pumps used by farmers to dispense herbicides do not readily allow delivery of compositions containing over 490g/L glyphosate. At high JO W:Veannie\pecies%09885 DOC concentrations glyphosate is also less stable in solution, particularly at low temperatures.
The glyphosate concentrate compositions of the invention will typically include at least 300g/L of glyphosate. The compositions of the invention are particularly advantageous when they include at least 360g/L glyphosate based on acid form and preferably they include at least 450g/L. Even more preferably the concentration is at least 490g/L and most preferably the glyphosate concentration is at least 500g/L. We have found that concentration of up to 540g/L or more may be formed with a viscosity allowing easy dispensing by the container pump systems used by farmers. Further the composition is generally stable even at low temperatures for example at Manufacturing concentrates may be prepared with concentrations of as high as 620g/L or more. Although concentrated compositions of at least 360g/L glyphosate are preferred the composition of the invention may be in the form of a diluted composition if desired. The concentration will preferably be at least 3.6g/L For example it may be in the form of a dilute formulation prepared from a concentrate before application or it may be a dilute solution of the type packaged for the domestic market.
The composition of the invention may and typically will contain other additives.
For example the composition may include a surfactant component. The surfactant component may include one or more surfactants and is preferably present in an amount of up to 20% by weight of the total composition. In cases where the surfactant is present at the upper end of this range the glyphosate concentration will be relatively low. More preferably the surfactant is present in an amount of up to 5% by weight of the total composition. At such surfactant concentrations higher amounts of glyphosate may be used to provide at least 500 g/L glyphosate.
Examples of surfactants which may be useful include alkanolamides, betaine derivatives, ethoxylated propoxylated block copolymers, glycerol esters, glycol JD W.eanniespeces\sO9885.DOC esters, imidazolines and imidazoline derivatives, lanolin derivatives, lecithin derivatives, tertiary or quaternary polyoxyalkylene alkylamines, polyoxyalkylene and non-polyoxyalkylene alkylamine oxides, polyoxyalkylene alkylethers, polyoxyalkylene alkylarylethers, polyoxyalkylene alkylesters, alkoxylated and nonalkoxylated sorbitan esters, alkyl glycosides, alkyl polyglycosides, sucrose esters, sucrose glycerides, alkyl sulfates or phosphates, olefin sulfonates, alkylaryl sulfonates, polyoxyalkylene alkylether sulfates or phosphates, sulfosuccinate derivatives, sulfosuccinamates, taurates, sulfates and sulfonates of oils, fatty acids, alcohols, alkoxylated alcohols, fatty esters and aromatic derivatives and mixtures thereof.
We have found the properties of the composition are particularly useful when the surfactant includes a phosphate ester, particularly an ethoxylated alcohol phosphate ester which may be in the form of a salt such as the ammonium or alkylamine salt such as the monoisopropylamine salt. It is particularly preferred that the surfactant includes the ammonium salt of the ethoxylated alcohol phosphate ester.
It is often desirable to use other herbicides in combination with glyphosate. In some cases these other herbicides can be mixed with the glyphosate composition and additives shortly before application. Dinitroanilines are one of the most commercially successful classes of herbicides. In particular, trifluralin is widely used in pre-sowing application to soil in many important crops. It is effective against both grassy weeds and broad-leave weeds. Herbicides of the triazine family, particulary atrazine, are also used at the time of sowing crops, particularly canola.
In order to kill the maximum number of weeds the timing for application of glyphosate needs to be left until shortly before sowing. This also coincides with the optimal timing for dinitroanilines and triazines. If glyphosate and dinitroanilines or triazines could be effectively applied together this has the potential to allow better knockdown. It would also allow farmers to sow a crop at the optimal time to maximise yield and reduce competition from weeds. Tank JD W:DeannielspeCies%09885 DOC mixing of the herbicides would reduce the labour and cost associated with separate applications which are currently required.
Existing formulations of glyphosate are generally incompatible with dinitroanilines and triazines. For example mixture with trifluralin or atrazine can result in phase separation when the herbicides are combined. Also their combined use has been found to seriously reduce the efficacy of the compositions.
Surprisingly we have found that when the ammonium salt of an ethoxylated alcohol phosphate ester is used as the surfactant in the compositions of the invention the formulation is compatible with dinitroanilines or triazines and mixtures of these herbicides with glyphosate do not generally suffer loss of efficacy to the same extent as conventional formulations. Indeed there is a significant improvement in efficacy when compared with combinations of the presently available herbicide compositions at corresponding concentrations.
Accordingly in a preferred embodiment of the invention we provide a glyphosate formulation including the monoisopropylamine salt of glyphosate and the ammonium salt of glyphosate wherein the ratio of said monoisopropylamine salt and ammonium salt is in the range from 80:20 to 97:3 (preferably 85:15 to 95:5) and therein the formulation includes a surfactant including the ammonium salt of an ethoxylated alcohol phosphate ester. The ethoxylated alcohol phosphate ester is preferably present in an amount of up to 5% by weight of the composition and most preferably from 0.5 to 5% by weight of the total composition.
The composition of the invention may be used as a stand alone product by diluting it with water to the required glyphosate concentration. It is desirable in many circumstances to use the herbicide composition in combination with an adjuvant. When the herbicide composition is to be used with other herbicides or with hard diluting water (over 1000 ppm) then use of an adjuvant is particularly preferred. Suitable adjuvants for use with glyphosate are known in the industry and they may be used if desired.
JD W.jeannie'speces609885.DOC 7 Suitable adjuvants include equivalently acceptable inorganic salts, dispersants, wetters and antifoam agents. Examples of acceptable inorganic salts include ammonium sulphate, ammonium nitrate, potassium phosphate, tetrapotassium pyrophosphate, sodium bisulphate, sodium sulfate, ammonium bicarbonate.
Ammonium sulphate is particularly preferred.
Examples of dispersants and wetters include the surfactants referred to above, however preferred dispersants include long aliphatic quaternary ammonium compounds, aliphatic amines, alkylpolysaccharides and ethoxylated phosphates.
Ethoxylated fatty amine surfactants such as soya amine ethoxylate and tallow amine ethoxylate alkylpolysaccharides and ethoxylated alcohol phosphate ester or mixtures, of two or more thereof, or with the above examples of surfactants are particularly useful.
The adjuvant may if desired contain crop oils such as paraffinic oils, vegetable oils or vegetable oil derivatives.
We have found that certain types of adjuvant components in combination provide compatibility with other herbicides such as triazine and dinitroanilines and a level of activity which is not readily obtained with existing adjuvants.
Accordingly in a further aspect the invention provides an adjuvant composition for use with glyphosate herbicide compositions the adjuvant including: ammonium sulphate or an alkylammonium sulphate; a surfactant component including an ammonium salt of an ethoxylated alcohol phosphate ester and an amphoteric surfactant.
The alkylammonium sulphate when present may be a mono-, di- or trialkylammonium sulphate. The alkyl group or groups preferably contain up to six carbon atoms, more preferably up to 4 carbon atoms and most preferably are isopropyl. Ammonium sulphate is preferably present.
JD W:eannie\species609885.DOC The amphoteric surfactant is preferably a phospholipid with an acidic buffer, particularly propionic acid.
The preferred concentration of components in the adjuvant are as follows: from 5 to 30% w/w of ammonium sulphate alkylammonium sulphate or mixture thereof; from 0 to 25% w/w, preferably from 0.5 to 25% w/w of ammonium salt of an ethoxylated alcohol phosphate ester and; from 0.5 to 10% w/w of amphoteric surfactant which is preferably a phospholipid.
The adjuvant of the invention may be used with the glyphosate composition of the invention or it may be used with other glyphosate compositions such as those which are commercially available from numerous sources. The adjuvant composition of the invention will generally be mixed with a glyphosate composition shortly before use. The composition will normally be mixed in the spray tank however it is preferred that at least a portion of the adjuvant to be used is added to the spray tank prior to the glyphosate. Preferably all of the adjuvant component to be used will be added to the spray tank prior to addition of the glyphosate composition.
The present invention will now be more fully described with reference to the following examples. It should be understood, however, that the description following is illustrative only and should not be taken in any way as a restriction on the generality of the invention described above. Where the concentration of glyphosate is expressed in grams per litre it is understood that this refers to grams of glyphosate as the acid form per litre of composition.
Examples 1 A glyphosate composition in accordance with the invention was prepared by combining the following components in the relative quantities specified: JD W.yeannie\species560988.DOC RAW MATERIAL-- Quantity
SKGIL
*Glyphosate Acid (Wetcake) 0.6287 2-Propanamine 100% w/w 0.1864 Ammonia (28% w/w) 0.0213 GERONOL CF/AR 0.0266 LUCONYL Green FK872 0.001 Process Water 0.3710 Specific Gravity 1.2350 *The glyphosate acid wetcake contained approximately 86% w/w glyphosate based on glyphosate acid (11% w/w water). The purity of the glyphosate was 96.5% on a dry basis.
The composition, which contains 540g/L glyphosate could readily be delivered using standard pumps used by farmers and was stable in solution at temperatures of 5°C for extended periods.
GERONOL CF/AR surfactant sold by Rhodia is the 2-propanamine salt of ethoxylated alcohol phosphate ester.
Example 2 An adjuvant formulation for use with a glyphosate composition was prepared by combining the following components in the relative quantities specified: RAW MATERIAL QUANTITY F-j KGIV-- Ammonium Sulphate 0.2550 RHODOFAC ARB-70 0.1786 Ammonia (28%w/w) 0.0510 Li-700 0.0455 Process Water 0.6320 Specific Gravity 1.162 JD W.jeannie\species'09885 DOC RHODOFAC ARB-70 sold by Rhodia is an ethoxylated alcohol phosphate ester and forms the ammonium salt in solution.
Li-700 from Loveland Industries Inc, U.S.A. is a mixture of soyal phospholipids and propionic acid.
The combination of components in the adjuvant composition generally allows for better physical compatibility and improved efficacy even in hard water.
It is to be understood that the invention described hereinabove is susceptible to variations, modifications and/or additions other than those specifically described and that the invention includes all such variations, modifications and/or additions which fall within the spirit and scope of the above description.
JD W.JeanniespedesW9885.DOC
Claims (3)
1. A glyphosate composition including the monoisopropylamine salt of glyphosate and the ammonium salt of glyphosate wherein the ratio of said monoisopropylamine salt to said ammonium salt is in the range of from 80:20 to 97:3 based on the weight of glyphosate acid in each form.
2. A glyphosate composition according to claim 1 in the form of an aqueous solution wherein the ratio of said monoisopropylamine salt to said ammonium salt is in the range of 85:15 to 95:5 and the glyphosate concentration is at least 490 g/l based on glyphosate acid.
3. A glyphosate composition according to claim 2 wherein the concentration of glyphosate in the aqueous solution is in the range of from 500 g/L to 620 g/L based on glyphosate acid. DATED: 24 February, 2000 PHILLIPS ORMONDE FITZPATRICK Attorneys for: NUFARM LIMITED. JD W:jeannie\species\609885DOC
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU19472/00A AU725067B3 (en) | 1999-10-13 | 2000-02-24 | Herbicidal composition and adjuvants |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AUPQ3393 | 1999-10-13 | ||
AUPQ3393A AUPQ339399A0 (en) | 1999-10-13 | 1999-10-13 | Herbicidal composition and adjuvant |
AUPQ4059A AUPQ405999A0 (en) | 1999-11-15 | 1999-11-15 | Herbicidal composition and adjuvant |
AUPQ4059 | 1999-11-15 | ||
AU19472/00A AU725067B3 (en) | 1999-10-13 | 2000-02-24 | Herbicidal composition and adjuvants |
Publications (1)
Publication Number | Publication Date |
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AU725067B3 true AU725067B3 (en) | 2000-10-05 |
Family
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Application Number | Title | Priority Date | Filing Date |
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AU19472/00A Ceased AU725067B3 (en) | 1999-10-13 | 2000-02-24 | Herbicidal composition and adjuvants |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007143788A1 (en) * | 2006-06-14 | 2007-12-21 | Eureka Agresearch Pty Ltd | Herbicidal composition and method for removing unwanted foliage |
US10736325B2 (en) | 2000-05-19 | 2020-08-11 | Monsanto Technology Llc | Surfactants and formulations |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0274369A1 (en) * | 1986-12-04 | 1988-07-13 | Monsanto Company | Glyphosate-ammonium sulfate herbicidal formulation |
EP0498145A1 (en) * | 1991-02-08 | 1992-08-12 | Monsanto Europe S.A./N.V. | Solid glyphosate compositions and their use |
WO1997036488A1 (en) * | 1996-03-29 | 1997-10-09 | Monsanto Europe S.A. | New use of n-(phosphonomethyl)glycine and derivatives thereof |
-
2000
- 2000-02-24 AU AU19472/00A patent/AU725067B3/en not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0274369A1 (en) * | 1986-12-04 | 1988-07-13 | Monsanto Company | Glyphosate-ammonium sulfate herbicidal formulation |
EP0498145A1 (en) * | 1991-02-08 | 1992-08-12 | Monsanto Europe S.A./N.V. | Solid glyphosate compositions and their use |
WO1997036488A1 (en) * | 1996-03-29 | 1997-10-09 | Monsanto Europe S.A. | New use of n-(phosphonomethyl)glycine and derivatives thereof |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10736325B2 (en) | 2000-05-19 | 2020-08-11 | Monsanto Technology Llc | Surfactants and formulations |
WO2007143788A1 (en) * | 2006-06-14 | 2007-12-21 | Eureka Agresearch Pty Ltd | Herbicidal composition and method for removing unwanted foliage |
AU2007260586B2 (en) * | 2006-06-14 | 2012-08-02 | Elders Toll Formulation Pty Ltd | Herbicidal composition and method for removing unwanted foliage |
US8461082B2 (en) | 2006-06-14 | 2013-06-11 | Eureka Agresearch Pty Ltd | Herbicidal composition and method for removing unwanted foliage |
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