GB1594991A

GB1594991A - Pesticidal formulation

Info

Publication number: GB1594991A
Application number: GB5319/77A
Authority: GB
Original assignee: Lilly Industries Ltd
Current assignee: Lilly Industries Ltd
Priority date: 1977-02-09
Filing date: 1977-02-09
Publication date: 1981-08-05
Also published as: CS195654B2; PL109495B1; NZ186408A; PT67624A; IE46401B1; BR7800768A; TR19841A; PH14580A; AU520655B2; PT67624B; HU184155B; FR2379981B1; IL53989A; JPS53101529A; DD133890A5; PL204533A1; SE7801423L; DE2805251A1; ES466798A1; IL53989A0

Abstract

The composition contains 10 to 75% of a herbicidal derivative of 2,6-dinitroaniline, such as trifluralin, 0 to 60% of a water-immiscible solvent (the herbicide and the solvent forming a homogenous disperse phase), 0.5 to 10% of an emulsifying agent and 15 to 70% of an aqueous solution of an inorganic salt such as NaCl, the salt representing at least 5% of the aqueous solution which may also contain urea (percentages expressed by weight). The compositions thus possess satisfactory storage stability characteristics while containing high herbicide concentrations. They can be used in agriculture, in pre-emergence treatment.

Description

(54) PESTICIDAL FORMULATION (71) We, LILLY INDUSTRIES LIMITED, a British company of Lilly House, Hanover Square, London, WIR OPA, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- This invention relates to pesticidal formulations, and more particularly to herbicidal formulations in the form of aqueous emulsions containing high concentrations of herbicidal 2,6 - dinitroaniline derivatives, such as trifluralin, and to methods of making such formulations.

Herbicidal 2,6 - dinitroaniline derivatives characteristically possess a melting point which is less than 200"C and a solubility in water at 25"C which is less than 100 parts per million by weight. Such herbicidal derivatives have hitherto been formulated in a concentrated solution in a substantially water-immiscible organic solvent such as xylene, together with an emulsifying agent. These concentrated formulations are dispersed in large volumes of water prior to spraying on crop land.

The preparation of 2,6 - dinitroaniline derivatives, such as trifluralin, and their activity as pre-emergent herbicides is described in, for example, U.K. Patent Specification No. 917,253.

Although the known concentrated formulations of herbicidal 2,6dinitroaniline derivatives have proved to be highly effective in enabling large quantities of the pesticides to be stored in a relatively compact form whilst being readily dispersible in large volumes of water in preparation for spraying, they do suffer from the disadvantage that bulk storage of such formulations carries the unavoidable fire risk associated with storage of organic solvents, and the commercial penalty of the high cost of organic solvents. Hitherto it has not been possible to provide an aqueous pesticidal formulation containing a high concentration of a herbicidal 2,6 - dinitroaniline derivative and having satisfactory storage stability.

According to the present invention there Is provided a herbicidal formulation in concentrate form being an aqueous emulsion comprising 10% to 75% by weight of a herbicide being at least one herbicidal 2,6 dinitroaniline derivative having a solubility in water at 250C less than 100 parts per million by weight and a melting point in the range from -100C to 1500C, 0% to 60% by weight of a substantially water-immiscible solvent, the herbicide and the solvent forming a homogeneous disperse phase, 0.5% to 10% by weight of an emulsifying agent, and 15% to 70% by weight of an aqueous solution of an inorganic salt, the concentration of the inorganic salt in the aqueous solution being at least 5% by weight.

The herbicide may be a single herbicidal 2,6 - dinitroaniline derivative or a mixture of two or more such derivatives. If the herbicide is a mixture of 2,6 dinitroaniline derivatives, it is the mixture which must fulfil the melting point and water-solubility requirements.

Similarly the inorganic salt may be a single salt, such as sodium chloride, a double salt, such as sodium alum, or a mixture of salts. The salts should be such that the aqueous solution is substantially neutral, i.e. it has a pH not greater than 9. Examples of salts which have been found to be useful include sodium chloride, potassium chloride, ammonium chloride, calcium chloride, magnesium chloride, ammonium nitrate, sodium acetate, ammonium carbonate, copper sulphate, magnesium sulphate, sodium sulphate, aluminium sulphate, sodium ferric sulphate and potassium dihydrogen phosphate. Salts giving rise to strongly alkaline aqueous solutions, i.e. solutions having a pH greater than 9, such as sodium carbonate, potassium carbonate and potassium monohydrogen phosphate should be avoided.

The emulsifying agent may consist of a single emulsifying agent or it may be a blend of emulsifying agents, and it may be a non-ionic, anionic or cationic surfactant, a blend of two or more non-ionic surfactants, a blend of non-ionic and anionic surfactants or a blend of non-ionic and cationic surfactants. Non-ionic surfactants are preferred. The hydrophile - lipophile balance (HLB) of the emulsifying agent should be at least 12.

The substantially water-immiscible solvent may be a single organic solvent or it may be a blend of two or more such materials. It is essential for the solvent to be such as will dissolve the herbicide in the formulation and to be substantially immiscible with the aqueous phase of the emulsion. Desirably the solvent should not be soluble in the aqueous phase to an extent greater than 0.2% w/w, and preferably the solubility of the solvent in the aqueous phase is 0.2% w/w or less. The solvent may have a melting point at or above ambient termperatures. However, if this is the case, a mixture of the herbicide and the solvent in relative proportions equal to their relative proportions in the herbicidal formulation should desirably be liquid at ambient temperature. Examples of suitable solvents include aromatic hydrocarbons, such as xylenes, trimethylbenzenes and polynuclear aromatic hydrocarbons, such as naphthalene, alkylnaphthalenes and anthracene, halogenated aromatic hydrocarbons, such as o- chlorotoluene, aliphatic hydrocarbons, such as decane, and other organic solvents such as camphor, and miscible blends of two or more of such solvents. In the event that the herbicide is a liquid such as isopropalin, in some circumstances a herbicidal formulation according to the invention may not include any water-immiscible solvent other than the herbicide itself.

Preferably formulations in accordance with the invention contain from 15% to 70% by weight of the herbicide, from 0% to 45% by weight of the solvent, from 0.9% to 6% by weight of the emulsifying agent and from 20% to 40% by weight of the aqueous solution, the concentration of the inorganic salt in the aqueous solution being from 10% to 20% by weight.

Examples of suitable 2,6 - dinitroaniline derivatives include trifluralin, benfluralin, isopropalin, ethalfluralin, dinitramine, dipropalin, oryzalin, 4 methylsulphonyl 2,6 - dinitro - N,N - dipropylaniline, fluchloralin, penoxalin, profluralin, and dibutalin. These derivatives fall within the scope of the formula I:

where R' is hydrogen, C24 alkyl or chloroethyl, R2 is C25 alkyl, chloroethyl, 2 methallyl or cyclopropylmethyl, R3 is hydrogen, methyl or amino and R4 is trifluoromethyl, C13 alkyl, -SO2NH2 or -SO2CH3.

Pesticidal formulations in accordance with the present invention preferably have one or more of the following features: (a) the herbicide is a 2,6 - dinitroaniline derivative of formula II:

where R' is C24 alkyl or chloroethyl R2 is C alkyl, chloroethyl or 2 - methallyl and R3 iS hydrogen or amino, (b) the herbicide is a 2,6 - dinitroaniline derivaitve of formula II wherein R' is ethyl or propyl, R2 is propyl, butyl or 2 - methallyl and R3 is hydrogen, (c) the herbicide is trifluralin, (d) the herbicide forms 15% to 65% by weight of the formulation, (e) the herbicide forms at least 40% by weight of the formulation, (f) the herbicide forms at least 45% by weight of the formulation, (g) the herbicide forms not more than 60% by weight of the formulation, (h) the solvent forms not more than 50% by weight of the formulation, (i) the solvent forms 10% to 45% by weight of the formulation, (j) the solvent forms at least 15% by weight of the formulation, (k) the solvent forms not more than 25% by weight of the formulation, (1) the solvent is an aromatic hydrocarbon solvent, (m) the solvent is xylene or a mixture of xylene and naphthalene, (n) the emulsifying agent forms at least 0.9% by weight of the formulation, (o) the emulsifying agent forms at least 2% by weight of the formulation, (p) the emulsifying agent forms at least 3% by weight of the formulation, (q) the emulsifying agent forms not more than 7% by weight of the formulation, (r) the emulsifying agent forms not more than 6% by weight of the formulation, (s) the emulsifying agent is a non-ionic surfactant or a blend of two or more non-ionic surfactants, (t) the emulsifying agent has a calculated hydrophile - lipophile balance of at least 12, (u) the emulsifying agent has a calculated hydrophile-lipophile balance in the range of from 14 to 18, (v) the emulsifying agent has a calculated hydrophile - lipophile balance in the range of from 15 to 17, (w) the emulsifying agent has a calculated hydrophile - lipophile balance of substantially 16, (x) the aqueous solution forms not more than 50% by weight of the formulation, (y) the aqueous solution forms not more than 40% by weight of the formulation, (z) the aqueous solution forms not more than 35% by weight of the formulation, (aa) the aqueous solution forms not more than 25% by weight of the formulation, (ab) the aqueous solution forms at least 10% by weight of the formulation, (ac) the aqueous solution forms at least 15% by weight of the formulation, (ad) the aqueous solution forms at least 20% by weight of the formulation, (ae) the aqueous solution additionally includes urea at a concentration up to 25% by weight of the aqueous solution, (af) the inorganic salt is selected from sodium chloride, potassium chloride and calcium chloride, (ag) the inorganic salt is sodium chloride.

(ah) the concentration of the inorganic salt is at least 10% by weight, (ai) the inorganic salt forms substantially 15% of the aqueous solution.

When the herbicide is isopropalin it preferably forms 60% to 75% by weight of the formulation, no solvent is included, the emulsifying agent forms 2% to 6% by weight of the formulation and the aqueous solution forms 19% to 38% by weight of the formulation.

In accordance with a preferred aspect of the present invention there is provided a herbicidal formulation in concentrate form being an aqueous emulsion comprising: 40% to 60% by weight of trifluralin, 15% to 25% by weight of a substantially water-immiscible aromatic hydrocarbon solvent, the trifluralin and the solvent forming a homogeneous disperse phase, 3% to 6% by weight of a non-ionic surfactant or a blend of such surfactants, having a calculated hydrophile-lipophile balance in the range of from 15 to 17, and 22% to 32% by weight of an aqueous solution of sodium chloride, the sodium chloride concentration being in the range 10% to 18% by weight of the aqueous solution, the aqueous solution additionally including 0% to 5% of urea by weight of the solution.

The invention also provides a process for preparing a herbicidal formulation in concentrate form which process comprises agitating together a homogeneous organic phase containing 10% to 75% by weight of the formulation of a herbicide being at least one herbicidal 2,6 - dinitroaniline having a solubility in water at 250C less than 100 parts per million by weight and a melting point in the range of from -10"C to 1500C, and 0% to 60% by weight of the formulation of a substantially water-immiscible solvent, and an aqueous phase consisting of 15% to 70% by weight of the formulation of an aqueous solution of an inorganic salt, the concentration of the inorganic salt in the aqueous solution being at least 5% by weight, with 0.5% to 10% by weight of the formulation of an emusifying agent, until a stable emulsion is formed therefrom.

In the method of the present invention it is preferred for at least part of the emulsifying agent to be dissolved in the organic phase prior to agitation of the organic phase and the aqueous phase. The herbicide is preferably dissolved in the solvent, the resulting solution is filtered and the emulsifying agent is dissolved therein before addition thereto of the aqueous phase and agitation. The agitation is desirably continued until the mean droplet diameter of the organic phase is observed to be in the range 8 to 14 microns. Urea may be dissolved in the aqueous solution up to 25% by weight of the aqueous solution prior to agitation of the organic phase and the aqueous phase.

The invention further includes a method of inhibiting growth of weeds which method comprises dispersing in a large volume of water a herbicidal formulation according to the invention, and applying the dispersion formed thereby to a locus in which it is desired to inhibit the growth of weeds.

In the examples of the invention a number of emulsifying agents and solvents are referred to by their commercial names. The emulsifying agents are Remcopal NP 30, Remcopal PONF, Remcopal 25, Remcopal 0.11, Remcopal 273, Tensagex DP24, Stepan agent 555--66A, Stepan agent 555-66B, Ethomeen T.25, Renex 650, Brij 72 and Brij 78. The solvents are Aromasol H and Solvesso 100. (the foregoing names in this paragraph are all Registered Trade Marks). The chemical natures of these commercial materials insofar as they are known to the Applicant are as follows: Remcopal NP30--an ethoxylated nonyl phenol containing on average 30 ethoxy groups and having a hydrophile - lipophile balance (HLB) of 17.5, Remcopal PONF-an ethoxylated nonyl phenol containing on average 11 ethoxy groups and having an HLB of 13.7.

Remcopal 25-an ethoxylated oleo-cetyl alcohol containing on average 25 ethoxy groups and having an HLB of 16.2.

Remcopal 0.11-an ethoxylated octyl phenol containing on average 10.5 ethoxy groups and having an HLB of 13.8, Remcopal 273-an ethoxylated tridecylalcohol containing on average three ethoxy groups and having an HLB of 8.6, Stepan agents 55566A and 555-66B-blends of calcium dodecylbenzene sulfonate and alkylphenoxy polyoxyethylene ethanols, Ethomeen T.25-ethylene oxide condensation product of primary fatty amines containing on average 15 ethoxy groups, Renex 650--an alkylaryl ether having an HLB of 17.1, Brij 72-a polyoxyethylene stearyl ether having an HLB of 4.9, Brij 78-a polyoxyethylene stearyl ether having an HLB of 15.3, Aromasol H-an aromatic hydrocarbon solvent consisting predominantly of isomeric trimethylbenzenes and having a specific gravity of 0.879 and distillation range from 1680C to 2000 C, Solvesso 100--an aromatic hydrocarbon solvent consisting predominantly of C9 hydrocarbons but also containing some C8 and C,0 hydrocarbon and having a specific gravity of 0.872 and distillation range from 156"C to 1800C.

The invention will be better understood from the following illustrative Examples: EXAMPLE I Trifluralin, technical (96% pure) 500 gms Xylene 230 gms Emulsifying agent-(blend of 24.4 gm "Remcopal NP30" and 15.6 gm "Remcopal PONF") 40 gms Aqueous solution of sodium chloride (15% w/w) 310 gms Total: 1080 gms (1 litre) The trifluralin was dissolved in the xylene with gentle warming to 500C and the resulting solution was filtered through a fine grade (Whatman No. 42) filterpaper.

The emulsifying agent was added to the solution of trifluralin in xylene, and dissolved with gentle warming to 500 C. The aqueous solution of sodium chloride was added to the xylene solution with agitation. The resulting emulsion was opaque and orange-yellow in colour.

EXAMPLE 2 Trifluralin 500 gms Xylene 180 gms Naphthalene (technical grade) 60 gms Emulsifying agent as in Example 1 40 gms Aqueous solution of sodium chloride (15% w/w) 310 gms Total: 1090 gms (1 litre) The trifluraiin and naphthalene were dissolved in the xylene with gentle warming to 50"C, and the remaining steps in forming the emulsion were as in Example 1. The emulsion was opaque and orange-yellow in colour.

The formulations of Examples 1 and 2 were tested for stability by storing for one month at temperatures of -10"C, -2"C, room temperature, 40"C and 50"C.

There was no noticeable deterioration of the formulations under these conditions.

Both formulations remained free flowing at --180C, which was the lowest temperature at which they were tested.

Both emulsions flowed easily and were readily dispersed with slight agitation in large volumes of water.

EXAMPLE 3 A formulation was prepared in identical manner as in Example I except that the emulsifying agent used was 40 gms of Tensagex DP 24 supplied by Tensia S.A.

This emulsifying agent is an anionic surfactant. The resulting formulation was a stable orange-yellow opaque emulsion.

EXAMPLE 4 A formulation was prepared as in Example 3 except that the emulsifying agent used was 40 gms of a blend of 75% by weight Stepan agent 555--66A and 25% by weight Stepan agent 555-66B supplied by Stepan Chemical Company. Both Stepan agents are blends of anionic and non-ionic surfactants. The resulting opaque emulsion was stable and was orange-yellow in colour.

EXAMPLE 5 A formulation was prepared as in Example 3, except that the emulsifying agent used was 40 gms of Ethomeen T.25 supplied by Armour Hess Chemicals Limited.

This emulsifying agent is a cationic surfactant. The resulting emulsion was stable, was opaque in appearance, and was orange-yellow in colour.

EXAMPLE 6 A formulation was prepared as in Example 2, except that the aqeuous solution was 310 gms of an aqueous solution of sodium chloride (17% w/w).

EXAMPLE 7 A formulation was prepared as in Example 1 except that the aqueous solution was 310 gms of an aqueous solution of sodium chloride (13 /O w/w) and urea (4% w/w), EXAMPLE 8 A formulation was prepared as in Example 1, except that the aqueous solution was 310 gms of an aqueous solution of potassium dihydrogen phosphate (13% w/w).

EXAMPLE 9 A formulation was prepared as in Example I except that the aqueous solution was 310 gms of an aqueous solution of ammonium ferric sulphate (13% w/w).

EXAMPLES 10 to 15 Formulations were prepared as in Example 1 except that the following were used as the emulsifying agents:

Example Emulsifying Agent 10 Remcopal 25(36.7 gms) + Remcopal (3.3 gms) 11 Renex 650 (36.4 gms) + Brij 72 (3.6 gms) 12 Renex 650(15.6 gms) + Brij 78 (24.4 gms) 13 RemcopalNP3O(18.3gms) + Remcopal PONF(11.7 gms) 14 Remcopal NP30 (12.2 gms) + Remcopal PONF (7.8 gms) 15 Remcopal NP30 (6.1 gms) + Remcopal PONF (3.9 gms) EXAMPLE 16 A formulation was prepared as in Example 1, except that in place of the xylene there was employed 235 gms of Solvesso 100.

EXAMPLE 17 A formulation was prepared as in Example 1, except that in place of the xylene there was employed 240 gms of Aromasol H.

EXAMPLE 18 Trifluralin, technical (96% pure) 625 gms Xylene 181 gms Emulsifying agent (36.7 gms of Remcopal 25 and 3.3 gms of Remcopal 0.11) 40 gms Aqueous solution of sodium chloride (15% w/w) 266 gms Total: 1112 gms (1 litre) The above formulation was prepared by a similar method to that used in Example 1.

EXAMPLE 19 Trifluralin, technical (96% pure) 688 gms Xylene 119 gms Emulsifying agent (24.4 gms of Remcopal NP30 and 15.6 gms of Remcopal PONF) 40 gms Aqueous solution of sodium chloride (15% w/w) 289 gms Total: 1136 gms (1 litre) This formulation was prepared by a similar method to that used in Example 1.

The emulsions of Examples 6 to 19 were all stable emulsions opaque in appearance and orange-yellow in colour.

EXAMPLE 20 Benfluralin, technical (95% pure) 190 gms Xylene 317 gms Naphthalene (technical grade) 104 gms Emulsifying agent (38.9 gms of Remcopal 25 and 1.1 gms of Remcopal 273) 40 gms Aqueous solution of ammonium chloride (13% w/w) 362 gms Total: 1013 gms (1 litre) The above formulation was prepared by a similar method to that used in Example 1. The resulting stable emulsion was opaque and was yellow in colour.

EXAMPLE 21 Benfluralin, technical (95% pure) 190 gms Xylene 277 gms Cyclohexanone 130 gms Emulsifying agent (33.3 gms of Remcopal NP30 and 6.7 gms of Remcopal 273) 40 gms Aqueous solution of sodium chloride (15% w/w) 362 gms Total: 999 gms (I litre) This formulation was prepared by a method similar to that used in Example 1.

The resulting emulsion was identical in appearance to that of Example 20.

EXAMPLE 22 Ethalfluralin, technical (95% pure) 347 gms Xylene 361 gms Emulsifying agent (33.3 gms of Remcopal NP30 and 6.7 gms of Remcopal 273) 40 gms Aqueous solution of sodium chloride (15% w/w) 289 gms Total: 1037 gms (1 litre) The above formulation was prepared by a similar method to that of Example 1.

The resulting stable emulsion was opaque in appearance and yellow in colour.

EXAMPLE 23 A formulation was prepared as in Example 22, except that the aqueous solution was 282 gms of an aqueous solution of potassium chloride (13% w/w). The resulting emulsion was similar in appearance to that of Example 22.

EXAMPLE 24 A formulation was prepared as in Example 22 except that the aqueous solution was 289 gms of an aqueous solution of calcium chloride (13% w/w). The resulting emulsion was similar in appearance to those of Examples 22 and 23.

EXAMPLE 25 Isopropalin, technical (90% pure) 800 gms Emulsifying agent (33.3 gms of Remcopal NP30 and 6.7 gms of Remcopal 273) 40 gms Aqueous solution of sodium chloride (15% w/w) 338 gms Total: 1178 gms (1 litre) The emulsifying agent was dissolved in the isopropalin with gentle warming.

The aqueous solution of sodium chloride was added with agitation. The resulting stable emulsion was opaque and dirty orange-yellow in colour.

It should be noted that the emulsifying agent of each of Examples I to 25 has a calculated hydrophile-lipophile balance of substantially 16.

In the emulsions of Examples 1 to 25 above it has been found that the mean droplet diameter of the organic phase is in the range of from 8 to 14 microns. These emulsions have been found to disperse readily when added to 100 volumes of water and to remain substantially dispersed for several hours. Such dispersions are readily applied to crop land by conventional means such as spraying, and are therefore usable in a similar manner to the known concentrated formulations.

The emulsions of Examples 1, 2 and 4 to 25 exhibit particularly good stability under a variety of storage conditions. Coalescence of droplets and formation of upper or lower aqueous layers is very slow and samples may be stored for at least a year at 250C or 40"C without appreciable coalescence. The emulsion of Example 7 has been found to have very good stability under high temperature storage conditions and has remained a stable emulsion after storage for several weeks at 60"C. At the lower ends of the temperature scale, these emulsions are generally stable at temperatures of -2"C to -100C and exhibit good resistance to crystallisation. In general they do not freeze until the temperature drops to about -25"C.

The formulations of Examples I to 25 present a reduced fire hazard compared with the known emulsifiable concentrate formulations of 2,6 - dinitroaniline herbicides in organic solvents such as xylene.

WHAT WE CLAIM IS: 1. A herbicidal formulation in concentrate form being an aqueous emulsion comprising 10% to 75% by weight of a herbicide being at least one herbicidal 2,6 dinitroaniline derivative having a solubility in water at 250C less than 100 parts per million by weight and a melting point in the range of from -10"C to 1500C.

0% to 60% by weight of a substantially water-immiscible solvent, the herbicide and the solvent forming a homogeneous disperse phase, 0.5% to 10% by weight of an emulsifying agent, and 15% to 70% by weight of an aqueous solution of an inorganic salt, the concentration of the inorganic salt in the aqueous solution being at least 5% by weight.

2. A formulation according to Claim I which contains from 15% to 70% by weight of the herbicide, from 0% to 45% by weight of the solvent, from 0.9% to 6% by weight of the emulsifying agent and from 20% to 40% by weight of the aqueous solution, the concentration of inorganic salt in the aqueous solution being from 10% to 20% by weight.

3. A formulation according to Claim 1 or 2 wherein no solvent is present, the herbicide is isopropalin which forms 60% to 75% by weight of the formulation, the emulsifying agent forms 2% to 6% by weight of the formulation and the aqueous solution forms 19% to 38% by weight of the formulation.

4. A formulation according to Claim I or 2 which contains 15% to 65% by weight of the herbicide which is a 2,6 - dinitroaniline derivative of formula

**WARNING** end of DESC field may overlap start of CLMS **.

Claims

**WARNING** start of CLMS field may overlap end of DESC **. EXAMPLE 25 Isopropalin, technical (90% pure) 800 gms Emulsifying agent (33.3 gms of Remcopal NP30 and 6.7 gms of Remcopal 273) 40 gms Aqueous solution of sodium chloride (15% w/w) 338 gms Total: 1178 gms (1 litre) The emulsifying agent was dissolved in the isopropalin with gentle warming. The aqueous solution of sodium chloride was added with agitation. The resulting stable emulsion was opaque and dirty orange-yellow in colour. It should be noted that the emulsifying agent of each of Examples I to 25 has a calculated hydrophile-lipophile balance of substantially 16. In the emulsions of Examples 1 to 25 above it has been found that the mean droplet diameter of the organic phase is in the range of from 8 to 14 microns. These emulsions have been found to disperse readily when added to 100 volumes of water and to remain substantially dispersed for several hours. Such dispersions are readily applied to crop land by conventional means such as spraying, and are therefore usable in a similar manner to the known concentrated formulations. The emulsions of Examples 1, 2 and 4 to 25 exhibit particularly good stability under a variety of storage conditions. Coalescence of droplets and formation of upper or lower aqueous layers is very slow and samples may be stored for at least a year at 250C or 40"C without appreciable coalescence. The emulsion of Example 7 has been found to have very good stability under high temperature storage conditions and has remained a stable emulsion after storage for several weeks at 60"C. At the lower ends of the temperature scale, these emulsions are generally stable at temperatures of -2"C to -100C and exhibit good resistance to crystallisation. In general they do not freeze until the temperature drops to about -25"C. The formulations of Examples I to 25 present a reduced fire hazard compared with the known emulsifiable concentrate formulations of 2,6 - dinitroaniline herbicides in organic solvents such as xylene. WHAT WE CLAIM IS:

1. A herbicidal formulation in concentrate form being an aqueous emulsion comprising 10% to 75% by weight of a herbicide being at least one herbicidal 2,6 dinitroaniline derivative having a solubility in water at 250C less than 100 parts per million by weight and a melting point in the range of from -10"C to 1500C.

where R' is C4 alkyl or chloroethyl, R2 is C24 alkyl, chloroethyl or 2 - methallyl and R3 is hydrogen or amino, 10% to 45% by weight of the solvent, 0.9% to 6% by weight of the emulsifying agent, and 20% to 40% by weight of the aqueous solution.

5. A formulation according to Claim 4 wherein R' is ethyl or propyl, R2 is propyl, butyl or 2 - methallyl and R3 is hydrogen.

6. A formulation according to any one of Claims 1, 2, 4 and 5 which contains 40% to 65% by weight of the herbicide, which is trifluralin, 10% to 25% by weight of the solvent, 0.9% to 6% by weight of the emulsifying agent and 20% to 35% by weight of the aqueous solution, the concentration of the inorganic salt being at least 10% by weight.

7. A formulation according to Claim 6 wherein the trifluralin forms from 40% to 60% by weight of the formulation, the solvent forms from 15% to 25% by weight of the formulation, and the emulsifying agent forms from 3% to 6% by weight of the formulation.

8. A formulation according to Claim 7 wherein the trifluralin forms from 40% to 50% of the formulation.

9. A formulation according to any one of Claims 1, 2 and 4 to 7 wherein the water-immiscible solvent is xylene or a mixture of xylene and naphthalene.

10. A formulation according to any one of Claims 1 to 9 wherein the emulsifying agent is a non-ionic surfactant or a blend of two or more non-ionic surfactants.

11. A formulation according to any one of Claims I to 10 wherein the emulsifying agent has a calculated hydrophile-lipophile balance in the range of from 14 to 18.

12. A formulation according to Claim 11 wherein the calculated hydrophilelipophile balance is in the range of from 15 to 17.

13. A formulation according to Claim 12 wherein the calculated hydrophilelipophile balance is substantially 16.

14. A formulation according to any one of Claims I to 13 wherein the inorganic salt forms substantially 15% of the aqueous solution.

15. A formulation according to any one of Claims 1 to 14 wherein the inorganic salt is selected from sodium chloride, potassium chloride and calcium chloride.

16. A formulation according to Claim 15 wherein the inorganic salt is sodium chloride.

17. A formulation according to any one of Claims 1 to 16 wherein the aqueous solution additionally includes urea at a concentration up to 25% by weight.

18. A herbicidal formulation in concentrate form being an aqueous emulsion comprising: 40% to 60% by weight of trifluralin, 15% to 25% by weight of a substantially water-immiscible aromatic hydrocarbon solvent, the trifluralin and the solvent forming a homogeneous disperse phase, 3% to 6% by weight of a non-ionic surfactant or a blend of such surfactants, having a calculated hydrophile-lipophile balance in the range of from 15 to 17, and 22% to 32% by weight of an aqueous solution of sodium chloride, the sodium chloride concentration being in the range 10% to 18% by weight of the aqueous solution, the aqueous solution additionally including 0% to 5% of urea by weight of the solution.

19. A process for preparing a herbicidal formulation in concentrate form which process comprises agitating together a homogeneous organic phase containing 10% to 75% by weight of the formulation of a herbicide being at least one herbicidal 2,6 - dinitroaniline derivative having a solubility in water at 25"C less than 100 parts per million by weight and a melting point in the range of from -10 C to 1500C, and 0% to 60% by weight of the formulation of a substantially water-immiscible solvent, and an aqueous phase consisting of 15% to 70 by weight of the formulation of an aqueous solution of an inorganic salt, the concentration of the inorganic salt in the aqueous solution being at least 5% by weight, with 0.5% to 10% by weight of the formulation of an emulsifying agent, until a stable emulsion is formed therefrom.

20. A process according to Claim 19 wherein at least part of the emulsifying agent is dissolved in the organic phase prior to agitation of the organic phase and the aqueous phase.

21. A process according to claim 19 or 20 which comprises dissolving 40% to 60% by weight of the formulation of herbicide, which is trifluralin, in 15% to 25% by weight of the formulation of the solvent, filtering the resulting solution to provide the organic phase, dissolving the emulsifying agent in the organic phase, adding the aqueous solution to the organic phase and agitating.

22. A process according to any one of Claims 19 to 21 wherein agitation is continued until the mean droplet diameter of the organic phase is observed to be in the range of from 8 to 14 microns.

23. A process according to any one of Claims 19 to 22 including the step of dissolving urea in the aqueous solution up to 25% by weight of the aqueous solution prior to agitation of the organic phase and the aqueous phase.

24. A process for preparing a herbicidal formulation according to Claim I substantially as hereinbefore described with reference to any one of Examples 1 to 5.

25. A process for preparing a herbicidal formulation according to Claim I substantially as hereinbefore described with reference to any one of Examples 6 to 25.

26. A herbicidal formulation whenever prepared by a process according to any one of Claims 19 to 25.

27. A herbicidal formulation according to Claim I substantially as hereinbefore described in any one of Examples 1 to 5.

28. A herbicidal formulation according to Claim I substantially as hereinbefore described in any one of Examples 6 to 25.

29. A method of inhibiting growth of weeds which method comprises dispersing in a large volume of water a herbicidal formulation according to any one of Claims I to 18 and 26 to 28, and applying the dispersion formed thereby to a locus in which it is desired to inhibit the growth of weeds.