Compositions containing glufosinate and a synthetic auxin herbicide
Aqueous herbicide compositions containing a salt of glufosinate and a salt of a synthetic auxin herbicide are described. Such compositions exhibit good compatibility and reduced viscosity. Methods of reducing the viscosity of an aqueous herbicide composition are also disclosed.
1 . An aqueous herbicide composition comprising:
(a) from about 1 to about 25 weight percent on an acid equivalent (wt % ae) basis of a water soluble salt of glufosinate;
(b) from about 1 to about 25 wt % ae of a water soluble salt of a synthetic auxin herbicide selected from the group including 2,4-D; and
(c) from about 1 to about 25 weight percent (wt %) of a surfactant selected from the group consisting of a sodium lauryl ether sulfate, an isopropyl ammonium lauryl ether sulfate, and combinations thereof,
wherein the composition exhibits a reduction in viscosity between about 40% to about 90% at a temperature between 15° C. to 25° C. when compared to a similar composition where the synthetic auxin herbicide salt is omitted,
wherein the composition includes, on an ae basis, a weight ratio of the synthetic auxin herbicide salt to the glufosinate salt of from 1:3 to 3:1,
wherein the water soluble salt of the synthetic auxin herbicide is derived by neutralizing the synthetic auxin herbicide acid with a choline cation,
wherein the composition has no phase separation at about 0° C., and
wherein the water soluble salt of glufosinate is derived by neutralizing glufosinate acid with either
(i) a cation selected from the group consisting of a quaternary organic ammonium cation of the formula
wherein R 1 , R 2 , R 3 , and R 4 independently are linear or branched (C 1 -C 16 ) alkyl, (C 1 -C 16 ) arylalkyl, or (CH 2 CH 2 O) n H, and n is an integer from 1-3; or
(ii) an organic amine compound of the formula
wherein:
R 1 , R 2 , and R 3 are each independently [(C n H 2n )O] m R 5 ;
R 4 ═[(C n H 2n )O] m R 5′ ;
R 5 ═H, OH or C 1 -C 6 alkyl;
R 5′ ═(CH 2 ) n ;
X═R 6 or R 7 NR 8 R 9 , where R 6 , R 8 , and R 9 are each independently [(C n H 2n )O] m R 5 ;
R 7 ═[(C n H 2n )O] m R 5′ ; and
n=1-4; m=0-10; z=0-3.
2 . The composition of claim 1 , wherein the water soluble salt of glufosinate is derived by neutralizing glufosinate acid with the organic amine compound of the formula
wherein:
R 1 , R 2 , and R 3 are each independently [(C n H 2n )O] m R 5 ;
R 4 ═[(C n H 2n )O] m R 5′ ;
R 5 ═H, OH or C 1 -C 6 alkyl;
R 5′ ═(CH 2 )n;
X═R 6 or R 7 NR 8 R 9 , where R 6 , R 8 , and R 9 are each independently [(C n H 2n )O] m R 5 ;
R 7 ═[(C n H 2n )O] m R 5′ ; and
n=1-4; m=0-10; z=0-3.
3 . The composition of claim 2 , wherein the organic amine compound is selected from the group consisting of monomethylamine, dimethylamine, triethylamine, propylamine, dipropylamine, tripropylamine, isopropylamine, diisopropylamine, triisopropylamine, n-butylamine, dibutylamine, tributylamine, sec-butylamine, isobutylamine, t-butylamine, methylethylamine, dimethylethylamine, methyldiethylamine, methyl-n-propylamine, ethyl-n-propylamine, methylethyl-n-propylamine, ethylenediamine, diethylenetriamine (CAS #111-40-0), triethylenetetramine (CAS #112-24-3), tetraethylenepentamine (CAS #112-57-2), ethanolamine, diethanolamine, triethanolamine, propanolamine, dipropanolamine, tripropanolamine, isopropanolamine, diisopropanolamine, triisopropanolamine, butanolamine, dibutanolamine, tributanolamine, isobutanolamine, dimethylethanolamine, diethyleneglycol amine (diglycolamine), triethyleneglycol amine, N-methyldiethanolamine, diethylethanolamine, N-ethyldiethanolamine, N-(2-hydroxyethyl) ethylenediamine, N,N-bis-(2-aminoethyl) methylamine, N,N-bis-(3-aminopropyl) methylamine, aminoethylethanolamine (CAS #111-41-1), N,N,N′,N′-tetraethyldiethylenetriamine (CAS #123-12-6), N,N′-bis-(3-aminopropyl)-1,3-propanediamine (CAS #4605-14-5), N,N-bis [3-(methylamino)propyl]methylamine (CAS #123-70-6), and combinations thereof.
4 . The composition of claim 1 , wherein the water soluble salt of glufosinate is derived by neutralizing glufosinate acid with the cation selected from the group consisting of a quaternary organic ammonium cation of the formula
wherein R 1 , R 2 , R 3 , and R 4 independently are linear or branched (C 1 -C 16 ) alkyl, (C 1 -C 16 ) arylalkyl, or (CH 2 CH 2 O) n H, and n is an integer from 1-3.
5 . The composition of claim 4 , wherein the quaternary organic ammonium cation is selected from the group including tetramethyl ammonium cation, tetraethyl ammonium cation, tetrapropyl ammonium cation, tetrabutyl ammonium cation, trimethylethyl ammonium cation, dimethyldiethyl ammonium cation, methyltriethyl ammonium cation, N-benzyltrimethyl ammonium cation, N-hexadecyltrimethylammonium cation, choline cation, and combinations thereof.
6 . The composition of claim 1 , wherein the surfactant is sodium lauryl ether sulfate of the formula
wherein:
M is Na;
n is an integer from 1 to 10; and
R is a saturated C 12 linear alkyl group.
7 . The composition of claim 1 , wherein the surfactant is isopropyl ammonium lauryl ether sulfate of the formula:
wherein M is isopropyl ammonium; n is an integer from 1 to 10; and R is a saturated C 12 linear alkyl group.
8 . The composition of claim 1 , further comprising one or more agriculturally acceptable adjuvants or carriers.
9 . The composition of claim 1 , wherein the aqueous herbicide composition is a aqueous liquid concentrate.
10 . A method of preparing the aqueous herbicide composition of claim 1 comprising combining the water-soluble salt of glufosinate, the water-soluble salt of the synthetic auxin herbicide, the surfactant, and water.
11 . A method of controlling undesirable vegetation comprising applying the aqueous herbicide composition of claim 1 to the undesirable vegetation or the locus of the undesirable vegetation after emergence of the undesirable vegetation, or to the soil to prevent the emergence of the undesirable vegetation.