IP Library Granted Patent US 10,173,943
Granted Patent B2
US 10,173,943 · App. 15/152,426 · Granted Jan 8, 2019

Non-corrosive nitrification inhibitor polar solvent formulation

Inventors: Hiteshkumar Dave (Carmel, IN); Lei Liu (Carmel, IN); Alex Williams (Indianapolis, IN); Rajesh Goyal (Bensalem, PA); Nicholas Fradette (Verona, NJ); Chloe Moreau (Pessac, FR); Samantha Armisen (Villenave d'Ornon, FR); Kevin Mayer (Quakertown, PA)
Assignee: Dow Agrosciences, LLC
C05G3/08C05C11/00C05G3/00C05G3/0064Y02P60/218
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Quick Facts
Patent No.
US 10,173,943
App. No.
15/152,426
Granted
Jan 8, 2019
Kind
B2
Abstract

This invention relates to stable liquid formulations of the nitrification inhibitor nitrapyrin comprising polar solvents that are stabilized with small amounts of compounds which help to reduce the tendency of polar solutions of nitrapyrin to corrode metal surfaces. Many of the formulations disclosed herein exhibit useful physical, chemical, and bioactive properties including reduced levels of corrosion when in contact with ferrous metals.

Claims (116)

1. A formulation, comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar first solvent and wherein the second solvent is no more polar than the first solvent;

wherein the polar first solvent is an alkoxybenzene compound selected from methoxybenzene and ethoxybenzene.

2. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 250 to about 300 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 40 to about 60 weight percent of a mixture of N,N-dimethyloctanamide (N,N-dimethylcaprylamide) and N,N-dimethyldecanamide (N,N-dimethylcapramide);

about 0.5 to about 1.5 weight percent of liquid epoxy resin and about 0.5 to about 1.5 weight percent 2,6-dimethylpyridine; and

about 5 to about 20 weight percent solvent naphtha.

3. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 230 to about 300 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 45 to about 55 weight percent of a mixture of N,N-dimethyloctanamide (N,N-dimethylcaprylamide) and N,N-dimethyldecanamide (N,N-dimethylcapramide);

about 0.75 to about 1.4 weight percent of liquid epoxy resin;

about 0.5 to about 1.5 weight percent 2,6-dimethylpyridine; and

about 10 to about 15 weight percent solvent naphtha.

4. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 50.0 to about 55 weight percent of a mixture of N,N-dimethyloctanamide (N,N-dimethylcaprylamide) and N,N-dimethyldecanamide (N,N-dimethylcapramide);

about 1.0 to about 1.1 weight percent of liquid epoxy resin oil;

about 0.5 to about 1.5 weight percent 2,6-dimethylpyridine; and

about 11.0 to about 14.0 weight percent solvent naphtha.

5. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 50.55 weight percent of a mixture of N,N-dimethyloctanamide (N,N-dimethylcaprylamide) and N,N-dimethyldecanamide (N,N-dimethylcapramide);

about 1.2 weight percent of liquid epoxy resin oil;

about 0.5 to about 1.5 weight percent 2,6-dimethylpyridine; and

about 12.64 weight percent solvent naphtha.

6. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 200 to about 400 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 20 to about 50 weight percent of a dibasic ester;

about 0.5 to about 2.5 weight percent of epoxidized linseed oil;

about 0.5 to about 2.5 weight percent of nicotinamide; and

about 20.0 to about 50.0 weight percent of cyclohexanone.

7. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L to about 350 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 20 to about 40 weight percent of a dibasic ester;

about 1.5 to about 2.5 weight percent of epoxidized linseed oil;

about 0.5 to about 1.5 weight percent nicotinamide; and

about 25.0 to about 45.0 weight percent cyclohexanone.

8. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 50.47 weight percent of a dibasic ester;

about 1.5 weight percent of epoxidized linseed oil;

about 0.8 weight percent nicotinamide; and

about 12.62 weight percent cyclohexanone.

9. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 200 to about 400 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 40 to about 60 weight percent of a dibasic ester;

about 0.5 to about 2.5 weight percent of epoxidized linseed oil; and

about 0.4 to about 1.5 weight percent nicotinamide.

10. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 63.08 weight percent of a dibasic ester;

about 1.5 weight percent of epoxidized linseed oil; and

about 0.6 to about 1.0 weight percent nicotinamide.

11. A formulation comprising:

an inhibitor of nitrification;

at least one corrosion inhibitor;

a polar first solvent capable of dissolving the nitrification inhibitor; and

a second solvent, the second solvent is miscible in the polar solvent and wherein the second solvent is no more polar than the first solvent; wherein said formulation comprises:

about 240 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 63.08 weight percent of a dibasic ester;

about 1.5 weight percent of epoxidized linseed oil; and

about 0.8 weight percent nicotinamide.

12. A formulation, comprising:

about 324 g/L of 2-chloro-6-(trichloromethyl)pyridine;

about 26.02 weight percent of a dibasic ester;

about 2.04 weight percent of epoxidized linseed oil;

about 0.98 weight percent nicotinamide; and

about 39.02 weight percent cyclohexanone.

13. A formulation, comprising;

the formulation according to claim 12 ; and

at least one additional agricultural ingredient selected from the group consisting of: herbicides, insecticides, mitocides, fungicides, and fertilizers.

14. The formulation according to claim 13 , wherein the agricultural ingredient is a fertilizer.

15. The formulation according to claim 14 , wherein the fertilizer includes nitrogen.

16. A method for treating soil, comprising the steps of:

applying at least one of the formulation of claim 12 to at least one area selected from the area consisting of: the surface of a portion of soil, beneath the surface of a portion of soil, a portion of a plant, and a portion of a surface adjacent to a plant.

17. The method according to claim 16 , wherein the applying step includes injecting the formulation into a portion of soil.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2024
From: RHODIA OPERATIONS
To: SPECIALTY OPERATIONS FRANCE
Reel/Frame 066374/0642 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2018
From: GOYAL, RAJESH; FRADETTE, NICHOLAS; MOREAU, CHLOE; ARMISEN, SAMANTHA; MAYER, KEVIN
To: RHODIA OPERATIONS
Reel/Frame 045538/0072 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2016
From: DAVE, HITESHKUMAR; LIU, LEI; WILLIAMS, ALEX
To: DOW AGROSCIENCES LLC
Reel/Frame 039584/0077 →
Continuity (6)
Provisional Application 62159884 · May 11, 2015
Provisional Application 62159885 · May 11, 2015
Provisional Application 62244901 · Oct 22, 2015
Provisional Application 62244902 · Oct 22, 2015
Provisional Application 62244903 · Oct 22, 2015
Related Publication 20160332931A1 · Nov 17, 2016