IP Library Granted Patent US 11,148,982
Granted Patent B2
US 11,148,982 · App. 16/164,198 · Granted Oct 19, 2021

Reaction products and methods for making and using the same

Inventors: Kurt D. Gabrielson (Lilburn, GA); Mary L. Epling (Conyers, GA)
Assignee: Koch Agronomic Services, LLC
C05G3/90C05C3/00C05C9/00C05C9/02Y02P60/21
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Quick Facts
Patent No.
US 11,148,982
App. No.
16/164,198
Granted
Oct 19, 2021
Kind
B2
Abstract

Reaction products and methods for making and using the same are provided. In at least one specific embodiment, the fertilizer can include a nitrogen source comprising urea, ammonia, ammonium nitrate, or any combination thereof and a reaction product of formaldehyde, an ammonia source, and a nitrification inhibitor.

Claims (32)

1. A method for producing a fertilizer, comprising:

reacting formaldehyde, an ammonia source, urea, and a nitrification inhibitor to produce a reaction product comprising the formaldehyde, ammonia, urea, and nitrification inhibitor; and

combining the reaction product with one or more nitrogen sources to produce the fertilizer;

wherein the amount of the reaction product in the fertilizer ranges from about 0.5 wt % to about 20 wt %, based on the total amount of nitrogen in the one or more nitrogen sources in the fertilizer.

2. The method of claim 1 , wherein the one or more nitrogen sources comprise urea, urea-formaldehyde polymers, anhydrous ammonia, aqueous ammonia, ammonium nitrate, or a combination thereof.

3. The method of claim 1 , wherein the ammonia source is ammonium hydroxide, ammonium chloride, ammonium nitrate, anhydrous ammonia, aqueous ammonia, or a combination thereof.

4. The method of claim 1 , wherein the nitrification inhibitor is 2-chloro-6-(trichloromethyl)-pyridine; 5-ethoxy-3-trichloromethyl-1,2,4-thiadiazol; dicyandiamide (DCD); 2-amino-4-chloro-6-methyl-pyrimidine; 1,3-benzothiazole-2-thiol; 4-amino-N-1,3-thiazol-2-ylbenzenesulfonamide; thiourea; guanidine; 3,4-dimethylpyrazophosphate; 2,4-diamino-6-trichloromethyl-5-triazine; polyetherionophores; 4-amino-1,2,4-triazole; 3-mercapto-1,2,4-triazole; potassium azide; carbon bisulfide; sodium trithiocarbonate; ammonium dithiocarbamate; 2,3, dihydro-2,2-dimethyl-7-benzofuranol methyl-carbamate; N-(2,6-dimethylphenyl)-N-(methoxyacetyl)-alanine methyl ester; ammonium thiosulfate; 1-hydroxypyrazole; 2-methylpyrazole-1-carboxamide; derivatives thereof, or any combination thereof.

5. The method of claim 1 , wherein the nitrogen source is a solid.

6. The method of claim 1 , wherein the nitrogen source is a liquid.

7. The method of claim 1 , wherein the nitrogen source is a mixture of a solid nitrogen source and a liquid nitrogen source.

8. The method of claim 1 , wherein the reaction product has a pH ranging from about 4 to about 6.

9. The method of claim 1 , wherein the formaldehyde, the ammonia source, urea, and the nitrification inhibitor are reacted under alkaline reaction conditions to produce a reaction product having a pH ranging from about 8 to about 11.

10. The method of claim 1 , wherein the formaldehyde, the ammonia source, urea, and the nitrification inhibitor are reacted in water under alkaline reaction conditions to produce an aqueous reaction product.

11. The method of claim 1 , wherein reacting the formaldehyde, ammonia source, urea, and nitrification inhibitor comprises:

combining the formaldehyde and the nitrification inhibitor at a molar ratio of from about 1:1 to about 3:1 to produce a first mixture;

heating the first mixture to a temperature ranging from about 50° C. to about 80° C.;

adding the urea to the first mixture;

introducing an ammonia source to the first mixture to produce a second mixture, wherein the total amount of ammonia source introduced to the first mixture provides a formaldehyde to ammonia source molar ratio ranging from about 3:1 to about 9:1; and

heating the second mixture to a temperature ranging from about 70° C. to about 90° C.; and cooling the second mixture to produce the reaction product.

12. The method of claim 1 , wherein a molar ratio of the formaldehyde to ammonia in the reaction product ranges from about 3:1 to about 9:1 and a molar ratio of the formaldehyde to nitrification inhibitor in the reaction product ranges from about 1:1 to about 3:1.

13. The method of claim 1 , wherein the reaction product comprises:

from about 30 mol % to about 70 mol % formaldehyde;

from about 5 mol % to about 25 mol % ammonia source; and

from about 15 mol % to about 45 mol % nitrification inhibitor;

based on the total weight of the formaldehyde, the ammonia source, and the nitrification inhibitor.

14. The method of claim 1 , wherein a molar ratio of the formaldehyde to the ammonia source in the reaction product ranges from about 1:1 to about 1:8 and a molar ratio of the formaldehyde to nitrification inhibitor in the reaction product ranges from about 1:1 to about 7:1.

15. The method of claim 1 , wherein the formaldehyde comprises an aqueous solution, and wherein the concentration of the formaldehyde in the aqueous solution ranges from about 37% to about 50%.

16. The method of claim 1 , wherein a concentration of the nitrification inhibitor in the fertilizer ranges from about 0.1 wt % to about 20 wt %, based on a total amount of nitrogen in the one or more nitrogen sources in the fertilizer.

17. The method of claim 1 , wherein a concentration of the nitrification inhibitor in the fertilizer ranges from about 1 wt % to about 10 wt %, based on a total amount of nitrogen in the one or more nitrogen sources in the fertilizer.

18. The method of claim 1 , further comprising one or more urease inhibitors, wherein the urease inhibitor is N-(n-butyl)thiophosphoric triamide, N-(butyl)phosphoric triamide, thiophosphoryl triamide, phenyl phophorodiamidate, cyclohexyl phosphoric triamide, cyclohexyl thiophosphoric triamide, phosphoric triamide, hydroquinone, p-benzoquinone, hexamidocyclotriphophazene, thiophyridines, thiophyrimidines, thiophyridine-N-oxides, N,N-dihalo-2-imidazolidinone, N-halo-2-oxazolidinone, derivatives thereof, or any combination thereof.

19. The method of claim 1 , wherein the reaction product further comprises a urease inhibitor reacted with the formaldehyde, ammonia source, urea, and nitrification inhibitor.

20. The method of claim 1 , wherein the fertilizer is further mixed with a fertilizer nutrient, pesticide, herbicide, fungicide, or combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2019
From: GABRIELSON, KURT D.; EPLING, MARY L.
To: KOCH AGRONOMIC SERVICES, LLC
Reel/Frame 048190/0771 →
Continuity (4)
Division 14929537 · Nov 2, 2015
Continuation 13098272 · Apr 29, 2011
Provisional Application 61329680 · Apr 30, 2010
Related Publication 20190047918A1 · Feb 14, 2019