Reaction products and methods for making and using the same

US11148982B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11148982-B2
Application numberUS-201816164198-A
CountryUS
Kind codeB2
Filing dateOct 18, 2018
Priority dateApr 30, 2010
Publication dateOct 19, 2021
Grant dateOct 19, 2021

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

What is claimed is: 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.

Assignees

Inventors

Classifications

  • Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures · CPC title

  • C05C3/00Primary

    Fertilisers containing other salts of ammonia or ammonia itself, e.g. gas liquor · CPC title

  • containing urea-formaldehyde condensates · CPC title

  • C05G3/90Primary

    for affecting the nitrification of ammonium compounds or urea in the soil · CPC title

  • Fertilisers containing urea or urea compounds · CPC title

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What does patent US11148982B2 cover?
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.
Who is the assignee on this patent?
Koch Agronomics Services Llc, Koch Agronomic Services Llc
What technology area does this patent fall under?
Primary CPC classification C05C3/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 19 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).