Process to conserve cyano-function and improve performance of low molecular weight nitrification inhibitors to improve fertilizer efficiency
US-2018170818-A1 · Jun 21, 2018 · US
US11084763B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11084763-B2 |
| Application number | US-201715622207-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 14, 2017 |
| Priority date | Jun 18, 2016 |
| Publication date | Aug 10, 2021 |
| Grant date | Aug 10, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A composition comprises a nonaqeuous, liquid carrier, an inhibitor compound, and a colorant composition comprising an azo colorant. A method for making the composition is also provided. A method for making a fertilizer composition using the disclosed composition is also provided.
Opening claim text (preview).
What is claimed is: 1. A composition comprising: (a) a nonaqueous, liquid carrier; (b) an inhibitor compound selected from the group consisting of urease inhibitors, nitrification inhibitors, and mixtures thereof; and (c) a colorant composition, the colorant composition comprising: (i) an azo colorant; and (ii) about 1 wt. % to about 60 wt. % of water, wherein the azo colorant is selected from the group consisting of (i) azo colorants comprising an azo chromophore and a polyoxyalkylene polymer covalently bound to the azo chromophore and (ii) azo colorants comprising a quaternary ammonium counterion having at least one polyoxyalkylene polymer covalently bound thereto. 2. The composition of claim 1 , wherein the nonaqueous, liquid carrier is selected from the group consisting of N-methylpyrrolidone, polyvinylpyrrolidone, propylene glycols, ethanolamine, propylene carbonate, alkyl-glycol ethers, alkyl-arylpolyether alcohols, and mixtures thereof. 3. The composition of claim 1 , wherein the urease inhibitor is selected from the group consisting of N-(n-butyl)thiophosphoric triamide, N-(n-butyl)phosphoric triamide, N-(2-nitrophenyl)phosphoric triamide, thiophosphoryl triamide, phenyl phosphorodiamidate, cyclohexyl thiophosphoric triamide, cyclohexyl phosphoric triamide, phosphoric triamide, hydroquinone, 1,4-benzoquinone, hexaamidocyclotriphosphazene, thiopyridines, thiopyrimidines, thiopyridine-N-oxides, N,N-dihalo-2-imidazolidinone, N-halo-2-oxazolidinone, and mixtures thereof. 4. The composition of claim 3 , wherein the urease inhibitor is N-(n-butyl) thiophosphoric triamide. 5. The composition of claim 1 , wherein the nitrification inhibitor is selected from the group consisting of 2-chloro-6-(trichloromethyl)pyridine, 2-amino-4-chloromethylpyrimidine, dicyandiamide, 3,4-dimethyl pyrazole phosphate, cyanoguanidine, N-2,5-dichlorophenylsuccinanilic acid, guanyl thiourea, sulfanyll-amidothiazole, 4-amino-1,2,4-triazole, 3-methylpyrazole, 1H-1,2,4-triazole, and mixtures thereof. 6. The composition of claim 1 , wherein the composition comprises a urease inhibitor and a nitrification inhibitor. 7. A method for making a composition, the method comprising the steps of: (a) providing a nonaqueous, liquid carrier; (b) providing an inhibitor compound selected from the group consisting of urease inhibitors, nitrification inhibitors, and mixtures thereof; (c) providing a colorant composition, the colorant composition comprising: (i) an azo colorant; and (ii) about 1 wt. % to about 60 wt. % of water; (d) mixing the nonaqueous, liquid carrier, the inhibitor compound, and the colorant composition to produce a composition, wherein the azo colorant is selected from the group consisting of (i) azo colorants comprising an azo chromophore and a polyoxyalkylene polymer covalently bound to the azo chromophore and (ii) azo colorants comprising a quaternary ammonium counterion having at least one polyoxyalkylene polymer covalently bound thereto. 8. The method of claim 7 , wherein the nonaqueous, liquid carrier is selected from the group consisting of N-methylpyrrolidone, polyvinylpyrrolidone, propylene glycols, ethanolamine, propylene carbonate, alkyl-glycol ethers, alkyl-arylpolyether alcohols, and mixtures thereof. 9. The method of claim 7 , wherein the urease inhibitor is selected from the group consisting of N-(n-butyl)thiophosphoric triamide, N-(n-butyl)phosphoric triamide, N-(2-nitrophenyl)phosphoric triamide, thiophosphoryl triamide, phenyl phosphorodiamidate, cyclohexyl thiophosphoric triamide, cyclohexyl phosphoric triamide, phosphoric triamide, hydroquinone, 1,4-benzoquinone, hexaamidocyclotriphosphazene, thiopyridines, thiopyrimidines, thiopyridine-N-oxides, N,N-dihalo-2-imidazolidinone, N-halo-2-oxazolidinone, and mixtures thereof. 10. The method of claim 9 , wherein the urease inhibitor is N-(n-butyl) thiophosphoric triamide. 11. The method of claim 7 , wherein the nitrification inhibitor is selected from the group consisting of 2-chloro-6-(trichloromethyl)pyridine, 2-amino-4-chloromethylpyrimidine, dicyandiamide, 3,4-dimethyl pyrazole phosphate, cyanoguanidine, N-2,5-dichlorophenylsuccinanilic acid, guanyl thiourea, sulfanyll-amidothiazole, 4-amino-1,2,4-triazole, 3-methylpyrazole, 1H-1,2,4-triazole, and mixtures thereof. 12. The method of claim 7 , wherein the inhibitor compound comprises a urease inhibitor and a nitrification inhibitor. 13. A method for producing a fertilizer composition, the method comprising the steps of: (a) providing a granular substrate having a surface, the granular substrate comprising a nitrogen source; (b) providing a coating composition, the coating composition comprising: (i) a nonaqueous, liquid carrier; (ii) an inhibitor compound selected from the group consisting of urease inhibitors, nitrification inhibitors, and mixtures thereof; and (iii) a colorant composition, the colorant composition comprising: (1) an azo colorant; and (2) about 1 wt. % to about 60 wt. % of water; and (c) applying the coating composition to at least a portion of the surface of the granular substrate; and (d) drying the granular substrate from step (c) to produce a coating on at least a portion of the surface of the granular substrate, wherein the azo colorant is selected from the group consisting of (i) azo colorants comprising an azo chromophore and a polyoxyalkylene polymer covalently bound to the azo chromophore and (ii) azo colorants comprising a quaternary ammonium counterion having at least one polyoxyalkylene polymer covalently bound thereto. 14. The method of claim 13 , wherein the nonaqueous, liquid carrier is selected from the group consisting of N-methylpyrrolidone, polyvinylpyrrolidone, propylene glycols, ethanolamine, propylene carbonate, alkyl-glycol ethers, alkyl-arylpolyether alcohols, and mixtures thereof. 15. The method of claim 13 , wherein the urease inhibitor is selected from the group consisting of N-(n-butyl)thiophosphoric triamide, N-(n-butyl)phosphoric triamide, N-(2-nitrophenyl)phosphoric triamide, thiophosphoryl triamide, phenyl phosphorodiamidate, cyclohexyl thiophosphoric triamide, cyclohexyl phosphoric triamide, phosphoric triamide, hydroquinone, 1,4-benzoquinone, hexaamidocyclotriphosphazene, thiopyridines, thiopyrimidines, thiopyridine-N-oxides, N,N-dihalo-2-imidazolidinone, N-halo-2-oxazolidinone, and mixtures thereof. 16. The method of claim 15 , wherein the urease inhibitor is N-(n-butyl) thiophosphoric triamide. 17. The method of claim 13 , wherein the nitrification inhibitor is selected from the group consisting of 2-chloro-6-(trichloromethyl)pyridine, 2-amino-4-chloromethylpyrimidine, dicyandiamide, 3,4-dimethyl pyrazole phosphate, cyanoguanidine, N-2,5-dichlorophenylsuccinanilic acid, guanyl thiourea, sulfanyll-amidothiazole, 4-amino-1,2,4-triazole, 3-methylpyrazole, 1H-1,2,4-triazole, and mixtures thereof. 18. The method of claim 13 , wherein the coating composition comprises a urease inhibitor and a nitrification inhibitor.
Layered or coated, e.g. dust-preventing coatings · CPC title
containing organic compounds · CPC title
Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures · CPC title
for affecting the nitrification of ammonium compounds or urea in the soil · CPC title
containing nitrogen and sulfur · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.