Increased longevity of the nitrogen content of soil through improved liquid delivery formulations of urease inhibitors and/or nitrification inhibitors designed for urea and manure based fertilizers

US9637420B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9637420-B2
Application numberUS-201414553107-A
CountryUS
Kind codeB2
Filing dateNov 25, 2014
Priority dateNov 26, 2013
Publication dateMay 2, 2017
Grant dateMay 2, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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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

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Increasing longevity of the nitrogen content of soil through improved liquid delivery formulations of urease inhibitors and/or nitrification inhibitors designed to apply to fertilizers, especially urea and manure based fertilizers These delivery formulations provide an environmentally sound and inherently safe solvating system that improves the storage stability of the urease inhibitors by utilizing aprotic solvents, maintain the urease inhibitors and/or nitrification inhibitors in solution to storage temperatures of at least 10° C. and provides improved application to fertilizer of urease and/or nitrification inhibitors. These delivery formulations enable safe storage, transport and subsequent application or blending with urea based or manure based fertilizers that can be applied to soil in either a liquid or granular form to provide improved nitrogen retention in the soil for uptake for plant life.

First claim

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We claim: 1. A composition comprising one or more nitrification inhibitors and one or more urease inhibitors in an organic liquid solvating system comprising a mixture of aprotic solvents wherein a first aprotic solvent is dimethyl sulfoxide, dialkyl sulfoxide, diaryl sulfoxide, or an alkylaryl sulfoxide having the formula R 1 —S(O)—R 2 , wherein R 1 is methyl, ethyl, n-propyl, phenyl or benzyl and R 2 is ethyl, n-propyl, phenyl or benzyl, and a second aprotic solvent is one or more members selected from the group consisting of: 1) a C 1 -C 12 ester of a) an alcohol or polyol from the family of C 1-10 alkynols and poly(C 1-10 alkylene) glycols, b) an alkylene glycol selected from the group consisting of ethylene, propylene, and butylene glycol, c) glycerin, d) an alkylene glycol alkyl ether selected from the group consisting of dipropylene glycol methyl ether, tripropylene glycol methyl ether, and tripropylene glycol butyl ether wherein the organic liquid solvating system meets the following criteria: a. environmentally safe b. has a flashpoint above 145° F. c. inherently rated safe for contact with humans and animals d. results in a composition comprising at least one of nitrification and urease inhibitors with a Chill Point <40° F. 2. The composition of claim 1 , wherein the nitrification inhibitor is one or more members selected from the group consisting of 1) dicyandiamide, 2) 2-chloro-6 trichloromethyl)pyridine, 3) 4-amino-1,2,4-6-triazole-HCl, 4) 2,4-diamino-6-trichloromethyltriazine, 5) thiourea, 6) 1-mercapto-1,2,4-triazole and 2-amino-4-chloro-6-methylpyrimidine, and 7) 3,4-dimethylpyrazole phosphate. 3. The composition of claim 1 , wherein one of the aprotic solvents in the mixture is dimethyl sulfoxide. 4. The composition of claim 3 , wherein dimethyl sulfoxide comprises between about 10 and 90% of the composition. 5. The composition of claim 1 wherein the one or more nitrification inhibitors comprises one or more members selected from the group consisting of 1) dicyandiamide, 2) 2-chloro-6 trichloromethyl)pyridine, 3) 4-amino-1,2,4-6-triazole-HCl, 4) 2,4-diamino-6-trichloromethyltriazine, 5) thiourea, 6) 1-mercapto-1,2,4-triazole and 2-amino-4-chloro-6-methylpyrimidine, and 7) 3,4 dimethylpyrazole phosphate; in a formulation wherein nitrification inhibitor(s) is/are present in an amount that is between about 5-45% of a total formulation amount and the composition also contains a mixture of DMSO and one or more aprotic solvents in ratios that are between about 20/80 to 80/20. 6. The composition of claim 1 , further comprising one or more members selected from the group consisting of protic solvents present in the amount of 0.5-15%, surfactants, buffers, fragrance/odor masking agents, colorants, micro-nutrients, dispersed nitrification inhibitors, dispersed urease inhibitor(s), crystallization inhibitors and flow modifiers. 7. The composition of claim 1 , wherein the one or more nitrification inhibitors comprises one or more members selected from the group consisting of 1) dicyandiamide, 2) 2-chloro-6 trichloromethyl)pyridine, 3) 4-amino-1,2,4-6-triazole-HCl, 4) 2,4-diamino-6-trichloromethyltriazine, 5) thiourea, 6) 1-Mercapto-1,2,4-triazole and 2-amino-4-chloro-6-methylpyrimidine, and 7) 3,4 dimethylpyrazole phosphate in a formulation wherein nitrification inhibitor(s) is/are present in an amount that is between about 5-45% of a total formulation amount and the formulation also comprises N-(n-butyl) thiophosphoric triamide in an amount that is between about 5-45% of the total formulation amount. 8. The composition of claim 4 , wherein the composition is substantially free of water. 9. A fertilizer granule additive or a liquid fertilizer additive, which comprises one or more nitrification inhibitors and one or more urease inhibitors in an organic liquid solvating system comprising a mixture of aprotic solvents wherein a first aprotic solvent is dimethyl sulfoxide, dialkyl sulfoxide, diaryl sulfoxide, or an alkylaryl sulfoxide having the formula R 1 —S(O)—R 2 , wherein R 1 is methyl, ethyl, n-propyl, phenyl or benzyl and R 2 is ethyl, n-propyl, phenyl or benzyl, and a second aprotic solvent is one or more members selected from the group consisting of 1) a C 1 -C 12 ester of a) an alcohol or polyol from the family of C 1-10 alkynols and poly(C 1-10 alkylene) glycols, b) an alkylene glycol selected from the group consisting of ethylene, propylene, and butylene glycol, c) glycerin, d) an alkylene glycol alkyl ether selected from the group consisting of dipropylene glycol methyl ether, tripropylene glycol methyl ether, and tripropylene glycol butyl ether; wherein the organo liquid solvating system meets the following criteria: a. Environmentally safe b. Have flashpoint above 145 F c. Inherently rated safe for contact with humans and animals d. That result in a composition comprising of nitrification and urease inhibitor with a Chill Point <40 F. 10. The fertilizer granule additive or the liquid fertilizer additive of claim 9 , wherein the one or more nitrification inhibitors is selected from the group consisting of 1) dicyandiamide, 2) 2-chloro-6 trichloromethyl)pyridine, 3) 4-amino-1,2,4-6-triazole-HCl, 4) 2,4-diamino-6-trichloromethyltriazine, 5) thiourea, 6) 1-mercapto-1,2,4-triazole and 2-amino-4-chloro-6-methylpyrimidine, and 7) 3,4 dimethylpyrazole phosphate. 11. The fertilizer granule additive or the liquid fertilizer additive of claim 9 , further comprising one or more urease inhibitors selected from the group consisting of phosphoric triamides, thiophosphoric triamides and alkylated thiophosphoric triamides, wherein the alkylated thiophosphoric triamides has one or more alkyl groups that independently contain between 1 and 6 carbon atoms. 12. The fertilizer granule additive or the liquid fertilizer additive of claim 11 , wherein the one or more nitrification inhibitors comprises 1) dicyandiamide, 2) 2-chloro-6 trichloromethyl)pyridine, 3) 4-amino-1,2,4-6-triazole-HCl, 4) 2,4-diamino-6-trichloromethyltriazine, 5) thiourea, 6) 1-mercapto-1,2,4-triazole and 2-Amino-4-chloro-6-methylpyrimidine, or 7) 3,4 dimethylpyrazole phosphate; and the one or more urease inhibitors comprises phosphoramides. 13. A method of making a composition to be added to a fertilizer comprising: heating a mixture comprising one or more nitrification inhibitors in an organic liquid solvating system comprising a mixture of aprotic solvents wherein a first aprotic solvent is dimethyl sulfoxide, dialkyl sulfoxide, diaryl sulfoxide, or an alkylaryl sulfoxide having the formula R 1 —S(O)—R 2 , wherein R 1 is methyl, ethyl, n-propyl, phenyl or benzyl and R 2 is ethyl, n-propyl, phenyl or benzyl, and a second aprotic solvent is one or more members selected from the group consisting of: 1) a C 1 -C 12 ester of a) an alcohol or polyol from the family of C 1-10 alkynols and poly(C 1-10 alkylene) glycols, b) an alkylene glycol selected from the group consisting of ethylene, propylene, and butylene glycol, c) glycerin, d) an alkylene glycol alkyl ethers selected from the group consisting of Dipropylene glycol methyl ether, Tripropylene glycol methyl ether, and Tripropylene glycol butyl ether, wherein the organo liquid solvating system meets the following criteria: a. Environmentally safe b. Have flashpoints above 145 F c. Inherently rated safe for contact with humans and animals e. That result in a composition comprising of nitrification and urease inhibitor with a chill point <40 F cooling the mixture to a temperature that optionally allows an addition of one or more of protic

Assignees

Inventors

Classifications

  • Liquid fertilisers (layered or coated C05G5/30; incorporated into a matrix C05G5/40) · CPC title

  • C05G3/90Primary

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

  • C05D9/02Primary

    containing trace elements · CPC title

  • containing nitrogen, oxygen and sulfur · CPC title

  • Fertilisers from human or animal excrements, e.g. manure · CPC title

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What does patent US9637420B2 cover?
Increasing longevity of the nitrogen content of soil through improved liquid delivery formulations of urease inhibitors and/or nitrification inhibitors designed to apply to fertilizers, especially urea and manure based fertilizers These delivery formulations provide an environmentally sound and inherently safe solvating system that improves the storage stability of the urease inhibitors by util…
Who is the assignee on this patent?
Mcknight Gary David, Rayborn Randall Linwood, Parker David Bruce, and 5 more
What technology area does this patent fall under?
Primary CPC classification C05G3/90. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 02 2017 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).