Solvent systems for dicyandiamide and/or alkyl thiophosphoric triamide and use in agricultural applications
US-2016107947-A1 · Apr 21, 2016 · US
US9834487B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9834487-B2 |
| Application number | US-201615206657-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 11, 2016 |
| Priority date | Jul 13, 2015 |
| Publication date | Dec 5, 2017 |
| Grant date | Dec 5, 2017 |
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.
The present disclosure relates to a novel highly concentrated phosphoric or thiophosphoric triamide formulation with enhanced stability against crystallization or freezing under extended exposure to low temperature of 0° C. or below. It also provides a method to make and use such formulations.
Opening claim text (preview).
We claim: 1. A highly concentrated phosphoric or thiophosphoric triamide composition comprising: i). a phosphoric or thiophosphoric triamide with a concentration range from 35% to 50% by weight, wherein said phosphoric or thiophosphoric triamide is a compound according to Formula I: (X═P)(NH 2 ) 2 NR 1 R 2 (Formula I) wherein X is oxygen or sulfur, and R 1 and R 2 are independently hydrogen, C 1 -C 12 alkyl, C 3 -C 12 cycloalkyl, C 6 -C 14 aryl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, C 5 -C 14 heteroaryl, C 1 -C 14 heteroalkyl, C 2 -C 14 heteroalkenyl, C 2 -C 14 heteroalkynyl, or C 3 -C 12 cycloheteroalkyl; ii). a glycol or glycol derivative with a concentration range from about 5% to about 30% by weight, wherein said glycol is a compound according to C n H 2n (OH) 2 (Formula II), and wherein n is 2-12; and iii). a liquid amide with a concentration range from about 20% to about 50% by weight, wherein said liquid amide is selected from the group consisting of 2-pyrrolidone, N—(C 1 -C 12 alkyl)-2-pyrrolidone, and an amide with the formula R 1 CONR 2 R 3 , wherein R 1 is a hydrogen or C 1 -C 4 alkyl, and R 2 and R 3 are independently hydrogen or C 1 -C 12 alkyl, wherein the ratio of the weight percentage of iii) to ii) is more than 1.0, and wherein said highly concentrated phosphoric or thiophosphoric triamide composition is physically stable at a temperature of 0° C., and there is substantially no freezing of the composition or crystallization of any solid for at least 14 days at 0° C. 2. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , further comprising a dye with a concentration range from about 1.0% to about 2.0% by weight. 3. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , wherein said phosphoric or thiophosphoric triamide is N-(n-butyl) thiophosphoric triamide (NBPT). 4. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , wherein said glycol or glycol derivative is a compound according to Formula II, and wherein n is 2-6. 5. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , wherein said glycol or glycol derivative is propylene glycol (PG). 6. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , wherein said liquid amide is N—(C 1 -C 12 alkyl)-2-pyrrolidone. 7. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , wherein said liquid amide is N-methyl-2-pyrrolidone (NMP). 8. The highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 , comprising: i). N-(n-butyl) thiophosphoric triamide (NBPT) with a concentration in the range from about 42% to about 48% by weight; ii). propylene glycol (PG) with a concentration in the range from about 8% to about 15% by weight; iii). N-methyl-2-pyrrolidone (NMP) with a concentration in the range from about 35% to about 45% by weight; and iv). a dye with a concentration in the range from about 1.2% to about 1.8% by weight. 9. A method comprising contacting a composition according to claim 1 with a urea-based fertilizer. 10. The method according to claim 9 , wherein said urea-based fertilizer is urea granules or prills. 11. The method according to claim 9 , wherein said urea-based fertilizer is molten urea. 12. A urea-based fertilizer comprising urea and a highly concentrated phosphoric or thiophosphoric triamide composition according to claim 1 . 13. A method of making the highly concentrated NBPT composition according to claim 1 by combining NBPT, PG, NMP and a dye to make a homogeneous solution.
Related publications grouped by family.
Answers are generated from the same data shown on this page.