IP Library Granted Patent US 11,684,067
Granted Patent B2
US 11,684,067 · App. 16/949,008 · Granted Jun 27, 2023

Generation of peroxyformic acid through polyhydric alcohol formate

Inventors: Junzhong Li (Saint Paul, MN); Allison Brewster (Saint Paul, MN); Richard Staub (Saint Paul, MN); Steven J. Lange (Saint Paul, MN); Taz Cheritu (Saint Paul, MN); Jonathan P. Fast (Saint Paul, MN); Catherine Hanson (Saint Paul, MN)
Assignee: ECOLAB USA INC.
A01N37/16A01N37/00A61K8/38A61L2/00A61L2/16A61Q17/005C07C407/00C07C409/24C11D3/00C11D3/3947C11D3/48C12P7/40
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Quick Facts
Patent No.
US 11,684,067
App. No.
16/949,008
Granted
Jun 27, 2023
Kind
B2
Abstract

The present invention relates generally to peroxyformic acid forming compositions, methods for forming peroxyformic acid, preferably in situ, using the peroxyformic acid forming compositions. The present invention also relates to the peroxyformic acid formed by the above compositions and methods. The present invention further relates to the uses of the peroxyformic acid, preferably in situ, for treating a surface or a target. The present invention further relates to methods for treating a biofilm using peroxyformic acid, including peroxyformic acid generated in situ.

Claims (28)

1. A peroxyformic acid composition comprising:

a) a first reagent that comprises a polyhydric alcohol ester of formic acid;

b) a second reagent that comprises hydrogen peroxide or an inorganic peroxo compound that generates hydrogen peroxide when contacted with an aqueous solution; and

c) a formed liquid comprising peroxyformic acid;

wherein the first reagent and the second reagent are kept separately prior to use;

wherein the formed liquid comprising peroxyformic acid is generated by contacting the first reagent and the second reagent; and

wherein the pH of the formed liquid becomes about 8 or lower within about 1 minute after the contacting between the first reagent and the second reagent.

2. The peroxyformic acid composition of claim 1 , wherein the polyhydric alcohol ester of formic acid is derived from a sugar alcohol and formic acid.

3. The peroxyformic acid composition of claim 2 , wherein the sugar alcohol is ethylene glycol, propylene glycol, or a combination thereof.

4. The peroxyformic acid composition of claim 1 , wherein the polyhydric alcohol ester of formic acid comprises glycerol formates, pentaerythritol formates, mannitol formates, propylene glycol formates, sorbitol formates, sugar formates, or a combination thereof.

5. The peroxyformic acid composition of claim 4 , wherein the sugar formates comprise sucrose formates, dextrin formates, maltodextrin formates, starch formates, or a combination thereof.

6. The peroxyformic acid composition of claim 1 , wherein the pH of the formed liquid is 8 or lower about instantaneously with the contacting between the first reagent and the second reagent.

7. The peroxyformic acid composition of claim 1 , wherein the pH of the formed liquid is between about 2 to about 7.

8. The peroxyformic acid composition of claim 1 , wherein the contacting occurs for a period of between about 10 seconds to about one week.

9. The peroxyformic acid composition of claim 1 , further comprising a catalyst or an enzyme that catalyzes formation of peroxyformic acid from the polyhydric alcohol ester of formic acid, and hydrogen peroxide.

10. The peroxyformic acid composition of claim 1 , wherein the catalyst or enzyme comprises a perhydrolytic enzyme, lipase, coronase, termanyl or esperease.

11. A method of using peroxyformic acid comprising:

generating a formed liquid comprising peroxyformic acid by contacting a first reagent comprising a polyhydric alcohol ester of formic acid and a second reagent comprising hydrogen peroxide or an inorganic peroxo compound that generates hydrogen peroxide when contacted with an aqueous solution, wherein the first reagent and the second reagent are kept separately prior to use, and wherein the pH of the formed liquid becomes about 8 or lower within about 1 minute after the contacting between the first reagent and the second reagent; and

contacting a target with an effective amount of the peroxyformic acid to form a treated target.

12. The method of claim 11 , wherein the treated target comprises from about 0.1 ppm to about 10,000 ppm of the peroxyformic acid.

13. The method of claim 11 , wherein the contacting between the target and the effective amount of the peroxyformic acid lasts for a sufficient time to bleach, remove soils and/or stabilize or reduce a microbial population in and/or on the treated target.

14. The method of claim 11 , wherein the target is a surface in need of high-level disinfecting.

15. The method of claim 14 , wherein the surface is a medical instrument in need of repurposing or reprocessing.

16. The method of claim 15 , wherein the medical instrument is an endoscope, and the treated surface comprises from about 10 ppm to about 500 ppm of the peroxyformic acid.

17. The method of claim 11 , wherein the target is water and/or at least a portion of a medium, a container, a piece of equipment, a system or a facility for producing, holding, processing, packaging, storing, or transporting pulp, and wherein the target is used in the papermaking, textiles, food, or pharmaceutical industry.

18. The method of claim 11 , wherein the target is a food item or a plant item and/or at least a portion of a medium, a container, an equipment, a system or a facility for growing, holding, processing, packaging, storing, transporting, preparing, cooking or serving the food item or the plant item.

19. The method of claim 11 , wherein the target is at least a portion of a medium, a surface, a container, an equipment, or a system in a health care facility.

20. The method of claim 11 , wherein the peroxyformic acid is applied to the target by means of a spray, a fog, or a foam, or by dipping all or part of the target in a composition comprising the peroxyformic acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2020
From: LI, JUNZHONG; BREWSTER, ALLISON; STAUB, RICHARD; LANGE, STEVEN J.; CHERITU, TAZ; FAST, JONATHAN P.
To: ECOLAB USA INC.
Reel/Frame 054601/0474 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2020
From: HANSON, CATHERINE
To: ECOLAB USA INC.
Reel/Frame 054601/0578 →
Continuity (5)
Continuation 16552323 · Aug 27, 2019
Continuation 15345263 · Nov 7, 2016
Continuation 14973389 · Dec 17, 2015
Provisional Application 62094048 · Dec 18, 2014
Related Publication 20210029996A1 · Feb 4, 2021
Cited By (1)
US 12,439,916