IP Library Granted Patent US 10,834,924
Granted Patent B2
US 10,834,924 · App. 16/552,323 · Granted Nov 17, 2020

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 10,834,924
App. No.
16/552,323
Granted
Nov 17, 2020
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 (18)

1. A method for forming peroxyformic acid comprising:

contacting a polyhydric alcohol ester of formic acid and hydrogen peroxide or an inorganic peroxo compound that generates hydrogen peroxide when contacted with an aqueous liquid to form a solution that comprises peroxyformic acid,

wherein the pH of the formed solution becomes about 8 or lower within about 1 minute after the contacting.

2. The method of claim 1 , wherein the polyhydric alcohol ester of formic acid is glycerol formate, pentaerythritol formate, mannitol formate, propylene glycol formate, sorbitol formate and/or a sugar formate.

3. The method of claim 2 , wherein the sugar formate comprises sucrose formates, dextrin formates, maltodextrin formates, or starch formates.

4. The method of claim 1 , wherein the formed solution has a pH ranging from about 2 to about 8.

5. The method of claim 4 , wherein the formed solution has a pH ranging from about 4 to about 8.

6. The method of claim 1 , wherein the formed solution comprises peroxyformic acid under ambient conditions and wherein said ambient conditions comprise the conditions of the surrounding environment.

7. The method of claim 1 , wherein the formed solution comprises peroxyformic acid at a temperature ranging from about 4° C. to about 60° C.

8. The method of claim 1 , further comprising contacting the polyhydric alcohol ester of formic acid and/or the hydrogen peroxide or inorganic peroxo compound that generates hydrogen peroxide with a catalyst that catalyzes the formation of peroxyformic acid from the polyhydric alcohol ester of formic acid and hydrogen peroxide.

9. The method of claim 8 , wherein the catalyst comprises a mineral acid or an enzyme, and wherein the enzyme comprises a perhydrolytic enzyme, lipase, coronase, termanyl or esperease.

10. The method of claim 1 , further comprising contacting the polyhydric alcohol ester of formic acid, and the hydrogen peroxide or inorganic peroxo compound that generates hydrogen peroxide with a stabilizing agent for peroxyformic acid and/or hydrogen peroxide, and/or a pH buffering agent.

11. The method of claim 10 , wherein the stabilizing agent is a pyridine carboxylic acid based stabilizer or salt thereof, a phosphonate based stabilizer or salt thereof, or combinations thereof.

12. The method of claim 1 , wherein the formed solution comprises about 1 ppm to about 500,000 ppm of the polyhydric alcohol ester of formic acid, and from about 150 ppm to about 150,000 ppm of the inorganic peroxo compound that generates hydrogen peroxide when contacted with the aqueous liquid.

13. The method of claim 1 , wherein the formed solution comprises from about 1 ppm to about 100,000 ppm of peroxyformic acid.

14. The method of claim 1 , wherein the formed solution comprises at least about 80% of the maximum experimental concentration of peroxyformic acid within from about 1 minute to about 15 minutes of the contact time.

15. The method of claim 1 , further comprising the step of adding a C 2 -C 22 peroxycarboxylic acid to the reagents.

16. The method of claim 15 , wherein the C 2 -C 22 peroxycarboxylic acid comprises peroxyacetic acid, peroxyoctanoic acid and/or peroxysulfonated oleic acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2019
From: LI, JUNZHONG; BREWSTER, ALLISON; STAUB, RICHARD; LANGE, STEVEN J.; CHERITU, TAZ; FAST, JONATHAN P.
To: ECOLAB USA INC.
Reel/Frame 050184/0729 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2019
From: HANSON, CATHERINE
To: ECOLAB USA INC.
Reel/Frame 050184/0747 →
Continuity (4)
Continuation 15345263 · Nov 7, 2016
Continuation 14973389 · Dec 17, 2015
Provisional Application 62094048 · Dec 18, 2014
Related Publication 20190387737A1 · Dec 26, 2019
Cited By (1)
US 12,439,916