Peracid/Peroxide Composition, Process for Accurately Making the Same, and Method for Use as an Evaporating Film Anti-Microbial Solution and as a Photosensitizer

• US 20130251590A1
• Filed: 09/21/2009
• Published: 09/26/2013
• Est. Priority Date: 01/11/2005
• Status: Abandoned Application

• Current Assignee: Contec, Inc
• Original Assignee: BioMed Protect, LLC
• Inventors: Golden, Jeffry, Brister, Paul, Martin, Charles, Stader, Joan
• Application Number:
  US13/383,067
• Publication Number:
  US 20130251590A1
• Time in Patent Office: Days
• US Class Current: 422/24
• CPC Class Codes: A01N 2300/00 Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
• CPC Class Codes: A01N 25/30 characterised by the surfactants
• CPC Class Codes: A01N 37/16 containing the group; Thio analogues thereof
• CPC Class Codes: A01N 59/00 Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds

Abstract

A method is provided for the microbicidal treatment of a surface such as sanitization, disinfection, sterilization, and decontamination of a surface or object by use of an anti-microbial composition comprising an aqueous solution of peracetic acid and hydrogen peroxide with acetic acid, water soluble polymer containing lactam, and phosphate ester surfactant and little or no stabilizer, and according to the method enhanced microbicidal efficacy is obtained when the composition is applied onto a surface as a thin film wetting the surface so that a shorter contact time for a desired fractional reduction in microbial population is obtained Still further, the compositions comprise photosensitizer for light-activated anti-microbial efficacy.

Claims

1. A method for the microbicidal treatment of a surface comprising the steps of:

applying a microbicidal composition to form a thin layer that wets said surface, wherein said microbicidal composition comprises;

hydrogen peroxide in concentration in a range of about 0.4 to 8% by weight,

peracetic acid in concentration in a range of about 0.02 to about 0.55% by weight,

acetic acid in concentration less that about 8% by weight,

phosphate ester surfactant in concentration in a range of about 0.01 to about 0.5% by weight,

water soluble polymer containing lactam in concentration in a range of about 0.01 to about 0.5% by weight,

less than 0.2% by weight of stabilizers selected from a group comprising inorganic phosphates, phosphonates, organic phosphonic acids or their salts, ethylenediaminetetracetic acid or its sodium salt,

less than about 1 ppm of mono- and divalent metal ions,

less than about 1 ppm of halide ions, and

a balance of water; and

contacting said surface with said microbicidal composition for a contact time that is greater than about 20% but less than or equal to 100% of an evaporation time of said thin layer, during said contact time said thin layer evaporating.

2. The method of claim 1, wherein said microbicidal composition further comprises less than 0.5% by weight of minors selected from a group comprising fragrance, colorant, and aesthetic enhancements.

3. The method of claim 1 further comprising:

illuminating said surface with light for photosensitized microbicidal effect.

4. The method of claim 1 further comprising:

rinsing said surface with clean water to substantially remove residue.

5. The method of claim 1 further comprising:

air-drying said surface.

6. The method of claim 1, wherein the step of applying said microbicidal composition is by a wipe that is wetted with said microbicidal composition just prior to use.

7. The method of claim 1, wherein the step of applying said microbicidal composition is by a packaged pre-wetted wipe with a ratio of a mass of said microbicidal composition and a mass of said wipe is in a range of 0.25 to about 10.

8. The method of claim 1 wherein in the step of contacting said surface with said microbicidal composition said contact time is about 100% of the evaporation time of said thin layer, and wherein the steps of applying said microbicidal composition and contacting said surface with said microbicidal composition are repeated one or more times.

9. The method of claim 3, wherein said surface is illuminated by ultraviolet light with a fluence of about 30 ml/cm² or greater for said photosensitized microbicidal effect.

10. The method of claim 1, wherein said thin layer has an initial thickness up to 150 μ

m.

11. The method of claim 1, wherein said thin layer has an initial thickness in a range of about 10 μ

m to 100 μ

m.

12. The method of claim 1, wherein said contact time is in a range of 25% to 70% of the said evaporation time.

13. A process for accurately making a batch of a microbicidal composition, wherein said batch of microbicidal composition comprises:

hydrogen peroxide in concentration in a range of about 2.0 to 6% by weight,

peracetic acid in concentration in a range of about 0.05 to about 0.74% by weight,

an equilibrium quantity of acetic acid,

phosphate ester surfactant in concentration in a range of about 0.025 to about 0.3% by weight,

water soluble polymer in concentration in a range of about 0.025 to about 0.3% by weight, and

a balance of water,

the resulting microbicidal composition having an equilibrium concentration quotient of about

14. The process of claim 13, wherein said water soluble polymer contains lactam.

15. The process of claim 13, wherein said batch of microbicidal composition further comprises:

acid catalyst in concentration in the range of 0 to about 1000 ppm by weight,

less than 0.2% by weight of stabilizers selected from a group comprising inorganic phosphates, phosphonates, organic phosphonic acids or their salts, ethylenediaminetetracetic acid or its sodium salt,

less than about 1 ppm by weight of mono- and divalent metal ions,

less than about 1 ppm by weight of halide ions, and

less than 0.5% by weight of minors selected from the group of fragrance, colorant, and aesthetic enhancements.

16. The process of claim 15, further comprising:

determining by calculation that includes decomposition of peracetic acid into acetic acid and oxygen and an evaporation of water during the process, an amount of a diluted solution of a more concentrated solution of known composition comprising peracetic acid, hydrogen peroxide, acetic acid, acid catalyst, and water, an amount of glacial acetic acid, an amount of an aqueous solution of hydrogen peroxide, amounts of surfactant, polymer, and minors, and an amount of de-ionized/reverse osmosis filtered water to be added to the batch to obtain said target concentrations.

17. The process of claim 16, further comprising:

heating about 75% to about 100% of the said amount of de-ionized/reverse osmosis filtered water in a clean, passivated blending vessel to said selected batching temperature and continuously mixing contents of said vessel to limit spatial temperature variation of said contents to less than about 5°

C.

18. The process of claim 17, further comprising:

adding the determined amount of water soluble polymer to and mixing with said heated water;

adding the determined amount of surfactant to and mixing with the contents of said vessel;

adding the determined amounts of hydrogen peroxide solution and glacial acetic acid to and mixing with the contents of said vessel;

adding the determined amount of peracetic acid solution to and mixing with the contents of said vessel; and

adding the determined amount of water to and mixing with the contents of said vessel.

19. The process of claim 18, further comprising:

maintaining the contents of said vessel at said batching temperature with less than about 5°

C. spatial or temporal variation in the temperature of the contents for a batching time in a range of about 2 to 4 equilibration times.

20. The process of claim 19, further comprising:

measuring concentrations of hydrogen peroxide, and peracetic acid.

21. The process of claim 20, further comprising:

cooling the contents of the contents of said vessel to a desired temperature or to ambient temperature in a time that is much less than an equilibration time.

22. The process of claim 18, further comprising a step of:

adjusting the microbicidal composition of the blended mixture to obtain said target concentrations;

23. The process of claim 18, further comprising a step of:

adding one or more said minors to and mixing with the contents of said vessel;

24. The process of claim 21, further comprising a step of:

storing the resulting microbicidal composition in said vessel, or transferring the contents to another vessel, or transferring the contents to a product package, or transferring the contents as an ingredient in one or more products.

25. The process of claim 13 wherein the selection of said target concentrations is made so that during the year following the making of the batch, the concentration of peracetic acid in the resulting microbicidal composition remains within an upper limit and a lower limit that are within ±

30% w/w of said target concentration and the concentration of hydrogen peroxide in the resulting microbicidal composition remains within an upper limit and a lower limit that are within ±

10% w/w of said target concentration.

26. A microbicidal composition comprising:

hydrogen peroxide in concentration in a range of about 2.0 to 6% by weight,

peracetic acid in concentration in a range of about 0.05 to about 0.74% by weight,

an equilibrium quantity of acetic acid,

phosphate ester surfactant in concentration in a range of about 0.025 to about 0.3% by weight,

water soluble polymer in concentration in a range of about 0.025 to about 0.3% by weight, and

a balance of water,

the resulting microbicidal composition having an equilibrium concentration quotient of about

27. The microbicidal composition of claim 26, wherein said soluble polymer contains lactam.

28. The microbicidal composition of claim 26, further comprising:

acid catalyst in concentration in a range of 0 to about 1000 ppm by weight,

less than 0.2% by weight of stabilizers selected from a group, comprising inorganic phosphates, phosphonates, organic phosphonic acids or their salts, ethylenediaminetetracetic acid or its sodium salt,

less than about 1 ppm by weight of mono- and divalent metal ions,

less than about 1 ppm by weight of halide ions, and

less than 0.5% by weight of minors selected from a group comprising fragrance, colorant, stabilizer, and aesthetic enhancements.

29. The microbicidal composition of claim 26, wherein the resulting microbicidal composition is made by a process for accurately making a batch of the microbicidal composition, the said process comprising the steps of:

selecting target concentrations of hydrogen peroxide, peracetic acid, polymer, and surfactant in the resulting microbicidal composition at a selected batching temperature in a range of about 40°

C. to about 55°

C.;

calculating target equilibrium concentration of acetic acid in the resulting microbicidal composition; and

selecting an initial concentration of peracetic acid, determining by calculation that includes decomposition of peracetic acid into acetic acid and oxygen and an evaporation of water during the batch process, an amount of a diluted solution of a more concentrated solution of known composition comprising from about 8% to about 25% w/w peracetic acid, about 10% to about 35% w/w hydrogen peroxide, from about 8% to about 28% w/w acetic acid, and water, an amount of glacial acetic acid, an amount of an aqueous solution of hydrogen peroxide, amounts of surfactant, polymer, and minors, and an amount of de-ionized/reverse osmosis filtered water to be added to the hatch to obtain the target concentrations.

30. The microbicidal composition of claim 29, wherein said process further comprising:

heating from about 75% to about 100% of an amount of de-ionized/reverse osmosis filtered water in a clean, passivated blending vessel to the selected botching temperature and continuously mixing the contents of said vessel to limit the spatial temperature variation of the contents to less than about 5°

C.;

adding the determined amount of water soluble polymer to and mixing with said heated water;

adding the determined amount of surfactant to and mixing with the contents of said vessel;

adding the determined amounts of hydrogen peroxide solution and glacial acetic acid to and mixing with the contents of said vessel;

adding the determined amount of peracetic acid solution to and mixing with the contents of said vessel;

adding the remainder of the determined amount of water to and mixing with the contents of said vessel;

maintaining the contents of said vessel at the batching temperature with less than about 5°

C. spatial or temporal variation in the temperature of the contents for a batching time in a range of about 2 to 4 equilibration times;

measuring the concentrations of hydrogen peroxide, and peracetic acid; and

cooling the contents of said vessel to a desired temperature or to ambient temperature in a time that is much less than an equilibration time,

31. The microbicidal composition of claim 30, wherein said process further comprises:

adjusting the composition of the blended mixture to obtain the target concentrations; and

adding one or more said minors to and mixing with the contents of said vessel;

32. The microbicidal composition of claim 30, wherein said process further comprises a step of:

storing the resulting microbicidal composition in said vessel, or transferring the contents to another vessel, or transferring the contents to a product package, or transferring the contents as an ingredient in one or more products.

33. The microbicidal composition of claim 26, wherein said microbicidal composition has a concentration of peracetic acid that remains within ±

30% w/w of a desired nominal value in a range of about 0.05 and 0.74% w/w and a concentration of hydrogen peroxide that remains within ±

10% w/w of a desired nominal value in a range of about 1 and 6% w/w for at least one year when stored within a temperature range of 10 to 30°

C.

34. A use of the microbicidal composition of claim 26 as a photosensitizer for ultraviolet light activated microbicidal effect.