IP Library Granted Patent US 11,330,818
Granted Patent B2
US 11,330,818 · App. 16/948,917 · Granted May 17, 2022

Water temperature as a means of controlling kinetics of onsite generated peracids

Inventors: Brandon Herdt (Saint Paul, MN); Richard Staub (Saint Paul, MN); Thomas C. Rustad (Saint Paul, MN); Junzhong Li (Saint Paul, MN); David D. McSherry (Saint Paul, MN); Paul R. Kraus (Saint Paul, MN); Richard Walsh (Saint Paul, MN)
Assignee: Ecolab USA Inc.
A01N37/16A01N37/02A01N59/00A61L2/18A61L2/186A61L2/24B01J4/001B01J4/008B01J14/00B01J19/0006B01J19/0013B01J19/24C02F1/50C02F1/722C07C407/00C07C409/24A61L2202/14B01J2219/00049B01J2219/00121B01J2219/00159B01J2219/24C02F2103/08
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Quick Facts
Patent No.
US 11,330,818
App. No.
16/948,917
Granted
May 17, 2022
Kind
B2
Abstract

Methods and systems for temperature-controlled, on-site generation of peracids, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions are disclosed. In particular, methods for using an adjustable biocide formulator or generator system overcome the limitations of temperature on the kinetics of the peracid generation and/or peracid decomposition inside an adjustable biocide formulator or generator system. The methods include the controlling of the temperature of at least one raw starting material, namely water, to improve upon methods of on-site generation of peracids. The methods allow for the generation of user-selected chemistry without regard to the ambient temperatures of the raw starting materials and/or the biocide formulator or generator system.

Claims (18)

1. A method for peroxycarboxylic acid forming composition generation or peroxycarboxylic acid generation comprising:

inputting a user-desired or system-controlled volume or mass of a peroxycarboxylic acid forming composition or peroxycarboxylic acid into a control software for on-site generation; and

combining one or more esters of a polyhydric alcohol and a C1 to C18 carboxylic acid, a source of alkalinity and an oxidizing agent at an alkaline pH of at least about 12 in an adjustable biocide formulator or generator system, wherein said system is an apparatus that is insensitive to environmental temperatures of the location of the apparatus and/or reagents comprising a reaction vessel, a series of feed pumps, an outlet for dosing the peroxycarboxylic acid forming composition or the peroxycarboxylic acid from said reaction vessel and a controller for a user- or system-inputted selection device; and

generating the peroxycarboxylic acid forming composition or peroxycarboxylic acid without an acid catalyst;

wherein said temperature insensitivity to the environmental temperatures of the location of the apparatus and/or reagents is controlled by a mechanism for maintaining a controlled temperature of said reaction vessel and/or one or more reagents;

wherein said feed pumps are in fluid connection with said reaction vessel and supply one or more reagents to produce said peroxycarboxylic acid forming composition in said reaction vessel; and

wherein said reaction vessel is in fluid connection with said outlet to dispense said peroxycarboxylic acid forming composition or peroxycarboxylic acid.

2. The method according to claim 1 , wherein the temperature control of said reaction vessel and supply of said reagents adjusts to a temperature of between about 4.4° C. to about 60° C.

3. The method according to claim 2 , wherein said temperature is adjusted to between about 21° C. to about 49° C.

4. The method according to claim 1 , wherein the source of alkalinity is sodium hydroxide, and wherein said sodium hydroxide is provided to said reaction vessel prior to the addition of said ester in a diluted solution.

5. The method according to claim 1 , wherein the peroxycarboxylic acid forming composition reaction goes to completion within less than about 30 minutes.

6. The method according to claim 1 , wherein the peroxycarboxylic acid forming composition maintains a peracid concentration within about 10% of its final completion concentration for at least about 1 minute.

7. The method according to claim 1 , wherein said temperature control mechanism is selected from the group consisting of external heating or cooling of the reaction vessel, internal heating of the reagents within the reaction vessel, preheating one or more of the reagents, and combinations of the same.

8. The method according to claim 7 , wherein said reaction vessel is a flow through reactor or a batch reactor and the heated reagent is water.

9. The method according to claim 1 , further comprising timing the addition of said esters in parallel or sequentially for reaction in said reaction manifold.

10. The method according to claim 1 , further comprising measuring the extent of said ester perhydrolysis reaction using one or more measurement devices, wherein said measurement device measures one or more reaction kinetics or system operations for said peroxycarboxylic acid generation selected from the group consisting of fluorescence, weight, flow, capacitive level, pH, oxidation reduction potential, pressure, temperature and combinations thereof, and wherein said measurement devices determine when to dilute said peroxycarboxylic acid forming composition with an acid or aqueous acidic solution to form said peroxycarboxylic acid.

11. The method according to claim 1 , further comprising providing an acid or aqueous acidic solution to form a peroxycarboxylic acid having a pH of about 0.1 to about 8.0, wherein the neutralization with the acid or aqueous acidic solution takes place when the concentration of peracid is within about 10% of its final concentration.

12. The method according to claim 1 , further comprising dispensing said peroxycarboxylic acid forming composition for use in a cleaning process, wherein said composition is dispensed from said reaction vessel when the concentration of peracid is within about 10% of its final concentration.

Continuity (6)
Continuation 16269820 · Feb 7, 2019
Division 15933161 · Mar 22, 2018
Division 14562960 · Dec 18, 2014
Division 13331385 · Dec 20, 2011
Provisional Application 61427951 · Dec 29, 2010
Related Publication 20210015096A1 · Jan 21, 2021
Cited By (1)
US 12,274,263