IP Library Granted Patent US 12680054
Granted Patent B2
US 12680054 · App. 18/295,399 · Granted Jul 14, 2026

Method of enhancing performance of a porous evaporative media

Inventors: Zhangzhang Yin (Monroeville, PA); Shawn Michael Dalke (Sugar Grove, IL); Michael J. Murcia (Sycamore, IL); Bingzhi Chen (Naperville, IL); Robert M. Lowe (Chicago, IL); Carter M. Silvernail (St. Paul, MN); Ashish Dhawan (St. Paul, MN); Thomas R. Mohs (St. Paul, MN)
Assignee: Ecolab USA Inc.
C11D3/361C11D3/3719C11D3/3723C11D3/3757F24F6/04F24F2221/22
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Quick Facts
Patent No.
US 12680054
App. No.
18/295,399
Filed
Apr 4, 2023
Granted
Jul 14, 2026
Kind
B2
Art Unit
1714
USPC
134/35
Abstract

The method of improving an evaporative performance of a porous evaporative media in a cooling system that utilizes water evaporation for heat transfer, the method comprising contacting the porous evaporative media with a nonionic surfactant, optionally in combination with an antiscalant.

Claims (21)

1 . A method of improving an evaporative performance of a porous evaporative media in a cooling system that utilizes water evaporation for heat transfer, the method comprising contacting the porous evaporative media with a scale relocating-effective amount of a nonionic surfactant and no antiscalant,

wherein the nonionic surfactant comprises a C 8 -C 22 alcohol ethoxylate, a C 8 -C 22 ethoxylate, a C 8 -C 22 alkyl phenol ethoxylate, a terminally blocked C 8 -C 22 alcohol polyethylene glycol ether, a monododecyl ether, a nonoxynol, an ethoxylated C 8 -C 22 ester, an ethoxylated amine, a C 8 -C 22 amide, a polyethoxylated tallow amine, a poloxamer, a C 8 -C 22 ester of a polyhydroxy compound, an alkyl polyglucoside, myristamine oxide, a polyethylene oxide polymer, a polypropylene polymer, a polyethylene oxide/polypropylene oxide copolymer, octaethylene glycol monododecyl ether, pentaethylene glycol monododecyl ether, Triton X-100, cocamide monoethanolamine, cocamide diethanolamine, glycerol monostearate, glycerol monolaurate, sorbitan monolaurate, sorbitan monostearate, sorbitan tristearate, Tween 20, Tween 40, Tween 60, Tween 80, decyl glucoside, lauryl glucoside, octyl glucoside, or a combination thereof.

2 . The method of claim 1 , comprising contacting the porous evaporative media with the nonionic surfactant and optionally a chelant before using the porous evaporative media in the cooling system.

3 . The method of claim 1 , wherein the cooling system comprises an adiabatic cooling system, an evaporative cooling system, or a humidification system.

4 . The method of claim 1 , wherein the cooling system is used in a data center, an automotive application, an industrial application, a commercial application, or an agricultural application.

5 . The method of claim 1 , wherein the nonionic surfactant comprises polyethylene oxide, polypropylene oxide, polyethylene oxide/polypropylene oxide, or a combination thereof.

6 . The method of claim 1 , wherein the nonionic surfactant comprises a C8-C22 alcohol ethoxylate, a C8-C22 ethoxylate, a C8-C22 alkyl phenol ethoxylate, a terminally blocked C8-C22 alcohol polyethylene glycol ether, a monododecyl ether, a nonoxynol, an ethoxylated C8-C22 ester, an ethoxylated amine, a C8-C22 amide, a polyethoxylated tallow amine, a poloxamer, a C8-C22 ester of a polyhydroxy compound, an alkyl polyglucoside, myristamine oxide, or a combination thereof.

7 . The method of claim 1 , wherein the nonionic surfactant comprises a polyethylene oxide polymer, a polypropylene polymer, a polyethylene oxide/polypropylene oxide copolymer, octaethylene glycol monododecyl ether, pentaethylene glycol monododecyl ether, Triton X-100, cocamide monoethanolamine, cocamide diethanolamine, glycerol monostearate, glycerol monolaurate, sorbitan monolaurate, sorbitan monostearate, sorbitan tristearate, Tween 20, Tween 40, Tween 60, Tween 80, decyl glucoside, lauryl glucoside, octyl glucoside, or a combination thereof.

8 . The method of claim 1 , comprising contacting the porous evaporative media in the cooling system with the nonionic surfactant and optionally a chelant continuously for a period of from about one day to about one year.

9 . The method of claim 1 , comprising contacting the porous evaporative media in the cooling system with the nonionic surfactant and optionally a chelant continuously for a period of from about one day to about three months.

10 . The method of claim 1 , comprising contacting the porous evaporative media in the cooling system with the nonionic surfactant and optionally a chelant continuously for a period of from about one day to about one month.

11 . The method of claim 1 , further comprising contacting the porous evaporative media with a chelant.

12 . The method of claim 11 , wherein the chelant comprises ethylenediaminetetraacetic acid (EDTA), ethyleneglycol bis(2-aminoethyl ether)-N,N,N′,N′ tetraacetic acid (EGTA), carboxymethyl cellulose (CMC), nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid (DTPA), methylglycinediacetic acid, [[(2-hydroxyethyl)imino]bis(methylene)]-bisphosphonic acid, 4-(phosphonomethyl)-2-hydroxy-2-oxo-1,4,2-oxazaphosphorinane, a salt thereof, or a combination thereof.

13 . The method of claim 1 , wherein the porous evaporative media comprises one or more corrugated sheets.

14 . The method of claim 13 , wherein the one or more corrugated sheets comprises a fibrous material, a filler, a polymer binder, or a combination thereof.

15 . The method of claim 1 , comprising contacting the porous evaporative media with the nonionic surfactant and optionally a chelant while the porous evaporative media is being used in the cooling system.

16 . The method of claim 15 , comprising combining water of the cooling system with the nonionic surfactant and optionally a chelant to produce a treated cooling water for relocating scale formation on the porous evaporative media.

17 . The method of claim 16 , comprising continuously feeding the treated cooling water through the porous evaporative media.

18 . The method of claim 16 , wherein the concentration of the nonionic surfactant in the treated cooling water is from about 10 ppm to about 200 ppm.

19 . The method of claim 16 , further comprising adjusting the pH of the treated cooling water with a pH adjusting agent.

20 . The method of claim 19 , wherein the pH adjusting agent comprises sulfuric acid, acetic acid, citric acid, nitric acid, propionic acid, tartaric acid, fumaric acid, phosphoric acid, salts thereof, or a combination thereof.