IP Library Granted Patent US 7,901,824
Granted Patent B2
US 7,901,824 · App. 12/571,943 · Granted Mar 8, 2011

Colorant treated ion exchange resins, method of making, heat transfer systems and assemblies containing the same, and method of use

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,901,824
App. No.
12/571,943
Granted
Mar 8, 2011
Kind
B2
Abstract

Disclosed is a colorant treated ion exchange resin comprising at least 15% of exchangeable groups comprising at least one of an ion, a Lewis acid, or a Lewis base resulting from a colorant having a pK a or pK b of greater than 5 in an aqueous solution at 25° C., based on the total number of exchangeable groups. Also disclosed are heat transfer systems, assemblies, fuel cell systems and methods of maintaining a conductivity of less than 200 μS/cm in a heat transfer fluid that employ the disclosed colorant treated ion exchange resins. Finally, a method of making the disclosed colorant treated ion exchange resins is provided.

Claims (74)

1. A heat transfer system, comprising

a circulation loop defining a flow path for a colored heat transfer fluid having a conductivity of less than 10 μS/cm, and

an ion exchange resin positioned in the flow path, the ion exchange resin comprising at least 15% by total number of the exchangeable groups comprising a colorant, based on the total number of the exchangeable groups,

wherein the colorant is of the formula:

R{A k [(B) n R 1 ] m } x

wherein

R is an organic chromophore selected from the group consisting of anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, xanthene, acridine, indene, phthalocyanine, azaannulene, nitroso, nitro, diarylmethane, triarylmethane, methine, indamine, azine, oxazine, thiazine, quinoline, indigoid, indophenol, lactone, aminoketone, hydroxyketone, stilbene, thiazole, one or more conjugated aromatic groups, one or more conjugated heterocyclic groups, one or more C-C double bonds, or combinations thereof;

A is a linking moiety in said chromophore and is selected from the group consisting of O, N or S;

k is 0 or 1;

B is selected from the group consisting of one or more alkyleneoxy or alkoxy groups containing from 1 to 8 carbon atoms;

n is an interger of from 1 to 100;

m is 1 or 2;

x is an integer of from 1 to 5; and

R 1 is selected from the group consisting of H, C 1 -C 6 alkyl or alkoxy groups containing from 1 to 8 carbon atoms, or combinations thereof.

2. The heat transfer system of claim 1 , wherein the colored heat transfer fluid comprises a non-conductive colorant and has a conductivity of no more than or equal to 10 μS/cm.

3. The heat transfer system of claim 2 , wherein the colored heat transfer fluid has a conductivity of less than 5 μS/cm.

4. The heat transfer system of claim 3 , wherein the colored heat transfer fluid has a conductivity from 0.02 to 5 μS/cm.

5. The heat transfer system of claim 4 , wherein the colored heat transfer fluid has a conductivity from 0.05 to 1 μS/cm.

6. The heat transfer system of claim 2 , wherein the non-conductive colorant is present in an amount of from 0.0001 to 0.2% by weight, based on the total weight of the colored heat transfer fluid.

7. The heat transfer system of claim 6 , wherein the non-conductive colorant is present in an amount of from 0.0005 to 0.1% by weight, based on the total weight of the colored heat transfer fluid.

8. The heat transfer system of claim 7 wherein the non-conductive colorant is present in an amount of from 0.0005 to 0.05% by weight, based on the total weight of the colored heat transfer fluid.

9. The heat transfer system of claim 8 wherein the colored heat transfer fluid further comprises an alcohol.

10. The heat transfer system of claim 9 wherein the alcohol is at least one of methanol, ethanol, propanol, butanol, furfurol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, dipropylene glycol, butylene glycol, glycrol, monoethylether of glycerol, dimethyl ether of glycerol, 1,2,6-hexanetriol, trimethylolpropane, methoxyethanol, or a combination thereof.

11. The heat transfer system of claim 9 wherein the colorant in the ion exchange resin and the non-conductive colorant in the colored heat transfer fluid are the same.

12. The heat transfer system of claim 11 wherein the colorant is substantially free of functional groups that will form an ionic species due to hydrolysis in an aqueous alcohol solution.

13. The heat transfer system of claim 12 wherein the colorant is substantially free of functional groups selected from the group consisting of carboxylate groups, sulfonate groups, phosphonate groups, quaternary amines, groups that carry a positive charge, or groups that carry a negative charge.

14. The heat transfer system of claim 11 wherein the colorant comprises at least one of the following chromophores: anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, xanthene, acridine, indene, phthalocyanine, azaannulene, nitroso, nitro, diarylmethane, triarylmethane, methine, indamine, azine, oxazine, thiazine, quinoline, indigoid, indophenol, lactone, aminoketone, hydroxyketone, stilbene, thiazole, one or more conjugated aromatic groups, one or more conjugated heterocyclic groups, one or more conjugated C-C double bond, or combinations thereof.

15. The heat transfer system of claim 14 wherein the colorant comprises the reaction product of a chromophore and a non-conductive alkoxy compound comprising from 1 to 30 carbons.

16. The heat transfer system of claim 15 wherein the colorant comprises the reaction product of at least one chromophore selected from the group consisting of anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, or combinations thereof.

17. A fuel cell system, comprising

at least one fuel cell comprising an anode, a cathode, and an electrolyte; and

a fuel cell heat transfer system in thermal communication with the at least one fuel cell, comprising

a circulation loop defining a flow path for a colored liquid heat transfer fluid having a conductivity of less than 10 μS/cm, and

an ion exchange resin positioned in the flow path, the ion exchange resin comprising ion exchangeable groups, wherein at least 15% of the total ion exchangeable groups comprise a colorant

wherein the colorant is of the formula:

R{A k [(B) n R 1 ] m } x

wherein

R is an organic chromophore selected from the group consisting of anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, xanthene, acridine, indene, phthalocyanine, azaannulene, nitroso, nitro, diarylmethane, triarylmethane, methine, indamine, azine, oxazine, thiazine, quinoline, indigoid, indophenol, lactone, aminoketone, hydroxyketone, stilbene, thiazole, one or more conjugated aromatic groups, one or more conjugated heterocyclic groups, one or more C-C double bonds, or combinations thereof;

A is a linking moiety in said chromophore and is selected from the group consisting of O, N or S;

k is 0 or 1;

B is selected from the group consisting of one or more alkyleneoxy or alkoxy groups containing from 1 to 8 carbon atoms;

n is an interger of from 1 to 100;

m is 1 or 2;

x is an integer of from 1 to 5; and

R 1 is selected from the group consisting of H, C 1 -C 6 alkyl or alkoxy groups containing from 1 to 8 carbon atoms, or combinations thereof.

18. A method of maintaining a conductivity of less than 10 μS/cm in a colored heat transfer fluid, comprising

passing a colored heat transfer fluid through a heat transfer system, wherein the colored heat transfer fluid has a conductivity of less than 10 μS/cm and the heat transfer system comprises

a circulation loop defining a flow path for the colored heat transfer fluid, and

an ion exchange resin positioned in the flow path, the ion exchange resin comprising at least 15% by total number of exchangeable groups comprising a colorant, based on the total number of exchangeable groups

wherein the colorant is of the formula:

R{A k [(B) n R 1 ] m } x

wherein

R is an organic chromophore selected from the group consisting of anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, xanthene, acridine, indene, phthalocyanine, azaannulene, nitroso, nitro, diarylmethane, triarylmethane, methine, indamine, azine, oxazine, thiazine, quinoline, indigoid, indophenol, lactone, aminoketone, hydroxyketone, stilbene, thiazole, one or more conjugated aromatic groups, one or more conjugated heterocyclic groups, one or more C-C double bonds, or combinations thereof;

A is a linking moiety in said chromophore and is selected from the group consisting of O, N or S;

k is 0 or 1;

B is selected from the group consisting of one or more alkyleneoxy or alkoxy groups containing from 1 to 8 carbon atoms;

n is an interger of from 1 to 100;

m is 1 or 2;

x is an integer of from 1 to 5; and

R 1 is selected from the group consisting of H, C 1 -C 6 alkyl or alkoxy groups containing from 1 to 8 carbon atoms, or combinations thereof.

19. The method of claim 18 wherein the colored heat transfer fluid has a color that is visible to the human eye.

20. A method of making a colorant treated ion exchange resin, comprising

contacting an ion exchange resin with an aqueous colorant solution for a period of time sufficient to exchange at least 15% of the exchange sites with colorant

wherein the colorant is of the formula:

R{A k [(B) n R 1 ] m } x

wherein

R is an organic chromophore selected from the group consisting of anthraquinone, triphenylmethane, diphenylmethane, azo containing compounds, disazo containing compounds, trisazo containing compounds, diazo containing compounds, xanthene, acridine, indene, phthalocyanine, azaannulene, nitroso, nitro, diarylmethane, triarylmethane, methine, indamine, azine, oxazine, thiazine, quinoline, indigoid, indophenol, lactone, aminoketone, hydroxyketone, stilbene, thiazole, one or more conjugated aromatic groups, one or more conjugated heterocyclic groups, one or more C-C double bonds, or combinations thereof;

A is a linking moiety in said chromophore and is selected from the group consisting of O, N or S;

k is 0 or 1;

B is selected from the group consisting of one or more alkyleneoxy or alkoxy groups containing from 1 to 8 carbon atoms;

n is an interger of from 1 to 100;

m is 1 or 2;

x is an integer of from 1 to 5; and

R 1 is selected from the group consisting of H, C 1 -C 6 alkyl or alkoxy groups containing from 1 to 8 carbon atoms, or combinations thereof.

Assignments (22)
GRANT OF SECURITY INTEREST IN PATENT RIGHTS Recorded Sep 8, 2024
From: PRESTONE PRODUCTS LLC
To: GOLDMAN SACHS MIDDLE MARKET LENDING CORP. II
Reel/Frame 068892/0272 →
GRANT OF SECURITY INTEREST IN PATENT RIGHTS Recorded Aug 15, 2024
From: PRESTONE PRODUCTS LLC
To: GOLDMAN SACHS MIDDLE MARKET LENDING CORP. II, AS COLLATERAL AGENT
Reel/Frame 068630/0147 →
RELEASE/TERMINATION OF INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 8, 2024
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: BIO-LAB, INC.; KIK CUSTOM PRODUCTS INC.; NC BRANDS, L.P.; PRESTONE PRODUCTS CORPORATION
Reel/Frame 068220/0306 →
RELEASE AND TERMINATION OF INTELLECTUAL PROPERTY SECURITY INTEREST Recorded Jul 8, 2024
From: BARCLAYS BANK PLC
To: AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIO-LAB, INC.; HI-LEX LLC; HOMECARE LABS, INC.; KIK CUSTOM PRODUCTS, INC.; KIK INTERNATIONAL, LLC; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; SUNBELT POOL PRODUCTS, LLC; JAMES AUSTIN COMPANY; NC BRANDS L.P.; CYGNUS CORPORATION
Reel/Frame 068220/0455 →
ENTITY CONVERSION Recorded Jun 25, 2024
From: PRESTONE PRODUCTS CORPORATION
To: PRESTONE PRODUCTS LLC
Reel/Frame 067826/0319 →
PARTIAL RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Jun 18, 2024
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: PRESTONE PRODUCTS CORPORATION
Reel/Frame 067777/0634 →
PARTIAL RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Jun 18, 2024
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
To: PRESTONE PRODUCTS CORPORATION
Reel/Frame 067777/0649 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Jun 18, 2024
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: PRESTONE PRODUCTS CORPORATION
Reel/Frame 067777/0671 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Jun 18, 2024
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: PRESTONE PRODUCTS CORPORATION
Reel/Frame 067777/0751 →
SECURITY AGREEMENT Recorded Dec 27, 2021
From: AQUA CLEAR INDUSTRIES, LLC; ASEPIS, INC.; BIO-LAB, INC.; HI-LEX LLC; HOMECARE LABS, INC.; KIK CUSTOM PRODUCTS INC.; KIK INTERNATIONAL LLC; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; SUNBELT POOL PRODUCTS, LLC; JAMES AUSTIN COMPANY; CYGNUS CORPORATION; NC BRANDS L.P.
To: BARCLAYS BANK PLC
Reel/Frame 058592/0835 →
RELEASE OF INTELLECTUAL PROPERTY SECURITY INTEREST Recorded Jul 29, 2021
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: BIO-LAB, INC.; HI-LEX LLC; HOMECARE LABS, INC.; JAMES AUSTIN COMPANY; KIK INTERNATIONAL LLC; NC BRANDS L.P.; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; SUNBELT POOL PRODUCTS, LLC
Reel/Frame 057650/0125 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT (NOTES) Recorded Dec 22, 2020
From: BIO-LAB, INC.; KIK CUSTOM PRODUCTS INC.; KIK INTERNATIONAL LLC; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; JAMES AUSTIN COMPANY; CYGNUS CORPORATION; NC BRANDS L.P.; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; HI-LEX LLC; HOMECARE LABS, INC.; SUNBELT POOL PRODUCTS, LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 055327/0754 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT (2019) Recorded Jan 28, 2019
From: APG, INC.; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIO-LAB, INC.; HI-LEX LLC; HOMECARE LABS, INC.; KIK CUSTOM PRODUCTS INC.; KIK CUSTOM PRODUCTS, INC; KIK INTERNATIONAL LLC; MARIETTA CORPORATION; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; SUNBELT POOL PRODUCTS, LLC; JAMES AUSTIN COMPANY; CBI LABORATORIES, INC.; CYGNUS CORPORATION; NC BRANDS L.P.
To: BARCLAYS BANK PLC, AS AGENT
Reel/Frame 048180/0101 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT (TERM LOAN) Recorded Jan 23, 2019
From: PRESTONE PRODUCTS CORPORATION
To: BARCLAYS BANK PLC
Reel/Frame 049517/0967 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT (ABL) Recorded Jan 23, 2019
From: PRESTONE PRODUCTS CORPORATION
To: BARCLAYS BANK PLC
Reel/Frame 049518/0001 →
RELEASE OF SECURITY INTEREST Recorded Sep 14, 2016
From: BARCLAYS BANK PLC
To: APG, INC.; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIO-LAB, INC.; CYGNUS CORPORATION; HI-LEX LLC; HOMECARE LABS, INC.; KIK CUSTOM PRODUCTS INC.; KIK CUSTOM PRODUCTS, INC; KIK INTERNATIONAL LLC; MARIETTA CORPORATION; SOLSKYN PERSONAL CARE LLC; KIK NEW JERSEY, LLC; PRESTONE PRODUCTS CORPORATION
Reel/Frame 040031/0793 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Apr 5, 2016
From: APG, INC.; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIO-LAB, INC.; CYGNUS CORPORATION; HI-LEX LLC; HOMECARE LABS, INC.; KIK CUSTOM PRODUCTS, INC. (TEXAS); KIK CUSTOM PRODUCTS INC. (DELAWARE); KIK INTERNATIONAL LLC; MARIETTA CORPORATION; PRESTONE PRODUCTS CORPORATION; SOLSKYN PERSONAL CARE LLC; KIK NEW JERSEY, LLC
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 038354/0938 →
TERM AND REL OF SEC INT IN PATS-2ND LIEN Recorded Apr 4, 2016
From: CREDIT SUISSE AG, AS COLLATERAL AGENT; PRESTONE PRODUCTS CORPORATION
To: FRAM GROUP IP LLC
Reel/Frame 038337/0762 →
TERM AND REL OF SEC INT IN PATS-1ST LIEN Recorded Apr 4, 2016
From: CREDIT SUISSE AG, AS COLLATERAL AGENT; PRESTONE PRODUCTS CORPORATION
To: FRAM GROUP IP LLC
Reel/Frame 038337/0741 →
SECURITY AGREEMENT Recorded Aug 12, 2011
From: FRAM GROUP IP LLC; PRESTONE PRODUCTS CORPORATION
To: CREDIT SUISSE AG, AS SECOND LIEN COLLATERAL AGENT
Reel/Frame 026740/0089 →
SECURITY AGREEMENT Recorded Aug 11, 2011
From: FRAM GROUP IP LLC; PRESTONE PRODUCTS CORPORATION
To: CREDIT SUISSE AG, AS FIRST LIEN COLLATERAL AGENT
Reel/Frame 026732/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2011
From: HONEYWELL INTERNATIONAL INC.
To: PRESTONE PRODUCTS CORPORATION
Reel/Frame 026671/0823 →