IP Library Granted Patent US 7,005,458
Granted Patent B2
US 7,005,458 · App. 10/601,088 · Granted Feb 28, 2006

Static dissipative polyurethane foams

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Quick Facts
Patent No.
US 7,005,458
App. No.
10/601,088
Granted
Feb 28, 2006
Kind
B2
Abstract

A static dissipative flexible polyurethane foam is formed under free rise expansion conditions from a polyether graft polyol and an isocyanate, wherein one or more anti-static additives are incorporated into the reaction mix in an amount from 0.10 to 20 parts by weight. Water is added in an amount of from 0.2 to 1.0 parts per weight. Upon curing, the foam has a density in the range of 6 to 20 pounds per cubic foot, a surface resistivity below 1×10 11 ohms/square, and a pore size in the range of 100 to 250 pores per inch. The foam may be fabricated (cut or shaped) to form a shaped article, such as a roller, a clean room wipe, a cosmetic applicator or a packaging element.

Claims (26)

1. A method for making a flexible polyurethane foam, comprising:

mixing at a mix head to react (i) a polyether graft polyol or a polyether graft polyol mixed with an ester polyol and/or a polyether polyol, wherein said polyol or combination of polyols has a number average molecular weight of from about 500 to about 8000, with (ii) an isocyanate selected from the group consisting of diphenylmethane 4,4′ diisocyanate, diphenyl methane 2,2′ diisocyanate, diphenylmethmne 2,4′ diisocyanate, toluene diisocyanate, higher molecular weight isocyanate oligomers, and mixtures thereof, with an isocyanate index in the range of 95 to 110 to form a reaction mix;

incorporating into the reaction mix water in an amount from 0.2 to 1.0 parts by weight per hundred parts polyol;

further incorporating into the reaction mix one or more anti-static additives in an amount from 0.1 to 20 parts by weight per hundred parts polyol, to form a foam-forming mixture; and

presenting the foam-forming mixture to an open container or a moving conveyor to permit free rise expansion of the polyurethane foam; wherein, upon curing, the polyurethane foam has a density in the range of 6 to 20 pounds per cubic foot, a surface resistivity below 1×10 11 ohms/square as determined at 12% relative humidity and 23° C., and a pore size in the range of 100 to 250 pores per inch.

2. The method of claim 1 , wherein the anti-static additive is selected from the group consisting of: quarternary ammonium compounds, metallic salts, complexes of metallic salts with polyhydric alcohols and their derivatives, complexes of metallic salts with mono-ols, hexahalogenated ionic compounds, and carbon black.

3. The method of claim 1 , wherein the graft polyol comprises at least 20 parts by weight per hundred parts of the polyol component of the reaction mix.

4. The method of claim 1 , further comprising incorporating into the reaction mix at the mix head a cross-linking agent selected from the group consisting of diethanolamine (DEOA), ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG), propylene glycol (PG), dipropylene glycol (DPG), 1,4 butanediol (BDO), and mixtures thereof, and in an amount from 0 to 25 parts by weight per hundred parts polyol.

5. The method of claim 1 , wherein the surface resistivity of the polyurethane foam is from 1×10 7 ohms/square to 1×10 7 ohms/square as determined at 12% relative humidity and 23° C.

6. The method of claim 1 , wherein the density of the polyurethane foam as from 7 to 9 pounds per cubic foot.

7. The method of claim 1 , wherein the isocyanate is diphenylmethane 4,4′ diisocyanate or diphenylmethmne 2,2′ diisocyanate or diphenylmethane 2,4′ diisocyanate, or mixtures thereof.

8. A method for making a shaped polyurethane foam part, comprising:

mixing at a mix head to react (i) a polyether graft polyol or polyol mixed with ester polyol and/or a polyether polyol, wherein said polyol or combination of polyols has a number average molecular weight of from about 500 to about 8000, with (ii) an isocyanate selected from the group consisting of diphenyl 4,4′ diisocyanate, diphenylmethane 2,2′ diisocyanate, diphenylmethane 2, 4′ diisocyanate, toluene diisocyanate, higher molecular weight isocyanate oligomers, and mixtures thereof, to form a reaction mix;

incorporating into the reaction mix water in an amount from 0.2 to 1.0 parts by weight per hundred parts polyol;

further incorporating into the reaction mix one or more anti-static additives in an amount from 0.1 to 20 parts by weight per hundred parts polyol, to form a foam-forming mixture;

presenting the foam-forming mixture to an open container or a moving conveyor to permit free rise expansion of the polyurethane foam, wherein, upon curing, the polyurethane foam has a density in the range of 6 to 20 pounds per cubic foot, a surface resistivity below 1×10 11 ohms/square as determined at 12% relative humidity and 23° C., and a pore size in the range of 100 to 250 pores per inch.; and

fabricating the polyurethane foam into the shaped polyurethane foam part.

9. The method of claim 8 , wherein the anti-static additive is selected from the group consisting of: quarternary ammonium compounds, metallic salts, complexes of metallic salts with polyhydric alcohols and their derivatives, complexes of metallic salts with mono-ols, hexahalogenated ionic compounds, and carbon black.

10. The method of claim 8 , wherein the graft polyol comprises at least 20 parts by weight per hundred parts of the polyol component of the reaction mix.

11. The method of claim 8 , further comprising incorporating into the reaction mix a cross-linking agent selected from the group consisting of: diethanolamine (DEOA), ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG), propylene glycol (PG), dipropylene glycol (DPG), 1,4 butanediol (BDO), and mixtures thereof, and in an amount from 0 to 25 parts by weight per hundred parts polyol.

12. The method of claim 8 , wherein the surface resistivity of the polyurethane foam is from 1×10 7 ohms/square to 1×10 9 ohms/square as determined at 12% relative humidity and 23° C.

13. The method of claim 8 , wherein the density of the polyurethane foam is from 7 to 9 pounds per cubic foot.

14. The method of claim 8 , wherein the isocyanate is diphenylmethane 4,4′ diisocyanate or diphenylmethane 2,2′ diisocyanate or diphenylmethane 2,4′ diisocyanate, or mixtures thereof.

15. The method of claim 8 , wherein fabricating comprises one or more of grinding, slicing, die-cutting, machining, peeling, convoluting, laser cutting, water pressure cutting or otherwise shaping by cutting.

16. A polyurethane foam produced by the method of claim 1 .

17. A polyurethane foam part produced by the method of claim 8 .

Assignments (26)
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT REEL/FRAME 052004/0277 Recorded Nov 25, 2025
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS SUCCESSOR IN INTEREST TO U.S. BANK NATIONAL ASSOCIATION
To: FXI, INC. (IN ITS OWN CAPACITY AND AS SUCCESSOR BY MERGER TO INNOCOR, INC.)
Reel/Frame 073698/0832 →
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT REEL/FRAME 063492/0830 Recorded Nov 25, 2025
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION
To: FXI, INC.
Reel/Frame 073698/0839 →
CORRECTIVE ASSIGNMENT TO CORRECT THE SUPPORTING DOCUMENTS PREVIOUSLY RECORDED AT REEL: 63492 FRAME: 830. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Nov 11, 2025
From: FXI, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 073572/0811 →
SECURITY INTEREST Recorded May 1, 2023
From: FXI, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 063492/0830 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 044779/0483 Recorded May 1, 2023
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS AGENT
To: FXI, INC.
Reel/Frame 063500/0738 →
SECURITY INTEREST Recorded Feb 25, 2020
From: FXI, INC.; INNOCOR, INC.
To: TRUIST BANK, AS AGENT
Reel/Frame 052019/0442 →
RELEASE OF SECURITY INTEREST Recorded Feb 25, 2020
From: TRUIST BANK, AS AGENT, SUCCESSOR-BY-MERGER TO SUNTRUST BANK
To: FXI, INC.
Reel/Frame 052019/0659 →
SECURITY INTEREST Recorded Feb 24, 2020
From: FXI, INC.; INNOCOR, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 052004/0277 →
RELEASE OF SECURITY INTEREST Recorded Nov 2, 2017
From: SUNTRUST BANK, AS AGENT
To: FXI, INC.
Reel/Frame 044360/0430 →
SECURITY INTEREST Recorded Nov 2, 2017
From: FXI, INC.
To: SUNTRUST BANK, AS AGENT
Reel/Frame 044360/0806 →
SECURITY INTEREST Recorded Nov 2, 2017
From: FXI, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 044779/0483 →
SECURITY INTEREST Recorded Dec 2, 2015
From: FXI, INC.
To: SUNTRUST BANK, AS AGENT
Reel/Frame 037189/0351 →
RELEASE OF SECURITY INTEREST Recorded Dec 2, 2015
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, SUCCESSOR BY MERGER TO WACHOVIA BANK, NATIONAL ASSOCIATION, AS AGENT
To: FXI, INC.
Reel/Frame 037186/0125 →
CHANGE OF NAME Recorded Dec 7, 2011
From: FOAMEX INNOVATIONS OPERATING COMPANY
To: FXI, INC.
Reel/Frame 027340/0565 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2009
From: FOAMEX INNOVATIONS, INC. (FORMERLY MP FOAM DIP LLC)
To: FOAMEX INNOVATIONS OPERATING COMPANY
Reel/Frame 023094/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2009
From: FOAMEX INTERNATIONAL INC.; FOAMEX L.P.
To: MP FOAM DIP LLC
Reel/Frame 023015/0187 →
SECURITY AGREEMENT Recorded Jul 20, 2009
From: FOAMEX INNOVATIONS OPERATING COMPANY
To: WACHOVIA BANK, NATIONAL ASSOCIATION
Reel/Frame 023056/0120 →
RELEASE OF LIEN ON PATENTS Recorded May 8, 2007
From: U.S. BANK NATIONAL ASSOCIATION
To: FOAMEX L.P.
Reel/Frame 019260/0287 →
RELEASE OF LIEN ON PATENTS Recorded May 8, 2007
From: BANK OF AMERICA, N.A.
To: FOAMEX L.P.
Reel/Frame 019260/0043 →
RELEASE OF LIEN ON PATENTS Recorded May 8, 2007
From: SILVER POINT FINANCE, LLC
To: FOAMEX L.P.
Reel/Frame 019260/0261 →
REVOLVING CREDIT PATENT SECURITY AGREEMENT Recorded Mar 15, 2007
From: FOAMEX L.P.
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 019019/0082 →
RELEASE OF SECURITY INTEREST Recorded Mar 9, 2007
From: SILVER POINT FINANCE, LLC
To: FOAMEX L.P.
Reel/Frame 018972/0891 →
RELEASE OF SECURITY INTEREST Recorded Mar 9, 2007
From: U.S. BANK NATIONAL ASSOCIATION
To: FOAMEX L.P.
Reel/Frame 018972/0917 →
RELEASE OF SECURITY INTEREST Recorded Mar 9, 2007
From: BANK OF AMERICA, N.A.
To: FOAMEX L.P.
Reel/Frame 018972/0866 →
SECOND LIEN TERM PATENT SECURITY AGREEMENT Recorded Mar 7, 2007
From: FOAMEX L.P.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 018972/0013 →
FIRST LIEN TERM PATENT SECURITY AGREEMENT Recorded Mar 2, 2007
From: FOAMEX L.P.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 018951/0057 →