IP Library Granted Patent US 7,666,254
Granted Patent B1
US 7,666,254 · App. 11/894,373 · Granted Feb 23, 2010

Borate compositions for wood preservation

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 7,666,254
App. No.
11/894,373
Granted
Feb 23, 2010
Kind
B1
Abstract

A wood preservation composition comprising an unexpectedly efficacious combination of a boron compound and bifenthrin is disclosed. A method of preserving wood, as well as the preserved wood, are also disclosed.

Claims (38)

1. Wood comprising:

a) a boron compound having a Boric Acid Equivalent (BAE) retention from greater than 0.15 to 0.7 wt % BAE;

b) bifenthrin having a retention in the range of from 1.5 to 10.0 grams per cubic meter of wood.

2. Wood as in claim 1 wherein the wood is preserved to a greater extent than wood treated to a BAE retention of 0.15 wt % and a bifenthrin retention in the range of from 1.5 to 10.0 grams per cubic meter of wood as measured by an ensis mean mass loss test protocol.

3. Wood as in claim 1 wherein the boron compound is present at a retention in the range of from 0.2 to 0.7 wt % BAE.

4. Wood as in claim 1 wherein the bifenthrin retention is in the range of from 5.0 to 10.0 grams per cubic meter of wood.

5. Wood as in claim 1 wherein the boron compound is boric acid or a sodium borate compound selected from the group consisting of disodium octaborate tetrahydrate, sodium borate pentahydrate, sodium borate decahydrate and anhydrous borax.

6. A method of preserving wood comprising the steps of:

a) contacting wood with a solution comprising a boron compound, such that the wood is impregnated with the boron compound to a Boric Acid Equivalent (BAE) retention in a range of from greater than 0.15 to 0.7 wt %;

b) contacting wood with a solution comprising bifenthrin, such that the wood is impregnated with the bifenthrin to a bifenthrin retention in a range of from 1.5 to 10.0 grams per cubic meter of wood.

7. The method of claim 6 wherein the wood is preserved to a greater extent than wood treated to a BAE retention of 0.15 wt % and a bifenthrin retention in the range of from 1.5 to 10.0 grams per cubic meter of wood as measured by an ensis mean mass loss test protocol.

8. The method of claim 6 wherein the boron compound retention is in the range of from 0.2 to 0.7 wt % BAE.

9. The method of claim 6 wherein the bifenthrin retention is in the range of from 5.0 to 10.0 grams per cubic meter of wood.

10. The method of claim 6 wherein the boron compound solution and the bifenthrin solution is a single solution.

11. The method of claim 6 wherein the boron compound is boric acid or a sodium borate compound selected from the group consisting of disodium octaborate tetrahydrate, sodium borate pentahydrate, sodium borate decahydrate, and anhydrous borax.

12. A composition comprising:

a) a boron compound; and

b) bifenthrin;

wherein the composition is a solution; and wherein the solution has a wt % Boric Acid Equivalent (BAE) in the range of from 0.09 to 12, and a bifenthrin concentration in a range of from 1 ppm to 5000 ppm.

13. The composition of claim 12 wherein the boron compound is present at concentration in the range of from 0.3 to 1 wt % BAE.

14. The composition of claim 12 wherein the bifenthrin is present at a concentration in the range of from 2 ppm to 100 ppm.

15. The composition of claim 13 wherein the bifenthrin is present at a concentration in the range of from 2 ppm to 100 ppm.

16. The composition of claim 12 wherein the boron compound is present at a concentration in the range of from 3 to 10 wt % BAE.

17. The composition of claim 12 wherein the bifenthrin is present at a concentration in the range of from 500 ppm to 3000 ppm.

18. The composition of claim 16 wherein the bifenthrin is present at a concentration in the range of from 500 ppm to 3000 ppm.

19. The composition of claim 13 wherein the boron compound is boric acid or a sodium borate compound selected from the group consisting of disodium octaborate tetrahydrate, sodium borate pentahydrate, sodium borate decahydrate, and anhydrous borax.

20. The composition of claim 12 wherein when the solution is applied to ensis samples with an ensis impregnation protocol, the sample has a BAE retention in the range of from 0.15 to 0.7 wt % and a bifenthrin retention in the range of from 1.5 to 10.0 grams per cubic meter of wood.

21. The composition of claim 12 wherein the composition further comprises a water repellent additive selected from the group consisting of waxes, wax emulsions and silicones.

22. The composition of claim 12 wherein the composition further comprises a pigment additive.

23. The composition of claim 22 wherein said pigment additive is selected from the group consisting of iron oxide pigments, dyes, azo dyes, acid dyes and basic dyes.

24. The composition of claim 12 wherein the composition further comprises an anti-foaming agent selected from the group consisting of siloxanes and oil soluble surfactants.

25. The composition of claim 12 wherein the composition further comprises a wetting agent.

26. The composition of claim 25 wherein said wetting agent is a surfactant.

27. The composition of claim 12 wherein the composition further comprises a penetration aide selected from the group consisting of chelating agents, imines and surfactants.

28. The composition of claim 12 wherein the composition further comprises a biocide.

29. The composition of claim 28 wherein the biocide is selected from the group consisting of octyl isothiazolin, dichloro octyl isothiazolin, methylisothiazolin, chloromethylisothiazolin, benzisothiazolin, methylene bis thiocyanate, 2-thiocyanomethylthio benzothiazole, and quaternary ammonium compounds.

30. The composition of claim 29 wherein said quaternary ammonium compounds are selected from the group consisting of didecyl dimethyl ammonium chloride, alkylbenzylammonium chloride, saccarine quats and carbo quats.

31. The composition of claim 30 wherein said carbo quats are selected from the group consisting of didecyl dimethyl ammonium carbonate and benzylammonium carbonate.

Assignments (12)
RELEASE (REEL 033591 / FRAME 0020) Recorded Jun 28, 2022
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: KOPPERS DELAWARE, INC. (F/K/A KOPPERS INDUSTRIES OF DELAWARE, INC.); KOPPERS PERFORMANCE CHEMICALS INC. (F/K/A OSMOSE, INC.); KOPPERS INC. (F/K/A KOPPERS INDUSTRIES, INC); KOPPERS PERFORMANCE CHEMICALS NEW ZEALAND LIMITED (F/K/A OSMOSE NEW ZEALAND); OSMOSE UTILITIES SERVICES, INC.
Reel/Frame 060448/0192 →
RELEASE OF PATENT SECURITY INTERESTS Recorded Jun 20, 2022
From: PNC BANK, NATIONAL ASSOCIATION
To: KOPPERS DELAWARE, INC.; KOPPERS PERFORMANCE CHEMICALS INC. (F/K/A OSMOSE, INC.); KOPPERS UTILITY AND INDUSTRIAL PRODUCTS INC. (F/K/A COX INDUSTRIES, INC.); KOPPERS INC. (F/K/A KOPPERS INDUSTRIES, INC.)
Reel/Frame 060390/0207 →
SECURITY AGREEMENT Recorded Jun 20, 2022
From: KOPPERS DELAWARE, INC.; KOPPERS PERFORMANCE CHEMICALS INC.
To: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 060390/0246 →
SECOND AMENDMENT TO CREDIT AGREEMENT AND JOINDER TO PATENT, TRADEMARK AND COPYRIGHT SECURITY AGREEMENT Recorded May 18, 2018
From: KOPPERS INC.; KOPPERS HOLDINGS INC.; KOPPERS DELAWARE, INC.; KOPPERS ASIA LLC; KOPPERS CONCRETE PRODUCTS, INC.; CONCRETE PARTNERS, INC.; KOPPERS PERFORMANCE CHEMICALS, INC.; KOPPERS RAILROAD STRUCTURES INC.; KOPPERS WORLD-WIDE VENTURES CORPORATION; M.A. ENERGY RESOURCES, LLC; KOPPERS VENTURES INC.; KOPPERS-NEVADA LIMITED-LIABILITY COMPANY; KOPPERS NZ LLC; WOOD PROTECTION MANAGEMENT LLC; WOOD PROTECTION LP; COX INDUSTRIES, INC.; COX WOOD PRESERVING COMPANY
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 046188/0895 →
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE PATENT NUMBER 8221797 PREVIOUSLY RECORDED AT REEL: 034036 FRAME: 0363. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Dec 9, 2014
From: OSMOSE, INC.
To: KOPPERS PERFORMANCE CHEMICALS INC.
Reel/Frame 034563/0407 →
CHANGE OF NAME Recorded Oct 23, 2014
From: OSMOSE, INC.
To: KOPPERS PERFORMANCE CHEMICALS INC
Reel/Frame 034036/0363 →
RELEASE OF SECURITY INTERST IN INTELLECTUAL PROPERTY Recorded Aug 27, 2014
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: OSMOSE, INC.
Reel/Frame 033645/0778 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Aug 27, 2014
From: CREDIT SUISSE AG, CAYMAND ISLANDS BRANCH, AS COLLATERAL AGENT
To: OSMOSE, INC. (FORMERLY OSMOSE WOOD PRESERVING, INC.)
Reel/Frame 033645/0796 →
PATENT, TRADEMARK AND COPYRIGHT SECURITY AGREEMENT Recorded Aug 22, 2014
From: KOPPERS INC.; KOPPERS HOLDINGS INC.; KOPPERS DELAWARE, INC.; KOPPERS ASIA LLC; KOPPERS CONCRETE PRODUCTS, INC.; CONCRETE PARTNERS, INC.; KOPPERS WORLD-WIDE VENTURES CORPORATION; KOPPERS VENTURES LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 033591/0020 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2014
From: ZHANG, JUN
To: OSMOSE, INC.
Reel/Frame 032626/0421 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 26, 2012
From: OSMOSE, INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 029351/0791 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 4, 2012
From: OSMOSE, INC. (FORMERLY OSMOSE WOOD PRESERVING, INC.)
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 028158/0611 →