IP Library Granted Patent US 6,881,814
Granted Patent B2
US 6,881,814 · App. 10/265,250 · Granted Apr 19, 2005

Borate modified phenolic resin for insulation material

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Quick Facts
Patent No.
US 6,881,814
App. No.
10/265,250
Granted
Apr 19, 2005
Kind
B2
Abstract

Phenolic resins and processes of making these phenolic resins that are useful for making binders for mineral wool insulation products are disclosed. The addition of a boron salt early in the process of making these phenolic resins leads to enhanced properties such as a reduction in the amount of tetradimers and an improvement in the stability of both the base resin and the pre-react.

Claims (52)

1. A process of making an alkaline phenol formaldehyde resin composition comprising the steps of

a) charging a reaction vessel with formaldehyde and phenol

b) adding a boron salt to the reaction vessel containing the formaldehyde and phenol to generate a reaction mix

c) adding a catalyst to the reaction mix

d) heating the reaction vessel

e) adding a base so as to generate the alkaline phenol formaldehyde resin.

2. A process of making an alkaline phenol formaldehyde resin composition comprising the steps of

a) charging a reaction vessel with formaldehyde and phenol

b) adding a catalyst to the reaction vessel containing the formaldehyde and the phenol

c) adding a boron salt to the reaction vessel containing the formaldehyde and the phenol and the catalyst

d) heating the reaction vessel to generate the alkaline phenol formaldehyde resin.

3. An alkaline phenol formaldehyde resin composition made by

a) charging a reaction vessel with formaldehyde and phenol

b) adding a boron salt to the reaction vessel containing the formaldehyde and phenol to generate a reaction mix

c) adding a catalyst to the reaction mix

d) heating the reaction vessel

e) adding a base so as to generate the alkaline phenol formaldehyde resin.

4. An alkaline phenolic resin composition made by

a) charging a reaction vessel with formaldehyde and phenol

b) adding a catalyst to the reaction vessel containing the formaldehyde and the phenol

c) adding a boron salt to the reaction vessel containing the formaldehyde and the phenol and the catalyst

d) heating the reaction vessel to generate the alkaline phenol formaldehyde resin.

5. The process according to claim 1 , wherein the boron salt is selected from the group consisting of ammonium, lithium, potassium and sodium boron salts.

6. The alkaline phenol formaldehyde resin according to claim 3 , wherein the boron salt is selected from the group consisting of ammonium, lithium, potassium and sodium boron salts.

7. The alkaline phenol formaldehyde resin according to claim 4 , wherein the boron salt is selected from the group consisting of ammonium, lithium, potassium and sodium boron salts.

8. The process according to claim 1 , wherein the boron salt is selected from the group consisting of ammonium, lithium, potassium and sodium boron salts.

9. The process according to claim 1 , wherein the boron salt is sodium tetraborate.

10. The process according to claim 2 wherein the boron salt is sodium tetraborate.

11. The alkaline phenol formaldehyde resin according to claim 3 , wherein the boron salt is sodium tetraborate.

12. The alkaline phenol formaldehyde resin according to claim 4 , wherein the boron salt is sodium tetraborate.

13. The process according to claim 1 , wherein the catalyst is a non-ortho directing catalyst.

14. The process according to claim 2 , wherein the catalyst is a non-ortho directing catalyst.

15. The alkaline phenol formaldehyde resin according to claim 3 , wherein the catalyst is a non-ortho directing catalyst.

16. The alkaline phenol formaldehyde resin according to claim 4 , wherein the catalyst is a non-ortho directing catalyst.

17. The process according to claim 13 , wherein the non-ortho directing catalyst is an organic base.

18. The process according to claim 13 , wherein the non-ortho directing catalyst is an inorganic base.

19. The process according to claim 1 , wherein a molar ratio of formaldehyde to phenol is between about 2.0 to about 5.0.

20. The process according to claim 2 , wherein a molar ratio of formaldehyde to phenol is between about 2.0 to about 5.0.

21. The alkaline phenol formaldehyde resin according to claim 3 , wherein a molar ratio of formaldehyde to phenol is between about 2.0 to about 5.0.

22. The alkaline phenol formaldehyde resin according to claim 4 , wherein a molar ratio of formaldehyde to phenol is between about 2.0 to about 5.0.

23. The process according to claim 1 , wherein a molar ratio of boron salt to phenol is between about 0.01 to about 0.30.

24. The process according to claim 1 , wherein a molar ratio of boron salt to phenol is between about 0.01 to about 0.30.

25. The alkaline phenol formaldehyde resin according to claim 3 , wherein a molar ratio of boron salt to phenol is between about 0.01 to about 0.30.

26. The alkaline phenol formaldehyde resin according to claim 4 , wherein a molar ratio of boron salt to phenol is between about 0.01 to about 0.30.

27. The process according to claim 1 , wherein the alkaline phenol formaldehyde resin has a pH of between from about 7.0 to 11.0.

28. The process according to claim 2 , wherein the alkaline phenol formaldehyde resin has a pH of between from about 7.0 to 11.0.

29. The alkaline phenol formaldehyde resin according to claim 3 , wherein the alkaline phenol formaldehyde resin has a pH of between from about 7.0 to 11.0.

30. The alkaline phenol formaldehyde resin according to claim 4 , wherein the alkaline phenol formaldehyde resin has a pH of between from about 7.0 to 11.0.

31. The process according to claim 1 , further comprising adding urea as a formaldehyde scavenger.

32. The process according to claim 2 , further comprising adding urea as a formaldehyde scavenger.

33. The alkaline phenol formaldehyde resin according to claim 3 , further comprising adding urea as a formaldehyde scavenger.

34. The alkaline phenol formaldehyde resin according to claim 4 , further comprising adding urea as a formaldehyde scavenger.

Assignments (18)
ABL PATENT SECURITY INTERESTS RELEASE AGREEMENT Recorded Oct 1, 2021
From: ROYAL BANK OF CANADA, AS AGENT
To: ARCLIN USA LLC; ARCLIN SURFACES LLC; ARCLIN CANADA HOLDINGS LTD.; COVERIGHT SURFACES CANADA INC.
Reel/Frame 057681/0704 →
FIRST LIEN PATENT SECURITY INTERESTS RELEASE AGREEMENT Recorded Oct 1, 2021
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
To: ARCLIN USA LLC; ARCLIN SURFACES LLC; ARCLIN CANADA HOLDINGS LTD.
Reel/Frame 057681/0696 →
SECOND LIEN PATENT SECURITY INTERESTS RELEASE AGREEMENT Recorded Feb 24, 2021
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT (SECOND LIEN)
To: ARCLIN USA LLC; ARCLIN CANADA HOLDINGS LTD.; ARCLIN SURFACES LLC
Reel/Frame 055402/0384 →
SECURITY INTEREST Recorded Feb 15, 2017
From: ARCLIN USA LLC; ARCLIN SURFACES LLC; ARCLIN CANADA LTD; COVERIGHT SURFACES CANADA INC.
To: ROYAL BANK OF CANADA, AS AGENT
Reel/Frame 041266/0073 →
SECURITY INTEREST Recorded Feb 15, 2017
From: ARCLIN USA LLC; ARCLIN SURFACES LLC; ARCLIN CANADA LTD
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT (FIRST LIEN)
Reel/Frame 041266/0192 →
SECURITY INTEREST Recorded Feb 15, 2017
From: ARCLIN USA LLC; ARCLIN SURFACES LLC; ARCLIN CANADA LTD
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT (SECOND LIEN)
Reel/Frame 041266/0255 →
RELEASE OF SECURITY INTEREST Recorded May 23, 2016
From: BANK OF AMERICA, N.A.
To: ARCLIN U.S.A., INC.; ARCLIN SURFACES, INC.; ARCLIN CANADA LTD.
Reel/Frame 038679/0334 →
RELEASE OF SECURITY INTEREST Recorded May 23, 2016
From: BANK OF AMERICA, N.A.
To: ARCLIN U.S.A., INC.; ARCLIN SURFACES, INC.; ARCLIN CANADA LTD.
Reel/Frame 038679/0387 →
RELEASE OF SECURITY INTEREST Recorded Jan 15, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: ARCLIN CANADA LTD.
Reel/Frame 023796/0863 →
RELEASE OF SECURITY INTEREST Recorded Jan 15, 2010
From: THE BANK OF NEW YORK MELLON
To: ARCLIN CANADA LTD.
Reel/Frame 023796/0856 →
RELEASE OF SECURITY INTEREST Recorded Jan 15, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: ARCLIN CANADA LTD.
Reel/Frame 023796/0866 →
SECURITY AGREEMENT Recorded Jan 15, 2010
From: ARCLIN U.S.A. INC.; ARCLIN SURFACES INC.; ARCLIN CANADA LTD.
To: BANK OF AMERICA, N.A.
Reel/Frame 023796/0883 →
PATENT SECURITY AGREEMENT Recorded Jul 29, 2009
From: ARCLIN CANADA LTD
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023015/0614 →
ASSIGNMENT AND ASSUMPTION FOR SECOND LIEN PATENT SECURITY AGREEMENT RECORDED AT REEL 019562 FRAME 0524 Recorded Mar 25, 2009
From: UBS AG, STAMFORD BRANCH
To: THE BANK OF NEW YORK MELLON
Reel/Frame 022449/0251 →
CHANGE OF NAME Recorded Aug 16, 2007
From: DYNEA CANADA LTD.
To: ARCLIN CANADA LTD.
Reel/Frame 019704/0252 →
SECOND LIEN PATENT SECURITY AGREEMENT Recorded Jul 17, 2007
From: DYNEA CANADA LTD.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 019562/0524 →
PATENT SECURITY AGREEMENT Recorded Jul 16, 2007
From: DYNEA CANADA LTD
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 019562/0115 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2003
From: TANG, KWOK; SANTOS, RUBEN A.; ZAPLETAL, BOHUMILA
To: DYNEA CANADA LTD.
Reel/Frame 013635/0775 →