IP Library Granted Patent US 9,458,349
Granted Patent B2
US 9,458,349 · App. 11/747,343 · Granted Oct 4, 2016

Phenol-formaldehyde novolac resin having low concentration of free phenol

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Quick Facts
Patent No.
US 9,458,349
App. No.
11/747,343
Granted
Oct 4, 2016
Kind
B2
Abstract

A phenol-formaldehyde novolac resin having a low concentration of free phenol prepared by distilling residual phenol from a molten novolac resin and replacing at least a portion of the phenol with a solvent having a volatility equal to or less than phenol. Such modified novolac resins are suitable for the production of resin coated molding sands for shell molding and sand cores, as well as for the production of resin coated proppants for use in oil and gas recovery operations.

Claims (40)

1. A solid phenol-formaldehyde novolac resin composition in flake form, comprising:

less than 1.5 wt % free phenol; and

a non-phenolic solvent in an amount sufficient to provide a solid phenol-formaldehyde novolac resin having a melt viscosity at 150° C. of less than 5,000 cps,

wherein the non-phenolic solvent is a dibasic ester selected from the group consisting of dimethyl adipate, dimethyl gluterate, dimethyl succinate, and mixtures thereof,

wherein the solid phenol-formaldehyde novolac resin has a melting point of from 77° C. to 93° C., and

wherein the solid phenol-formaldehyde novolac resin contains no other non-phenolic solvent.

2. The solid phenol-formaldehyde novolac resin composition of claim 1 , wherein the free phenol is less than 1.0 wt % and the melt viscosity at 150° C. is less than 4,000 cps.

3. The solid phenol-formaldehyde novolac resin composition of claim 1 , wherein the free phenol is less than 0.5 wt % and the melt viscosity at 150° C. is less than 3,000 cps.

4. The solid phenol-formaldehyde novolac resin of claim 1 , further comprising a phenol to formaldehyde mole ratio (P:F) of 1:0.6 to 1:0.8.

5. The solid phenol-formaldehyde novolac resin composition of claim 1 , comprising about 1 wt % to about 8 wt % of the non-phenolic solvent.

6. The solid phenol-formaldehyde novolac resin of claim 5 , wherein the non-phenolic solvent contains about 20% to about 35% dimethyl adipate, about 65% to about 80% dimethyl gluterate, and up to 3% dimethyl succinate.

7. A coated particle having a coating comprising a cured mixture of the solid phenol-formaldehyde novolac resin of claim 1 and a cross-linking agent.

8. The coated particle of claim 7 wherein the particle is a proppant.

9. The coated particle of claim 7 wherein the particle is a foundry mold aggregate.

10. The coated particle of claim 7 wherein the cross-linking agent is hexamine.

11. A coated particle comprising a mixture of the solid phenol-formaldehyde novolac resin of claim 1 and a cross-linking agent.

12. The coated particle of claim 11 wherein the particle is a proppant.

13. The coated particle of claim 11 wherein the particle is a foundry mold aggregate.

14. The coated particle of claim 11 wherein the cross-linking agent is hexamine.

15. A solid phenol-formaldehyde novolac resin in flake form, comprising:

less than 1.5 wt % free phenol; and

about 1 wt % to about 8 wt % of a dibasic ester solvent selected from the group consisting of dimethyl adipate, dimethyl gluterate, dimethyl succinate, and mixtures thereof, wherein the solid phenol-formaldehyde novolac resin contains no other non-phenolic solvent, wherein the solid phenol-formaldehyde novolac resin has a melting point of from 77° C. to 93° C., and wherein the solid phenol-formaldehyde novolac resin has a melt viscosity at 150° C. of less than 4,000 cps.

16. The solid phenol-formaldehyde novolac resin of claim 15 , wherein the solid phenol-formaldehyde novolac resin is a thermoplastic resin.

17. A phenol-formaldehyde novolac resin composition in flake form consisting essentially of:

less than 1.5 wt % free phenol; and

a dibasic ester selected from the group consisting of dimethyl adipate, dimethyl gluterate, dimethyl succinate, and mixtures thereof;

wherein the dibasic ester was added to the phenol-formaldehyde novolac resin while the phenol-formaldehyde novolac resin was in a molten state after a level of free phenol was reduced to less than 1.5%, wherein the phenol-formaldehyde novolac resin has a melting point of from 77° C. to 93° C., and wherein the phenol-formaldehyde novolac resin has a melt viscosity at 150° C. that is not greater than 10% higher than the melt viscosity at 150° C. of the phenol-formaldehyde novolac resin before both the non-phenolic solvent was added and the level of free phenol was reduced.

18. The composition of claim 17 , further comprising a wax and salicylic acid.

19. A solid phenol-formaldehyde novolac resin, comprising:

a phenol to formaldehyde mole ratio (P:F) of 1:0.6 to 1:0.8;

a melting point of from 77° C. to 93° C.,

about 0.1 wt % to about 1.5 wt % free phenol;

about 1 wt % to about 8 wt % of at least one non-phenolic solvent selected from the group consisting of: dimethyl adipate, dimethyl gluterate, and dimethyl succinate; and

no other non-phenolic solvents, wherein the resin has a melt viscosity at 150° C. of less than 4,000 cps and is in flake form.

20. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the non-phenolic solvent comprises about 2 wt % to about 6 wt % of the at least one non-phenolic solvent.

21. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the free phenol is less than 0.5 wt % and the melt viscosity at 150° C. is less than 3,000 cps, and wherein the phenol to formaldehyde mole ratio (P:F) is 1:0.7 to 1:0.8.

22. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the non-phenolic solvent contains about 20% to about 35% dimethyl adipate, about 65% to about 80% dimethyl gluterate, and up to 3% dimethyl succinate.

23. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the non-phenolic solvent consists of dimethyl gluterate.

24. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the non-phenolic solvent consists of dimethyl adipate.

25. The solid phenol-formaldehyde novolac resin of claim 19 , wherein the non-phenolic solvent consists of dimethyl succinate.

Assignments (5)
ASSIGNMENT OF PATENT AND TRADEMARK SECURITY INTEREST Recorded May 12, 2025
From: MACQUARIE CAPITAL FUNDING LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071276/0379 →
CHANGE OF NAME Recorded Mar 13, 2025
From: GEORGIA-PACIFIC CHEMICALS LLC
To: BAKELITE CHEMICALS LLC
Reel/Frame 070495/0222 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.; SURFACE TECH LLC
To: GOLDMAN SACHS BANK USA, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0250 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.
To: MACQUARIE CAPITAL FUNDING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0327 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 3, 2007
From: REDIGER, RICHARD; LUCAS, EDWARD
To: GEORGIA-PACIFIC CHEMICALS LLC
Reel/Frame 019514/0915 →