IP Library Granted Patent US 7,494,718
Granted Patent B2
US 7,494,718 · App. 10/529,902 · Granted Feb 24, 2009

Method for improving the surface hardness of a wooden body using an aqueous solution of an impregnating agent

Assignee: BASF Aktiengesellschaft
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Quick Facts
Patent No.
US 7,494,718
App. No.
10/529,902
Granted
Feb 24, 2009
Kind
B2
Abstract

A process for the production of a wood body having increased surface hardness, in which an untreated wood body is impregnated with an aqueous solution of A) an impregnating agent consisting of a 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one modified with a C 1-5 -alcohol, a polyol or mixtures thereof, and B) a catalyst from the group consisting of ammonium or metal salts, organic or inorganic acids or mixtures thereof, dried and then hardened at elevated temperature is described.

Claims (35)

1. A process for the production of a wood body, comprising

impregnating an untreated wood body with an aqueous solution of

A) an impregnating agent selected from the group consisting of a reaction product of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one with a C 1-5 -alcohol selected from the group consisting of methanol, ethanol, n-propanol, isopropanol, n-butanol, and n-pentanol, or a polyol selected from the group consisting of ethylene glycol, diethylene glycol, 1,2- and 1,3-propylene glycol, 1,2-, 1,3- and 1,4-butylene glycol, glycerol, and polyethylene glycols of the formula HO(CH 2 CH 2 O) n H, where n is from 3 to 20 and mixtures thereof, and

B) a catalyst selected from the group consisting of ammonium salts, metal salts, organic acids, inorganic acids and mixtures thereof, and

drying and then hardening at elevated temperature.

2. The process according to claim 1 , wherein an impregnating agent C) selected from the group consisting of 1,3-bis(hydroxymethyl)-4,5dihydroxyimidazolidin-2-one, 1,3-dimethyl-4,5-dihydroxyimidazolidin-2-one, dimethylolurea, bis(methoxymethyl)urea, tetramethylolacetylenediurea, 1,3-bis(hydroxymethyl)imidazolidin-2-one, methylolmethylurea and mixtures thereof is concomitantly used.

3. The process according to claim 1 , wherein an impregnating agent D) selected from the group consisting of a C l-5 -alcohol, a polyol and mixtures thereof is concomitantly used.

4. The process according to claim 3 , wherein methanol, ethanol, n-propanol, isopropanol, n-butanol, n-pentanol, ethylene glycol, diethylene glycol, 1,2- and 1,3-propylene glycol, 1,2-, 1,3- and 1 ,4-butylene glycol, glycerol, polyethylene glycols of the formula HO(CH 2 CH 2 O) n H, where n is from 3 to 20, or mixtures thereof are concomitantly used.

5. The process according to claim 4 , wherein methanol, diethylene glycol or a mixture thereof is concomitantly used.

6. The process according to claim 1 , wherein the impregnating agents A) and, optionally, C) and D) are used in a concentration of from 1 to 60% by weight in the aqueous solution.

7. The process according to claim 1 , wherein metal salts selected from the group consisting of metal halides, metal sulfates, metal nitrates, metal tetrafluoroborates, metal phosphates and mixtures thereof are used as catalyst B).

8. The process according to claim 7 , wherein metal salts selected from the group consisting of magnesium chloride, magnesium sulfate, zinc chloride, lithium chloride, lithium bromide, boron trifluoride, aluminum sulfate, aluminum chloride, zinc nitrate, sodium tetrafluoroborate and mixtures thereof are used as catalyst B).

9. The process according to claim 1 , wherein ammonium salts selected from the group consisting of ammonium chloride, ammonium sulfate, ammonium oxalate, diammonium phosphate and mixtures thereof are used as catalyst B).

10. The process according to claim 1 , wherein organic or inorganic acids selected from the group consisting of maleic acid, formic acid, citric acid, tartaric acid, oxalic acid, p-toluenesulfonic acid, hydrochloric acid, sulfuric acid, boric acid and mixtures thereof are used as catalyst B).

11. The process according to claim 1 , wherein magnesium chloride is used as catalyst B).

12. The process according to claim 1 , wherein the catalyst B) is used in a concentration of from 0.1 to 10% by weight, based on the amount of the impregnating agent A) and, optionally, C) and D).

13. The process according to claim 1 , wherein the impregnated wood body is dried at a temperature of from 20 to 60° C.

14. The process according to claim 1 , wherein the impregnated and dried wood body is hardened at a temperature of from 80 to 170° C.

15. The process according to claim 14 , wherein the impregnated and dried wood body is hardened at a temperature of from 90 to 150° C.

16. The process according to claim 1 , wherein the impregnated and dried wood body is hardened over a period of from 10 min to 72 hours.

17. The process according to claim 1 , wherein, after the impregnation and drying, the wood body is fixed so that a change in the shape of the wood body during the hardening is counteracted.

18. The process according to claim 17 , wherein the wood body is fixed in a heatable press.

19. A wood body, obtained by the process according to claim 1 .

20. A process for the production of a wood body, comprising

impregnating an untreated wood body with an aqueous solution consisting of

A) an impregnating agent selected from the group consisting of a reaction product of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one with a C 1-5 -alcohol selected from the group consisting of methanol, ethanol, n-propanol, isopropanol, n-butanol, and n-pentanol, or a polyol selected from the group consisting of ethylene glycol, diethylene glycol, 1,2- and 1,3-propylene glycol, 1,2-, 1,3- and 1,4-butylene glycol, glycerol, and polyethylene glycols of the formula HO(CH 2 CH 2 O) n H, where n is from 3 to 20, and mixtures thereof;

B) a catalyst selected from the group consisting of ammonium salts, metal salts, organic acids, inorganic acids and mixtures thereof,

C) an impregnating agent selected from the group consisting of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one, 1,3-dimethyl-4,5-dihydroxyimidazolidin-2-one, dimethylolurea, bis(methoxymethyl)urea, tetramethylolacetylenediurea, 1,3-bis(hydroxymethyl)imidazolidin-2-one, methylolmethylurea and mixtures thereof,

D) a C 1-5 -alcohol selected from the group consisting of methanol, ethanol, n-propanol, isopropanol, n-butanol and n-pentanol, or a polyol selected from the group consisting of ethylene glycol, diethylene glycol, 1,2- and 1,3-propylene glycol, 1,2-, 1,3- and 1,4-butylene glycol, glycerol and polyethylene glycols of the formula HO(CH 2 CH 2 O) n H, where n is from 3 to 20, or mixtures thereof; and

water, and

drying and then hardening at elevated temperature.

21. A wood body, obtained by the process according to claim 20 .

22. The process according to claim 1 , wherein the impregnating agent A) is a reaction product of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one with methanol.

23. The process according to claim 1 , wherein the impregnating agent A) is a reaction product of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one with diethylene glycol.

24. The process according to claim 1 , wherein the impregnating agent A) is a reaction product of 1,3-bis(hydroxymethyl)-4,5-dihydroxyimidazolidin-2-one with a mixture of methanol and diethylene glycol.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2017
From: BASF SE
To: GEORG-AUGUST-UNIVERSITÄT GÖTTINGEN
Reel/Frame 042422/0666 →
CHANGE OF NAME Recorded May 18, 2017
From: BASF AKTIENGESELLSCHAFT
To: BASF SE
Reel/Frame 042493/0460 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2005
From: KRAUSE, ANDREAS; MILITZ, HOLGER
To: BASF AKTIENGESELLSCHAFT
Reel/Frame 016530/0293 →
Priority Claims (1)
DE 102 46 400 · Oct 4, 2002 · national
Continuity (1)
Related Publication 20060051607A1 · Mar 9, 2006