IP Library Granted Patent US 8,366,863
Granted Patent B2
US 8,366,863 · App. 11/993,750 · Granted Feb 5, 2013

Method for producing bonded mineral wool and binder therefor

Inventors: Hagen Huenig (Dosseinheim, DE); Eva Wagner (Altrip, DE)
Assignee: Saint-Gobain Isover
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Quick Facts
Patent No.
US 8,366,863
App. No.
11/993,750
Granted
Feb 5, 2013
Kind
B2
Abstract

The present invention relates to a binder for the production of bonded mineral wool, wherein a phenol-formaldehyde-binder is applied onto the still hot fibers after the fiberization of a mineral wool, using a binder that comprises hydroxylamine or an amino alcohol with the following general formula (I) wherein R1 and R2 are the same or different from each other, and independently are hydrogen, a linear or branched, saturated or unsaturated aliphatic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a chain-like or branched alkylether with 1-50 alkoxy units or a chain-like or branched alkylamine with 1-50 alkylamine units; and R3 is a linear or branched, saturated or unsaturated aliphatic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a chain-like or branched alkylether with 1-50 alkoxy units or a chain-like or branched alkylamine with 1-50 alkylamine units.

Claims (24)

1. A method for producing bonded mineral wool, in which a phenol-formaldehyde-binder is applied onto the still hot fibers after the fiberization of a mineral melt,

a binder, which is essentially free of ammonia, and contains hydroxylamine or an amino alcohol with the following general formula:

wherein R1 and R2 are the same or different from each other, and independently are hydrogen, a linear or branched, saturated or unsaturated alipathic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a straight chain or branched alkylether with 1-50 alkoxy units or a straight chain or branched alkylamine with 1-50 alkylamine units; and

R3 is a linear or branched, saturated or unsaturated aliphatic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a straight chain or branched alkylether with 1-50 alkoxy units or a straight chain or branched alkylamine with 1-50 alkylamine units; and

wherein a sugar-containing preparation is added.

2. The method according to claim 1 , wherein the ethanolamine is an amino alcohol.

3. The method according to claim 1 , wherein the sugar-containing preparation is added in the concentration of 0.5 to 25 percent by weight.

4. The method according to claim 1 , wherein an acidic salt is additionally added to the binder.

5. The method according to claim 1 , wherein a binder with a content of approximately 0.05 to 4 percent by weight of an amino alcohol is used.

6. The method according to claim 1 , wherein a binder with additionally approximately 0.1 to 3.0 percent by weight of an acid salt is used.

7. The method according to claim 6 , wherein a binder with a concentration of ammonium sulphate of approximately 1.0 percent by weight is used.

8. The method according to claim 7 , wherein the binder has an ethanolamine concentration of approximately 0.5 percent by weight and a ammonium sulphate concentration of approximately 1.0 percent by weight.

9. A bonded mineral wool product that is obtainable according to the procedure in accordance with claim 1 .

10. A binder for the preparation of a phenol-formaldehyde resin based bonded mineral wool, comprising a sugar-containing preparation and an hydroxylamine or an amino alcohol of the following general formula:

wherein R1 and R2 are the same or different from each other, and independently are hydrogen, a linear or branched, saturated or unsaturated aliphatic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a straight chain or branched alkylether with 1-50 alkoxy units or a straight chain or branched alkylamine with 1-50 alkylamine units; and

R3 is a linear or branched, saturated or unsaturated aliphatic hydrocarbon with 1-12 carbon atoms, a saturated or unsaturated alicyclic or heterocyclic hydrocarbon with 5-8 carbon atoms, a carbocyclic or heterocyclic aromatic hydrocarbon with 5-12 ring members or a straight chain or branched alkylether with 1-50 alkoxy units or a straight chain or branched alkylamine with 1-50 alkylamine units,

wherein the binder is essentially free of ammonia.

11. The binder according to claim 10 , which comprises ethanolamine.

12. The binder according to claim 10 , further comprising an ammonium salt.

13. The binder according to claim 10 , comprising an amino alcohol content of approximately 0.05 to 2.5 percent by weight.

14. The binder according to claim 10 , comprising an ammonium salt in a concentration of approximately 0.1 to 3.0 percent by weight.

15. The binder according to claim 14 , comprising an ammonium salt concentration of approximately 1.0 percent by weight.

16. The binder according to claim 14 , comprising concentration of the amino alcohol in an amount of approximately 0.5 percent by weight and ammonium salt in an amount of approximately 1.0 percent by weight.

17. The binder according to claim 10 , wherein the sugar containing preparation is present in the binder in a concentration of 0.5 to 25 percent by weight.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2008
From: HUENIG, HAGEN; WAGNER, EVA
To: SAINT-GOBAIN ISOVER
Reel/Frame 021008/0375 →
Priority Claims (1)
DE 10 2005 029 479 · Jun 24, 2005 · national
Continuity (1)
Related Publication 20100175826A1 · Jul 15, 2010