Process for producing porous materials based on polyurea

Patent metadata

Field	Value
Publication number	US-9260580-B2
Application number	US-201113169245-A
Country	US
Kind code	B2
Filing date	Jun 27, 2011
Priority date	Jun 28, 2010
Publication date	Feb 16, 2016
Grant date	Feb 16, 2016

Abstract

The present invention relates to a process for producing porous materials, which comprises reaction of at least one polyfunctional isocyanate with an amine component comprising at least one polyfunctional substituted aromatic amine and also water in the presence of a solvent.
The invention further relates to the porous materials which can be obtained in this way and the use of the porous materials as insulation material and in vacuum insulation panels.

First claim

The invention claimed is:

1. A process for producing a porous material, which comprises reacting the following components:
(a1) at least one polyfunctional isocyanate, and
(a2) at least one polyfunctional substituted aromatic amine (a2-s) having the general formula I

where R 1 and R 2 can be identical or different and are each selected independently from among hydrogen and linear or branched alkyl groups having from 1 to 6 carbon atoms and all substituents Q 1 to Q 5 and Q 1 ′ to Q 5 ′ are identical or different and are each selected independently from among hydrogen, a primary amino group and a linear or branched alkyl group having from 1 to 12 carbon atoms, where the alkyl group can bear further functional groups, with the proviso that
the compound having the general formula I comprises at least two primary amino groups, where at least one of Q 1 , Q 3 and Q 5 is a primary amino group and at least one of Q 1 ′, Q 3 ′ and Q 5 ′ is a primary amino group, and
Q 2 , Q 4 , Q 2 ′ and Q 4 ′ are selected so that the compound having the general formula I has at least one linear or branched alkyl group, which can bear further functional groups, having from 1 to 12 carbon atoms in the α position relative to at least one primary amino group bound to the aromatic ring, and
optionally at least one further polyfunctional aromatic amine (a2-u) which differs from the amines (a2-s) having the general formula I and

(a3) water in the presence of a solvent (C) and optionally in the presence of at least one catalyst (a4);
wherein a total amount of the component (a1), the component (a2) and the water account for no more than 40% by weight in the solvent, based on the total weight of the components (a1) and (a2), the water and the solvent.

2. The process according to claim 1 , wherein Q 2 , Q 4 , Q 2 ′ and Q 4 ′ are selected so that the substituted aromatic amine (a2-s) comprises at least two primary amino groups which each have a linear or branched alkyl group having from 1 to 12 carbon atoms, which can bear further functional groups, in the α position.

3. The process according to claim 1 , wherein the amine component (a2) comprises at least one compound (a2-s) selected from the group consisting of 3,3′,5,5′-tetraalkyl-4,4′-diaminodiphenylmethane, 3,3′,5,5′-tetraalkyl-2,2′-diaminodiphenylmethane and 3,3′,5,5′-tetraalkyl-2,4′-diaminodiphenylmethane, where the alkyl groups in the 3,3′,5 and 5′ positions can be identical or different and are selected independently from among linear or branched alkyl groups which have from 1 to 12 carbon atoms and can bear further functional groups.

4. The process according to claim 1 , wherein the alkyl groups of the polyfunctional aromatic amines (a2-s) having the general formula I are selected from among methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl and tert-butyl.

5. The process according to claim 1 , wherein the polyfunctional aromatic amines (a2-s) having the general formula 1 are 3,3′,5,5′-tetraalkyl-4,4′-diaminodiphenylmethanes, preferably 3,3′,5,5′-tetraethyl-4,4′-diaminodiphenylmethane and/or 3,3′,5,5′-tetramethyl-4,4′-diaminodiphenylmethane.

6. The process according to claim 1 , wherein the amount of component (a1) used is from 40 to 99.8% by weight based on the total weight of the components (a1), (a2) and (a3), which is 100% by weight.

7. The process according to claim 1 , wherein the amount of component (a2) used is from 0.1 to 30% by weight, that of the component (a1) is from 40 to 99.8% by weight and that of the component (a3) is from 0.1 to 30% by weight, in each case based on the total weight of the components (a1), (a2) and (a3), which is 100% by weight.

8. The process according to claim 1 , wherein component (a2) consists exclusively of compounds of the type (a2-s) having the general formula 1.

9. The process according to claim 1 , wherein the reaction is carried out in the presence of a catalyst (a4).

10. The process according to claim 1 , wherein the reaction is carried out in the presence of at least one tertiary amine as catalyst (a4).

11. The process according to claim 1 , which comprises:
a) provision of the components (a1), (a2) and (a3) and the solvent (C),
b) reaction of the components (a1), (a2) and (a3) in the presence of the solvent (C) to form a gel and
c) drying of the gel obtained in the preceding step.

12. The process according to claim 11 , wherein the components (a1) and (a2) are provided separately, in each case in a partial amount of the solvent (C).

13. The process according to claim 11 , wherein the drying of the gel obtained is carried out by converting the liquid comprised in the gel into the gaseous state at a temperature and a pressure below the critical temperature and the critical pressure of the liquid comprised in the gel.

14. The process according to claim 11 , wherein the drying of the gel obtained is carried out under supercritical conditions.

15. The process according to claim 1 , wherein the amount of component (a1) used is from 55 to 99.3% by weight, based on the total weight of the components (a1), (a2) and (a3), which is 100% by weight.

16. A process for producing a porous material, which comprises reacting component (a1) with component (a2) in the presence of water and a solvent to provide an organic gel, wherein the solvent is a liquid under the temperature and pressure conditions of a reaction of the components (a1) and (a2), and which can dissolve the organic gel, or provide a dispersion of the organic gel,
the component (a1) is at least one polyfunctional isocyanate, and
the component (a2) is at least one polyfunctional substituted aromatic amine (a2-s) having the general formula I

where R 1 and R 2 can be identical or different and are each selected independently from among hydrogen and linear or branched alkyl groups having from 1 to 6 carbon atoms and all substituents Q 1 to Q 5 and Q 1 ′ to Q 5 ′ are identical or different and are each selected independently from among hydrogen, a primary amino group and a linear or branched alkyl group having from 1 to 12 carbon atoms, where the alkyl group can bear further functional groups, with the proviso that
the compound having the general formula I comprises at least two primary amino groups, where at least one of Q 1 , Q 3 and Q 5 is a primary amino group and at least one of Q 3 ′ and Q 5 ′ is a primary amino group, and
Q 2 , Q 4 , Q 2 ′ and Q 4 ′ are selected so that the compound having the general formula I has at least one linear or branched alkyl group, which can bear further functional groups, having from 1 to 12 carbon atoms in the αposition relative to at least one primary amino group bound to the aromatic ring, and
optionally at least one further polyfunctional aromatic amine (a2-u) which differs from the amines (a2-s);

wherein a total amount of the component (a1), the component (a2) and the water account for no more than 40% by weight in the solvent, based on the total weight of the components (a1) and (a2), the water and the solvent; and
drying the organic gel to provide the porous material.

17. The process according to claim 16 wherein the total amount of the component (a1), the component (a2) and the water account for 10% to 20% by weight in the solvent, to provide the porous material having a desired pore structure, low thermal conductivity and low shrinking upon dryi

Assignees

• Fricke Marc
• Elbing Mark
• Basf Se

Inventors

• Fricke Marc
• Elbing Mark

Classifications

• C08G18/3243

  containing two or more aromatic rings · CPC title

• C08J9/28 Primary

  by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum · CPC title

• C08G2101/0083

  Chemistry & Metallurgy · mapped topic

• C08J2201/0502

  the liquid phase being organic · CPC title

• C08J2205/024

  Organogel, i.e. a gel containing an organic composition · CPC title