(Super)hydrophobic isocyanate based porous materials

Patent metadata

Field	Value
Publication number	US-11434344-B2
Application number	US-201615776163-A
Country	US
Kind code	B2
Filing date	Oct 12, 2016
Priority date	Nov 16, 2015
Publication date	Sep 6, 2022
Grant date	Sep 6, 2022

Abstract

A (super)hydrophobic isocyanate based organic aerogel/xerogel/cryogel having a water contact angle of at least 90° comprising:
a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, and hydrophobic compounds having before the gelling step at least one isocyanate-reactive group and no isocyanate groups

Characterized in that said hydrophobic compounds are covalently bonded within the porous network of the aerogel/xerogel/cryogel and wherein said bondings are created during the gelling step of the formation of the isocyanate based organic aerogel/xerogel/cryogel cross-linked porous network structure.

First claim

The invention claimed is:

1. A process for making a hydrophobic isocyanate based organic porous material having water repellent properties, and a water contact angle >90°, wherein the hydrophobic isocyanate based porous material comprises a cross-linked porous network structure comprising: polyurethane, polyisocyanurate, polyurea, or a combination thereof; and a hydrophobic compound covalently bonded within the porous network, said process comprising;
a) providing a polyisocyanate compound;
b) optionally, providing an isocyanate-reactive compound;
c) optionally, providing at least one catalyst compound promoting polyurethane, polyurea, and/or polyisocyanurate formation;
d) providing a first solvent selected from the group consisting of a hydrocarbon, a dialkyl ether, a cyclic ether, a dialkyl ketone, an alkyl alkanoate, a hydrochlorocarbon, a chlorofluorocarbon, a halogenated aromatic, an aromatic, a fluorine-containing ether, N-methyl pyrrolidone, and a combination thereof;
e) providing a hydrophobic compound having a solubility in water <10 g/L at 20° C., at least 1 isocyanate-reactive group, and no isocyanate groups, said hydrophobic compound is different from the isocyanate-reactive compound optionally provided in step b) and is able to impart hydrophobicity to the porous material obtained in a subsequent step j), wherein said hydrophobic compound is selected from the group consisting of siloxanes, polyethylene, polypropylene, polybutadiene, polyisoprene, or combinations thereof;
f) optionally, providing further additives;
g) combining the compounds provided in steps a), d), e) and optionally b) and/or c) and/or f) at a temperature of about 10° C. to about 50° C. to form a gel comprising a porous cross-linked polyurethane, polyurea, or polyisocyanurate network having the hydrophobic compound covalently bonded in the network, wherein the hydrophobic compound is covalently bonded in the network during step g;
h) optionally, removing unreacted species;
i) optionally, exchanging the first solvent with a second solvent; and
j) removing the first solvent or second solvent from the porous cross-linked polyurethane, polyurea, or polyisocyanurate network in order to obtain the porous material;
and wherein the porous material is an aerogel, a xerogel, or cryogel.

2. The process according to claim 1 , wherein the hydrophobic porous material has superhydrophobic properties and a water contact angle >150°.

3. The process according to claim 1 , wherein the hydrophobic porous material comprises:
50-99.9% by weight polyurethane, polyisocyanurate, or polyurea calculated on the total dry weight of the hydrophobic porous material.

4. The process according to claim 1 , wherein said hydrophobic compounds are incorporated within the porous structure by means of a urethane and/or urea bonding.

5. The process according to claim 1 , wherein the hydrophobic porous material cross-linked porous network structure has the following properties:
Porosity: 20 to 99%;
Density: lower than 800 kg/m 3 ; and
Average pore diameter: 0.1 nm to 1 mm.

6. The process according to claim 1 , wherein the hydrophobic porous material has a lambda value under atmospheric pressure in the range 9-50 mW/m.K at 10° C. together with a density in the range of 50-300 kg/m 3 .

7. The process according to claim 1 , wherein the amount of hydrophobic compound is in the range of 0.1 to 30%, by weight calculated on the total weight of the compounds provided in steps (a) and (e) and, when present, steps (b), (c), and/or (f).

8. The process according to claim 1 , wherein the porous material is a monolithic gel and the process further comprising, after the step g), a step wherein the obtained gel is optionally broken or grinded into particles having smaller dimensions than the obtained porous material.

9. The process according to claim 1 , further comprising, after step g), a step wherein the porous material is aged is performed.

10. The process according to claim 1 , wherein the polyisocyanate compound is an organic polyisocyanate selected from the group consisting of hexamethylene diisocyanate, m-phenylene diisocyanate, tolylene-2,4-diisocyanate, tolylene-2,6-diisocyanate, diphenylmethane-4,4′-diisocyanate, or combinations thereof.

11. The process according to claim 1 , wherein the optional isocyanate-reactive compound, when present, is selected from the group consisting of a monoamine compound, a polyamine compound, an aromatic or aliphatic polyether polyol compound, an aromatic or aliphatic polyester polyol compound, or combinations thereof.

12. The process according to claim 1 , wherein in step g) the compounds are added to a reaction vessel and the compounds are mixed at temperatures of about at least 10° C. below the boiling point of the solvent used in step d) by shaking the reaction vessel or by slowly stirring the compounds in the reaction vessel.

13. The process according to claim 1 , wherein the at least one catalyst compound, when present, is selected from the group consisting of quaternary ammonium hydroxides, quaternary salts, alkali metal or alkaline earth metal hydroxides, alkali metal or alkaline earth metal alkoxides, and alkali metal or alkaline earth metal carboxylates, lead octoate, and symmetrical triazine derivatives, and wherein the obtained isocyanate based organic aerogel/xerogel/cryogel is prepared at an isocyanate index greater than 100.

14. The process according to claim 1 , wherein the at least one catalyst compound is selected from the group consisting of N,N-dimethylcyclohexylamine, organometallic compounds, and alkali metal salts, and wherein the isocyanate based organic aerogel/xerogel/cryogel is prepared at an isocyanate index in the range of 50-200.

15. The process according to claim 1 , wherein the step of removing the solvent in step j) is performed by drying the porous material until the weight of the porous material remains constant by using supercritical CO 2 , evaporating the organic solvents being present in the gel by air-drying under ambient pressure and ambient temperature, drying under vacuum, drying in an oven at elevated temperatures, microwave drying, radiofrequency drying, sublimation, freeze drying, or any combination thereof.

16. The process according to claim 1 , wherein the first solvent used in step d) is selected from the group consisting of a hydrocarbon, a dialkyl ether, a ketone and a combination thereof.

17. The process according to claim 1 , wherein the second solvent used in step i), when present, is selected from the group consisting of hydrocarbons, dialkyl ethers, cyclic ethers, ketones, alkyl alkanoates, aliphatic hydrofluorocarbons, cycloaliphatic hydrofluorocarbons, hydrochlorofluorocarbons, chlorofluorocarbons, hydrochlorocarbons, halogenated aromatic compounds, fluorine-containing ethers, and combinations thereof.

Assignees

• Huntsman Int Llc

Inventors

• Joncheray Thomas Julien
• Vandenbroeck Jan
• Geumez Gilles Jean

Classifications

• C08G18/7664

  containing alkylene polyphenyl groups · CPC title

• C08J9/35 Primary

  Composite foams, i.e. continuous macromolecular foams containing discontinuous cellular particles or fragments · CPC title

• C08L75/00

  Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers · CPC title

• C08J2475/02

  Polyureas · CPC title

• C08J2205/042

  Nanopores, i.e. the average diameter being smaller than 0,1 micrometer · CPC title