Composite body

Patent metadata

Field	Value
Publication number	US-11596904-B2
Application number	US-201916702752-A
Country	US
Kind code	B2
Filing date	Dec 4, 2019
Priority date	Dec 20, 2018
Publication date	Mar 7, 2023
Grant date	Mar 7, 2023

Abstract

The present invention provides a composite body having, on a porous substrate and in the interstices of the substrate that includes fibers, preferably of an electrically nonconductive material, a porous layer (1) composed of oxide particles bonded to one another and partly to the substrate that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, preferably selected from Al2O3, ZrO2, TiO2 and SiO2, and having, at least on one side, a further porous layer (2) including oxide particles bonded to one another and partly to layer (1) that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, preferably selected from Al2O3, ZrO2, TiO2 and SiO2, where the oxide particles present in layer (1) have a greater median particle size than the oxide particles present in layer (2), which is characterized in that the median particle size (d50) of the oxide particles in layer (1) is from 0.5 to 4 μm and the median particle size (d50) of the oxide particles in layer (2) is from 0.015 to 0.15 μm, preferably 0.04 to 0.06 μm, a process for producing corresponding composite bodies and for the use thereof, especially in gas separation.

First claim

The invention claimed is:

1. A flexible composite gas separation membrane body having, on a porous substrate and in the interstices of the substrate that includes fibers,
a porous layer (1) composed of oxide particles bonded to one another and partly to the substrate that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, and having, at least on one side, a further porous layer;
(2) including oxide particles bonded to one another and partly to layer (1) that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, where the oxide particles present in layer (1) have a greater median particle size than the oxide particles present in layer (2), wherein the median particle size (d50) of the oxide particles in layer (1), is from 0.5 to 4 μm and the median particle size (d50) of the oxide particles in layer (2), is from 0.015 to 0.15 μm;
and wherein the flexible composite gas separation membrane body has a Gurley number of from 250 to 1200 sec, and a gas flow of greater than 50 GPU for carbon dioxide as clean gas; and
further comprises a silicone polymer layer; and
the flexible composite gas separation membrane body has a thickness of from 100 to 400 μm and can be wound around a bar or tube having a diameter of 15 mm or greater.

2. The flexible composite gas separation membrane body according to claim 1 , wherein the flexible composite body has a Gurley number of from 300 to 800 sec.

3. The flexible composite gas separation membrane body according to claim 1 , wherein the flexible composite body has a thickness of from 100 to 400 μm and has a Gurley number of from 300 to 800 sec.

4. The flexible composite gas separation membrane body according to claim 1 , wherein the substrate is a nonwoven fabric, knit or laid scrim.

5. The flexible composite gas separation membrane body according to claim 1 , wherein the fibers have a dimension of from 1 to 200 g/km of fiber and are composed of polyacrylonitrile, polyamide, polyester and/or polyolefin.

6. The flexible composite gas separation membrane body according to claim 1 , wherein the substrate has a thickness of from 50 to 150 μm and a basis weight of from 40 to 150 g/m 2 .

7. The flexible composite gas separation membrane body according to claim 1 , wherein the flexible composite body has an average pore size of from 60 to 140 nm.

8. The flexible composite gas separation membrane body according to claim 1 , wherein the flexible composite body, on the surface of the layer (2), has a surface roughness Sdq of less than 10 μm.

9. The flexible composite gas separation membrane body according to claim 8 , wherein a polymer layer (PS) is present atop or above layer (2).

10. The flexible composite gas separation membrane body according to claim 8 having a gas flow of gas flow of greater than 80 GPU for carbon dioxide as clean gas, wherein the silicone in the silicone layer is selected from the group consisting of polydimethylsilicone, polyethylmethylsilicone, nitrile silicone, rubbers, poly(4-methyl-1-pentene), and polytrimethylsilylpropenes.

11. A process for producing a flexible composite gas separation membrane body of claim 1 , wherein the process comprises the following steps:
(a) applying a coating composition (BM1) to and into a substrate having fibers and interstices between the fibers, where the coating composition is produced by combining
(a1) a dispersion (D1) of oxide particles produced by mixing oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter (d50) of from 0.5 to 4 μm with water, an inorganic acid, and a dispersing aid,
(a2) a dispersion (D2) of oxide particles produced by mixing oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter (d50) of from 15 to 150 nm, with water,
(a3) a binder formulation (BF1), produced by mixing at least two organofunctional silanes with an alkanol, an inorganic acid, and water,
(b) consolidating the coating composition (BMI) at a temperature of from 100° C. to 275° C., in order to create a first layer (SI′),
(c) optionally applying a coating composition (BM2) to at least layer (S1′), where the coating composition (BM2) is produced by combining
(c1) a dispersion (D3) of oxide particles produced by mixing oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter (d50) of from 0.5 to 4 μm with water, an inorganic acid, and a dispersing aid,
(c2) a dispersion (D4) of oxide particles produced by mixing oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter (d50) of from 15 to 150 nm, with water,
(c3) a binder formulation (BF2), produced by mixing at least two organofunctional silanes with an alkanol, an inorganic acid, and water,
(d) optionally consolidating the coating composition (BM2) at a temperature of from 100° C. to 275° C., in order to create a second layer (S2′),
(e) applying a coating composition (BM3) to layer (S1′) or, if present, layer (S2′), where the coating composition (BM3) has been produced by combining water and an inorganic acid with an
(e1) aqueous dispersion (D5) including oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter (d50) of from 15 to 150 nm, and with ethanol and with a
(e2) binder formulation (BF3) comprising at least two organofunctional silanes,
(f) consolidating the coating composition at a temperature of from 100° C. to 275° C., in order to create a layer (S3′),
(g) optionally applying a coating composition (BM4) to layer (S3′), where the coating composition (BM4) has been produced by combining water and an inorganic acid with an
(g1) aqueous dispersion (D6) including oxide particles selected from the oxides of the elements Ti, Al, Zr and/or Si and having a median particle diameter of from 15 to 150 nm, and with ethanol and with a
(g2) binder formulation (BF4) comprising at least two organofunctional silanes,
(h) optionally consolidating the coating composition at a temperature of from 100° C. to 275° C., in order to create a layer (S4′), and
(i) conducted after step (0 or after step (h), a polymer layer (PS) including a polymer is applied to layer (S3′) or to layer (S4′).

12. The process according to claim 11 , wherein the organofunctional silanes are selected from the group consisting of 3-glycidyloxytriethoxysilane, methyltriethoxysilane and tetraethoxysilane.

13. The process according to claim 11 , wherein 3-glycidyloxytriethoxysilane, methyltriethoxysilane and tetraethoxysilane are used in binder formulation (BF1) and (BF2) in a mass ratio of from 2 to 4:0.5 to 1.5:1.

14. The process according to claim 11 , wherein 3-glycidyloxytriethoxysilane, methyltriethoxysilane and tetraethoxysilane are used in binder formulation (BF3) and (BF4) in amass ratio of from 0.5 to 1.5:1.5 to 2.5:1.

15. The process according to claim 11 , wherein the coating compositions (BM3) and (BM4) are of identical composition.

16. The process according to claim 11 , wherein the coating compositions (BM1) and (BM2) are of identical composition.

17. The process according to claim 11 , wherein the substrate used is a polymer nonwoven including fibers selected from the group consisting of polyacrylonitrile, polyester, polyamide and polyolefin.

18. The process according to claim 11 , wherein the consolidating is affected by passage through a hot air oven or an IR oven.

19. The p

Assignees

• Evonik Operations Gmbh

Inventors

• Hying Christian
• Grzenia David
• Terwonne Rolf-Walter
• Brugger Bastian Matthias
• Khaletskaya Kira
• Conradi Oliver
• Nettelnbreker Hans-Jürgen
• Paasche Alexander

Classifications

• B01D67/0049 Primary

  by evaporation · CPC title

• B01D71/701

  Polydimethylsiloxane · CPC title

• B01D71/024

  Oxides · CPC title

• B01D69/12

  Composite membranes; Ultra-thin membranes · CPC title

• B01D2256/10

  Nitrogen · CPC title