System, process and reactor for conducting a synthesis gas conversion reaction
US-2015038598-A1 · Feb 5, 2015 · US
US12280340B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12280340-B2 |
| Application number | US-202017784580-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 10, 2020 |
| Priority date | Dec 11, 2019 |
| Publication date | Apr 22, 2025 |
| Grant date | Apr 22, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
It is provided a water-saturated carbon molecular sieve membrane obtainable by a) providing a hydrophilic carbon molecular sieve membrane (CMSM) comprising pores of a pore size from 0.25 nm to 0.55 nm for molecular sieving, pores of a pore size from 0.55 nm to 0.90 nm for adsorption diffusion and a negligible amount of pores larger than 0.90 nm such that a plot of N 2 permeance versus pressure of permeation at room temperature and at a pressure from 1 to 4 bar has zero or negative slope; and b) humidifying the membrane until obtaining a water-saturated carbon molecular sieve membrane. It is also provided a process for the separation of a gas from a gas mixture with such a water-saturated membrane, and its use for solvent dehydration, and as a membrane reactor.
Opening claim text (preview).
The invention claimed is: 1. A water-saturated carbon molecular sieve membrane obtainable by a process comprising: i) providing a hydrophilic carbon molecular sieve membrane (CMSM) comprising pores of a pore size as defined herein from 0.25 nm to 0.55 nm for molecular sieving, and of a pore size from higher than 0.55 nm to 0.90 nm for adsorption diffusion and a negligible amount of pores larger than 0.90 nm, such that a plot of N 2 permeance as defined herein versus pressure of permeation at room temperature and at a pressure from 1 to 4 bar has zero or negative slope; and ii) humidifying the CMSM obtained in step i) to obtain a water-saturated CMSM by: treating it with water vapor at a temperature from 5° C. to 180° C. and at atmospheric pressure and a relative humidity higher than 95% during a period of time such that after further treatment with water vapor, the permeation flux of a non-adsorbable gas at 4 bar at the temperature at which the CMSM has been treated with water vapor is constant during a particular period of time; or alternatively, by exposing the CMSM to a N 2 or He gas stream saturated with water by bubbling the gas at a temperature from 5° C. to 180° C. into a tank filled with water such that after further exposure to the N 2 or He gas stream saturated with water, the permeation flux of a non-adsorbable gas at 4 bar and at the mentioned temperature is constant during a particular period of time. 2. The water-saturated carbon molecular sieve membrane of claim 1 , wherein the CMSM is a composite alumina-carbon molecular sieve membrane (Al-CMSM). 3. The water-saturated carbon molecular sieve membrane of claim 2 , wherein the Al-CMSM has a nitrogen content from 0.1 wt % to 4.0 wt %, an alumina content from 2.5% to 50% and a carbon content from 50 wt % to 95 wt %, with respect to the total weight of the membrane. 4. A process for the preparation of water-saturated composite alumina-carbon molecular sieve membrane (water-saturated Al-CMSM) comprising: i) preparing a hydrophilic Al-CMSM by: providing a porous α-Al 2 O 3 support; preparing a solution containing from 5 to 20 wt % of phenol formaldehyde resin, from 0.5 to 5 wt % of formaldehyde, from 0.1 to 2 wt % of ethylenediamine, from 0.1 to 5 wt % of boehmite in N-methyl-2-pyrrolidone, and heating the solution to carry out a pre-polymerization process in order to obtain a coating solution; dip-coating the porous α-Al 2 O 3 support in the coating solution in order to obtain a coated support; drying the coated support at a temperature from 70 to 120° C. in order to complete the polymerization process; and carbonizing the dried coated support at a carbonization temperature from 450° C. to 750° C. in order to obtain the hydrophilic Al-CMSM; and ii) humidifying the hydrophilic Al-CMSM prepared in step i) to obtain a water-saturated Al-CMSM by: treating the hydrophilic Al-CMSM with water vapor at a temperature from 5° C. to 180° C. and at atmospheric pressure and a relative humidity higher than 95% during a period of time such that, after further treatment with water vapor, the permeation flux of a non-adsorbable gas at 4 bar at the temperature at which the hydrophilic Al-CMSM has been treated with water vapor is constant during a particular period of time; or alternatively, by exposing the hydrophilic Al-CMSM to a N 2 or He gas stream saturated with water by bubbling the gas at a temperature from 5° C. to 180° C. into a tank filled with water such that after further exposure to the N 2 or He gas stream saturated with water, the permeation flux of a non-adsorbable gas at 4 bar and at the mentioned temperature is constant during a particular period of time. 5. The process according to claim 4 , wherein the phenol formaldehyde resin is a novolac resin. 6. The process according to claim 4 , wherein the carbonization temperature is from 450° C. to 700° C. 7. A water-saturated Al-CMSM obtainable by the process defined in claim 4 . 8. A process for the separation of a gas from a gas mixture, the process comprising: a) providing the water-saturated membrane as defined in claim 1 ; b) providing a gas mixture comprising at least two gases; and c) feeding the gas mixture to the water-saturated CMSM at a temperature from 5° C. to 300° C. in order to get a retentate and a permeate, wherein feeding is carried out at a pressure such that the partial pressure of the gas in the retentate is higher than the partial pressure of the gas in the permeate and such that a difference in permeation is observed compared to the same CMSM without having been subjected to an humidifying step in order to get a water saturated membrane at the feeding temperature and pressure. 9. The process according to claim 8 , wherein the at least two gases have a polarizability from 2 to 27 and at least one of the at least two gases have a kinetic diameter less than 0.55 nm, and wherein if the at least two gases have a kinetic diameter lower than 0.55 nm, the difference of the kinetic diameter between the at least two gases is equal to or more than 0.01 nm and/or the difference of the polarizability between the at least two gases is equal to or more than 1 m 3 . 10. The process according to claim 9 , wherein the at least two gases are selected from the group consisting of He, H 2 O, Ne, H 2 , NO, Ar, NH 3 , N 2 , O 2 , CO, CO 2 , CH 4 , C 2 H 4 , C 2 H 6 , propene, propane, H 2 S, methanol, and ethanol. 11. The process according to claim 8 , wherein the gas mixture comprising at least two gases is selected from the group consisting of H 2 /CH 4 , H 2 /N 2 ; H 2 /CO 2 ; CO 2 /CH 4 , CO 2 /N 2 ; O 2 /N 2 ; and biogas. 12. The process according to claim 11 , wherein the gas mixture comprises from 5% to 20% of H 2 and from 95% to 80% of CH 4 , and wherein step c) is carried out at a hydrogen partial pressure difference equal to or higher than 3 bars and at a temperature of 40° C. or below. 13. The process according to claim 11 , wherein the at least two gases are CO 2 and N 2 and the gas mixture comprises from 10% to 20% of CO 2 and from 65% to 75% of N 2 . 14. The process according to claim 11 , wherein the at least two gases are H 2 and CO 2 and the gas mixture comprises from 55% to 65% of H 2 and from 30% to 40% of CO 2 . 15. The process according to claim 11 , wherein the gas mixture comprising at least two gases is biogas, and CO 2 is removed from biogas, wherein biogas is a gas mixture comprising methane and carbon dioxide. 16. A process for removal of water from an organic solvent, the process comprising: applying vacuum from a permeated side of the water-saturated CMSM as defined in claim 1 . 17. A process for in situ removal of water during a catalytic reaction in which water is produced, the process comprising: carrying out the catalytic reaction in a membrane reactor, wherein the membrane reactor is the water-saturated CMSM as defined in claim 1 . 18. A process for the separation of a gas from a gas mixture, the process comprising: a) providing a water-saturated membrane as defined in claim 7 ; b) providing a gas mixture comprising at least two gases; and c) feeding the gas mixture to the water-saturated CMSM at a temperature from 5° C. to 300° C. in order to get a retentate and a permeate, wherein feeding is carried out at a pressure such that the partial pressure of the gas in the retentate is higher than the partial pressure of the gas in the permeate and such that a difference in permeation is observed compared to the same CMSM without having been subjected to an humidifying step in order to ge
by dialysis, osmosis or reverse osmosis {(general membrane separation processes B01D61/00, membrane modules B01D63/00, electrodialysis C02F1/4693, combination of membrane modules and bioreactors C02F3/1268)} · CPC title
Hydrophilic membranes · CPC title
Hydrophilization · CPC title
Composite membranes; Ultra-thin membranes · CPC title
characterised by their properties · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.