# US 11,992,805 B2 · Humidity as a method for controlling CO2 adsorption with step-shaped adsorbents

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- Number: US 11,992,805 B2
- Document ID: US11992805B2
- Status: Granted
- Kind: B2
- Application number: 17/120,796
- Filed: 2020-12-14
- Published: 2021-06-17
- Granted: 2024-05-28
- Earliest claimed: 2019-12-17
- Assignees: Mosaic Materials, Inc.
- Applicants: Mosaic Materials, Inc.
- Inventors: Thomas Michael McDonald; Graham Benjamin Wenz
- Web page: https://patentgrep.com/patent/US11992805B2

## CPC

- B01D 53/62: Carbon oxides
- B01D 53/02: by adsorption, e.g. preparative gas chromatography {(solid sorbent compositions B01J20/00, preparation of inorganic compounds or elements C01)}
- B01D 53/0462: {Temperature swing adsorption}
- B01J 20/226: {Coordination polymers, e.g. metal-organic frameworks [MOF], zeolitic imidazolate frameworks [ZIF] (preparation of metal complexes containing carboxylic acid moieties C07C51/418; MOF's per se C07F)}
- B01J 20/3425: {of sorbents or filter aids comprising organic materials}
- B01J 20/3466: {with steam}
- B01D 53/0476: {Vacuum pressure swing adsorption}
- B01D 2253/204: Metal organic frameworks (MOF's)
- B01D 2256/12: Oxygen
- B01D 2256/245: Methane
- B01D 2257/504: Carbon dioxide
- Y02C 20/40: of CO2
- B01D: SEPARATION (separating solids from solids by wet methods B03B, B03D; by pneumatic jigs or tables B03B; by other dry methods B07; magnetic or electrostatic separation of solid materials from solid materials or fluids, separation by high-voltage electric fields B03C; centrifuges, vortex apparatus B04; presses per se for squeezing-out liquid from liquid-containing material B30B9/02; treatment of water C02F, e.g. softening by ion-exchange C02F1/42; {arrangements of air intake cleaners in gas turbine plants F02C7/05} ; arrangements or mounting of filters in air-conditioning, air-humidification or ventilation F24F13/28)
- B01J: CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- Y02C: CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]

## Abstract

The present disclosure relates to improved solid state sorbent materials and methods for controlling and enhancing carbon dioxide adsorption performance for selected metal-organic framework (MOF) materials. The present disclosure further relates to inventive methods using a novel class of diamine-appended metal-organic frameworks MOF absorbents displaying step-shaped adsorption isotherms with large carbon dioxide capacities. More specifically, the present disclosure relates to diamine-appended MOF materials exhibiting step-shaped adsorption isotherms that are employed in a method utilizing humidity to control and improve carbon dioxide adsorption performance. In addition, the present disclosure relates to diamine-appended MOF materials used in a process including a regeneration step with carbon dioxide and humidity level control to achieve deep carbon dioxide removal even from dilute, near ambient condition carbon dioxide streams as well as more concentrated industrial output streams spanning multiple orders of magnitude. The present disclosure also relates to scrubbing apparatus and methods employing the inventive MOF materials, methods, process steps and apparatus as disclosed to achieve rapid and deeper carbon dioxide capture without the need to pretreat column materials.

## Claims

### Claim 1

A method for removing CO2 from an effluent gas stream, the method comprising:
(a) contacting the effluent gas stream with an adsorption material located within an adsorption system to reversibly adsorb CO2 from said effluent gas stream thereby generating an adsorption material with improved CO2 capacity;
wherein said adsorption material is an amine-functionalized solid sorbent comprising an amine-appended metal-organic framework composed of a plurality of
(i) amine-containing ligands;
(ii) polytopic organic linkers; and
(iii) metal ions;
wherein said amine-functionalized solid sorbent is present in the form of a packed bed of solids selected from particles, granules, agglomerates thereof, and combinations thereof;
wherein said improved CO2 capacity is achieved by means of pre-saturating said adsorption material using water vapor prior to contact with said effluent gas stream;
(b) removing a major portion of the CO2 from said effluent gas stream to generate a treated effluent gas stream exiting said adsorption system; and
(c) retaining said major portion of said CO2 on said amine-functionalized solid sorbent prior to a regeneration process to renew said adsorption material;
wherein said means of pre-saturating said adsorption material is achieved by means of a humidification unit that functions to control the amount of water present within said adsorption material, and
wherein the method further comprises measuring a relative humidity level of the treated effluent gas stream exiting the adsorption system to obtain a measured relative humidity of the treated effluent gas stream; and
based on the measured relative humidity of the treated effluent gas stream, changing the temperature of the incoming effluent gas stream, changing the velocity of said incoming effluent gas stream, or changing the temperature of the adsorption material to maintain a humidity level within said adsorption material at an optimum level during usage, and
wherein the optimum level in the adsorption material is a relative humidity with respect to water present on said amine-functionalized solid sorbent, and the optimum level corresponds to between 1.5 and 3.5 mole percent H2O.

### Claim 2 (depends on 1)

The method of claim 1, wherein the amine-containing ligands are selected from diamines, triamines, tetraamines, polyamines, and amine-alcohols.

### Claim 3 (depends on 1)

The method of claim 1, wherein the amine-containing ligands are selected from ethylene diamine, N-methylethylenediamine, N-ethylethylenediamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, di(N-methyl)ethylene diamine, N-isopropylethylenediamine, N,N-dimethyl-N-methylethylenediamine, di(N,N-dimethyl)ethylenediamine, N,N-diisopropylethylenediamine, 2,2-dimethyl-1,3-diaminopropane, 1,3-diaminopentane, diethylenetriamine, N-(2-aminoethyl)-1,3-propanediamine, bis(3-aminopropyl)amine, N-(3-aminopropyl)-1,4-diaminobutane, triethylenetetramine, N,N′-bis(2-aminoethyl)-1,3-propanediamine, 1,2-bis(3-aminopropylamino)ethane, N,N′-bis(3-aminopropyl)-1,3-propanediamine, N,N′-bis(3-aminopropyl)-1,4-diaminobutane, tetraethylenepentamine, and combinations thereof.

### Claim 4 (depends on 1)

The method of claim 1, wherein said humidity level within said adsorption material is maintained at an optimum level during usage by continuously monitoring the relative humidity level of the treated effluent gas stream exiting said adsorption system and adjusting said humidity level within said adsorption material to said optimum level by changing the temperature of the adsorption material.

### Claim 5 (depends on 1)

The method of claim 1, wherein said adsorption material is synthesized by a method comprising grafting a plurality of said amine-containing ligands onto a metal-organic framework, wherein the metal-organic framework comprises a plurality of metal cations and a plurality of polytopic organic linkers, wherein the grafting comprises exposing an amount of the metal-organic framework to a solution comprising the polyamine amine-containing ligands diluted with a solvent thereby forming an unactivated adsorption material.

### Claim 6 (depends on 1)

The method of claim 1, wherein
said diamine-containing ligands are selected from ethylene diamine, N-methylethylenediamine, N-ethylethylenediamine, N,N-dimethylethylenediamine, N,N-diethylethylenediamine, di(N-methyl)ethylenediamine, N-isopropylethylenediamine, N,N-dimethyl-N-methylethylenediamine, di(N,N-dimethyl)ethylenediamine, N,N-diisopropylethylenediamine, 2,2-dimethyl-1,3-diaminopropane, 1,3-diaminopentane, and combinations thereof;
wherein said polytopic organic linker is selected from 4,4′-dihydroxy-(1,1′-biphenyl)-3,3′-dicarboxylic acid, its deprotonated mono-carboxylate form, its di-carboxylate form, and combinations thereof; and
wherein said metal ions are cationic metal ions selected from Mg, Ca, Mn, Cr, Fe, Co, Ni, Cu, Zn, and combinations thereof.

### Claim 7 (depends on 6)

The method of claim 6,
wherein said adsorption material is saturated by the continuous introduction of water to said adsorption material in the form of water vapor introduced by means of injecting said water vapor into said effluent gas stream prior to contact with said adsorption material to achieve a higher relative humidity level than the effluent gas stream prior to said injection of water;
wherein said means of injecting said water vapor is achieved by use of said humidification unit; and
wherein said humidification unit is located between the source of said effluent gas stream and said adsorption system.

### Claim 8 (depends on 6)

The method of claim 6, wherein said adsorption material is pre-saturated by first introducing water to an unactivated adsorption material in the form of water vapor introduced by means of first exposing said adsorption material to a neutral carrier gas containing water vapor to produce an activated adsorption material prior to exposing said activated adsorption material to said effluent gas stream.

### Claim 9 (depends on 8)

The method according to claim 8, wherein said adsorption material is regenerated in a repeatable cyclic process comprising the steps of
(a) adsorbing CO2 from either an effluent gas stream or gaseous environment;
(b) regenerating said adsorbent material using at least one step of applying heat to said adsorbent material, heating the effluent gas stream, heating an inert gas stream, applying vacuum to said adsorbent material, or combinations thereof to release adsorbed carbon dioxide and water;
(c) flowing an inert gas stream containing water vapor over said adsorption material or contacting said adsorption material with water, water vapor or combinations thereof to achieve an optimum level of relative humidity; and
(d) repeating steps (a)-(c) until acceptable extraction has been achieved.

### Claim 10 (depends on 8)

The method of claim 8, wherein said step of pre-saturating said adsorption material using water vapor by means of a humidification unit prior to contacting with the effluent gas stream results in an activated adsorption material exhibiting at least one improvement in performance relative to said unactivated adsorption material wherein said improvement is selected from (i) an increased CO2 capacity, (ii) increased gas velocity at constant CO2 capacity, (iii) depth of CO2 adsorption, and combinations thereof.

### Claim 11 (depends on 10)

The method of claim 10, wherein said at least one improvement in performance relative to said unactivated adsorption material is achieved by maintaining the humidity level within said adsorption material to the optimum level during dynamic contact with said effluent gas stream.