IP Library Granted Patent US 8,889,589
Granted Patent B2
US 8,889,589 · App. 14/149,210 · Granted Nov 18, 2014

Layered solid sorbents for carbon dioxide capture

Inventors: Bingyun Li (Morgantown, WV); Bingbing Jiang (Morgantown, WV); McMahan L. Gray (Pittsburgh, PA); Daniel J. Fauth (Pittsburgh, PA); Henry W. Pennline (Bethel Park, PA); George A. Richards (Morgantown, WV)
Assignee: West Virginia University
B01D53/62B05D1/04B01J20/3289B01J20/264B01J20/28014B01D2253/202B01D53/02B01J20/327B01J20/3272B01D2257/504B01D2253/25Y02C10/08B01J20/26
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Quick Facts
Patent No.
US 8,889,589
App. No.
14/149,210
Granted
Nov 18, 2014
Kind
B2
Abstract

A solid sorbent for the capture and the transport of carbon dioxide gas is provided having at least one first layer of a positively charged material that is polyethylenimine or poly(allylamine hydrochloride), that captures at least a portion of the gas, and at least one second layer of a negatively charged material that is polystyrenesulfonate or poly(acryclic acid), that transports the gas, wherein the second layer of material is in juxtaposition to, attached to, or crosslinked with the first layer for forming at least one bilayer, and a solid substrate support having a porous surface, wherein one or more of the bilayers is/are deposited on the surface of and/or within the solid substrate. A method of preparing and using the solid sorbent is provided.

Claims (26)

1. A method of preparing a solid sorbent comprising:

employing electrostatic layer by layer nanoassembly of drawing a positively charged polymer in aqueous media through a porous sorbent support material under sufficient vacuum pressure for a period of time ranging from one minute to greater than fifteen minutes for forming a positively charged layer of said positively charged polymer on the surface of and/or within said porous sorbent support material resulting in a treated porous sorbent support material, wherein said positively charged polymer is selected from the group consisting of polyethylenimine and poly(allylamine hydrochloride);

rinsing said treated porous sorbent support material with water;

employing electrostatic layer by layer nanoassembly of drawing a negatively charged polymer in aqueous media through said treated porous sorbent support material under sufficient vacuum pressure for a period of time ranging from 1 minute to greater than fifteen minutes for forming a negatively charged layer of said negatively charged polymer in juxtaposition to, attached to or crosslinked with said positively charged layer resulting in the formation of one bilayer of said positively charged layer and said negatively charged layer, wherein said negatively charged polymer is selected from the group consisting of polystyrenesulfonate and poly(acryclic acid), or wherein said positively charged polymer and said negatively charged polymer are selected from the group of ionic liquid monomers and poly-ionic liquid polymers; and

rinsing said solid sorbent having said bilayer resulting in one cycle of deposition of said bilayer on said surface of and/or within said porous sorbent support material; and optionally repeating said above steps for forming one or more successive cycles of bilayer deposition; and optionally including wherein said layer formation is based on interactions of hydrogen bonding; and optionally including wherein said layers go through post-assembly treatment including crosslinking and deprotonation treatment of said positively charged polymers via pH shift.

2. The method of claim 1 wherein said poly ionic liquid polymer is formed from monomers selected from the group consisting of 2-(methacryloyloxy)ethyl-trimethylammonium chloride, p-vinylbenzonyltrimethylammonium chloride, arginine, aspartic acid, PLGA, EMIM, and combinations thereof.

3. The method of claim 1 including wherein said positively charged polymer is polyethylenimine and wherein said negatively charged polymer is polystyrenesulfonate.

4. The method of claim 2 wherein said poly ionic liquid polymer is selected from the group of poly[p-vinylbenzonyltrimethylammonium chloride][Cl], poly[p-vinylbenzonyltrimethylammonium chloride][Arg], poly[2-(methacryloyloxy)ethyl-trimethylammonium chloride][Cl], [PLGA][EMIM], and [PLGA-Arginine][EMIM].

5. The method of claim 2 including wherein said poly ionic liquid polymer is poly [METMA][Arginine][Aspartic acid] a copolymer synthesized from polymerization of [2-(methacryloyloxy)ethyltrimethylammonium chloride][Arginine] and [2-(methacryloyloxy)ethyltrimethylammonium chloride][Aspartic acid].

6. A method of capturing carbon dioxide from a pollutant source comprising:

passing an effluent stream of gas containing carbon dioxide through or in contact with a solid sorbent comprising at least one first layer of a material that captures at least a portion of a gas, wherein said first layer of said material is selected from the group consisting of polyethylenimine and poly(allylamine hydrochloride); and at least one second layer of a second material that transports said gas, wherein said second layer of said material is selected from the group consisting of polystyrenesulfonate and poly(acryclic acid), or wherein said first and said second layers of materials are selected from the group of ionic liquid monomers and poly-ionic liquid polymers said second layer of material is in juxtaposition to, attached to, or crosslinked with said first layer such that said first layer of material and said second layer of material form one bilayer; and a solid substrate support having a porous surface, wherein said bilayer is deposited on the surface of said substrate or deposited into said solid substrate; and

capturing said carbon dioxide on said surface of said substrate or depositing said carbon dioxide into said solid substrate.

7. The method of claim 6 including wherein said solid sorbent of has alternating layers of said first layer of material and said second layer of material forming more than one bilayer.

8. The method of claim 6 including wherein said first layer of said material is different than said second layer of said material.

9. The method of claim 6 including wherein said first layer of material is a positively charged material and wherein said second layer of material is an oppositely charged material relative to the first layer of material.

10. The method of claim 9 including wherein the first layer of material is a positively charged polyelectrolyte and wherein said second layer of material is a negatively charged polyelectrolyte.

11. The method of claim 6 including wherein said first layer is a positively charged polymer and wherein said second layer is an oppositely charged polymer relative to the polymer of said first layer.

12. The method of claim 6 including wherein said solid substrate support is selected from the group consisting of polymethylmethacrylate, silica, silicone, glass, a metal, and a colloid of an inorganic and organic material.

13. The method of claim 6 including wherein said porosity of said solid substrate support has a diameter ranging from 1 nanometer to greater than 200 nanometers.

14. The method of claim 6 including wherein said bilayer has a thickness of at least 1 nanometer.

15. The method of claim 14 including wherein there are from 2 to 10 bilayers wherein each bilayer has a thickness of from 1 to 10 nanometers.

16. The method of claim 6 including wherein the ionic liquid monomers are selected from the group of noncrosslinked and crosslinked monomers.

17. The method of claim 6 including wherein said first layer of material is polyethylenimine and said second layer of material is polystyrenesulfonate.

18. The method of claim 6 including wherein said poly ionic liquid polymer is formed from monomers selected from the group consisting of 2-(methacryloyloxy)ethyl-trimethylammonium chloride, p-vinylbenzonyltrimethylammonium chloride, arginine, aspartic acid, PLGA, EMIM, and combinations thereof.

19. The method of claim 18 including wherein said poly ionic liquid polymer is selected from the group of poly[p-vinylbenzonyltrimethylammonium chloride][Cl], poly[p-vinylbenzonyltrimethylammonium chloride][Arg], poly[2-(methacryloyloxy)ethyl-trimethylammonium chloride][Cl], [PLGA][EMIM], and [PLGA-Arginine][EMIM].

20. The method of claim 18 including wherein said poly ionic liquid polymer is poly [METMA][Arginine][Aspartic acid] a copolymer synthesized from polymerization of [2-(methacryloyloxy)ethyltrimethylammonium chloride][Arginine] and [2-(methacryloyloxy)ethyltrimethylammonium chloride][Aspartic acid].

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2014
From: LI, BINGYUN; JIANG, BINGBING
To: WEST VIRGINIA UNIVERSITY
Reel/Frame 031906/0676 →
Continuity (3)
Division 13611651 · Sep 12, 2012
Provisional Application 61573746 · Sep 12, 2011
Related Publication 20140127104A1 · May 8, 2014