Metal organic frameworks for the capture of volatile organic compounds

Patent metadata

Field	Value
Publication number	US-11426704-B2
Application number	US-201816646357-A
Country	US
Kind code	B2
Filing date	Sep 12, 2018
Priority date	Sep 12, 2017
Publication date	Aug 30, 2022
Grant date	Aug 30, 2022

Abstract

The use of porous crystalline solids constituted of a metal-organic framework (MOF) for the capture of polar volatile organic compounds (VOCs). In particular, the MOF of interest are material having an average pores sizes of 0.4 to 0.6 nm and an hydrophobic core formed by a metal oxide and/or hydroxide network connected by linkers, the linkers being selected from the group including (i) C6-C24 aromatic polycarboxylate linkers, such as benzyl or naphtyl di-, tri- or tetracarboxylate, and (ii) C6-C16 polycarboxylate aliphatic linkers; the linkers bearing or not apolar fluorinated groups, e.g. —(CF2)n—CF3 groups, n being a integer from 0 to 5, preferably 0 ou 3, and/or apolar C1-C20 preferably C1-C4 alkyl groups, e.g. —CH3 or —CH2—CH3, grafted directly to the linkers and pointing within the pores of the MOF. The MOF solids used in the present invention can be used for the purification of air, for example for the capture of polar VOCs like acetic acid and aldehydes from indoor air in cars, museums and archives, much more efficiently than common adsorbents, particularly in presence of above normal levels of humidity. They can in particular be used for the preservation of cultural heritage.

First claim

The invention claimed is:

1. A process for adsorbing polar volatile organic compounds present at a concentration in the range of 10 ppb to 100 ppm (volume/volume) in a gaseous environment comprising the step of contacting with said environment a porous Metal-Organic Framework (MOF) material comprising an average pore size of 0.4 to 0.6 nm and an hydrophobic core formed by a metal oxide and/or hydroxide network connected by linkers, said linkers being selected from the group consisting of:
C 6 -C 24 aromatic polycarboxylate linkers;
C 6 -C 16 polycarboxylate aliphatic linkers;
C 4 -C 16 polycarboxylate aliphatic linkers; and
imidazole-based linkers;

each of the aforementioned linkers optionally bearing apolar fluorinated groups and/or apolar C 1 -C 20 groups grafted directly to the linkers and pointing within the pores of the MOF.

2. The process according to claim 1 , wherein the C 6 -C 24 aromatic polycarboxylate linkers are selected from the group consisting of C 6 H 4 (CO 2 − ) 2 (terephthalate), C 10 H 6 (CO 2 − ) 2 (naphthalene-2,6-dicarboxylate), C 12 H 8 (CO 2 − ) 2 (biphenyl-4,4′-dicarboxylate), C 6 H 3 (CO 2 − ) 3 (benzene-1,2,4-tricarboxylate), C 6 H 3 (CO 2 − ) 3 (benzene-1,3,5-tricarboxylate), C 24 H 15 (CO 2 − ) 3 (benzene-1,3,5-tribenzoate), C 6 H 2 (CO 2 − ) 4 (benzene-1,2,4,5-tetracarboxylate, C 10 H 4 (CO 2 − ) 4 (naphtalene-2,3,6,7-tetracarboxylate), C 10 H 4 (CO 2 − ) 4 (naphtalene-1,4,5,8-tetracarboxylate), C 12 H 6 (CO 2 − ) 4 (biphenyl-3,5,3′,5′-tetracarboxylate), and modified analogues selected from 2-methyl terephthalate, 2,5-dimethyl terephthalate, tetramethyl terephthalate, perfluoromethyl terephthalate, diperfluoromethyl terephthalate, 2-chloroterephthalate, 2-bromoterephthalate, 2,5-tetrafluoroterephthalate, tetrafluoroterephthalate, dimethyl-4,4′-biphenyldicarboxylate, tetramethyl-4,4′-biphenyldicarboxylate, dicarboxy-4,4′-biphenyldicarboxylate, azobenzene dicarboxylate, and azobenzene tetracarboxylate.

3. The process according to claim 1 , wherein the C 4 -C 16 polycarboxylate alkyl linkers are selected from di-, tri- and tetracarboxylate or carboxylic acid linkers.

4. The process according to claim 2 , wherein the linkers optionally bear apolar fluorinated —(CF 2 )—CF 3 or —CF 3 groups grafted directly to the linkers and pointing within the pores of the MOF.

5. The process according to claim 1 , wherein the linkers optionally bear —CH 3 or —CH 2 —CH 3 , groups grafted directly to the linkers and pointing within the pores of the MOF.

6. The process according to claim 1 , wherein the metal atom of the metal oxide and/or hydroxide is selected from Li, Na, Rb, Mg, Ca, Sr, Ba, Sc, Ti, Zr, Ta, Cr, Mo, W, Mn, Fe, Ru, Os, Co, Ni, Pd, Pt, Cu, Au, Zn, Al, Ga, In, Si, Ge, Sn, Bi, Cd, Mn, Tb, Gd, Ce, La, and Cr.

7. The process according to claim 1 , wherein the MOF is selected from the group consisting of MIL-140B, MIL-140C, UiO-66-2CF 3 , UiO-NDC, UiO-66-(CH 3 ) 2 , ZIF, ZIF-8, MIL-53, MIL-69 and MIL-88B-4CH 3 .

8. The process according to claim 1 , wherein the polar volatile organics compounds are selected from the group consisting of acetic acide, acetaldehyde, formaldehyde and a mixture of two or three thereof.

9. The process according to claim 1 , wherein the MOF is in the form of a powder or granules or embedded in the form of a composite material, or embedded in or applied onto the surface of a paper sheet or a polymer or a fiber.

10. The process according to claim 1 , wherein the gaseous environment is air having >30% relative humidity.

11. The process according to claim 1 , wherein the linkers are selected from the group consisting of:
C 6 -C 24 aromatic polycarboxylate linkers,
C 6 -C 16 polycarboxylate aliphatic linkers, and
C 4 -C 16 polycarboxylate aliphatic linkers.

12. The process according to claim 1 , wherein the C 6 -C 24 aromatic polycarboxylate linkers are benzyl or naphthyl di-, tri- or tetracarboxylates.

13. The process according to claim 1 , wherein the apolar fluorinated groups are —(CF 2 ) n —CF 3 groups, n being an integer from 0 to 5.

14. The process according to claim 1 , wherein the apolar C 1 -C 20 groups are C 1 -C 4 alkyl groups.

15. The process according to claim 13 , wherein the apolar C 1 -C 20 groups are —CH 3 or —CH 2 —CH 3 .

16. The process according to claim 3 , wherein the C 4 -C 16 polycarboxylate alkyl linkers are selected from C 2 H 2 (CO 2 − ) 2 (fumarate), C 2 H 4 (CO 2 − ) 2 (succinate), C 3 H 6 (CO 2 − ) 2 (glutarate), (C 4 H 4 )(CO 2 − ) 2 (muconate), and C 4 H 8 (CO 2 − ) 2 (adipate).

17. The process according to claim 7 , wherein the MOF is selected from the group consisting of MIL-140B, MIL-140C, UiO-66-2CF 3 , UiO-NDC, UiO-66-(CH 3 ) 2 , MIL-53, and MIL-88B-4CH 3 .

Assignees

• Centre Nat Rech Scient
• Ecole Normale Superieure De Paris
• Ecole Superieure Physique & Chimie Ind Ville De Paris
• Univ De Versailles—Saint Quentin En Yvelines
• Inst Superior Tecnico

Inventors

• Serre Christian
• Pinto Moisés L

Classifications

• B01D2253/204

  Metal organic frameworks (MOF's) · CPC title

• B01J20/226 Primary

  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) · CPC title

• B01D2253/306

  Surface area, e.g. BET-specific surface · CPC title

• B01D2257/708

  Volatile organic compounds V.O.C.'s · CPC title

• B01D2258/06

  Polluted air · CPC title