Granted Patent B2

US 12,263,464 · App. 16/980,660 · Granted Apr 1, 2025

Inventors: Deepak Pahwa (Delhi, IN); Varun Pahwa (Delhi, IN); Anil Kumar Choudhary (Gurgaon, IN); Sonia (New Delhi, IN); Vivek Kumar Jha (Gurgaon, IN); Anjali Chauhan (Gurgaon, IN); Annu Yadav (Gurgaon, IN)

Assignee: DESICCANT ROTORS INTERNATIONAL PRIVATE LIMITED

B01J20/226B01J20/28045B01J20/3204B01J20/3206B01J20/3236B01J20/3265B01J20/3289

Abstract

Claims (43)

1. A method for the in situ synthesis of MOFs, COFs, or ZIFs, onto and within a porous substrate comprising: contacting the porous substrate with a first solution and a second solution, wherein the first and the second solutions are capable of forming the said MOFs, COFs, or ZIFs, and wherein the ratio of in situ synthesized adsorbent to bare substrate is in the range of 0.1 to 6 times by weight of the in situ synthesized adsorbent to the bare substrate.

2. The method as claimed in claim 1 , wherein the porous substrate is contacted with the first solution and the second solution, sequentially in any order or simultaneously as a mixture of the two solutions.

3. The method as claimed in claim 1 , wherein the first solution and/or the second solution comprise a mixture of two or more solutions, wherein the resulting adsorbent synthesized in situ is either one or more MOFs, COFs, or ZIFs or a combination of one or more of MOFs, COFs or ZIFs with an inorganic adsorbent.

4. The method as claimed in claim 1 , wherein the contacting is done by dipping or soaking.

5. The method as claimed in claim 4 , wherein dipping/soaking time, temperature, pressure, concentration, and viscosity for both the first solution and the second solution are optimized with or without use of enhancers or retarders.

6. The method as claimed in claim 1 , wherein the substrate is pretreated with a rigidifying agent selected from the group consisting of silica sol, alumina sol, polyvinyl alcohol, polyvinyl acetate, acrylate, water glass and any combination thereof.

7. The method as claimed in claim 1 , wherein the substrate is washed after in situ synthesis to remove unreacted or excess starting material or byproducts formed during the synthesis, drying, and activation.

8. The method as claimed in claim 4 , wherein the substrate is converted into a desired geometry after dipping in a first solution, followed by dipping/soaking the shaped substrate into a second solution to result in the in situ formation of the adsorbent.

9. The method as claimed in any of claim 4 , wherein the substrate is first shaped into a desired geometry, followed by sequential dipping of the shaped substrate into a first solution and a second solution or a mixture of the first and second solutions to result in the in situ formation of an adsorbent.

10. The method as claimed in claim 1 , wherein a dosing amount of titanium silicate is added to the first solution or the second solution prior to treatment of the substrate.

11. The method as claimed in claim 1 , wherein the substrate is subjected to burn-off of substantially all organic binding material without affecting the adsorbent properties.

12. The method as claimed in claim 1 , wherein the in situ synthesized MOF comprises any one of MIL-100 (Fe), AIF, MOF-5, Cu-BTC, MIL-53, MIL-68, Mg-MOF-74, MIL-101 (Cr), MOF 801, MOF 177, CAU-10H, MOF 808, IR-MOF-8, CPO-Ni (27), MOF 199, DMOF (Zn), DUT-4, and a combination thereof.

13. The method as claimed in claim 1 , wherein the COF formed in situ is selected from the group consisting of COF-202, COF-1, COF-5, PcPBBA, TpPa-1, TpPa-2, TpPa-NO2, TpPa-F4, TpBD, TpBD-(NO2), and a combination thereof.

14. A method as claimed in claim 1 , wherein the ZIF is selected from the group consisting of ZIF-1, ZIF-7, ZIF-8, ZIF-35, ZIF-67, ZIF-69, ZIF-71, ZIF-90, ZIF-95 and ZIF-100, and a combination thereof.

15. The method as claimed in claim 1 , wherein the substrate is a porous substrate selected from the group consisting of glass fibers, ceramic fibres, natural fibers, synthetic fibers, biosoluble fibers, pulp and any combination thereof, and if desired strengthened with 2 to 8% by weight of a rigidifying agent selected from the group consisting of silica sol, alumina sol, polyvinyl alcohol, polyvinyl acetate, and acrylate.

16. The method as claimed in claim 1 , wherein the loaded substrate is dried at a temperature of up to 90° C.

17. The method as claimed in claim 1 , wherein the substrate treated with both solutions is dried at a temperature in the range of 80° C. to 160° C.

18. The method as claimed in claim 1 , further comprises 0.25 to 15% by weight of an additive selected from the group consisting of xanthan gum, sodium alginate, hydroxypropylmethylcellulose, guar gum, starch, and ethylene glycol, been added to the substrate via the solution containing the organic component.

19. The method as claimed in claim 1 , further comprises an organic linker used to impregnate the substrate that is a bidentate or tridentate ligand derived from a dicarboxylic acid selected from the group consisting of oxalic acid, tartaric acid, succinic acid, 1,4-butanedicarboxylic acid, 1,4-butene-dicarboxylic acid, 4-oxopyran-2,6-dicarboxylic acid, decanedicarboxylic acid, 1,8-heptadecanedicarboxylic acid, 1,6-hexanedicarboxylic acid, heptadecanedicarboxylic acid, acetylene dicarboxylic acid, 1,9-heptadecanedicarboxylic acid, 1,2-benzenedicarboxylic acid, 1,3-benzenedicarboxylic acid, 2,3-pyridinedicarboxylic acid, pyridine-2,3-dicarboxylic acid, 1,4-benzenedicarboxylic acid, p-benzenedicarboxylic acid, imidazole-2,4-dicarboxylic acid, 2-methylquinoline-3,4-dicarboxylic acid, quinoline-2,4-dicarboxylic acid, quinoxaline-2,3-dicarboxylic acid, 6-chloroquinoxaline-2,3-dicarboxylic acid, 1,3-butadiene-1,4-dicarboxylic acid, 4,4′-diaminophenylmethane-3,3′-dicarboxylic acid, quinoline-3,4-dicarboxylic acid, di imidedicarboxylic acid, pyridine-2,6-dicarboxylic acid, 2-methylimidazole-4,5-dicarboxylic acid, 7-chloro-4-hydroxyquinoline-2,8-dicarboxylic acid, thiophene-3,4-dicarboxylic acid, tetrahydropyran-4,4-dicarboxylic acid, perylene-3,9-dicarboxylic acid, 2-isopropylimidazole-4,5-dicarboxylic acid, perylenedicarboxylic acid, Pluriol E 200-dicarboxylic acid, 3,5-cyclohexadiene-1,2-dicarboxylic acid, octanedicarboxylic acid, pentane-3,3-carboxylic acid, 3,6-dioxaoctanedicarboxylic acid, 4,4′-diamino-1,1′-biphenyl-3,3′-dicarboxylic acid, 4,4′-diaminobiphenyl-3,3′-dicarboxylic acid, benzidine-3,3′-dicarboxylic acid, 1,1′-binaphthyldicarboxylic acid, 1,4-bis(phenylamino)benzene-2,5-dicarboxylic acid, 7-chloro-8-methylquinoline-2,3-dicarboxylic acid, 1-anilinoanthraquinone-2,4′-dicarboxylic acid, 1,4-bis(carboxymethyl) piperazine-2,3-dicarboxylic acid, phenylinanedicarboxylic acid, 7-choroquinoline-3,8-dicarboxylic acid, polytetrahydrofuran 250-dicarboxylic acid, 1-(4-carboxy)phenyl-3-(4-chloro)phenylpyrazoline-4,5-dicarboxylic acid, 1,4,5,6,7,7-hexachloro-5-norbornene-2,3-dicarboxylic acid, 1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, naphthalene-1,8-dicarboxylic acid, 1,3-dibenzyl-2-oxoimidazolidine-4,5-cis-dicarboxylic acid, 2,2′-biquinoline-4,4′-dicarboxylic acid, 2-benzoylbenzene-1,3-dicarboxylic acid, pyridine-3,4dicarboxylic acid, 3,6,9-trioxaundecanedicarboxylic acid, Pluriol E 300 dicarboxylic acid, Pluriol E 400-dicarboxylic acid, hydroxybenzophenonedicarboxylic acid, Pluriol E 600-dicarboxylic acid, pyrazole-3,4-dicarboxylic acid, bis(4-aminophenyl) sulfone diimide-dicarboxylic acid, 5,6-dimethyl-2,3-pyrazinedicarboxylic acid, bis(4-aminophenyl) ether diimide-dicarboxylic acid, 2,3-pyrazinedicarboxylic acid, 4,4′-diaminodiphenylmethane diimide-dicarboxylic acid, 1,4-naphthalenedicarboxylic acid, 1,3-adamantanedicarboxylic acid, 1,8-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 2,3-naphthalenedicarboxylic acid, 8-methoxy-2,3-naphthalenedicarboxylic acid, 8-sulfo-2,3-naphthalenedicarboxylic acid, anthracene-2,3-dicarboxylic acid, 8-nitro-2,3-naphthalenecarboxylic acid, 2′,3′-diphenyl-p-terphenyl-4,4″-dicarboxylic acid, (diphenyl ether)-4,4′-dicarboxylic acid, 4 (1H)-oxothiochromene-2,8-dicarboxylic acid, imidazole-4,5-dicarboxylic acid, 5-tert-butyl-1,3-benzenedicarboxylic acid, 7,8-quinolinedicarboxylic acid, 4,5-imidazoledicarboxylic acid, 1,3,5-benzenetricarboxylic acid, 1,3,5-tris(4-carboxyphenyl)benzene, and comprises heterocyclic aromatic organic compounds for in situ synthesis of ZIFs selected from the group consisting of imidazole, benzimidazole, chlorobenzimidazole, nitroimidazole, 2-methylimidazole, and imidazole-2-carboxyaldehyde.

20. The method as claimed in claim 1 , further comprises metal salt selected from the group consisting of ferric nitrate, ferric chloride, ferrous chloride, chromium nitrate, chromium chloride, aluminium sulphate, aluminium chloride, aluminium bromide, aluminium hydrogensulfate, aluminium dihydrogen phosphate, aluminium monohydrogen phosphate, aluminium phosphate, aluminium nitrate, nickel acetate, zirconium oxychloride, zinc nitrate, zinc acetate, copper acetate, copper nitrate, cobalt nitrate and magnesium nitrate.

21. The method as claimed in claim 20 , wherein the concentration of the metal salt in solution is in the range of 5% to 50% by weight of the solution.

22. The method as claimed in claim 1 , further comprises solvent selected from the group consisting of water, methanol, ethanol, n-propanol, iso-propanol, n-butanol, isobutanol, t-butanol, pentanol, hexanol, dimethyl sulfoxide, N,N-dimethyl formamide, N,N-diethyl formamide, toluene, acetonitrile, dioxane, N,N-dimethylacetamide, benzene, chlorobenzene, tetrahydrofuran, ethyl acetate, methyl ethyl ketone, pyridine, sulfolane, glycol, N-methylpyrrolidone, diethyl amine, triethyl amine, gamma-butyrolactone, cyclohexanol, acetylacetonate, mesitylene and other similar aqueous, non-aqueous, aliphatic, aromatic, organic, in-organic solvents and mixture thereof.

23. The method as claimed in claim 1 , wherein the reaction temperature is in the range of 5 to 120° C., and a reaction time is in the range of 10 min to 24 hours.

24. A porous substrate having MOFs, COFs, or ZIFs synthesized in situ onto and within the substrate by a method as claimed in claim 1 , for use in gas separation membranes, dehumidification applications, drug delivery systems, energy storage devices, CO2 capture, sensors, lithium batteries.

25. An adsorbent matrix comprising one or more adsorbents selected from the group consisting of MOFs, COFs, ZIFs, and a combination thereof, with and optionally an inorganic adsorbent, synthesized by a method as claimed in claim 1 , wherein the ratio of the in situ synthesized adsorbent to substrate is in the range of 0.1 to 6 times by weight of the adsorbent to the bare substrate.

26. The adsorbent matrix as claimed in claim 25 wherein the matrix is in the form of a honeycomb.

27. The adsorbent matrix as claimed in claim 25 wherein the MOF comprises any one of MIL-100 (Fe), AIF, MOF-5, Cu-BTC, MIL-53, MIL-68, Mg-MOF-74, MIL-101 (Cr), MOF 801, MOF 177, CAU-10H, MOF 808, IR-MOF-8, CPO-Ni (27), MOF 199, DMOF (Zn), DUT-4, and a combination thereof.

28. The adsorbent matrix as claimed in claim 25 wherein the COF is selected from the group consisting of COF-202, COF-1, COF-5, PcPBBA, TpPa-1, TpPa-2, TpPa-NO2, TpPa-F4, TpBD, TpBD-(NO2), and a combination thereof.

29. The adsorbent matrix as claimed in claim 25 wherein ZIF is selected from the group consisting of ZIF-1, ZIF-7, ZIF-8, ZIF-35, ZIF-67, ZIF-69, ZIF-71, ZIF-90, ZIF-95 and ZIF-100, and a combination thereof.

30. The adsorbent matrix as claimed in claim 25 wherein the substrate is a porous substrate selected from the group consisting of glass fibers, ceramic fibres, natural fibers, synthetic fibers, biosoluble fibers, pulp and combination thereof, and optionally strengthened with 2 to 8% by weight of a rigidifying agent selected from the group consisting of silica sol, alumina sol, polyvinyl alcohol, polyvinyl acetate, and acrylate.

31. A method for the manufacture of an adsorbent matrix as claimed in claim 26 , wherein one or more adsorbents selected from the group consisting of MOFs, COFs, ZIFs, and a combination of one or more MOFs, COFs, ZIFs, and optionally an inorganic adsorbent are synthesized onto and within a substrate thereon; wherein the ratio of the in situ synthesized adsorbent to bare substrate is in the range of 0.1 to 6 times by weight of the adsorbent to the bare substrate.

32. The method as claimed in claim 31 , wherein the in situ synthesis or impregnation is followed by washing to remove unreacted or excess starting material or byproducts formed during the synthesis, and, drying and/or activation.

33. The method as claimed in claim 31 , comprising dipping the substrate in a first solution, converting the dipped substrate into a shaped matrix, followed by dipping the shaped matrix into a second solution.

34. The method as claimed in claim 33 , wherein the first solution or the second solution is a combination of two or more solutions.

35. The method as claimed in claim 33 , wherein the contacting with the first and second solutions can be sequential in any order or simultaneous with a mixture of the first and second solutions.

36. The method as claimed in claim 31 , wherein the adsorbent substrate is treated with a rigidifying agent.

37. The method as claimed in claim 31 , wherein the adsorbent is present in the form of a slurry and wherein the impregnation is carried out using a suitable binder selected from the group consisting of inorganic or organic binders.

38. The method as claimed in claim 37 , wherein the dipping/soaking time and concentration/viscosity for the adsorbent slurry at synthesis are adjusted.

39. A method for filtering an adsorbate from a fluid using an adsorbent laden matrix as claimed in claim 26 .

40. The method as claimed in claim 39 , wherein the fluid can be liquid or a gas, or a combination of liquids or a combination of gases.

41. The method as claimed in claim 39 , wherein the adsorbate can be a liquid or gas or a combination of liquids or a combination of gases.

42. The method as claimed in claim 39 , wherein the adsorbate is water vapour, CO2, VOCs and other gaseous matter and the adsorbent laden matrix is provided in a desiccant/adsorbent shaped wheel or a shaped matrix of any geometry.

43. A desiccant wheel having an adsorbent matrix as claimed in claim 25 .

Assignments (1)

Priority Claims (1)

Continuity (1)

References Cited (38)