IP Library Granted Patent US 11,155,473
Granted Patent B2
US 11,155,473 · App. 16/208,785 · Granted Oct 26, 2021

Nanostructured mixed metal oxides as catalysts and method of making thereof

Inventors: Eranda Nikolla (Troy, MI); Bingwen Wang (Riverview, MI); Ayad Nacy (Sterling Heights, MI)
Assignee: Wayne State University
C01G53/006B01J23/002B01J23/63B01J23/83B01J35/00B01J35/0013B01J37/009B01J37/03B01J37/031B01J37/036B01J37/08C01G53/68C01G53/70C01G55/002H01M4/9033B01J23/894B01J35/026B01J2523/3706B01J2523/3718B01J2523/828B01J2523/847B82Y30/00B82Y40/00C01P2002/34C01P2002/72C01P2002/85C01P2004/03C01P2004/04C01P2004/16
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Quick Facts
Patent No.
US 11,155,473
App. No.
16/208,785
Granted
Oct 26, 2021
Kind
B2
Abstract

A method of forming a metal oxide material having a rod shape or polyhedral nanostructure includes preparing a first reverse micro-emulsion system comprising an aqueous precipitating agent dispersion and a second reverse micro-emulsion system containing an aqueous metal salt dispersion; combining the micro-emulsions together to initiate a reaction; allowing the reaction to continue to form a product mixture comprising a metal oxide gel and aqueous media; separating the metal oxide gel from the aqueous media; collecting the metal oxide gel; and calcining the metal oxide gel to form the metal oxide material. The metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , Pr 2-y A y NiO 4 , or La 2-z D z NiO 4 , wherein M is copper, cobalt, iron, manganese, chromium, aluminum, or platinum; A is lanthanum or neodymium; D is calcium, barium or strontium; x ranges from 0 to 1; y ranges from 0 to 2; and z ranges from 0 to 0.25.

Claims (38)

1. A method of forming a metal oxide material having a rod shape or a polyhedral nanostructure; the method comprising:

preparing a first reverse micro-emulsion system comprising a precipitating agent dispersed in a first aqueous medium;

preparing a second reverse micro-emulsion system containing a metal salt dispersed in a second aqueous medium, wherein preparing the second reverse micro-emulsion system includes ultrasonicating to obtain a transparent micro-emulsion suspension of the metal salt dispersed in the second aqueous medium;

combining the first and second reverse micro-emulsions together to initiate a reaction;

allowing the reaction to continue for a predetermined amount of time to form a product mixture comprising a metal oxide gel and the first and second aqueous media;

separating the metal oxide gel from the first and second aqueous media;

collecting the metal oxide gel; and

calcining the metal oxide gel to form the metal oxide material;

wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , Pr 2-y A y NiO 4 , or La 2-z D z NiO 4 , wherein M is copper (Cu), cobalt (Co), iron (Fe), manganese (Mn), chromium (Cr), aluminum (Al), or platinum (Pt); A is lanthanum (La) or neodymium (Nd); D is calcium (Ca), barium (Ba) or strontium (Sr); x ranges from 0 to 1; y ranges from 0 to 2; and z ranges from 0 to 0.25.

2. The method according to claim 1 , wherein the first and second aqueous media further comprises one or more of a surfactant, a co-surfactant, and a co-solvent, such that the surfactant is cetyl tetrammoniabromide (CTAB), the co-surfactant is an aliphatic hydrocarbon that has at least six carbon atoms, and the co-solvent is an aliphatic alcohol.

3. The method according to claim 2 , wherein the co-surfactant is hexane and the co-solvent is n-butanol.

4. The method according to claim 1 , wherein the first and second aqueous media comprises a molar ratio (Wo) of water to surfactant that is controlled at a value of about 1.6.

5. The method according to claim 1 , wherein the metal salt comprises a combination of metal cations that are independently selected from the elements of La, Pr, Mn, Cr, Ni, Fe, Co, Cu, Pt, Nd, Ca, Ba, or Sr, and an anion that is independently selected from a nitrate, an acetate, a chloride, or a combination thereof.

6. The method according to claim 1 , wherein the precipitating agent is an alkali metal hydroxide, an alkali metal carbonate, or a combination thereof.

7. The method according to claim 1 , wherein the predetermined amount of time is at least 4 hours.

8. The method according to claim 1 , wherein separating the metal oxide gel from the first and second aqueous media comprises filtering or centrifuging the product mixture.

9. The method according to claim 1 , wherein the method further comprises washing the metal oxide gel with water/ethanol and drying the metal oxide gel in an oven at 80° C. prior to calcination.

10. The method according to claim 1 , wherein the calcination is performed at a temperature that is in the range of about 700° C. to about 1,000° C.

11. The method according to claim 1 , wherein at least one of the metal salt and the precipitating agent are present in a stoichiometric amount.

12. The method according to claim 1 , wherein the metal oxide material is a Ruddlesden-Popper (R-P) oxide material.

13. The method according to claim 1 , wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , wherein M is Co, Fe, or Mn, and x ranges from greater than 0 to 1.

14. The method according to claim 1 , wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , wherein M is Al, Mn, Fe, Co, or Cu, and x is 0.5.

15. The method according to claim 1 , wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , wherein M is Fe, Cu, Cr, Mn, or Co, and x is 0.12.

16. The method according to claim 1 , wherein the metal oxide material corresponds to the chemical formula of La 2-z D z NiO 4 , wherein D is Ca, Ba, or Sr and z ranges from greater than 0 to 0.25.

17. The method according to claim 1 , further comprising washing the metal oxide gel after separating the metal oxide gel from the first and second aqueous media, wherein washing the metal oxide gel includes adding a solvent and ultrasonicating the metal oxide gel in the solvent.

18. A method of forming a metal oxide material having a rod shape or a polyhedral nanostructure; the method comprising:

preparing a first reverse micro-emulsion system comprising a precipitating agent dispersed in a first aqueous medium;

preparing a second reverse micro-emulsion system containing a metal salt dispersed in a second aqueous medium; wherein preparing the second reverse microemulsion system includes ultrasonicating to obtain a transparent micro-emulsion suspension of the metal salt dispersed in the second aqueous medium

combining the first and second reverse micro-emulsions together to initiate a reaction;

allowing the reaction to continue for a predetermined amount of time to form a product mixture comprising a metal oxide gel and the first and second aqueous media;

separating the metal oxide gel from the first and second aqueous media;

collecting the metal oxide gel; and

calcining the metal oxide gel to form the metal oxide material;

wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 or La 2-z D z NiO 4 , wherein M is copper (Cu), cobalt (Co), iron (Fe), manganese (Mn), chromium (Cr), aluminum (Al), or platinum (Pt); D is calcium (Ca), barium (Ba) or strontium (Sr); x ranges from greater than 0 to 1; and z ranges from greater than 0 to 0.25.

19. The method according to claim 18 , wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , wherein M is Al, Mn, Fe, Co, or Cu, and x is 0.5.

20. The method according to claim 18 , wherein the metal oxide material corresponds to the chemical formula of La 2 M x Ni 1-x O 4 , wherein M is Fe, Cu, Cr, Mn, or Co, and x is 0.12.

21. The method according to claim 18 , wherein the metal oxide material corresponds to the chemical formula of La 2-z D z NiO 4 , wherein D is Sr and z ranges from greater than 0 to 0.25.

22. The method according to claim 18 , further comprising washing the metal oxide gel after separating the metal oxide gel from the first and second aqueous media, wherein washing the metal oxide gel includes adding a solvent and ultrasonicating the metal oxide gel in the solvent.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 16, 2024
From: WAYNE STATE UNIVERSITY
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 068957/0757 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2018
From: NIKOLLA, ERANDA; WANG, BINGWEN; NACY, AYAD
To: WAYNE STATE UNIVERSITY
Reel/Frame 047868/0913 →
Continuity (2)
Provisional Application 62594140 · Dec 4, 2017
Related Publication 20190169043A1 · Jun 6, 2019