Nanostructured mixed metal oxides as catalysts and method of making thereof

Patent metadata

Field	Value
Publication number	US-11155473-B2
Application number	US-201816208785-A
Country	US
Kind code	B2
Filing date	Dec 4, 2018
Priority date	Dec 4, 2017
Publication date	Oct 26, 2021
Grant date	Oct 26, 2021

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 La2MxNi1-xO4, Pr2-yAyNiO4, or La2-zDzNiO4, 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.

First claim

What is claimed is:

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.

Assignees

• Univ Wayne State

Inventors

• Nikolla Eranda
• Wang Bingwen
• Nacy Ayad

Classifications

• B01J2235/15

  X-ray diffraction · CPC title

• B01J2235/30

  Scanning electron microscopy; Transmission electron microscopy · CPC title

• B01J35/45

  Nanoparticles · CPC title

• B01J35/55

  Cylinders or rings · CPC title

• B01J2235/00

  Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title