System and method for two and three way mixed metal oxide ZPGM catalyst
US-9216408-B2 · Dec 22, 2015 · US
US11319232B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11319232-B2 |
| Application number | US-201816499097-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 30, 2018 |
| Priority date | Mar 31, 2017 |
| Publication date | May 3, 2022 |
| Grant date | May 3, 2022 |
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Disclosed is a method for preparing a solid material including manganese, the method including the following steps: a. bringing into contact an aqueous effluent including manganese, for example at least 5 mg/L, typically at least 5 to 50 mg/L, and preferably 7 to 25 mg/L of manganese, with an oxidizing agent, manganese, preferably at a temperature between 10° C. and 50° C., and obtaining an oxidized aqueous solution; b. adding a base to the oxidized aqueous solution obtained at the end of step a) until a pH of between 8 and 12, preferably greater than 9, and preferably from 9 to 10.5, and obtaining a solution including a precipitate; c. filtration of the solution obtained at the end of step b); and d. obtaining a solid material including manganese, and especially manganese (IV) and/or Mn (III).
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The invention claimed is: 1. Method for the preparation of a solid material comprising manganese, said method comprising the following steps: a. bringing into contact an aqueous effluent comprising manganese, with an agent capable of oxidizing manganese, and obtaining an aqueous solution comprising oxidized manganese; b. adding to the aqueous solution comprising oxidized manganese obtained at the end of step a) of a base until a pH of between 9.5 and 12, and obtaining a solution comprising a precipitate that comprises manganese; c. filtration of the solution obtained at the end of step b); and d. obtaining a solid material comprising manganese. 2. Method according to claim 1 , wherein the solid material obtained at the end of step d) comprises oxides of manganese. 3. Method according to claim 1 , wherein the agent capable of oxidizing manganese is chosen from hydrogen peroxide, dioxygen or sodium percarbonate. 4. Method according to claim 1 , wherein the agent capable of oxidizing manganese is added in a concentration of between 0.015 mL/L and 2 mL/L. 5. Method according to claim 1 wherein the base is selected from potassium hydroxide, sodium hydroxide, calcium carbonate, sodium carbonate and calcium hydroxide. 6. Method according to claim 1 wherein the effluent further comprises one or more of the elements selected from aluminum, calcium, copper, iron, potassium, magnesium, sodium, zinc, nickel, arsenic and silicon. 7. The method of claim 1 , wherein: the step of bringing into contact the aqueous effluent comprises at least 5 mg/L of manganese, with an agent capable of oxidizing manganese, at a temperature between 10° C. and 50° C.; the step of adding to the aqueous solution comprising oxidized manganese a base is performed until a pH greater than 9.5 is achieved; and the solid material obtained is manganese (IV) and/or Mn (III). 8. Method according to claim 1 , wherein the agent capable of oxidizing manganese is hydrogen peroxide. 9. Method according to claim 1 wherein the base is sodium hydroxide. 10. Method according to claim 1 wherein in step b) the base is added until a pH 9.5 is obtained. 11. Method according to claim 1 wherein the effluent further comprises one or more of the elements selected from aluminum, calcium, copper, iron, potassium, magnesium and sodium. 12. Method of carrying out an organic synthesis reaction comprising the following steps: i) preparing a solid material comprising manganese according to claim 1 ; ii) carrying out an organic synthesis reaction by contacting the solid material comprising manganese obtained at the end of stage i) as a catalyst with a reaction medium. 13. Method according to claim 12 , in which the organic synthesis reaction is chosen from the oxidation reactions; the oxidative cleavage reactions; and the epoxidation reactions of alkenes. 14. Method according to claim 13 , wherein the organic synthesis reaction is carried out in the presence of ambient oxygen. 15. Method according to claim 12 , in which the organic synthesis reaction is chosen from the reactions for the oxidation of alcohols to aldehydes or ketones, said alcohols being selected from alcohols in alpha of an aromatic ring, in alpha of heterocyclic, in alpha of a double bond, and aliphatic alcohols; the oxidative cleavage reactions of diols, of alpha hydroxy acids, of alpha hydroxylated carbonyl derivatives, of dicarbonyl derivatives; and the epoxidation reactions of mono, di-, tri or tetrasubstituted alkenes.
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