Non-pgm ammonia slip catalyst
US-2015352492-A1 · Dec 10, 2015 · US
US11045792B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-11045792-B1 |
| Application number | US-202017038367-A |
| Country | US |
| Kind code | B1 |
| Filing date | Sep 30, 2020 |
| Priority date | Sep 30, 2020 |
| Publication date | Jun 29, 2021 |
| Grant date | Jun 29, 2021 |
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Highly efficient nanosized mesoporous CuMgAl ternary oxide catalysts are provided.
Opening claim text (preview).
We claim: 1. A method of catalyzing a chemical reaction comprising contacting reactants of the chemical reaction with a catalytically effective amount of a CuMgAl ternary oxide catalyst, wherein the reactants include a nitroalkane and an aldehyde or a ketone. 2. The method of claim 1 , wherein the reaction is conducted in the presence of ultrasonic irradiation. 3. The method of claim 1 , wherein the nitroalkane is nitromethane, the aldehyde is an aryl aldehyde and reaction products include one or more β-nitro-alcohols. 4. The method of claim 1 , further comprising, after the reaction is complete, recovering and reusing the CuMgAl ternary oxide catalyst, wherein the steps of recovering and reusing are performed at least 5 times without diminished catalytic activity of the CuMgAl ternary oxide catalyst. 5. The method of claim 4 , further comprising, after the step of recovering, reusing the CuMgAl ternary oxide catalyst to catalyze another chemical reaction. 6. A method of making one or more β-nitro-alcohols, comprising combining 4-nitrobenzaldehyde, nitromethane and a CuMgAl ternary oxide catalyst in a reaction vessel; exposing the reaction vessel to ultrasonic energy for a period of time sufficient to convert the 4-nitrobenzaldehyde and the nitromethane to the one or more β-nitro-alcohols; and recovering the one or more β-nitro-alcohols. 7. The method of claim 6 , wherein the CuMgAl ternary oxide catalyst is CuMgAl-I or CuMgAl-II. 8. The method of claim 6 , wherein the CuMgAl ternary oxide catalyst is CuMgAl-I. 9. The method of claim 6 , wherein the β-nitro-alcohols include 2-Nitro-1-(4-nitrophenyl)ethan-1-ol, 2-Nitro-1-(3-nitrophenyl)ethan-1-ol, 2-Nitro-1-(2-nitrophenyl)ethan-1-ol, 1-(3,5-Dibromophenyl)-2-nitroethan-1-ol, 4-Bromo-2-(1-hydroxy-2-nitroethyl)-6-nitrophenol, 1-[4-(Dimethylamino)phenyl]-2-nitroethan-1-ol, 1-(4-Bromophenyl)-2-25 nitroethan-1-ol, 1-(4-Methoxyphenyl)-2-nitroethan-1-ol, 1-(3,5-Dimethoxyphenyl)-2-nitroethan-1-ol and 4-(1-Hydroxy-2-nitroethyl)-2-methoxyphenol.
X-ray diffraction · CPC title
Infrared [IR] · CPC title
Scanning electron microscopy; Transmission electron microscopy · CPC title
having a two-dimensional [2D] layered crystalline structure, e.g. layered double hydroxide [LDH] · CPC title
Mechanical properties · CPC title
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