Fluid catalytic cracking process including adsorption of hydrogen and a catalyst for the process
US-2015166431-A1 · Jun 18, 2015 · US
US11628432B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11628432-B2 |
| Application number | US-201816640947-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 13, 2018 |
| Priority date | Sep 15, 2017 |
| Publication date | Apr 18, 2023 |
| Grant date | Apr 18, 2023 |
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The invention discloses a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst, a preparation method and use thereof. The preparation method comprises the steps of: dissolving an organic ligand and Ti(OC3H7)4 in a mixture of methanol and DMF at a certain ratio, performing a hydrothermal reaction, centrifuging and drying to obtain a Titanium-based metal organic framework (Ti-MOF); pyrolyzing the obtained Ti-MOF under an inert atmosphere, and oxidizing the same for etching to obtain a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst. The obtained composite photocatalyst not only facilitates the adsorption, enrichment and mass transfer of low concentration VOCs, but also efficiently degrades VOCs under sunlight. It has high degradation activity and stability when performing photocatalytic removal of VOCs in the presence of visible light, is simple in synthesis, low in preparation cost, and has strong potential for the use in environmental protection.
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What is claimed is: 1. A method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst, characterized in that it comprises the steps of: S1. mixing an organic ligand, Ti(OC 3 H 7 ) 4 , methanol and DMF into a reaction vessel with polytetrafluoroethylene; S2. placing the reaction vessel containing the mixed solution in S1 in an oven, rising the temperature to 120-160° C., maintaining this temperature for 24-72 hours, and then cooling to room temperature to obtain a precipitate; S3. cross washing the precipitate obtained in S2 with an alcohol and DMF, centrifuging, and drying under vacuum to obtain an activated Titanium-based MOF material; S4. heating the activated Titanium-based MOF material obtained in S3 to 500-800° C. in an inert gas atmosphere and maintaining the temperature for 2-12 h; after lowering the temperature to 300-500° C., replacing the inert gas with a weak oxidizing gas; maintaining the condition for 30-120 min, adjusting the atmosphere back to the original inert gas atmosphere and the temperature to room temperature, so as to prepare a nitrogen-doped mesoporous carbon-coated TiO 2 composite photocatalyst. 2. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that the organic ligand in S1 is a mixture of 2-aminoterephthalic acid and terephthalic acid or 2-aminoterephthalic acid alone. 3. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that the molar ratio of the organic ligand, Ti(OC 3 H 7 ) 4 , methanol and DMF in S1 is 3:2: (23-25): (118-120). 4. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that the rate of said rising temperature in S2 is 0.1-10° C/min. 5. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that the alcohol in S3 is methanol or ethanol. 6. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that said drying under vacuum in S3 is carried out under 100-170° C. for 8-24 h. 7. The method for preparing a nitrogen-doped mesoporous carbon-coated Titanium dioxide composite photocatalyst according to claim 1 , characterized in that the inert gas in S4 is Ar or N 2 , and the weak oxidizing gas is CO 2 or air; the rate of said heating is 1-10° C/min, and the rate of said lowering temperature is 1-10° C/min.
Titanium · CPC title
Oxidising · CPC title
Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp · CPC title
Aromatic hydrocarbons · CPC title
Coordination polymers, e.g. metal-organic frameworks [MOF] (preparation of metal complexes containing carboxylic acid moieties C07C51/418; MOF's per se C07F) · CPC title
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