Cerium-based composite oxide VOCs (volatile organic compounds) combustion catalyst using metal organic framework as template and preparation method thereof
A metal-organic framework, composite oxide technology, applied in catalyst activation/preparation, combustion method, physical/chemical process catalyst, etc., can solve the problems of long reaction time, large energy consumption, complex process, etc., and achieve good catalytic performance, The effect of improved catalytic ability and broad application prospects
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[0040] In the specific embodiment of the present invention, the cerium-based metal organic framework material used is Ce-BTC (the molecular formula is Ce(1,3, 5-BTC)(H 2 O) 6 ); The preparation method of Ce-BTC includes the following steps:
[0041] Take the cerium-based salt and organic ligand (mesitylene), configure the metal organic framework compound Ce(1, 3, 5-BTC) (H 2 O) 6 Precursor mixture of, stand, centrifuge, wash with solvent, filter, dry, and grind to obtain powdered sample Ce(1, 3,5-BTC)(H 2 O) 6 .
[0042] In the specific embodiment, for the decomposition temperature range of the cerium-based metal organic framework material Ce-BTC between 300°C and 500°C, the firing temperature is selected between 300°C and 500°C, the firing time is 6h, and the firing rate is 2°C / min. .
Example Embodiment
[0043] Example 1
[0044] MnOx-CeO 2 The specific steps for preparing the composite catalyst are as follows:
[0045] (1) Weigh 4.34 g Ce(NO 3 ) 3 • 6H 2 O was dissolved in 50 mL of deionized water, 2.10 g of mesitylene was dissolved in a mixture of 150 mL of deionized water and 200 mL of ethanol, and the above two solutions were mixed to obtain the precursor solution. The mixture was allowed to stand for 24 hours. Wash with deionized water 3 times, filter and dry to obtain Ce(1, 3, 5-BTC)(H 2 O) 6 , After X-ray diffraction structure analysis and comparison with simulated powder XRD diffraction patterns, it is determined as Ce(1, 3, 5-BTC)(H 2 O) 6 ;
[0046] Ce(1, 3, 5-BTC)(H 2 O) 6 The specific surface area is 715 m 2 / g;
[0047] (2) Weigh 0.8 g Ce(1, 3, 5-BTC)(H 2 O) 6 And 182μL 50wt% Mn(NO 3 ) 2 The solution was dispersed in a mixed solution of 20 mL of ethanol and water (ethanol: water = 1:1, v / v), allowed to stand at room temperature for 24 hours and then dried at 60°C. After g...
Example Embodiment
[0050] Example 2
[0051] MnOx-CeO 2 The specific steps for preparing the composite catalyst are as follows:
[0052] (1) Weigh 4.34 g Ce(NO 3 ) 3 • 6H 2 O was dissolved in 50 mL of deionized water, 2.10 g of mesitylene was dissolved in a mixture of 150 mL of deionized water and 200 mL of ethanol, and the above two solutions were mixed to obtain a precursor mixed solution. Let it stand for 24 hours and use it after centrifugation. Washed with ionized water 3 times, filtered and dried to obtain Ce(1, 3, 5-BTC)(H 2 O) 6 , After X-ray diffraction structure analysis and comparison with simulated powder XRD diffraction patterns, it is determined as Ce(1, 3, 5-BTC)(H 2 O) 6 ;
[0053] Ce(1, 3, 5-BTC)(H 2 O) 6 The specific surface area is 715 m 2 / g;
[0054] (2) Weigh 0.8 g Ce(1, 3, 5-BTC)(H 2 O) 6 And 182μL 50wt% Mn(NO 3 ) 2 The solution was dispersed in a mixed solution of 20 mL of ethanol and water (ethanol: water = 1:1, v / v). After standing for 24 hours at room temperature, the powder w...
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