Core-shell CO oxidation catalyst as well as preparation method and application thereof
An oxidation catalyst, core-shell type technology, applied in the direction of catalyst activation/preparation, physical/chemical process catalyst, metal/metal oxide/metal hydroxide catalyst, etc., can solve the complex preparation process, high production cost, Less storage capacity and other issues, to achieve the effects of avoiding catalyst deactivation, prolonging service life, and low preparation cost
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Embodiment 1
[0039] Example 1: Preparation of core-shell catalyst derived from MnBDC@ZiF-67
[0040] First, dissolve 0.6125g of manganese acetate tetrahydrate and 0.4150g of terephthalic acid in 25mL of N,N-dimethylformamide, mix them uniformly by ultrasonic, and record it as solution A; then mix 1.4550g of cobalt nitrate hexahydrate with 1.6460g 2-Methylimidazole was dissolved in 40 mL of methanol respectively, and mixed evenly after complete dissolution, which was recorded as solution B; the mixed solutions A and B were ultrasonically stirred, and placed in an autoclave at 150 °C for 5 h. After centrifugal washing with DMF for 2-3 times, washing with methanol until the supernatant was colorless, and drying at 80°C, the MnBDC@ZiF-67 core-shell material was obtained, which was purple in color. Then calcined at 350° C. for 2 h in a muffle furnace to obtain the final catalyst, which was black in color.
[0041] The CO catalytic test analysis was carried out on the core-shell catalyst derive...
Embodiment 2
[0044] Example 2: Preparation of core-shell catalyst derived from FeBTC (hydrothermal)@ZiF-67
[0045] First, dissolve 0.4000g of FeBTC (hydrothermal) in 40mL of ethanol, mix it uniformly by ultrasonic, and record it as solution A; then dissolve 1.4550g of cobalt nitrate hexahydrate and 1.6420g of 2-methylimidazole in 40mL of methanol, and completely dissolve After mixing evenly, record it as solution B; mix A and B solutions, and stir at room temperature for 24 hours. After centrifugation and washing with ethanol, the supernatant was washed with methanol until it was colorless, and dried at 80° C. to obtain an uncalcined product with a purple color. Then calcined at 350° C. for 2 h in a muffle furnace to obtain the final catalyst, which was black in color.
[0046] The CO catalytic test analysis was carried out on the core-shell catalyst derived from FeBTC (hydrothermal)@ZiF-67, and CO was completely oxidized at 110 °C.
Embodiment 3
[0047] Example 3: Preparation of core-shell catalyst derived from CuBTC (nitrate, 100°C, hydrothermal)@ZiF-67
[0048] First, dissolve 0.4000g CuBTC (nitrate, 100°C, hydrothermal) in 40mL of ethanol, mix it uniformly by ultrasonic, and record it as solution A; then dissolve 1.4550g of cobalt nitrate hexahydrate and 1.6420g of 2-methylimidazole in 40mL In methanol, completely dissolved and mixed evenly, recorded as solution B; mix A and B solutions, and stir at room temperature for 24 hours. After centrifugation and washing with ethanol, the supernatant was washed with methanol until it was colorless, and dried at 80° C. to obtain an uncalcined product with a purple color. Then it was calcined at 350°C for 2 h in a muffle furnace to obtain the final catalyst, which was black in color.
[0049] The CO catalytic test analysis was carried out on the core-shell catalyst derived from CuBTC (nitrate, 100 °C, hydrothermal) @ZiF-67, and CO was completely oxidized at 110 °C. Scanning ...
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