Spinel-structured catalyst with capability of simultaneous desulfurization and denitrification as well as preparation method and application of catalyst
A spinel structure, desulfurization and denitration technology, which is applied in the field of simultaneous desulfurization and denitration catalysts with spinel structure and its preparation, can solve the problem of no transition metal active components and the like, and achieve the effects of low cost, wide source and easy acquisition.
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[0020] The catalyst with spinel structure capable of desulfurization and denitrification simultaneously of the present invention, its preferred embodiment is:
[0021] Including: the active components are CoO, Fe 2 o 3 、Al 2 o 3 Two or three of them, the additive is CeO 2 , Y 2 o 3 One or two of them, the carrier is activated carbon;
[0022] The active components of the catalyst form a spinel structure on the surface of the carrier.
[0023] The active components are CoO, Fe 2 o 3 、Al 2 o 3 Two or three of them, the content of each component accounts for between 5% and 15% of the mass of the carrier;
[0024] The auxiliary agent is CeO 2 , Y 2 o 3 One or two of them, the content of each component accounts for 1-5% of the mass of the carrier.
[0025] The specific surface area of the catalyst: 800 ~ 1500m 2 / g.
[0026] The above-mentioned preparation method of the catalyst with spinel structure capable of simultaneous desulfurization and denitrification of ...
Embodiment 1、10
[0050] Example 1, 10Fe 2 o 3 6CoO3Y 2 o 3 / AC
[0051] where Fe 2 o 3 Accounting for 10% of the mass of the carrier, CoO accounts for 6% of the mass of the carrier, Y 2 o 3 Accounting for 3% of the mass of the carrier, that is, the total load of active components and auxiliary agents is 19%.
[0052] First take 20-40 mesh AC500g in a beaker, and use a certain concentration and a certain proportion (mass ratio to AC) of HNO 3 Pretreat for 12 hours, then wash to neutral dryness, cool to room temperature and set aside.
[0053] Accurately weigh 2.5299gFe(NO 3 ) 3 9H 2 O, 1.0532g Co(NO 3 ) 2 ·6H 2 O, 0.3393g Y (NO 3 ) 3 ·6H 2 O, add 7ml of deionized water to dissolve to form a mixed solution; accurately weigh 5.0000g of pretreated AC, dip into the prepared mixed solution, soak at 40°C for 12h, and then dry in a 110°C drying oven 12h, and finally roasted at 500°C for 4h in a nitrogen-protected tubular roaster to obtain a catalyst sample.
[0054] The prepared cat...
Embodiment 2、10
[0056] Example 2, 10CoO15Al 2 o 3 2CeO 2 / AC
[0057] where Al 2 o 3 Accounting for 15% of the mass of the carrier, CoO accounts for 10% of the mass of the carrier, CeO 2 Accounting for 2% of the mass of the carrier, that is, the total loading of active components and auxiliary agents is 27%.
[0058] First take 20-40 mesh AC500g in a beaker, and use a certain concentration and a certain proportion (mass ratio to AC) of HNO 3 Pretreat for 12 hours, then wash to neutral dryness, cool to room temperature and set aside.
[0059] Accurately weigh 5.5166g Al(NO 3 ) 3 9H 2 Og, 2.5053Co(NO 3 ) 2 ·6H 2 O, 0.2523g Ce(NO 3 ) 2 ·6H 2 O, add 7ml of deionized water to dissolve to form a mixed solution; accurately weigh 5.0000g of pretreated AC, dip into the prepared mixed solution, soak at 40°C for 12h, and then dry in a 110°C drying oven 12h, and finally roasted at 500°C for 4h in a nitrogen-protected tubular roaster to obtain a catalyst sample.
[0060] The prepared cata...
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