Barium-transition metal-cerium base oxide catalyst for eliminating carbon smoke
A technology of cerium-based oxides and transition metals, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, catalyst activation/preparation, etc., can solve the problem of harmful soot particles threatening human health , to achieve the effects of convenient control of the reaction process, low production cost, and meeting the exhaust temperature requirements
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Embodiment 1
[0025] Add 2.777g of ammonium cerium nitrate, 0.241g of cobalt acetate and 15ml of water into a 200ml beaker, stir to dissolve, then add 2.836g of citric acid under stirring at room temperature, and then add 0.3g of polyethylene glycol (molecular weight 400) after dissolving After the dropwise addition, heat and stir at 80°C until the water evaporates to produce a viscous colloid. Then the obtained colloid was dried in the air atmosphere at 110°C for 12 hours, taken out and pulverized, pre-calcined at 300°C for 1 hour, calcined at 500°C for 3 hours, and cooled in the furnace to obtain a Co-Ce composite oxide, abbreviated as (CoO y ) 0,1 (CeO 2 ) 0.9 . Take 0.241g of barium nitrate and dissolve it in 0.9g of deionized water. Add 1.5g of the prepared Co-Ce composite oxide into the barium nitrate solution, stir evenly, heat and dry at 110°C for 3 hours, calcinate at 550°C for 1 hour, and cool in the furnace to prepare Ba-loaded barium-cobalt-cerium Ba 0.1 / (CoO) 0,1 (CeO ...
Embodiment 2
[0027] Add 2.777g of ceric ammonium nitrate, 0.230g of nickel chloride and 15ml of water in a 200ml beaker, stir and dissolve, then add 2.836g of citric acid under stirring at room temperature, and then add 0.3g of polyethylene glycol (molecular weight 200 ), after the dropwise addition, heat and stir at 80°C until the water evaporates to produce a viscous colloid. Then dry the obtained colloid in air atmosphere at 110°C for 12 hours, take it out and grind it finely, pre-calcine at 300°C for 1 hour, calcinate at 500°C for 3 hours, and cool in the furnace to obtain Ni-Ce composite oxide, abbreviated as (NiO) 0,1 (CeO 2 ) 0.9 . Take 0.241g of barium nitrate and dissolve it in 0.9g of deionized water. Add the prepared 1.5g Ni-Ce composite oxide into the barium nitrate solution, stir evenly, heat and dry at 110°C for 3 hours, calcinate at 550°C for 1 hour, and cool in the furnace to prepare Ba-loaded barium-nickel-cerium Ba 0.1 / (NiO) 0,1 (CeO 2 ) 0.9 catalyst. The conten...
Embodiment 3
[0029] Add 2.777g of ammonium cerium nitrate, 0.272g of ferric sulfate and 15ml of water into a 200ml beaker, stir to dissolve, then add 2.836g of citric acid under stirring at room temperature, and then add 0.3g of polyethylene glycol (molecular weight 600) after dissolving After the dropwise addition, heat and stir at 80°C until the water evaporates to produce a viscous colloid. Then the obtained colloid was dried at 110°C for 12 hours in an air atmosphere, taken out and ground into fine pieces, pre-calcined at 300°C for 1 hour, calcined at 500°C for 3 hours, and cooled in the furnace to obtain Fe-Ce composite oxide, abbreviated as (FeO 1.5 ) 0,1 (CeO 2 ) 0.9 . Take 0.247g of barium nitrate and dissolve it in 0.9g of deionized water. Add 1.5g of the Fe-Ce composite oxide prepared into the barium nitrate solution, stir evenly, heat and dry at 110°C for 3 hours, calcinate at 550°C for 1 hour, and cool in the furnace to prepare Ba-loaded barium-iron-cerium Ba 0.1 / (FeO 1...
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