Iron-based catalyst for ft synthesis and preparation thereof
An iron-based catalyst and Fischer-Tropsch synthesis technology, applied in physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, and hydrocarbon production from carbon oxides, can solve the problem of low selectivity and achieve The effect of increasing the specific surface area and increasing the pore volume
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[0018] When the catalyst contains a substrate, the preparation method of the catalyst further includes the step of introducing the substrate into the catalyst. As for the method of introducing the substrate, the present invention is not particularly limited. When there are optional water-soluble precursors (such as aluminum oxide precursor water-soluble aluminum-containing salt, silicon oxide precursor water glass, magnesium oxide precursor water-soluble magnesium salt, etc.), the preferred method can be In step (1) of the method, the water-soluble precursor of the matrix, the water-soluble iron-containing compound and the organic reducing agent are simultaneously mixed with water and dissolved into a mixed solution, or the water-soluble After the precursor of the matrix is separately mixed with water and dissolved into a solution, the solution is introduced with the solution formed by mixing and dissolving the iron-containing compound, the organic reducing agent, and water; it ...
Example Embodiment
[0031] Example 1
[0032] Dissolve 50 grams of ferric nitrate, 2 grams of copper nitrate, and 5 grams of aluminum nitrate in deionized water to prepare a 70 ml solution; weigh urea [CO(NH 2 ) 2 , The same below] 32 grams, prepared into 50 ml solution; mix the two solutions and stir them evenly, put them in a muffle furnace and heat until fire and burn, the organic reducing agent is burned to obtain a fluffy foamy powder, and then at 500 ℃ and In the presence of air, the powder material was calcined in a muffle furnace for 3 hours to obtain catalyst A. The composition, specific surface area and pore volume of Catalyst A are listed in Table 1.
Example Embodiment
[0033] Example 2
[0034] Add 50 grams of ferric nitrate, 2 grams of manganese nitrate [Mn(NO 3 ) 2 ·6H 2 O], 5 grams of aluminum nitrate, dissolved in deionized water to make a 70 ml solution; weigh citric acid (C 6 H 8 O 7 ·H 2 O, the same below) 26 g, prepared into 50 ml solution; mix the two solutions and stir them evenly, put them in a muffle furnace and heat until they catch fire. After the organic reducing agent is burned, a fluffy foamy powder is obtained, and then heated at 500°C In the presence of air, the powder material was calcined in a muffle furnace for 4 hours to obtain catalyst B. The composition, specific surface area and pore volume of Catalyst B are listed in Table 1.
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