Catalyst for Fischer-Tropsch synthesis reaction and preparation method thereof
A Fischer-Tropsch synthesis and catalyst technology, which is used in the preparation of liquid hydrocarbon mixtures, chemical instruments and methods, organic compounds/hydrides/coordination complex catalysts, etc. Increased surface area and improved selectivity
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Embodiment 1
[0036] (1) Get 3g nanometer red phosphorus, 10.8g ferric chloride (FeCl 3 ·6H 2 O), 2.4g nickel chloride (NiCI 2 ·6H 2 O) adding 25Ml ethanolamine, stirring evenly, ultrasonic treatment for 3h, then transferring the mixed solution to a polytetrafluoroethylene-lined reactor, adding ethanolamine to 80% of the volume, putting it into a blast drying oven, and hydrothermally treating it for 5h, The treatment temperature was 160°C. After the reaction, the product was taken out, cooled to room temperature and filtered, washed three times with ethanol and deionized water and dried to obtain iron nickel phosphide (FeP, Ni 2 P) Nanoparticles, the molar ratio of iron to nickel in the iron-nickel phosphide is Fe:Ni=4:1, and the molar ratio of red phosphorus to iron-nickel is P:(Fe,Ni)=2:1.
[0037] (2) Dissolve 3.93g of iron-nickel phosphide in 36g of deionized water, add 2.31g of deceth-4 phosphate, then add 5.24g of zinc nitrate (Zn(NO 3 )·6H 2 O) stirring at 50° C. in a water bath...
Embodiment 2
[0041] (1) Get 4.5g nanometer red phosphorus, 10.8g ferric chloride (FeCl 3 ·6H 2 O), 2.4g nickel chloride (NiCI 2 ·6H 2 O) adding 25Ml ethanolamine, stirring evenly, ultrasonic treatment for 3h, then transferring the mixed solution to a polytetrafluoroethylene-lined reactor, adding ethanolamine to 80% of the volume, putting it into a blast drying oven, and hydrothermally treating it for 8h, The treatment temperature was 180°C. After the reaction, the product was taken out, cooled to room temperature and filtered, washed 3 times with ethanol and deionized water and dried to obtain iron nickel phosphide (FeP, Ni 2 P), the molar ratio of iron to nickel in the iron-nickel phosphide is Fe:Ni=4:1, and the molar ratio of red phosphorus to iron-nickel is P:(Fe, Ni)=3:1.
[0042] (2) Dissolve 4.93g of iron-nickel phosphide in 36g of deionized water, add 3.89g of deceth-4 phosphate, and then add 5.24g of zinc nitrate (Zn(NO 3 )·6H 2 O) stir 30min under 50 ℃ of water-baths; The 2-m...
Embodiment 3
[0046] (1) Get 6g nanometer red phosphorus, 10.8g ferric chloride (FeCl 3 ·6H 2 O), 2.4g nickel chloride (NiCI 2 ·6H 2 O) Adding 25Ml ethanolamine, stirring evenly, ultrasonic treatment for 3h, then transferring the mixed solution to a polytetrafluoroethylene-lined reactor, adding ethanolamine to 80% of the volume, putting it into a blast drying oven, and hydrothermally treating it for 11h, The treatment temperature was 200°C. After the reaction, the product was taken out, cooled to room temperature and filtered, washed three times with ethanol and deionized water and dried to obtain iron-nickel phosphide (FeP, Ni 2 P), the molar ratio of iron to nickel in the iron-nickel phosphide is Fe:Ni=4:1, and the molar ratio of red phosphorus to iron-nickel is P:(Fe, Ni)=4:1.
[0047] (2) Dissolve 5.93g of iron-nickel phosphide in 36g of deionized water, add 5.87g of deceth-4 phosphate, then add 5.24g of zinc nitrate (Zn(NO 3 )·6H 2 O) stir 30min under 50 ℃ of water-baths; The 2-me...
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