Load typed varadium catalyst and its preparing method and application
A catalyst and a supported technology, which are applied in the application field of a supported vanadium oxide catalyst and the coupling reaction of ethylbenzene dehydrogenation to styrene
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Embodiment 1
[0022] Example 1 Accurately weigh and dry at 120°C, the specific surface area is 942m 2 2.0000 g of activated carbon (20-40 mesh) per gram, accurately measure 0.579 mol / L of NH with a pipette 4 VO 3 3.00ml solution impregnated carrier, let stand for 24 hours, dry in oven at 120°C for 4-6 hours, N 2 Under the atmosphere of 500 ° C, calcined for 5 hours, put it into a dryer to obtain a V / AC catalyst, the V content is 0.87mmol / g activated carbon, which is designated as catalyst A. The reaction temperature is 550°C, and the space velocity of ethylbenzene is 2.17h -1 , CO 2 The / EB molar ratio was 11. The analysis method is: the product is analyzed by a GC-7A gas chromatograph on a 1m×φ3mm dinonyl phthalate column, detected by a hydrogen flame (FID), the tail gas is analyzed by a 2m×φ3mm carbon molecular sieve column, and detected by a thermal conductivity (TCD) . The results are shown in Table 1.
Embodiment 2
[0023] Example 2 Accurately weighed and dried at 120°C, the specific surface area was 942m 2 2.0000 g of activated carbon (20-40 mesh) per gram, accurately measure 0.579 mol / L of NH with a pipette 4 VO 3 Solution 3.00ml and 1.50mol / L LiNO 3 Solution 0.20ml, mix evenly, co-impregnate carrier, let stand for 24 hours, dry in oven at 120°C for 4-6 hours, N 2 Under the atmosphere of 500 ℃, roast for 5 hours, put into the desiccator. The VLi / AC catalyst with a V content of 0.87mmol / g activated carbon and a lithium content of 0.15mmol / g activated carbon was obtained, which was designated as catalyst B. Other conditions are with embodiment 1.
Embodiment 3
[0024] Embodiment 3 Accurately weighed 120 ℃ drying, specific surface area is 1200m 2 2.0000 g of activated carbon (20-40 mesh) per gram, accurately measure 0.579 mol / L of NH with a pipette 4 VO 3 Solution 3.00ml and 1.50mol / L NaNO 3 Solution 0.20ml, mix evenly, co-impregnate carrier, let stand for 24 hours, dry in oven at 120°C for 4-6 hours, N 2 Under the atmosphere of 500 ℃, roast for 5 hours, put into the desiccator. The obtained V content is 0.87mmol / g activated carbon, and the VNa / AC catalyst whose sodium content is 0.15mmol / g activated carbon is denoted as catalyst C. Other conditions are with embodiment 1.
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