Method for increasing butene-2 yield through C4 fraction containing small amount of butadiene
A carbon four fraction, butadiene technology, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, organic chemistry, etc., to achieve good resistance to impurities and poisons, high isomerization rate, and reduce olefin loss. Effect
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Embodiment 1
[0014] Hydrogenation and isomerization operations are carried out in fixed-bed adiabatic reactors. The nickel-based catalyst prepared according to the method described in claim 2 is filled in the reactor, and the catalyst is sulfurized and activated in situ. The selective hydrogenation and isomerization operations of the ether C4 fraction containing 1.56% butadiene were carried out in a continuous manner.
[0015] During the hydroisomerization process, the operating conditions are as follows: Reactor inlet temperature: 60 o C; Reactor pressure: 1.2MPa
[0016] Liquid phase space velocity: 6h -1 , hydrogen / butadiene molar ratio: 2.15; see Table 1 for the composition of the material and the effluent of the hydroisomerization reactor operated under the above conditions.
[0017] Table 1
[0018]
Embodiment 2
[0020] Hydrogenation and isomerization operations are carried out in fixed-bed adiabatic reactors. The nickel-based catalyst prepared according to the method described in claim 2 is filled in the reactor, and the catalyst is sulfurized and activated in situ. The selective hydrogenation and isomerization operations of the raffinate C4 fraction containing 0.60% butadiene are carried out in a continuous manner.
[0021] During the hydroisomerization process, the operating conditions are as follows: Reactor inlet temperature: 60 o C; Reactor pressure: 1.4MPa; Liquid phase space velocity: 6h -1 Hydrogen / butadiene molar ratio: 2.67; See Table 2 for the composition of the hydroisomerization reactor effluent operated under the above-mentioned conditions.
[0022] Table 2
[0023]
Embodiment 3
[0025] Hydrogenation and isomerization operations are carried out in fixed-bed adiabatic reactors. The nickel-based catalyst prepared according to the method described in claim 2 is filled in the reactor, and the catalyst is sulfurized and activated in situ. The selective hydrogenation and isomerization operations of the ether C4 C4 fraction containing butadiene with a mass fraction of 0.21% were carried out in a continuous manner.
[0026] The operating conditions of hydroisomerization are as follows: Reactor inlet temperature: 70 o C; Reactor pressure: 1.6MPa; Liquid phase space velocity: 6h -1 , Hydrogen / butadiene molar ratio: 2.8; See Table 3 for the composition of the material and the effluent of the hydroisomerization reactor operated under the above conditions.
[0027] table 3
[0028]
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