Catalytic cracking method for increasing liquid yield
A catalytic cracking and catalytic cracking device technology, which is applied in the field of catalytic cracking to increase liquid yield, can solve problems such as poor thermal stability, and achieve significant economic benefits
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[0028] One embodiment, the oxidation synthesis method is used to carry out the oxidation treatment; the conditions of the oxidation synthesis method include: the oxidant is hydrogen peroxide, the oxidation synthesis catalyst is ferric oxide, and the weight ratio of hydrogen peroxide to distillate oil is 1: (1- 150), preferably 1:(2-100); the weight ratio of oxidation synthesis catalyst to distillate oil is 1:(1-15), preferably 1:(2-10), and the reaction temperature is 40-55°C, preferably 50-55°C, and the reaction time is 1-10 hours, preferably 5-10 hours.
[0029] According to the present invention, in step d, the hydroxylated oil and the hydrocarbon oil feedstock can be mixed in conventional mixing conditions and equipment in the art, such as feedstock oil mixing tanks or static mixers, etc., preferably the obtained hydroxylated oil and hydrocarbon oil The raw materials are mixed in a static mixer. Static mixer is a kind of high-efficiency mixing equipment without moving par...
Embodiment 1
[0042] This example is used to illustrate the catalytic cracking method for increasing the liquid yield provided by the present invention.
[0043] According to the ratio of m (atmospheric residual oil): m (hydroxylated oil A) of 4:1, the two are fully mixed in a static mixer to obtain a mixed raw oil at 200 ° C, and then the mixed raw oil is injected into the fluidized bed for reaction The catalytic cracking reaction is carried out in the reactor, wherein the reaction temperature is 510°C, and the weight hourly space velocity is 20h -1 , the mass ratio of agent to oil is 6. The resulting product distribution is shown in Table 4.
Embodiment 2
[0045] This example is used to illustrate the catalytic cracking method for increasing the liquid yield provided by the present invention.
[0046] The reaction device adopted is the same as in Example 1, and the atmospheric residue and main experimental steps used are the same as in Example 1. The difference is that the atmospheric residue is mixed with hydroxylated oil B, and m (atmospheric residue): m (hydroxylated oil B) was 20:3, and the main results are listed in Table 4.
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