Processing method and processing system of diesel oil raw material
A technology for raw materials and diesel oil, applied in the petroleum industry, hydrotreating process, processing hydrocarbon oil, etc., can solve the problems of low olefin yield and unreasonable utilization of coking diesel light fractions, and achieve the effect of high yield
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Embodiment 1
[0104] This embodiment adopts figure 1 The process flow diagram shown is carried out, and the specific steps are as follows:
[0105] The diesel raw material D is introduced into the diesel fractionation tower 2 and separated into light diesel oil fraction E with a distillation range 230 °C according to the cut point of 230 °C, diesel raw material D, light diesel oil fraction E and heavy diesel oil fraction The properties of diesel fraction F are shown in Table 1. The heavy diesel oil fraction is introduced into the hydrofinishing reactor 5 for hydrofinishing treatment to obtain a hydrofinishing reaction effluent.
[0106] The hydrotreating reaction effluent is introduced into the separator 10 for separation, and the hydrogen-rich gas in the gas phase product at the top of the separator 10 obtained after separation is processed by the circulating hydrogen compressor 6 and then mixed with new hydrogen to obtain mixed hydrogen. For recycling back to the hydrofinishing reactor ...
Embodiment 2
[0118] Embodiment 2 adopts the technological process identical with embodiment 1 to carry out, and difference is, the reaction conditions and the product distribution of the hydrofinishing reactor of embodiment 2 are as shown in table 3, and the reaction conditions of catalytic cracking reactor are as shown in table shown in 4. The product distribution obtained by the method of Example 2 is shown in Table 4.
Embodiment 3
[0123] Present embodiment adopts the method similar to embodiment 1 to carry out, difference is, the reaction temperature in the 3rd catalytic cracking reactor of the catalytic cracking reaction zone of present embodiment is higher than the reaction temperature in the second catalytic cracking reactor 50 °C, specifically, the reaction conditions and product distribution of the hydrofinishing reactor in this embodiment are shown in Table 3, and the reaction conditions of the catalytic cracking reactor are shown in Table 4. The product distribution obtained by the method of this embodiment is shown in Table 4.
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Abstract
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