Hydrogenation modification method for faulty gasoline
A technology for hydrogenation upgrading and low-quality gasoline, which is applied in the fields of hydrotreating process, petroleum industry, and hydrocarbon oil treatment. Achieve sulfur and olefin content and reduce olefin effect
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Embodiment 1
[0047] The catalyst prepared in this embodiment includes:
[0048] Based on the total weight of the catalyst, the selective hydrodesulfurization catalyst (catalyst I-A) in the first stage reaction zone comprises: 4wt.% CoO-12wt.% MoO 3 -3wt.%K 2 O-2wt.%P 2 o 5 / 67wt.%Al 2 o 3 -8wt.%TiO 2 -4wt.% MgO; The desulfurization of the second stage reaction zone-hydrocarbon multi-branched hydroisomerization catalyst (II-A), its composition includes: 1wt.% CoO-6wt.%MoO 3 -3wt.% NiO / 64wt.% SAPO-11 molecular sieve -22wt.% Al 2 o 3 -4wt.%TiO 2 , wherein, SAPO-11 molecular sieves are formed on Al-Ti composite oxides through in-situ crystallization; the supplementary desulfurization-hydrocarbon single branched chain isomerization / aromatization catalyst (catalyst III-A) in the third stage reaction zone, its The composition includes: 2wt.% CoO-6wt.% MoO 3 -1wt.%P 2 o 5 / 65wt.%HZSM-5-21wt.%Al 2 o 3 -5wt.%TiO 2 , which is a modified HZSM-5 zeolite-aluminum titanium catalyst.
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Embodiment 2
[0066] The difference between this example and Example 1 is that the full cut FCC gasoline (raw material oil 2) is cut into light and heavy cut FCC gasoline at 55°C, and the heavy cut FCC gasoline is used as the reaction raw material to react with the above-mentioned three-stage catalyst in sequence, and then heavy cut FCC gasoline Distillate FCC gasoline reaction products are mixed with light fraction FCC gasoline to obtain low-sulfur, low-olefin clean gasoline;
[0067] The three-stage series reaction conditions of heavy distillate FCC gasoline are as follows: the pressure of the three reactors is 1.8MPa, the volume ratio of hydrogen to oil is 500, the temperature of the first reactor is 250°C, and the volume space velocity is 5.0h -1 , the temperature of the second reactor is 290℃, the volume space velocity is 3.5h -1 , the temperature of the third reactor is 380℃, the volume space velocity is 3.5h -1 .
Embodiment 3
[0069] The difference between this example and Example 1 is that the first stage reaction zone is catalyst I-B: 2.5wt.% CoO-10wt.% MoO 3 -2wt.%K 2 O-3wt.%P 2 o 5 / 60wt.%Al 2 o 3 -15.5wt.%TiO 2 -7wt.% MgO, the second stage reaction zone is catalyst II-B: 2.0wt.% CoO-8wt.% MoO 3 -4wt.%NiO / 60wt.%SAPO-11-20wt.%Al 2 o 3 -6wt.%TiO 2 , the third reaction zone is Catalyst III-B: 1.0wt.% CoO-5wt.% MoO 3 -3wt.%P 2 o 5 / 60wt.%HZSM-5-22wt.%Al 2 o 3 -9wt.%TiO 2 ;
[0070] The reaction conditions are: the pressure of the three reactors is 2.3MPa, the volume ratio of hydrogen to oil is 400, the temperature of the first reactor is 260°C, and the volume space velocity is 6.0h -1 , the temperature of the second reactor is 280℃, the volume space velocity is 4.0h -1 , the temperature of the third reactor is 380℃, the volume space velocity is 3.0h -1 .
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