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Coker gasoline hydrorefining process

A technology for hydrofining and coking gasoline, which is applied in the petroleum industry, treating hydrocarbon oil, molecular sieve catalysts, etc. It can solve the problems of large loss of metal components of catalysts, reduction of active components, and increase in pressure drop.

Inactive Publication Date: 2017-01-04
锡山区绿春塑料制品厂
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In the existing desulfurization process, hydrofining has been widely used due to its mature environment-friendly technology. However, the sulfur content of the raw materials targeted by the existing hydrogenation process is mostly at the level of several hundred ppm, and for as high as 6000ppm-10,000 The sulfur content in ppm, the catalyst used in the existing hydrorefining process is difficult to adapt to such a high sulfur content, generally there will be two problems: first, the activity of the catalyst decreases rapidly, and the device is under the condition of processing other raw materials The service life of the catalyst can reach 6a (6 years) or even longer, but after dealing with coked gasoline, the service life of the catalyst is only 1-2a
[0005] After analysis, it is found that when the catalyst used in the existing hydrofinishing is used for the hydrofinishing of coked gasoline, the loss of the metal components of the catalyst is relatively large, indicating that the active components on the catalyst are reduced, and the pore volume is much smaller, resulting in the reaction between the reactant and the catalyst. The contact area of ​​the catalyst decreases, which is directly reflected in the decrease of the catalyst activity
At the same time, when producing ethylene feedstock, reformate feedstock, and synthetic ammonia feedstock, coking gasoline requires high operating severity and high hydrogenation depth, which leads to aggravated carbon deposition in the catalyst bed and a rapid increase in pressure drop

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] The catalyst is prepared by impregnation method, and the carrier is doped Co 2+ SAPO-5, Co 2+ The doping amount in SAPO-5 was controlled at 0.65% of the mass of the carrier. The active component is molybdenum nitride MO 2 N, tungsten nitride W 2 N, molybdenum carbide Mo 2 The total content of C and tungsten carbide WC is 10% of the mass of the carrier, and its molar ratio is 1:0.4:0.3:0.8.

[0044] The catalyst is loaded into a fixed-bed reactor, the reaction tube of the reactor is made of stainless steel with an inner diameter of 50 mm, the catalyst bed is set to 3 layers, the temperature of the catalyst bed is measured with a UGU808 temperature control meter, and the raw material is coker gasoline. The double-piston micro-pump manufactured by the Beijing Satellite Manufacturing Plant is continuously transported, and the hydrogen is supplied from a high-pressure gas cylinder and the flow rate is controlled by a Beijing Qixing Huachuang D07-11A / ZM gas mass flowmeter...

Embodiment 2

[0049] The catalyst is prepared by impregnation method, and the carrier is doped Co 2+ SAPO-5, Co 2+ The doping amount in SAPO-5 was controlled at 0.7% of the carrier mass. The active component is molybdenum nitride MO 2 N, tungsten nitride W 2 N, molybdenum carbide Mo 2 The total content of C and tungsten carbide WC is 10% of the mass of the carrier, and its molar ratio is 1:0.6:0.45):1.2.

[0050] The remaining conditions are the same as in Example 1.

[0051] The final product was tested, and the total sulfur content was reduced to 3 ppm, and the pressure drop of the catalyst bed did not change after half a year of operation.

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PUM

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Abstract

The invention discloses a coker gasoline hydrorefining process. According to the process, a fixed bed reactor is adopted and is filled with hydrogen desulfurization and denitrification catalyst; the catalyst comprises a carrier and an active ingredient; the carrier is SAPO-5 doped with heteroatom Co<2+> in a synthetic framework structure; the active ingredient is a mixture of dimolybdenum nitride MO2N, tungsten nitride, molybdenum carbide and tungsten carbide WC; the reaction conditions of the fixed bed reactor comprise the reaction temperature of 240-350 DEG C, the hydrogen partial pressure of 2-3.5MPa, the hydrogen to oil volume ratio of 450-700 and the volume space velocity of 1-2h<-1>. According to the process, the total sulfur content of coker gasoline is controlled to be lower than 5ppm, and the service life of the catalyst is prolonged to be 8a or longer.

Description

technical field [0001] The invention relates to a coking gasoline hydrodesulfurization refining process, in particular to a coking gasoline hydrorefining process using a specific catalyst. Background technique [0002] Coker naphtha, also known as coker naphtha, is a fraction with an initial boiling point to 180 (205°C) produced in a delayed coking process. Coker gasoline has high sulfur content and high olefin content, low motor octane number (about 60), and poor stability (bromine value 40-60gBr / 100g). The stabilized coker gasoline can only be used as a semi-finished product. Hydrorefining removes nitrogen-containing, sulfur-containing compounds and diolefins before it can be used as a gasoline blending component for vehicles or as a petrochemical raw material (light oil) to produce ethylene, as a raw material for ammonia synthesis or as a raw material for catalytic reforming . [0003] The sulfur content of coker gasoline is generally 0.6%-1.0%, that is, 6,000 to 10,000...

Claims

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Application Information

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IPC IPC(8): C10G45/08B01J29/03
CPCC10G45/08B01J29/0341B01J2229/18C10G2300/202C10G2400/02
Inventor 朱忠良
Owner 锡山区绿春塑料制品厂