Coking naphtha hydrofining method

A technology for coking naphtha and hydrotreating, which is applied in the petroleum industry, hydrotreating process, and hydrocarbon oil treatment, etc., can solve the problems of short start-up period and increased pressure drop due to colloidal coking in the upper part.

Active Publication Date: 2022-05-06
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In the above scheme, the conventional hydrofining catalyst bed is a single bed. Considering that the exothermic heat of the olefin hydrogenation reaction is concentrated on

Method used

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  • Coking naphtha hydrofining method
  • Coking naphtha hydrofining method
  • Coking naphtha hydrofining method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] After preparing 1000g aluminum nitrate, 100g zirconium nitrate, 6g cerium nitrate and 3000g water to form an aqueous solution, flow it together with a 20% sodium hydroxide solution into a reaction kettle containing 1L of pure water. The temperature of the reaction kettle is controlled at 50°C . Control the liquid flow rate, keep the pH value of the solution in the reaction tank constant at 7.4, neutralize and react the aluminum nitrate mixed solution for 180 minutes, and obtain a slurry.

[0032] A small amount of tetramethylammonium hydroxide was added to the obtained slurry to adjust the pH value of the slurry to 8.8. Put it in a closed autoclave, age at 185°C for 24 hours, take it out, wash and filter, and dry at 120°C to obtain a composite powder.

[0033] After the obtained composite powder was crushed and sieved (200 mesh), 2g of scallop powder, 15g of 10% nitric acid and 110mL of deionized water were added, and the carrier was obtained after molding, drying at 1...

Embodiment 2

[0036] After preparing 30g of zirconium sulfate, 16g of lanthanum sulfate and 1000g of water into an aqueous solution, add 1L of sodium metaaluminate solution with a concentration of 400g / L into a reaction kettle containing 1L of pure water in parallel, and the temperature of the reaction kettle is controlled at 65°C. At the same time, sulfuric acid with a concentration of 10% is added in parallel and the liquid flow rate is controlled to keep the pH value of the reaction tank solution constant at 8.0. After 90 minutes of neutralization, the mixed solution of zirconium and lanthanum is reacted with the sodium metaaluminate solution to obtain a slurry.

[0037] A small amount of triethanolamine was added to the obtained slurry to adjust the pH value of the slurry to 9.2. Put it in a closed autoclave, age at 160°C for 30 hours, take it out, wash and filter, and dry at 110°C to obtain a composite powder.

[0038] After the obtained composite powder was crushed and sieved (200 mes...

Embodiment 3

[0041] After making 1000g aluminum nitrate, 150g zirconium nitrate, 12g cerium nitrate and 3000g water into an aqueous solution, it is mixed with 20% sodium hydroxide solution into a reaction kettle containing 1L of pure water, and the temperature of the reaction kettle is controlled at 75°C. Control the liquid flow rate to keep the pH value of the solution in the reaction tank constant at 8.6. After 180 minutes of neutralization and reaction of the aluminum nitrate mixed solution, a slurry is obtained.

[0042] A small amount of ethylenediamine was added to the obtained slurry to adjust the pH value of the slurry to 9.6. Put it in a closed autoclave, age at 170°C for 24 hours, take it out, wash and filter, and dry at 110°C to obtain a composite powder.

[0043] After the obtained composite powder was crushed and sieved (200 mesh), 2.6g of scallop powder, 19g of 10% nitric acid and 130mL of deionized water were added, shaped, dried at 110°C, and calcined at 500°C to obtain the...

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Abstract

The invention discloses a coker naphtha hydrofining method which comprises the following steps: coker naphtha and hydrogen flow into a hydrogenation reactor in parallel to react with a catalyst; a hydrodesilication catalyst bed layer and n hydrofining catalyst bed layers are sequentially arranged in the hydrogenation reactor along the material flowing direction, wherein n is greater than or equal to 2; the n hydrofining catalyst bed layers are sequentially a first hydrofining catalyst bed layer, a second hydrofining catalyst bed layer,..., and an Nth hydrofining catalyst bed layer along a material flowing direction; the hydrodesiliconization catalyst bed accounts for 10-50% of the total catalyst bed volume; catalyst active metals in the n hydrofining catalyst bed layers are increased layer by layer from the first to the Nth. According to the method, the hydrodesiliconization agent and the hydrofining catalyst are combined and graded in stages and the hydrogen feeding mode is adjusted aiming at the technological processes of removal of impurity silicon in the coked naphtha and olefin hydrogenation saturation, so that the carbon deposition resistance and the desiliconization capability of the catalyst bed layers are improved.

Description

technical field [0001] The invention belongs to the field of petrochemical industry, and in particular relates to a method for hydrofining coking naphtha. Background technique [0002] Delayed coking is one of the important means of processing inferior heavy oil. The naphtha yield in the delayed coking process is usually about 15%, and these coking naphthas contain relatively high levels of impurities such as sulfur, nitrogen, olefins, and colloids. Poor stability, not suitable for motor gasoline, so many refineries are equipped with coker naphtha hydrogenation unit. In the process of coking naphtha hydrofining, on the one hand, due to the high content of olefins and colloids in coking naphtha, olefins are easy to be hydrogenated and saturated, and most of the reactions are usually completed in the upper part of the catalyst bed, resulting in a huge heat release. Taking coking gasoline containing 40% as an example, if it is fully reacted, the adiabatic reaction temperature ...

Claims

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Application Information

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IPC IPC(8): C10G65/04
CPCC10G65/04C10G2300/4006C10G2300/4012C10G2300/4018C10G2300/70Y02P20/52
Inventor 孙进郭蓉李扬郑步梅段为宇
Owner CHINA PETROLEUM & CHEM CORP
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