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C2 fraction selective hydrogenation method

A carbon distillate, selective hydrogenation technology, applied in the fields of hydrocarbons, chemical instruments and methods, hydrocarbon purification/separation, etc., can solve the problems of easy coking, catalyst coking deactivation, and no catalyst

Active Publication Date: 2014-10-15
PETROCHINA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0021] However, in the carbon two hydrogenation reaction, the generation of green oil and the coking of the catalyst are important factors affecting the reaction life of the catalyst. The activity, selectivity and service life of the catalyst constitute the overall performance of the catalyst. The above methods may be useful for improving catalyst activity, Selectivity proposes a better method, but it does not solve the problem that the catalyst is easy to coke, or it solves the problem that the catalyst is easy to generate green oil and coke, but it does not solve the problem of selectivity
Although the carrier with a macroporous structure can improve the selectivity, the larger molecules generated by the polymerization and chain growth reactions tend to accumulate in the macropores of the carrier, causing coking and deactivation of the catalyst and affecting the service life of the catalyst.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] A commercially available bimodal pore distribution cylindrical alumina carrier with a diameter of 4 mm and a length of 4 mm was used. After calcination at 1200°C for 4 hours, the bimodal peaks of pore diameters are at 40nm and 100nm respectively, the pore volume is 0.6ml / g, and the specific surface area is 30m 2 / g.

[0050] The post-hydrogenation process is adopted, and the raw material composition is shown in Table 1.

[0051] Table 1 hydrogenation raw material composition

[0052] Hydrogenation feedstock

C 2 h 4

C 2 h 2

C 2 h 6

Content (mol%)

75.5

1.5

23

[0053] Process conditions: Two-stage adiabatic bed reactors are used.

[0054] Material air speed: 2000h -1 , Operating pressure: 1.5MPa, catalyst filling volume: 300ml. The inlet temperature of the first stage reactor is 50°C, and the inlet temperature of the first stage reactor is H 2 / C 2 h 2 =1:1 (V / V); the inlet temperature of the second stage ...

Embodiment 2

[0056] A commercially available bimodal pore distribution spherical alumina carrier with a diameter of 4 mm was used. After calcination at 1120°C for 4 hours, the bimodal peaks of the pore diameters are at 20nm and 150nm respectively, the pore volume is 0.4ml / g, and the specific surface area is 40m 2 / g.

[0057] The post-hydrogenation process is adopted, and the process flow chart is as attached figure 1 Shown, raw material composition is as shown in table 2:

[0058] Table 2 hydrogenation raw material composition

[0059] Hydrogenation feedstock

C 2 h 4

C 2 h 2

C 2 h 6

Content (mol%)

80

1.5

18.5

[0060] Process conditions: Two-stage adiabatic bed reactors are connected in series, that is, the material from the outlet of the first-stage reactor enters the second-stage reactor. Each reactor has an independent gas distribution system.

[0061] Material gas space velocity: 5000h -1 , Operating pressure: 1.9MPa, ea...

Embodiment 3

[0063] A commercially available bimodal pore distribution four-leaf clover-shaped alumina carrier was used, with a diameter of 5.5 mm and a length of 4 mm. After calcination at 1150°C for 4 hours, the bimodal peaks of the pore diameters are 30nm and 200nm respectively, the pore volume is 0.3ml / g, and the specific surface area is 20m 2 / g.

[0064] Adopt post-hydrogenation process, reaction raw material composition is as shown in table 4 and is:

[0065] Table 3 hydrogenation raw material composition

[0066] Hydrogenation feedstock

C 2 h 4

C 2 h 2

C 2 h 6

Content (mol%)

80

2.5

17.5

[0067] Reaction conditions: Three-stage adiabatic bed reactor series process, that is, the outlet material of the first-stage reactor enters the second-stage reactor, and the outlet material of the second-stage reactor enters the third-stage reactor. Each reactor has an independent gas distribution system.

[0068] Material air speed: 8...

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Abstract

The invention relates to a C2 fraction selective hydrogenation method. The C2 fraction selective hydrogenation method comprises the following steps of feeding an effluent which is in an ethylene device and is discharged from the top of a demethanizer into an adiabatic bed reactor, and carrying out selective hydrogenation to remove ethyne. The C2 fraction selective hydrogenation method is characterized in that selective hydrogenation catalyst carriers comprise alumina or mainly comprising alumina, have a double-humped hole distributed structures and contain double active components of Pd and Ni. In catalyst preparation, a coking-resistant component Ni in the form of microemulsion enters into large holes of the carriers so that the coking-resistant component Ni is mainly distributed in the large holes of the carriers and thus a catalyst surface coking degree is greatly reduced, the compound subjected to hydrogenation saturation is gradually diffused into catalyst channels, channel blocking is avoided, a catalyst service life is greatly prolonged, a green oil yield and catalyst coking are obviously reduced and device operation economic benefits are improved.

Description

technical field [0001] The invention relates to a method for selective hydrogenation, in particular to a method for selective hydrogenation of carbon distillates to remove acetylene. Background technique [0002] The production of polymer grade ethylene is the leader of the petrochemical industry, and polymer grade ethylene and propylene are the most basic raw materials for downstream polymerization units. Among them, the selective hydrogenation of acetylene has an extremely important impact on the ethylene processing industry. In addition to ensuring that the acetylene content at the outlet of the hydrogenation reactor reaches the standard, it is also necessary to ensure that the catalyst has excellent selectivity, so that ethylene can generate as little ethane as possible, and improve the overall efficiency. The ethylene yield of the process. In addition, the high anti-coking performance of the catalyst can prolong the service life of the catalyst, which is of great signi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C11/04C07C7/167B01J23/89B01J21/04B01J35/10B01J32/00
CPCY02P20/52
Inventor 谭都平梁琨景喜林钱颖高源韩伟梁玉龙车春霞常晓昕李赫张峰王书峰胡晓丽刘晓兰林宏
Owner PETROCHINA CO LTD
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