Catalytic distillation process for olefin production device

A production device and a technology for catalytic rectification, which are applied in the fields of catalytic rectification and selective hydrogenation of carbon three highly unsaturated hydrocarbon components, and carbon two, and can solve the problem of poor gas-liquid flow conditions, uneven catalyst distribution, and bed pressure drop. too big problem

Active Publication Date: 2006-09-13
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The hydrogen used in the post-hydrogenation can be added as needed, which improves the hydrogenation selectivity, reduces the loss of the target product, and the quality of the hydrogenation product is stable, but its disadvantage is that the process of the separation system is relatively complicated. In order to obtain high-purity ethylene products , it is necessary to set up a second demethanizer or adopt the side discharge technology of the ethylene rectification tower
However, this process also hydrogenates diolefins with high industrial value such as butadiene in the feed, and the loss is relatively large
In addition, the catalyst loading method of this process adopts the CDTECH bundled structure, the catalyst is unevenly distributed, the utilization rate is not high, the local pressure drop of the bed is too large, the gas-liquid flow is not good, and the liquid distribution is uneven, which affects the reaction efficiency.

Method used

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  • Catalytic distillation process for olefin production device
  • Catalytic distillation process for olefin production device
  • Catalytic distillation process for olefin production device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0063] For a schematic diagram of the process, see figure 2 .

[0064] The high-pressure depropanizer 1 is a 35-layer sieve tray tower, and the low-pressure depropanizer 4 is a 57-layer sieve tray tower. The cracked gas a after compression, alkali washing and drying enters the 14th plate of the high-pressure depropanizer 1, and the liquid hydrocarbon b produced by compressing the cracked gas enters the 20th plate of the high-pressure depropanizer 1, and the reflux liquid returns to the 1st plate, the top of the tower The gas phase stream c includes hydrogen, methane, carbon distillate, carbon three distillate, etc., and the liquid phase stream d in the bottom of the tower includes propane, propylene, propyne, propadiene, C4, C5, C6, benzene, toluene and other components. The stream c is mined and compressed in five stages, and after being compressed by the compressor 2, it enters the gas-phase hydrogenation reactor 3, and the stream d is mined out of the 28th plate of the lo...

Embodiment 2

[0069] For a schematic diagram of the process flow, see image 3 .

[0070] The high-pressure depropanizer 1 is a 35-layer sieve tray tower, and the low-pressure depropanizer 4 is a 57-layer sieve tray tower. The cracked gas a enters the 14th plate of the high-pressure depropanizer 1, the liquid hydrocarbon b enters the 20th plate of the high-pressure depropanizer 1, the reflux liquid returns to the 1st plate, the gaseous phase stream c at the top of the tower is extracted and compressed in five stages, and the liquid phase stream in the tower bottom d Mining out of the 28th plate of the low-pressure depropanizer 4. The gas phase stream e (containing C3 and C4 fractions) at the top of the low-pressure depropanizer 4 returns to the 20th plate of the high-pressure depropanizer 1 after condensation except part of the reflux; the liquid phase stream f in the bottom of the tower goes to the debutanizer. The pressure at the top of the high-pressure depropanizer 1 is 1.4 MPa, and t...

Embodiment 3

[0074] For a schematic diagram of the process flow, see image 3 .

[0075] The high-pressure depropanizer 1 is a 35-layer sieve tray tower, and the low-pressure depropanizer 4 is a 57-layer sieve tray tower. The cracked gas a enters the 14th plate of the high-pressure depropanizer 1, the liquid hydrocarbon b enters the 20th plate of the high-pressure depropanizer 1, the reflux liquid returns to the 1st plate, the gaseous phase stream c at the top of the tower is extracted and compressed in five stages, and the liquid phase stream in the tower bottom d Mining out of the 28th plate of the low-pressure depropanizer 4. After condensation, except for reflux, 50% (weight) of the stream returns to the 20th plate of the high-pressure de-propanizer 1, and the rest of the stream goes to the propylene refining tower; Phase stream f goes to the debutanizer. The pressure at the top of the high-pressure depropanizer 1 is 1.4 MPa, and the catalytic reaction temperature is 5-40°C. The pr...

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Abstract

The catalytic rectification method for olefin production includes setting catalytic reaction area in the pre-depropanizing column of the olefin producing apparatus; selectively hydrogenating C3- acetylene hydrocarbons and diene while separating C3, C3-, C4 and C4+ fractions; making top gaseous matter flow into gaseous hydrogenating reactor for further eliminating C3- acetylene hydrocarbons and diene; and feeding the cauldron liquid C4+ to the further separation area. The said method of the present invention can convert most of the C3- acetylene hydrocarbons and diene into corresponding olefin, reduce the hydrogen amount into the deeply freezing system, lower the power consumption, simplify technological process, reduce investment, raise the selectivity of catalytic hydrogenation and raise olefin yield, and has prolonged catalyst operating period, stable operation and no loss of butadiene.

Description

technical field [0001] The present invention relates to a method used in an olefin production unit, in particular to a method used in catalytic rectification and selective hydrogenation of C2 and C3 highly unsaturated hydrocarbon components in the hydrogenation process before depropanization before olefin production method. Background technique [0002] In the process of hydrocarbon cracking to olefins, a small amount of alkynes and dienes will be produced along with ethylene, propylene, and butene. These alkynes and diolefins will reduce the activity of the polymerization catalyst and deteriorate the physical properties of the polymer during the post-processing of olefins, especially during the polymerization of olefins, so they must be removed. In industry, catalytic selective hydrogenation and solvent absorption are usually used to remove alkynes and dienes in cracked gas. Due to the simple process of selective hydrogenation, less energy consumption, no environmental po...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C11/02C07C5/03C07C7/04
CPCY02P20/10
Inventor 杨元一戴伟李东风陈硕程建民郭彦来廖丽华彭晖李振虎穆玮
Owner CHINA PETROLEUM & CHEM CORP
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