CN102516007A - Process and device for processing and preparing hydrocarbon by utilizing liquefied gas - Google Patents
Process and device for processing and preparing hydrocarbon by utilizing liquefied gas Download PDFInfo
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- CN102516007A CN102516007A CN201110387102XA CN201110387102A CN102516007A CN 102516007 A CN102516007 A CN 102516007A CN 201110387102X A CN201110387102X A CN 201110387102XA CN 201110387102 A CN201110387102 A CN 201110387102A CN 102516007 A CN102516007 A CN 102516007A
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- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 47
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 43
- 239000004215 Carbon black (E152) Substances 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 35
- 238000010521 absorption reaction Methods 0.000 claims abstract description 128
- 238000005899 aromatization reaction Methods 0.000 claims abstract description 112
- 238000000926 separation method Methods 0.000 claims abstract description 86
- 238000005336 cracking Methods 0.000 claims abstract description 52
- 239000002994 raw material Substances 0.000 claims abstract description 50
- 230000006641 stabilisation Effects 0.000 claims abstract description 48
- 238000011105 stabilization Methods 0.000 claims abstract description 48
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 35
- 238000006243 chemical reaction Methods 0.000 claims abstract description 28
- 238000000746 purification Methods 0.000 claims abstract description 12
- 239000007789 gas Substances 0.000 claims description 307
- 238000010992 reflux Methods 0.000 claims description 109
- 230000000087 stabilizing effect Effects 0.000 claims description 98
- 239000007788 liquid Substances 0.000 claims description 85
- 238000003795 desorption Methods 0.000 claims description 76
- 239000000047 product Substances 0.000 claims description 63
- 239000003921 oil Substances 0.000 claims description 37
- 229910052799 carbon Inorganic materials 0.000 claims description 33
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 29
- 239000003502 gasoline Substances 0.000 claims description 27
- 238000010438 heat treatment Methods 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000003381 stabilizer Substances 0.000 claims description 14
- 239000012071 phase Substances 0.000 claims description 12
- 238000003860 storage Methods 0.000 claims description 12
- 239000012295 chemical reaction liquid Substances 0.000 claims description 11
- 239000007795 chemical reaction product Substances 0.000 claims description 11
- 238000000197 pyrolysis Methods 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 8
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 7
- 239000002737 fuel gas Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 230000002745 absorbent Effects 0.000 claims description 6
- 239000002250 absorbent Substances 0.000 claims description 6
- 239000000295 fuel oil Substances 0.000 claims description 6
- 238000005086 pumping Methods 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000007791 liquid phase Substances 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 10
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract description 10
- 238000005265 energy consumption Methods 0.000 abstract description 7
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- 239000003245 coal Substances 0.000 description 3
- 239000001282 iso-butane Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- -1 and finally Substances 0.000 description 1
- 238000012824 chemical production Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The invention discloses a process and a device for processing and preparing hydrocarbon by utilizing liquefied gas. The process comprises the processes of cracking reaction, absorption and stabilization, aromatization reaction, gas separation raw material gas stripping concentration and aromatic hydrocarbon purification. The device comprises a cracking reaction system, an absorption and stabilization system, an aromatization reaction system, a gas separation raw material gas stripping concentration system and an aromatic hydrocarbon purification system. The process and the device have the advantages that the energy consumption is low, and after the process is adopted, a deisobutanizer stops running, 90 kilograms of standard coals consumed by a carton-4 raw material per ton are treated, and 48.5 percent of energy is saved; gas separation raw material gas propylene is high in content and is improved from 15 percent to 50 percent in mass fraction; the requirements on equipment and heat energy are low and are easily realized; and the device is simple in process, is easy in operation and control and stable in running.
Description
Technical Field
The invention relates to a liquefied gas deep processing technology, in particular to a technology and a device for preparing hydrocarbon by processing liquefied gas, belonging to the field of hydrocarbon preparation by processing liquefied gas.
Background
Various methods are used for processing and separating liquefied gas in chemical production. At present, the main common adopted in the industry is: firstly, pretreating raw materials, extracting three carbon and carbon components in liquefied petroleum gas from the top of a depropanization tower, feeding mixed carbon and four components at the bottom of the tower into a deisobutanizer, separating isobutane from the deisobutanization tower, feeding components with the carbon number of more than or equal to four at the bottom of the tower into a cracking reaction system for cracking reaction, and feeding the obtained low-carbon hydrocarbons containing propylene and the like into an absorption stabilization system; the absorption tower, the desorption tower and the stabilization tower in the absorption stabilization system circularly separate materials, and finally, gas component feed gas containing 15% of propylene mass fraction, aromatic hydrocarbon at the bottom of the stabilization tower and dry gas at the top of the absorption tower are obtained from the top of the stabilization tower, aromatic hydrocarbon and fuel gas are obtained after aromatization reaction of the dry gas, and the gas component feed gas is extracted after passing through a reflux pump of the stabilization tower and is sent to a gas component device or a gas component feed tank for storage.
The method has high requirements on equipment and heat energy, and particularly when the isobutane is separated in the deisobutanizer, 200 layers of trays are needed, the height of the whole tower reaches 160 meters, and the temperature requirement of the tower top is not lower than 50 ℃, so that the method has harsh heat supply conditions, high energy consumption which accounts for 50 percent of the total energy consumption, uncoordinated device operation, and the quality of the isobutane product can not meet the requirement; meanwhile, the propylene content of the produced gas component feed gas is low, which is only 15%, so that the operation of a downstream gas component device is unstable. Meanwhile, the aromatic hydrocarbon impurity content after aromatization reaction is high, the market competitiveness of the product is weak, and the price is low.
Disclosure of Invention
In order to solve the problems, the invention designs a process and a device for processing and preparing hydrocarbon by using liquefied gas, and the process is simple, easy to control, low in energy consumption and high in product quality.
The technical scheme of the invention is as follows:
a process for preparing hydrocarbon from liquefied gas includes cracking reaction, absorption stabilizing, aromatization, gas-separating raw gas concentrating and purifying aromatic hydrocarbon.
Wherein:
(1) a cracking reaction process:
conveying liquefied gas of a carbon four raw material in a cracking raw material tank to a device area through a raw material pump, exchanging heat with a cracking reaction product through a first heat exchanger and a second heat exchanger, then feeding the heat-exchanged carbon four raw material into a heating furnace, further heating to 500 ℃, and feeding the heated gas into a cracking reactor from the top of the cracking reactor to perform a cracking reaction;
the pyrolysis reaction product sequentially passes through a second heat exchanger, a first heat exchanger, a hot water heat exchanger and a pyrolysis product cooler from the bottom of the pyrolysis reactor for heat exchange and cooling until the temperature is reduced to 40 ℃, and then enters a gas-liquid separation tank for separation; the separated condensate is pumped into an absorption tower by a reaction liquid pump and is used for further absorbing the rich gas sent by the compressor; and compressing and cooling the separated gas by a rich gas compressor, and then sending the gas to an absorption tower for further absorption.
(2) An absorption stabilization step:
the gas compressed by the rich gas compressor in the step (1) and the absorption oil from the bottom of the absorption tower and the desorption gas from the top of the desorption tower sequentially pass through an air cooler at the outlet of the gas compressor and a cooler at the outlet of the gas compressor, are cooled to 40 ℃ and then enter a liquid separation tank at the outlet of the gas compressor, so that the oil and the gas are separated;
separating out rich gas from the top of the liquid separating tank at the outlet of the gas compressor and conveying the rich gas to the lower part of the absorption tower, wherein the rich gas is in countercurrent contact with an absorbent entering from the upper part of the absorption tower in the absorption tower, the absorbed lean gas enters the dry gas liquid separating tank from the top of the absorption tower for gas-liquid separation, the liquid flows into a stabilizing tower for reflux, and the dry gas coming out from the top of the dry gas liquid separating tank is conveyed to an aromatization reactor;
in order to take away the heat released in the absorption tower, the gasoline which circularly reflows from the middle section is pumped out by an absorption tower middle section pump at the middle part of the absorption tower, cooled to 20 ℃ by an absorption tower middle section cooler and then returned to the absorption tower;
the condensate coming out of the bottom of the liquid separating tank at the outlet of the gas compressor is divided into two paths by a feeding pump of the desorption tower: one path directly enters the top of the desorption tower, and the other path enters the upper part of the desorption tower after heat exchange is carried out to 70 ℃ by a feeding heat exchanger of the desorption tower;
the desorption gas escapes from the tower top and is merged with the compressed rich gas of the rich gas compressor to enter an air cooler at the outlet of the gas compressor; the desorbed gasoline is pumped out from the bottom of the desorption tower by a stabilizing tower feed pump, exchanges heat with the stabilized gasoline at the bottom of the stabilizing tower through a stabilizing tower feed heat exchanger to 125 ℃, and then enters the middle part of the stabilizing tower;
and C4, distilling out the components of C four and C four from the top of the stabilizing tower, passing through an air cooler at the top of the stabilizing tower and a condenser at the top of the stabilizing tower, entering a reflux tank at the top of the stabilizing tower, and pumping the gas component feed gas from the bottom of the reflux tank at the top of the stabilizing tower through a reflux pump of the stabilizing tower to divide the gas component feed gas into two paths: one path of the reflux returns to the top of the stabilizing tower, and the other path of the reflux enters a feed preheater of the depropanizing tower;
the stabilized gasoline of the stabilizing tower is discharged from the bottom of the tower, and is cooled to 30 ℃ by a stabilizing tower feeding heat exchanger, a desorption tower feeding heat exchanger and a light hydrocarbon cooler in sequence, and then is divided into two parts: one part enters a feeding heat exchanger of the stripping tower to exchange heat with light aromatic hydrocarbon, namely product gasoline extracted by reflux at the top of the stripping tower, and then enters the stripping tower, and the other part is pressurized by an absorption oil pump, cooled to 20 ℃ by an absorption oil cooler and then sent to the top of an absorption tower to be used as an absorbent.
Furthermore, the desorption tower supplies heat to the tower from a desorption tower reboiler at the bottom of the tower.
Further, the stabilization tower supplies heat to the tower from a stabilization tower reboiler at the bottom of the tower.
(3) An aromatization reaction process:
the dry gas from the top of the dry gas liquid separation tank in the step (2) is merged with the fuel gas of the dry gas circulating machine and then is divided into two parts: one part of the main line firstly enters a dry gas feeding heat exchanger to exchange heat with the gas after aromatization reaction, then enters the aromatization reactor from the top of the aromatization reactor after being further heated to 300 ℃ by a dry gas electric heater to contact with an aromatization catalyst for aromatization reaction; the other part is that the internal temperature of the aromatization reactor is controlled, and the aromatization reactor is directly fed into the aromatization reactor from the middle part for aromatization reaction without heat exchange and temperature raising;
the gas after aromatization reaction comes out from the bottom of the aromatization reactor and enters a dry gas feeding heat exchanger to exchange heat with raw dry gas, and then is cooled to 20 ℃ through an aromatization product cooler and an aromatization product deep cooler, and then enters an aromatization product gas-liquid separation tank to be subjected to gas-liquid separation, wherein the gas phase is divided into two parts: one part of the mixture enters a heating furnace to be used as fuel gas, and the other part of the mixture is compressed by a dry gas circulator and then returns to the aromatization reactor; the liquid phase aromatic hydrocarbon, namely crude gasoline directly enters a feeding heat exchanger of the stripping tower by means of the pressure difference between an aromatization reaction system and a stripping tower system.
(4) Gas separation raw material gas concentration process
The gas component feed gas in the step (2) directly enters a depropanizing tower feeding preheater from the bottom of a stabilizing tower top reflux tank through a stabilizing tower reflux pump to be heated by the pressure difference of the stabilizing tower connected with the depropanizing tower, and then enters the depropanizing tower to separate carbon three and carbon four components;
the carbon three-fraction, namely gas component feed gas, is evaporated from the top of the depropanizing tower, is cooled by a depropanizing tower top air cooler and a condenser, and then enters a depropanizing tower top reflux tank, and condensate is divided into two parts after being pumped by a depropanizing tower reflux pump: one part is used as the reflux of the depropanizing tower, and the other part is used as the gas component raw material and sent to a gas component device or a gas component raw material tank for storage;
the carbon four components from the bottom of the depropanizing tower directly enter an MTBE device by virtue of pressure difference to be used as raw materials to participate in reaction or are sent into a carbon four raw material tank to be stored.
Furthermore, the depropanizing tower supplies heat to the tower from a reboiler of the depropanizing tower at the bottom of the tower, and the heat source adopts heat-conducting oil.
(5) Purification of aromatic hydrocarbons
The aromatic hydrocarbon coming out from the light hydrocarbon cooler of the stabilizing tower in the working procedure (2) and the aromatization product gas-liquid separation tank of the working procedure (3) enters the stripping tower from the middle section of the stripping tower after heat exchange between a feeding heat exchanger, namely a product cooler at the top of the tower, and the gas phase at the top of the stripping tower;
the aromatic hydrocarbon entering the stripping tower and the original light aromatic hydrocarbon in the tower, namely the product gasoline, carry out mass transfer and heat transfer and are divided into a heavy component and a light component;
the heavy component moves down to the bottom of the tower and is further heated by a reboiler of a stripping tower, and meanwhile, part of the heavy component is extracted and sent to a heavy oil tank for storage after being subjected to pressure increase by a forced circulation pump;
the light components are evaporated and lifted and fully vaporized, the lifted light components escape from the top of the tower to the feeding heat exchanger, are further cooled to 30 ℃ by a condenser at the top of the tower, enter a reflux tank, and are divided into two parts after being pressurized by a reflux pump: one part is extracted as an aromatic hydrocarbon product and sent to a gasoline tank for storage, and the other part enters a stripping tower from the top of the tower as reflux.
The raw material directly enters a cracking reaction system for reaction, low-carbon hydrocarbon obtained after the cracking reaction enters a depropanizing tower after being treated by an absorption stabilizing system, and gas component raw material gas with 15 percent of original propylene content is extracted from the top of the depropanizing tower; and the stripping tower is used for carrying out light and heavy component separation on the aromatic hydrocarbon obtained at the bottom of the aromatization and stabilization tower to obtain light aromatic hydrocarbon with purer components. The low-carbon hydrocarbon liquefied gas obtained after passing through the absorption stabilization system enters a depropanizing tower, the gas component feed gas is separated from the top of the tower, and the content of propylene reaches 50 percent.
The device for realizing the process for preparing the hydrocarbon by utilizing the liquefied gas comprises a cracking reaction system, an absorption stabilizing system, an aromatization reaction system, a gas component feed gas concentrating system and an aromatic hydrocarbon purifying system.
Wherein,
the cracking reaction system comprises: the system comprises a raw material pump, a first heat exchanger, a second heat exchanger, a heating furnace, a cracking reactor, a reaction product cooler, a hot water heat exchanger, a gas-liquid separation tank, a reaction liquid pump, a rich gas compressor, a gas compressor outlet air cooler, a gas compressor outlet cooler and a gas compressor outlet liquid separation tank;
the outlet of the raw material pump is connected with a pipe orifice at the bottom of the shell pass of the first heat exchanger, a pipe orifice at the top of the shell pass of the first heat exchanger is connected with a pipe orifice at the bottom of the shell pass of the second heat exchanger, and a pipe orifice at the top of the shell pass of the second heat exchanger is respectively connected with the inlet of the heating furnace and the middle part of the cracking reactor; the outlet of the heating furnace is connected with the top of the cracking reactor;
the bottom of the cracking reactor is connected with a tube orifice at the top of a tube pass of a second heat exchanger, a tube orifice at the bottom of the tube pass of the second heat exchanger is connected with a tube orifice at the top of a tube pass of a first heat exchanger, a tube orifice at the bottom of the tube pass of the first heat exchanger is connected with a tube orifice at the top of a tube pass of a hot water heat exchanger, a tube orifice at the bottom of the tube pass of the hot water heat exchanger is connected with a tube orifice at the top of a shell pass of a cracking product cooler, a tube orifice at the bottom of the shell pass of the cracking product cooler; the outlet of the reaction liquid pump is connected with the upper part of the absorption tower; the gas-phase outlet at the top of the gas-liquid separation tank is connected with a rich gas compressor; the rich gas compressor, the air cooler at the outlet of the air compressor, the cooler at the outlet of the air compressor and the liquid separating tank at the outlet of the air compressor are sequentially connected; the gas phase outlet at the top of the liquid separating tank at the outlet of the gas compressor is connected with the lower part of the absorption tower; the outlet at the bottom of the outlet liquid-separating tank of the gas compressor is connected with a feed pump of the desorption tower.
The absorption stabilization system comprises: the system comprises an absorption tower, an absorption tower middle-section pump, an absorption tower middle-section cooler, an absorption tower bottom oil pump, a desorption tower feed pump, a desorption tower feed heat exchanger, a desorption tower reboiler, a stabilization tower feed pump, a stabilization tower feed heat exchanger, a stabilization tower reboiler, a stabilization tower top air cooler, a stabilization tower top reflux tank, a stabilization tower reflux pump, a light hydrocarbon cooler, an absorption oil pump, an absorption oil cooler and a dry gas liquid separation tank;
the bottom of the absorption tower is connected with an inlet of an air cooler at the outlet of the air compressor through an oil pump at the bottom of the absorption tower, and the top of the absorption tower is connected with a dry gas separating tank; the top of the dry gas liquid separation tank is connected with a pipe orifice at the bottom of the shell pass of the dry gas feeding heat exchanger; the bottom of the dry gas liquid separation tank is connected with the inlet of a reflux pump of the stabilizing tower; the outlet of the reflux pump of the stabilizing tower is respectively connected with the upper part of the stabilizing tower and the pipe orifice at the bottom of the pipe pass of the feed preheater of the depropanizing tower;
an absorption tower middle section pump and an absorption tower middle section cooler are sequentially connected in parallel in the middle of the absorption tower;
the desorption tower feed pump is connected with the top of the desorption tower and is also connected with the upper part of the desorption tower through a desorption tower feed heat exchanger;
the desorption tower and the rich gas compressor are both connected with an air cooler at the outlet of the gas compressor; the bottom of the desorption tower is connected with the middle part of the stabilizing tower through a stabilizing tower feed pump and a stabilizing tower feed heat exchanger in sequence;
the top of the stabilizing tower, an air cooler at the top of the stabilizing tower, a condenser of the stabilizing tower and a reflux tank at the top of the stabilizing tower are connected in sequence; the bottom of the stabilizing tower top reflux tank is respectively connected with the top of the stabilizing tower and a depropanizing tower feeding preheater through a stabilizing tower top reflux pump;
the bottom of the stabilizing tower, a stabilizing tower feeding heat exchanger, a desorption tower feeding heat exchanger and a light hydrocarbon cooler are connected in sequence; the light hydrocarbon cooler is connected with the feeding heat exchanger of the stripping tower, and is also connected with the top of the absorption tower through the absorption oil pump and the absorption oil cooler in sequence.
Furthermore, the desorption tower is provided with a desorption tower reboiler at the bottom of the desorption tower.
Further, the stabilizer is provided with a stabilizer reboiler at the bottom of the tower.
The aromatization reaction system comprises: the system comprises a dry gas feeding heat exchanger, a dry gas electric heater, an aromatization reactor, an aromatization product cooler, an aromatization product deep cooler, an aromatization product gas-liquid separation tank and a dry gas circulator;
a tube orifice at the top of the shell pass of the dry gas feeding heat exchanger is sequentially connected with the top of the aromatization reactor through a dry gas electric heater; the tube orifice at the top of the tube pass of the dry gas feeding heat exchanger is also connected with the bottom of the aromatization reactor; the bottom of the tube pass of the dry gas feeding heat exchanger, an aromatization product cooler, an aromatization product deep cooler and an aromatization product gas-liquid separation tank are connected in sequence; the top of the dry gas liquid separation tank is respectively connected with the dry gas circulator and the middle part of the aromatization reactor;
the top of the aromatization product gas-liquid separation tank is connected with a heating furnace, and the aromatization product gas-liquid separation tank is also sequentially connected with an aromatization reactor through a dry gas circulator, a dry gas feeding heat exchanger and a dry gas electric heater.
The gas separation feed gas concentration system comprises: a depropanizing tower feeding preheater, a depropanizing tower reboiler, a depropanizing tower top air cooler, a depropanizing tower top condenser, a depropanizing tower top reflux tank and a depropanizing tower reflux pump;
the bottom of the reflux tank at the top of the stabilizing tower is sequentially connected with a feed preheater of the depropanizing tower and the depropanizing tower through a reflux pump of the stabilizing tower;
the top of the depropanizing tower is sequentially connected with a depropanizing tower top air cooler, a depropanizing tower top condenser, a depropanizing tower top reflux tank and a depropanizing tower top reflux pump to form a loop; the top reflux pump of the depropanization tower is also connected with a gas separation device.
Furthermore, the depropanizing tower supplies heat to the tower from a reboiler of the depropanizing tower at the bottom of the tower, and the heat source adopts heat-conducting oil.
The light hydrocarbon purification system comprises: the system comprises a feeding heat exchanger, an electric heater, a stripping tower reboiler, a stripping tower top condenser, a stripping tower top reflux tank, a stripping tower reflux pump and a forced circulation pump;
the feeding heat exchanger of the stripping tower is connected with the stripping tower; the forced circulation pump is connected with the heavy oil tank;
the top of the stripping tower is connected with a feeding heat exchanger, a condenser, a reflux tank and a reflux pump of the stripping tower in turn to form a loop; the stripping tower reflux pump is also connected with a gasoline tank.
Furthermore, the stripping tower is provided with a stripping tower reboiler at the bottom.
Compared with the existing hydrocarbon preparation process, the invention removes a deisobutanizer and accessory supporting equipment thereof, the raw materials are not pretreated any more, and directly enter a cracking reaction system for reaction, the reacted low-carbon hydrocarbon enters a depropanizer after being treated by an absorption stabilizing system for gas separation raw material gas concentration, and the propylene gas separation raw material gas with the weight content of more than or equal to 15 percent is extracted from the top of the depropanizer; and (3) carrying out light and heavy component separation on the aromatic hydrocarbon obtained at the bottom of the aromatization and stabilization tower through a stripping tower in the aromatic hydrocarbon purification process, and further concentrating to obtain light aromatic hydrocarbon with purer components, wherein the propylene content reaches 50 percent by weight.
The invention has the advantages that:
(1) the energy consumption is low: when the existing deisobutanizer process is adopted, 175kg of standard coal consumed for treating carbon four per ton of raw material is processed, after the process disclosed by the invention is adopted, the deisobutanizer stops running, 90kg of standard coal consumed for treating carbon four per ton of raw material is processed, and the energy consumption is saved by 48.5%;
(2) the gas component feed gas has high propylene content, and the mass fraction content is improved from 15% to 50%;
(3) the device has low requirements on equipment and heat energy, is easy to realize, has simple device flow, is easy to control and operates stably.
The invention is further illustrated by the following figures and examples.
Drawings
FIG. 1 is a schematic view showing the connection of the apparatus of a liquefied gas processing hydrocarbon manufacturing apparatus according to an embodiment of the present invention;
in the figure: 1-raw material pump, 2-first heat exchanger, 3-second heat exchanger, 4-heating furnace, 5-cracking reactor, 6-reaction product cooler, 7-hot water heat exchanger, 8-gas-liquid separating tank, 9-reaction liquid pump, 10-rich gas compressor, 11-gas compressor outlet air cooler, 12-gas compressor outlet cooler, 13-gas compressor outlet liquid separating tank, 14-absorption tower, 15-absorption tower middle section pump, 16-absorption tower middle section cooler, 17-absorption tower bottom oil pump, 18-desorption tower, 19-desorption tower feeding pump, 20-desorption tower feeding heat exchanger, 21-desorption tower reboiler, 22-stabilizing tower, 23-stabilizing tower feeding pump, 24-stabilizing tower feeding heat exchanger, 25-stabilizing tower reboiler, 26-stable tower top air cooler, 27-stable tower top condenser, 28-stable tower top reflux tank, 29-stable tower reflux pump, 30-light hydrocarbon cooler, 31-absorption oil pump, 32-absorption oil cooler, 33-dry gas liquid separation tank, 34-dry gas feeding heat exchanger, 35-dry gas electric heater, 36-aromatization reactor, 37-aromatization product cooler, 38-aromatization product deep cooler, 39-aromatization product gas-liquid separation tank, 40-dry gas circulator, 41-depropanizer feeding preheater, 42-depropanizer, 43-depropanizer reboiler, 44-depropanizer top air cooler, 45-depropanizer top condenser, 46-depropanizer top reflux tank, 47-depropanizer reflux pump reflux tank, 48-stripper feeding heat exchanger, 49-electric heater, 50-stripper, 51-stripper reboiler, 52-stripper overhead condenser, 53-stripper overhead reflux tank, 54-stripper reflux pump and 55-forced circulation pump.
Detailed Description
Example 1
A process for preparing hydrocarbon by using liquefied gas comprises the following steps:
(1) a cracking reaction process:
conveying a carbon four raw material in a cracking raw material tank to a device area through a raw material pump, exchanging heat with a cracking reaction product through a first heat exchanger and a second heat exchanger, then feeding the carbon four raw material subjected to heat exchange into a heating furnace, further heating to 500 ℃, and feeding the gas subjected to temperature increase from the top of a cracking reactor for cracking reaction;
the pyrolysis reaction product sequentially passes through a second heat exchanger, a first heat exchanger, a hot water heat exchanger and a pyrolysis product cooler (namely a reaction condenser) from the bottom of the pyrolysis reactor for heat exchange and cooling, and enters a gas-liquid separation tank for separation after the temperature is reduced to 40 ℃ (the pyrolysis reaction product exchanges heat with the carbon four raw material in the second heat exchanger and the first heat exchanger, and exchanges heat with hot water and circulating water in the hot water heat exchanger and the pyrolysis product cooler respectively); the separated condensate is pumped into an absorption tower by a reaction liquid pump and is used for further absorbing the rich gas sent by the compressor; compressing and cooling the separated gas by a rich gas compressor, and then sending the gas to an absorption tower for further absorption;
(2) an absorption stabilization step:
the gas compressed by the rich gas compressor in the step (1) and the absorption oil from the bottom of the absorption tower and the desorption gas from the top of the desorption tower sequentially pass through an air cooler at the outlet of the gas compressor and a cooler at the outlet of the gas compressor, are cooled to 40 ℃ and then enter a liquid separation tank at the outlet of the gas compressor, so that the oil and the gas are separated;
separating out rich gas from the top of the liquid separating tank at the outlet of the gas compressor and conveying the rich gas to the lower part of the absorption tower, wherein the rich gas is in countercurrent contact with an absorbent (such as stabilized gasoline) entering from the upper part of the absorption tower in the absorption tower, the absorbed lean gas enters the dry gas liquid separating tank from the top of the absorption tower for gas-liquid separation, liquid is converged into the stabilization tower for reflux, and the dry gas coming out from the top of the dry gas liquid separating tank is conveyed to an aromatization reactor;
in order to take away the heat released in the absorption tower, the gasoline which circularly reflows from the middle section is pumped out by an absorption tower middle section pump at the middle part of the absorption tower, cooled to 20 ℃ by an absorption tower middle section cooler and then returned to the absorption tower;
the condensate coming out of the bottom of the liquid separating tank at the outlet of the gas compressor is divided into two paths by a feeding pump of the desorption tower: one path directly enters the top of the desorption tower, and the other path enters the upper part of the desorption tower after heat exchange is carried out to 70 ℃ by a feeding heat exchanger of the desorption tower;
the desorption tower supplies heat to the tower from a desorption tower reboiler at the bottom of the tower; the desorption gas escapes from the tower top and is merged with the compressed rich gas of the rich gas compressor to enter an air cooler at the outlet of the gas compressor; the desorbed gasoline is pumped out from the bottom of the desorption tower by a stabilizing tower feed pump, exchanges heat with the stabilized gasoline at the bottom of the stabilizing tower through a stabilizing tower feed heat exchanger to 125 ℃, and then enters the middle part of the stabilizing tower;
the stabilizing tower supplies heat to the tower from a stabilizing tower reboiler at the bottom of the tower; and C4, distilling out the components of C four and C four from the top of the stabilizing tower, passing through an air cooler at the top of the stabilizing tower and a condenser at the top of the stabilizing tower, entering a reflux tank at the top of the stabilizing tower, and pumping the gas component feed gas from the bottom of the reflux tank at the top of the stabilizing tower through a reflux pump of the stabilizing tower to divide the gas component feed gas into two paths: one path of the reflux returns to the top of the stabilizing tower, and the other path of the reflux enters a feed preheater of the depropanizing tower;
the stabilized gasoline of the stabilizing tower is discharged from the bottom of the tower, and is cooled to 30 ℃ by a stabilizing tower feeding heat exchanger, a desorption tower feeding heat exchanger and a light hydrocarbon cooler in sequence, and then is divided into two parts: one part of the gas enters a feeding heat exchanger (namely a product cooler at the top of the tower) of the stripping tower to exchange heat with light aromatic hydrocarbon, namely product gasoline extracted by reflux at the top of the stripping tower, and then enters the stripping tower, and the other part of the gas is pressurized by an absorption oil pump, cooled to 20 ℃ by an absorption oil cooler and then sent to the top of an absorption tower to be used as an absorbent;
(3) an aromatization reaction process:
the dry gas from the top of the dry gas liquid separation tank in the step (2) is merged with the fuel gas of a dry gas circulator (a screw compressor) and then is divided into two parts: one part of the main line firstly enters a dry gas feeding heat exchanger to exchange heat with the gas after aromatization reaction, then enters the aromatization reactor from the top of the aromatization reactor after being further heated to 300 ℃ by a dry gas electric heater to contact with an aromatization catalyst for aromatization reaction; the other part is that the internal temperature of the aromatization reactor is controlled, and the aromatization reactor is directly fed into the aromatization reactor from the middle part for aromatization reaction without heat exchange and temperature raising;
the gas after aromatization reaction comes out from the bottom of the aromatization reactor and enters a dry gas feeding heat exchanger to exchange heat with raw dry gas, and then is cooled to 20 ℃ through an aromatization product cooler and an aromatization product deep cooler, and then enters an aromatization product gas-liquid separation tank to be subjected to gas-liquid separation, wherein the gas phase is divided into two parts: one part of the mixture enters a heating furnace to be used as fuel gas, and the other part of the mixture is compressed by a dry gas circulator and then returns to the aromatization reactor; liquid-phase aromatic hydrocarbon, namely crude gasoline directly enters a feeding heat exchanger of a stripping tower by means of the pressure difference between an aromatization reaction system and a stripping tower system;
(4) gas separation raw material gas concentration process
The gas component feed gas in the step (2) directly enters a depropanizing tower feeding preheater from the bottom of a stabilizing tower top reflux tank through a stabilizing tower reflux pump to be heated by the pressure difference of the stabilizing tower connected with the depropanizing tower, and then enters the depropanizing tower to separate carbon three and carbon four components;
the carbon three-fraction, namely gas component feed gas, is evaporated from the top of the depropanizing tower, is cooled by a depropanizing tower top air cooler and a condenser, and then enters a depropanizing tower top reflux tank, and condensate is divided into two parts after being pumped by a depropanizing tower reflux pump: one part is used as the reflux of the depropanizing tower, and the other part is used as the gas component raw material and sent to a gas component device or a gas component raw material tank for storage;
directly feeding the four carbon components discharged from the bottom of the depropanizing tower into an MTBE (methyl tert-butyl ether) device by virtue of pressure difference to be used as raw materials to participate in reaction or be fed into a four carbon raw material tank for storage;
the depropanizing tower supplies heat to the tower from a reboiler at the bottom of the depropanizing tower, and the heat source adopts heat-conducting oil
(5) Purification of aromatic hydrocarbons
The aromatic hydrocarbon coming out from the light hydrocarbon cooler of the stabilizing tower in the working procedure (2) and the aromatization product gas-liquid separation tank of the working procedure (3) enters the stripping tower from the middle section of the stripping tower after heat exchange between a feeding heat exchanger, namely a product cooler at the top of the tower, and the gas phase at the top of the stripping tower;
the aromatic hydrocarbon entering the stripping tower and the original light aromatic hydrocarbon in the tower, namely the product gasoline, carry out mass transfer and heat transfer and are divided into a heavy component and a light component;
the heavy component moves down to the bottom of the tower and is further heated by a reboiler of a stripping tower, and meanwhile, part of the heavy component is extracted and sent to a heavy oil tank for storage after being subjected to pressure increase by a forced circulation pump;
the light components are evaporated and lifted and fully vaporized, the lifted light components escape from the top of the tower to the feeding heat exchanger, are further cooled to 30 ℃ by a condenser at the top of the tower, enter a reflux tank, and are divided into two parts after being pressurized by a reflux pump: one part is extracted as an aromatic hydrocarbon product and sent to a gasoline tank for storage, and the other part enters a stripping tower from the top of the tower as reflux.
As a result: the standard coal consumption for treating four raw materials per ton of carbon is 90kg, and the energy consumption is saved by 48.5%; the propylene content of the gas component feed gas is improved to 50 percent by mass.
Example 2
As shown in fig. 1, an apparatus for implementing the process for producing hydrocarbons by using liquefied gas processing according to example 1 includes a cracking reaction system, an absorption stabilization system, an aromatization reaction system, a gas component raw material gas concentration system, and an aromatic hydrocarbon purification system.
The cracking reaction system comprises: the system comprises a raw material pump 1, a first heat exchanger 2, a second heat exchanger 3, a heating furnace 4, a cracking reactor 5, a reaction product cooler 6, a hot water heat exchanger 7, a gas-liquid separation tank 8, a reaction liquid pump 9, a rich gas compressor 10, a gas compressor outlet air cooler 11, a gas compressor outlet cooler 12 and a gas compressor outlet liquid separation tank 13;
an outlet of the raw material pump 1 is connected with a shell pass bottom pipe orifice of the first heat exchanger 2, a shell pass top pipe orifice of the first heat exchanger 2 is connected with a shell pass bottom pipe orifice of the second heat exchanger 3, and a shell pass top pipe orifice of the second heat exchanger 3 is respectively connected with an inlet of the heating furnace 4 and the middle part of the cracking reactor 5; the outlet of the heating furnace 4 is connected with the top of the cracking reactor 5;
the bottom of the cracking reactor 5 is connected with a tube orifice at the top of a tube pass of a second heat exchanger 3, a tube orifice at the bottom of a tube pass of the second heat exchanger 3 is connected with a tube orifice at the top of a tube pass of a first heat exchanger 2, a tube orifice at the bottom of a tube pass of the first heat exchanger 2 is connected with a tube orifice at the top of a tube pass of a hot water heat exchanger 7, a tube orifice at the bottom of a tube pass of the hot water heat exchanger 7 is connected with a tube orifice at the top of a shell pass of a cracking product cooler 6, a tube orifice at the bottom of a shell pass of the cracking product cooler 6 is connected with an; the outlet of the reaction liquid pump 9 is connected with the upper part of the absorption tower 14; a gas phase outlet at the top of the gas-liquid separation tank 8 is connected with a rich gas compressor 10; the rich gas compressor 10, the air cooler 11 at the outlet of the gas compressor, the cooler 12 at the outlet of the gas compressor and the liquid separation tank 13 at the outlet of the gas compressor are sequentially connected; the gas phase outlet at the top of the liquid separation tank 13 at the outlet of the gas compressor is connected with the lower part of the absorption tower 14; the outlet at the bottom of the liquid separation tank 13 at the outlet of the gas compressor is connected with a feed pump 19 of the desorption tower.
The absorption stabilization system comprises: an absorption tower 14, an absorption tower middle-section pump 15, an absorption tower middle-section cooler 16, an absorption tower bottom oil pump 17, a desorption tower 18, a desorption tower feed pump 19, a desorption tower feed heat exchanger 20, a desorption tower reboiler 21, a stabilization tower 22, a stabilization tower feed pump 23, a stabilization tower feed heat exchanger 24, a stabilization tower reboiler 25, a stabilization tower top air cooler 26, a stabilization tower top cooler 27, a stabilization tower top reflux tank 28, a stabilization tower reflux pump 29, a light hydrocarbon cooler 30, an absorption oil pump 31, an absorption oil cooler 32 and a dry gas liquid separation tank 33;
the bottom of the absorption tower 14 is connected with the inlet of an air cooler 11 at the outlet of the air compressor through an oil pump 17 at the bottom of the absorption tower, and the top of the absorption tower 14 is connected with a dry gas liquid separation tank 33; the top of the dry gas liquid separation tank 33 is connected with a shell pass bottom pipe orifice of a dry gas feeding heat exchanger 34; the bottom of the dry gas liquid separation tank 33 is connected with the inlet of the reflux pump 29 of the stabilizing tower; the outlet of the reflux pump 29 of the stabilizing tower is respectively connected with the upper part of the stabilizing tower 22 and the pipe orifice at the bottom of the pipe pass of the feed preheater 41 of the depropanizing tower;
an absorption tower middle section pump 15 and an absorption tower middle section cooler 16 are sequentially connected in parallel in the middle of the absorption tower 14;
a desorption tower feed pump 19 is connected with the top of the desorption tower 18, and the desorption tower feed pump 19 is also connected with the upper part of the desorption tower 18 through a desorption tower feed heat exchanger 20;
the desorption tower 18 is provided with a desorption tower reboiler 21 at the bottom of the tower; the desorption tower 18 and the rich gas compressor 10 are both connected with an outlet air cooler 11 of the gas compressor; the bottom of the desorption tower 18 is connected with the middle part of the stabilizing tower 22 through a stabilizing tower feeding pump 23 and a stabilizing tower feeding heat exchanger 24 in sequence;
the stabilizer tower 22 is provided with a stabilizer reboiler 25 at the bottom of the tower; the top of the stabilizer 22 is sequentially connected with a stabilizer top air cooler 26, a stabilizer condenser 27 and a stabilizer top reflux tank 28 in turn; the bottom of the stabilizing tower top reflux tank 28 is respectively connected with the top of the stabilizing tower 22 and the feed preheater 41 of the depropanizer through a stabilizing tower top reflux pump 29;
the bottom of the stabilizing tower 22, the stabilizing tower feeding heat exchanger 24, the desorption tower feeding heat exchanger 20 and the light hydrocarbon cooler 30 are connected in sequence; the light hydrocarbon cooler 30 is connected with the stripper feeding heat exchanger 48, and the light hydrocarbon cooler 30 is also connected with the top of the absorption tower 14 through the absorption oil pump 31 and the absorption oil cooler 32 in sequence.
The aromatization reaction system comprises: a dry gas feeding heat exchanger 34, a dry gas electric heater 35, an aromatization reactor 36, an aromatization product cooler 37, an aromatization product deep cooler 38, an aromatization product gas-liquid separation tank 39 and a dry gas circulator 40;
a tube orifice at the top of the shell pass of the dry gas feeding heat exchanger 34 is sequentially connected with the top of the aromatization reactor 36 through a dry gas electric heater 35; the tube side top orifice of the dry gas feed heat exchanger 34 is also connected with the bottom of the aromatization reactor 36; the bottom of the tube pass of the dry gas feeding heat exchanger 34, an aromatization product cooler 37, an aromatization product deep cooler 38 and an aromatization product gas-liquid separation tank 39 are connected in sequence; the top of the dry gas liquid separation tank 33 is respectively connected with the dry gas circulator 40 and the middle part of the aromatization reactor 36;
the aromatization product gas-liquid separation tank 39 is connected with the heating furnace 4, and the aromatization product gas-liquid separation tank 39 is also connected with the aromatization reactor 36 through a dry gas circulator 40, a dry gas feeding heat exchanger 34 and a dry gas electric heater 35 in sequence.
The gas separation feed gas concentration system comprises: a depropanizing tower feeding preheater 41, a depropanizing tower 42, a depropanizing tower reboiler 43, a depropanizing tower top air cooler 44, a depropanizing tower top condenser 45, a depropanizing tower top reflux tank 46 and a depropanizing tower reflux pump 47;
the bottom of the stabilizing tower top reflux tank 28 is sequentially connected with a depropanizer feeding preheater 41 and a depropanizer 42 through a stabilizing tower reflux pump 29;
the top of the depropanizing tower 42 is connected with a depropanizing tower top air cooler 44, a depropanizing tower top condenser 45, a depropanizing tower top reflux tank 46 and a depropanizing tower top reflux pump 47 in sequence to form a loop; the depropanizer overhead reflux pump 47 is also connected with a gas separation device;
the depropanizing tower 42 supplies heat to the tower from a depropanizing tower reboiler 43 at the bottom of the tower, and the heat source adopts heat-conducting oil.
The light hydrocarbon purification system comprises: a feed heat exchanger 48, an electric heater 49, a stripping tower 50, a stripping tower reboiler 51, a stripping tower top condenser 52, a stripping tower top reflux tank 53, a stripping tower reflux pump 54 and a forced circulation pump 55;
stripper feed heat exchanger 48 is connected to stripper 50; the forced circulation pump 55 is connected with the heavy oil tank;
the stripping column 50 is provided with a stripping column reboiler 51 at the bottom. The top of the stripping tower 50 is connected with a feeding heat exchanger 48 of the stripping tower, a condenser 52 of the stripping tower, a reflux tank 53 of the stripping tower and a reflux pump 54 of the stripping tower in sequence to form a loop; stripper reflux pump 54 is also connected to a gasoline tank.
It should be noted that: the various devices adopted in the invention are conventional devices used in the production process in the field, and the operation, parameters and the like of each device are carried out according to the conventional operations without special points.
Claims (10)
1. A process for preparing hydrocarbon by utilizing liquefied gas comprises a cracking reaction process, an absorption stabilization process and an aromatization reaction process, and is characterized in that: also comprises a gas separation raw material gas concentration process and an aromatic hydrocarbon purification process;
wherein, the gas separation feed gas concentration process comprises the following steps:
the gas component feed gas in the absorption stabilization procedure enters a depropanizing tower feeding preheater from the bottom of a stabilization tower top reflux tank through a part of a stabilization tower reflux pump to be heated and then enters the depropanizing tower to separate carbon three and carbon four components;
the carbon three fraction is evaporated from the top of the depropanizing tower, cooled by a depropanizing tower top air cooler and a condenser and then enters a depropanizing tower top reflux tank, and condensate is divided into two parts after being pumped by a depropanizing tower reflux pump: one part is used as the reflux of the depropanizing tower, and the other part is used as the gas component raw material and sent to a gas component device or a gas component raw material tank for storage;
and (3) feeding the four carbon components discharged from the bottom of the depropanizing tower into an MTBE device to be used as raw materials to participate in reaction or feeding the raw materials into a four carbon raw material tank for storage.
2. The process for preparing hydrocarbons by processing liquefied gas according to claim 1, wherein the aromatic hydrocarbon purification process comprises:
aromatic hydrocarbon discharged from a light hydrocarbon cooler of a stabilizing tower in the absorption stabilizing procedure and an aromatization product gas-liquid separation tank in the aromatization reaction procedure exchanges heat with the gas phase at the top of a stripping tower through a feeding heat exchanger, and then enters the stripping tower from the middle section of the stripping tower;
the aromatic hydrocarbon entering the stripping tower and the original gasoline light aromatic hydrocarbon in the tower carry out mass transfer and heat transfer and are divided into a heavy component and a light component;
the heavy component moves down to the bottom of the tower and is further heated, and meanwhile, part of the heavy component is extracted and sent to a heavy oil tank for storage after being subjected to pressure increase by a forced circulation pump;
the light components are evaporated and lifted and fully vaporized, the lifted light components escape from the tower top to the feeding heat exchanger, are further cooled to 30 ℃ by a tower top condenser, enter a reflux tank, and are divided into two parts after being pressurized by a reflux pump: one part is extracted as an aromatic hydrocarbon product and sent to a gasoline tank for storage, and the other part enters a stripping tower from the top of the tower as reflux.
3. The process for producing hydrocarbons using liquefied gas according to claim 1, wherein the cracking reaction comprises:
a carbon four liquefied gas raw material in a cracking raw material tank passes through a raw material pump, sequentially passes through a first heat exchanger and a second heat exchanger to exchange heat with a cracking reaction product, the heat-exchanged carbon four raw material enters a heating furnace, the temperature is further raised to 500 ℃, and the gas with the raised temperature enters a cracking reactor from the top of the cracking reactor to perform cracking reaction;
the pyrolysis reaction product sequentially passes through a second heat exchanger, a first heat exchanger, a hot water heat exchanger and a pyrolysis product cooler from the bottom of the pyrolysis reactor for heat exchange and cooling until the temperature is reduced to 40 ℃, and then enters a gas-liquid separation tank for separation; the condensate obtained by separation is pumped into an absorption tower by a reaction liquid pump; and compressing and cooling the separated gas by a rich gas compressor.
4. The process for producing hydrocarbons using liquefied gas according to claim 1, wherein the absorption stabilization step comprises:
the gas compressed by the rich gas compressor in the cracking reaction process, the absorption oil from the bottom of the absorption tower and the desorption gas from the top of the desorption tower sequentially pass through an air cooler at the outlet of the gas compressor and a cooler at the outlet of the gas compressor, are cooled to 40 ℃ and then enter a liquid separation tank at the outlet of the gas compressor, so that the oil and the gas are separated;
separating out rich gas from the top of the liquid separating tank at the outlet of the gas compressor and conveying the rich gas to the lower part of the absorption tower, wherein the rich gas is in countercurrent contact with an absorbent entering from the upper part of the absorption tower in the absorption tower, the absorbed lean gas enters the dry gas liquid separating tank from the top of the absorption tower for gas-liquid separation, the liquid flows into a stabilizing tower for reflux, and the dry gas coming out from the top of the dry gas liquid separating tank is conveyed to an aromatization reactor;
pumping gasoline which circularly reflows from the middle section of the absorption tower by using a middle section pump of the absorption tower, cooling to 20 ℃ by a middle section cooler of the absorption tower, and returning to the absorption tower;
the condensate coming out of the bottom of the liquid separating tank at the outlet of the gas compressor is divided into two paths by a feeding pump of the desorption tower: one path directly enters the top of the desorption tower, and the other path enters the upper part of the desorption tower after heat exchange is carried out to 70 ℃ by a feeding heat exchanger of the desorption tower;
the desorption gas escapes from the tower top and is merged with the compressed rich gas of the rich gas compressor to enter an air cooler at the outlet of the gas compressor; the desorbed gasoline is pumped out from the bottom of the desorption tower by a stabilizing tower feed pump, exchanges heat with the stabilized gasoline at the bottom of the stabilizing tower through a stabilizing tower feed heat exchanger to 125 ℃, and then enters the middle part of the stabilizing tower;
and C4, distilling out the components of C four and C four from the top of the stabilizing tower, passing through an air cooler at the top of the stabilizing tower and a condenser at the top of the stabilizing tower, entering a reflux tank at the top of the stabilizing tower, and pumping the gas component feed gas from the bottom of the reflux tank at the top of the stabilizing tower through a reflux pump of the stabilizing tower to divide the gas component feed gas into two paths: one path of the reflux returns to the top of the stabilizing tower, and the other path of the reflux enters a feed preheater of the depropanizing tower;
the stabilized gasoline of the stabilizing tower is discharged from the bottom of the tower, and is cooled to 30 ℃ by a stabilizing tower feeding heat exchanger, a desorption tower feeding heat exchanger and a light hydrocarbon cooler in sequence, and then is divided into two parts: one part enters a feeding heat exchanger of the stripping tower to exchange heat with the product gasoline light aromatic hydrocarbon extracted by reflux at the top of the stripping tower, and then enters the stripping tower, and the other part is pressurized by an absorption oil pump, cooled to 20 ℃ by an absorption oil cooler and then sent to the top of the absorption tower to be used as an absorbent.
5. The process for producing hydrocarbons by using liquefied gas as claimed in claim 1, wherein the aromatization reaction comprises the following steps:
the dry gas from the top of the dry gas liquid separation tank in the absorption stabilization procedure is merged with the fuel gas of the dry gas circulator and then is divided into two parts: one part of the main line firstly enters a dry gas feeding heat exchanger to exchange heat with the gas after aromatization reaction, then enters the aromatization reactor from the top of the aromatization reactor after being further heated to 300 ℃ by a dry gas electric heater to contact with an aromatization catalyst for aromatization reaction; the other part of the mixture directly enters an aromatization reactor to carry out aromatization reaction;
the gas after aromatization reaction comes out from the bottom of the aromatization reactor and enters a dry gas feeding heat exchanger to exchange heat with raw dry gas, and then is cooled to 20 ℃ through an aromatization product cooler and an aromatization product deep cooler, and then enters an aromatization product gas-liquid separation tank to be subjected to gas-liquid separation, wherein the gas phase is divided into two parts: one part of the mixture enters a heating furnace to be used as fuel gas, and the other part of the mixture is compressed by a dry gas circulator and then returns to the aromatization reactor; the liquid phase enters a stripper feed heat exchanger.
6. An apparatus for implementing a process for preparing hydrocarbons by processing liquefied gas according to claim 1, comprising a cracking reaction system, an absorption stabilization system, an aromatization reaction system, a gas component feed gas concentration system, an aromatic hydrocarbon purification system which are sequentially communicated;
wherein, gas divides feed gas concentration system, include: a depropanizing tower feeding preheater (41), a depropanizing tower (42), a depropanizing tower top air cooler (44), a depropanizing tower top condenser (45), a depropanizing tower top reflux tank (46) and a depropanizing tower reflux pump (47);
the bottom of a reflux tank (28) at the top of the stabilizing tower is sequentially connected with a feed preheater (41) of a depropanizing tower and a depropanizing tower (42) through a reflux pump (29) of the stabilizing tower;
the top of the depropanizing tower (42) is connected with a depropanizing tower top air cooler (44), a depropanizing tower top condenser (45), a depropanizing tower top reflux tank (46) and a depropanizing tower top reflux pump (47) in sequence to form a loop; the top reflux pump (47) of the depropanization tower is also connected with a gas separation device.
7. An apparatus for processing hydrocarbons using liquefied gas according to claim 6, wherein:
the light hydrocarbon purification system comprises: a feeding heat exchanger (48), an electric heater (49), a stripping tower (50), a stripping tower top condenser (52), a stripping tower top reflux tank (53), a stripping tower reflux pump (54) and a forced circulation pump (55);
the stripper column feed heat exchanger (48) is connected with the stripper column (50); the forced circulation pump (55) is connected with the heavy oil tank;
the top of the stripping tower (50) is connected with a stripping tower feeding heat exchanger (48), a stripping tower top condenser (52), a stripping tower top reflux tank (53) and a stripping tower reflux pump (54) in sequence to form a loop; the stripper return pump (54) is also connected to the gasoline tank.
8. An apparatus for processing hydrocarbons using liquefied gas according to claim 6, wherein:
the cracking reaction system comprises: the system comprises a raw material pump (1), a first heat exchanger (2), a second heat exchanger (3), a heating furnace (4), a cracking reactor (5), a reaction product cooler (6), a hot water heat exchanger (7), a gas-liquid separation tank (8), a reaction liquid pump (9), a rich gas compressor (10), a gas compressor outlet air cooler (11), a gas compressor outlet cooler (12) and a gas compressor outlet liquid separation tank (13);
an outlet of the raw material pump (1) is connected with a shell pass bottom pipe orifice of the first heat exchanger (2), a shell pass top pipe orifice of the first heat exchanger (2) is connected with a shell pass bottom pipe orifice of the second heat exchanger (3), and a shell pass top pipe orifice of the second heat exchanger (3) is respectively connected with an inlet of the heating furnace (4) and the middle part of the cracking reactor (5); the outlet of the heating furnace (4) is connected with the top of the cracking reactor (5);
the bottom of the cracking reactor (5) is connected with a tube side top pipe orifice of the second heat exchanger (3), a tube side bottom pipe orifice of the second heat exchanger (3) is connected with a tube side top pipe orifice of the first heat exchanger (2), a tube side bottom pipe orifice of the first heat exchanger (2) is connected with a tube side top pipe orifice of the hot water heat exchanger (7), a tube side bottom pipe orifice of the hot water heat exchanger (7) is connected with a shell side top pipe orifice of the cracking product cooler (6), a shell side bottom pipe orifice of the cracking product cooler (6) is connected with a top inlet of the gas-liquid separation tank (8), and a bottom outlet of the gas-liquid separation tank (8) is connected with an inlet of a reaction liquid pump (9); the outlet of the reaction liquid pump (9) is connected with the upper part of the absorption tower (14); a gas phase outlet at the top of the gas-liquid separation tank (8) is connected with a rich gas compressor (10); the rich gas compressor (10), the air cooler (11) at the outlet of the aerostatic press, the cooler (12) at the outlet of the aerostatic press and the liquid separation tank (13) at the outlet of the aerostatic press are connected in sequence; a gas phase outlet at the top of the gas compressor outlet liquid separation tank (13) is connected with the lower part of the absorption tower (14); the outlet at the bottom of the liquid separation tank (13) at the outlet of the gas compressor is connected with a feed pump (19) of the desorption tower.
9. An apparatus for processing hydrocarbons using liquefied gas according to claim 6, wherein:
the absorption stabilization system comprises: the device comprises an absorption tower (14), an absorption tower middle-section pump (15), an absorption tower middle-section cooler (16), an absorption tower bottom oil pump (17), a desorption tower (18), a desorption tower feed pump (19), a desorption tower feed heat exchanger (20), a stabilization tower (22), a stabilization tower feed pump (23), a stabilization tower feed heat exchanger (24), a stabilization tower top air cooler (26), a stabilization tower top cooler (27), a stabilization tower top reflux tank (28), a stabilization tower reflux pump (29), a light hydrocarbon cooler (30), an absorption oil pump (31), an absorption oil cooler (32) and a dry gas liquid separation tank (33);
the bottom of the absorption tower (14) is connected with the inlet of an air cooler (11) at the outlet of the air compressor through an oil pump (17) at the bottom of the absorption tower, and the top of the absorption tower (14) is connected with a dry gas liquid separation tank (33); the top of the dry gas liquid separation tank (33) is connected with a shell pass bottom pipe orifice of a dry gas feeding heat exchanger (34); the bottom of the dry gas liquid separation tank (33) is connected with the inlet of a reflux pump (29) of the stabilizing tower; the outlet of the stabilizing tower reflux pump (29) is connected with the upper part of the stabilizing tower (22) and the pipe orifice at the bottom of the pipe pass of the depropanizing tower feeding preheater (41);
an absorption tower middle section pump (15) and an absorption tower middle section cooler (16) are sequentially connected in parallel in the middle of the absorption tower (14);
a desorption tower feed pump (19) is connected with the top of the desorption tower (18), and the desorption tower feed pump (19) is also connected with the upper part of the desorption tower (18) through a desorption tower feed heat exchanger (20);
the desorption tower (18) and the rich gas compressor (10) are both connected with an air cooler (11) at the outlet of the gas compressor; the bottom of the desorption tower (18) is connected with the middle part of the stabilizing tower (22) through a stabilizing tower feeding pump (23) and a stabilizing tower feeding heat exchanger (24) in sequence;
the top of the stabilizer (22) is connected with a reflux tank (28) at the top of the stabilizer through an air cooler (26) at the top of the stabilizer and a condenser (27) at the top of the stabilizer in sequence; the bottom of the stabilizing tower top reflux tank (28) is respectively connected with the top of the stabilizing tower (22) and a depropanizer feeding preheater (41) through a stabilizing tower top reflux pump (29);
the bottom of the stabilizer (22) is connected with the stabilizer feeding heat exchanger (24), the desorber feeding heat exchanger (20) and the light hydrocarbon cooler (30) in sequence: the light hydrocarbon cooler (30) is connected with the feeding heat exchanger (48) of the stripping tower, and the light hydrocarbon cooler (30) is also connected with the top of the absorption tower (14) through the absorption oil pump (31) and the absorption oil cooler (32) in sequence.
10. An apparatus for processing hydrocarbons using liquefied gas according to claim 6, wherein: the aromatization reaction system comprises: a dry gas feeding heat exchanger (34), a dry gas electric heater (35), an aromatization reactor (36), an aromatization product cooler (37), an aromatization product deep cooler (38), an aromatization product gas-liquid separation tank (39) and a dry gas circulating machine (40);
a shell side top pipe orifice of the dry gas feeding heat exchanger (34) is connected with the top of the aromatization reactor (36); the tube side top orifice of the dry gas feeding heat exchanger (34) is connected with the bottom of the aromatization reactor (36); the bottom of the tube pass of the dry gas feeding heat exchanger (34) is connected with an aromatization product cooler (37), an aromatization product deep cooler (38) and an aromatization product gas-liquid separation tank (39) in sequence; the top of the dry gas liquid separation tank (33) is respectively connected with the dry gas circulator (40) and the middle part of the aromatization reactor (36);
the aromatization product gas-liquid separation tank (39) is connected with the heating furnace (4), and the aromatization product gas-liquid separation tank (39) is also connected with the aromatization reactor (36) through a dry gas circulator (40).
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| CN201310485574.8A CN103755508B (en) | 2011-11-29 | 2011-11-29 | A kind of technique utilizing liquefied gas processing and preparing hydrocarbon |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105859530A (en) * | 2015-01-23 | 2016-08-17 | 上海优华系统集成技术有限公司 | Stabilizer tower and MTBE device catalytic distillation column combined cycle system |
| CN106365946A (en) * | 2016-10-09 | 2017-02-01 | 宁夏龙江化工科技有限公司 | Technology and equipment for preparing propylene and olefin by desulfurizing high-sulfur liquefied gas |
| CN107603669A (en) * | 2017-10-26 | 2018-01-19 | 中国石油化工股份有限公司 | The ethylene recovery system of catalytic cracked dry gas |
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| CN107603669B (en) * | 2017-10-26 | 2019-08-27 | 中国石油化工股份有限公司 | The ethylene recovery system of catalytic cracked dry gas |
| CN108865212A (en) * | 2018-07-13 | 2018-11-23 | 佛山市三水区精联自动化设备有限公司 | A kind of crude flashing device |
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