CN1962576A - Method for producing propylene ethane by carbon-containing olefin catalytic cracking - Google Patents
Method for producing propylene ethane by carbon-containing olefin catalytic cracking Download PDFInfo
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- CN1962576A CN1962576A CN 200510110293 CN200510110293A CN1962576A CN 1962576 A CN1962576 A CN 1962576A CN 200510110293 CN200510110293 CN 200510110293 CN 200510110293 A CN200510110293 A CN 200510110293A CN 1962576 A CN1962576 A CN 1962576A
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- catalytic cracking
- carbon
- tower
- knockout tower
- containing olefin
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- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 37
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 24
- 150000001336 alkenes Chemical class 0.000 title claims description 41
- 238000004523 catalytic cracking Methods 0.000 title claims description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims description 15
- IIPKBWQWKYOKRA-UHFFFAOYSA-N ethane;prop-1-ene Chemical compound CC.CC=C IIPKBWQWKYOKRA-UHFFFAOYSA-N 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 36
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 36
- 238000000034 method Methods 0.000 claims abstract description 33
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 11
- 239000007791 liquid phase Substances 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims description 30
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 16
- 238000009833 condensation Methods 0.000 claims description 10
- 230000005494 condensation Effects 0.000 claims description 10
- 241000282326 Felis catus Species 0.000 claims description 8
- 239000001294 propane Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 238000000926 separation method Methods 0.000 claims description 4
- 238000007233 catalytic pyrolysis Methods 0.000 claims description 3
- 238000002309 gasification Methods 0.000 claims description 3
- 230000001112 coagulating effect Effects 0.000 claims description 2
- 238000005520 cutting process Methods 0.000 claims description 2
- 238000012856 packing Methods 0.000 claims description 2
- 238000004227 thermal cracking Methods 0.000 claims description 2
- 239000012808 vapor phase Substances 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims 1
- 238000005336 cracking Methods 0.000 abstract description 14
- 239000005977 Ethylene Substances 0.000 abstract description 8
- -1 carbon olefin Chemical class 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract 2
- 238000002156 mixing Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 21
- 238000005516 engineering process Methods 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- 239000002808 molecular sieve Substances 0.000 description 5
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 238000010504 bond cleavage reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000004230 steam cracking Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention discloses a preparing method of propylene and ethylene through catalyzing and cracking carbon olefin, which comprises the following steps: adopting liquid phase raw material carbon olefin composition to exchange heat of cracking product; gasifying; preheating; heating through heating furnace to reacting temperature; exchanging heat for cracking product through blending with carbon olefin; condensing partially; separating partial C5 fraction; compressing residual cracking product to 1.0-4.0Mpa; transmitting to subsequent separating unit to separate further; obtaining propylene with density over 90-99%, ethylene with density at 90-99% and component over C4; fitting for industrial device to manufacture propylene and ethylene.
Description
Technical field
The present invention relates to a kind of method of producing propylene ethane by carbon-containing olefin catalytic cracking.
Background technology
Propylene, ethene are one of important basic Organic Chemicals.Propylene is mainly used in many products such as producing PP, isopropyl benzene, vinyl cyanide, vinylformic acid; Ethene is the main raw material of producing polyethylene (PE), polyvinyl chloride (PVC) and ethylene oxide/ethylene glycol important organic chemical industry's products such as (EO/EG).As important light olefin, propylene, ethene year demand in continuous growth.Hydrocarbon pyrolysis is still one of main method of producing ethene, but and the general overview of the technology of production propylene is byproduct technology and proprietary technology.Byproduct technology mainly is meant the propylene that obtains by steam cracking and catalytic cracking system ethylene unit.Proprietary technology refers to the technology of special Development and Production propylene, mainly contains Technologies such as dehydrogenating propane, low-carbon alkene disproportionation, low-carbon alkene cracking, preparing propylene from methanol at present.Low-carbon alkene cracking system propylene technology not only can be used for producing propylene, ethene, and can improve the added value of low-carbon alkene, has very big development prospect.The ultimate principle of low-carbon alkene preparing propylene by catalytic cracking technology is to utilize to have uniqueness and select type and tart ZSM-5 molecular sieve catalyst, selectively low-carbon alkene is cracked into propylene and ethene.
Document WO 2004096439 has been introduced a kind of technology of mixed olefins cracking system light olefin.This technology does not adopt shared material, and the raw material mixed olefins carries out scission reaction under the high-speed condition.This technology can obtain multiple light olefin, but very not high to propylene, selectivity of ethylene.
Document EP 109059 has been introduced a kind of C
4~C
12The technology of mixed olefins system propylene, ethene, this technology does not have shared material equally, and the raw material mixed olefins is directly greater than 50 hours
-1Weight space velocity under carry out scission reaction.This production technique is not very high to the selectivity of propylene, and to C
5The selectivity of above cut is on the contrary greater than 33%.
The described technology of above-mentioned document all is under the condition that does not need shared material mixed olefins to be carried out cracking, produces propylene and ethylene.Except scission reaction not high this shortcoming of selectivity to propylene, the both does not relate to the separation of split product, as technology independently, and all can't apparatus for establishing.
Summary of the invention
Technical problem to be solved by this invention is the independence and the not strong problem of combinableness of the not high and carbonaceous olefin cracking technology of carbonaceous olefin mixture added value in the conventional art, and a kind of method of new producing propylene ethane by carbon-containing olefin catalytic cracking is provided.This method has when carbonaceous olefin mixture carried out catalytic cracking reaction, can obtain the advantage of highly selective propylene, cracking of ethylene product; Simultaneously, this method increases separating step by split product is carried out condensation, compression, can obtain propylene, ethene that different purity requires, can not only improve self independence, and can combine with multiple device, improves economy.
In order to solve the problems of the technologies described above, the technical solution used in the present invention is as follows: a kind of method of producing propylene ethane by carbon-containing olefin catalytic cracking may further comprise the steps:
(1) gasification and preheating after liquid phase feed carbonaceous olefin and the split product heat exchange, and then be heated to 400~600 ℃, enter reactor and carry out catalytic cracking reaction;
(2) with the heat exchange of raw material carbonaceous olefin after split product, partial condensation enters knockout drum then again; Gas-liquid separation pot bottom cutting out partial liquid phase C
5Above cut after the vapor-phase thermal cracking product that obtains is compressed into 1.0~4.0MPa, enters first knockout tower in the knockout drum top portion;
(3) obtaining weight concentration at the first knockout tower cat head is 90~99% ethene, the C that obtains at the bottom of the tower
3Above cut is sent into second knockout tower;
(4) C that obtains at the second knockout tower cat head
3Cut enters the 3rd knockout tower; Obtain C at the bottom of the tower
4Above cut;
(5) at the 3rd knockout tower cat head for not coagulating gas, side line is extracted out and obtained weight concentration is 90~99% propylene, obtains weight concentration at the bottom of the tower and be 80~95% propane.
In the technique scheme, the carbon-contained alkene by catalytic cracking preferred catalyst is the shape-selective molecular sieve catalyzer; Reacting used liquid phase feed preferred version is C
4~C
8Carbonaceous olefin mixture; The reaction feed preferred version is heated to 450~550 ℃, enters reactor and carries out catalytic cracking reaction; The reactor preferred version is one or more snippets fixed-bed reactor; Reaction weight space velocity preferable range is 5~100 hours in the reactor
-1, more preferably scope is 5~50 hours
-1The reaction pressure preferable range is 0.02~0.3MPa in the reactor, and more preferably scope is 0.05~0.15MPa.The reaction product preferred version enters the first knockout tower stage casing for being compressed into 2.0~3.0MPa; First separates the C that obtains at the bottom of the Tata
3Above cut, preferred version is for sending into the second knockout tower stage casing; The second knockout tower preferred version is the C that cat head obtains
3Cut enters the 3rd knockout tower 1/4th places at the bottom of tower, the C that obtains at the bottom of the tower
422~76 weight % of above cut, preferable range is 30~66 weight %, circulation is as the catalytic pyrolysis raw material.The 3rd knockout tower preferred version is extracted out for the top of tower side line and is obtained propylene; First to the 3rd knockout tower preferred version is packing tower, tray column or valve tray column.The split product partial condensation, the temperature preferable range is 10~80 ℃ after the condensation, more preferably scope is 20~60 ℃.
Propylene that the inventive method obtains and ethene are no less than 52% of alkene total amount in the raw material.The first, the 3rd knockout tower obtains propylene, ethene respectively, and both purity can be optimized by the parameter of regulating knockout tower.If as self-contained system, the purity that then can regulate propylene, ethene is polymerization-grade; If be incorporated into preparing ethylene by steam cracking device, FCC apparatus and other propylene enhancing device such as preparing propylene from methanol device, then the propylene in present method, ethene purity can reduce, and carry out high precision by these main devices again and purify.Therefore, production technique of the present invention has very high independence, combinableness, has obtained better technical effect.
Description of drawings
Fig. 1 is the inventive method process flow diagram;
Fig. 2 is document EP 109059 process flow diagrams;
1 is the raw material carbonaceous olefin mixture among Fig. 1 or Fig. 2, and 2 is process furnace, and 3 is reactor, and 4 is feed exchanger, and 5 is fractional distillating tube, and 6 is gas-liquid separator, and 7 is compressor, and 8 is first knockout tower, and 9 is C
5Above cut, 10 gaseous ethene products, 11 is second knockout tower, and 12 is the 3rd knockout tower, and 13 is noncondensable gas, and 14 is the liquid propylene product, and 15 is propane, and 16 are the outer C of out-of-bounds
4Above cut, 17 are circulation C
4Above cut, 18 is C
2Following cut, 19 is C
3Cut, 20 is other cut, 21 is mixed C
4~C
8
Among Fig. 1, carbonaceous olefin mixture 1 and reactor split product are heated to temperature of reaction through process furnace 2 in interchanger 4 heat exchange after gasification, the preheating again.The reactor split product enters knockout drum 6 again after fractional distillating tube 5 partial condensations after interchanger 4 heat exchange.Gas-liquid separator 6 bottom liquid phases 9 are C
5Above cut.Enter first knockout tower 8 after compressed machine 7 compressions of gas-liquid separator 6 top gas phases, obtain the gaseous ethene 10 of different purity at the first knockout tower top, the bottom is C
3Above cut is sent into second knockout tower 11.At the second knockout tower top is C
3Cut is sent into the 3rd knockout tower 12; The bottom is C
4Above cut, portion C
4Above cut 17 is circulated to reactor 3 as cracking stock, and rest part 16 is sent out-of-bounds.The top of the 3rd knockout tower 12 is a noncondensable gas 13, and side line is extracted the liquid propylene 14 of different purity out, and the bottom is the liquid phase propane 15 of different purity.
The invention will be further elaborated below by embodiment.
Embodiment
[comparative example 1]
By shown in Figure 2, carbonaceous olefin mixture is formed (weight %) and is: iso-butylene: 45%, and Trimethylmethane: 55%.Adopt document EP 109059 technical process, weight hourly space velocity is 80 hours
-1, temperature of reaction is 575 ℃, reaction pressure is 0.05MPa, experimental results show that the product (weight %) that will obtain following ratio:
C
2Alkene: 0.11%
C
3Alkene: 23.3%
C
4:28.5%
C
5More than: 48.09%
[comparative example 2]
By shown in Figure 2, carbonaceous olefin mixture is formed (weight %) and is: iso-butylene: 45%, and Trimethylmethane: 55%.Adopt document EP 109059 technical process, weight hourly space velocity 60 hours
-1, temperature of reaction is 550 ℃, and reaction pressure is 0.15MPa, and evidence will obtain the product (weight %) of following ratio:
C
2Alkene: 0.07%
C
3Alkene: 34.11%
C
4:18.25%
C
5More than: 47.64%
[embodiment 1]
By shown in Figure 1, carbonaceous olefin mixture is formed (weight %) and is: iso-butylene: 45%, and Trimethylmethane: 55%.Adopt technical process of the present invention, catalyzer is the ZSM-5 molecular sieve of silica alumina ratio 200, and reactor is one section fixed-bed reactor, and the reaction weight hourly space velocity is 15 hours
-1, temperature of reaction is 450 ℃, and reaction pressure is 0.08MPa, and the temperature behind the fractional distillating tube 5 is 25 ℃, and split product is compressed into 1.5MPa, the C of 28 weight %
4Above cut circulation is as cracking stock, and the pilot plant proof will obtain the product (weight %) of following ratio:
Weight concentration is 90% ethene: 12.3%
Weight concentration is 92% propylene: 43.0%
Non-condensable gas: 0.08%
Weight concentration is 95% propane: 2.2%
C
4Above cut: 42.4%
[embodiment 2]
By shown in Figure 1, carbonaceous olefin mixture is formed with embodiment 1.Adopt technical process of the present invention, catalyzer is the ZSM-5 molecular sieve of silica alumina ratio 200, and reactor is one section fixed-bed reactor, and the reaction weight hourly space velocity is 60 hours
-1, temperature of reaction is 500 ℃, and reaction pressure is 0.15MPa, and the temperature behind the fractional distillating tube 5 is 45 ℃, and split product is compressed into 2.0MPa, the C of 48 weight %
4Above cut circulation will obtain the product (weight %) of following ratio as cracking stock:
Weight concentration is 95% ethene: 12.1%
Weight concentration is 96% propylene: 42.2%
Non-condensable gas: 0.06%
Weight concentration is 92% propane: 5.5%
C
4Above cut: 40.2%
[embodiment 3]
By shown in Figure 1, carbonaceous olefin mixture is formed with embodiment 1.Adopt technical process of the present invention, catalyzer is the ZSM-5 molecular sieve of silica alumina ratio 200, and reactor is one section fixed-bed reactor, and the reaction weight hourly space velocity is 100 hours
-1, temperature of reaction is 550 ℃, and reaction pressure is 0.30MPa, and the temperature behind the fractional distillating tube 5 is 55 ℃, and split product is compressed into 3.5MPa, and the above cut circulation of the C4 of 68 weight % will obtain the product (weight %) of following ratio as cracking stock:
Weight concentration is 98% ethene: 13.1%
Weight concentration is 99% propylene: 38.6%
Non-condensable gas: 0.05%
Weight concentration is 82% propane: 3.0%
C
4Above cut: 45.2%
Claims (10)
1, a kind of method of producing propylene ethane by carbon-containing olefin catalytic cracking may further comprise the steps:
(1) gasification and preheating after liquid phase feed carbonaceous olefin and the split product heat exchange, and then be heated to 400~600 ℃, enter reactor and carry out catalytic cracking reaction;
(2) with the heat exchange of raw material carbonaceous olefin after split product, partial condensation enters knockout drum then again; Gas-liquid separation pot bottom cutting out partial liquid phase C
5Above cut after the vapor-phase thermal cracking product that obtains is compressed into 1.0~4.0MPa, enters first knockout tower in the knockout drum top portion;
(3) obtaining weight concentration at the first knockout tower cat head is 90~99% ethene, the C that obtains at the bottom of the tower
3Above cut is sent into second knockout tower;
(4) C that obtains at the second knockout tower cat head
3Cut enters the 3rd knockout tower; Obtain C at the bottom of the tower
4Above cut;
(5) at the 3rd knockout tower cat head for not coagulating gas, side line is extracted out and obtained weight concentration is 90~99% propylene, obtains weight concentration at the bottom of the tower and be 80~95% propane.
2, according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1, it is characterized in that reacting used liquid phase feed is C
4~C
8Carbonaceous olefin mixture; Reaction feed is heated to 450~550 ℃, enters reactor and carries out catalytic cracking reaction; Reactor is one or more snippets fixed-bed reactor.
3,, it is characterized in that the reaction weight space velocity is 5~100 hours in the reactor according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1
-1, reaction pressure is 0.02~0.3MPa.
4,, it is characterized in that the reaction weight space velocity is 5~50 hours in the reactor according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 3
-1, reaction pressure is 0.05~0.15MPa.
5, according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1, it is characterized in that split product is compressed into 2.0~3.0MPa, enter the first knockout tower stage casing; First separates the C that obtains at the bottom of the Tata
3Above cut is sent into the second knockout tower stage casing; The C that the second knockout tower cat head obtains
3Cut enters the 3rd knockout tower 1/4th places at the bottom of tower, the C that obtains at the bottom of the tower
422~76 weight % circulation of above cut is as the catalytic pyrolysis raw material.
6,, it is characterized in that the 3rd knockout tower top side line extraction obtains propylene according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1.
7,, it is characterized in that first to the 3rd knockout tower is packing tower, tray column or valve tray column according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1.
8,, it is characterized in that obtaining C at the bottom of the 3rd separation Tata according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 5
430~66 weight % circulation of above cut is as the catalytic pyrolysis raw material.
9, according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 1, it is characterized in that the split product partial condensation, temperature is 10~80 ℃ after the condensation.
10, according to the method for the described producing propylene ethane by carbon-containing olefin catalytic cracking of claim 9, it is characterized in that the split product partial condensation, temperature is 20~60 ℃ after the condensation.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101545890B (en) * | 2009-04-16 | 2012-04-25 | 中国石油兰州石油化工公司 | Method for online determination of sec-butyl alcohol content in butene hydration product |
CN110526797A (en) * | 2018-05-24 | 2019-12-03 | 中国石油化工股份有限公司 | A kind of method and apparatus that steam cracking device depressurizes gasified raw material carbon four and recycles cooling capacity |
CN112694383A (en) * | 2019-10-22 | 2021-04-23 | 中国石油化工股份有限公司 | Method for producing ethylene and propylene by catalytic cracking of olefin |
-
2005
- 2005-11-11 CN CNB200510110293XA patent/CN100506760C/en active Active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101545890B (en) * | 2009-04-16 | 2012-04-25 | 中国石油兰州石油化工公司 | Method for online determination of sec-butyl alcohol content in butene hydration product |
CN110526797A (en) * | 2018-05-24 | 2019-12-03 | 中国石油化工股份有限公司 | A kind of method and apparatus that steam cracking device depressurizes gasified raw material carbon four and recycles cooling capacity |
CN110526797B (en) * | 2018-05-24 | 2021-12-14 | 中国石油化工股份有限公司 | Method and device for gasifying carbon four as raw material through decompression of steam cracking device and recovering cold energy |
CN112694383A (en) * | 2019-10-22 | 2021-04-23 | 中国石油化工股份有限公司 | Method for producing ethylene and propylene by catalytic cracking of olefin |
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