US2111900A - Process for the manufacture of ethylene from oil - Google Patents
Process for the manufacture of ethylene from oil Download PDFInfo
- Publication number
- US2111900A US2111900A US62932A US6293236A US2111900A US 2111900 A US2111900 A US 2111900A US 62932 A US62932 A US 62932A US 6293236 A US6293236 A US 6293236A US 2111900 A US2111900 A US 2111900A
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- US
- United States
- Prior art keywords
- oil
- ethylene
- hydrocarbons
- temperature
- yield
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title description 32
- 239000005977 Ethylene Substances 0.000 title description 31
- 238000000034 method Methods 0.000 title description 17
- 238000004519 manufacturing process Methods 0.000 title description 7
- 239000003921 oil Substances 0.000 description 35
- 229930195733 hydrocarbon Natural products 0.000 description 24
- 150000002430 hydrocarbons Chemical class 0.000 description 24
- 239000007789 gas Substances 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 16
- 238000007600 charging Methods 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 230000035939 shock Effects 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G9/34—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts
- C10G9/36—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/20—C2-C4 olefins
Definitions
- the subject matter of this invention. is a new method for producing et lene, a hydrocarbon gas C2H4 of the-olefin series, from liquid hydrocarbon mixtures of. the type found in petroleum, 5 in which new process the correlation of temperatures, reaction velocities and reaction periods of time produce yields of ethylene far in excess of the yields by the current methods of producing g ethylene from hydrocarbons.
- ethylene is a by-product i converting heavy oil' to gasoline by pyrolysis and the yield of ethylene, depending upon whether the liquid or the vapor phase methodoi cracking is employed, varies in" amounts up to approximate1y,6% by weight or the charging stock.
- the ethylene yield as above indicated is, only about 6%; in'the chemical industry the yield of liquids is in-theorder of 40% by weight of the;
- charging stock and the ethylene yield is in the order of v10% by weight 01' the charging'stock.
- the present invention provides a method wherein substantially all ofthe oil charging stock is converted to fixed gas of less than four carbon atoms, the major constituent at which is ethylene, the
- One of the objects of this invention is the production of ethylene as the primary'product of the operation in converting. substantially all of the charging stock to gases, the yield of condensible polymers being inhibited substantially to ex- 40 clusion.
- This operation is not of necessity an adjunct to oil refinery operations but can be convenientiy located wherever ethyleneis desired for use either directly or as a process material.
- Another object of this inventit in is the pro-'- duction oi'ethylene from liquid hydrocarbons, wherein Iv obtain a yield 01 ethylene as high as 45% by weight of the hydrocarbons charged,- my method providing for the flash system oracking oipreheated liquid hydrocarbons, the ethylenethus produced being preventedirom polymerizing .to heavier. hydrocarbons, thereby insuring the maximum yield of ethylene and the minimum yield of liquids.
- the oil to be processed is taken e from any suitable source ofsupply l and supplied 20 to thepressure preheater 2 at a pressure in the order of, for example, 20 atmospheres or higher pressure, flowing continuously through the preheater to the reaction zone '3.
- the oil' is preheated to a temper'aturein-the order of 850 F.
- preheated oil is continuously injected into the hotter reaction zone 3, flashing into vapor the 30 temperature of, the hotter reaction zone being so controlled that substantially all of the .oil
- vapor is converted tocthylene and hydrocarbons vof less than four carbonatoms at a temperature of in the order 021400" F.
- the hot gases are shock chilled to below 1000 F. preferably by means of water or steam injected as a continuous flow into the: gas
- the cooled gas flows to a fractional distillation unit which separates the ethylene irom the productsof pyrolysis, orthe ethylene by chemical reaction is separated as ethylene derivatives from" 50 the fixed gas.
- a fractional distillation unit which separates the ethylene irom the productsof pyrolysis, orthe ethylene by chemical reaction is separated as ethylene derivatives from" 50 the fixed gas.
- the liquid hydrocarbons used-as the charging I stock are-preferably gas oil and oils heavier than -The hot oil to be converted "toethylene and .55
- the temperature should not exceed 1600 F. because at such temperature ethylene decreases.
- the temperature ranges between 1300 F. and 1500 F. and the time varies in inverse relation to the temperature, preferably ranging from approximately one and one-half seconds to less than one-half second in order to obtain the optimum yield of ethylene.
- shock chilling may be made at different points along the length of the hot reaction zone cracking race 3 for the purpose of regulating the oil vapor heat treatment time before shock chilling takes place.
- the present invention provides a process for converting oil to a fixed gas of less than four carbon atoms, the major constituent of which is .ethylene, the process being such that substantially all of the oil is converted to the desired fixed gas.
- the process of producing ethylene from oil comprises preheating the oil under superatrnospheric pressure while maintaining the oil slightly below its vaporizing temperature at that pressure, injecting all of the preheated liquid oil into a flowing superheated condensible vapor which contains suflicient heat for heat exchange to the preheated oil to flash heat the preheated oil' to within the temperature range of 1300 F. to 1600 F., at which temperature all of the hydrocarbons of the oil are instantly decomposed to ethylene and hydrocarbons of not more than four carbon atoms, and immediately upon attaining this temperature shock cooling the gaseous mixture to below 1000 F. to exclude polymerizing reactions forming gasoline hydrocarbons and to retain the hydrocarbons as ethylene and hydrocarbons of not more than four carbon atoms.
- the process of producing ethylene from heavy oil comprises preheating the oil to a temperature in the order of 850 F. while subjected to superatmospheric pressure, controlling pressure and time conditions while preheating so that the oil remains in the liquid phase, injecting all of the preheated oil into a flowing superheated condensible vapor which contains suflicient heat for heat exchange to the preheated oil to flash heat the preheated oil to within the temperature range of'1300 F. to 1600 F., at which temperature all of the hydrocarbons of the oil are instantly decomposed to ethylene and hydrocarbons of not more than four carbon atoms, and immediately upon attaining this temperature shock cooling to below 1000 F. to exclude polymerizing reactions forming gasoline hydrocarbons and to retain the hydrocarbons as ethylene and hydrocarbons of not more than four carbon atoms.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
PROCESS *FOR .THE MANUFACTURE OF ETHYLENE FRoMoIL Filed F'eb. -8', 136
INVEN+0R ATTORNEYS Patented Mar; 22 .1938 1 umrap. ST T S PATENT crews 2,111,900 4 rnoonss FOR 'rnE MANUFACTURE or ETHYLENE mom on.
Theodore Nagei, N. Y. ,Applicationl 'ebrnary a, 19cc, Serial No. 62,932 *2 Claims." (01;. zoo-17o) The subject matter of this invention. is a new method for producing et lene, a hydrocarbon gas C2H4 of the-olefin series, from liquid hydrocarbon mixtures of. the type found in petroleum, 5 in which new process the correlation of temperatures, reaction velocities and reaction periods of time produce yields of ethylene far in excess of the yields by the current methods of producing g ethylene from hydrocarbons. I
In the oil industry ethylene is a by-product i converting heavy oil' to gasoline by pyrolysis and the yield of ethylene, depending upon whether the liquid or the vapor phase methodoi cracking is employed, varies in" amounts up to approximate1y,6% by weight or the charging stock.
In the'chemical'industry, in the operation dinoted to the production of ethylene from liquid hydrocarbons, a variation of the vapor phase method used in the ofl industry is employed.
1 In the oil industry the yield of liquids is in the order of 75% by weight of the charging stock and.
the ethylene yield as above indicated is, only about 6%; in'the chemical industry the yield of liquids is in-theorder of 40% by weight of the;
charging stock and the ethylene yield is in the order of v10% by weight 01' the charging'stock.
- As distinguished from these prior processea' the present invention provides a method wherein substantially all ofthe oil charging stock is converted to fixed gas of less than four carbon atoms, the major constituent at which is ethylene, the
yield of ethylene being substantially 45% by weight of the hydrocarbon content of the charg ing stock with practically no yield of condensate One of the objects of this invention is the production of ethylene as the primary'product of the operation in converting. substantially all of the charging stock to gases, the yield of condensible polymers being inhibited substantially to ex- 40 clusion. This operation is not of necessity an adjunct to oil refinery operations but can be convenientiy located wherever ethyleneis desired for use either directly or as a process material. i
Another object of this inventit in is the pro-'- duction oi'ethylene from liquid hydrocarbons, wherein Iv obtain a yield 01 ethylene as high as 45% by weight of the hydrocarbons charged,- my method providing for the flash system oracking oipreheated liquid hydrocarbons, the ethylenethus produced being preventedirom polymerizing .to heavier. hydrocarbons, thereby insuring the maximum yield of ethylene and the minimum yield of liquids.
My new process produces these novel results I from liquid hydrocarbons in acontinuous operation, the process comprising the operations ofpreheating the oil to a sufiiciently high-tempera-' j ture, while subj'ectedto suitable pressure and velocity so that uponflashing the preheated'oil chilled below the polymerizationdemperature 10 zone to practically exclude polymerization before a substantial amount of ethylene is polymer- In the accompanying drawing 1 have illustrated diagrammatically an embodiment of my linvention.
- -As an example of the practice of my invention for the production of ethylene from heavy oil.
charging stock: The oil to be processed is taken e from any suitable source ofsupply l and supplied 20 to thepressure preheater 2 at a pressure in the order of, for example, 20 atmospheres or higher pressure, flowing continuously through the preheater to the reaction zone '3. The oil'is preheated to a temper'aturein-the order of 850 F.
In the preheating step of my process'temperature and pressure conditions are so controlled that the oil remains inthe liquid. phase. The
preheated oil is continuously injected into the hotter reaction zone 3, flashing into vapor the 30 temperature of, the hotter reaction zone being so controlled that substantially all of the .oil
vapor is converted tocthylene and hydrocarbons vof less than four carbonatoms at a temperature of in the order 021400" F.
Before 'a substantial amount or ethylene is polymerized, the hot gases are shock chilled to below 1000 F. preferably by means of water or steam injected as a continuous flow into the: gas
' as indicated at 4 on the drawing, so as to practically exclude polymerization, thereby avoiding yield of a substantial quantity oi condensate, oil, tar, etc., i. e., not in'excess 01' 10% condensate by weight of the charging stock. -'I'hereby practically'all' the charging stock is converted by 45 pyrolysisto gas and maintained as a fixed gas.
The cooled gas flows to a fractional distillation unit which separates the ethylene irom the productsof pyrolysis, orthe ethylene by chemical reaction is separated as ethylene derivatives from" 50 the fixed gas. Y Y
The liquid hydrocarbons used-as the charging I stock are-preferably gas oil and oils heavier than -The hot oil to be converted "toethylene and .55
other gases of less than four carbon atoms is flashed into a hotter reaction zone, the source of the heat of this hotter reaction zone being a superheated condensiblejvaporor gas 5 as a heat carrying medium acting as a sweep gas flowing through the hot reaction zone or cracking race 3 into which the hot oil is flashed. Through convection by diffusion with the superheated condensible vapor or gas as for example superheated steam, practically all of the hot oil instantly attains a temperature that practically instantly gasifies substantially all of the hydrocarbons to less than four carbon atoms, and before a substantial amount of polymerization takes place the gases are shock chilled with a cool condensible vapor, water or steam 4, to practically exclude the formation of condensate oils, tar, etc. and retain practically all of the oil in the form of fixed gas.
In the example given above I have mentioned temperature in the order of 1400 F. with reference to the gas in the reaction zone. It is to be understood that with difierent charging stocks the temperature at which the reaction takes place and the time necessary to obtain the optimum yield of ethylene therefrom vary, but in any case the temperature should not be less than approximately 1200 F. andthe reaction time should not exceed approximately one and one-half seconds to avoid producing condensates. Furthermore, the
30 temperature should not exceed 1600 F. because at such temperature ethylene decreases. Preferably the temperature ranges between 1300 F. and 1500 F. and the time varies in inverse relation to the temperature, preferably ranging from approximately one and one-half seconds to less than one-half second in order to obtain the optimum yield of ethylene.
Several connections for shock chilling may be made at different points along the length of the hot reaction zone cracking race 3 for the purpose of regulating the oil vapor heat treatment time before shock chilling takes place.
When the condensible vapor used as the sweep gas in the reaction zone is superheated steam, before any substantial amount of said reactions between the steam and hydrocarbons takes place,
' the gases are shock chilled as hereinabove described, this shock chilling also practically inhibiting to exclusion such side reactions.
It will be seen from all of the foregoing that the present invention provides a process for converting oil to a fixed gas of less than four carbon atoms, the major constituent of which is .ethylene, the process being such that substantially all of the oil is converted to the desired fixed gas.
What I claim is:--
1. The process of producing ethylene from oil, which process comprises preheating the oil under superatrnospheric pressure while maintaining the oil slightly below its vaporizing temperature at that pressure, injecting all of the preheated liquid oil into a flowing superheated condensible vapor which contains suflicient heat for heat exchange to the preheated oil to flash heat the preheated oil' to within the temperature range of 1300 F. to 1600 F., at which temperature all of the hydrocarbons of the oil are instantly decomposed to ethylene and hydrocarbons of not more than four carbon atoms, and immediately upon attaining this temperature shock cooling the gaseous mixture to below 1000 F. to exclude polymerizing reactions forming gasoline hydrocarbons and to retain the hydrocarbons as ethylene and hydrocarbons of not more than four carbon atoms.
2. The process of producing ethylene from heavy oil, which process comprises preheating the oil to a temperature in the order of 850 F. while subjected to superatmospheric pressure, controlling pressure and time conditions while preheating so that the oil remains in the liquid phase, injecting all of the preheated oil into a flowing superheated condensible vapor which contains suflicient heat for heat exchange to the preheated oil to flash heat the preheated oil to within the temperature range of'1300 F. to 1600 F., at which temperature all of the hydrocarbons of the oil are instantly decomposed to ethylene and hydrocarbons of not more than four carbon atoms, and immediately upon attaining this temperature shock cooling to below 1000 F. to exclude polymerizing reactions forming gasoline hydrocarbons and to retain the hydrocarbons as ethylene and hydrocarbons of not more than four carbon atoms.
' THEODORE NAGEL
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62932A US2111900A (en) | 1936-02-08 | 1936-02-08 | Process for the manufacture of ethylene from oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62932A US2111900A (en) | 1936-02-08 | 1936-02-08 | Process for the manufacture of ethylene from oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2111900A true US2111900A (en) | 1938-03-22 |
Family
ID=22045797
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US62932A Expired - Lifetime US2111900A (en) | 1936-02-08 | 1936-02-08 | Process for the manufacture of ethylene from oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2111900A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2648875A (en) * | 1951-03-27 | 1953-08-18 | John D Gibson | Clearer tensioning device |
| US2889384A (en) * | 1954-11-11 | 1959-06-02 | Ici Ltd | Production of olefinic gases from hydrocarbon oils |
| US2926077A (en) * | 1955-05-02 | 1960-02-23 | Totzek Friedrich | Process of thermally cracking liquid hydrocarbons |
| US4479869A (en) * | 1983-12-14 | 1984-10-30 | The M. W. Kellogg Company | Flexible feed pyrolysis process |
| US4599480A (en) * | 1985-07-12 | 1986-07-08 | Shell Oil Company | Sequential cracking of hydrocarbons |
-
1936
- 1936-02-08 US US62932A patent/US2111900A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2648875A (en) * | 1951-03-27 | 1953-08-18 | John D Gibson | Clearer tensioning device |
| US2889384A (en) * | 1954-11-11 | 1959-06-02 | Ici Ltd | Production of olefinic gases from hydrocarbon oils |
| US2926077A (en) * | 1955-05-02 | 1960-02-23 | Totzek Friedrich | Process of thermally cracking liquid hydrocarbons |
| US4479869A (en) * | 1983-12-14 | 1984-10-30 | The M. W. Kellogg Company | Flexible feed pyrolysis process |
| US4599480A (en) * | 1985-07-12 | 1986-07-08 | Shell Oil Company | Sequential cracking of hydrocarbons |
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