US2111900A - Process for the manufacture of ethylene from oil - Google Patents

Process for the manufacture of ethylene from oil Download PDF

Info

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
Authority
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.)
Expired - Lifetime
Application number
US62932A
Inventor
Nagel Theodore
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US62932A priority Critical patent/US2111900A/en
Application granted granted Critical
Publication of US2111900A publication Critical patent/US2111900A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/34Thermal 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
    • C10G9/36Thermal 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/20C2-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.

Landscapes

  • 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
US62932A 1936-02-08 1936-02-08 Process for the manufacture of ethylene from oil Expired - Lifetime US2111900A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (5)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US2378067A (en) Process of cracking petroleum
US2904502A (en) Method of cracking hydrocarbons
US2111900A (en) Process for the manufacture of ethylene from oil
US2656307A (en) Conversion of hydrocarbon materials
US3353920A (en) High severity pyrolysis apparatus
US2176962A (en) Process for producing ethylene from oil
US1613010A (en) Conversion process
US2111899A (en) Process for the manufacture of ethylene from oil
US2899475A (en) Thermal cracking process with an improved
GB479438A (en) Improvements in the production of acetylene
US2147399A (en) Process for cracking hydrocarbons
US2431485A (en) Process for converting hydrocarbons
US1893774A (en) Process of manufacturing lubricating oil
US1659930A (en) Combined distilling and cracking process and apparatus therefor
US3576734A (en) Process for production of synthetic crude oil from low temperature coal tars
US2358912A (en) Conversion of hydrocarbons
US2097489A (en) Process of gasifying oils and coals
US2391117A (en) Process for the production of butadiene
US2233951A (en) Process of producing low boiling hydrocarbons
US1963264A (en) Conversion of hydrocarbon oil
US2913504A (en) Vapor phase cracking of cyclopentadiene dimer
US1830963A (en) Distilling petroleum residuum
US1974683A (en) Process of cracking hydrocarbon oil
US1946739A (en) Process of treating hydrocarbons to produce carbon black
US2045255A (en) Manufacture of unsaturated hydrocarbons