[go: up one dir, main page]

US1891619A - Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series - Google Patents

Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series Download PDF

Info

Publication number
US1891619A
US1891619A US173253A US17325327A US1891619A US 1891619 A US1891619 A US 1891619A US 173253 A US173253 A US 173253A US 17325327 A US17325327 A US 17325327A US 1891619 A US1891619 A US 1891619A
Authority
US
United States
Prior art keywords
oil
metallic halide
action
carbo
reaction
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
US173253A
Inventor
Marvin L Chappell
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.)
Standard Oil Company of California
Original Assignee
Standard Oil Company of California
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 Standard Oil Company of California filed Critical Standard Oil Company of California
Priority to US173253A priority Critical patent/US1891619A/en
Application granted granted Critical
Publication of US1891619A publication Critical patent/US1891619A/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
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/02Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils characterised by the catalyst used
    • C10G11/08Halides

Definitions

  • This invention relates to the treatment of mineral oils, such as petroleum oil, with metallic halides, such as aluminum or ferric chloride.
  • the petroleum oil and metallic halide admixture is heated to a temperature of from 300 to 600 F.
  • a large percentage of the high boiling point unsaturated components of the petroleum oil are polymerized with the formation of tars.
  • the formation of such tars hinders, to a large extent, further reaction of the metallic halide on the oil and increases considerably the difficulty of securing proper contact with the metallic halide and the oil, thereby necessitating the employment of excessive amounts of a uminum chloride to treat the oil or resulting in the production of a small yield of gasoline or motor fuel.
  • the unsaturated high boiling point h drocarbons are also polymerized and are difficult to separate from the lubricating oil stock and, moreover, both increase the difiiculty of obtaining contact between the hydro carbon oil and metallic halide and also hinder the further action of the metallic halide on the oil by rendering said metallic halide less active.
  • the apparatus is indicated as in diagrammatic elevation and with certain parts in vertical section.
  • 2 indicates a reaction chamber preferably provided with some suitable heating means, being indicated as set over a furnace 3 provided With a burner 4.
  • 5 indicates a line having a valve 6, which line may be employed for introducing mineral or'petroleum oil into the reaction chamber 2.
  • the reaction chamber 2 is also provided with a line 7 controlled by a valve 8 for introducing chlorine into the reaction chamber 2, said line 7 preferably I
  • I have heremafter set forth an example of a process with a vapor withdrawal line 10, controlled by a valve 11, by which means petroleum vapors and unreacted chlorine or other products may be withdrawn from the reaction chamber 2 as desired.
  • the reaction chamber 2 is indicated as connected by a line 12 including a pump 13 to a second reaction chamber 14.
  • the re action chamber 14 is indicated as provided with an aluminum chloride charger 15 including the hopper 16 and spaced valves 17 and 18 by which solid metallic halide may be' introduced into the reaction chamber against the pressure employed therein.
  • the charger is also indicated as provided with a valve controlled line 19 by which metallic halide in liquid form may be introduced if desired.
  • the reaction chamber 14 is preferably provided with suitable heating means and for this purpose, is indicated as mounted over a furnace 20 having the burner 21.
  • Thereaction chamber 14 also preferably includes suitable means, such as the rotary agitator22 for agitating the contents of the reaction chamber.
  • 23 indicates a vapor line lead'ng from the reaction chamber 14 to a dcphlegmator or reflux tower 24.
  • the reflux tower 24 is provided at its lower end with a line 25 which may be utilized for assing reflux or condensed materials either y line 26, controlled by valve 27, back into reaction chamber 14 or through line 28, controlled by valve 29 to a receiver 30.
  • the receiver 30 is indicated as having a valve controlled draw-ofi line 31.
  • the dephlegmator 24 is preferably provided with a planer 32 having inlet and outlet passages 33 and 34 by means of which the temperature of the va ors discharged from the dephlegmator may e controlled. If desired, the oil either in line 5 or in line 12 may be pased through this planer.
  • the dephleginator is connected with a vapor withdrawal line 35 leading through a condenser 36 to a receiving tank 37 for the gasoline or other low boiling point oil reduced in the process.
  • Said receiving tan" 3? ⁇ is rovided with a valve controlled vent line 38 y means of which the pressure imposed upon the system may be controlled.
  • the reaction chamber 1% is also connected 1 with a residual withdrawal line 39 controlled lgy a valve 401 which line leads to a receiver 41 meters constituents.
  • the mineral hydrocarbon oil and chlorine which are continuously fed therein are maintained at a temperature ranging from approximately to 212 F. and suliicient chlorine is added to substantially combine with all of the unsaturated oils to form therefrom saturated chlorinated hydrocarbon compounds.
  • T he reaction is generally as indicated in the following equation, in which R indicates any hydrocarbon radical:
  • the partially chlorinated mineral or hydrocarbon oil which always contains a quantity of saturated mineral or hydrocarbon compounds which have not been chlorinated is continuously passed into reaction chamber 14 in which chamber it is subjected to reaction with a metallic halide, preferably aluminum chloride.
  • a metallic halide preferably aluminum chloride.
  • the temperature of the reaction in the reaction chamber 14 and the relative quantities of metallic halide and partially chlorinated mineral oil fed into the reaction chamber will depend upon the kind of reaction desired to effect in said reaction chamber.
  • the process of the presentinvention is of a vanta e in case it is desired to produce refined lu ricatin oil stock or other refined viscous stock andis also of advantage when it is'desired to conduct the metallic halide reaction to effect the catalytic decomposition of the oils into lower boiling point oils.
  • the partially chlorinated mineral oil is heated in reaction chamber 14 to a temperature ranging from 300 to 650 F.
  • the reaction is preferably conducted under a pressure above atmospheric, such as 20 pounds gage.
  • a metallic halide such as aluminum chloride, I prefer to employ around 0.2 to 0.8
  • the vaporsevolved in the reaction charm ber 14 are preferably passed to the dephlegmator 24 in which the motor fuel or naphtha is separated from the higher boiling point oils and passed from the dephlegmator together with the hydrogen chloride produced,
  • the hydrogen chloride gas is withdrawn from the vent line 38 and, of course, may be recovered in any preferred or suitable manner.
  • the condensed high boiling point oils with or without some vaporized and condensed metallic halide may be passed either from the dephlegmator 24 to receiver 30 for. a later separation or processing, or where it is desired to conduct the reaction to produce only naphthaor motor fuel and unrefined high boiling point oil, such condensed material from dephlegmator 24 may be passed to the evaporating chamber 14.
  • the process may be carried on mainly for the production of naphtha or mainly for the production of a refined viscous stock or for the simultaneous production of both naphtha and a refined viscous oil stock.
  • the quantity of metallic halide necessary for such refining or decomposition is materially reduced over that required where the metallic halide iscontacted with a normal mineral hydrocarbon oil iii-place of the chlorinated or partially chlorinated oil employed in the present process.
  • a process of converting mineral oils of relatively high boiling point into motor fuels, while a par-it of the oils are simultaneously polymerized into refined viscous oils which comprises first contacting the same with chlorine at a temperature sufiicient to chlorinate substantially only the unsaturated oils while separating the light petroleum vapors, and thereafter subjecting the liquid chlorinated mineral oils to reaction with a metallic halide at a temperature between 300 650 F., and at a pressure about seventy pounds per square inch above atmospheric.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (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

Dec. 20, 1932. CHAPPELL 1,891,619 PROCESS OF PRODUCING HYDROCARBON PRODUCTS BY THE ACTION OF A METALLIC HALIDE AND A PARTIALLY CHLORINATED MINERAL oIL OF THE CARBO-CYCLIC SERIES Filed'March 7. 1927 Patented Dec. 20, 1932 UNITED STATES PATENT OFFICE MARVIN L. CHAPPELL, 0F LOS ANGELES, CALIFORLIIA, .ASSIGNQR TO STANDARD OIL COMPANY OF CALIFORNIA, OF SAN FRANCISCO, CALIFORNIA, A CORPORATION OF DELAWARE PROCESS OF PRODUCING HYDROCARBON PRODUCTS BY THE ACTION OF A METALLIC HALIDE AND A PARTIALLY CHLORINATIEI) MINERAL OIL OF ZIH'E CARBO-CYCLIC SERIES Application filed March 7,
This invention relates to the treatment of mineral oils, such as petroleum oil, with metallic halides, such as aluminum or ferric chloride.
In the conventional method of reaction upon petroleum oils by metallic halides, such as aluminum chloride, the petroleum oil and metallic halide admixture is heated to a temperature of from 300 to 600 F. Particularly when the process is carried out for the production of gasoline or motor fuel, a large percentage of the high boiling point unsaturated components of the petroleum oil are polymerized with the formation of tars. The formation of such tars hinders, to a large extent, further reaction of the metallic halide on the oil and increases considerably the difficulty of securing proper contact with the metallic halide and the oil, thereby necessitating the employment of excessive amounts of a uminum chloride to treat the oil or resulting in the production of a small yield of gasoline or motor fuel.
Furthermore, when hydrocarbon oil is subjected to the action of metallic halides for the purpose of refining the oil for the production, for example, of high grade lubricating oils, the unsaturated high boiling point h drocarbons are also polymerized and are difficult to separate from the lubricating oil stock and, moreover, both increase the difiiculty of obtaining contact between the hydro carbon oil and metallic halide and also hinder the further action of the metallic halide on the oil by rendering said metallic halide less active.
I have discovered that this tar formation can be decreased and a higher percentage of motor fuel or refined oil produced by first treating the mineral or petroleum oil to be processed with chlorine under conditions to form with the unsaturated compounds of the oil, a partially chlorinated or addition product. Such a reaction has been found to proceed when such mineral or petroleum oils are treated with chlorine at a temperature ranging approximately from to 212 F. Under such conditions, suflicient chlorine combines with the unsaturated oils of the mineral oil body to form substantially satu- 1927. Serial No. 173,253.
rated chlorinated hydrocarbons. When such partially chlorinated mineral or petroleum is thereafter subjected to reaction With metallic halide, particularly in the presence of nonchlorinated compounds of saturated nature, they may be refined to produce a high grade lubricating stock with a minimum production of tar and with great efliciency insofar as the consumption of aluminum chloride is concerned.
Moreover, when such partially chlorinated mineral or hydrocarbon oils are treated with a metallic halide, particularly in the presence of non-chlorinated saturated oil at temperatures ranging from 300 to 650 F., and preferably under evolved pressure of about 20 pounds per square inch gage, a high yield of gasoline or motor fuel may beobtained with a low production of tar and a low consumption of metallic halide.
form or example of a process which embodies the 1nvent:on.
which embodies the invention. The process is described in connection with the accompanying drawing, Which illustrates diagrammatically an apparatus suitable for conducting the process.
In the drawing:
The apparatus is indicated as in diagrammatic elevation and with certain parts in vertical section.
Referring to the drawing, 2 indicates a reaction chamber preferably provided with some suitable heating means, being indicated as set over a furnace 3 provided With a burner 4. 5 indicates a line having a valve 6, which line may be employed for introducing mineral or'petroleum oil into the reaction chamber 2. The reaction chamber 2 is also provided with a line 7 controlled by a valve 8 for introducing chlorine into the reaction chamber 2, said line 7 preferably I For this purpose, I have heremafter set forth an example of a process with a vapor withdrawal line 10, controlled by a valve 11, by which means petroleum vapors and unreacted chlorine or other products may be withdrawn from the reaction chamber 2 as desired.
The reaction chamber 2 is indicated as connected by a line 12 including a pump 13 to a second reaction chamber 14. The re action chamber 14 is indicated as provided with an aluminum chloride charger 15 including the hopper 16 and spaced valves 17 and 18 by which solid metallic halide may be' introduced into the reaction chamber against the pressure employed therein. The charger is also indicated as provided with a valve controlled line 19 by which metallic halide in liquid form may be introduced if desired.
The reaction chamber 14 is preferably provided with suitable heating means and for this purpose, is indicated as mounted over a furnace 20 having the burner 21. Thereaction chamber 14 also preferably includes suitable means, such as the rotary agitator22 for agitating the contents of the reaction chamber. 23 indicates a vapor line lead'ng from the reaction chamber 14 to a dcphlegmator or reflux tower 24.
The reflux tower 24 is provided at its lower end with a line 25 which may be utilized for assing reflux or condensed materials either y line 26, controlled by valve 27, back into reaction chamber 14 or through line 28, controlled by valve 29 to a receiver 30. The receiver 30 is indicated as having a valve controlled draw-ofi line 31.
The dephlegmator 24 is preferably provided with a planer 32 having inlet and outlet passages 33 and 34 by means of which the temperature of the va ors discharged from the dephlegmator may e controlled. If desired, the oil either in line 5 or in line 12 may be pased through this planer. The dephleginator is connected with a vapor withdrawal line 35 leading through a condenser 36 to a receiving tank 37 for the gasoline or other low boiling point oil reduced in the process. Said receiving tan" 3?} is rovided with a valve controlled vent line 38 y means of which the pressure imposed upon the system may be controlled.
The reaction chamber 1% is also connected 1 with a residual withdrawal line 39 controlled lgy a valve 401 which line leads to a receiver 41 meters constituents. Within the reaction chamber 2, the mineral hydrocarbon oil and chlorine which are continuously fed therein are maintained at a temperature ranging from approximately to 212 F. and suliicient chlorine is added to substantially combine with all of the unsaturated oils to form therefrom saturated chlorinated hydrocarbon compounds. T he reaction is generally as indicated in the following equation, in which R indicates any hydrocarbon radical:
n H n n .aaamaaaas Upon certain mineral or hydrocarbon oils, a considerable portion of the chlorine fed into the reaction chamber 2 will not react with the oilsfupona single passage through the body of oils and it is understood that the same is then merely recirculated through'the body of the oil to secure eilicient use of the chlorine.
The partially chlorinated mineral or hydrocarbon oil which always contains a quantity of saturated mineral or hydrocarbon compounds which have not been chlorinated is continuously passed into reaction chamber 14 in which chamber it is subjected to reaction with a metallic halide, preferably aluminum chloride. The temperature of the reaction in the reaction chamber 14 and the relative quantities of metallic halide and partially chlorinated mineral oil fed into the reaction chamber will depend upon the kind of reaction desired to effect in said reaction chamber. The process of the presentinvention is of a vanta e in case it is desired to produce refined lu ricatin oil stock or other refined viscous stock andis also of advantage when it is'desired to conduct the metallic halide reaction to effect the catalytic decomposition of the oils into lower boiling point oils. In case a catailiytic decomposition reaction is desired to be e ected, the partially chlorinated mineral oil is heated in reaction chamber 14 to a temperature ranging from 300 to 650 F. The reaction is preferably conducted under a pressure above atmospheric, such as 20 pounds gage. As an example of suitable proportions of a metallic halide, such as aluminum chloride, I prefer to employ around 0.2 to 0.8
pounds of aluminum chloride per gallon of oil to be treated.
In case alubricating stock only is desired, a smaller amount of the metallic halide or aluminum chloride is used and a lower temperature range is generally employed. For
' LBQLMQ In case the higher temperaturesare em-.
ployed to produce motor fuel, a further reaction proceeds between the hydrocarbon formed and the metallic halide, such as indicated by the following equation:
residuum The vaporsevolved in the reaction charm ber 14 are preferably passed to the dephlegmator 24 in which the motor fuel or naphtha is separated from the higher boiling point oils and passed from the dephlegmator together with the hydrogen chloride produced,
the naphtha being condensed in the condenser 36v and collected in the receiving tank 3?. The hydrogen chloride gas is withdrawn from the vent line 38 and, of course, may be recovered in any preferred or suitable manner.
The condensed high boiling point oils with or without some vaporized and condensed metallic halide may be passed either from the dephlegmator 24 to receiver 30 for. a later separation or processing, or where it is desired to conduct the reaction to produce only naphthaor motor fuel and unrefined high boiling point oil, such condensed material from dephlegmator 24 may be passed to the evaporating chamber 14.
It will thus be seen that the process may be carried on mainly for the production of naphtha or mainly for the production of a refined viscous stock or for the simultaneous production of both naphtha and a refined viscous oil stock. In any case, the quantity of metallic halide necessary for such refining or decomposition is materially reduced over that required where the metallic halide iscontacted with a normal mineral hydrocarbon oil iii-place of the chlorinated or partially chlorinated oil employed in the present process.
It may be advantageous to employ pressures below atmospheric in certain cases, particularly when the process is being run for the production of lubricating stock.
\Vhile the process herein described is well adapted for carrying out the objects of the present invention, it is understood that numerous modifications may be made and all such modifications come withinthe scope of the following claim.
I claim:
.A process of converting mineral oils of relatively high boiling point into motor fuels, while a par-it of the oils are simultaneously polymerized into refined viscous oils which comprises first contacting the same with chlorine at a temperature sufiicient to chlorinate substantially only the unsaturated oils while separating the light petroleum vapors, and thereafter subjecting the liquid chlorinated mineral oils to reaction with a metallic halide at a temperature between 300 650 F., and at a pressure about seventy pounds per square inch above atmospheric.
Signed at Los Angeles this 28 day of Feb ruary, 1927.
MARVIN L. CHAPPELL.
CERTIFICATE OF CORRECTION Patent No. 1,891,619. December 20, 1932.
MARVIN L. GHAPPELL.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as fellows: Page 3, line 86, the claim, for "seventy" read "twenty"; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 16th day of May, A. D. 1933.
' (go (Seal) Acting 'G-ornn'sissiener of Patents.
US173253A 1927-03-07 1927-03-07 Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series Expired - Lifetime US1891619A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US173253A US1891619A (en) 1927-03-07 1927-03-07 Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US173253A US1891619A (en) 1927-03-07 1927-03-07 Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series

Publications (1)

Publication Number Publication Date
US1891619A true US1891619A (en) 1932-12-20

Family

ID=22631192

Family Applications (1)

Application Number Title Priority Date Filing Date
US173253A Expired - Lifetime US1891619A (en) 1927-03-07 1927-03-07 Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series

Country Status (1)

Country Link
US (1) US1891619A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2457457A (en) * 1942-02-13 1948-12-28 Alais & Froges & Camarque Cie Methods for treating bituminous shales

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2457457A (en) * 1942-02-13 1948-12-28 Alais & Froges & Camarque Cie Methods for treating bituminous shales

Similar Documents

Publication Publication Date Title
US1891619A (en) Process of producing hydrocarbon products by the action of a metallic halide and a partially chlorinated mineral oil of the carbo-cyclic series
US1944236A (en) Process for simultaneously producing high grade motor fuels and lubricants from heavy hydrocarbons by the action of hydrogen
US1940725A (en) Process for treating carbonaceous material
US1893774A (en) Process of manufacturing lubricating oil
US1872446A (en) Process of producing low boiling point oils or motor fuel from hydrocarbon oils by the employment of metallic halides
US1681321A (en) Process and apparatus for treating oil
US1869799A (en) Process of converting heavy hydrocarbons
US1881901A (en) Process for the treatment of hydrocarbon oils with aluminum chloride
US1745155A (en) Asphalt and road oil and process of producing the same
US1878262A (en) Process of treating hydrocarbons with alpha chlorinated hydrocarbon in the presence of alpha metallic halide
US1835280A (en) Process of treating petroleum oil to produce low boiling point oil
US2377107A (en) Chemical process
US1974301A (en) Treatment of hydrocarbon oils
US1936539A (en) Process of continuously treating hydrocarbon products
US2173376A (en) Catalyst
US1803670A (en) Process of treating hydrocarbon oil with metallic halides
US1825270A (en) Treating hydrocarbons
US1811257A (en) Method of producing motor fuel or gasoline from petroleum oil
US1692203A (en) Process of treating hydrocarbons
US1823967A (en) Process of producing naphtha from hydrocarbon oils
US1606246A (en) Process of treating hydrocarbons
US1756153A (en) Manufacture of lubricating oils
US2066685A (en) Process of recovering sulphuric acid from separated sludge acid
US1950721A (en) Treatment of hydrocarbon oils
US1936633A (en) Continuous process of treating hydrocarbon products