US2079158A - Treatment of hydrocarbon oils - Google Patents

Treatment of hydrocarbon oils Download PDF

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US2079158A
US2079158A US498650A US49865030A US2079158A US 2079158 A US2079158 A US 2079158A US 498650 A US498650 A US 498650A US 49865030 A US49865030 A US 49865030A US 2079158 A US2079158 A US 2079158A
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Rachat Nicholas G De
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Universal Oil Products Co
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Universal Oil Products Co
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    • 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
    • C10G25/00Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents

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  • This invention relates to the treatment of hydrocarbon oils and particularly reiersl tothe treatment of oils such as distillates, lubricating oils and the like, with adsorbent materials such 5 as clay or otheradsorbent earths, to improve the quality of the oil.
  • the principles of the present invention are applicable to the treatment of many oils, and in the present embodiment are particularly directed to the treatment of distillates such as straight run or cracked products containin'g'motor fuel, end point distillates, either cracked or straight run, such as gasoline, kerosene, naphtha and the like, and'lubricating oils.
  • distillates such as straight run or cracked products containin'g'motor fuel, end point distillates, either cracked or straight run, such as gasoline, kerosene, naphtha and the like, and'lubricating oils.
  • the distillate to be treated which in this case may fall within the boiling range of commercial motor fuel, may be supplied directly from the fractionato'r of a cracking system, not shown, through lines I and 2 and valve 3, to treater 4. Allor any desired portion of the distillate vapors may, however, be directed through valve 5 in line I to heating element 6, disposed within any suitable furnace,
  • heatingelement B passes from storage or elsewhere in -a' -liuuid' state it is preferably directed through,., he'ating to enact its complete or substantial ya before it is introduced into treater l 1 eat '1 4 may comprise a'cylindricai shell ll,
  • distillate to be reated element I in the manner hereinbefore zation thereon and extends through the upper head of treater 4, through a suitable stumng box I4 and, during the operation of the process, is driven at a relatively high rate 'of speed by any suitable means such as an electric motor l5.
  • Perforated bafiies or deflectors l6 may be conical in shape and extend from the shell In of the treater to its central portion, terminating in openings ll through which shaft l2 extends.
  • the treating agent in this case adsorbent clay, may be introduced into the treater from hopper l8 by means of helical conveyor l9 and through line 20.
  • a bed of the treating material may be maintained within conveyor l8 and hopper 18 to serve as a seal, preventing the escape of vapors from the zone of treatment or, especially when it is desirable to operate under a substantial super-atmospheric pressure, any other well known means of introducing the treating material and, at the same time, preventing the escape of vapors may beemployed;
  • the adsorbent clay may be introduced into the upper portion of treater 4 to the uppermost of the battles l6, which directs said material to the central portion of the uppermost disc I3.
  • Said disc' may be rapidly rotated and may hurl the clay, in a finely dispersed state, into the body of vapors passing through the treater.
  • the finely dispersed clay may be collected upon the next lower baflle l6 and may be directed to another rapidly rotating disc l3 where it is again dispersed.
  • a deflector l6 and a rapidly rotating disc l3, arranged'as illustrated, comprise one treating stage or step and, any desired numberof said stages or steps may be employed, depending upon the material undergoing treatment and the results desired.
  • the vapors to be treated,v entering treater .4 through line 2 are preferably discharged beneath a deflector 2
  • the vapors may.
  • the slope of the ballles may be greater than the angle of repose of the adsorbentclay andmay be of sum-Q cient' magnitude to allow the clay," together with any-adsorbed oil and reflux condensate to flow downwardly over-the upper-surface of the battles to the rapidly rotating disc of the next lower step and thus continuously downwardly through the zone of treatment substantially countercurrent to the vapors undergoing treatment.
  • the vapors may be contacted in the succeeding treating stages with the adsorbent material in a finely dispersed form and by means of the perforated bailies It the vapors undergoing treatment may successively be contacted with moving beds of the adsorbent treating agent.
  • positive contact is effected between the hydrocarbon vapors and the treating agent insuring efficient treatmentregulated inv extent by the number of treating stages employed, the speed of rotation of discs l3, the relative sizes of the various component parts of the treating zone, the temperature of the vapors, and the pressure conditions maintained within'the treater.
  • Stages comprising bailles l6 and discs I3 may, if desired, be provided below the inlet of the vapors to the treating zone. Three such stages are here illustrated, although any desired number may be employed, or this phase of the treatment may, if desired, be eliminated.
  • the purpose of these lower treating stages is to substantially devolatilize the spent treating material and, to assist in this devolatilization, steam, preferably in a superheated state may be introduced as illustrated, through line 23 controlled by valve 24.
  • the treating material may come in contact with the steam in the lower stages of the treating zone in the same manner as it is contacted with hydrocarbon vapors in the upper stages of the treating zone.
  • Another means of drying and assisting devolatilization of the spent clay comprises a steam jacket 25 which may surround the lower portion of treater 4, steam being introduced through line 26 and valve 21 and exhausted through line 28 controlled by valve 29.
  • the methods here illustrated and described, or any other suitable well known means of substantially drying the clay may be utilized separately or Jointly.
  • the spent treating material may be removed by means of screw conveyor 30 actuated by any suitable means, not illustrated, through gears 3i.
  • Conveyor 30 may also furnish a means of maintaining a seal at the point of discharge of the spent treating agent from the treater by maintaining a body of the clay within the conveyor or any other well known means of removing the spent treating material and preventing leakage at this point may be employed.
  • Hydrocarbons driven from the treating material by the drying and devolatilizing action may be removed as vapors from the treater together with the steam, if used in direct contact, through line and valve 38. These volatilized hydrocarbons may however, be collected as liquid, together with any reflux condensate from the vapors undergoing treatment which are not entrained in the treating material upon deck 31 and may be removed from the treater through line 38 and valve 33.
  • the treated vapors may be removed from the upper portion of treater 4 through line 32 controlled by valve 33 and may be passed to any desired further treatment such as fractionation or passed directly, after condensation and cooling, to storage.
  • the pressures employed within the treating system may range fromsubatmospheric to substantial superatmospheric pressures of several hundred pounds per square inch. Heating of the oil. to betreated, if employed, may be accomplished under any desired pressure conditions. Temperatures-employed within the treating zone will depend upon the oil undergoing treatment and the desired results and may range, for example, from a temperature suflicient only to substantially vaporize the oil to temperatures as high'as 800 F., or thereabouts. Preferably, the oil is introduced to the treater at a temperature sufllcient to maintain its components which boil 'within the range of the finished product in a vaporized state throughout the treatment, permitting withdrawal of the treated product as vapors.
  • vapors are taken directly from the fracticnator of a cracking system at a temperature of about 375 F., and before their introduction into the treater are superheated to a temperature of approximately 500 F. under a superatmospheric pressure of about 60 pounds per square inch.
  • the hot vapors are contacted in successive stages of the treating zone with an adsorbent clay of about 60 mesh under substantially atmospheric pressure and the treated vapors are condensed and cooled without redistillation or further chemical treatment. This treatment produces a sweet, color stable motor fuel of low gum and low sulphur content.
  • Thetreating loss is often less than 2%, based on the vapors treated, and a ton of clay may treat some 2500 to 3000 barrels of distillate and in some cases as high as 10,000 barrels, depending largely upon the-refining required by the raw or untreated vapors.
  • a process of treating hydrocarbon oils to remove objectionable constituents therefrom which comprises introducing said oils into a treatingzone in a substantially vaporous state, passing said vapors in a substantially vertical direction upwardly through said zone introducing absorbent material into said zone and centrifugally hurling said material in stages radially from the center of said zone into intimate contact with the vapors and devolitalizing the spent absorbent material beforeremoval from said treating zone.
  • a continuous process of intimately contacting vapors and an absorbent material and devolatilizing spent absorbent material which comprises introducing said vapors into the intermediate portion of an enclosed zone, introducing steam into the lower portion of said zone, introducing absorbent material into the upperportion of said zone, and centrifugally hurling 1d material in stages radially from the center of said zone into the ascending vapors and the steam.
  • a continuous process of intimately contact ing vapors and an absorbent material and devolatilizing spent absorbent material which comprises introducing said vapors into the interme dlate portion of an enclosed zone, introducing steam into the lower portion of said zone, introducing absorbent material into the upper por-

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  • 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)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

May 4, 1937. N. a. DE RACHAT 2,079,15fi
TREATMENT OF HYDROCARBON OILS Filed Nov.28, 1930 Patented May 4, 1937 UNITED 1 STATES 2,079,158 TREATMENT or nrnaoesnnori oms Nicholas G. de Rachat,
Chicago, 111., assignor, by
mesne assignments, to Universal Oil Products Company, Chicago, 111., a corporation of Delaware Application November 28, 1930, Serial No. 498,650
3 Claims.
This invention relates to the treatment of hydrocarbon oils and particularly reiersl tothe treatment of oils such as distillates, lubricating oils and the like, with adsorbent materials such 5 as clay or otheradsorbent earths, to improve the quality of the oil.
The principles of the present invention-are applicable to the treatment of many oils, and in the present embodiment are particularly directed to the treatment of distillates such as straight run or cracked products containin'g'motor fuel, end point distillates, either cracked or straight run, such as gasoline, kerosene, naphtha and the like, and'lubricating oils.
The principles of the invention as adapted to the treatment of a cracked distillate of motor fuel boiling range are shown in the attached diagrammatic drawing, which will serve to more clearly illustrate the features and novelty of the invention, although it should be understood that the invention is not limited to the use of the apparatus illustrated nor to the treatment of any specific type of oil. The invention is, rather, di-
rected to an improved method and means of continuously treating hydrocarbon oils with adsorbent materials by dispersing said adsorbent material throughout the body of the oil, preferably 1 maintained in a vaporized state, said dispersion Referring now to the drawing, the distillate to be treated, which in this case may fall within the boiling range of commercial motor fuel, may be supplied directly from the fractionato'r of a cracking system, not shown, through lines I and 2 and valve 3, to treater 4. Allor any desired portion of the distillate vapors may, however, be directed through valve 5 in line I to heating element 6, disposed within any suitable furnace,
setting 'I,- to increase their temperature to any desired degree, passing from heatingelement B is supplied from storage or elsewhere in -a' -liuuid' state it is preferably directed through,., he'ating to enact its complete or substantial ya before it is introduced into treater l 1 eat '1 4 may comprise a'cylindricai shell ll,
preferably insulated as indicated at l'l Shaft being effected by means of one or a plurality of through line 8 and valve 9 to line 2, midi-thence. to treater 4. In case the distillate to be reated element I in the manner hereinbefore zation thereon and extends through the upper head of treater 4, through a suitable stumng box I4 and, during the operation of the process, is driven at a relatively high rate 'of speed by any suitable means such as an electric motor l5. Perforated bafiies or deflectors l6 may be conical in shape and extend from the shell In of the treater to its central portion, terminating in openings ll through which shaft l2 extends. i
The treating agent, in this case adsorbent clay, may be introduced into the treater from hopper l8 by means of helical conveyor l9 and through line 20. A bed of the treating material may be maintained within conveyor l8 and hopper 18 to serve as a seal, preventing the escape of vapors from the zone of treatment or, especially when it is desirable to operate under a substantial super-atmospheric pressure, any other well known means of introducing the treating material and, at the same time, preventing the escape of vapors may beemployed;
The adsorbent clay may be introduced into the upper portion of treater 4 to the uppermost of the battles l6, which directs said material to the central portion of the uppermost disc I3. Said disc'may be rapidly rotated and may hurl the clay, in a finely dispersed state, into the body of vapors passing through the treater. The finely dispersed clay may be collected upon the next lower baflle l6 and may be directed to another rapidly rotating disc l3 where it is again dispersed. A deflector l6 and a rapidly rotating disc l3, arranged'as illustrated, comprise one treating stage or step and, any desired numberof said stages or steps may be employed, depending upon the material undergoing treatment and the results desired. The vapors to be treated,v entering treater .4 through line 2, are preferably discharged beneath a deflector 2|, which may distribute the vapors and prevent clay from lodging within line 2 and restricting the flow of vapors. The vapors may.
pass upward through the several treating stages,- in each of which they are intimately commingled with theadsorbent clay-as it is dispersed through-- put their mass, as hereinbefore described, by means of rapidly rotating discs l3. Barnes It may be provided with perforations 22 H ndi with screens 34 of somewhat smaller mesh than the size of the adsorbent clay. The slope of the ballles may be greater than the angle of repose of the adsorbentclay andmay be of sum-Q cient' magnitude to allow the clay," together with any-adsorbed oil and reflux condensate to flow downwardly over-the upper-surface of the battles to the rapidly rotating disc of the next lower step and thus continuously downwardly through the zone of treatment substantially countercurrent to the vapors undergoing treatment.
By means of the action of the discs It the vapors may be contacted in the succeeding treating stages with the adsorbent material in a finely dispersed form and by means of the perforated bailies It the vapors undergoing treatment may successively be contacted with moving beds of the adsorbent treating agent. In this manner positive contact is effected between the hydrocarbon vapors and the treating agent insuring efficient treatmentregulated inv extent by the number of treating stages employed, the speed of rotation of discs l3, the relative sizes of the various component parts of the treating zone, the temperature of the vapors, and the pressure conditions maintained within'the treater. It is evident that these variables render the treating process very flexible and insure the eflicient treatment of oils which vary widely in characteristics, also a wide variety of treating agents is permitted, such as, for example, adsorbent clay, diatomaceous earths, iullers earth, bentonite and similar materials.
Stages comprising bailles l6 and discs I3 may, if desired, be provided below the inlet of the vapors to the treating zone. Three such stages are here illustrated, although any desired number may be employed, or this phase of the treatment may, if desired, be eliminated. The purpose of these lower treating stages is to substantially devolatilize the spent treating material and, to assist in this devolatilization, steam, preferably in a superheated state may be introduced as illustrated, through line 23 controlled by valve 24. The treating material may come in contact with the steam in the lower stages of the treating zone in the same manner as it is contacted with hydrocarbon vapors in the upper stages of the treating zone.
Another means of drying and assisting devolatilization of the spent clay comprises a steam jacket 25 which may surround the lower portion of treater 4, steam being introduced through line 26 and valve 21 and exhausted through line 28 controlled by valve 29. The methods here illustrated and described, or any other suitable well known means of substantially drying the clay may be utilized separately or Jointly.
The spent treating material may be removed by means of screw conveyor 30 actuated by any suitable means, not illustrated, through gears 3i. Conveyor 30 may also furnish a means of maintaining a seal at the point of discharge of the spent treating agent from the treater by maintaining a body of the clay within the conveyor or any other well known means of removing the spent treating material and preventing leakage at this point may be employed.
Hydrocarbons driven from the treating material by the drying and devolatilizing action may be removed as vapors from the treater together with the steam, if used in direct contact, through line and valve 38. These volatilized hydrocarbons may however, be collected as liquid, together with any reflux condensate from the vapors undergoing treatment which are not entrained in the treating material upon deck 31 and may be removed from the treater through line 38 and valve 33.
If steam is used as described in the lower stages of the treater it may be permitted to commingle with the hydrocarbon vapors in the upper stages of the treater assisting in the treatment and often resulting in the production of a sweeter and more stable final product. I
The treated vapors may be removed from the upper portion of treater 4 through line 32 controlled by valve 33 and may be passed to any desired further treatment such as fractionation or passed directly, after condensation and cooling, to storage. I
The pressures employed within the treating system may range fromsubatmospheric to substantial superatmospheric pressures of several hundred pounds per square inch. Heating of the oil. to betreated, if employed, may be accomplished under any desired pressure conditions. Temperatures-employed within the treating zone will depend upon the oil undergoing treatment and the desired results and may range, for example, from a temperature suflicient only to substantially vaporize the oil to temperatures as high'as 800 F., or thereabouts. Preferably, the oil is introduced to the treater at a temperature sufllcient to maintain its components which boil 'within the range of the finished product in a vaporized state throughout the treatment, permitting withdrawal of the treated product as vapors.
As a specific example of the operation of the improved process of the present invention, as applied to the treatment of a cracked distillate of motor fuel boiling range, vapors are taken directly from the fracticnator of a cracking system at a temperature of about 375 F., and before their introduction into the treater are superheated to a temperature of approximately 500 F. under a superatmospheric pressure of about 60 pounds per square inch. The hot vapors are contacted in successive stages of the treating zone with an adsorbent clay of about 60 mesh under substantially atmospheric pressure and the treated vapors are condensed and cooled without redistillation or further chemical treatment. This treatment produces a sweet, color stable motor fuel of low gum and low sulphur content. Thetreating loss is often less than 2%, based on the vapors treated, and a ton of clay may treat some 2500 to 3000 barrels of distillate and in some cases as high as 10,000 barrels, depending largely upon the-refining required by the raw or untreated vapors.
It is to be understood of course, that the above example is given merely for purposes of illustration and is not intended to serve as a limitation upon my invention.
I claim as my invention:-
1. A process of treating hydrocarbon oils to remove objectionable constituents therefrom which comprises introducing said oils into a treatingzone in a substantially vaporous state, passing said vapors in a substantially vertical direction upwardly through said zone introducing absorbent material into said zone and centrifugally hurling said material in stages radially from the center of said zone into intimate contact with the vapors and devolitalizing the spent absorbent material beforeremoval from said treating zone.
2. A continuous process of intimately contacting vapors and an absorbent material and devolatilizing spent absorbent material which comprises introducing said vapors into the intermediate portion of an enclosed zone, introducing steam into the lower portion of said zone, introducing absorbent material into the upperportion of said zone, and centrifugally hurling 1d material in stages radially from the center of said zone into the ascending vapors and the steam.
3. A continuous process of intimately contact ing vapors and an absorbent material and devolatilizing spent absorbent material which comprises introducing said vapors into the interme dlate portion of an enclosed zone, introducing steam into the lower portion of said zone, introducing absorbent material into the upper por-
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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2419204A (en) * 1940-01-22 1947-04-22 Elkington Frank Production of concentrated slurries of magnesium hydroxide
US2430245A (en) * 1940-12-28 1947-11-04 Socony Vacuum Oil Co Inc Method for continuous catalytic operation
US2443190A (en) * 1944-03-21 1948-06-15 Standard Oil Dev Co Contacting solid particles with gaseous fluids
US2444990A (en) * 1941-09-12 1948-07-13 Standard Oil Dev Co Contacting solid particles and gaseous fluids
US2488032A (en) * 1941-05-10 1949-11-15 Standard Oil Co Catalytic conversion of hydrocarbons and apparatus therefor
US2593495A (en) * 1946-11-01 1952-04-22 Houdry Process Corp Art of applying an atomized hydrocarbon mixture to contact material during passage thereof through a reaction zone
US2661322A (en) * 1946-07-10 1953-12-01 Houdry Process Corp Process and apparatus for reacting gaseous media in the presence of hot contact material
US2686110A (en) * 1951-02-15 1954-08-10 Standard Oil Dev Co Reactor
US2703275A (en) * 1951-01-08 1955-03-01 Martin A Elliott Apparatus for conducting heterogeneous chemical reactions
US2731398A (en) * 1951-05-24 1956-01-17 Kellogg M W Co Catalytic conversion of hydrocarbons with the stripping of the fouled catalyst particles
US2760916A (en) * 1947-09-04 1956-08-28 Kellogg M W Co Catalytic conversion of hydrocarbons
US2783187A (en) * 1954-12-01 1957-02-26 William W Odell Contacting fluids with solids
DE970874C (en) * 1950-09-23 1958-11-06 Ruhrchemie Ag Process for the catalytic splitting of hydrocarbons in the vapor phase
US3007545A (en) * 1955-12-21 1961-11-07 Exxon Research Engineering Co Method of extracting hydrocarbons

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2419204A (en) * 1940-01-22 1947-04-22 Elkington Frank Production of concentrated slurries of magnesium hydroxide
US2430245A (en) * 1940-12-28 1947-11-04 Socony Vacuum Oil Co Inc Method for continuous catalytic operation
US2488032A (en) * 1941-05-10 1949-11-15 Standard Oil Co Catalytic conversion of hydrocarbons and apparatus therefor
US2444990A (en) * 1941-09-12 1948-07-13 Standard Oil Dev Co Contacting solid particles and gaseous fluids
US2443190A (en) * 1944-03-21 1948-06-15 Standard Oil Dev Co Contacting solid particles with gaseous fluids
US2661322A (en) * 1946-07-10 1953-12-01 Houdry Process Corp Process and apparatus for reacting gaseous media in the presence of hot contact material
US2593495A (en) * 1946-11-01 1952-04-22 Houdry Process Corp Art of applying an atomized hydrocarbon mixture to contact material during passage thereof through a reaction zone
US2760916A (en) * 1947-09-04 1956-08-28 Kellogg M W Co Catalytic conversion of hydrocarbons
DE970874C (en) * 1950-09-23 1958-11-06 Ruhrchemie Ag Process for the catalytic splitting of hydrocarbons in the vapor phase
US2703275A (en) * 1951-01-08 1955-03-01 Martin A Elliott Apparatus for conducting heterogeneous chemical reactions
US2686110A (en) * 1951-02-15 1954-08-10 Standard Oil Dev Co Reactor
US2731398A (en) * 1951-05-24 1956-01-17 Kellogg M W Co Catalytic conversion of hydrocarbons with the stripping of the fouled catalyst particles
US2783187A (en) * 1954-12-01 1957-02-26 William W Odell Contacting fluids with solids
US3007545A (en) * 1955-12-21 1961-11-07 Exxon Research Engineering Co Method of extracting hydrocarbons

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