US1991750A - Process for the pyrolytic treatment of hydrocarbons and carboniferous material - Google Patents

Process for the pyrolytic treatment of hydrocarbons and carboniferous material Download PDF

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US1991750A
US1991750A US586573A US58657332A US1991750A US 1991750 A US1991750 A US 1991750A US 586573 A US586573 A US 586573A US 58657332 A US58657332 A US 58657332A US 1991750 A US1991750 A US 1991750A
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combustion
treating
air
gases
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William O Keeling
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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
    • 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
    • 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
    • C10G9/38Thermal 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 produced by partial combustion of the material to be cracked or by combustion of another hydrocarbon
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S208/00Mineral oils: processes and products
    • Y10S208/951Solid feed treatment with a gas other than air, hydrogen or steam
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S48/00Gas: heating and illuminating
    • Y10S48/05Diffusion membrane for gas reaction or separation

Definitions

  • One object of my invention is to provide a process of pyrolytic treatment of material by means of hot gases of combustion which will obviate the disadvantages which exist in the present processes.
  • Another object of my invention is to provide a process of pyrolytic treatment of hydrocarbons or carboniferous material in general in which the hot gases' of combustion used to treat the material are generated at uniform temperature and composition, and at a controlled pressure somewhat above the system pressure.
  • a further object of my invention is to provide Y a means oi reducing or tempering the hotgases of combustion to bring them to the desired temperature for eifecting ment.
  • Figure 1 represents a diagrammatic view of one apparatus capable of carrying out my invention.
  • Figure 2 is a diagrammatic view ofl a surface combustion burner used in carrying out my invention.
  • my invention contemplates, taking for example treating hydrocarbons, introducing the charging stock in heat exchange with the products of treatment and its introduction into a reaction chamber.
  • the hot products of combustion are brought to the desired temperature by means of the introduction of a cooler inert gas.
  • the volume and. quantity or gas will, of course, control the temperature at which the hot products of combustion enter the reaction stage.
  • diierent temperatures are required for dierent kinds of pyrolytic treatment.
  • the temperature should be between' '700 and 1500 F.
  • the temperature of the gases enthe contemplated treattering the reaction stage should be such that the f resulting temperature in thereaction stage will be not above 700 F.
  • the kind of oil or material being treated will necessitate different temperatures as will be obvious to those skilled in the art.
  • the charging stock enters through pipe l and passes through heat exchanger 2, through pipe 3, into heat exchanger 4, through pipe 5, into pipe 6 to the iirst treating stage 7.
  • the treating stage may consist of an enlarged chamber lined with refractory material.
  • I provide means for passing the charging stock through the heat exchangers either' in series, in parallel, or in one or the other of said heat exchangers. I am enabledy to do this by a valve and pipe arrangement. In the mode of charging in series as above described, it will be understood that valves 8, 9, 10, and 11 are open and that valves 12 and 13 are closed.
  • valves 8 and 12 will be left open so that the charging stock will enter the two heat exchangers in a divided stream through valve 8 and pipe 5.
  • the products leaving the heat exchangers are passed through valves 9 and 10, .through valve 13, into line 6, whence they will be discharged into the first reaction stage. If it is desired to use only heat exchanger 2, valves 10, 11 and 12 will be closed, while valves 8, 9, and 13v will be left open. If it is desired to use only heat exchanger 4, valves 8, 9, and 1'1 will be closed, while valves 10, 12, and 13 -will be left open.
  • I provide combustion burners 14 which consist of a combustion space 15 lined with a refractory material 16 and an inspirator device 17.
  • the inspirator device consists of fuel and air lines 17 and 18 through which air and fuel iiow.
  • the regulating valves comprise a diaphragm controlled valve consisting of a valve 21,
  • each diaphragm I provides a spring 30 which maybe adjusted to various tensions by adjusting screws 31 and 32.
  • the adjusting screws 32 on the air control valves are set to exert lesser pressure than the adjusting screws of the fuel control valves.
  • I may use a weight on the control valves of the air lines tending to hold the valves open. The employment of the weight, however, necessitates the mounting of the valves lll D9 understood 1r ciently high to overcome any prospective pressure which might be reached'within the system.
  • the air and fuel are obtained from tanks or any other suitable source of supply.. not shown. If.
  • the source of supply becomes disrupted, the action above described, whereby the valves in the air and fuel lines will tend to close by a reduction of pressure in the respective lines, is for the purpose of shutting off the system, in case of a break in the air and fuel lines.
  • the gas and air supply is sufficiently high to overcome any pressure which may exist in the system. Y).
  • the fuel and air which is drawn in through my Vinspirator is passed through mixing lines 33 to insure a perfect mixture of the fuel and air.
  • the mixture will burn with surface combustion along the surfaces of the refractory material packed in the combustion space 34, and issue into the enlarged space 15.
  • Above the zone of perfect combustion I provide inlet pipesv 35 for the admission ofthe tempering gases which will serve to bring the products of, combustion to the desired temperature depending upon the nature of the process being practiced. This temperature will vary, as pointed out above.
  • the hot gases of combustion thus generated and tempered to the desired temperature by the tempering gases issuing Vfrom lines'35 enter the iirst treating zone 'I Where a pyrolytic treatment is effected.
  • vaporized portions resulting from the pyrolytic treatment will pass from the reaction stage 7 through line 36 to a suitable condenser not shown. 'I'he unvaporized portions will pass through line 37 into a second treating zone 38 in which a fresh supply of hot gases of combustion generated in second burner 14 enter after being tempered through line 39. The vaporized portions in the second treating stage will pass through line 40 to a second condenser not shown. The unvaporized portions may be withdrawn through line 41 and passed to a third treating stage, not shown, it being understood that I may use as many treating stages as desired.
  • the unvaporized portions may be recycled, that is added to the cool incoming charging stock or introduced directly into the first treating zone and the cycle repeated.-
  • I avoid large pieces of equipment.
  • I am enabled to get a more uniform product due to the fact that I do not have to supply the total quantity 0f heat necessary for the treating in one stage.
  • a process as in claim 1 which includes the further step of tempering the hot combustion gases with a cooler inert gas before employing the hot products of combustion in the treating stage.
  • a process as in claim 4 which includes the additional step of passing the hydrocarbon oil to be treated in heat exchange relationship with the products evolved in the treating stages.
  • A-processas in claim 4 in which the hot gases of combustion are tempered with a cooler inert gas before employing the hot products of combustion in the treating stages.

Description

Feb. 19, 1935. w o. KEELING PROCESS FOR THE PYROLYTIC TREATMENT OF HYDROCARBO AND CARBONIFEROUS MATERIAL Filed Jan.
A TTORNEY.
Patented Feb. 19, 19.35
UNITED STATES PATENT OFFICE PROCESS F01?. THE PAYROLYTIC TREATMENT 0F BYDBOCARBONS AND GARBUNIFEB- My invention relates to a process for the pyrolytic treatment of hydrocarbons and carboniferous material in general and more particularly to a process wherein hot gases of combustion.
are used to supply the heat for treatment.
This application is a continuation in part of my copending application, Serial No. 369,174, filed June 7, 1929.
In the processes of the prior art in which hot gases of combustion are used for the pyrolytic treatment of hydrocarbons, no provision is made to generate the gases at a uniform temperature, pressure and composition. The gases are generated in a combustion space into which the fuel and air are admitted through hand controlled valves. 'Ihe success of any process of pyrolytic treatment depends upon more or less correct and constant pressure and a uniformity of temperature. If imperfect combustion is obtained, due to an excess, oxygen will be present in the combustion gases resulting in the formation of aldehydes, ketones, acids, gum forming compounds and color forming bodies. If imperfect combustion results, due to deciency of air, an excess of carbon monoxide will be present which represents a loss of valuable fuel. Ivhave discovered that, in order to obtain perfect combustion, it is necessary to use a surface combustion burner and that the mixture admitted to the burner must be of explosive proportions, that is, the air and gas must be properly proportioned to give substantially perfect combustion. It 'm impossible to obtain perfect combustion at all times Without an automatic control means due to the fact that pressure ductuations will result, due to variations in the charging stock, the presence of moisture, or to temperature changes which take place within the system. A sudden rise of pressure might extinguish the burner.
One object of my invention is to provide a process of pyrolytic treatment of material by means of hot gases of combustion which will obviate the disadvantages which exist in the present processes.
Another object of my invention is to provide a process of pyrolytic treatment of hydrocarbons or carboniferous material in general in which the hot gases' of combustion used to treat the material are generated at uniform temperature and composition, and at a controlled pressure somewhat above the system pressure.
the pyrolytic A further object of my invention is to provide Y a means oi reducing or tempering the hotgases of combustion to bring them to the desired temperature for eifecting ment.
Further objects o1' my invention will appear from the following description. In the drawing:
Figure 1 represents a diagrammatic view of one apparatus capable of carrying out my invention.
Figure 2 is a diagrammatic view ofl a surface combustion burner used in carrying out my invention.
In general, my invention contemplates, taking for example treating hydrocarbons, introducing the charging stock in heat exchange with the products of treatment and its introduction into a reaction chamber. I contemplate providing one or more reaction chambers in which the material will be treated in a stepwise manner. While I have shown two reaction chambers, it is to be understood that any number of successive stages of reaction may be provided. I make provision for the introduction of hot gases of combustion which are generated by an automatic system into each reaction chamber to supply the heat required for the pyrolytic treatment. While I have shown the use of separate burners for each successive reaction stage, it lis to be understood that I may employ va single burner to supply the gases to each reaction stage.
The hot products of combustion are brought to the desired temperature by means of the introduction of a cooler inert gas. The volume and. quantity or gas will, of course, control the temperature at which the hot products of combustion enter the reaction stage. It will be understood that diierent temperatures are required for dierent kinds of pyrolytic treatment. For example, in the cracking operation, the temperature should be between' '700 and 1500 F. For distillation, the temperature of the gases enthe contemplated treattering the reaction stage should be such that the f resulting temperature in thereaction stage will be not above 700 F. The kind of oil or material being treated will necessitate different temperatures as will be obvious to those skilled in the art. More particularly referring now to the drawing and again, taking for example the treatment of hydrocarbon oil, the charging stock enters through pipe l and passes through heat exchanger 2, through pipe 3, into heat exchanger 4, through pipe 5, into pipe 6 to the iirst treating stage 7. The treating stage may consist of an enlarged chamber lined with refractory material. I provide means for passing the charging stock through the heat exchangers either' in series, in parallel, or in one or the other of said heat exchangers. I am enabledy to do this by a valve and pipe arrangement. In the mode of charging in series as above described, it will be understood that valves 8, 9, 10, and 11 are open and that valves 12 and 13 are closed. If it be desired, for example, to charge the charging stock in parallel, valves 8 and 12 will be left open so that the charging stock will enter the two heat exchangers in a divided stream through valve 8 and pipe 5. The products leaving the heat exchangers are passed through valves 9 and 10, .through valve 13, into line 6, whence they will be discharged into the first reaction stage. If it is desired to use only heat exchanger 2, valves 10, 11 and 12 will be closed, while valves 8, 9, and 13v will be left open. If it is desired to use only heat exchanger 4, valves 8, 9, and 1'1 will be closed, while valves 10, 12, and 13 -will be left open.
I provide combustion burners 14 which consist of a combustion space 15 lined with a refractory material 16 and an inspirator device 17. The inspirator device consists of fuel and air lines 17 and 18 through which air and fuel iiow. I interpose regulating valves 19 and 20 in the air and fuel lines. The regulating valves comprise a diaphragm controlled valve consisting of a valve 21,
and valve stem22, to which is secured a diaphragm 23. The diaphragm is mounted in an enclosed chamber 24 which is divided into two parts by the diaphragm 23. The lower part of the chamber is exposed to the pressure of the fuel or gas, and air supply through branch lines 25 and 26 respectively. The upper portions of the diaphragms are in communication with the pressure of the system. through lines 27 and branch lines, 28 and 29. Above each diaphragm I provide a spring 30 which maybe adjusted to various tensions by adjusting screws 31 and 32. Inasmuch as the air is to act as an inspirating agent, that is the velocity of the air stream will serve to draw in the desired quantity of fuel, the adjusting screws 32 on the air control valves are set to exert lesser pressure than the adjusting screws of the fuel control valves. If desired, instead of using a spring to obtain the differential pressure contemplated, I may use a weight on the control valves of the air lines tending to hold the valves open. The employment of the weight, however, necessitates the mounting of the valves lll D9 understood 1r ciently high to overcome any prospective pressure which might be reached'within the system. The air and fuel are obtained from tanks or any other suitable source of supply.. not shown. If. for any reason, the source of supply becomes disrupted, the action above described, whereby the valves in the air and fuel lines will tend to close by a reduction of pressure in the respective lines, is for the purpose of shutting off the system, in case of a break in the air and fuel lines. Normally the gas and air supply is sufficiently high to overcome any pressure which may exist in the system. Y).
The fuel and air which is drawn in through my Vinspirator is passed through mixing lines 33 to insure a perfect mixture of the fuel and air. The mixture will burn with surface combustion along the surfaces of the refractory material packed in the combustion space 34, and issue into the enlarged space 15. Above the zone of perfect combustion I provide inlet pipesv 35 for the admission ofthe tempering gases which will serve to bring the products of, combustion to the desired temperature depending upon the nature of the process being practiced. This temperature will vary, as pointed out above. The hot gases of combustion thus generated and tempered to the desired temperature by the tempering gases issuing Vfrom lines'35 enter the iirst treating zone 'I Where a pyrolytic treatment is effected. The
vaporized portions resulting from the pyrolytic treatment will pass from the reaction stage 7 through line 36 to a suitable condenser not shown. 'I'he unvaporized portions will pass through line 37 into a second treating zone 38 in which a fresh supply of hot gases of combustion generated in second burner 14 enter after being tempered through line 39. The vaporized portions in the second treating stage will pass through line 40 to a second condenser not shown. The unvaporized portions may be withdrawn through line 41 and passed to a third treating stage, not shown, it being understood that I may use as many treating stages as desired. Il' desired, the unvaporized portions may be recycled, that is added to the cool incoming charging stock or introduced directly into the first treating zone and the cycle repeated.- By using a plurality of successive steps, I avoid large pieces of equipment. Furthermore, I am enabled to get a more uniform product due to the fact that I do not have to supply the total quantity 0f heat necessary for the treating in one stage.
It will be appreciated that my process provides Y a method of pyrolytic treatment by hotcombustion gases enabling the treatment to be carried If, for example. it is desired to treat oil shale,
a very slight modification of my apparatus can be made. All that is necessary is to providel means for introducing the oil shale into my treating chambers and means for periodically' removing the exhausted shale. I may employ my process in the destructive distillation oi' wood, coal or other carboniferous material.
It will be understood that certain features, subcombinations. and Voperations are of utility and may be employed without reference to other features and subcombinations. This is contemplated by and is withinthe scope of my claims.
It is further obviousl that various changes may be made in the details within the scope of my claims without departing from the spirit of myinvention. It is, therefore, tobe understood that my invention is not to be limited to the specific details shown and described.
Having thus described my invention, what I claimjs: v
1. In a process for the pyrolytic treatment of hydrocarbon oil with hot combustion gases the steps oi' mixing fuel and air in such proportions that an explosive mixture will result capable of producing substantially perfect combustion in a surface combustion burner whereby hot combustion gases substantially devoid of free oxygen and carbon monoxide will result, automatically continuously governing the respective pressures of the gas and air entering the mixing stage responsive to the pressure existing in the treating system, maintaining the pressure of the entering air above the pressure of the incoming fuel, buming said mixture `)Vith surface combustion to obtain hot combustion gases substantially devoid of'free oxygen and carbon monoxide, passing said gasesintocontactwiththeoilto be treatedin a treatlngstagaallowingsaidgasestoeffecta pyrolytic treatment of said material, and withdrawing the vaporized and unvaporized products from said treating stage separately.
2. A process as in claim 1 which includes the further step of tempering the hot combustion gases with a cooler inert gas before employing the hot products of combustion in the treating stage.
3. A process as in claim 1 in which the hydrocarbons to be treated are passed in heat exchange relation with the vapors withdrawn from the treating stage.
4. Isn a process for the pyrolytic treatment of hydrocarbon oil with hot combustion gases, the steps of mixing fuel and air insuch proportions that an explosive mixture will result, capable of substantially perfect combustion in a surface combustion burner, automatically continuously governing the respective pressures of the gas and air entering the mixing stage responsive to the pressure existing in the treating system, maintaining the pressure of the entering air above the pressure of the incoming fuel, burning said mixture with surface combustion to produce hot gases substantially devoid of free oxygen and carbon monoxide, passing said hot gases into contact with the hydrocarbon oil to be treated in a rst treating stage, withdrawing the vapors evolved in said ilrst treating stage, passing the unvaporized product into a second treating stage,
adding afresh supply of generated hot'combustion gases into said second treating stage, allowing a pyrolytic treatment to take place in said second treating stage, and withdrawing the products evolved in said second treating stage.
5. A process as in claim 4 which includes the additional step of passing the hydrocarbon oil to be treated in heat exchange relationship with the products evolved in the treating stages.
6. A process as in claim 4 in which the hot gases of combustion entering the second treating stage are generated in a separatesurface combustion burner.
'7. A-processas in claim 4 in which the hot gases of combustion are tempered with a cooler inert gas before employing the hot products of combustion in the treating stages.
8. A process as in claim 1 in which the un-r vaporized oil is withdrawn from the first treating stage and similarly treated by hot gases of stage.
.combustion in at least one subsequent treating WILLIAM o. mma.
US586573A 1932-01-14 1932-01-14 Process for the pyrolytic treatment of hydrocarbons and carboniferous material Expired - Lifetime US1991750A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2443402A (en) * 1942-02-10 1948-06-15 Phillips Petroleum Co Process for hydrocarbon conversion
US2583736A (en) * 1946-02-23 1952-01-29 Selas Corp Of America Gas heater
US2618533A (en) * 1948-07-22 1952-11-18 Union Oil Co Manufacture of carbon black
US2700016A (en) * 1950-11-27 1955-01-18 Naumann Carl Distillation of high boiling hydrocarbons and products therefrom
DE1010682B (en) * 1953-05-21 1957-06-19 Anton Gruschka Dr Ing Process for splitting high-boiling hydrocarbons at high temperatures
WO2002086024A1 (en) * 2001-04-20 2002-10-31 Exxonmobil Upstream Research Company Heavy oil upgrade method and apparatus
US20040104147A1 (en) * 2001-04-20 2004-06-03 Wen Michael Y. Heavy oil upgrade method and apparatus

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2443402A (en) * 1942-02-10 1948-06-15 Phillips Petroleum Co Process for hydrocarbon conversion
US2583736A (en) * 1946-02-23 1952-01-29 Selas Corp Of America Gas heater
US2618533A (en) * 1948-07-22 1952-11-18 Union Oil Co Manufacture of carbon black
US2700016A (en) * 1950-11-27 1955-01-18 Naumann Carl Distillation of high boiling hydrocarbons and products therefrom
DE1010682B (en) * 1953-05-21 1957-06-19 Anton Gruschka Dr Ing Process for splitting high-boiling hydrocarbons at high temperatures
WO2002086024A1 (en) * 2001-04-20 2002-10-31 Exxonmobil Upstream Research Company Heavy oil upgrade method and apparatus
US20040104147A1 (en) * 2001-04-20 2004-06-03 Wen Michael Y. Heavy oil upgrade method and apparatus
US6852215B2 (en) 2001-04-20 2005-02-08 Exxonmobil Upstream Research Company Heavy oil upgrade method and apparatus

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