CA1320467C - Process for the thermal cracking of residual hydrocarbon oils - Google Patents
Process for the thermal cracking of residual hydrocarbon oilsInfo
- Publication number
- CA1320467C CA1320467C CA000590680A CA590680A CA1320467C CA 1320467 C CA1320467 C CA 1320467C CA 000590680 A CA000590680 A CA 000590680A CA 590680 A CA590680 A CA 590680A CA 1320467 C CA1320467 C CA 1320467C
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- Prior art keywords
- synthesis gas
- asphaltenes
- thermal cracking
- hydrocarbon oils
- line
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G9/34—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts
- C10G9/36—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours
- C10G9/38—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours produced by partial combustion of the material to be cracked or by combustion of another hydrocarbon
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
- C10G49/007—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 in the presence of hydrogen from a special source or of a special composition or having been purified by a special treatment
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
- C10G67/04—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only including solvent extraction as the refining step in the absence of hydrogen
- C10G67/0454—Solvent desasphalting
- C10G67/049—The hydrotreatment being a hydrocracking
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S208/00—Mineral oils: processes and products
- Y10S208/95—Processing of "fischer-tropsch" crude
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)
- Combustion & Propulsion (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Industrial Gases (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
A B S T R A C T
PROCESS FOR THE THERMAL CRACKING OF
RESIDUAL HYDROCARBON OILS
Process for thermal cracking of residual hydro-carbon oils by 1) feeding the oil and a synthesis gas to a thermal cracking zone, the gas having a temperature suffi-ciently high to maintain the temperature in the cracking zone by means of direct heat exchange at 420-850 °C, 2) separating the cracked products into (a) a gas, (b) one or more distillates and (c) a cracked residue, 3) separating the cracked residue into one or more heavy hydrocarbon oils poor in asphaltenes and one or more heavy hydrocarbon oils rich in asphaltenes, 4) gasifying the oil(s) rich in asphaltenes in the presence of oxygen and steam to produce synthesis gas, and 5) applying synthesis gas from 4) as synthesis gas in 1).
PROCESS FOR THE THERMAL CRACKING OF
RESIDUAL HYDROCARBON OILS
Process for thermal cracking of residual hydro-carbon oils by 1) feeding the oil and a synthesis gas to a thermal cracking zone, the gas having a temperature suffi-ciently high to maintain the temperature in the cracking zone by means of direct heat exchange at 420-850 °C, 2) separating the cracked products into (a) a gas, (b) one or more distillates and (c) a cracked residue, 3) separating the cracked residue into one or more heavy hydrocarbon oils poor in asphaltenes and one or more heavy hydrocarbon oils rich in asphaltenes, 4) gasifying the oil(s) rich in asphaltenes in the presence of oxygen and steam to produce synthesis gas, and 5) applying synthesis gas from 4) as synthesis gas in 1).
Description
PROCESS FOR THE THERMAL CRACKING OF
RESIDUAL HYDROCARBON OILS
The invention relates to a process for the thermal cracking of residual hydrocarbon oils.
Residual hydrocarbon oils may be obtained by distillation at atmospheric pressure of a crude mineral oil, producing straight run distillate fractions and a residual oil, also called "long residue". The long residue is usually distilled at sub-atmospheric pressure to yield one or more so called "vacuum distillates" and a residual oil, also called "short residue". Both residual oils and also other residual oils such as those obtained from tar sands and shale oils have been subject of much research aiming at conversion thereof into more valuable products.
The article in "Wissenschaft und Technik, Erdoel und Kohle-Erdgas-Petrochemie vereinigt mit Brennstoff-Chemie", 36, October 1983, 457-461 concerns thermal cracking of residual hydrocarbon oils in the presence of hydrogen. A tar sand heavy oil is cracked in this manner with formation of cracked products from which a gaseous fraction containing hydrocarbons having one to four carbon atoms per molecule and a liquid residual fraction were separated. The liquid residual fraction contained 70% by weight of distillate with a final boiling point of 592 C. The experiments were carried out by preheating the tar sand heavy oil to a tempera-ture of 375 C and the hydrogen to a temperature of 1200 C and introducing the preheated material into a reaction vessel, the temperature of the hydrogen being sufficiently high to provide the heat required for the thermal cracking.
Japanese patent application publication No. 62-96589 concerns a process in which a mixture of a heavy hydrocarbon oil, hydrogen and carbonaceous fine particles is thermally cracked, the cracked products are separated into a gas, a light oil, a middle oil and a cracked residue, the cracked residue is deasphalted with formation of a deasphalted oil and a fraction relatively rich in asphaltenes, the hydrocarbon fraction relatively rich in asphaltenes is gasified in the presence of oxygen and steam with formation of synthesis gas, carbonaceous fine particles are separated from the synthesis gas and the separated particles are recycled to the thermal cracking. The presence of hydrogen in the thermal cracking zone reduces problems brought about by formation of carbon-aceous products in thermal cracking and yields oilhaving a high stability and a low olefin content. In this known process the material to be thermally cracked is indirectly heated to the cracking temperature, that is to say via a wall through which heat is transmitted.
A disadvantage thereof is the possibility of a gradual buildup of carbonaceous deposits on the inner wall by the mixture to be thermally cracked, resulting in a reduced on-stream time of the furnace in which heating takes place. This disadvantage is particularly important in those cases where high conversions of the heavy hydrocarbon oil are aimed at. Another dis-advantage is that particles of metals and ash which are usually present in synthesis gas are not removed there-from. Consequently, metals and ash will be present inincreasing concentration.
It is an object of the present invention to avoid the disadvantages of indirect heating of the residual hydrocarbon oil to the cracking temperature.
Another object is to avoid concentration of particles of metals and ash in the process.
A further object is to use hydrogen in an easily available form.
Accordingly, the invention provides a process for the thermal cracking of residual hydrocarbon oils which process comprises the following steps:-step 1:- feeding the residual hydrocarbon oil and a synthesis gas to a thermal cracking zone, the synthesis gas having a sufficiently high temperature to maintain the temperature in the thermal cracking zone by means of direct heat exchange at a value in the range of from 420 C to 850 C;
step 2:- separating the cracked products from step 1 into (a) a gaseous fraction containing synthesis gas, (b) one or more hydrocarbon distillate fractions and (c~ a cracked residue;
step 3:- separating the cracked residue from step 2 into one or more heavy hydrocarbon oils relatively poor in asphaltenes and one or more heavy hydrocarbon oils relatively rich in asphaltenes;
step 4:- gasifying one or more heavy hydrocarbon oils relatively rich in asphaltenes from step 3 in the presence of oxygen and steam with production of synthesis gas; and step 5:- applying synthesis gas from step 4 as synthesis gas in step 1.
The residual hydrocarbon oil is directly contacted in step 1 with hot synthesis gas, thus providing heat for the thermal cracking, and avoiding the dis-advantages of indirect heating of the residual hydro-carbon oil to the ~racking temperature. Efficient contacting is an important means to reduce formation of carbonaceous products; contacting may take place efficiently by providing a high oil to gas interface in the thermal cracking zone, by using, for example, a spray reactor in which the residual hydrocarbon oil and the hot synthesis gas are separately introduced.
The temperature in step 1 is an important process variable in thermal cracking. The desirable effect of thermal cracking, i.e. the decrease of molecular weight and viscosity of the residual hydrocarbon oil, arise from the fact that the larger molecules have a higher cracking rate than the smaller molecules. It is known from Sachanen, "Conversion of Petroleum", 1948, Chapter 3, that at lower temperatures the difference in crack-ing rates between larger and smaller molecules increases and, hence, the resultant desirable effect will be greater. At very low temperatures, say, below 400 C, the cracking rate decreases to uneconomically small values and a considerable amount of ethylenically unsaturated products is formed. At very high tempera-tures, that is to say above 850 C, much gas andcarbonaceous products will be formed and less hydrocarbon distillate fractions will be produced in step 2, and less heavy hydrocarbon oils relatively poor in asphaltenes in step 3. To achieve a relatively high production of distillate fractions in step 2 and heavy hydrocarbon oils relatively poor in asphaltenes in step 3, which, moreover, have a considerably reduced content of ethylenically unsaturated products, the temperature in the thermal cracking zone is preferably in the range of from 420 C to 645 C, more preferably in the range of from 460 C to 550 C.
The residual hydrocarbon oil and the synthesis gas are fed to the thermal cracking zone in which a react-ion mixture is formed which is allowed a certain average residence time. This average residence time isanother important process variable in thermal cracking.
Generally, the average residence time is set in accord-ance with the temperature. The thermal cracking in step l is preferably carried out at an average residence time in the range of from l sec to lO min, more prefer-ably in the range of from lO sec to lO min. At resi-dence times below l sec the thermal cracking will not make sufficient progress and at a residence time of more than lO min the amount of gas and carbonaceous products will increase and less hydrocarbon distillate fractions will be produced in step 2, and less heavy hydrocarbon oils relatively poor in asphaltenes in step 3. The average residence time is defined herein as V:F, in which "V" is the volume of the thermal cracking zone and "F" is the volume of residual hydrocarbon oil that is fed to this zone per unit of time.
The pressure in step l is preferably chosen in the range of from 2 to 50 bar, and in particular from 3 to lO bar so as to provide a high oil to gas interphase in the thermal cracking zone and to enhance the production of heavy hydrocarbon oil relatively poor in asphaltenes in step 3.
Examples of residual hydrocarbon oils which may be used in step l of the process according to the present invention are long residues, short residues, residues obtained by distillation of hydrocarbon mixtures formed by thermal cracking of hydrocarbon oils in the absence of added hydrogen and residual oils obtained from tar sands or shale oils. If desired, the residual hydrocarbon oil may be blended with a heavy distillate fraction, for example a cycle oil obtained by catalytic cracking of a hydrocarbon oil fraction, or with a heavy hydrocarbon oil obtained by extraction from a residual hydrocarbon oil.
The cracked products from step 1 are separated in step 2 into a gaseous fraction, one or more hydrocarbon distillate fractions and a cracked residue. This may, for example, be effected by withdrawing gas from the top and the cracked residue from the bottom of the thermal cracking zone. The gas withdrawn from the top may be separated by means of distillation at atmos-pheric pressure into (a) a gaseous fraction containing synthesis gas, hydrocarbons having in the range of from one to four carbon atoms per molecule and hydrogen sulphide if the hydrocarbon fraction relatively rich in asphaltenes to be gasified in step 4 also contains sulphur, (b) a naphtha fraction, (c) a kerosine fraction, (d) a gas oil fraction and (e) a small amount of a residue. This small amount of residue may be mixed with the cracked residue obtained in step 2. The hydrogen sulphide may be removed from the gaseous fraction by means of any suitable conventional technique. After removal thereof the gaseous fraction may be separated by means of conventional separation techniques into synthesis gas and hydrocarbons. The synthesis gas may be reused in step 1, if desired after enrichment with hydrogen, and/or used as, for example, fuel gas or gas to drive a turbine for generation of power.
The cracked residue from step 2 contains, i.a., heavy hydrocarbon oil, asphaltenes, suspended carbon-aceous particles and, if any, heavy metals.
According to a preferred embodiment of the present invention the cracked residue from step 2 is separated in step 3 by means of distillation at sub-atmospheric pressure into one or more heavy hydrocarbon oil distillates relatively poor in asphaltenes and a heavy residual hydrocarbon oil relatively rich in asphaltenes. This distillation is suitably a flash and may take place in one or more columns or flash vessels.
According to another preferred embodiment of the present invention the cracked residue from step 2 is contacted in step 3 with an extractant with formation of an extract phase containing the heavy hydrocarbon oils relatively poor in asphaltenes and an extraction residue comprising a heavy hydrocarbon oil relatively rich in asphaltenes. The extractant is preferably an alkane or a mixture of alkanes, in particular propane, butane, isobutane and/or pentane. Preference is given to pentane. Such extraction processes are well known in the art. The extract phase and the extraction residue being the heavy hydrocarbon oil relatively rich in asphaltenes may be separated by means of gravity settling and the separated extract phase may be separated by means of distillation into extractant and the heavy hydrocarbon oil relatively poor in asphaltenes.
The hydrocarbon fraction relatively rich in asphaltenes also contains suspended particles of carbonaceous products and, if present at all, heavy metals, for example vanadium and nickel. This fraction is gasified in step 4 in the presence of oxygen and steam with production of synthesis gas which has as main components carbon monoxide and hydrogen, the gasification being a partial oxidation. The hydrogen is thus easily available and need not be separated from carbon monoxide. The synthesis gas contains particles of carbonaceous products and of ash and usually of heavy metals.
The gasification in step 4 may be carried out, for example, at a weight ratio of oxygen to hydrocarbon fraction in the range of from 0.5 to 1.5 and of steam to hydrocarbon fraction in the range of from 0.2 to l;
both weight ratios depend on the molecular composition of the fuel and on the temperature at which the gasification is carried out. These weight ratios also determine the amount of carbonaceous products formed.
Gasification may be carried out at a pressure in the range of, for example, l to lO0 bar and a temperature in the range of, for example, lO00 C to 1600 C.
Preferably, particles of metals and ash present in the synthesis gas from step 4 are removed therefrom before the gas is applied in step 5. Removal may be effected from the main synthesis gas stream but is suitably effected from a by-pass stream thereof. Suit-ably, removal is effected at the temperature at which the synthesis gas becomes available.
The particles of metals and ash are preferably selectively removed from the synthesis gas from step 4 before application thereof in step 5, that is to say selectively with respect to the particles of carbon-aceous products therein. An advantage thereof is that the particles of carbonaceous products end up in the heavy hydrocarbon oil relatively rich in asphaltenes separated in step 3 and are then gasified in step 4. It is a favourable feature of the present process that particles of carbonaceous products need not be disposed of as a waste product. The selective removal may be based on the differences in size and density between the particles of carbonaceous products and those of metals and ash. The particles of carbonaceous products usually have a relatively small size and relatively low density, whilst the particles of metals and ash usually have a relatively large size and relatively high density. This separation may be carried out by means of, for example, a cyclone separator. The particles of metals and ash thus separated may be used for recovery of these metals.
_ 9 The synthesis gas should have a sufficiently high temperature to maintain the temperature in the thermal cracking zone at a value in the range of from 420 C to 850 C. It is a favourable feature of the present invention that, with respect of this requirement, a surplus heat is usually available in the synthesis gas.
Therefore, heat present in the synthesis gas from step 4 can usually be withdrawn therefrom, preferably by means of indirect heat exchange with a cooling medium, for example water. This offers the possibility to produce steam of relatively high pressure and to control the temperature in the thermal cracking zone.
Alternatively, the synthesis gas is split into two portions, one of which is used in step l to maintain the temperature in the thermal cracking zone at a value in the range of from 420 C to 850 C and the other is given any other suitable destination. For example, the other portion may be burned in a turbine for generation of power.
The hydrocarbon fraction relatively poor in asphaltenes separated in step 3 may be given any suit-able desti~ation. For example, as it has a relatively low density, viscosity and Conradson carbon content and does not contain carbon particles or has a very low content thereof, this fraction is very suitable as a blending component for commercial fuels. Alternatively, it may be catalytically cracked or hydrocracked for producing gasoline and kerosine fractions, or it can be recycled to the thermal cracking zone in step l for thermal cracking to lighter hydrocarbon distillate fractions.
The invention will now be described in more detail with reference to the accompanying drawings, wherein Figures l and 2 each depict a simplified flow scheme of the process according to the present invention in which auxiliary equipment such as, for example, heat ex-changers and valves is not shown. Figure l depicts the embodiment of distilling the cracked residue at sub--atmospheric pressure and Figure 2 the embodiment of deasphalting the cracked residue.
Referring to Figure 1, a heavy hydrocarbon oil is introduced via a line 1 and a line 2 into a thermal cracker 3. Synthesis gas is supplied via a line 4 to the thermal cracker 3 (step l).
From the thermal cracker 3 a gaseous phase and a cracked residue are withdrawn via a line 5 and a line 6, respectively. The gaseous phase is introduced via the line 5 into a distillation column 7 in which it is separated at atmospheric pressure into a synthesis gas-containing top fraction, a full range naphtha fraction, a gas oil fraction and a bottom fraction, withdrawn from the distillation column 7 via a line 8, a line 9, a line 10 and a line 11, respectively (step 2).
The cracked residue is introduced via the line 6 and a line 12 into a vacuum distillation column 13 in which it is separated at sub-atmospheric pressure into a vacuum top fraction, one or more vacuum distillates and a bottom fraction containing asphaltenes, withdrawn from the vacuum distillation column 13 via a line 14, a line 15 and a line 16, respectively (step 3~. The top fraction and distillate are substantially free from asphaltenes and the bottom fraction contained particles of carbonaceous products.
The fraction containing asphaltenes is introduced via the line 16, a pump 17 and a line 18 into a gasifier 19 to which oxygen and steam are supplied via a line 20. Synthesis gas produced in the gasifier 19 is withdrawn therefrom via a line 21 (step 4).
The synthesis gas is conducted via the line 21 into a separator 22 in which particles of metals and ash are selectively removed from the gas. Synthesis gas substantially free from particles of metals and ash but still containing particles of carbonaceous products is withdrawn from the separator 22 via a line 23 and introduced into a waste heat boiler 24 in which excess heat is withdrawn from the synthesis gas. Synthesis gas having a reduced temperature is withdrawn from the waste heat boiler 24 via the line 4 and, as stated hereinbefore, introduced into the thermal cracker 3 (step 5).
The particles of metals and ash removed from the synthesis gas in the separator 22 are withdrawn there-from via a line 25. Water is supplied to the waste heatboiler 24 via a line 26 and high pressure steam is removed therefrom via a line 27.
The vacuum medium distillate conducted through the line 15 is, in this case, partly conducted via a line 28 to a destination outside the process and partly recirculated via a line 29 to the line 2, to increase the production of full range naphtha fraction and gas oil fraction via the lines 9 and 10, respectively.
Alternatively, all of the vacuum medium distillate from the line 15 may be withdrawn via the line 28. The latter possibility is usually preferred.
The bottom fraction conducted via the line 11 is introduced via a pump 30 and a line 31 into the line 12.
In Figures 1 and 2 reference numerals relating to corresponding parts are the same.
Referring to Figure 2, the cracked residue from the thermal cracker 3 is introduced via the line 6 into a solvent deasphalting unit 50 in which it is separated into a deasphalted oil substantially free from particles of carbonaceous products and a fraction containing asphaltenes and particles of carbonaceous products, withdrawn from the unit 50 via the line 15 and the line 16, respectively (step 3), the carbon-aceous products originating from the gasifier 19 and the thermal cracker 3.
The deasphalted oil withdrawn via the line 15 is partly conducted via a line 28 to a destination outside the process and partly recirculated via the line 29 to the line 2 to increase the production of full range naphtha fraction and gas oil fraction via the lines 9 and 10, respectively. Alternatively, all of the de-asphalted oil from the line 15 may be withdrawn via the line 28. The latter possibility is usually preferred.
Example 1 This example was carried out with reference to Figure 1. The heavy hydrocarbon oil conducted through the line 1 was a short residue having the following properties:
Density , 25 C/25 C 1.028 Viscosity , 150 C 154 cS
Initial boiling point, C520 Vanadium content , ppm 135.8 Nickel content , ppm 43.3 Sulphur content , % by weight 5.30 Conradson Carbon , % by weight 21.7 C5-asphaltenes , % by weight 19.9 "The abbreviation ppm" means parts per million by weight. The thermal cracker 3 was a cylindrical vessel operated at a temperature of 475 C, a pressure of 6.0 bar and an average residence time of 3 min. The gasi-fier 19 was operated at a temperature of 1400 C, a pressure of 30 bar and a residence time of 5 sec, and the distillation column 14 at a pressure of 0.013 bar.
High pressure steam was withdrawn via the line 27.
The following overall material balance was found:
In Out Line kg/hLine kg/h 1 Short residue 125.0 8 Light hydrocarbons 116.6 and synthesis gas 20 Oxygen 37.99 Naphtha, C5-165 C 13.3 20 Steam 28.410 Gas oil, 165-370 C12.1 28 Vacuum flashed distil-late, 370-550 C 48.3 25 Solid particles of metals and ash 191.3 191.3 The material balance around the thermal cracker 3 was as follows:
In Out Line kg/hLine kg/h 4 112.5 5 142.0 2 125.0 6 95.5 237._ 237.5 The material balance around the vacuum distillation column 13 was as follows:
In Out Line kg/h Line kg/h 12 95.5 14 negligible 48.25 16 47.25 95.5 95.5 Some properties of the vacuum flashed distillate in line 28 and of the fraction containing asphaltenes in line 16 are as follows:
Fraction Vacuum Flashed Containing DistillateAsphaltenes Density, 25 C/25 C 1.015 1.116 Viscosity , cS 30.2 at 100 C 779 at 200 C
Vanadium content, ppm 0.4355 Nickel content , ppm 0.6113 Sulphur content , ~ by weight 4.06.1 Conradson Carbon, % by weight 0.856.2 C5-asphaltenes , % by weight 0.0263.6 The vacuum flashed distillate was free from particles of carbonaceous products. The composition of the fraction containing asphaltenes excludes the particles of carbonaceous products.
The gas in line 4 had the following composition in %mol (at 20 C), excluding particles of carbonaceous products:
C0 46.6 C2 3-4 H2S 1.4 H2 41.5 H2O 6.5 N2 0.6 ExamPle 2 This example was carried out with reference to Figure 2. The heavy hydrocarbon oil conducted throuqh the line 1 was the same short residue as used in Example 1. The thermal cracker 3 was operated at a temperature of 475 C, a pressure of 6.0 bar and a cold oil residence time of 3 min. The gasifier 19 was operated at a temperature of 1400 C, a pressure of 30 bar and a residence time of 5 sec. The extraction column 50 was a rotating disc contactor operated isothermally at a temperature of 185 C and a pressure of 40 bar with n-pentane as extractant. An extractant to feed weight ratio of 2.0 was applied, using a rotator speed of 100 revolutions per minute.
The following overall material balance was found:
In Out Line kg/h Line kg/h 1 Short residue 125.08 Light hydrocarbons 72.4 and synthesis gas 20 Oxygen 23~09 Naphtha, C5-165 C13.3 20 Steam 17.410 Gas oil, 165-370 C12.1 28 Deasphalted oil 66.8 _ 25 Solid particles 0.8 165.4 of metals and ash 165.4 The material balance around the thermal cracker 3 was as follows:
In Out Line kg/h Line kg/h 4 68.3 5 97.8 2 125.0 6 95.5 193.3 193.3 The material balance around the solvent de-asphalting unit 50 was as follows:
In Out Line kg/g Line kg/h 12 95.5 15 66.8 16 28.7 95.5 95.5 The gas in line 4 had the following composition in %mol (at 20 C), excluding particles of carbonaceous products:
CO 48.2 C2 3-1 H2S 1-6 H2 40 9 H2O 6.0 N2 0.2 Some prop~rties of the deasphalted oil in line 28 and of the fraction containing asphaltenes in line 16 are as follows:
fraction deasphalted containing oil asPhaltenes Density 25 C/25 C 1.007 1.221 Viscosity cS 65 at 100 C 75110 at 200 C
Vanadium content ppm 26.5 530 Nickel content ppm12.9 159 Sulphur content % by weight 4.2 7.1 Conradson carbo ~ by weight 10.4 70.7 C5-asphaltenes % by weight 5.7 92~7 The composition of the fraction containing asphaltenes excludes the particles of carbonaceous products. The deasphalted oil was free from particles of carbonaceous products.
RESIDUAL HYDROCARBON OILS
The invention relates to a process for the thermal cracking of residual hydrocarbon oils.
Residual hydrocarbon oils may be obtained by distillation at atmospheric pressure of a crude mineral oil, producing straight run distillate fractions and a residual oil, also called "long residue". The long residue is usually distilled at sub-atmospheric pressure to yield one or more so called "vacuum distillates" and a residual oil, also called "short residue". Both residual oils and also other residual oils such as those obtained from tar sands and shale oils have been subject of much research aiming at conversion thereof into more valuable products.
The article in "Wissenschaft und Technik, Erdoel und Kohle-Erdgas-Petrochemie vereinigt mit Brennstoff-Chemie", 36, October 1983, 457-461 concerns thermal cracking of residual hydrocarbon oils in the presence of hydrogen. A tar sand heavy oil is cracked in this manner with formation of cracked products from which a gaseous fraction containing hydrocarbons having one to four carbon atoms per molecule and a liquid residual fraction were separated. The liquid residual fraction contained 70% by weight of distillate with a final boiling point of 592 C. The experiments were carried out by preheating the tar sand heavy oil to a tempera-ture of 375 C and the hydrogen to a temperature of 1200 C and introducing the preheated material into a reaction vessel, the temperature of the hydrogen being sufficiently high to provide the heat required for the thermal cracking.
Japanese patent application publication No. 62-96589 concerns a process in which a mixture of a heavy hydrocarbon oil, hydrogen and carbonaceous fine particles is thermally cracked, the cracked products are separated into a gas, a light oil, a middle oil and a cracked residue, the cracked residue is deasphalted with formation of a deasphalted oil and a fraction relatively rich in asphaltenes, the hydrocarbon fraction relatively rich in asphaltenes is gasified in the presence of oxygen and steam with formation of synthesis gas, carbonaceous fine particles are separated from the synthesis gas and the separated particles are recycled to the thermal cracking. The presence of hydrogen in the thermal cracking zone reduces problems brought about by formation of carbon-aceous products in thermal cracking and yields oilhaving a high stability and a low olefin content. In this known process the material to be thermally cracked is indirectly heated to the cracking temperature, that is to say via a wall through which heat is transmitted.
A disadvantage thereof is the possibility of a gradual buildup of carbonaceous deposits on the inner wall by the mixture to be thermally cracked, resulting in a reduced on-stream time of the furnace in which heating takes place. This disadvantage is particularly important in those cases where high conversions of the heavy hydrocarbon oil are aimed at. Another dis-advantage is that particles of metals and ash which are usually present in synthesis gas are not removed there-from. Consequently, metals and ash will be present inincreasing concentration.
It is an object of the present invention to avoid the disadvantages of indirect heating of the residual hydrocarbon oil to the cracking temperature.
Another object is to avoid concentration of particles of metals and ash in the process.
A further object is to use hydrogen in an easily available form.
Accordingly, the invention provides a process for the thermal cracking of residual hydrocarbon oils which process comprises the following steps:-step 1:- feeding the residual hydrocarbon oil and a synthesis gas to a thermal cracking zone, the synthesis gas having a sufficiently high temperature to maintain the temperature in the thermal cracking zone by means of direct heat exchange at a value in the range of from 420 C to 850 C;
step 2:- separating the cracked products from step 1 into (a) a gaseous fraction containing synthesis gas, (b) one or more hydrocarbon distillate fractions and (c~ a cracked residue;
step 3:- separating the cracked residue from step 2 into one or more heavy hydrocarbon oils relatively poor in asphaltenes and one or more heavy hydrocarbon oils relatively rich in asphaltenes;
step 4:- gasifying one or more heavy hydrocarbon oils relatively rich in asphaltenes from step 3 in the presence of oxygen and steam with production of synthesis gas; and step 5:- applying synthesis gas from step 4 as synthesis gas in step 1.
The residual hydrocarbon oil is directly contacted in step 1 with hot synthesis gas, thus providing heat for the thermal cracking, and avoiding the dis-advantages of indirect heating of the residual hydro-carbon oil to the ~racking temperature. Efficient contacting is an important means to reduce formation of carbonaceous products; contacting may take place efficiently by providing a high oil to gas interface in the thermal cracking zone, by using, for example, a spray reactor in which the residual hydrocarbon oil and the hot synthesis gas are separately introduced.
The temperature in step 1 is an important process variable in thermal cracking. The desirable effect of thermal cracking, i.e. the decrease of molecular weight and viscosity of the residual hydrocarbon oil, arise from the fact that the larger molecules have a higher cracking rate than the smaller molecules. It is known from Sachanen, "Conversion of Petroleum", 1948, Chapter 3, that at lower temperatures the difference in crack-ing rates between larger and smaller molecules increases and, hence, the resultant desirable effect will be greater. At very low temperatures, say, below 400 C, the cracking rate decreases to uneconomically small values and a considerable amount of ethylenically unsaturated products is formed. At very high tempera-tures, that is to say above 850 C, much gas andcarbonaceous products will be formed and less hydrocarbon distillate fractions will be produced in step 2, and less heavy hydrocarbon oils relatively poor in asphaltenes in step 3. To achieve a relatively high production of distillate fractions in step 2 and heavy hydrocarbon oils relatively poor in asphaltenes in step 3, which, moreover, have a considerably reduced content of ethylenically unsaturated products, the temperature in the thermal cracking zone is preferably in the range of from 420 C to 645 C, more preferably in the range of from 460 C to 550 C.
The residual hydrocarbon oil and the synthesis gas are fed to the thermal cracking zone in which a react-ion mixture is formed which is allowed a certain average residence time. This average residence time isanother important process variable in thermal cracking.
Generally, the average residence time is set in accord-ance with the temperature. The thermal cracking in step l is preferably carried out at an average residence time in the range of from l sec to lO min, more prefer-ably in the range of from lO sec to lO min. At resi-dence times below l sec the thermal cracking will not make sufficient progress and at a residence time of more than lO min the amount of gas and carbonaceous products will increase and less hydrocarbon distillate fractions will be produced in step 2, and less heavy hydrocarbon oils relatively poor in asphaltenes in step 3. The average residence time is defined herein as V:F, in which "V" is the volume of the thermal cracking zone and "F" is the volume of residual hydrocarbon oil that is fed to this zone per unit of time.
The pressure in step l is preferably chosen in the range of from 2 to 50 bar, and in particular from 3 to lO bar so as to provide a high oil to gas interphase in the thermal cracking zone and to enhance the production of heavy hydrocarbon oil relatively poor in asphaltenes in step 3.
Examples of residual hydrocarbon oils which may be used in step l of the process according to the present invention are long residues, short residues, residues obtained by distillation of hydrocarbon mixtures formed by thermal cracking of hydrocarbon oils in the absence of added hydrogen and residual oils obtained from tar sands or shale oils. If desired, the residual hydrocarbon oil may be blended with a heavy distillate fraction, for example a cycle oil obtained by catalytic cracking of a hydrocarbon oil fraction, or with a heavy hydrocarbon oil obtained by extraction from a residual hydrocarbon oil.
The cracked products from step 1 are separated in step 2 into a gaseous fraction, one or more hydrocarbon distillate fractions and a cracked residue. This may, for example, be effected by withdrawing gas from the top and the cracked residue from the bottom of the thermal cracking zone. The gas withdrawn from the top may be separated by means of distillation at atmos-pheric pressure into (a) a gaseous fraction containing synthesis gas, hydrocarbons having in the range of from one to four carbon atoms per molecule and hydrogen sulphide if the hydrocarbon fraction relatively rich in asphaltenes to be gasified in step 4 also contains sulphur, (b) a naphtha fraction, (c) a kerosine fraction, (d) a gas oil fraction and (e) a small amount of a residue. This small amount of residue may be mixed with the cracked residue obtained in step 2. The hydrogen sulphide may be removed from the gaseous fraction by means of any suitable conventional technique. After removal thereof the gaseous fraction may be separated by means of conventional separation techniques into synthesis gas and hydrocarbons. The synthesis gas may be reused in step 1, if desired after enrichment with hydrogen, and/or used as, for example, fuel gas or gas to drive a turbine for generation of power.
The cracked residue from step 2 contains, i.a., heavy hydrocarbon oil, asphaltenes, suspended carbon-aceous particles and, if any, heavy metals.
According to a preferred embodiment of the present invention the cracked residue from step 2 is separated in step 3 by means of distillation at sub-atmospheric pressure into one or more heavy hydrocarbon oil distillates relatively poor in asphaltenes and a heavy residual hydrocarbon oil relatively rich in asphaltenes. This distillation is suitably a flash and may take place in one or more columns or flash vessels.
According to another preferred embodiment of the present invention the cracked residue from step 2 is contacted in step 3 with an extractant with formation of an extract phase containing the heavy hydrocarbon oils relatively poor in asphaltenes and an extraction residue comprising a heavy hydrocarbon oil relatively rich in asphaltenes. The extractant is preferably an alkane or a mixture of alkanes, in particular propane, butane, isobutane and/or pentane. Preference is given to pentane. Such extraction processes are well known in the art. The extract phase and the extraction residue being the heavy hydrocarbon oil relatively rich in asphaltenes may be separated by means of gravity settling and the separated extract phase may be separated by means of distillation into extractant and the heavy hydrocarbon oil relatively poor in asphaltenes.
The hydrocarbon fraction relatively rich in asphaltenes also contains suspended particles of carbonaceous products and, if present at all, heavy metals, for example vanadium and nickel. This fraction is gasified in step 4 in the presence of oxygen and steam with production of synthesis gas which has as main components carbon monoxide and hydrogen, the gasification being a partial oxidation. The hydrogen is thus easily available and need not be separated from carbon monoxide. The synthesis gas contains particles of carbonaceous products and of ash and usually of heavy metals.
The gasification in step 4 may be carried out, for example, at a weight ratio of oxygen to hydrocarbon fraction in the range of from 0.5 to 1.5 and of steam to hydrocarbon fraction in the range of from 0.2 to l;
both weight ratios depend on the molecular composition of the fuel and on the temperature at which the gasification is carried out. These weight ratios also determine the amount of carbonaceous products formed.
Gasification may be carried out at a pressure in the range of, for example, l to lO0 bar and a temperature in the range of, for example, lO00 C to 1600 C.
Preferably, particles of metals and ash present in the synthesis gas from step 4 are removed therefrom before the gas is applied in step 5. Removal may be effected from the main synthesis gas stream but is suitably effected from a by-pass stream thereof. Suit-ably, removal is effected at the temperature at which the synthesis gas becomes available.
The particles of metals and ash are preferably selectively removed from the synthesis gas from step 4 before application thereof in step 5, that is to say selectively with respect to the particles of carbon-aceous products therein. An advantage thereof is that the particles of carbonaceous products end up in the heavy hydrocarbon oil relatively rich in asphaltenes separated in step 3 and are then gasified in step 4. It is a favourable feature of the present process that particles of carbonaceous products need not be disposed of as a waste product. The selective removal may be based on the differences in size and density between the particles of carbonaceous products and those of metals and ash. The particles of carbonaceous products usually have a relatively small size and relatively low density, whilst the particles of metals and ash usually have a relatively large size and relatively high density. This separation may be carried out by means of, for example, a cyclone separator. The particles of metals and ash thus separated may be used for recovery of these metals.
_ 9 The synthesis gas should have a sufficiently high temperature to maintain the temperature in the thermal cracking zone at a value in the range of from 420 C to 850 C. It is a favourable feature of the present invention that, with respect of this requirement, a surplus heat is usually available in the synthesis gas.
Therefore, heat present in the synthesis gas from step 4 can usually be withdrawn therefrom, preferably by means of indirect heat exchange with a cooling medium, for example water. This offers the possibility to produce steam of relatively high pressure and to control the temperature in the thermal cracking zone.
Alternatively, the synthesis gas is split into two portions, one of which is used in step l to maintain the temperature in the thermal cracking zone at a value in the range of from 420 C to 850 C and the other is given any other suitable destination. For example, the other portion may be burned in a turbine for generation of power.
The hydrocarbon fraction relatively poor in asphaltenes separated in step 3 may be given any suit-able desti~ation. For example, as it has a relatively low density, viscosity and Conradson carbon content and does not contain carbon particles or has a very low content thereof, this fraction is very suitable as a blending component for commercial fuels. Alternatively, it may be catalytically cracked or hydrocracked for producing gasoline and kerosine fractions, or it can be recycled to the thermal cracking zone in step l for thermal cracking to lighter hydrocarbon distillate fractions.
The invention will now be described in more detail with reference to the accompanying drawings, wherein Figures l and 2 each depict a simplified flow scheme of the process according to the present invention in which auxiliary equipment such as, for example, heat ex-changers and valves is not shown. Figure l depicts the embodiment of distilling the cracked residue at sub--atmospheric pressure and Figure 2 the embodiment of deasphalting the cracked residue.
Referring to Figure 1, a heavy hydrocarbon oil is introduced via a line 1 and a line 2 into a thermal cracker 3. Synthesis gas is supplied via a line 4 to the thermal cracker 3 (step l).
From the thermal cracker 3 a gaseous phase and a cracked residue are withdrawn via a line 5 and a line 6, respectively. The gaseous phase is introduced via the line 5 into a distillation column 7 in which it is separated at atmospheric pressure into a synthesis gas-containing top fraction, a full range naphtha fraction, a gas oil fraction and a bottom fraction, withdrawn from the distillation column 7 via a line 8, a line 9, a line 10 and a line 11, respectively (step 2).
The cracked residue is introduced via the line 6 and a line 12 into a vacuum distillation column 13 in which it is separated at sub-atmospheric pressure into a vacuum top fraction, one or more vacuum distillates and a bottom fraction containing asphaltenes, withdrawn from the vacuum distillation column 13 via a line 14, a line 15 and a line 16, respectively (step 3~. The top fraction and distillate are substantially free from asphaltenes and the bottom fraction contained particles of carbonaceous products.
The fraction containing asphaltenes is introduced via the line 16, a pump 17 and a line 18 into a gasifier 19 to which oxygen and steam are supplied via a line 20. Synthesis gas produced in the gasifier 19 is withdrawn therefrom via a line 21 (step 4).
The synthesis gas is conducted via the line 21 into a separator 22 in which particles of metals and ash are selectively removed from the gas. Synthesis gas substantially free from particles of metals and ash but still containing particles of carbonaceous products is withdrawn from the separator 22 via a line 23 and introduced into a waste heat boiler 24 in which excess heat is withdrawn from the synthesis gas. Synthesis gas having a reduced temperature is withdrawn from the waste heat boiler 24 via the line 4 and, as stated hereinbefore, introduced into the thermal cracker 3 (step 5).
The particles of metals and ash removed from the synthesis gas in the separator 22 are withdrawn there-from via a line 25. Water is supplied to the waste heatboiler 24 via a line 26 and high pressure steam is removed therefrom via a line 27.
The vacuum medium distillate conducted through the line 15 is, in this case, partly conducted via a line 28 to a destination outside the process and partly recirculated via a line 29 to the line 2, to increase the production of full range naphtha fraction and gas oil fraction via the lines 9 and 10, respectively.
Alternatively, all of the vacuum medium distillate from the line 15 may be withdrawn via the line 28. The latter possibility is usually preferred.
The bottom fraction conducted via the line 11 is introduced via a pump 30 and a line 31 into the line 12.
In Figures 1 and 2 reference numerals relating to corresponding parts are the same.
Referring to Figure 2, the cracked residue from the thermal cracker 3 is introduced via the line 6 into a solvent deasphalting unit 50 in which it is separated into a deasphalted oil substantially free from particles of carbonaceous products and a fraction containing asphaltenes and particles of carbonaceous products, withdrawn from the unit 50 via the line 15 and the line 16, respectively (step 3), the carbon-aceous products originating from the gasifier 19 and the thermal cracker 3.
The deasphalted oil withdrawn via the line 15 is partly conducted via a line 28 to a destination outside the process and partly recirculated via the line 29 to the line 2 to increase the production of full range naphtha fraction and gas oil fraction via the lines 9 and 10, respectively. Alternatively, all of the de-asphalted oil from the line 15 may be withdrawn via the line 28. The latter possibility is usually preferred.
Example 1 This example was carried out with reference to Figure 1. The heavy hydrocarbon oil conducted through the line 1 was a short residue having the following properties:
Density , 25 C/25 C 1.028 Viscosity , 150 C 154 cS
Initial boiling point, C520 Vanadium content , ppm 135.8 Nickel content , ppm 43.3 Sulphur content , % by weight 5.30 Conradson Carbon , % by weight 21.7 C5-asphaltenes , % by weight 19.9 "The abbreviation ppm" means parts per million by weight. The thermal cracker 3 was a cylindrical vessel operated at a temperature of 475 C, a pressure of 6.0 bar and an average residence time of 3 min. The gasi-fier 19 was operated at a temperature of 1400 C, a pressure of 30 bar and a residence time of 5 sec, and the distillation column 14 at a pressure of 0.013 bar.
High pressure steam was withdrawn via the line 27.
The following overall material balance was found:
In Out Line kg/hLine kg/h 1 Short residue 125.0 8 Light hydrocarbons 116.6 and synthesis gas 20 Oxygen 37.99 Naphtha, C5-165 C 13.3 20 Steam 28.410 Gas oil, 165-370 C12.1 28 Vacuum flashed distil-late, 370-550 C 48.3 25 Solid particles of metals and ash 191.3 191.3 The material balance around the thermal cracker 3 was as follows:
In Out Line kg/hLine kg/h 4 112.5 5 142.0 2 125.0 6 95.5 237._ 237.5 The material balance around the vacuum distillation column 13 was as follows:
In Out Line kg/h Line kg/h 12 95.5 14 negligible 48.25 16 47.25 95.5 95.5 Some properties of the vacuum flashed distillate in line 28 and of the fraction containing asphaltenes in line 16 are as follows:
Fraction Vacuum Flashed Containing DistillateAsphaltenes Density, 25 C/25 C 1.015 1.116 Viscosity , cS 30.2 at 100 C 779 at 200 C
Vanadium content, ppm 0.4355 Nickel content , ppm 0.6113 Sulphur content , ~ by weight 4.06.1 Conradson Carbon, % by weight 0.856.2 C5-asphaltenes , % by weight 0.0263.6 The vacuum flashed distillate was free from particles of carbonaceous products. The composition of the fraction containing asphaltenes excludes the particles of carbonaceous products.
The gas in line 4 had the following composition in %mol (at 20 C), excluding particles of carbonaceous products:
C0 46.6 C2 3-4 H2S 1.4 H2 41.5 H2O 6.5 N2 0.6 ExamPle 2 This example was carried out with reference to Figure 2. The heavy hydrocarbon oil conducted throuqh the line 1 was the same short residue as used in Example 1. The thermal cracker 3 was operated at a temperature of 475 C, a pressure of 6.0 bar and a cold oil residence time of 3 min. The gasifier 19 was operated at a temperature of 1400 C, a pressure of 30 bar and a residence time of 5 sec. The extraction column 50 was a rotating disc contactor operated isothermally at a temperature of 185 C and a pressure of 40 bar with n-pentane as extractant. An extractant to feed weight ratio of 2.0 was applied, using a rotator speed of 100 revolutions per minute.
The following overall material balance was found:
In Out Line kg/h Line kg/h 1 Short residue 125.08 Light hydrocarbons 72.4 and synthesis gas 20 Oxygen 23~09 Naphtha, C5-165 C13.3 20 Steam 17.410 Gas oil, 165-370 C12.1 28 Deasphalted oil 66.8 _ 25 Solid particles 0.8 165.4 of metals and ash 165.4 The material balance around the thermal cracker 3 was as follows:
In Out Line kg/h Line kg/h 4 68.3 5 97.8 2 125.0 6 95.5 193.3 193.3 The material balance around the solvent de-asphalting unit 50 was as follows:
In Out Line kg/g Line kg/h 12 95.5 15 66.8 16 28.7 95.5 95.5 The gas in line 4 had the following composition in %mol (at 20 C), excluding particles of carbonaceous products:
CO 48.2 C2 3-1 H2S 1-6 H2 40 9 H2O 6.0 N2 0.2 Some prop~rties of the deasphalted oil in line 28 and of the fraction containing asphaltenes in line 16 are as follows:
fraction deasphalted containing oil asPhaltenes Density 25 C/25 C 1.007 1.221 Viscosity cS 65 at 100 C 75110 at 200 C
Vanadium content ppm 26.5 530 Nickel content ppm12.9 159 Sulphur content % by weight 4.2 7.1 Conradson carbo ~ by weight 10.4 70.7 C5-asphaltenes % by weight 5.7 92~7 The composition of the fraction containing asphaltenes excludes the particles of carbonaceous products. The deasphalted oil was free from particles of carbonaceous products.
Claims (12)
1. A process for the thermal cracking of residual hydrocarbon oils which process comprises the following steps:-step 1:- feeding the residual hydrocarbon oil and a synthesis gas to a thermal cracking zone, the synthesis gas having a sufficiently high temperature to maintain the temperature in the thermal cracking zone by means of direct heat exchange at a value in the range of from 420 °C to 850 °C:
step 2:- separating the cracked products from step 1 into (a) a gaseous fraction containing synthesis gas, (b) one or more hydrocarbon distillate fractions and (c) a cracked residue;
step 3:- separating the cracked residue from step 2 into one or more heavy hydrocarbon oils relatively poor in asphaltenes and one or more heavy hydrocarbon oils relatively rich in asphaltenes;
step 4:- gasifying one or more heavy hydrocarbon oils relatively rich in asphaltenes from step 3 in the presence of oxygen and steam with production of synthesis gas; and step 5:- applying synthesis gas from step 4 as synthesis gas in step 1.
step 2:- separating the cracked products from step 1 into (a) a gaseous fraction containing synthesis gas, (b) one or more hydrocarbon distillate fractions and (c) a cracked residue;
step 3:- separating the cracked residue from step 2 into one or more heavy hydrocarbon oils relatively poor in asphaltenes and one or more heavy hydrocarbon oils relatively rich in asphaltenes;
step 4:- gasifying one or more heavy hydrocarbon oils relatively rich in asphaltenes from step 3 in the presence of oxygen and steam with production of synthesis gas; and step 5:- applying synthesis gas from step 4 as synthesis gas in step 1.
2. A process as claimed in claim 1 in which the thermal cracking in step 1 is carried out at a temperature in the range of from 420 °C to 645 °C.
3. A process as claimed in claim 2 in which the thermal cracking in step 1 is carried out at a temperature in the range of from 460 °C to 550 °C.
4. A process as claimed in claim 1, 2 or 3, in which step 1 is carried out at a pressure in the range of from 3 to 10 bar.
5. A process as claimed in claim 1, 2 or 3, in which the thermal cracking in step 1 is carried out at an average residence time in the range of from 1 sec to 10 min.
6. A process as claimed in claim 5 in which the thermal cracking in step 1 is carried out at an average residence time in the range of from 10 sec to 10 min.
7. A process as claimed in claim 1, 2, 3 or 6, in which heat present in the synthesis gas from step 4 is withdrawn therefrom by means of indirect heat exchange with a cooling medium before the gas 1 applied in step 5.
8. A process as claimed in claim 1, 2, 3 or 6, in which particles of metals and ash present in the synthesis gas from step 4 are selectively removed therefrom with respect to particles of carbonaceous products before the gas is applied in step 5.
9. A process as claimed in claim 1, 2, 3 or 6, in which the cracked residue from step 2 is separated in step 3 by means of distillation at sub-atmospheric pressure into one or more heavy hydrocarbon oil distillate relatively poor in asphaltenes and a heavy residual hydrocarbon oil relatively rich in asphaltenes.
10. A process as claimed in claim 1, 2, 3 or 6 in which the cracked residue from step 2 is contacted in step 3 with an extractant with formation of an extract phase containing the heavy hydrocarbon oils relatively poor in asphaltenes and an extraction residue comprising a heavy hydrocarbon oil relatively rich in asphaltenes.
11. A process as claimed in claim 10 in which the extractant is propane, butane, isobutane and/or pentane.
12. Hydrocarbon oils whenever obtained by a process as claimed in claim 1, 2, 3, 6 or 11.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8803156 | 1988-02-11 | ||
| GB888803156A GB8803156D0 (en) | 1988-02-11 | 1988-02-11 | Process for thermal cracking of residual hydrocarbon oils |
Publications (1)
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|---|---|
| CA1320467C true CA1320467C (en) | 1993-07-20 |
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| CA000590680A Expired - Lifetime CA1320467C (en) | 1988-02-11 | 1989-02-10 | Process for the thermal cracking of residual hydrocarbon oils |
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| US (1) | US4938862A (en) |
| EP (1) | EP0328216B1 (en) |
| JP (1) | JP2588772B2 (en) |
| KR (1) | KR970010860B1 (en) |
| CN (1) | CN1020626C (en) |
| AT (1) | ATE69256T1 (en) |
| AU (1) | AU606779B2 (en) |
| CA (1) | CA1320467C (en) |
| DE (1) | DE68900393D1 (en) |
| ES (1) | ES2025838T3 (en) |
| GB (1) | GB8803156D0 (en) |
| GR (1) | GR3003193T3 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8828335D0 (en) * | 1988-12-05 | 1989-01-05 | Shell Int Research | Process for conversion of heavy hydrocarbonaceous feedstock |
| BR9508692A (en) * | 1994-09-05 | 1998-01-06 | Shell Int Research | Process for thermal cracking of a residual hydrocarbon oil |
| FR2764300B1 (en) * | 1997-06-10 | 1999-07-23 | Inst Francais Du Petrole | PROCESS FOR THE CONVERSION OF OIL HEAVY FRACTIONS COMPRISING A HYDRODESULFURIZATION STEP AND A STEP OF CONVERSION INTO A BOILING BED |
| ES2229752T3 (en) * | 1998-07-29 | 2005-04-16 | Texaco Development Corporation | INTRODUCTION OF DISASPHALTATION AND SOLVENT GASIFICATION. |
| AR021966A1 (en) * | 1998-12-22 | 2002-09-04 | Texaco Development Corp | USE OF MEMBRANES AND EXPANSORS / COMPRESSORS IN GASIFICATION |
| US6171473B1 (en) * | 1999-04-08 | 2001-01-09 | Abb Lummus Global Inc. | Integrated residue thermal cracking and partial oxidation process |
| WO2001074268A1 (en) * | 2000-03-30 | 2001-10-11 | Align Technology, Inc. | System and method for separating three-dimensional models |
| CN1333044C (en) * | 2003-09-28 | 2007-08-22 | 中国石油化工股份有限公司 | Method for cracking hydrocarbon oil |
| WO2005073346A1 (en) | 2004-02-02 | 2005-08-11 | Boris Nikolaevich Ulko | Process and installation for high temperature processing of heavy petroleum residues |
| US7964090B2 (en) * | 2008-05-28 | 2011-06-21 | Kellogg Brown & Root Llc | Integrated solvent deasphalting and gasification |
| US8690977B2 (en) | 2009-06-25 | 2014-04-08 | Sustainable Waste Power Systems, Inc. | Garbage in power out (GIPO) thermal conversion process |
| US9056771B2 (en) * | 2011-09-20 | 2015-06-16 | Saudi Arabian Oil Company | Gasification of heavy residue with solid catalyst from slurry hydrocracking process |
| ES2441691B1 (en) | 2013-10-21 | 2014-08-11 | Eqtec Iberia S.L. | Procedure for the conditioning of a gas stream from a gasifier, thermal cracking of tars and steam reforming and reactor used |
| KR20220109780A (en) * | 2021-01-29 | 2022-08-05 | 주식회사 엘지화학 | Method for preparing synthesis gas |
| KR20220109784A (en) * | 2021-01-29 | 2022-08-05 | 주식회사 엘지화학 | Method for preparing synthesis gas |
| KR20230000240A (en) * | 2021-06-24 | 2023-01-02 | 주식회사 엘지화학 | Method for preparing synthesis gas and aromatic hydrocarbon |
| KR20230000227A (en) * | 2021-06-24 | 2023-01-02 | 주식회사 엘지화학 | Method for preparing synthesis gas and aromatic hydrocarbon |
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| US2539434A (en) * | 1947-02-25 | 1951-01-30 | Hydrocarbon Research Inc | Synthesis of hydrocarbons |
| US2605215A (en) * | 1949-01-15 | 1952-07-29 | Texas Co | Conversion of heavy carbonaceous oils to motor fuels, fuel gas, and synthesis gas |
| US2917532A (en) * | 1957-08-13 | 1959-12-15 | Universal Oil Prod Co | Combination process for hydrotreating and synthesizing hydrocarbons |
| US3928170A (en) * | 1971-04-01 | 1975-12-23 | Kureha Chemical Ind Co Ltd | Method for manufacturing petroleum pitch having high aromaticity |
| JPS5230283B2 (en) * | 1973-12-17 | 1977-08-06 | ||
| GB1518085A (en) * | 1974-08-19 | 1978-07-19 | Shell Int Research | Process for the production of hydrogen carbon monoxide and light hydrocarbon-containing gases |
| JPS59152992A (en) * | 1983-02-18 | 1984-08-31 | Mitsubishi Heavy Ind Ltd | Thermal decomposition for producing olefin from hydrocarbon |
| JPS59159887A (en) * | 1983-03-03 | 1984-09-10 | Mitsubishi Heavy Ind Ltd | Thermal cracking of hydrocarbon to produce olefin |
| JPS6011585A (en) * | 1983-06-30 | 1985-01-21 | Mitsubishi Heavy Ind Ltd | Thermal cracking to produce petrochemicals selectively from hydrocarbon |
| JPS61163992A (en) * | 1985-01-16 | 1986-07-24 | Fuji Standard Res Kk | Continuously producing pitch suitable for use as raw material of carbon fiber |
| JPH06296589A (en) * | 1992-09-22 | 1994-10-25 | Olympus Optical Co Ltd | Medical treatment system |
-
1988
- 1988-02-11 GB GB888803156A patent/GB8803156D0/en active Pending
-
1989
- 1989-02-06 AT AT89200274T patent/ATE69256T1/en not_active IP Right Cessation
- 1989-02-06 EP EP89200274A patent/EP0328216B1/en not_active Expired - Lifetime
- 1989-02-06 DE DE8989200274T patent/DE68900393D1/en not_active Expired - Lifetime
- 1989-02-06 ES ES198989200274T patent/ES2025838T3/en not_active Expired - Lifetime
- 1989-02-09 AU AU29798/89A patent/AU606779B2/en not_active Expired
- 1989-02-09 JP JP1028838A patent/JP2588772B2/en not_active Expired - Lifetime
- 1989-02-09 KR KR1019890001594A patent/KR970010860B1/en not_active IP Right Cessation
- 1989-02-10 CA CA000590680A patent/CA1320467C/en not_active Expired - Lifetime
- 1989-02-10 CN CN89100741A patent/CN1020626C/en not_active Expired - Lifetime
- 1989-02-10 US US07/309,757 patent/US4938862A/en not_active Expired - Lifetime
-
1991
- 1991-11-25 GR GR91401812T patent/GR3003193T3/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2588772B2 (en) | 1997-03-12 |
| AU606779B2 (en) | 1991-02-14 |
| ES2025838T3 (en) | 1992-04-01 |
| ATE69256T1 (en) | 1991-11-15 |
| GB8803156D0 (en) | 1988-03-09 |
| AU2979889A (en) | 1989-08-17 |
| DE68900393D1 (en) | 1991-12-12 |
| US4938862A (en) | 1990-07-03 |
| EP0328216B1 (en) | 1991-11-06 |
| CN1036787A (en) | 1989-11-01 |
| KR890013163A (en) | 1989-09-21 |
| JPH01252696A (en) | 1989-10-09 |
| GR3003193T3 (en) | 1993-02-17 |
| EP0328216A1 (en) | 1989-08-16 |
| KR970010860B1 (en) | 1997-07-01 |
| CN1020626C (en) | 1993-05-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed | ||
| MKEC | Expiry (correction) |
Effective date: 20121205 |