Classifications

• • 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
  • C10G9/28—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid material
  • C10G9/30—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid material according to the "moving bed" method
• • 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
  • C10G55/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one refining process and at least one cracking process
  • C10G55/02—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one refining process and at least one cracking process plural serial stages only
  • C10G55/04—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one refining process and at least one cracking process plural serial stages only including at least one thermal cracking step

Definitions

• the present invention relates to a process for the conversion of a heavy asphaltenes-containing hydrocarbonaceous feedstock comprising at least 25 %wt of hydrocarbons with a boiling point of at least 520 °C into products with a lower boiling point.
• Thermal cracking is a suitable process for the conversion of heavy asphaltenes-containing hydrocarbonaceous feedstocks into products with a lower average boiling point.
• Thermal cracking is a fairly simple process and comprises preheating the feedstock to the appropriate temperature and sending the preheated feedstock to a thermal cracking zone. There the cracking takes place. At the outlet of the thermal cracking zone the effluent is usually quenched to stop the cracking reactions and the effluent is fractionated to yield one or more distillate fractions and a residue. The residue contains virtually all asphaltenes present in the cracked product and is normally not treated any further but disposed of as refinery or commercial fuel.
• An important aspect of the process relates to the stability of the cracked residue after blending with suitable diluents to give the resulting fuel the desired product specifications such as viscosity, sulphur content, density and Conradson Carbon Number. It is known that if the cracking is too severe, the character of the asphaltenes and the oils changes such that sludge formation occurs. Sludge formation especially occurs in the thermal cracking of asphaltenes-containing feedstocks. If the feedstock has been deasphalted and the deasphalted oil is thermally cracked, only at extremely high conversions some sludge is formed. The sludge basically comprises coke particles that are not soluble in the cracked oil and/or in the fuel when the cracked residue has been blended to yield a fuel. If the sludge formation is above a certain specified limit, the fuel does not comply with commercial fuel specifications.
• a way to prevent sludge resides in the moderation of the severity of the thermal cracking process. Therefore, dependent on the type of feedstock the severity of the thermal cracking is selected such that the conversion of the heavy hydrocarbons, i.e. the hydrocarbons with a boiling point of 520 °C and above, is below about 30 %wt. The problem of sludge formation will be avoided at this conversion level. It will be evident that then the yield on distillates is not optimal.
• Another way to prevent sludge formation is to deasphalt the feedstock prior to the thermal cracking process. Conversion levels higher than 30 %wt are then attainable. However, the asphaltenes that have been removed can no longer contribute to the production of distillates and hence also in this case the yield on distillates is not optimal.
• a batch process in which it is attempted to maximise the yield on distillates is delayed coking.
• the feedstock is allowed to stay in so-called coker drums to crack and yield distillates and coke.
• Heavy products are recycled and when the coker drum is filled with coke, the process continues in another coke drum.
• the coker drums are filled/emptied batchwise. It will be evident that the facts that delayed coking is operated batchwise and that more or less solid coke has to be handled form drawbacks of this process.
• the present invention provides a process in which the conversion can be increased without incurring the problems of an unstable residue and a batchwise operation, whilst the yield of distillates is enhanced.
• the present invention provides a process for the conversion of a heavy asphaltenes-containing hydrocarbonaceous feedstock comprising at least 25 %wt of hydrocarbons with a boiling point of at least 520 °C into products with a lower boiling point, which process comprises preheating the hydrocarbonaceous feedstock, passing the preheated feedstock through a thermal cracking zone so that a conversion of the hydrocarbons with a boiling point of 520 °C and above of at least 35 %wt is obtained, separating the effluent from the cracking zone into one or more distillate fractions and a residual fraction, and deasphalting the residual fraction to obtain an asphalt and a deasphalted oil.
• the asphalt obtained contains the solid coke particles that may have formed during the cracking reactions, and the deasphalted oil contains virtually no asphaltenes and has a lower viscosity, a lower density and a lower Conradson Carbon Number than the residual fraction obtained in the separation of the effluent from the thermal cracking zone.
• the deasphalted oil does not have any stability problems and can be used directly as blending component in the preparation of a commercial fuel, or be used for different purposes.
• the heavy hydrocarbonaceous feedstock that is used in the process according to the present invention comprises at least 25 %wt of hydrocarbons with a boiling point of at least 520 °C (520 °C+ hydrocarbons). When the percentage of 520 °C + hydrocarbons is lower the stability problem is less likely to occur.
• Convenient feedstocks include atmospheric residues of crude oils, so-called long residues.
• the feedstock comprises more than 37.5 %wt of 520 °C+ hydrocarbons, more preferably more than 75 %wt and most advantageously more than 90 %wt.
• a very convenient feedstock is a vacuum residue of a crude oil, a so-called short residue.
• the heavy feedstock may comprise a cycle oil obtained by catalytic cracking and/or residual oils obtained from tar sands and shale oils.
• the feedstock contains asphaltenes.
• asphaltenes in this specification refers to C5-asphaltenes, determined analogous to the method of IP 143 but using C5 hydrocarbons.
• Another way to express the asphaltenes content is by using C7-asphaltenes in accordance with IP 143. It is appreciated that the number for C5-asphaltenes will be higher than for C7-asphaltenes.
• the process can be carried out with a feedstock that does not contain asphaltenes, it is observed that thermal cracking of feedstocks without asphaltenes is less prone to causing stability problems and/or sludge formation.
• the asphaltenes content of a typical deasphalted oil is less than 5 %wt.
• the asphaltenes content in the feedstock of the present process may vary, dependent on the source from which it originates.
• the C5-asphaltenes content in the feedstock ranges from 5 to 50 %wt, determined according to the modified IP 143 method.
• the feedstock Before being passed into the thermal cracking zone the feedstock is preheated. Usually this is done in one or more furnaces or furnace sections, provided with heat exchange tubes or coils through which the feedstock to be preheated is passed.
• the temperature to which the feedstock is preheated is preferably from 350 to 600 °C.
• the thus preheated feedstock is passed through the thermal cracking zone.
• the feedstock may be passed in an upward or a downward direction through the cracking zone.
• the flow is upward.
• the feedstock may be passed through a cracking zone that is constituted as an empty vessel, e.g. as described in US-A 1,899,889.
• the thermal cracking zone is situated in a soaking vessel containing internals.
• the internals are preferably in the form of perforated plates. In such a soaking vessel the internals provide compartments by means of which the occurrence of back-mixing is decreased.
• a very suitable soaking vessel is described in EP-A 7656. For more detailed information on the internals reference to this specification is made.
• the present invention provides a high conversion of the 520 °C+ hydrocarbons. That means that the yield on distillate fractions will be high.
• the conversion of the 520 °C+ hydrocarbons is preferably from 35 to 70 %wt. At a conversion below 30 %wt hardly any stability problem will occur, whereas at a conversion above 70 %wt the residual fraction will be so viscous and rich of coke that handling thereof will be very cumbersome. Very good results have been obtained at a conversion of 520 °C+ hydrocarbons from 40 to 60 %wt.
• the thermal cracking is generally carried out in the absence of reducing gases, such as hydrogen.
• the cracking can be carried out in the presence of steam.
• the conditions at which the thermal cracking may be carried out can be varied. One might adjust the temperature, pressure and residence time at will in such a way that the desired conversion occurs. It will be evident to a person skilled in the art that the same conversion can be obtained at a high temperature and a short residence time on the one hand and at a lower temperature but at a longer residence time at the other hand. Further, the cracking reactions are endothermic and therefore the temperature tends to decrease over the cracking zone in the case of soaker cracking. Hence, the person skilled in the art will be able to select the conditions in the cracking zone such that the desired conversion level will be obtained. Suitable cracking conditions include a temperature of 350 to 600 °C, a pressure of 1 to 100 bar and a residence time of 0.5 to 60 min. The residence time relates to the cold feedstock.
• Quenching may be carried out by contacting the effluent with a colder quench fluid.
• Suitable quench fluids include relatively light hydrocarbon oils, such as gasoline or a recycled cool residual fraction obtained from the effluent.
• the effluent is separated into one or more distillate fractions and a residual fraction.
• the distillate fractions comprise e.g. gas (C1 ⁇ 4 hydrocarbons), gasoline, middle distillates and optionally one or more vacuum distillates.
• the residual fraction obtained will contain the heavy 520 °C+ hydrocarbons.
• the residual fraction obtained may be very viscous.
• the residual fraction may be blended with a diluent to facilitate handling of the resulting mixture.
• Suitable diluents include cutter oils, such as gasoline, gasoil and other hydrocarbon streams from both straight run and catalytic cracking origin.
• the deasphalting of the residual fraction may be carried out in a conventional manner. Solvent deasphalting is known in the art.
• the extracting medium which is usually a light hydrocarbon solvent containing paraffinic compounds, preferably C3 ⁇ 8 paraffinic hydrocarbons, more preferably butane, pentane and/or hexane, in particular pentane.
• a rotating disc contactor or a plate column can be used with the residual fraction entering at the top and the extracting medium entering at the bottom.
• the paraffinic compounds dissolve in the extracting medium and are withdrawn at the top of the apparatus.
• the asphaltenes that are insoluble in the extracting medium are withdrawn at the bottom of the apparatus.
• the conditions at the deasphalting are suitably a total solvent to residual fraction ratio of 1.5 to 8.0 wt/wt, a pressure from 1 to 50 bar and a temperature from 160 to 230 °C. These conditions allow the production of very heavy asphalts. To enable the handling of such heavy asphalts the addition of cutter oils to the asphalt may be desirable.
• the deasphalting will suitably be carried out such that more than 35 %wt of the asphaltenes of the residual fraction are removed therefrom. Preferably more than 50 %wt of the asphaltenes are removed, more preferably more than 80 %wt.
• more than 15 %wt of the residual fraction is recovered as asphalt. That ensures a complete removal of all solid particles and a removal of the vast majority of the asphaltenes.
• the resulting deasphalted oil will then have excellent properties as to the density, Conradson Carbon number and viscosity, and therefore will not incur any problem when used in the preparation of a fuel.
• Dependent on the type of feedstock and the conversion level of the thermal cracking conveniently from 15 to 50 %wt, preferably from 20 to 45 %wt of the residual fraction is separated as asphalt.
• the deasphalted oil resulting from the deasphalting step can be used as residual fuel or can be used as a blending component for a residual fuel.
• the specifications for a fuel may be such that the deasphalted oil is preferably blended with a so-called cutter oil to bring the resulting mixture on the desired product specifications.
• the specifications relate not only to the stability, but also to other characteristics such as the Conradson Carbon content, viscosity and density.
• deasphalted oil examples include the use of the oil as feed for a hydrotreatment or a hydrocracking process, for a catalytic cracking process or for a thermal cracking process.
• the asphalt can suitably be combusted, e.g. in a fluid bed combustion unit, or in the form of an emulsified fuel.
• Another useful outlet for the asphalt is the use as feed for a gasification unit to yield synthesis gas or fuel gas.
• the thermal cracking experiments were carried out in a pilot plant apparatus comprising a coil which was heated while the feedstock was passed through it, and a soaking vessel.
• the feed rate of the feedstock was selected such that the residence time (based on the cold feedstock) in the heating coil was 2 min. and the residence time in the soaking vessel was 38 min.
• the temperature was varied in accordance with the desired conversion.
• a heat exchanger was arranged and a fractionator to cool the effluent from the soaking vessel and subsequently to separate the effluent into a gaseous (C1 ⁇ 4) fraction, a gasoline (C5 - 165 °C) fraction, a gasoil (165 - 350°C) fraction and a residual (350 °C+) fraction.
• the deasphalting experiments were carried out in a rotating disc contactor operating at a pentane:residual fraction weight ratio of 2.0-2.2, a feed rate of about 2.0 kg of residual fraction/h, and at a pressure of 40 bar.
• the temperature in the contactor was varied between 170 and 210 °C.
• Feedstock I Middle East short residue
• Venezuela short residue Venezuela short residue
• Feedstock III North Sea short residue

Landscapes

• Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=10647963

Family Applications (1)

Country Status (8)

Cited By (7)

Families Citing this family (8)

Citations (3)

• 1988
  • 1988-12-05 GB GB888828335A patent/GB8828335D0/en active Pending
• 1989
  • 1989-12-04 FI FI895789A patent/FI99022C/fi not_active IP Right Cessation
  • 1989-12-04 CA CA002004480A patent/CA2004480A1/en not_active Abandoned
  • 1989-12-04 RU SU894742598A patent/RU2024586C1/ru active
  • 1989-12-04 EP EP89203073A patent/EP0372652A1/de not_active Ceased
  • 1989-12-05 JP JP1314504A patent/JP2926415B2/ja not_active Expired - Lifetime
  • 1989-12-05 CN CN89109072A patent/CN1022254C/zh not_active Expired - Fee Related
  • 1989-12-05 KR KR1019890017986A patent/KR0148566B1/ko not_active IP Right Cessation

Patent Citations (3)

Also Published As

Similar Documents

Legal Events