US20140202826A1 - Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations - Google Patents

Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations Download PDF

Info

Publication number
US20140202826A1
US20140202826A1 US14/220,634 US201414220634A US2014202826A1 US 20140202826 A1 US20140202826 A1 US 20140202826A1 US 201414220634 A US201414220634 A US 201414220634A US 2014202826 A1 US2014202826 A1 US 2014202826A1
Authority
US
United States
Prior art keywords
stage
solvent
separator
asphaltene
bitumen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US14/220,634
Inventor
Geoff Stevens
Ray REIPAS
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TotalEnergies E&P Canada Ltd
Original Assignee
Total E&P Canada Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Total E&P Canada Ltd filed Critical Total E&P Canada Ltd
Priority to US14/220,634 priority Critical patent/US20140202826A1/en
Publication of US20140202826A1 publication Critical patent/US20140202826A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G21/00Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
    • C10G21/02Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents with two or more solvents, which are introduced or withdrawn separately
    • 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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • C10G1/045Separation of insoluble materials
    • 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
    • C10G53/00Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes
    • 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
    • C10G53/00Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes
    • C10G53/02Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only
    • C10G53/04Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural serial stages only including at least one extraction step
    • 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
    • C10G53/00Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes
    • C10G53/16Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more refining processes plural parallel stages only

Definitions

  • the invention relates to the separation of bitumen, solvent, water, solids and asphaltenes in a paraffinic froth treatment process. More particularly, solvent is added to the influent of each of at least two stages of three stages of separation. The overflows of the first and second stages combine at the third stage for recovery of a diluted bitumen product stream and an asphaltene by-product stream.
  • Recovery of bitumen from mined oilsands involves separation of a bitumen-rich froth from an oilsand slurry, and treatment of the froth to remove impurities and produce a marketable product.
  • Known paraffinic froth treatment processes involve the addition of a paraffinic solvent to the bitumen-rich froth which enables separation of the mineral and water contaminants and production of a marketable bitumen product.
  • Asphaltenes in the bitumen precipitate if sufficient paraffinic solvent is mixed with froth.
  • a froth settler vessel the precipitated asphaltenes settle along with the mineral and water contaminants.
  • This gravity settling process separates the diluted froth into two streams; a diluted bitumen product at a top and an underflow at a bottom.
  • the underflow is a mixture of solids, water, bitumen, solvent and precipitated asphaltenes.
  • the paraffinic froth treatment process can be sub-divided into three components: froth settler/separation, solvent recovery and tailings solvent recovery.
  • the diluted bitumen product is sent to a solvent recovery unit (SRU) where solvent is recovered for re-use and clean bitumen is obtained as the feed to an upgrading process.
  • Underflow from froth settling/separation is sent to a tailing solvent recovery unit (TSRU) to recover residual solvent.
  • SRU solvent recovery unit
  • TSRU tailing solvent recovery unit
  • Conventional settler/separation operations implement a counter-current, multi-stage system to produce two streams, a solvent-rich diluted bitumen product (which includes some asphaltenes), and an underflow tailings stream containing solids, water, bitumen, solvent and precipitated asphaltenes.
  • a distillation column is employed for recovering relatively volatile solvent from the solvent-rich diluted bitumen product and delivering a clean, solvent-free, bitumen product and solvent stream for reuse.
  • a tailings solvent recovery unit In a tailings solvent recovery unit (TSRU), residual solvent in the settler underflow stream is recovered to ensure that a final tailings stream contains minimal amounts of residual solvent.
  • a TSRU vessel is a flash tower into which the hot, pressurized tailings stream is released, resulting in rapid vaporization of the bulk of the residual solvent from the tailings. Steam may be added to further scavenge solvent from the tailings.
  • CA 2,454,942 describes a process in which a low-molecular weight paraffin is used as the solvent in a two-stage settler configuration. Underflow from a first stage settler is directed as influent to a second stage settler. In this process, the only introduction of solvent is by addition to the influent of the second stage settler, and the second stage settler overflow is recycled to the influent of the first stage settler. The overflow product of the first stage settler is the final product to the SRU. Accordingly, solvent is only added to the first stage settler by recycling back from the second stage settler overflow. The process is known as a counter-current process as the solvent flows counter-currently to the flow of froth. The second stage underflow is the influent to the TSRU.
  • CA 2,521,248 describes a process which applies three settlers. As in the True North process, there is a recycling of the overflow from the second stage settler to the influent of the first stage settler.
  • the second stage overflow contains mainly solvent and diluted bitumen.
  • the overflow of the third stage settler is recycled back to the influent of the second stage settler.
  • the overflow product of the first stage settler is the final product to the SRU.
  • the only introduction of solvent is by addition to the influent of the third stage settler, and therefore solvent is only recycled to the first and second stage settlers by recycling back from the third stage settler.
  • a counter-current process is described with the overflow product of the first stage settler being the final diluted bitumen product to the SRU and the third stage underflow being the influent to the TSRU.
  • each of the True North and Shell processes result in a single, high water content waste stream for downstream processing in the TSRU.
  • the True North process results in about 7% of the bitumen in the froth being precipitated as asphaltenes and lost to the tailings. Asphaltenes are not a desirable component in a tailings stream or the bitumen product stream.
  • the present invention provides a system, process and arrangement of separator stages and staged solvent addition which redirects asphaltenes preferentially from waste tailings to a new asphaltene by-product stream.
  • the waste tailings contain a lower proportion of asphaltenes than heretofore achieved.
  • Much of said asphaltenes are recovered in the asphaltene by-product stream that were otherwise lost to waste tailings in the prior art processes.
  • Paraffinic solvent is known to precipitate asphaltenes from bitumen froth. However, as disclosed herein, it has been discovered that use of controlled and multiple points of addition of paraffinic solvent, split between multiple stages of separators, and the arrangement of the separators cooperate to control the precipitation.
  • At least three stages of separation are provided.
  • a first stage and a second stage are arranged in series, the underflow of the first stage flowing as influent to the second stage.
  • the overflows of the first and second stages are combined as the influent to a third stage.
  • Paraffinic solvent is added to the influent of the first stage and to the influent of at least one of the second or third stages.
  • the solvent to bitumen ratio (S/B ratio) is controlled.
  • three product streams are recovered: a waste tailings from the underflow of the second stage which is high in water and low in hydrocarbon fractions, a solvent-diluted bitumen stream from the overflow of the third stage and an asphaltene by-product stream from the underflow of the third stage which is also low in solids and low in water fractions.
  • asphaltene is a constituent of the bitumen
  • the recovery of bitumen in the diluted bitumen stream may be reduced slightly as asphaltenes are precipitated and redistributed between the waste tailings and asphaltene by-product stream.
  • the precipitation of asphaltenes from the froth yields an improved quality or cleanliness of the diluted bitumen.
  • asphaltene precipitation manipulate asphaltene precipitation to best advantage.
  • solvent addition to the first stage can result in precipitation of asphaltenes which are lost to waste tailings, however, some asphaltene precipitation also aids in water and solids separation from the froth.
  • asphaltenes can precipitate from bitumen in the first stage underflow and be lost to waste tailings, but will also result in additional recovery of bitumen from the second stage overflow for delivery to the third stage. All bitumen, including asphaltenes, reporting to the third stage is now recoverable.
  • An overall S/B ratio achieved by confluence of at least the first and second stage overflows at the third stage, and optionally of a third stage solvent addition. This overall S/B ratio aids in the precipitation of asphaltenes for further asphaltene-cleaning of the bitumen for recovery as a dilute bitumen product and recovery of the precipitated asphaltenes as an asphaltene by-product.
  • the paraffinic solvent is split between the first and second stages. Paraffinic solvent is added to the first stage in an S/B ratio which is below or in the vicinity of about a conventional asphaltene precipitation threshold. On the other hand, when paraffinic solvent is then added to the second stage, as a result of the influent to said second stage having a reduced bitumen fraction, this second solvent addition S/B ratio is much higher than a conventional asphaltene precipitation threshold.
  • the overall S/B ratio for the system remains comparable to that applied in conventional counter-current processes, however, having been applied in several stages.
  • solvent is added to the influent of the first stage and to each of the influents of the second and third stages of separation.
  • Each stage of the separation can be conducted in conventional froth settlers.
  • Alternate separators include centrifuges and hydrocyclones where appropriate. Centrifuges could be particularly suited at the first stage.
  • a process for treating bitumen froth comprises: directing the froth and a first paraffinic solvent as a first influent to a first stage separator.
  • a first underflow from the first stage separator is directed to a second stage separator.
  • a first overflow from the first stage separator is combined with a second overflow from the second stage separator as a third influent to a third stage separator.
  • a second underflow is produced from the second stage separator as a waste tailings.
  • At least a second paraffinic solvent is added to at least one of the second influent or third influent.
  • a third overflow from the third stage separator is produced as a diluted bitumen product, and a third underflow from the third stage separator is produced as an asphaltene by-product.
  • the at least a second paraffinic solvent is a second solvent added to the second influent. In another embodiment, the at least a second paraffinic solvent is a second solvent added to the third influent. In yet another embodiment, the at least a second paraffinic solvent comprises two solvent additions: a second solvent added to the second influent and a third solvent added to the third influent.
  • the first paraffinic solvent is added for precipitating little or substantially no asphaltenes, thereby minimizing losses to tailings.
  • the at least a second paraffinic solvent is added to control the fraction of asphaltene reporting at the third underflow. Hydrocarbon loss is minimized at the waste tailings and overall bitumen recovery is maximized.
  • FIG. 1 is a flow diagram of an embodiment of a froth treatment process of the present invention having two stages of solvent addition;
  • FIG. 2 is a flow diagram of an embodiment of a froth treatment process of the present invention having three stages of solvent addition.
  • Paraffinic solvent is added to a bitumen-rich froth which enables separation of the mineral and water contaminants and production of a marketable bitumen product.
  • Paraffinic solvent is admixed with froth and introduced to a froth separator. The solvent dissolves in the bitumen fraction of the froth.
  • An amount of solvent added is typically referred to in terms of a solvent to bitumen ratio (S/B ratio).
  • a flow-through froth treatment process comprises a process and system for introducing paraffinic solvent to bitumen-rich froth and separating a solvent-diluted bitumen therefrom in at least three stages of separation, one result being the formation of a new, asphaltene by-product stream.
  • each of multiple stages of separation may also be referred to as settlers, although other separation processes could also be employed including centrifuges and hydrocyclones. Accordingly, except where the context is expressly otherwise, the term “settlers” is also to be read broadly as a separator which happens to include at least settlers, centrifuges and hydrocyclones.
  • froth F is directed as a part of a first stage influent or first influent 5 to a first stage separator 10 .
  • a first solvent S1 is added to the froth F to form part of the first influent 5 .
  • a first underflow 12 from the first stage settler 10 is directed to form part of a second stage influent or second influent 15 to a second stage settler 20 .
  • a second solvent S2 is added to the first underflow 12 and forms part of the second influent 15 to the second stage settler 20 .
  • a second underflow 22 from the second stage settler 20 is produced as a waste tailings T.
  • a first overflow 11 from the first stage settler 10 is directed to form part of a third stage influent or third influent 25 which is directed to a third stage settler 30 .
  • a second overflow 21 from the second stage settler 20 is also directed to and forms a part of the third influent stream 25 to the third stage settler 30 .
  • a third overflow 31 from the third stage settler 30 is produced as a diluted bitumen product P.
  • a third underflow 32 from the third stage settler 30 is produced as an asphaltene by-product A.
  • asphaltene precipitation can now be controlled so as to aid in froth treatment and yet also to redistribute precipitated asphaltenes for reducing losses in the waste tailing T and recovering precipitated asphaltenes in the new asphaltene by-product A.
  • the diluted bitumen product P is cleaner, having been liberated of some asphaltenes.
  • the asphaltene by-product stream A happens to be characterized by a low water and low mineral content.
  • any one or more of the first, second or third stage settlers 10 , 20 , 30 can comprise one or more physical separators to meet the process requirements.
  • Conventional separation vessels can be employed including settlers such as vertical and inclined plate settlers.
  • Other separation vessels include centrifuges or hydrocyclones.
  • the waste tailing stream T is directed to a tailing treatment process such as a TSRU.
  • the diluted bitumen product P is directed to a SRU.
  • the asphaltene by-product stream A is directed for further processing or use.
  • solvent is added in at least two stages, the first solvent stream S1 being added to the froth F as part of the first influent 5 to the first stage settler 10 .
  • the second solvent stream S2 is added to at least a further stage, shown in FIG. 1 as forming part of the second influent 15 directed to the second stage settler 20 .
  • the adding of a second paraffinic solvent S2 to the second influent 15 comprises controlling a fraction of asphaltene reporting at the third underflow 32 from the third stage settler 30 .
  • the combined, target or overall S/B ratio, that is (S1+S2)/B, provided to the froth treatment operations, can be conventional as is known by those of skill in the art.
  • Various ranges of S/B ratios are known for other paraffinic froth treatment processes and which are dependant upon various parameters including the grade of the bituminous ore, the particular paraffinic solvent being used and the temperature of the operations.
  • Known paraffinic solvents include C4 though C7, various mixtures thereof and natural gas condensate which includes alkanes of C5 through C16.
  • Asphaltenes tend to exhibit greater solubility in longer chain paraffinic solvents than in shorter chain paraffinic solvents, with the result that the amount of asphaltenes precipitated decreases as the selected paraffinic solvent becomes heavier or longer chained. Asphaltene precipitation is therefore generally greater in pentane than it is in hexane, heptane or octane.
  • the precipitation of asphaltenes from the bitumen froth stream is also dependent upon the selection of the operating temperature for the separating step. The amount of asphaltenes precipitated from a particular solvent will generally decrease as the operating temperature is increased.
  • the precipitation of asphaltenes from the bitumen froth stream is also dependent upon the amount of diluent solvent which is added to the bitumen froth stream.
  • the amount of asphaltenes precipitated from a particular solvent will generally increase as the amount of the solvent, S/B ratio, increases.
  • a common and conventional range of overall S/B ratio is about 1 to about 2.
  • the solvent S1,S2 is introduced as part of the first and second influents 5 , 15 respectively and the total solvent is therefore split between the first and second stage settlers 10 , 20 .
  • the amount of solvent S1,S2 added is controlled through the control of the S/B ratio.
  • the first solvent S1 is added to the bitumen froth F and the mixture forms the first influent 5 to the first stage settler 10 .
  • the amount of the first solvent S1 is controlled in order to have an S/B ratio below, up to or in the vicinity of about an asphaltene precipitation threshold.
  • a typical S/B ratio would be selected so as to be at or above an asphaltene precipitation threshold, for example at about 1.5 for the conventional two-stage, counter-current froth treatment process.
  • the prior art process has one opportunity, at the first stage vessel, to recover a diluted bitumen product. Greater S/B ratios are known to result in greater asphaltene precipitation.
  • one embodiment applies an S/B ratio of the first solvent S1 at a first addition S/B ratio which is non-zero and can be up to and about the asphaltene precipitation threshold for the conditions present at the first stage settler.
  • this approach results in little or substantially no asphaltene precipitation.
  • the first addition S/B ratio ranges from about 0.7 to about 0.9.
  • the first stage settler 10 produces a first underflow 12 containing mainly solids, water, with a small amount of bitumen, and the possibility of a small amount of precipitated asphaltenes. Most of the water and solids are separated or dropped out, at least in part as a result of the first solvent S1. As discussed, the first additional S/B ratio is generally lower compared to the prior art and the asphaltene precipitation threshold.
  • the first overflow 11 produced by the first stage settler 10 contains diluted bitumen, water, and solids. The diluted bitumen includes any asphaltenes not reporting to the first underflow 12 .
  • the second solvent S2 is then added at a second addition S/B ratio to the first stage settler's first underflow 12 and the mixture is directed as second influent 15 to the second stage settler 20 .
  • the low magnitude of the bitumen denominator results in a second addition S/B ratio, entering the second stage settler 20 , which is very high. Consequently, a large fraction or substantially all the residual asphaltenes in the bitumen flowing to the second stage settler 20 are precipitated.
  • Precipitated asphaltenes are removed with the second underflow 22 to the waste tailings T along with essentially all the mineral and water entering the second stage settler 20 .
  • the amount of solvent S2 added in the second stage settler 20 is adjusted to control the rejection of asphaltene from the overall process.
  • the first and second overflows 11 and 21 from the first and second stage settlers 10 , 20 respectively are combined and directed as the influent stream 25 to the third stage settler 30 with an overall S/B ratio which is at about conventional S/B ratios.
  • the overall S/B ratio is about 1.25 or could be higher.
  • a third stream of solvent S3 could be added to form part of the third stage influent stream 25 .
  • Solvent S3 is added so as to more finely manage asphaltene precipitation and control the asphaltene by-product stream A from the third settler 30 .
  • the second addition S/B ratio is reduced to accommodate a third addition S/B ratio, the overall S/B ratio (S1+S2+S3)/B still being about conventional for known paraffinic froth treatment operations.
  • the water content in the third settler underflow 32 can be controlled by controlling the S/B ratios in each of the first and second stage settlers 10 , 20 , and optionally the third stage settler 30 .
  • the S/B ratio at the third influent stream 25 to the third stage settler 30 can be increased by adjusting the solvent S2 addition to the second stage settler 20 , or also by adding the optional solvent S3 to the third influent 25 of the third stage settler 30 .
  • water and solids content in the third stage settler underflow 32 can be about 25% or less which means that, having a hydrocarbon content contributed mostly by asphaltene and residual solvent, this asphaltene by-product stream A can be used as fuel either before or after additional processing to remove solvent and/or water.
  • Bitumen comprises maltenes and asphaltenes.
  • Froth F comprises bitumen, water and minerals. All percentages are in weight %.
  • Table 2 outlines the parameters in the paraffinic tests for the embodiment shown in FIG. 1 and Tables 2A, 2B and 3C present the results.
  • the solvent used was substantially pentane and the tests were conducted at 80° C. Each test happens to have been repeated using a demulsifier introduced to the first stage without significant adverse or beneficial effect.
  • Tables 2A, 2B and 2C report the recovery of the original bitumen in the froth to the various products, rounded to the nearest 0.1%.
  • the bitumen was recovered as follows: 88.6% to the diluted bitumen product P, 1.7% loss to waste tailings T and the balance of 9.7% in the asphaltene by-product A, for a total of 100% of the bitumen in the froth F.
  • Asphaltenes are concentrated in the asphaltene by-product A. From Table 1, initially 17.9 wt % of the bitumen in the froth F was asphaltenes.
  • Test A of the 9.7% of the bitumen recovered in the asphaltene by-product A, 42.5% was asphaltenes.
  • the asphaltene by-product A is further characterized by a low water and a low mineral content.
  • the asphaltene by-product A of Table 2C is combustible, having value as a fuel or other source of hydrocarbon.
  • Example D like Examples A-C, has solvent addition to two stages of separation according to FIG. 1 .
  • Example E is a test using solvent addition to all three stages of separation according to FIG. 2 . It was expected that the use of solvent addition to the third stage settler 30 would further decrease the amount of precipitated asphaltene lost to the waste tailings T. Accordingly, the second addition S/B ratio to second settler 20 was decreased with third addition S/B ratios of ⁇ 3 targeted with the objective of decreasing the amount of asphaltene precipitated in the second stage settler 20 and accordingly reporting to waste tailings T.

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)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

A process for treating bitumen froth with paraffinic solvent is provided which uses three stages of separation. Froth and a first solvent are directed to a first stage at a solvent/bitumen ratio for precipitating few or substantially no asphaltenes. A first stage underflow is directed to a second stage and a first stage overflow is directed to a third stage. A second stage underflow is directed to waste tailings and the second stage overflow joins the first stage overflow. A third stage underflow is recovered as an asphaltene by-product and a third stage overflow is recovered as a diluted bitumen product. At least a second solvent is added to one or both of the second or third stages for controlling a fraction of asphaltenes in the third stage underflow. Asphaltene loss to waste tailings is minimized and asphaltenes are now recovered as asphaltene by-product.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a divisional application of U.S. patent application Ser. No. 12/582,662, filed Oct. 20, 2009 (allowed), which was a non-provisional application based on U.S. Provisional Patent Application Ser. No. 61/107,617, filed Oct. 22, 2008, both of which are incorporated by reference in their entirety.
  • FIELD OF THE INVENTION
  • The invention relates to the separation of bitumen, solvent, water, solids and asphaltenes in a paraffinic froth treatment process. More particularly, solvent is added to the influent of each of at least two stages of three stages of separation. The overflows of the first and second stages combine at the third stage for recovery of a diluted bitumen product stream and an asphaltene by-product stream.
  • BACKGROUND OF THE INVENTION
  • Recovery of bitumen from mined oilsands involves separation of a bitumen-rich froth from an oilsand slurry, and treatment of the froth to remove impurities and produce a marketable product. Known paraffinic froth treatment processes involve the addition of a paraffinic solvent to the bitumen-rich froth which enables separation of the mineral and water contaminants and production of a marketable bitumen product. Asphaltenes in the bitumen precipitate if sufficient paraffinic solvent is mixed with froth. In a froth settler vessel the precipitated asphaltenes settle along with the mineral and water contaminants. This gravity settling process separates the diluted froth into two streams; a diluted bitumen product at a top and an underflow at a bottom. The underflow is a mixture of solids, water, bitumen, solvent and precipitated asphaltenes.
  • Typically, the paraffinic froth treatment process can be sub-divided into three components: froth settler/separation, solvent recovery and tailings solvent recovery. After the froth settling/separation, the diluted bitumen product is sent to a solvent recovery unit (SRU) where solvent is recovered for re-use and clean bitumen is obtained as the feed to an upgrading process. Underflow from froth settling/separation is sent to a tailing solvent recovery unit (TSRU) to recover residual solvent.
  • Conventional settler/separation operations implement a counter-current, multi-stage system to produce two streams, a solvent-rich diluted bitumen product (which includes some asphaltenes), and an underflow tailings stream containing solids, water, bitumen, solvent and precipitated asphaltenes.
  • In a solvent recovery unit (SRU), a distillation column is employed for recovering relatively volatile solvent from the solvent-rich diluted bitumen product and delivering a clean, solvent-free, bitumen product and solvent stream for reuse.
  • In a tailings solvent recovery unit (TSRU), residual solvent in the settler underflow stream is recovered to ensure that a final tailings stream contains minimal amounts of residual solvent. Conventionally, a TSRU vessel is a flash tower into which the hot, pressurized tailings stream is released, resulting in rapid vaporization of the bulk of the residual solvent from the tailings. Steam may be added to further scavenge solvent from the tailings.
  • Two prior art processes which implement counter-current processes are Canadian Patent application 2,454,942 to True North Energy and Canadian patent 2,521,248 to Shell et al.
  • CA 2,454,942 describes a process in which a low-molecular weight paraffin is used as the solvent in a two-stage settler configuration. Underflow from a first stage settler is directed as influent to a second stage settler. In this process, the only introduction of solvent is by addition to the influent of the second stage settler, and the second stage settler overflow is recycled to the influent of the first stage settler. The overflow product of the first stage settler is the final product to the SRU. Accordingly, solvent is only added to the first stage settler by recycling back from the second stage settler overflow. The process is known as a counter-current process as the solvent flows counter-currently to the flow of froth. The second stage underflow is the influent to the TSRU.
  • CA 2,521,248 describes a process which applies three settlers. As in the True North process, there is a recycling of the overflow from the second stage settler to the influent of the first stage settler. The second stage overflow contains mainly solvent and diluted bitumen. Further, the overflow of the third stage settler is recycled back to the influent of the second stage settler. The overflow product of the first stage settler is the final product to the SRU. The only introduction of solvent is by addition to the influent of the third stage settler, and therefore solvent is only recycled to the first and second stage settlers by recycling back from the third stage settler. Again, a counter-current process is described with the overflow product of the first stage settler being the final diluted bitumen product to the SRU and the third stage underflow being the influent to the TSRU.
  • Other than the diluted bitumen product stream, each of the True North and Shell processes result in a single, high water content waste stream for downstream processing in the TSRU. The True North process results in about 7% of the bitumen in the froth being precipitated as asphaltenes and lost to the tailings. Asphaltenes are not a desirable component in a tailings stream or the bitumen product stream.
  • There is a need for recovering at least some of the asphaltenes otherwise lost to the tailings for reducing environmental impact, or for other beneficial purposes. Further, improved handling of the asphaltenes fraction can result in reduced asphaltene content in the diluted bitumen product. Simply, there are synergistic objectives to reduce hydrocarbon loss in tailings and to recover a valuable product from what is otherwise wasted.
  • SUMMARY OF THE INVENTION
  • The present invention provides a system, process and arrangement of separator stages and staged solvent addition which redirects asphaltenes preferentially from waste tailings to a new asphaltene by-product stream. As a result, the waste tailings contain a lower proportion of asphaltenes than heretofore achieved. Much of said asphaltenes are recovered in the asphaltene by-product stream that were otherwise lost to waste tailings in the prior art processes.
  • Paraffinic solvent is known to precipitate asphaltenes from bitumen froth. However, as disclosed herein, it has been discovered that use of controlled and multiple points of addition of paraffinic solvent, split between multiple stages of separators, and the arrangement of the separators cooperate to control the precipitation.
  • In embodiments of froth treatment disclosed herein, at least three stages of separation are provided. A first stage and a second stage are arranged in series, the underflow of the first stage flowing as influent to the second stage. The overflows of the first and second stages are combined as the influent to a third stage. Paraffinic solvent is added to the influent of the first stage and to the influent of at least one of the second or third stages. The solvent to bitumen ratio (S/B ratio) is controlled. As a result, three product streams are recovered: a waste tailings from the underflow of the second stage which is high in water and low in hydrocarbon fractions, a solvent-diluted bitumen stream from the overflow of the third stage and an asphaltene by-product stream from the underflow of the third stage which is also low in solids and low in water fractions. As asphaltene is a constituent of the bitumen, the recovery of bitumen in the diluted bitumen stream may be reduced slightly as asphaltenes are precipitated and redistributed between the waste tailings and asphaltene by-product stream. The precipitation of asphaltenes from the froth yields an improved quality or cleanliness of the diluted bitumen.
  • Simply, the embodiments herein manipulate asphaltene precipitation to best advantage. For example, solvent addition to the first stage can result in precipitation of asphaltenes which are lost to waste tailings, however, some asphaltene precipitation also aids in water and solids separation from the froth. Further, in an embodiment adding solvent addition to the second stage, asphaltenes can precipitate from bitumen in the first stage underflow and be lost to waste tailings, but will also result in additional recovery of bitumen from the second stage overflow for delivery to the third stage. All bitumen, including asphaltenes, reporting to the third stage is now recoverable. An overall S/B ratio achieved by confluence of at least the first and second stage overflows at the third stage, and optionally of a third stage solvent addition. This overall S/B ratio aids in the precipitation of asphaltenes for further asphaltene-cleaning of the bitumen for recovery as a dilute bitumen product and recovery of the precipitated asphaltenes as an asphaltene by-product.
  • In one embodiment, the paraffinic solvent is split between the first and second stages. Paraffinic solvent is added to the first stage in an S/B ratio which is below or in the vicinity of about a conventional asphaltene precipitation threshold. On the other hand, when paraffinic solvent is then added to the second stage, as a result of the influent to said second stage having a reduced bitumen fraction, this second solvent addition S/B ratio is much higher than a conventional asphaltene precipitation threshold.
  • In embodiments, the overall S/B ratio for the system remains comparable to that applied in conventional counter-current processes, however, having been applied in several stages.
  • In another embodiment, solvent is added to the influent of the first stage and to each of the influents of the second and third stages of separation.
  • Each stage of the separation can be conducted in conventional froth settlers. Alternate separators include centrifuges and hydrocyclones where appropriate. Centrifuges could be particularly suited at the first stage.
  • Accordingly, in one aspect of the invention, a process for treating bitumen froth comprises: directing the froth and a first paraffinic solvent as a first influent to a first stage separator. A first underflow from the first stage separator is directed to a second stage separator. A first overflow from the first stage separator is combined with a second overflow from the second stage separator as a third influent to a third stage separator. A second underflow is produced from the second stage separator as a waste tailings. At least a second paraffinic solvent is added to at least one of the second influent or third influent. Finally, a third overflow from the third stage separator is produced as a diluted bitumen product, and a third underflow from the third stage separator is produced as an asphaltene by-product.
  • In one embodiment, the at least a second paraffinic solvent is a second solvent added to the second influent. In another embodiment, the at least a second paraffinic solvent is a second solvent added to the third influent. In yet another embodiment, the at least a second paraffinic solvent comprises two solvent additions: a second solvent added to the second influent and a third solvent added to the third influent.
  • The first paraffinic solvent is added for precipitating little or substantially no asphaltenes, thereby minimizing losses to tailings. The at least a second paraffinic solvent is added to control the fraction of asphaltene reporting at the third underflow. Hydrocarbon loss is minimized at the waste tailings and overall bitumen recovery is maximized.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a flow diagram of an embodiment of a froth treatment process of the present invention having two stages of solvent addition; and
  • FIG. 2 is a flow diagram of an embodiment of a froth treatment process of the present invention having three stages of solvent addition.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Paraffinic solvent is added to a bitumen-rich froth which enables separation of the mineral and water contaminants and production of a marketable bitumen product. Paraffinic solvent is admixed with froth and introduced to a froth separator. The solvent dissolves in the bitumen fraction of the froth. An amount of solvent added is typically referred to in terms of a solvent to bitumen ratio (S/B ratio).
  • Conventionally, sufficient paraffinic solvent is added to the froth to precipitate asphaltenes. The diluted solvent/bitumen hydrocarbon phase is less dense than the mineral, water and precipitated asphaltenes. Further, during the separation process, precipitated asphaltenes have the beneficial effect of capturing incremental mineral and water that would otherwise not have been separated out of the hydrocarbon phase. Generally speaking, the greater the asphaltene precipitation, the cleaner will be the diluted bitumen product obtained after the separation is complete, this cleaner diluted bitumen product having a lower asphaltene content.
  • In an embodiment of the invention, a flow-through froth treatment process comprises a process and system for introducing paraffinic solvent to bitumen-rich froth and separating a solvent-diluted bitumen therefrom in at least three stages of separation, one result being the formation of a new, asphaltene by-product stream.
  • In the embodiments described herein, each of multiple stages of separation may also be referred to as settlers, although other separation processes could also be employed including centrifuges and hydrocyclones. Accordingly, except where the context is expressly otherwise, the term “settlers” is also to be read broadly as a separator which happens to include at least settlers, centrifuges and hydrocyclones.
  • Having reference to FIG. 1, froth F is directed as a part of a first stage influent or first influent 5 to a first stage separator 10. A first solvent S1 is added to the froth F to form part of the first influent 5. A first underflow 12 from the first stage settler 10 is directed to form part of a second stage influent or second influent 15 to a second stage settler 20.
  • A second solvent S2 is added to the first underflow 12 and forms part of the second influent 15 to the second stage settler 20. A second underflow 22 from the second stage settler 20 is produced as a waste tailings T.
  • A first overflow 11 from the first stage settler 10 is directed to form part of a third stage influent or third influent 25 which is directed to a third stage settler 30.
  • A second overflow 21 from the second stage settler 20 is also directed to and forms a part of the third influent stream 25 to the third stage settler 30.
  • A third overflow 31 from the third stage settler 30 is produced as a diluted bitumen product P.
  • A third underflow 32 from the third stage settler 30 is produced as an asphaltene by-product A.
  • The introduction of an asphaltene by-product A permits the process to control asphaltene distribution. The prior art is constrained to balance the need for asphaltene precipitation between competing objectives. On one hand, the prior art encourages precipitation of asphaltenes to aid in froth separation but, on the other hand, precipitated asphaltenes are lost with the tailings. In CA 2,454,942 at page 24, it was recognized that since asphaltenes are essentially hydrocarbons, their precipitation during the separating step should be managed to minimize loss of hydrocarbons from the diluted bitumen component and to minimize the amount of precipitated asphaltenes which are contained in the tailings component. The process disclosed in CA 2,454,942 limited their implementation of those objectives.
  • Herein, asphaltene precipitation can now be controlled so as to aid in froth treatment and yet also to redistribute precipitated asphaltenes for reducing losses in the waste tailing T and recovering precipitated asphaltenes in the new asphaltene by-product A. Further, the diluted bitumen product P is cleaner, having been liberated of some asphaltenes. Further, the asphaltene by-product stream A happens to be characterized by a low water and low mineral content.
  • Herein, any one or more of the first, second or third stage settlers 10,20,30 can comprise one or more physical separators to meet the process requirements. Conventional separation vessels can be employed including settlers such as vertical and inclined plate settlers. Other separation vessels include centrifuges or hydrocyclones.
  • In an embodiment of the invention, the waste tailing stream T is directed to a tailing treatment process such as a TSRU. The diluted bitumen product P is directed to a SRU. The asphaltene by-product stream A is directed for further processing or use.
  • As shown, solvent is added in at least two stages, the first solvent stream S1 being added to the froth F as part of the first influent 5 to the first stage settler 10. The second solvent stream S2 is added to at least a further stage, shown in FIG. 1 as forming part of the second influent 15 directed to the second stage settler 20. The adding of a second paraffinic solvent S2 to the second influent 15 comprises controlling a fraction of asphaltene reporting at the third underflow 32 from the third stage settler 30.
  • The combined, target or overall S/B ratio, that is (S1+S2)/B, provided to the froth treatment operations, can be conventional as is known by those of skill in the art. Various ranges of S/B ratios are known for other paraffinic froth treatment processes and which are dependant upon various parameters including the grade of the bituminous ore, the particular paraffinic solvent being used and the temperature of the operations. Known paraffinic solvents include C4 though C7, various mixtures thereof and natural gas condensate which includes alkanes of C5 through C16.
  • Again, as set forth in CA 2,454,942, one view is that asphaltenes tend to exhibit greater solubility in longer chain paraffinic solvents than in shorter chain paraffinic solvents, with the result that the amount of asphaltenes precipitated decreases as the selected paraffinic solvent becomes heavier or longer chained. Asphaltene precipitation is therefore generally greater in pentane than it is in hexane, heptane or octane. The precipitation of asphaltenes from the bitumen froth stream is also dependent upon the selection of the operating temperature for the separating step. The amount of asphaltenes precipitated from a particular solvent will generally decrease as the operating temperature is increased. Finally, the precipitation of asphaltenes from the bitumen froth stream is also dependent upon the amount of diluent solvent which is added to the bitumen froth stream. The amount of asphaltenes precipitated from a particular solvent will generally increase as the amount of the solvent, S/B ratio, increases.
  • A common and conventional range of overall S/B ratio is about 1 to about 2.
  • In the embodiment of FIG. 1, the solvent S1,S2 is introduced as part of the first and second influents 5,15 respectively and the total solvent is therefore split between the first and second stage settlers 10,20. The amount of solvent S1,S2 added is controlled through the control of the S/B ratio.
  • The first solvent S1 is added to the bitumen froth F and the mixture forms the first influent 5 to the first stage settler 10. The amount of the first solvent S1 is controlled in order to have an S/B ratio below, up to or in the vicinity of about an asphaltene precipitation threshold. In prior art processes, a typical S/B ratio would be selected so as to be at or above an asphaltene precipitation threshold, for example at about 1.5 for the conventional two-stage, counter-current froth treatment process. The prior art process has one opportunity, at the first stage vessel, to recover a diluted bitumen product. Greater S/B ratios are known to result in greater asphaltene precipitation.
  • Herein, in contrast to the prior art processes, one embodiment applies an S/B ratio of the first solvent S1 at a first addition S/B ratio which is non-zero and can be up to and about the asphaltene precipitation threshold for the conditions present at the first stage settler. In contra-distinction to the prior art, this approach results in little or substantially no asphaltene precipitation. In the exemplary embodiment of FIG. 1 and corresponding Examples A, B, C and D, using substantially pentane as the first stage solvent S1, the first addition S/B ratio ranges from about 0.7 to about 0.9.
  • Consequently, the first stage settler 10 produces a first underflow 12 containing mainly solids, water, with a small amount of bitumen, and the possibility of a small amount of precipitated asphaltenes. Most of the water and solids are separated or dropped out, at least in part as a result of the first solvent S1. As discussed, the first additional S/B ratio is generally lower compared to the prior art and the asphaltene precipitation threshold. The first overflow 11 produced by the first stage settler 10 contains diluted bitumen, water, and solids. The diluted bitumen includes any asphaltenes not reporting to the first underflow 12.
  • The second solvent S2 is then added at a second addition S/B ratio to the first stage settler's first underflow 12 and the mixture is directed as second influent 15 to the second stage settler 20. As the amount of diluted bitumen remaining in the first underflow 12 is already low, the low magnitude of the bitumen denominator results in a second addition S/B ratio, entering the second stage settler 20, which is very high. Consequently, a large fraction or substantially all the residual asphaltenes in the bitumen flowing to the second stage settler 20 are precipitated. Precipitated asphaltenes are removed with the second underflow 22 to the waste tailings T along with essentially all the mineral and water entering the second stage settler 20. In this embodiment, the amount of solvent S2 added in the second stage settler 20, the second addition S/B ratio, is adjusted to control the rejection of asphaltene from the overall process.
  • The first and second overflows 11 and 21 from the first and second stage settlers 10,20 respectively are combined and directed as the influent stream 25 to the third stage settler 30 with an overall S/B ratio which is at about conventional S/B ratios. For paraffinic solvents which are substantially pentane, the overall S/B ratio is about 1.25 or could be higher.
  • As a result, the water and solids content in the third stage underflow 32 is low, and the asphaltenes therein are recoverable in the asphaltene by-product A.
  • With reference to FIG. 2, in an optional embodiment, a third stream of solvent S3 could be added to form part of the third stage influent stream 25. Solvent S3 is added so as to more finely manage asphaltene precipitation and control the asphaltene by-product stream A from the third settler 30. The second addition S/B ratio is reduced to accommodate a third addition S/B ratio, the overall S/B ratio (S1+S2+S3)/B still being about conventional for known paraffinic froth treatment operations.
  • The water content in the third settler underflow 32 can be controlled by controlling the S/B ratios in each of the first and second stage settlers 10,20, and optionally the third stage settler 30. For example, if it is desirable to reduce water and solid content, more solvent S1 can be added in the first stage settler 10. If more asphaltene precipitation is desired, the S/B ratio at the third influent stream 25 to the third stage settler 30 can be increased by adjusting the solvent S2 addition to the second stage settler 20, or also by adding the optional solvent S3 to the third influent 25 of the third stage settler 30.
  • Test results have shown that water and solids content in the third stage settler underflow 32 can be about 25% or less which means that, having a hydrocarbon content contributed mostly by asphaltene and residual solvent, this asphaltene by-product stream A can be used as fuel either before or after additional processing to remove solvent and/or water.
  • EXAMPLES
  • Bitumen comprises maltenes and asphaltenes. Froth F comprises bitumen, water and minerals. All percentages are in weight %.
  • Exemplary samples used in testing were as follows in Table 1:
  • TABLE 1
    Froth for Examples A-E
    Examples
    A, B, C D, E
    Component wt % wt %
    Bitumen 67.4 57.2
    Water 23.8 34.7
    Mineral 8.8 8.1
    Total 100.0 100.0
    Of the bitumen in the froth, 17.9 19.5
    % asphaltenes
  • Laboratory programs were conducted to assess different locations for multiple solvent addition and the effect on the redistribution of asphaltenes.
  • Examples A, B and C
  • Table 2 outlines the parameters in the paraffinic tests for the embodiment shown in FIG. 1 and Tables 2A, 2B and 3C present the results. The solvent used was substantially pentane and the tests were conducted at 80° C. Each test happens to have been repeated using a demulsifier introduced to the first stage without significant adverse or beneficial effect.
  • TABLE 2
    Examples A, B, C - Test Matrix for Paraffin Solvent
    S/B in each stage based on FIG. 1
    Overall S/B
    First stage Second Stage Target by Third
    10 20 Stage 30
    TEST S1/B S2/B (S1 + S2)/B
    A 0.7 11.5 1.25
    B 0.8 9.8 1.25
    C 0.9 5.5 1.25
  • Tables 2A, 2B and 2C report the recovery of the original bitumen in the froth to the various products, rounded to the nearest 0.1%. For example, for Test A, the bitumen was recovered as follows: 88.6% to the diluted bitumen product P, 1.7% loss to waste tailings T and the balance of 9.7% in the asphaltene by-product A, for a total of 100% of the bitumen in the froth F. Asphaltenes are concentrated in the asphaltene by-product A. From Table 1, initially 17.9 wt % of the bitumen in the froth F was asphaltenes. In Test A, of the 9.7% of the bitumen recovered in the asphaltene by-product A, 42.5% was asphaltenes.
  • TABLE 2A
    Examples A, B, C - Diluted Bitumen Product
    Diluted Bitumen Product P
    (Stream 31)
    Bitumen Water Solid
    S/B recovery Content Content
    TEST 10 (%) (wt %) (wt %)
    A 0.7 88.6 <0.1 0.024
    B 0.8 91.2 <0.1 0.021
    C 0.9 90.3 <0.1 0.048
  • TABLE 2B
    Examples A, B, C - Waste Tailings
    Waste Tailings T (stream 22)
    Bitumen Solvent Water
    S/B loss Content Content
    TEST 10 (%) (wt %) (wt %)
    A 0.7 1.7 2.9 82.8
    B 0.8 2.0 2.7 93.5
    C 0.9 3.7 0.3 86.0
  • It is understood that the prior art processes result in 8 to 10% of the bitumen reporting to the waste tailings stream, see J. H. Masliyah, “Extraction and Upgrading of Bitumen”, workshop Jun. 24 & 25, 2009, Calgary, p. B5-23. Examples A-C illustrate that bitumen loss to the waste tailings is significantly reduced and, correspondingly, difficulties and environmental aspects are reduced also.
  • TABLE 2C
    Examples A, B, C - Asphaltene By-Product
    Asphaltene By-Product A (Stream 32) Overall
    Asphaltene Bitumen
    Bitumen Content Water Solids Recovery
    S/B Recovery (wt % of Content Content (31 + 32)
    TEST 10 (%) Bitumen) (wt %) (wt %) (wt %)
    A 0.7 9.7 42.5 18.5 6.5 98.3
    B 0.8 6.8 40.9 20.0 5.2 98.0
    C 0.9 6.0 41.3 18.9 5.8 96.4
  • The asphaltene by-product A is further characterized by a low water and a low mineral content. In the prior art, there is no asphaltene by-product A at all, and this otherwise recoverable bitumen is needlessly lost to tailings.
  • As noted above, the asphaltene by-product A of Table 2C is combustible, having value as a fuel or other source of hydrocarbon.
  • Examples D, E
  • Tests for Examples D and E are additional tests performed at a different laboratory and using a different froth composition (see Table 1). Example D, like Examples A-C, has solvent addition to two stages of separation according to FIG. 1.
  • Example E is a test using solvent addition to all three stages of separation according to FIG. 2. It was expected that the use of solvent addition to the third stage settler 30 would further decrease the amount of precipitated asphaltene lost to the waste tailings T. Accordingly, the second addition S/B ratio to second settler 20 was decreased with third addition S/B ratios of <3 targeted with the objective of decreasing the amount of asphaltene precipitated in the second stage settler 20 and accordingly reporting to waste tailings T.
  • With reference to Tables 3A, 3B and 3C, the recovery of the original bitumen in the froth 5 is illustrated for the various product streams 22, 31 and 32.
  • TABLE 3A
    Examples D, E - Diluted Bitumen Product
    Diluted Bitumen Product P
    (Stream 31)
    Bitumen Water Solid
    S/B recovery Content Content
    TEST 10 (%) (wt %) (wt %)
    D 0.8 92.5 0.04 0.05
    E 0.8 92.9 0.01 0
  • In this additional testing of Examples D and E, both the two-way split solvent addition and the three-way split solvent addition, respectively, produced comparable diluted bitumen recovery relative to Examples A, B and C.
  • TABLE 3B
    Examples D, E - Waste Tailings
    Waste Tailings T (stream 22)
    Bitumen Solvent Water
    S/B loss Content Content
    TEST 10 (%) (wt %) (wt %)
    D 0.8 2.9 8.11 70.1
    E 0.8 4.1 17.7 62.8
  • Similarly, the Examples D and E consistently resulted in low bitumen losses to the wasted tailings.
  • TABLE 4C
    Examples D, E - Asphaltene By-Product
    Asphaltene By-Product (Stream 32) A Overall
    Asphaltene Bitumen
    Bitumen Content Water Solids Recovery
    S/B Recovery (wt % of Content Content (31 + 32)
    TEST 10 (%) Bitumen) (wt %) (wt %) (wt %)
    D 0.8 4.6 35.0 5.6 6.0 97.1
    E 0.8 3.0 46.0 0.35 0.8 95.9
  • The water and solids content in the asphaltene by-product of Examples D and E were consistently low, the overall recovery of bitumen at streams 31 and 32 was comparable to those from Examples A, B and C, the overall recovery of bitumen was improved over those recovered at the sole diluted bitumen product stream of the prior art.

Claims (17)

The embodiments of the invention for which an exclusive property or privilege is claimed are defined as follows:
1. A system for treating bitumen froth with paraffinic solvent comprising:
in a flow-through process,
a first stage froth treatment separator for receiving the froth and a paraffinic first solvent;
a second stage froth treatment separator for receiving, as a second stage influent, at least a first underflow from the first stage separator and producing a waste tailings from a second stage underflow; and
a third stage froth treatment separator for receiving a third stage influent of at least a first overflow from the first stage froth treatment separator and a second overflow from the second stage froth treatment separator, wherein
at least a second paraffinic solvent is combined with at least one of the second stage influent or the third stage influent,
the third stage froth treatment separator produces a diluted bitumen product from a third stage overflow and produces an asphaltene by-product from a third stage underflow;
the first underflow flows through to the second stage froth treatment separator to report as either the second overflow or the waste tailings,
the first overflow flows through to the third stage froth treatment separator to report as either the diluted bitumen product or the asphaltene by-product; and
the second overflow directly flows through to the third stage froth treatment separator to report as either the diluted bitumen product or the asphaltene by-product.
2. The system of claim 1, wherein the second stage influent comprises the at least a second paraffinic solvent.
3. The system of claim 1, wherein the third stage influent comprises the at least a second paraffinic solvent.
4. The system of claim 1, wherein the second stage influent and the third stage influent each comprises the at least a second paraffinic solvent.
5. The system of claim 1, wherein the second stage influent comprises the at least a second paraffinic solvent and the third stage influent comprises a third paraffinic solvent.
6. The system of claim 5, wherein the first paraffinic solvent, the at least a second paraffinic solvent and the third paraffinic solvent are substantially pentane and wherein an overall solvent/bitumen ratio is about 1.25 or higher.
7. The system of claim 1, wherein the first paraffinic solvent and the at least a second paraffinic solvent are substantially pentane and wherein an overall solvent/bitumen ratio is about 1.25 or higher.
8. The system of claim 1, wherein the first paraffinic solvent is added to the first stage froth treatment separator in a first addition S/B ratio for minimizing asphaltene precipitation in the first stage froth treatment separator.
9. The system of claim 8, wherein the first addition S/B ratio is controlled between an S/B ratio below an asphaltene precipitation threshold and an S/B ratio up to about the asphaltene precipitation threshold.
10. The system of claim 9, wherein the first paraffinic solvent is substantially pentane and the first addition S/B ratio is non-zero and up to about 0.9.
11. The system of claim 8, wherein the at least a second paraffinic solvent being added to the second stage froth treatment separator or the third stage froth separator is controlled in order to control the fraction of asphaltene reporting at the third underflow.
12. The system of claim 1, wherein the at least a second paraffinic solvent being added to the second stage froth treatment separator or the third stage froth separator is controlled in order to control the fraction of asphaltene reporting at the third underflow.
13. The system of claim 1, wherein the first stage separator, the second stage separator and the third stage separator are settlers.
14. The system of claim 1, wherein the first stage separator is selected from the group of separators consisting of settlers, centrifuges and hydrocyclones.
15. The system of claim 1, wherein the first stage separator, the second stage separator and the third stage separator are selected from the group consisting of settlers, centrifuges and hydrocyclones.
16. The system of claim 1, wherein the waste tailings is substantially free of precipitated asphaltenes.
17. The system of claim 1, wherein at least the first stage and second stage froth treatment separators are arranged in series.
US14/220,634 2008-10-22 2014-03-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations Abandoned US20140202826A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US14/220,634 US20140202826A1 (en) 2008-10-22 2014-03-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US10761708P 2008-10-22 2008-10-22
CA2683123 2009-10-20
CA2683123A CA2683123C (en) 2008-10-22 2009-10-20 Process and system for production of asphaltene by-product in paraffinic froth treatment operations
US12/582,662 US8709237B2 (en) 2008-10-22 2009-10-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations
US14/220,634 US20140202826A1 (en) 2008-10-22 2014-03-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US12/582,662 Division US8709237B2 (en) 2008-10-22 2009-10-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations

Publications (1)

Publication Number Publication Date
US20140202826A1 true US20140202826A1 (en) 2014-07-24

Family

ID=42107790

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/582,662 Active 2032-11-08 US8709237B2 (en) 2008-10-22 2009-10-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations
US14/220,634 Abandoned US20140202826A1 (en) 2008-10-22 2014-03-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/582,662 Active 2032-11-08 US8709237B2 (en) 2008-10-22 2009-10-20 Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations

Country Status (2)

Country Link
US (2) US8709237B2 (en)
CA (1) CA2683123C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016008025A1 (en) * 2014-07-14 2016-01-21 Total E&P Canada, Ltd. Solvent to bitumen ratio assurance during froth separation

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8114274B2 (en) * 2008-07-21 2012-02-14 Syncrude Canada Ltd. Method for treating bitumen froth with high bitumen recovery and dual quality bitumen production
CN102712848B (en) 2009-08-17 2016-01-13 布拉克卡培都能源科技有限公司 Oil-sand extracts
CA2682109C (en) * 2009-10-27 2011-01-25 Imperial Oil Resources Limited Method and system for reclaiming waste hydrocarbon from tailings using solvent sequencing
CA2729457C (en) 2011-01-27 2013-08-06 Fort Hills Energy L.P. Process for integration of paraffinic froth treatment hub and a bitumen ore mining and extraction facility
CA2853070C (en) 2011-02-25 2015-12-15 Fort Hills Energy L.P. Process for treating high paraffin diluted bitumen
CA2931815C (en) 2011-03-01 2020-10-27 Fort Hills Energy L.P. Process and unit for solvent recovery from solvent diluted tailings derived from bitumen froth treatment
CA2865139C (en) 2011-03-04 2015-11-17 Fort Hills Energy L.P. Process for co-directional solvent addition to bitumen froth
CA2735311C (en) 2011-03-22 2013-09-24 Fort Hills Energy L.P. Process for direct steam injection heating of oil sands bitumen froth
CA2815785C (en) 2011-04-15 2014-10-21 Fort Hills Energy L.P. Heat recovery for bitumen froth treatment plant integration with temperature circulation loop circuits
CA2805804C (en) 2011-04-28 2014-07-08 Fort Hills Energy L.P. Process and tsru with inlet with multiple nozzle configuration for distribution of solvent diluted tailings
CA2857702C (en) 2011-05-04 2015-07-07 Fort Hills Energy L.P. Process for operating a bitumen froth treatment operation in turndown mode
CA2832269C (en) 2011-05-18 2017-10-17 Fort Hills Energy L.P. Temperature control of bitumen froth treatment process with trim heating of solvent streams
US9150795B2 (en) * 2011-09-22 2015-10-06 Total E&P Canada Ltd. Multi-stage counter-current froth settler and method of use
US10808183B2 (en) 2012-09-12 2020-10-20 The University Of Wyoming Research Corporation Continuous destabilization of emulsions
CA2887363A1 (en) * 2012-09-12 2014-03-20 John F. Schabron Methods for changing stability of water and oil emulsions
AR106171A1 (en) 2015-10-01 2017-12-20 Ecolab Usa Inc METHOD FOR SIMULATING HIGH PRESSURE PARAFFINAL FOAM TREATMENTS
US10954448B2 (en) 2017-08-18 2021-03-23 Canadian Natural Resources Limited High temperature paraffinic froth treatment process

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2200899A1 (en) * 1997-03-25 1998-09-25 Shell Canada Limited Method for processing a diluted oil sand froth
US20090200209A1 (en) * 2008-02-11 2009-08-13 Sury Ken N Upgrading Bitumen In A Paraffinic Froth Treatment Process

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5876592A (en) 1995-05-18 1999-03-02 Alberta Energy Co., Ltd. Solvent process for bitumen separation from oil sands froth
US6214213B1 (en) * 1995-05-18 2001-04-10 Aec Oil Sands, L.P. Solvent process for bitumen seperation from oil sands froth
CA2232929C (en) 1997-03-25 2004-05-25 Shell Canada Limited Method for processing a diluted oil sand froth
CA2217300C (en) 1997-09-29 2002-08-20 William Edward Shelfantook Solvent process for bitumen separation from oil sands froth
US6007709A (en) * 1997-12-31 1999-12-28 Bhp Minerals International Inc. Extraction of bitumen from bitumen froth generated from tar sands
CA3036668C (en) 2004-01-08 2021-07-06 Fort Hills Energy L.P. Paraffinic froth treatment techniques
ITMI20042446A1 (en) * 2004-12-22 2005-03-22 Eni Spa PROCEDURE FOR CONVERSION OF PESANTYI CHARGES SUCH AS HEAVY CRATES AND DISTILLATION RESIDUES
US20060196812A1 (en) * 2005-03-02 2006-09-07 Beetge Jan H Zone settling aid and method for producing dry diluted bitumen with reduced losses of asphaltenes
CA2521248C (en) 2005-09-26 2012-01-31 Shell Canada Limited Method for separating bitumen from an oil sand froth
CA2640914C (en) * 2008-10-10 2011-08-09 Northern Lights Partnership A multi-stage process for treating bitumen froth using a paraffinic diluent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2200899A1 (en) * 1997-03-25 1998-09-25 Shell Canada Limited Method for processing a diluted oil sand froth
US20090200209A1 (en) * 2008-02-11 2009-08-13 Sury Ken N Upgrading Bitumen In A Paraffinic Froth Treatment Process

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016008025A1 (en) * 2014-07-14 2016-01-21 Total E&P Canada, Ltd. Solvent to bitumen ratio assurance during froth separation

Also Published As

Publication number Publication date
US8709237B2 (en) 2014-04-29
CA2683123C (en) 2016-08-09
US20100096297A1 (en) 2010-04-22
CA2683123A1 (en) 2010-04-22

Similar Documents

Publication Publication Date Title
US8709237B2 (en) Process and system for recovery of asphaltene by-product in paraffinic froth treatment operations
US7998342B2 (en) Separation of tailings that include asphaltenes
CA1068228A (en) Process for recovery of bitumen from a bituminous froth
US7736501B2 (en) System and process for concentrating hydrocarbons in a bitumen feed
US9321967B2 (en) Oil sands extraction
US8382976B2 (en) Recovery of bitumen from froth treatment tailings
CA2573633C (en) Bitumen froth treatment process
CN104919024B (en) The selective deasphalting method of heavy feedstocks
CA2638120C (en) Method for treating bitumen froth with high bitumen recovery and dual quality bitumen production
US8114274B2 (en) Method for treating bitumen froth with high bitumen recovery and dual quality bitumen production
CA2693879A1 (en) A method for processing froth treatment tailings
CN105765035A (en) Method of selective deasphalting in series
CA2719865C (en) Oil sand slurry solids reduction to enhance extraction performance for problem ores
US9150795B2 (en) Multi-stage counter-current froth settler and method of use
US9296954B2 (en) Treatment of poor processing bitumen froth using supercritical fluid extraction
CA2590300C (en) System and process for concentrating hydrocarbons in a bitumen feed
US9371490B2 (en) Method for extracting bitumen from an oil sand stream
CA2738560C (en) Enhancing fine capture in paraffinic froth treatment process
CA2933966C (en) Paraffinic froth treatment with controlled aggregation
CA2900794C (en) Paraffinic froth pre-treatment
US9376630B2 (en) Method for extracting bitumen from an oil sand stream
CA3107143C (en) Process and system for treating bitumen-containing emulsions, such as bitumen froth, integrating naphthenic and paraffinic treatments
US5013428A (en) Recovery of oil from a shale containing the same
JPH0362753B2 (en)

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION