[go: up one dir, main page]

US3422000A - Phosphate additives in a tar sand water separation process - Google Patents

Phosphate additives in a tar sand water separation process Download PDF

Info

Publication number
US3422000A
US3422000A US508439A US3422000DA US3422000A US 3422000 A US3422000 A US 3422000A US 508439 A US508439 A US 508439A US 3422000D A US3422000D A US 3422000DA US 3422000 A US3422000 A US 3422000A
Authority
US
United States
Prior art keywords
oil
water
sand
range
zone
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.)
Expired - Lifetime
Application number
US508439A
Inventor
John A Bichard
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
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 Exxon Research and Engineering Co filed Critical Exxon Research and Engineering Co
Application granted granted Critical
Publication of US3422000A publication Critical patent/US3422000A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • 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
    • 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
    • C10G1/047Hot water or cold water extraction processes

Definitions

  • the present invention is broadly concerned with the recovery of hydrocarbons from tar sands.
  • the invention is more particularly concerned with an improved technique for the maximum removal of oil from tar sand utilizing a particular combination of phosphate additives.
  • a maximum amount of oil is removed from the sand which is associ ated with the froth separated from the treated sand.
  • tar sands exist which contain various types of hydrocarbons as, for example, the heavy oil deposits of Athabaska tar sands existing in Canada. These sands constitute tremendous reserves of hydrocarbon constituents.
  • the oil in the sands may vary from about 5% to 21% by volume, generally in the range of about 12% by volume.
  • the gravity of the oil ranges from about 6 to 10 API, generally about 8 API.
  • These sands lie from about 200 to 300 ft. below an overburden and the beds may range from about 100 to 400 ft. thick.
  • a typical oil recovered from the sands has an initial boiling point of about 300 F. 1.0% distilled to 430 F., 20.0% distilled to 650 F. and 50.0% distilled to 980 F.
  • a particular class of sodium phosphate compounds wherein the sodium concentration is maintained in a critical range from about 0.4 wt. percent to about 0.8 wt. percent preferably about 0.4 to 0.6 wt. percent, such as about 0.5 wt. percent, as compared with the sand in an initial stage wherein the amount of water utilized is in the range from about to 30% by weight based upon the sand.
  • the preferred amount of water is from about 18% to 26% by weight, preferably about 22% by weight.
  • the phos- 3,422,000 Patented Jan. 14, 1969 phate compound utilized is selected from the class of sodium phosphate compounds wherein the ratio of phosphorous to sodium varies from about 1:1 to 1:2, preferably about 121.7.
  • tar sands are introduced into initial stage 10 by means of feed line 1.
  • Water is introduced into initial stage or mixing zone 10 by means of line 2.
  • the amount of water utilized in initial stage 10 based upon the sand is in the range from about 15 to 30% preferably in the range of about 20 to 22% by weight.
  • Initial stage 10 is maintained at a temperature in the range from about 120 to 200 F., preferably at about 140 F., by any suitable means.
  • a sodium polyphosphate compound is introduced into initial stage 10 by means of line 3.
  • the amount of sodium polyphosphate utilized is such as to secure a sodium concentration based upon the amount of sand in the range from about 0.4 to 0.8 wt. percent, preferably about 0.5 wt. percent.
  • the sodium polyphosphate compound utilized is selected from the class of compounds wherein the phosphorous-to-sodium ratio is in the range from about 1:1 to 1:2, preferably about 111.7. Any suitable means of mixing may be utilized in zone 10 such as stirrers and the like.
  • the mixture is withdrawn from initial zone 10 by means of line 4 and mixed with additional water which is introduced by means of line 5.
  • the amount of additional water utilized is sufiicient to have from about -300% by weight of water, preferably about 200% by weight of water based upon the sand.
  • the mixture is then introduced into a secondary stage or separation zone 20.
  • the temperature in secondary stage 20 is in the range of from about to 200 F., preferably about F. Under these conditions sand and water substantially free of oil, is removed from secondary stage 20 by means of line 6 while an aqueous froth containing substantially all of the oil and a relatively small quantity of water is removed from zone 20 by means of line 7.
  • the Water phase and and removed by means of line 6 is passed into a sand separation zone 30 wherein a water phase free of sand is separated and preferably recycled to the system. Since this water phase contains the added phosphate the sand is removed from separation zone 30 by means of line 8 and disposed of as desired.
  • the oil-rich froth is then handled or processed in order to secure an oil phase.
  • One preferred method is to introduce the oil froth into a distillation zone 40 in order to remove overhead water by means of line 9. It is preferred that the oil phase withdrawn from distillation zone 40 by means of line 11 be at a temperature in the range from about 250 to 400 P. such as about 300 F.
  • a hydrocarbon diluent such as a hydrocarbon fraction boiling in the range from about 250 to 600 F. is added to the oil phase by means of line 12.
  • Other hydrocarbons may be added such as benzene, toluene, and the like.
  • the amount of diluent added is about 0.5 to 2.0 volumes of diluent per volume of oil.
  • Separation zone 50 may comprise filters or settling means.
  • a diluent oil phase is removed from separation zone 50 by means of line 14 and introduced into a diluent-heavy oil separation zone 60 wherein the diluent is separated and removed by means of line 15 and preferably recycled to the system.
  • the heavy oil phase is removed by means of line 16 and further processed as desired.
  • the oil froth contained a far greater concentration of oil when utilizing a sodium concentration in the range from about 0.4 to 0.8, and when using a phosphorous-to-sodium ratio as defined by the present invention.
  • Improved process for the recovery of oil from tar sands which comprises mixing said tar sand with from about wt. percent to 30 wt. percent of water in an initial mixing zone maintained at a temperature of about 120 F. to 200 F., adding a sodium phosphate compound to mixing zone so as to have a sodium concentration based upon the weight of the tar sand in the range from about 0.4 to about 0.8 wt.

Landscapes

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

Description

Jan. 14, 1969 J. A. BICHARD 3,422,000
PHOSPHATE ADDITIVES IN A TAR SAND WATER SEPARATION PROCESS Filed Nov. 18, 1965 l5 L TAR SAND M 40 I IO r 6O 7 FROTH- DILUENT 3O SAND MM 4. Maw/1v mvsmon PATENT ATTORNEY United States Patent 3,422,000 PHOSPHATE ADDITIVES IN A TAR SAND WATER SEPARATION PROCESS John A. Bichard, Point Edward, Ontario, Canada, as-
signor to Esso Research and Engineering Company, a
corporation of Delaware Filed Nov. 18, 1965, Ser. No. 508,439
US. Cl. 20811 Int. Cl. C10g N00 5 Claims ABSTRACT OF THE DISCLOSURE The present invention is broadly concerned with the recovery of hydrocarbons from tar sands. The invention is more particularly concerned with an improved technique for the maximum removal of oil from tar sand utilizing a particular combination of phosphate additives. In accordance with the present invention by utilizing critical amounts of particular phosphate additives, a maximum amount of oil is removed from the sand which is associ ated with the froth separated from the treated sand.
In various areas of the world, tar sands exist which contain various types of hydrocarbons as, for example, the heavy oil deposits of Athabaska tar sands existing in Canada. These sands constitute tremendous reserves of hydrocarbon constituents. For example, the oil in the sands may vary from about 5% to 21% by volume, generally in the range of about 12% by volume. The gravity of the oil ranges from about 6 to 10 API, generally about 8 API. These sands lie from about 200 to 300 ft. below an overburden and the beds may range from about 100 to 400 ft. thick. A typical oil recovered from the sands has an initial boiling point of about 300 F. 1.0% distilled to 430 F., 20.0% distilled to 650 F. and 50.0% distilled to 980 F.
However, the recovery of hydrocarbons in the past has not been effective to any great extent due to the deficiencies in operating techniques for the recovery of these hydrocarbons. For example, a relatively small amount of clay (from about 0% to 30%, usually 5%) in the sand greatly retards recovery of the oil utilizing conventional water techniques. Apparently the oil and the clay form skins which envelop small pockets of water often containing finely divided sand; then the enveloped pockets are distributed in water, thus forming a type of emulsion. Since large amounts of material must be treated and handled to recover the oil, any technique or process which improves the yield of oil even slightly will result in great economic benefits.
In accordance with the present invention, a particular class of sodium phosphate compounds is used wherein the sodium concentration is maintained in a critical range from about 0.4 wt. percent to about 0.8 wt. percent preferably about 0.4 to 0.6 wt. percent, such as about 0.5 wt. percent, as compared with the sand in an initial stage wherein the amount of water utilized is in the range from about to 30% by weight based upon the sand. The preferred amount of water is from about 18% to 26% by weight, preferably about 22% by weight. The phos- 3,422,000 Patented Jan. 14, 1969 phate compound utilized is selected from the class of sodium phosphate compounds wherein the ratio of phosphorous to sodium varies from about 1:1 to 1:2, preferably about 121.7.
The process of the present invention may be readily understood by reference to the drawing illustrating an embodiment of the same. Referring specifically to the drawing, tar sands are introduced into initial stage 10 by means of feed line 1. Water is introduced into initial stage or mixing zone 10 by means of line 2. The amount of water utilized in initial stage 10 based upon the sand is in the range from about 15 to 30% preferably in the range of about 20 to 22% by weight.
Initial stage 10 is maintained at a temperature in the range from about 120 to 200 F., preferably at about 140 F., by any suitable means. In accordance with the present invention, a sodium polyphosphate compound is introduced into initial stage 10 by means of line 3. The amount of sodium polyphosphate utilized is such as to secure a sodium concentration based upon the amount of sand in the range from about 0.4 to 0.8 wt. percent, preferably about 0.5 wt. percent. The sodium polyphosphate compound utilized is selected from the class of compounds wherein the phosphorous-to-sodium ratio is in the range from about 1:1 to 1:2, preferably about 111.7. Any suitable means of mixing may be utilized in zone 10 such as stirrers and the like.
The mixture is withdrawn from initial zone 10 by means of line 4 and mixed with additional water which is introduced by means of line 5. The amount of additional water utilized is sufiicient to have from about -300% by weight of water, preferably about 200% by weight of water based upon the sand. The mixture is then introduced into a secondary stage or separation zone 20.
The temperature in secondary stage 20 is in the range of from about to 200 F., preferably about F. Under these conditions sand and water substantially free of oil, is removed from secondary stage 20 by means of line 6 while an aqueous froth containing substantially all of the oil and a relatively small quantity of water is removed from zone 20 by means of line 7. The Water phase and and removed by means of line 6 is passed into a sand separation zone 30 wherein a water phase free of sand is separated and preferably recycled to the system. Since this water phase contains the added phosphate the sand is removed from separation zone 30 by means of line 8 and disposed of as desired.
The oil-rich froth is then handled or processed in order to secure an oil phase. One preferred method is to introduce the oil froth into a distillation zone 40 in order to remove overhead water by means of line 9. It is preferred that the oil phase withdrawn from distillation zone 40 by means of line 11 be at a temperature in the range from about 250 to 400 P. such as about 300 F. A hydrocarbon diluent such as a hydrocarbon fraction boiling in the range from about 250 to 600 F. is added to the oil phase by means of line 12. Other hydrocarbons may be added such as benzene, toluene, and the like. The amount of diluent added is about 0.5 to 2.0 volumes of diluent per volume of oil. Sufficient pressure is maintained on the system to keep the diluent in the liquid phase. The mixture is then passed into a final solids separation zone 50 wherein the remaining traces of solids separate and are removed by means of line 13. Separation zone 50 may comprise filters or settling means. A diluent oil phase is removed from separation zone 50 by means of line 14 and introduced into a diluent-heavy oil separation zone 60 wherein the diluent is separated and removed by means of line 15 and preferably recycled to the system. The heavy oil phase is removed by means of line 16 and further processed as desired. Sepa- OIL REC. IN FROTH, WT. PERCENT Na con. wt. percent (based on tar sand) P/Na 0 From the above it is apparent that the oil froth contained a far greater concentration of oil when utilizing a sodium concentration in the range from about 0.4 to 0.8, and when using a phosphorous-to-sodium ratio as defined by the present invention.
What is claimed is:
1. Improved process for the recovery of oil from tar sands which comprises mixing said tar sand with from about wt. percent to 30 wt. percent of water in an initial mixing zone maintained at a temperature of about 120 F. to 200 F., adding a sodium phosphate compound to mixing zone so as to have a sodium concentration based upon the weight of the tar sand in the range from about 0.4 to about 0.8 wt. percent and to have a phosphorous-to-sodium ratio in the range from about 1:1 to 1:2, withdrawing the mixture from said mixing zone and adding additional water so as to have a water concentration in the range from about 100% to 300% by weight based upon the tar sand, thereafter passing the mixture to a secondary zone maintained at a temperature in the range from about 120 to 200 F., removing an oil-rich froth and a sands-water phase from said secondary zone, passing said froth to a distillation zone and removing water overhead from said distillation zone, removing an oil phase from the bottom of said distillation Zone and adding a hydrocarbon diluent boiling in the range from about 250 to 600 F. thereto, passing the mixture to a tertiary zone and separating the final traces of solids therefrom, and thereafter separating said oil from said diluent.
2. Process as defined by claim 1 wherein the sodium concentration in said mixing zone is about 0.5% by weight and wherein the phosphorous-to-sodium ratio is about 1 to 1.7.
3. Process as defined by claim 1 wherein the amount of diluent added is about one volume of diluent per one volume of bottoms oil phase.
4. Process as defined by claim 1 wherein said diluent consists essentially of benzene.
5. Process as defined by claim 1 wherein from about 0.5 to 2 volumes of diluent are added per volume of oil.
References Cited UNITED STATES PATENTS 1,820,917 9/1931 Langford et a1. 208-11 2,453,060 11/1948 Bauer et a1 208-11 3,152,979 10/1964 Bichard et al. 208--11 3,208,930 9/1965 Andrassy 208-11 3,296,117 1/1967 Ross et a1. 20811 FOREIGN PATENTS 488,928 12/ 1952 Canada. 602,087 7/ 1960 Canada.
OTHER REFERENCES Canadian Chemical Processing, Sun Oil Company, August, 1964.
DANIEL E. WYMAN, Primary Examiner.
PAUL E. KONOPKA, Assistant Examiner.
US. Cl. X.R. 209166
US508439A 1965-11-18 1965-11-18 Phosphate additives in a tar sand water separation process Expired - Lifetime US3422000A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50843965A 1965-11-18 1965-11-18

Publications (1)

Publication Number Publication Date
US3422000A true US3422000A (en) 1969-01-14

Family

ID=24022756

Family Applications (1)

Application Number Title Priority Date Filing Date
US508439A Expired - Lifetime US3422000A (en) 1965-11-18 1965-11-18 Phosphate additives in a tar sand water separation process

Country Status (1)

Country Link
US (1) US3422000A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3509037A (en) * 1967-08-11 1970-04-28 Sun Oil Co Tar sand separation process using solvent,hot water and correlated conditions
US4229281A (en) * 1978-08-14 1980-10-21 Phillips Petroleum Company Process for extracting bitumen from tar sands
US4425227A (en) 1981-10-05 1984-01-10 Gnc Energy Corporation Ambient froth flotation process for the recovery of bitumen from tar sand
US4648964A (en) * 1985-08-30 1987-03-10 Resource Technology Associates Separation of hydrocarbons from tar sands froth
US4765885A (en) * 1984-12-21 1988-08-23 Eneresource, Inc. Treatment of carbonaceous materials
WO1989004356A3 (en) * 1987-11-11 1989-06-01 Dvgw Forschungsstelle Am Engle Improved process for eliminating hazardous substances from soils
US4891131A (en) * 1984-12-21 1990-01-02 Tar Sands Energy Ltd. Sonication method and reagent for treatment of carbonaceous materials
US4968413A (en) * 1985-08-22 1990-11-06 Chevron Research Company Process for beneficiating oil shale using froth flotation
US5017281A (en) * 1984-12-21 1991-05-21 Tar Sands Energy Ltd. Treatment of carbonaceous materials
US5152885A (en) * 1990-12-18 1992-10-06 Exxon Research And Engineering Company Hydrotreating process using noble metal supported catalysts
US5376182A (en) * 1993-03-17 1994-12-27 Remsol (U.S.A.) Corporation Surfactant soil remediation

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1820917A (en) * 1927-04-29 1931-09-01 Continental Oil Co Method for separating bitumen from bituminous sands and similar bituminous materials
US2453060A (en) * 1944-08-26 1948-11-02 Union Oil Co Process and apparatus for treating bituminous sands
CA488928A (en) * 1952-12-16 Colin Ferguson James Apparatus for the recovery of tar sands
CA602087A (en) * 1960-07-19 Oyen Albert Process for the separation of oil from bituminous sands and like oil bearing materials
US3152979A (en) * 1961-09-07 1964-10-13 Exxon Research Engineering Co Process for the efficient removal of oil from tar sands
US3208930A (en) * 1963-07-19 1965-09-28 Andrassy Stella Process and apparatus for the separation of hydrocarbons from tar sands
US3296117A (en) * 1964-03-09 1967-01-03 Exxon Research Engineering Co Dewatering/upgrading athabaska tar sands froth by a two-step chemical treatment

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA488928A (en) * 1952-12-16 Colin Ferguson James Apparatus for the recovery of tar sands
CA602087A (en) * 1960-07-19 Oyen Albert Process for the separation of oil from bituminous sands and like oil bearing materials
US1820917A (en) * 1927-04-29 1931-09-01 Continental Oil Co Method for separating bitumen from bituminous sands and similar bituminous materials
US2453060A (en) * 1944-08-26 1948-11-02 Union Oil Co Process and apparatus for treating bituminous sands
US3152979A (en) * 1961-09-07 1964-10-13 Exxon Research Engineering Co Process for the efficient removal of oil from tar sands
US3208930A (en) * 1963-07-19 1965-09-28 Andrassy Stella Process and apparatus for the separation of hydrocarbons from tar sands
US3296117A (en) * 1964-03-09 1967-01-03 Exxon Research Engineering Co Dewatering/upgrading athabaska tar sands froth by a two-step chemical treatment

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3509037A (en) * 1967-08-11 1970-04-28 Sun Oil Co Tar sand separation process using solvent,hot water and correlated conditions
US4229281A (en) * 1978-08-14 1980-10-21 Phillips Petroleum Company Process for extracting bitumen from tar sands
US4425227A (en) 1981-10-05 1984-01-10 Gnc Energy Corporation Ambient froth flotation process for the recovery of bitumen from tar sand
US4765885A (en) * 1984-12-21 1988-08-23 Eneresource, Inc. Treatment of carbonaceous materials
US4891131A (en) * 1984-12-21 1990-01-02 Tar Sands Energy Ltd. Sonication method and reagent for treatment of carbonaceous materials
US5017281A (en) * 1984-12-21 1991-05-21 Tar Sands Energy Ltd. Treatment of carbonaceous materials
US4968413A (en) * 1985-08-22 1990-11-06 Chevron Research Company Process for beneficiating oil shale using froth flotation
US4648964A (en) * 1985-08-30 1987-03-10 Resource Technology Associates Separation of hydrocarbons from tar sands froth
WO1989004356A3 (en) * 1987-11-11 1989-06-01 Dvgw Forschungsstelle Am Engle Improved process for eliminating hazardous substances from soils
US5152885A (en) * 1990-12-18 1992-10-06 Exxon Research And Engineering Company Hydrotreating process using noble metal supported catalysts
US5376182A (en) * 1993-03-17 1994-12-27 Remsol (U.S.A.) Corporation Surfactant soil remediation

Similar Documents

Publication Publication Date Title
US4250016A (en) Recovery of bitumen from tar sand
US4035282A (en) Process for recovery of bitumen from a bituminous froth
US2825677A (en) Process for separating oil from bituminous sands, shales, etc.
US4722781A (en) Desalting process
US3331765A (en) Treatment of athabasca tar sands froth
US3330757A (en) Chemical treatment of athabaska froth
CA1143686A (en) Solvent extraction method
US3716474A (en) High pressure thermal treatment of waste oil-containing sludges
US3131141A (en) Non-aqueous process for the recovery of bitumen from tar sands
US3422000A (en) Phosphate additives in a tar sand water separation process
US3392105A (en) Use of a soluble oil in the extraction of hydrocarbons from oil sands
US3296117A (en) Dewatering/upgrading athabaska tar sands froth by a two-step chemical treatment
US2968603A (en) Hot water process for the extraction of oil from bituminous sands and like oil bearing material
CA1293465C (en) Purification process for bitumen froth
US3661774A (en) Separation of solids from a liquid
US3594306A (en) Separation cell and scavenger cell froths treatment
US3509037A (en) Tar sand separation process using solvent,hot water and correlated conditions
US3075913A (en) Processing of bituminous sands
US3152979A (en) Process for the efficient removal of oil from tar sands
US2601257A (en) Continuous process for thermal extraction of oil shale
US3607721A (en) Process for treating a bituminous froth
US3969220A (en) Aerating tar sands-water mixture prior to settling in a gravity settling zone
US3547803A (en) Recovery of oil from bituminous sands
US3884829A (en) Methods and compositions for refining bituminous froth recovered from tar sands
US4456533A (en) Recovery of bitumen from bituminous oil-in-water emulsions