US3422000A - Phosphate additives in a tar sand water separation process - Google Patents
Phosphate additives in a tar sand water separation process Download PDFInfo
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- 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
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- oil
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 25
- 238000000926 separation method Methods 0.000 title description 10
- 239000011275 tar sand Substances 0.000 title description 8
- 229910019142 PO4 Inorganic materials 0.000 title description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title description 6
- 239000010452 phosphate Substances 0.000 title description 6
- 239000000654 additive Substances 0.000 title description 5
- 239000003921 oil Substances 0.000 description 28
- 239000004576 sand Substances 0.000 description 14
- 239000003085 diluting agent Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 239000012071 phase Substances 0.000 description 11
- 239000011734 sodium Substances 0.000 description 11
- 229910052708 sodium Inorganic materials 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 9
- 150000002430 hydrocarbons Chemical class 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 239000011269 tar Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 235000019830 sodium polyphosphate Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical class [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 238000012993 chemical processing Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- -1 sodium phosphate compound Chemical class 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/04—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
- C10G1/045—Separation of insoluble materials
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/04—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
- C10G1/047—Hot 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.
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- 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.
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
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)
| 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)
| 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 |
-
1965
- 1965-11-18 US US508439A patent/US3422000A/en not_active Expired - Lifetime
Patent Citations (7)
| 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)
| 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 |
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