MX2008014630A - Process for simultaneous recovery and cracking/upgrading of oil from solids. - Google Patents
Process for simultaneous recovery and cracking/upgrading of oil from solids.Info
- Publication number
- MX2008014630A MX2008014630A MX2008014630A MX2008014630A MX2008014630A MX 2008014630 A MX2008014630 A MX 2008014630A MX 2008014630 A MX2008014630 A MX 2008014630A MX 2008014630 A MX2008014630 A MX 2008014630A MX 2008014630 A MX2008014630 A MX 2008014630A
- Authority
- MX
- Mexico
- Prior art keywords
- oil
- sand
- solids
- recovery
- disintegration
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 36
- 230000008569 process Effects 0.000 title claims abstract description 35
- 239000007787 solid Substances 0.000 title claims abstract description 29
- 238000011084 recovery Methods 0.000 title claims abstract description 21
- 238000005336 cracking Methods 0.000 title abstract 2
- 239000011275 tar sand Substances 0.000 claims abstract description 29
- 239000004058 oil shale Substances 0.000 claims abstract description 11
- 239000004576 sand Substances 0.000 claims description 34
- 239000007789 gas Substances 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 230000006872 improvement Effects 0.000 claims description 11
- 239000000567 combustion gas Substances 0.000 claims description 8
- 239000003208 petroleum Substances 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 238000000889 atomisation Methods 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 5
- 238000002485 combustion reaction Methods 0.000 claims description 4
- 230000001133 acceleration Effects 0.000 claims description 3
- 239000000571 coke Substances 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 3
- 239000007924 injection Substances 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000010454 slate Substances 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 238000005393 sonoluminescence Methods 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000000265 homogenisation Methods 0.000 claims 1
- 238000005516 engineering process Methods 0.000 abstract description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 5
- 229910001385 heavy metal Inorganic materials 0.000 abstract description 4
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 46
- 239000010426 asphalt Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 239000010779 crude oil Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000011269 tar Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000005416 organic matter Substances 0.000 description 3
- 230000032258 transport Effects 0.000 description 3
- 238000005265 energy consumption Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
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
- C10G1/02—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by distillation
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)
Abstract
The present invention relates to a process for the simultaneous recovery and cracking/upgrading of oil from solids such as tar sand and oil shale. With this process a number of the obstacles with the existing technology are solved, and the process upgrades the oil into a lighter product than the existing technology, remove sulphur in the order of 40% and heavy metals in the order of 90%.
Description
PROCESS FOR THE RECOVERY AND DEBUGGATION / SIMULTANEOUS IMPROVEMENT OF OIL FROM SOLIDS
FIELD OF THE INVENTION The present invention relates to a process for the recovery of petroleum from tar sand (also called petroleum sands) and / or oil shale and the improvement of petroleum in the same process. BACKGROUND OF THE INVENTION Tar sand is found in huge quantities in a number of countries, the largest resources are found in Canada and consists of extra heavy crude oil and sand in natural resources at different depths. These resources have been the subject of intense research in an effort to develop technologies for the recovery of oil from sand. In this way, there are a number of different technologies. Alberta's most important mineral resources are oil and natural gas and account for 90 percent of Alberta's income from mining. Alberta produces approximately two thirds of Canada's oil and more than three quarters of its natural gas. Almost half of Alberta's oil is extracted from tar sands, which are deposits of extra-heavy crude oil called bitumen. The tar sands of
Alberta represent the largest known deposits of bitumen in the world. Tar sands are found in three major areas of the province: the Athabasca River Valley in the northeast, the Peace River area in the north, and the Cold Lake region in eastern central Alberta. Bitumen is more expensive to extract than conventional crude oil, which flows naturally or is pumped from the ground. This is because the thick black oil must be separated from the surrounding sand and water to produce a crude oil that can also be refined. During the 1950's and 1960's, oil deposits were discovered in other regions, such as the Peace River area and Swan Hills, south of Lesser Slave Lake. At the end of 1960 's the last most important deposits were found. Bitumen, unlike normal crude found in deep reservoirs, does not have the same light fractions as this one, it has been evaporated for thousands of years. Bitumen consists of heavy molecules with a density that exceeds 1000 kg / dm3 (less than 10API) and a viscosity 1000 s greater than light crude. In addition, tar sand contains more than 4% sulfur by weight and hundreds of ppm of heavy metals. The content of organic matter in the tar sand can be, oscillate, between
% by weight up to 20% by weight and also the extraction of oil from the tar sand involves a huge mass transport. Because the bitumen composition has to be improved before it can be refined in a light crude refinery. Due to the economic potential of these huge resources, there are a number of different processes for oil recovery from tar sand. Such technologies involve biological, solvent, thermal and processes where oil is washed (extracted) from the sand by superheated water. Due to the huge amounts of sand (waste) associated with the extraction of tar mines, the different processes face a number of environmental obligations. Contrary to tar sand, shale is shale (slate) containing organic matter known as kerosene which can not be washed or dissolved as the bitumen of tar sand. To recover the oil from the oil shale, it must be heated to a temperature of 500-600 ° C through which the organic matter is disintegrated into liquid products. As for tar sand, the oil shale contains a number of unwanted components,
which cause environmental restrictions. And as for oil recovery technologies from tar sand, there exists a number of different technologies for the recovery of oil from the oil shale. SUMMARY OF THE INVENTION The present invention relates to a self-sustaining energy process where a number of the obstacles with the existing technologies are solved and in which in addition to recovering the oil, the oil is improved in a lighter product than any other of the existing technologies, the sulfur is removed in the order of 40% and heavy metals in the order of 90%. In addition, the process has waste with limited environmental restrictions, as inorganic matter (sand) is disposed in a dry condition. BRIEF DESCRIPTION OF THE FIGURES Fig. 1.- It is a simplified flow chart of the process. Fig. 2.- It shows an illustration of a plant of
10000 bbl / day Fig. 3.- It is the design of the platform Fig. 4.- It shows the platform during the test Fig. 5.- It shows the tar sand, recovered oil and clean sand from the test
DETAILED DESCRIPTION OF THE INVENTION The process is a fast fluidized "drying" process where the sand is mixed in a fluidized reactor supplied with part of the organic components in the tar sand. The combustion gases separate the oil from the sand, together they act as a pneumatic conveyor that transports sand and its associated gases to a cyclone reactor where the sand is separated from the gaseous current, which is also guided to a condensing system. A portion of the condensed oil can be guided back to the flow path, an atomization nozzle for a second disintegration through which the process recovers and improves the oil in an operation without the need for improvement units. To optimize the collisions between the particles in order to obtain maximum shear forces between the solids, the sand stream, the combustion gases and the hydrocarbon gases are accelerated and delayed in a variable diameter riser. The collisions between the particles cause a moderate hydrogenation of the oil by sono-luminescence of the microscopic current of bubbles trapped between the solid particles that collide. When current bubbles are trapped between the turbulence of the particles, the current is subject to a compression
Adiabatic through which the temperature and pressure in the bubbles is elevated several hundred times above the global temperature and pressure in a supercritical state where the water is disintegrated to hydrogen and hydroxyl radicals. Hydrogen, which is absorbed by superheavy oil chains, reduces its bonds through which the turbulence impact forces of grains can break down molecules and the "explosion" of the microscopic bubble current takes place . Most of the hydrogen is then released and reacts back with the hydroxyl radicals in water, but a part of the hydrogen causes a moderate hydrogenation of the product. It is very desirable to perform a good sand / oil mix as soon and as quickly as possible. The described method to carry out requires the acceleration mentioned above and the current delay. Traditionally, the current is the means used to keep the solid bed fluidized and moving in the elevator. The current, however, has a destructive effect on the very hot solids found in the residues of the disintegration processes. Under these conditions the current causes the hydrothermal deactivation of the catalyst in, for example FCC-disintegrators (catalysts of
disintegration of fluids, FCC-crackers for its acronym in English). This is overcome by the present invention which utilizes the exhaust gases of the fluidized bed reactor regenerator (CO / CO and hydrocarbon gases) as the solids carrier, which will act as a catalyst in the disintegration of the oil. In order to have the process verified, a test platform of 2.5 x 2.5 x 3 m was built and is located in SINTEF ENERGY RESEARCH AS in Trondheim, Norway with a maximum power of 125 kW. The energy required to process one kg of tar sand is given by: Q = xs * cs * dt + x0 (cs * dt + r0) + xw * H Where: xs = the weight part of sand (including metals and sulfur) ), example 80% xo = part by weight of oil, example 15% xw = part by weight of water, example 5% cs = specific heat of the sand kJ / kgK = 1 kJ / kgK c0 = specific heat of the oil to the operating temperature kJ / kgK = approximately 2.25 kJ / kgK r0 = evaporation heat kJ / kg = approximately 225 kJ / kg dt = temperature differential between operating temperature and sand feed temperature K
H = enthalpy of water at operating temperature kJ / h = 3500 kJ Operating temperature 360 ° C = 633 K Supply temperature 90 ° C = 363 K dt = 270 ° CQ = 516 kJ / kg and to which a capacity of the test platform of 872 kg / hr of sand containing 130 kg of oil which offers a capacity of approximately 20 bbl / day. The tests were carried out with tar sand from the Athabasca River Valley deposits with the properties listed above where the following results were obtained: • Density of oil recovered from the fluidizer: 21 API. • Density of oil recovered in the elevator: 29.3 API. • Density of oil drained from the oil condenser: 25.15 API. • Coke remaining in the spent sand: 1.25% by weight
• Reduction of sulfur in oil: 45% • Reduction of heavy metals: 87% • Energy consumption in% of recovered oil: 9.3 = approximately 12.5 kg of oil / hr
approximately 3.93 USD per bbl. (Price of oil 50 USD per bbl) The process is described below as it appears in the simplified flow diagram of Figure 1. A) It shows the vertical fluidized reactor which has a fluidizing mesh B) placed at a distance from the bottom of the cell. The space between the bottom and the fluidized mesh B) is a plenum C) which receives the combustion gases from a combustor D) which can be fed by gas and / or recovered oil. The combustion gases will heat and fluidize the solids (sand) E) entrained in reactor A). the pressure of the combustion gases accumulated in the reactor will cause the solids and the entrained gases, which consist of combustion gases, steam and hydrocarbon gases, to be pneumatically transported through the elevator JJ) in a cyclonic reactor G) which is designed in such a way, contrary to ordinary cyclones, the solids are rotated several hundred times in the cylindrical part of the cyclone before falling to the conical part H) and returning to the fluidizer. At the bottom of the conical part of the cyclone, the superheated steam is injected into the cyclone by the pipe I) to remove the hydrocarbons between the solids that fall into the cyclone which falls into reactor A) via a dipleg.
The tar sand is injected into reactor A) by a feed system Ce) and Dd). The same amount of sand injected into reactor A) has to be drained from the reactor. This is done through the adapted pipe K) where the sand is transported to a combustor that fluidizes it L) where the remaining coke is burned by air injection through M). The exhausted gases of L) pass through a gas cleaner and the recovery heat system N) is first vented in air. The "clean" solids of L) are guided to a solid / liquid hot exchanger O) which is heated, cooled with water from the heat exchanger Z) transported from the pump supplying water P). the hot water is also transported to a boiler Q) located in the combustor L). The boiler is producing steam where a part of it is guided to a superheater R) located in plenum C) of reactor A). the superheated steam is guided to the injection nozzle S) for the atomization of the petroleum vapor, the dipleg J) in the cyclone of the reactor H) and the dipleg T) in the separation cyclone U). The "clean" chilled sand can be disposed from the heat exchanger 0) to a landfill as the sand will be dried and released from any volatile hydrocarbon.
The excess steam that was not superheated is guided through the pipe V) by feed preheating, process purposes or by electricity generation through a turbine steam system. From the cyclone of the reactor G) and the separation cyclone U) the gaseous vapor is guided to a condenser W) tends to approximately 95 ° C through which the main part of the petroleum gas is condensed to liquid petroleum. The gas is condensed to half the recovered oil as the oil collected at the bottom of the condenser is pumped by the pump X) through a heat exchanger Z) and cooled by water carried by the pump P). From the heat exchanger Z), the cooled oil is guided to the top of the condenser and condenses the incoming oil gases. As the level of oil rises in the condenser, the product is drained through the pipe BB). The non-condensable gases and steam are guided to a second condenser CC) which is cooled by the water injected from pump P). the condensed water is drained from the condenser through the pipe DD) and collected in a sedimentation tank EE). In the decant tank EE), the light oil brought from the petroleum condenser CC) will be decanted through the pipe FF) to the product line from the oil condenser W) and guided to a receiver via the
AA pipe). The water is drained through the pipe GG) to drain. The non-condensable in the condenser CC) is exhausted through the pipe HH) by an air or gas cleaning system depending on local emission requirements. A portion of the product is returned to the elevator JJ) through the pipe NN) by a high pressure pump LL) to the atomization nozzle S) attached to the elevator JJ). The atomization nozzle S) receives the vapor- for the atomization of the oil from the superheater R). The combustion gases formed in excess in the reactor which are not necessary for the transport of the sand in the elevator JJ), can be ventilated from the reactor via the pipe 00) in a system of recovery of gas cleaner and heat not shown . When the reactor is heated to the operational temperature by combustor D), the supply of gas or oil by combustion can be gradually cut through which the injected air will cause internal combustion of the hydrocarbon gases formed in reactor A ) through which the process will be self-sustained by the energy extracted from the tar sand itself. Alternatively the combustor can be fed with a part of the recovered oil transported by the pump LL).
To obtain the acceleration and delay of the current in the elevator, mentioned above, you can use elevators of variable diameters. A preferred embodiment is to form a part of the elevator as a Laval nozzle where the atomization nozzle (s) S) is (are) located in a very narrow part of the ejector or where the ejector begins to expand. The entire process is a highly intensive thermal process with a high energy density due to gas velocity and sand flow. Because of the process speeds, intense heat exchange; between sand and oil; and the low partial pressure of hydrocarbon gases, caused by gases and steam. combustion, the process can operate at a temperature in the range of 300-500 ° C. Apart from the reduced thermal stress and the energy consumption, this low temperature reduces the polymerization of the disintegrated products.
Claims (9)
- NOVELTY OF THE INVENTION Having described the invention as above, property is claimed as contained in the following:
- CLAIMS 1. - A process for the simultaneous recovery and disintegration / improvement of oil from solids, such as tar sand and oil shale, characterized in that the oil-containing solids are injected into a fluidized bed reactor where they are evaporated the hydrocarbons and where the heat for evaporation is transported by the internal combustion of a part of the hydrocarbons in the solids by an external combustor and that the combustion gases together with the evaporated hydrocarbons act as a pneumatic conveyor of the solids and reduce the partial pressure of the hydrocarbon gases and where the current is guided by a cyclonic reactor and also by a solids removal separator and also by a condensation system for the condensable gases. 2. - A process - for the recovery and simultaneous disintegration / improvement of oil from solids, such as tar sand and oil shale, according to claim 1, characterized in that a portion of the product from the
- The condenser system is guided back into the current in an elevator via an atomization nozzle through which the stream of solids acts as a means of disintegration by shear forces, heat exchange and sono-luminescence. 3. - A process for the recovery and disintegration / simultaneous operation of the oil from solids, such as tar sand and bituminous shale, according to claims 1 and 2, characterized in that the elevator has different diameters to obtain the acceleration , delay and optimized collisions between the particles of the solid in the stream.
- 4. A process for the simultaneous recovery and disintegration / improvement of petroleum from solids, such as tar sand and oil shale, according to claim 1, characterized by the temperature in the regenerator is controlled by the Dry tar sand injected into the regenerator.
- 5. - A process for the recovery and simultaneous disintegration / improvement of oil from solids, such as tar sand and oil shale, according to claim 1, characterized in that the unbleached tar sand is guided to a fluidized combustor where the coke remaining on the sand is burned by the injection of air into the combustor and where the spent gas from the combustor is alternatively guided to the plenum of the removal reactor to participate with heat and fluidized gas in the removal of the oil trapped on the sand.
- 6. A process for the recovery and simultaneous disintegration / improvement of oil from solids, such as tar sand and oil shale, according to claim 1, characterized in that a portion of the unmade sand is mixed with tar sand for heat recovery and homogenization of the sand, improving the reactor feed.
- 7. A process for the recovery and simultaneous disintegration / improvement of oil from solids, such as tar sand and oil shale, according to claim 1, characterized in that the fluidised bed reactor has two diameters , where 'the lower part of the regenerator has a diameter so small that the top part in order to reduce the velocities of the gas in the upper part of the regenerator.
- 8.- A process for the recovery and disintegration / simultaneous improvement of petroleum from solids, such as tar sand and bituminous slate, according to claim 1, characterized in that the sand disposed in the regenerator is discharged continuously from the regenerator via a pipe outside the regenerator which has a trap " water "which can be U-shaped and where the steam or gas is ejected in the pipe opposite the" water trap "by pneumatic transport of the sand that falls into the trap.
- 9.- A process for the recovery and simultaneous disintegration / improvement of oil from solids, such as the tar sand and the bituminous slate, according to claim 1, characterized in that a battery of regenerators are arranged around a joint charging system and a joint reception sand collector and a recovery fluidizer of heat (L) and where the exhaust gases of the regenerator divides a joint sand separation system and an open joint condenser and where the condensed cooled oil acts as a condensing medium in the condenser by direct contact between the hot gases of oil and condensed chilled oil.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA2546940A CA2546940C (en) | 2006-05-15 | 2006-05-15 | Process for simultaneous recovery and cracking/upgrading of oil from solids |
| PCT/NO2007/000170 WO2007133089A1 (en) | 2006-05-15 | 2007-05-10 | Process for simultaneous recovery and cracking/upgrading of oil from solids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2008014630A true MX2008014630A (en) | 2009-02-06 |
Family
ID=38686899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2008014630A MX2008014630A (en) | 2006-05-15 | 2007-05-10 | Process for simultaneous recovery and cracking/upgrading of oil from solids. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20090120844A1 (en) |
| EP (1) | EP2029695A4 (en) |
| CN (1) | CN101484550A (en) |
| AU (1) | AU2007250630B2 (en) |
| BR (1) | BRPI0711480A2 (en) |
| CA (1) | CA2546940C (en) |
| MX (1) | MX2008014630A (en) |
| NO (1) | NO20085143L (en) |
| RU (1) | RU2434049C2 (en) |
| WO (1) | WO2007133089A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO331801B1 (en) * | 2009-01-09 | 2012-04-02 | Tarblaster As | Process for simultaneous recovery and cracking of oil from oil / solid mixtures |
| GB201200155D0 (en) | 2012-01-06 | 2012-02-15 | Statoil Asa | Process |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2537153A (en) * | 1946-10-08 | 1951-01-09 | Standard Oil Dev Co | Fluidized carbonization process |
| US2534051A (en) * | 1946-11-22 | 1950-12-12 | Standard Oil Dev Co | Method for fluidized low-temperature carbonization of coal |
| US2729597A (en) * | 1949-04-30 | 1956-01-03 | Hydrocarbon Research Inc | Process for rendering solid carbonaceous materials non-agglomerative |
| US2764531A (en) * | 1952-08-01 | 1956-09-25 | Exxon Research Engineering Co | Process and apparatus for retorting oil shale |
| US3501394A (en) * | 1967-04-17 | 1970-03-17 | Mobil Oil Corp | Gas lift retorting process for obtaining oil from fine particles containing hydrocarbonaceous material |
| SU1029830A3 (en) * | 1974-05-31 | 1983-07-15 | Стандарт Ойл Компани (Фирма) | Process for producing hydrocarbon fraction from carbonaceous feedstock |
| US4105502A (en) * | 1976-06-25 | 1978-08-08 | Occidental Petroleum Corporation | Simplified liquefaction pyrolysis process and apparatus therefor |
| US4094767A (en) * | 1976-11-10 | 1978-06-13 | Phillips Petroleum Company | Fluidized bed retorting of tar sands |
| US4369100A (en) * | 1977-09-27 | 1983-01-18 | Sawyer Harold T | Method for enhancing chemical reactions |
| US4264435A (en) * | 1978-04-05 | 1981-04-28 | The Dow Chemical Company | Crude oil cracking using partial combustion gases |
| US4276021A (en) * | 1979-08-08 | 1981-06-30 | Dravo Corporation | Method of recovering heat from hot granular solids |
| US4326944A (en) * | 1980-04-14 | 1982-04-27 | Standard Oil Company (Indiana) | Rapid hydropyrolysis of carbonaceous solids |
| DE3023670C2 (en) * | 1980-06-25 | 1982-12-23 | Veba Oel Entwicklungsgesellschaft mbH, 4660 Gelsenkirchen-Buer | Method and device for smoldering oil shale |
| US4412910A (en) * | 1981-10-21 | 1983-11-01 | Westinghouse Electric Corp. | Recovery of fuel from oil shale |
| US4415433A (en) * | 1981-11-19 | 1983-11-15 | Standard Oil Company (Indiana) | Fluid bed retorting process with multiple feed lines |
| US4507195A (en) * | 1983-05-16 | 1985-03-26 | Chevron Research Company | Coking contaminated oil shale or tar sand oil on retorted solid fines |
| US5076910A (en) * | 1990-09-28 | 1991-12-31 | Phillips Petroleum Company | Removal of particulate solids from a hot hydrocarbon slurry oil |
| US5914027A (en) * | 1994-09-12 | 1999-06-22 | Thermtech A/S | Thermo-mechanical cracking and hydrogenation |
| KR0171501B1 (en) * | 1996-08-28 | 1999-03-20 | 이성래 | Waste oil regeneration device and method |
| US6709573B2 (en) * | 2002-07-12 | 2004-03-23 | Anthon L. Smith | Process for the recovery of hydrocarbon fractions from hydrocarbonaceous solids |
| NO20040615L (en) * | 2004-02-11 | 2005-08-12 | Ellycrack As | Low temperature catalytic cracking and conversion process for upgrading heavy crude oil |
-
2006
- 2006-05-15 CA CA2546940A patent/CA2546940C/en not_active Expired - Fee Related
-
2007
- 2007-05-10 BR BRPI0711480-0A patent/BRPI0711480A2/en not_active IP Right Cessation
- 2007-05-10 RU RU2008149093/04A patent/RU2434049C2/en not_active IP Right Cessation
- 2007-05-10 EP EP07747631A patent/EP2029695A4/en not_active Withdrawn
- 2007-05-10 AU AU2007250630A patent/AU2007250630B2/en not_active Ceased
- 2007-05-10 MX MX2008014630A patent/MX2008014630A/en active IP Right Grant
- 2007-05-10 WO PCT/NO2007/000170 patent/WO2007133089A1/en not_active Ceased
- 2007-05-10 US US12/300,549 patent/US20090120844A1/en not_active Abandoned
- 2007-05-10 CN CNA2007800174764A patent/CN101484550A/en active Pending
-
2008
- 2008-12-10 NO NO20085143A patent/NO20085143L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20085143L (en) | 2008-12-15 |
| RU2008149093A (en) | 2010-06-20 |
| RU2434049C2 (en) | 2011-11-20 |
| AU2007250630B2 (en) | 2011-08-18 |
| CA2546940A1 (en) | 2007-11-15 |
| EP2029695A4 (en) | 2011-11-02 |
| CN101484550A (en) | 2009-07-15 |
| AU2007250630A1 (en) | 2007-11-22 |
| US20090120844A1 (en) | 2009-05-14 |
| CA2546940C (en) | 2010-09-21 |
| EP2029695A1 (en) | 2009-03-04 |
| WO2007133089A1 (en) | 2007-11-22 |
| BRPI0711480A2 (en) | 2011-11-16 |
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