Abstract: A method for processing asphaltenes is disclosed. The method can include separating asphaltenes from an asphaltene-containing composition and oxidizing the separated asphaltenes to form oxidation products. Alternatively, the method can include oxidizing asphaltenes within an asphaltene-containing composition without first separating the asphaltenes. Once formed, the oxidation products can be combined with other hydrocarbons. The amount of oxidation can be limited to an amount sufficient to produce a mixture suitable for the desired application. This method can be used to upgrade asphaltenes from a variety of sources, including oil sands. The oxidation step can be performed, for example, by introducing an oxidizing agent and, in some cases, a catalyst into the asphaltenes. A solvent or miscibility agent also can be introduced to improve mixing between the oxidizing agent and the asphaltenes.

Abstract: Methods for obtaining bitumen from bituminous material. The methods may include a dissolution step where a first solvent is added to material comprising bitumen to dissolve the bitumen contained therein. The majority of the dissolved bitumen is then removed from the mixture of first solvent and material comprising bitumen by filtering or settling the mixture of first solvent and material comprising bitumen. Any residual dissolved bitumen is then removed from the mixture of first solvent and material comprising bitumen by adding additional first solvent to the mixture to displace the residual dissolved bitumen from the mixture.

Abstract: Methods for preparing solvent-dry, stackable tailings. The methods may include a primary leaching or extraction process that separates most of the bitumen from a material comprising bitumen and produces first solvent-wet tailings. The first solvent-wet tailings are washed with a second solvent that removes the first solvent from the tailings. Second solvent remaining in the tailings is removed to thereby produce solvent-dry, stackable tailings.

Abstract: A nozzle reactor system for increasing the conversion rate of material feed injected into the nozzle reactor system. The system includes two or more nozzle reactors aligned in series, such that material exiting a first nozzle reactor may be injected into a second nozzle reactor, Each nozzle reactor includes an interior reactor chamber and an injection passage and a material feed passage that are each in material injecting communication with the interior reactor chamber. Furthermore, the injection passage is aligned transversely to the injection passage. The injection passage is configured to accelerate cracking material passed therethrough to a supersonic speed. A method of increasing the conversion rate of material feed utilizing multiple cracking steps is also described.

Abstract: Embodiments of a method and a system for recovering energy, materials or both from asphaltene-containing tailings are disclosed. The asphaltene-containing tailings can be generated, for example, from a process for recovering hydrocarbons from oil sand. Embodiments of the method can include a flotation separation and a hydrophobic agglomeration separation. Flotation can be used to separate the asphaltene-containing tailings into an asphaltene-rich froth and an asphaltene-depleted aqueous phase. The asphaltene-rich froth, or an asphaltene-rich slurry formed from the asphaltene-rich froth, then can be separated into a heavy mineral concentrate and a light tailings. Hydrophobic agglomeration can be used to recover an asphaltene concentrate from the light tailings. Another flotation separation can be included to remove sulfur-containing minerals from the heavy mineral concentrate. Oxygen-containing minerals also can be recovered from the heavy mineral concentrate.

Abstract: Embodiments of a method and a system for recovering energy, materials or both from asphaltene-containing tailings are disclosed. The asphaltene-containing tailings can be generated, for example, from a process for recovering hydrocarbons from oil sand. Embodiments of the method can include a flotation separation and a hydrophobic agglomeration separation. Flotation can be used to separate the asphaltene-containing tailings into an asphaltene-rich froth and an asphaltene-depleted aqueous phase. The asphaltene-rich froth, or an asphaltene-rich slurry formed from the asphaltene-rich froth, then can be separated into a heavy mineral concentrate and a light tailings. Hydrophobic agglomeration can be used to recover an asphaltene concentrate from the light tailings. Another flotation separation can be included to remove sulfur-containing minerals from the heavy mineral concentrate. Oxygen-containing minerals also can be recovered from the heavy mineral concentrate.

Abstract: Embodiments of a method and a system for recovering energy, materials or both from asphaltene-containing tailings are disclosed. The asphaltene-containing tailings can be generated, for example, from a process for recovering hydrocarbons from oil sand. Embodiments of the method can include a flotation separation and a hydrophobic agglomeration separation. Flotation can be used to separate the asphaltene-containing tailings into an asphaltene-rich froth and an asphaltene-depleted aqueous phase. The asphaltene-rich froth, or an asphaltene-rich slurry formed from the asphaltene-rich froth, then can be separated into a heavy mineral concentrate and a light tailings. Hydrophobic agglomeration can be used to recover an asphaltene concentrate from the light tailings. Another flotation separation can be included to remove sulfur-containing minerals from the heavy mineral concentrate. Oxygen-containing minerals also can be recovered from the heavy mineral concentrate.

Abstract: Various systems and methods are described that can be used as part of a process to separate bitumen from oil sands. The process may include adding a hydrocarbon solvent to a bitumen containing extract. The tailings from this process may contain a significant amount of solvent. The solvent may be recovered from the tailings with a tailings solvent recovery unit that utilizes negative pressure to significantly reduce the cost of the process in comparison to a conventional steam stripping unit. In one embodiment, the tailings may also separated prior to entering the tailings solvent recovery unit with a gravity separation apparatus or a cyclonic separation apparatus, such as a hydrocyclone.

Abstract: A method for obtaining heavy oil is disclosed. The method includes mixing a material including heavy oil (e.g., oil sand) with a solvent including biodiesel to form a mixture and separating the mixture into a oil-enriched solvent phase and a residual sand phase. The method also can include introducing a solvent including biodiesel into an in-situ geological formation including heavy oil and collecting a mixture including biodiesel and heavy oil from the formation. For example, the mixture can be collected after the solvent travels through at least a portion of the formation by gravity. A method for producing biodiesel also is disclosed. The method includes microbially digesting asphaltenes to form a liquor including a fatty acid and reacting the fatty acid with an alcohol to produce biodiesel. This method can be used to convert petroleum asphaltenes and/or coal asphaltenes into biodiesel.

Abstract: A method for processing asphaltenes is disclosed. The method can include separating asphaltenes from an asphaltene-containing composition and oxidizing the separated asphaltenes to form oxidation products. Alternatively, the method can include oxidizing asphaltenes within an asphaltene-containing composition without first separating the asphaltenes. Once formed, the oxidation products can be combined with other hydrocarbons. The amount of oxidation can be limited to an amount sufficient to produce a mixture suitable for the desired application. This method can be used to upgrade asphaltenes from a variety of sources, including oil sands. The oxidation step can be performed, for example, by introducing an oxidizing agent and, in some cases, a catalyst into the asphaltenes. A solvent or miscibility agent also can be introduced to improve mixing between the oxidizing agent and the asphaltenes.

Abstract: A hydrometallurgical process is provided for producing pigment grade TiO2 from titanium containing solutions. Generally, the solution is an aqueous solution. The process includes hydrolyzing the solution via complete evaporation in well-controlled conditions of temperature to form titanium oxide of well-defined characteristics. The hydrolyzing can be achieved by spray hydrolysis in a spray dryer. After hydrolyzing, the titanium oxide is calcined to transform the titanium oxide to the desired form of titanium dioxide. The titanium dioxide can be either anatase or rutile. Following calcination, the titanium dioxide is milled to provide the desired particle size distribution and then finished.

Abstract: A hydrometallurgical process is provided for producing ultrafine or nano-sized titanium dioxide from titanium containing solutions, particularly titanium chloride solutions. The process is conducted by total evaporation of the solution, above the boiling point of the solution and below the temperature where there is significant crystal growth. Chemical control additives may be added to control particle size. Nano-sized elemental particles are formed after calcination. The titanium dioxide can be either anatase or rutile. Following calcination, the titanium dioxide is milled to liberate the elemental particles and provide a high quality nano-sized TiO2 with a narrow particle size distribution.

Abstract: A process for leaching an ore that contains nickel and magnesium includes mixing a microorganism that is capable of producing an organic acid, a nutrient, and an ore that contains nickel and magnesium for a period of time to dissolve the nickel and form a solution containing a nickel salt and a magnesium salt, separating the nickel from the magnesium in the salt solution.

Abstract: A bio-leaching method is provided for recovering metal from a metal containing ore. The ore is subjected to contact with a microorganism selective to the oxidation of sulfur. A sulfur containing compound is mixed with the microorganism before, during or after contact with the ore to systemically form sulfuric acid to leach the metal from the ore. The ore is in the form of a slurry, a heap, a charge in a vat and is bioleached for a time sufficient to dissolve the metal in the ore and form a metal-rich leachate and an ore residue. The metal can then be extracted from the metal-rich leachate. The metal containing ore may contain base metals, precious metals, or platinum group metals. Upon formation of the metal-rich leachate, the ore residue may be further processed to recover any precious metals or platinum group metals that may be present.

Abstract: A hydrometallurgical process is provided for producing pigment grade TiO2 from titaniferous mineral ores, and in particular from ilmenite ore. The ore is leached with a hydrochloric acid, preferably a recycled solution at high hydrochloric acid concentration, to form a leachate containing titanium and iron chloride and a residue. The leachate may be filtered to separate the leachate from the residue. The leachate is cooled to a temperature sufficient to form crystals of FeCl2, which are separated from the leachate. The leachate may be subjected to a reduction step to reduce Fe+3 to Fe+2, before crystallizing. The leachate is subjected to a first solvent extraction to form a pregnant strip solution containing titanium and ferric ions and a raffinate containing ferrous ions. This strip solution is subjected to a second solvent extraction to form a second strip solution containing ferric ions and a raffinate containing titanium ions.

Abstract: A process is provided for the direct recovery of nickel and cobalt from a nickeliferous oxide ore leach slurry by ion exchange. A nickeliferous ore is leached with mineral acid to solubilize the metals. The resulting leach slurry is contacted with ion exchange resin, which selectively loads the nickel and cobalt from the pulp. The resin is separated from the leach slurry by screening and then stripped with an acidic solution. After stripping, the resin is returned to the loading cycle. Nickel and/or cobalt can be recovered in substantially pure form from the eluate by known processes. The metal-depleted slurry proceeds to waste treatment and disposal. This process eliminates the difficult solid/liquid separation, which would otherwise be required to recover metals values from the pregnant leach slurry.

Abstract: Raw lead to be refined is leached in a leach apparatus with a leach solution containing fluoro compounds. During the leaching step, lead is dissolved, with ferric fluro compounds being reduced to ferrous fluro compounds. The leaching solution resulting from the leaching step is sent to the cathodic compartment of a diaphragm cell in which lead is deposited on a cathode, in compact, highly pure form. The solution that is depleted of lead is sent to the anodic compartment in which a suitable anode oxidizes the ferrous fluro compound to ferric fluro compounds that can be recycled to the leaching step.

Abstract: A process is provided for heap leaching ore to recover nickel. The process is particularly effective for ores that have a tangible clay component (i.e., greater than about 10% by weight). The process includes sizing the ore (where necessary), forming pellets by contacting ore with a lixiviant and agglomerating. The pellets are formed into a heap and leached with sulfuric acid to extract the metal values, including nickel. The leachate may be subjected to a nickel recovery operation without the need for intermediate neutralization.

Abstract: A process is provided for the selective recovery from an impure solution of pure nickel and cobalt solutions, suitable for electrolysis of the respective metals. The impure solution may be that obtained from acid leaching of nickel/cobalt bearing laterite or oxide ore. The impure solution is contacted with a solid ion exchange resin to selectively extract nickel and cobalt, while rejecting at least one element of the group manganese, magnesium, calcium, iron(II), and chromium(III). The ion exchange resin contains bis-picolyl amine as the primary chelating group. The impure solution has sufficiently low levels of chromium(VI) and copper to allow repeated use of the ion exchange resin. The metal-bearing resin is washed and then stripped with an acid solution. This solution is then contacted with a water-immiscible organic phase for the selective extraction of cobalt, leaving nickel in the raffinate as a substantially pure nickel solution.

Abstract: A process for the biological treatment of bitumen froth tailings produced from a tar sands treatment and bitumen froth extraction process is disclosed. In this process bitumen froth tailings, containing native hydrocarbon metabolizing microorganisms, are mixed with a growth media to form an inoculum which is then incubated under isothermal conditions for an amount of time to produce a mixed bacterial culture containing bioliquor and a water product containing a reduced amount of asphaltenes as well as solids such as clays and sands. The bioliquor produced in this process is then utilized in the initial tar sands conditioning process from which bitumen froth is produced as well as in the initial tar sands mining process via bioliquor injection directly into the tar sands formation. Because the mixed bacterial culture is made up of a number of hydrocarbon metabolizing microorganisms, the bioliquor is also used in the degradation of the asphaltenes.