456results about "Tar working-up by chemical refining" patented technology

deposition in a formation, wellbore, near wellbore region, and production tubing. Compositions of the invention comprise an asphaltene solvent and a viscosity reducing agent, the asphaltene solvent and viscosity reducing agent present in a ratio so as to substantially reduce viscosity of an asphaltene-containing material while substantially negating deposition of asphaltenes either in a reservoir, in production tubing, or both when mixed or otherwise contacting the asphaltene-containing material Methods of the invention comprise forcing a composition comprising an asphaltene solvent and a viscosity reducing agent to contact an asphaltene-containing hydrocarbon in an underground geologic formation, and producing from the formation a production composition comprising at least some of the treatment composition and at least some of the asphaltene-containing hydrocarbon under conditions sufficient to substantially negate deposition of asphaltenes in the formation.

A process derived hydrogen donor solvent is used to increase the maximum resid conversion and conversion rate in an ebullated bed resid hydrocracker. The hydrogen donor solvent precursor is produced by hydroreforming reactions within the resid hydrocracker, recovered as the resin fraction from a solvent deasphalting unit, regenerated in a separate hydrotreater reactor, and recycled to the ebullated bed resid hydrocracker. The major advantage of this invention relative to earlier processes is that hydrogen is more efficiently transferred to the resin residual oil in the separate hydrotreater and the hydrogen donor solvent effectively retards the formation of coke precursors at higher ebullated bed resid hydrocracker operating temperatures and resid cracking rates.

A method of recovering hydrocarbons from hydrocarbonaceous materials can include forming a constructed permeability control infrastructure. This constructed infrastructure defines a substantially encapsulated volume. A comminuted hydrocarbonaceous material can be introduced into the control infrastructure to form a permeable body of hydrocarbonaceous material. The permeable body can be heated sufficient to remove hydrocarbons therefrom. During heating the hydrocarbonaceous material is substantially stationary as the constructed infrastructure is a fixed structure. Removed hydrocarbons can be collected for further processing, use in the process, and/or use as recovered.

A continuous process for upgrading sour crude oil by treating the sour crude oil in a two step process that includes a hydro-demetallization section and a hydro-desulfurization section, both of which are constructed in a permutable fashion so as to optimize the operating conditions and catalyst lifespan to produce a high value crude oil having low sulfur and low organometallic impurities.

One exemplary embodiment can include a slurry hydrocracking process. The process can include combining one or more hydrocarbons and a slurry hydrocracking catalyst as a feed to a slurry hydrocracking reaction zone, fractionating an effluent from the slurry hydrocracking reaction zone, separating the pitch from at least a portion of the slurry hydrocracking catalyst, and recycling the suspension to the slurry hydrocracking reaction zone. The slurry hydrocracking catalyst may include a support. Fractionating the effluent may provide a light vacuum gas oil, a heavy vacuum gas oil, and a mixture comprising a pitch and the slurry hydrocracking catalyst. Generally, the separated slurry hydrocracking catalyst is comprised in a suspension.

Provided is a hydrocarbon tar. The tar has 75 wt % or more of aromatics of 10 carbons to 75 carbons based on the total weight of the tar. The aromatics exhibit 40% to 80% aromaticity. The tar has a boiling point of from 300° F. to 1350° F. There is also a fuel oil composition having the tar therein. There are also processes for making the hydrocarbon tar.

A method of produced water treatment in an in-situ recovery method of producing bitumen from oil sand, the method has the steps of: separating bitumen from bitumen-mixed fluid so as to leave produced water, the bitumen-mixed fluid having been recovered from the oil sand wells; and filtering the produced water via a microfiltration membrane made of polytetrafluoroethylene.

Novel amine-chelate complexes are useful in significantly reducing the viscosity of heavy crude oils, facilitating the recovery and transportation of such heavy crude oils. The amine-chelate complexes are formed by heating together an organic amine with a chelating agent.

The invention relates to the use of steam cracked tar with the bottoms product of a flash drum integrated with a pyrolysis furnace. In embodiments, the steam cracked tar is added to fuel oil.

A process and apparatus to remove asphaltenic contaminants from bitumen, heavy oil or residue to produce lower viscosity petroleum products and high purity asphaltenes.

A process for the solvent separation of hydrocarbons from tar sand or contaminated soils comprises extracting the hydrocarbons from the sand or soil in a solvent extraction means to form a hydrocarbon rich solvent solution. The rich solvent is separated from the hydrocarbon in a process that utilizes flashing of the solvent in a heated flashing column at ambient pressure. The hydrocarbon is withdrawn from the bottom of the column and the flashed solvent vapors are strategicly withdrawn and passed into a condensation column from which the condensed solvent may be recycled. The flashing column is divided by a series of horizontal, vertically aligned apertured trays. The solution is introduced into the top of the column and the flashing operation is facilitated by the increase in the surface area of the solution as it flows by gravity from tray to tray. The column is maintained at a temperature, preferably above the boiling temperature of the solvent. The process is particularly adapted to the use of chlorinated hydrocarbon solvents and most particularly to the use of methylene chloride.

Hydrogenation for processing and utilizing coal tar is carried out by dewatering for coal tar raw material to water content<0.05%, removing mechanical impurities to obtain purified coal tar raw material, mixing cal tar with hydrogen at 300-427 degree, 10.0-17.0 MPa and 0.15-1.0h-1 liquid volume air speed, hydrogenation reacting to obtain gas-phase and liquid-phase products under hydrogenation protector and loaded hydrogenation catalyst existence, in proportion of hydrogen: coal tar=1000:1-3500:1, and fractioning to obtain gasoline, middle fraction oil and modified coal asphalt. It's reasonable and flexible and has high supplementary value.

A mercury removal apparatus for a liquid hydrocarbon of the present invention includes a conversion device 2 which converts a mercury component in a raw liquid hydrocarbon into elemental mercury to obtain a first liquid hydrocarbon containing the elemental mercury; and a first stripping device 4 which brings the first liquid hydrocarbon into counter-current contact with a first stripping gas, thereby transferring the elemental mercury in the first liquid hydrocarbon to the first stripping gas to obtain a second liquid hydrocarbon in which the amount of the elemental mercury decreases and a first gaseous hydrocarbon containing the elemental mercury.

Methods for upgrading a hydrocarbon feed are disclosed. The methods include a hydrocarbon feed having an insolubility number, I_feed, with at least a first fluid to form a fluid-feed mixture; and inducing a centrifugal force to the fluid-feed mixture sufficient to form at least a higher density portion and a lower density portion, said lower density portion having an insolubility number, I_LD, wherein I_LD/I_feed≦0.95. Methods and apparatus for hydroprocessing the treated feed and blending with a fuel oil blend-stock are also described.

Disclosed is an apparatus for extracting sulfur compounds from a hydrocarbon stream. A prewash section for converting hydrogen sulfide to sodium sulfide by reaction with an alkali such as caustic prepares the hydrocarbon stream for extraction. Spent alkali is continuously withdrawn and regenerated alkali is continuously added to the prewash section.