Compositions consisting of block copolymers α,ω-di-aryl or alkyl sulfonates of poly(ethylene oxide).sub.w-poly(propylene oxide)-poly(ethylene oxide).sub.w of bis-ammonium and block copolymers α,ω-di-amine of poly(ethylene oxide).sub.w-poly(propylene oxide)-poly(ethylene oxide).sub.w, are provided that are effective in the dewatering and desalting crude oils whose specific gravities are within the range of 14 to 20° API. A method of dewatering and desalting heavy crude oil adds a mixture of the copolymer bifunctionalized with an aliphatic or aromatic secondary amine and a copolymer bifunctionalized with an aliphatic or aromatic tertiary amine.

Compositions consisting of block copolymers α,ω-di-aryl or alkyl sulfonates of poly(ethylene oxide).sub.w-poly(propylene oxide)-poly(ethylene oxide).sub.w of bis-ammonium and block copolymers α,ω-di-amine of poly(ethylene oxide).sub.w-poly(propylene oxide)-poly(ethylene oxide).sub.w, are provided that are effective in the dewatering and desalting crude oils whose specific gravities are within the range of 14 to 20° API. A method of dewatering and desalting heavy crude oil adds a mixture of the copolymer bifunctionalized with an aliphatic or aromatic secondary amine and a copolymer bifunctionalized with an aliphatic or aromatic tertiary amine.

A process for optimising the removal of calcium from a hydrocarbon feedstock in a refinery desalting process, the refinery desalting process comprising the following steps: (a) mixing one or more wash water streams with one or more hydrocarbon feedstock streams; (b) at least partially separating the wash water from the hydrocarbons in a refinery desalter; and (c) removing the separated water and hydrocarbons from the refinery desalter as one or more desalted hydrocarbon streams and one or more effluent water streams; the process optimisation comprising: (i) providing at least one x-ray fluorescence analyser at at least one point in the refinery desalting process; (ii) measuring the concentration of calcium at the at least one point in the process using the at least one x-ray fluorescence analyser; and (iii) optionally adjusting at least one process condition of the refinery desalting process in response to the calcium concentration measurement in step (ii). An apparatus comprises a desalter; a line through which one or more hydrocarbon feedstock streams are passed to the desalter; optionally a line through which one or more wash water streams are passed to the desalter; and one or more x-ray fluorescence analysers configured so as to measure the concentration of calcium in water or hydrocarbons at one or more positions within the apparatus.

A process for optimising the removal of calcium from a hydrocarbon feedstock in a refinery desalting process, the refinery desalting process comprising the following steps: (a) mixing one or more wash water streams with one or more hydrocarbon feedstock streams; (b) at least partially separating the wash water from the hydrocarbons in a refinery desalter; and (c) removing the separated water and hydrocarbons from the refinery desalter as one or more desalted hydrocarbon streams and one or more effluent water streams; the process optimisation comprising: (i) providing at least one x-ray fluorescence analyser at at least one point in the refinery desalting process; (ii) measuring the concentration of calcium at the at least one point in the process using the at least one x-ray fluorescence analyser; and (iii) optionally adjusting at least one process condition of the refinery desalting process in response to the calcium concentration measurement in step (ii). An apparatus comprises a desalter; a line through which one or more hydrocarbon feedstock streams are passed to the desalter; optionally a line through which one or more wash water streams are passed to the desalter; and one or more x-ray fluorescence analysers configured so as to measure the concentration of calcium in water or hydrocarbons at one or more positions within the apparatus.

An apparatus for separating hydrocarbons from solid particles includes a slurry inlet for receiving a slurry including water, hydrocarbons and solid particles, a water supply for rinsing water, and a slurry outlet. The apparatus further includes a plurality of nozzles configured to provide rinsing water as droplets with sufficient speed to induce cavitation in the slurry, and a separator for extracting a liquid containing water and hydrocarbons from the slurry and a separate liquid outlet for the extracted liquid.

Heavy hydro-carbonaceous materials such as bitumen are upgraded in supercritical water in a continuous-flow reactor system. The present invention provides a reactor arrangement for and a method of converting bitumen and other highly viscous hydrocarbon containing materials into pumpable liquids to enable further processing of such materials while avoiding production of char. The process can be carried out in an underground reactor based on oil well technology. The reactor design and method facilitates mass transfer to dissolve bitumen in heated water and breaks down heavy hydrocarbons by controlling the temperature and pressure in zones within the flowing stream. The reactor may include an embedded electric heater.

The present disclosure provides a process and system for removing at least a portion of organosulfur compounds from an oil sands produced gas and transferring the organosulfur compounds to a bitumen-based liquid. One example of the system includes an absorber to contact the gas with an amount of liquid hydrocarbon sufficient to absorb some of the organosulfur compounds, producing an organosulfur enriched liquid hydrocarbon. The system includes a separator that accepts the organosulfur enriched liquid hydrocarbon and an emulsion that includes water and the bitumen-based liquid. The separator separates produced water from a bitumen-based mixture of organosulfur enriched liquid hydrocarbon and bitumen-based liquid. The system adds an amount of additional liquid hydrocarbon to separate the produced water from the bitumen-based mixture when the amount of liquid hydrocarbon added is less than the amount of liquid hydrocarbon needed to separate the produced water from the bitumen-based mixture.

The present disclosure provides a process and system for removing at least a portion of organosulfur compounds from an oil sands produced gas and transferring the organosulfur compounds to a bitumen-based liquid. One example of the system includes an absorber to contact the gas with an amount of liquid hydrocarbon sufficient to absorb some of the organosulfur compounds, producing an organosulfur enriched liquid hydrocarbon. The system includes a separator that accepts the organosulfur enriched liquid hydrocarbon and an emulsion that includes water and the bitumen-based liquid. The separator separates produced water from a bitumen-based mixture of organosulfur enriched liquid hydrocarbon and bitumen-based liquid. The system adds an amount of additional liquid hydrocarbon to separate the produced water from the bitumen-based mixture when the amount of liquid hydrocarbon added is less than the amount of liquid hydrocarbon needed to separate the produced water from the bitumen-based mixture.

The invention relates to a class of novel surfactants that have utility in the recovery and/or extraction of oil.

A process for conversion of a hydro-carbonaceous feed including ionic halides to a hydrocarbon product stream by hydrotreatment, wherein the stream is combined with wash water, the weight ratio between wash water and hydrocarbon product stream water is between 1:10 and 10:1, wherein the combined hydrocarbon product stream and wash water are separated in a non-polar stream of hydrocarbon product and a polar stream of wash water including ionic halides, such that from 50% of the ionic halides are transferred from the hydrocarbon product stream to the polar stream of wash water including ionic halides, wherein the polar stream of wash water is directed to a means of concentrating, to provide a stream of purified water and a stream of brine having a concentration of ionic halides being more than 2 times and less than 100 times above that of the polar stream of waste water including ionic halides.