A process for producing blown asphalt comprising the steps of mixing a heated hydrocarbon stream and a supercritical water in to produce a mixed stream, operating the supercritical water reactor to produce a reactor effluent, reducing the temperature of the reactor effluent in the cooler to produce a cooled effluent, feeding the cooled effluent through a depressurizing device to produce a depressurized stream, separating the depressurized stream in the flash drum to produce a light fraction stream and a heavy fraction stream, the heavy fraction stream contains a maltene fraction, an asphaltene fraction, and water, introducing the heavy fraction stream to a storage tank, withdrawing an oxidizing reactor feed from the storage tank, introducing the oxidizing reactor feed to an oxidation reactor, and operating the oxidation reactor at an oxidation temperature and an oxidation pressure to produce a product effluent that comprises an oxidized asphaltene fraction.

A process for producing blown asphalt comprising the steps of mixing a heated hydrocarbon stream and a supercritical water in to produce a mixed stream, operating the supercritical water reactor to produce a reactor effluent, reducing the temperature of the reactor effluent in the cooler to produce a cooled effluent, feeding the cooled effluent through a depressurizing device to produce a depressurized stream, separating the depressurized stream in the flash drum to produce a light fraction stream and a heavy fraction stream, the heavy fraction stream contains a maltene fraction, an asphaltene fraction, and water, introducing the heavy fraction stream to a storage tank, withdrawing an oxidizing reactor feed from the storage tank, introducing the oxidizing reactor feed to an oxidation reactor, and operating the oxidation reactor at an oxidation temperature and an oxidation pressure to produce a product effluent that comprises an oxidized asphaltene fraction.

The present invention relates to a method for reducing the cloud point of a Fischer-Tropsch derived fraction to below 0 C., wherein the method comprises subjecting the Fischer-Tropsch derived fraction to a cloud point reduction step comprising mixing the Fischer-Tropsch derived fraction, which comprises more than 80 wt. % of paraffins and 90 wt. % of saturates, with a solvent mixture (16), wherein the solvent mixture (16) comprises a paraffinic naphtha fraction (7) and a co-solvent (15); and subjecting the solvent treatment mixture (23) to a solvent de-waxing step (17).

The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid hydrocarbon feedstock stream, which comprises aliphatic hydrocarbons and additionally comprises aromatic hydrocarbons and/or polar components, said process comprising the steps of: feeding the liquid hydrocarbon feedstock stream to a first column; feeding a first solvent stream which comprises an organic solvent to the first column at a position which is higher than the position at which the liquid hydrocarbon feedstock stream is fed; contacting at least a portion of the liquid hydrocarbon feedstock stream with at least a portion of the first solvent stream; and recovering at least a portion of the aliphatic hydrocarbons by liquid-liquid extraction of aromatic hydrocarbons and/or polar components with organic solvent, resulting in a stream comprising recovered aliphatic hydrocarbons and optionally organic solvent and a bottom stream from the first column comprising organic solvent and aromatic hydrocarbons and/or polar components.

The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid hydrocarbon feedstock stream, which comprises aliphatic hydrocarbons and additionally comprises aromatic hydrocarbons and/or polar components, said process comprising the steps of: feeding the liquid hydrocarbon feedstock stream to a first column; feeding a first solvent stream which comprises an organic solvent to the first column at a position which is higher than the position at which the liquid hydrocarbon feedstock stream is fed; contacting at least a portion of the liquid hydrocarbon feedstock stream with at least a portion of the first solvent stream; and recovering at least a portion of the aliphatic hydrocarbons by liquid-liquid extraction of aromatic hydrocarbons and/or polar components with organic solvent, resulting in a stream comprising recovered aliphatic hydrocarbons and optionally organic solvent and a bottom stream from the first column comprising organic solvent and aromatic hydrocarbons and/or polar components.

Non-acidic sulfur compounds (e.g., thiols) can be selectively extracted from a hydrocarbon stream containing them (e.g., crude oil) by contacting the hydrocarbon stream with a carbonate solvent that contains at least one organic carbonate (e.g., propylene carbonate) in an amount effective to selectively absorb and extract the non-acidic sulfur compounds therefrom. The carbonate solvent may optionally also comprise an additional solvent (e.g., caprolactam), a soluble metal salt (e.g., a metal salt where the metal is iron), and/or a mercaptan scavenger that is a heterocyclic amine (e.g., oxazolidine).

Non-acidic sulfur compounds (e.g., thiols) can be selectively extracted from a hydrocarbon stream containing them (e.g., crude oil) by contacting the hydrocarbon stream with a carbonate solvent that contains at least one organic carbonate (e.g., propylene carbonate) in an amount effective to selectively absorb and extract the non-acidic sulfur compounds therefrom. The carbonate solvent may optionally also comprise an additional solvent (e.g., caprolactam), a soluble metal salt (e.g., a metal salt where the metal is iron), and/or a mercaptan scavenger that is a heterocyclic amine (e.g., oxazolidine).

Described is a novel process for fractionating biomass pyrolysis oil quantitatively into energy dense hydrophobic aromatic fraction and water-soluble organics in an economical and energy efficient manner. Using the concepts of solvents and anti-solvent behaviours to separate the pyrolysis oil, which is an emulsion, a method utilising minimal quantities of solvents and water is proposed, By comparison with the existing methods to isolate the hydrophobic aromatic fraction, there is a volume reduction of greater than 50:1. Additionally, there is a significant time saving over the 24 hours for the accepted method as a solvent, and the anti-solvent system is pontaneous.

Described is a novel process for fractionating biomass pyrolysis oil quantitatively into energy dense hydrophobic aromatic fraction and water-soluble organics in an economical and energy efficient manner. Using the concepts of solvents and anti-solvent behaviours to separate the pyrolysis oil, which is an emulsion, a method utilising minimal quantities of solvents and water is proposed, By comparison with the existing methods to isolate the hydrophobic aromatic fraction, there is a volume reduction of greater than 50:1. Additionally, there is a significant time saving over the 24 hours for the accepted method as a solvent, and the anti-solvent system is pontaneous.

Settling unconverted pitch from a SHC reactor effluent before fractionation improves efficiency of fractionation of slurry hydrocracked products. The recycle of soft pitch to the SHC reactor results in improved reactor operation by avoiding the recycle of lighter products which vaporize in the reactor to occupy reactor space and the recycle of hard pitch which will not convert. The settling step facilitated by mixing with a solvent can achieve a separation between soft pitch and hard pitch not achievable in a fractionation column.