The present invention describes a process for the simultaneous removal of arsenic and sulphur compounds from hydrocarbon streams of fossil origin, wherein hydrocarbon streams of fossil origin resulting from the retorting process of schist are purified by direct contact with hydrated iron oxide, such as goethite (-FeOOH) in its raw natural form (limonite ore particles).

A catalyst preparation unit for producing an activated hydrocarbon-catalyst mixture. The catalyst preparation unit includes one or more catalyst reactant input conduits; a hydrocarbon input conduit; a water input conduit; one or more catalyst reactant mixing and conveyance systems for receiving and mixing catalyst reactants from the catalyst component input conduits and water provided by the water input conduit to provide one or more catalyst reactant solutions; one or more hydrocarbon mixing and conveyance systems for receiving and mixing the catalyst reactant solutions and hydrocarbons provided by the hydrocarbon input conduit to produce a hydrocarbon-catalyst reactant mixture; at least one reactor located downstream of the mixers, for receiving and activating the hydrocarbon-catalyst reactant mixture, thereby producing the activated hydrocarbon catalyst mixture; a gas/liquid separator located downstream of the reactor, for removing vapors and gas from the activated hydrocarbon-catalyst mixture; and an output conduit for transporting the activated hydrocarbon-catalyst mixture away from the catalyst preparation unit.

A catalyst preparation unit for producing an activated hydrocarbon-catalyst mixture. The catalyst preparation unit includes one or more catalyst reactant input conduits; a hydrocarbon input conduit; a water input conduit; one or more catalyst reactant mixing and conveyance systems for receiving and mixing catalyst reactants from the catalyst component input conduits and water provided by the water input conduit to provide one or more catalyst reactant solutions; one or more hydrocarbon mixing and conveyance systems for receiving and mixing the catalyst reactant solutions and hydrocarbons provided by the hydrocarbon input conduit to produce a hydrocarbon-catalyst reactant mixture; at least one reactor located downstream of the mixers, for receiving and activating the hydrocarbon-catalyst reactant mixture, thereby producing the activated hydrocarbon catalyst mixture; a gas/liquid separator located downstream of the reactor, for removing vapors and gas from the activated hydrocarbon-catalyst mixture; and an output conduit for transporting the activated hydrocarbon-catalyst mixture away from the catalyst preparation unit.

A system for steam cracking a whole crude that may include a volatilization device, a control system, a separator, and a steam pyrolysis reactor. The volatilization device may be configured to separate a vapor phase from a liquid phase. The control system may be configured to maintain a flow rate of the whole crude and steam, at an initial relative velocity of less than 30 m/s. The separator may be fluidly connected to the volatilization device and configured to separate the liquid phase into a second vapor phase, and a second liquid phase. The steam pyrolysis reactor may include a convection section and a steam pyrolysis heater section, the convection section configured to heat the vapor phase, the liquid phase, and the second vapor phase, and the steam pyrolysis heater section configured to steam crack hydrocarbons in the vapor phase thereby generating a cracked hydrocarbon product.

A system for steam cracking a whole crude that may include a volatilization device, a control system, a separator, and a steam pyrolysis reactor. The volatilization device may be configured to separate a vapor phase from a liquid phase. The control system may be configured to maintain a flow rate of the whole crude and steam, at an initial relative velocity of less than 30 m/s. The separator may be fluidly connected to the volatilization device and configured to separate the liquid phase into a second vapor phase, and a second liquid phase. The steam pyrolysis reactor may include a convection section and a steam pyrolysis heater section, the convection section configured to heat the vapor phase, the liquid phase, and the second vapor phase, and the steam pyrolysis heater section configured to steam crack hydrocarbons in the vapor phase thereby generating a cracked hydrocarbon product.

In accordance with one or more embodiments herein, an integrated process for upgrading a hydrocarbon oil feed stream utilizing a delayed coker, steam enhanced catalytic cracker, and an aromatics complex includes solvent deasphalting the hydrocarbon oil stream; delayed coking the heavy residual hydrocarbons; hydrotreating the delayed coker product stream and the deasphalted oil stream to form a light C.sub.5+ hydrocarbon stream and a heavy C.sub.5+ hydrocarbon stream; steam enhanced catalytically cracking the light C.sub.5+ hydrocarbon stream; steam enhanced catalytically cracking the heavy C.sub.5+ hydrocarbon stream; passing at least a portion of the light steam enhanced catalytically cracked stream, the heavy steam enhanced catalytically cracked stream, or both to a product separator to produce a olefin product stream, a naphtha product stream, and a BTX product stream; and processing the naphtha product stream in the aromatics complex to produce benzene and xylenes.

A method is provided involving altering the viscosity of bio-derived paraffins to produce a paraffinic fluid, where the altering step includes chlorinating the bio-derived paraffins; the bio-derived paraffins include a hydrodeoxygenated product produced by hydrodeoxygenating a bio-based feed where the bio-based feed includes bio-derived fatty acids, fatty acid esters, or a combination thereof; the bio-derived paraffins include n-paraffins; and the n-paraffins have a biodegradability of at least 40% after about 23 days of exposure to microorganisms. Also provided are methods of protecting and/or cleaning a substance by applying the paraffinic fluid.

A method is provided involving altering the viscosity of bio-derived paraffins to produce a paraffinic fluid, where the altering step includes chlorinating the bio-derived paraffins; the bio-derived paraffins include a hydrodeoxygenated product produced by hydrodeoxygenating a bio-based feed where the bio-based feed includes bio-derived fatty acids, fatty acid esters, or a combination thereof; the bio-derived paraffins include n-paraffins; and the n-paraffins have a biodegradability of at least 40% after about 23 days of exposure to microorganisms. Also provided are methods of protecting and/or cleaning a substance by applying the paraffinic fluid.

The present application provides a porous carbon material and a preparation method and application thereof, which includes following steps: choosing a distillate of ethylene tar in a range of 250? C.?550? C.and performing hydrogenation treatment on the distillate to obtain hydrofined ethylene tar; performing pre-carbonization treatment on part of the hydrofined ethylene tar to obtain coke; mixing the remaining hydrofined ethylene tar and the coke to form a mixture, and performing activating treatment on the mixture to obtain the porous carbon material. The present application can realize the preparation of high purity porous carbon with simple preparation process and low cost.

Processes herein may be used to thermally crack various hydrocarbon feeds, and may eliminate the refinery altogether while making the crude to chemicals process very flexible in terms of crude. In embodiments herein, crude is progressively separated into at least light and heavy fractions. Depending on the quality of the light and heavy fractions, these are routed to one of three upgrading operations, including a fixed bed hydroconversion unit, a fluidized catalytic conversion unit, or a residue hydrocracking unit that may utilize an ebullated bed reactor. Products from the upgrading operations may be used as feed to a steam cracker.