The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid hydrocarbon feedstock stream comprising aliphatic hydrocarbons, heteroatom containing polar components and optionally aromatic hydrocarbons, said process comprising the steps of: a) mixing the liquid hydrocarbon feedstock stream with a solvent resulting in a liquid mixture; b) cooling the liquid mixture obtained in step a) to a temperature in the range of from +5° C. to −30° C. to obtain wax crystals in the mixture; c) separating wax crystals from the cooled liquid mixture obtained in step b) to produce a wax comprising aliphatic hydrocarbons and a dewaxed liquid mixture comprising solvent, heteroatom containing polar components and optionally aromatic hydrocarbons; d) separating solvent from the liquid mixture obtained in step c) and optionally recycling the separated solvent to step a). Further, the present invention relates to a process for the recovery of aliphatic hydrocarbons from plastics, and to a process for steam cracking a hydrocarbon feed.

The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid hydrocarbon feedstock stream comprising aliphatic hydrocarbons, heteroatom containing polar components and optionally aromatic hydrocarbons, said process comprising the steps of: a) mixing the liquid hydrocarbon feedstock stream with a solvent resulting in a liquid mixture; b) cooling the liquid mixture obtained in step a) to a temperature in the range of from +5° C. to −30° C. to obtain wax crystals in the mixture; c) separating wax crystals from the cooled liquid mixture obtained in step b) to produce a wax comprising aliphatic hydrocarbons and a dewaxed liquid mixture comprising solvent, heteroatom containing polar components and optionally aromatic hydrocarbons; d) separating solvent from the liquid mixture obtained in step c) and optionally recycling the separated solvent to step a). Further, the present invention relates to a process for the recovery of aliphatic hydrocarbons from plastics, and to a process for steam cracking a hydrocarbon feed.

The present disclosure discloses a crosslinked polymer for dewaxing the lubricating oils, the polymer derived from (a) 70-77 weight percentage of at least one alkyl acrylate; (b) 23-28 weight percentage of at least one vinyl aromatic hydrocarbon; (c) 0.1-2.5 weight percentage of at least one crosslinker; and (d) 0.75-2.5 weight percentage of at least one initiator and wherein the polymer has a number average molecular weight in the range of 5000-15000. The present disclosure discloses a convenient process for preparing the crosslinked polymer. The present disclosure further reveals a method for dewaxing the lubricating oil.

The present disclosure discloses a crosslinked polymer for dewaxing the lubricating oils, the polymer derived from (a) 70-77 weight percentage of at least one alkyl acrylate; (b) 23-28 weight percentage of at least one vinyl aromatic hydrocarbon; (c) 0.1-2.5 weight percentage of at least one crosslinker; and (d) 0.75-2.5 weight percentage of at least one initiator and wherein the polymer has a number average molecular weight in the range of 5000-15000. The present disclosure discloses a convenient process for preparing the crosslinked polymer. The present disclosure further reveals a method for dewaxing the lubricating oil.

Systems and methods are provided for performing solvent dewaxing using a dewaxing solvent that is not fully miscible with the feed being dewaxed. It has been unexpectedly discovered that by operating with a ketone solvent mixture that is beyond the miscibility limit by a small amount, the rate of solvent dewaxing can be substantially increased. Additionally, the difference between the filtration temperature during solvent dewaxing and the pour point of the resulting dewaxed product is unexpectedly reduced. The dewaxing solvent beyond the miscibility limit can correspond to, for example, a solvent mixture where the weight percent of methyl ethyl ketone is beyond the miscibility limit by 0.1 vol % to 5.0 vol %.

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 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).

Systems and methods are provided for performing solvent dewaxing using a dewaxing solvent that is not fully miscible with the feed being dewaxed. It has been unexpectedly discovered that by operating with a ketone solvent mixture that is beyond the miscibility limit by a small amount, the rate of solvent dewaxing can be substantially increased. Additionally, the difference between the filtration temperature during solvent dewaxing and the pour point of the resulting dewaxed product is unexpectedly reduced. The dewaxing solvent beyond the miscibility limit can correspond to, for example, a solvent mixture where the weight percent of methyl ethyl ketone is beyond the miscibility limit by 0.1 vol % to 5.0 vol %.

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 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).