Abstract: This invention relates to a process for hydrogenation of benzene contained in a catalytic reformate, in which: The hydrogen that is present in the catalytic reformate is separated from the remainder of the reformate with separation means, A light benzene-enriched fraction is separated from the heavy reformate, The light reformate that contains the benzene is brought into contact with a nickel-based hydrogenation catalyst at a temperature of between 90° C. and 150° C., a VVH of between 0.5 and 10, and with at least one portion of hydrogen that is obtained during the separation stage of the hydrogen at the top of the separator tank and used at the output pressure of said separator.

Abstract: The invention concerns a process for purification by elimination of chlorine in the form of hydrogen chloride and organochlorine compounds by contacting in the presence of hydrogen of at least a part of the effluent from a reforming, aromatics production, dehydrogenation, isomerisation or hydrogenation zone, said part of the effluent comprising olefins, hydrogen chloride and organochlorine compounds, on an elimination zone comprising a chain arrangement of two masses, the first mass being a mass comprising at least one metal from group VIII deposited on a mineral carrier and the second mass being a hydrogen chloride adsorbent.

Abstract: A process in which the paraffinic effluent derived from a Fischer-Tropsch synthesis unit is separated to obtain a heavy C5+ fraction, said heavy fraction then being hydrogenated in the presence of a hydrogenation catalyst at a temperature in the range 80° C to 200° C, at a total pressure in the range 0.5 to 6 MPa, at an hourly space velocity in the range 1 to 10 h-1, and at a hydrogen flow rate corresponding to a hydrogen/hydrocarbons volume ratio in the range 5 to 80 NI/I/h, the liquid hydrogenated effluent then being brought into contact with a hydroisomerization/hydrocracking catalyst, with no prior separation step, the hydroisomerized/hydrocracked effluent then being distilled to obtain middle distillates and possibly oil bases.

Abstract: The invention describes a process for treatment of a feedstock that is obtained from a renewable source that comprises a hydrotreatment stage in the presence of at least one fixed-bed catalyst, whereby said catalyst comprises a hydro-dehydrogenating function and an amorphous substrate, at a temperature of between 50 and 450° C., at a pressure of between 1 MPa and 10 MPa, at an hourly volumetric flow rate of between 0.1 h?1 and 10 h?1, and in the presence of a total quantity of hydrogen that is mixed with the feedstock such that the hydrogen/feedstock ratio is between 50 and 1000 Nm3 of hydrogen/m3 of feedstock, followed by a separation from the hydrotreated effluent that is obtained from stage a) of hydrogen, gases, and at least one liquid hydrocarbon effluent that consists of at least 50% linear n-paraffins, and a steam-cracking of at least one portion of the liquid hydrocarbon effluent that is obtained from stage b).

Abstract: The invention describes a two-step process for hydrotreatment of a feed derived from a renewable source, comprising: a) a first step, termed a mild pre-hydrogenation step, operating in the presence of a first, metallic, catalyst comprising an active hydrodehydrogenating phase constituted by at least one metal from group VIII and/or at least one metal from group VIB and an amorphous mineral support; and b) a second step, termed the second treatment step, operating in the presence of a second, sulphurized, catalyst comprising an active hydrodehydrogenating phase constituted by at least one non-noble metal from group VIII and/or at least one metal from group VIB and an amorphous mineral support.

Abstract: Process for the production of high-quality kerosene and diesel fuels and for the coproduction of hydrogen from a so-called light naphtha cut to which any quantity of LPG cut can be added where the steps of the process include: separating normal and iso-paraffins, dehydrogenation of the paraffins, oligomerization of the olefins and hydrogenation of the oligomerized olefins, the process permitting the production of kerosene and diesel fuels meeting market specifications, or even improved relative to the latter.

Abstract: Process mainly for the production of high-quality kerosene and diesel fuels and for the coproduction of hydrogen from a so-called light naphtha cut to which any quantity of LPG cut can be added, employing the following successive stages: dehydrogenation of the paraffins, oligomerization of the olefins and hydrogenation of the oligomerized olefins, the process permitting the production of kerosene and diesel fuels meeting market specifications, or even improved relative to the latter.

Abstract: The invention concerns a process for purification by elimination of chlorine in the form of hydrogen chloride and organochlorine compounds by contacting in the presence of hydrogen of at least a part of the effluent from a reforming, aromatics production, dehydrogenation, isomerisation or hydrogenation zone, said part of the effluent comprising olefins, hydrogen chloride and organochlorine compounds, on an elimination zone comprising a chain arrangement of two masses, the first mass being a mass comprising at least one metal from group VIII deposited on a mineral carrier and the second mass being a hydrogen chloride adsorbent.

Abstract: The invention describes a process in which the paraffinic effluent derived from a Fischer-Tropsch synthesis unit is separated to obtain a heavy C5+ fraction, said heavy fraction then being hydrogenated in the presence of a hydrogenation catalyst at a temperature in the range 80° C. to 200° C., at a total pressure in the range 0.5 to 6 MPa, at an hourly space velocity in the range 1 to 10 h?1, and at a hydrogen flow rate corresponding to a hydrogen/hydrocarbons volume ratio in the range 5 to 80 Nl/l/h, the liquid hydrogenated effluent then being brought into contact with a hydroisomerization/hydrocracking catalyst, with no prior separation step, the hydroisomerized/hydrocracked effluent then being distilled to obtain middle distillates and possibly oil bases.

Abstract: The invention describes a process for treatment of a feedstock that is obtained from a renewable source that comprises a hydrotreatment stage in the presence of at least one fixed-bed catalyst, whereby said catalyst comprises a hydro-dehydrogenating function and an amorphous substrate, at a temperature of between 50 and 450° C., at a pressure of between 1 MPa and 10 MPa, at an hourly volumetric flow rate of between 0.1 h?1 and 10 h?1, and in the presence of a total quantity of hydrogen that is mixed with the feedstock such that the hydrogen/feedstock ratio is between 50 and 1000 Nm3 of hydrogen/m3 of feedstock, followed by a separation from the hydrotreated effluent that is obtained from stage a) of hydrogen, gases, and at least one liquid hydrocarbon effluent that consists of at least 50% linear n-paraffins, and a steam-cracking of at least one portion of the liquid hydrocarbon effluent that is obtained from stage b).

Abstract: The invention describes a two-step process for hydrotreatment of a feed derived from a renewable source, comprising: a) a first step, termed a mild pre-hydrogenation step, operating in the presence of a first, metallic, catalyst comprising an active hydrodehydrogenating phase constituted by at least one metal from group VIII and/or at least one metal from group VIB and an amorphous mineral support; and b) a second step, termed the second treatment step, operating in the presence of a second, sulphurized, catalyst comprising an active hydrodehydrogenating phase constituted by at least one non-noble metal from group VIII and/or at least one metal from group VIB and an amorphous mineral support.

Abstract: This invention relates to a process for hydrogenation of benzene contained in a catalytic reformate, in which: The hydrogen that is present in the catalytic reformate is separated from the remainder of the reformate with separation means, A light benzene-enriched fraction is separated from the heavy reformate, The light reformate that contains the benzene is brought into contact with a nickel-based hydrogenation catalyst at a temperature of between 90° C. and 150° C., a VVH of between 0.5 and 10, and with at least one portion of hydrogen that is obtained during the separation stage of the hydrogen at the top of the separator tank and used at the output pressure of said separator.

Abstract: A facility for converting an olefinic C4 cut to isobutene and propylene comprising, in succession: 1) a zone 1 for selective hydrogenation of olefins in the olefinic C4 cut with simultaneous isomerisation of butene-1 to butene-2, said zone comprising at least one device for introducing the olefinic C4 cut to be converted, at least one device for removing an effluent, and at least one device for introducing hydrogen, said zone also comprising at least one catalyst bed; 2) a separation zone, comprising at least one device for introducing the effluent from zone 1 directly connected to said at least one device for removing an effluent, at least one device for removing a first fraction comprising isobutene and butene-1, and at least one device for removing a second fraction comprising butene-2 and n-butane, wherein the second fraction comprises at most 1% by weight of isobutene and at most 1% by weight of butene-1; 3) a metathesis zone for metathesis of butene-2 with ethylene to produce propylene, wherein the m

Abstract: A process for producing a gasoline with a low sulphur content comprises: separating a sulphur-containing gasoline into a light fraction and a heavy fraction, hydrodesulphurising the light gasoline on a nickel-based catalyst, hydrodesulphurising the heavy fraction on a catalyst comprising at least one group VIII metal and/or at least one group VIB metal, and mixing the desulphurised fractions.

Abstract: An aliphatic alkylate with a high octane number is prepared from a C4 catalytic cracking or steam-cracking fraction that contains mainly isobutane, isobutene, butene-1 and butenes-2 by: (a) hydro-isomerizing said C4 fraction, obtaining a mixture that contains for the most part butenes-2, isobutene and isobutane; (b) separating, by distillation of the hydro-isomerized fraction, of a butene-2-rich effluent that is collected at the bottom and an isobutane- and isobutene-rich effluent that is collected at the top; (c) sending said isobutene- and isobutane-rich effluent into a hydrogenation zone that produces an effluent that for the most part contains isobutane; (d) sending of said butenes-2-rich effluent that is derived from (b) and of said effluent that for the most part contains the isobutane that is derived from (c) into an alkylation zone producing, by addition of isobutane to butenes-2, an isooctane mixture that contains excess isobutane; (e) separating by distillation of excess isobutane, which comes

Abstract: The invention concerns a process for purifying naphthalene. The process comprises selective hydrotreatment corresponding to hydrodesulphuration and/or hydrodenitrogenation and/or hydrodehydroxylation and/or hydrogenation of olefins while limiting naphthalene hydrogenation. The catalyst used comprises a matrix, at least one group VIII metal, at least one group VI metal and optionally phosphorous. It has a specific surface area of at most 220 m2/g, a pore volume of 0.35-0.7 ml/g and an average pore diameter of over 10 nm. The process is carried out at 150-325° C. at a pressure of 0.1-0.9 MPa, with an HSV of 0.05-10 h−1, and a H2/naphthalene ratio of 0.1-1.3 mole/mole. The effluent, freed of H2S, NH3 and water, undergoes a naphthalene separation process by distillation or, as is preferable, by crystallisation. Further, recycling the separated tetralin to the hydrotreatment step can substantially increase the naphthalene yield.

Abstract: A process for processing a feedstock comprising a major amount of olefinic hydrocarbons having 4 carbon atoms per molecule, including isobutene as well as but-1-ene and but-2-enes, wherein the process comprises processing said feedstock in a distillation zone associated with a hydroisomerization reaction zone located at least partly external to the distillation zone, said processing comprising drawing at the height of a draw-off level of the distillation zone at least part of the liquid flowing in the distillation zone, passing said liquid into the external hydroisomerization reaction zone to form a hydroisomerized effluent, and reintroducing at least part of the effluent from said reaction zone reintroduced into the distillation zone at one or more reintroduction level(s), so as to ensure the continuity of the distillation.

Abstract: The present invention concerns a process for the conversion of an olefinic C4 cut to polyisobutene and to propylene by metathesis. The process comprises three successive steps: (1) selective hydrogenation of diolefins with simultaneous isomerisation of 1-butene to 2-butenes, (2) polymerisation of the isobutene, including optional prior extraction of the isobutene, (3) metathesis of 2-butene with ethylene. Part or all of the C4 cut may originate from the metathesis of an olefinic C5 cut with ethylene after hydroisomerisation of the C5 cut. Application to C4 and C5 steam cracking cuts.

Abstract: The present invention concerns a plant for the conversion of an olefinic C.sub.4 or C.sub.5 cut to an alkyl-tertiobutylether or alkyl-tertioamylether and to propylene, by metathesis. The plant comprises four successive stages: (1) selective hydrogenation of the diolefins with simultaneous isomerisation of the alpha olefins to internal olefins; (2) etherification of the isoolefins; (3) elimination of oxygen-containing impurities; (4) metathesis of internal olefins with ethylene. Application to C.sub.4 and C.sub.5 steam cracking units.

Abstract: The invention relates to a process for producing high purity isobutene from a hydrocarbon cut essentially comprising olefinic hydrocarbons containing 4 carbon atoms per molecule including isobutene, also butene-1 and butene-2 compounds in a ratio which substantially corresponds to the thermodynamic equilibrium. The process comprises passing the cut into a distillation zone (3) associated with a hydroisomerisation reaction zone, the bottom product of the distillation zone comprising butene-2 compounds being passed into a skeletal isomerisation zone (2) where the linear butenes are at least partially isomerised to isobutene, at least part of the principal effluent from the skeletal isomerisation zone being recycled upstream of the reactive distillation zone (3).