Abstract: The disclosure concerns a process to perform a catalytic dehydration of alcohols having at least two carbon atoms into olefins, said process comprising the steps of a) providing one fluidized bed reactor and a bed comprising particles; b) putting the particles in a fluidized state to obtain a fluidized bed; c) heating the fluidized bed to a temperature ranging from 200° C. to 500° C.; remarkable in that the particles of the bed comprise electrically conductive particles and particles of one or more solid acid catalysts, wherein at least 10 wt. % of the particles based on the total weight of the particles of the bed are electrically conductive particles and have a resistivity ranging from 0.001 Ohm·cm to 500 Ohm·cm at 400° C.; and in that the step c) of heating the fluidized bed is performed by passing an electric current through the fluidized bed.

Abstract: A process to produce olefins and aromatics via a purification of a hydrocarbon stream including: a) Providing a hydrocarbon stream having a starting boiling point of at least 15° C., a diene value of at least 1.0 preferably at least 1.5 g I2/100 g and a bromine number of at least 5 g Br2/100 g and containing at least 10 wt % of pyrolysis plastic oil where preferably at least 10 wt. % of said hydrocarbon stream has a boiling point of at least 150° C. based on the total weight of said hydrocarbon stream; c) Performing a first hydrotreating step; e) performing a second hydrotreating step; and f) recovering a purified hydrocarbon stream wherein at least a part of this purified hydrocarbon stream is sent to a steam cracker to produce olefins, such as ethylene and propylene, and aromatics.

Abstract: A process to produce olefins including: (a) Providing a hydrocarbon stream containing at least 10 wt % of pyrolysis plastic oil; (b) Optionally contacting the effluent obtained in step a) with silica gel, clays, alkaline or alkaline earth metal oxide, iron oxide, ion exchange resins, active carbon, active aluminium oxide, molecular sieves, alkaline oxide and/or porous supports containing lamellar double hydroxide modified or not and silica gel, or any mixture thereof; (c) performing a selective hydrogenation step; (d) contacting the stream obtained in step c) with a cracking catalyst to crack the olefins and/or paraffins into olefins having 2 to 4 carbon atoms (e) separating from the effluents obtained at the step d) a first stream containing olefins and saturated hydrocarbons having at most 3 carbon atoms, and a second stream containing hydrocarbons having 4 or more carbon atoms and (f) recovering from said first stream the ethylene and propylene.

Abstract: A process to produce olefins and aromatics via a purification of a hydrocarbon stream including: a) Providing a hydrocarbon stream having a starting boiling point of at least 15° C., a diene value of at least 1.0 preferably at least 1.5 g I2/100 g and a bromine number of at least 5 g Br2/100 g and containing at least 10 wt % of pyrolysis plastic oil where preferably at least 10 wt. % of said hydrocarbon stream has a boiling point of at least 150° C. based on the total weight of said hydrocarbon stream; c) Performing a first hydrotreating step; e) performing a second hydrotreating step; and f) recovering a purified hydrocarbon stream wherein at least a part of this purified hydrocarbon stream is sent to a steam cracker to produce olefins, such as ethylene and propylene, and aromatics.

Abstract: A process to produce olefins including: (a) Providing a hydrocarbon stream containing at least 10 wt % of pyrolysis plastic oil; (b) Optionally contacting the effluent obtained in step a) with silica gel, clays, alkaline or alkaline earth metal oxide, iron oxide, ion exchange resins, active carbon, active aluminium oxide, molecular sieves, alkaline oxide and/or porous supports containing lamellar double hydroxide modified or not and silica gel, or any mixture thereof; (c) performing a selective hydrogenation step; (d) contacting the stream obtained in step c) with a cracking catalyst to crack the olefins and/or paraffins into olefins having 2 to 4 carbon atoms (e) separating from the effluents obtained at the step d) a first stream containing olefins and saturated hydrocarbons having at most 3 carbon atoms, and a second stream containing hydrocarbons having 4 or more carbon atoms and (f) recovering from said first stream the ethylene and propylene.

Abstract: A process for the preparation of olefin by alcohol dehydration, for making polymer, fuel or fuel additive and use of olefin obtainable by said process for making polymer, fuel or fuel additive. Preferred olefin is C5 olefin obtained from dehydration of an alcohol or alcohol mixture, preferably from fusel oil.

Abstract: A process for purification a hydrocarbon stream including: (a) Providing a hydrocarbon stream having a diene value of at least 1.0, a bromine number of at least 5 g and containing at least 10 wt % of pyrolysis plastic oil; b) contacting the effluent obtained in step a) with a silica gel, clays, alkaline or alkaline earth metal oxide, iron oxide, ion exchange resins, active carbon, active aluminium oxide, molecular sieves, alkaline oxide and/or porous supports, and/or silica gel, or any mixture thereof; c) performing a first hydrotreating step; d) contacting the effluent obtained in step c) with silica gel, clays, alkaline or alkaline earth metal oxide, iron oxide, ion exchange resins, active carbon, active aluminium oxide, molecular sieves, alkaline oxide and/or porous supports and silica gel, or any mixture thereof; e) performing a second hydrotreating step; and f) recovering a purified hydrocarbon stream.

Abstract: A process for the purification of a hydrocarbon stream including: (a) Providing a hydrocarbon stream having a diene value of at least 1.0 and a bromine number of at least 5 gBr2/100 g and containing pyrolysis plastic oil; (b) Optionally contact the hydrocarbon stream obtained in step (a) with a silica gel, clays, alkaline or alkaline earth metal oxide, iron oxide, ion exchange resins, active carbon, active aluminum oxide, molecular sieves, alkaline oxide and/or porous supports and silica gel, or any mixture thereof; (c) Heating the stream obtained in step a) or b) followed by a mixing of the heated stream with a second diluent heated at a temperature of at least 300° C. preferably at least 330° C.; (d) performing an hydroprocessing step at a temperature of at least 250° C. in the presence of H2; and (e) recovering a purified hydrocarbon stream.

Abstract: The present disclosure relates to a novel staged-synthesis method for introduction of various metals in the structure of zeolite frameworks by isomorphous substitution. This new method is based on a hydrothermal synthesis in which the metal addition to the precursor suspensions (gel) is delayed. This so-called “staged-synthesis method” allows to obtain nanosized silanol highly homo-geneous crystalline zeolite structures with a control of the metal location.

Abstract: Method for the preparation of a composition enriched in 2-methyl-but-2-ene and use for making a polymer.

Abstract: The present disclosure relates to a novel method for introducing various metals in the structure of zeolite frameworks by isomorphous substitution. This new method is based on a hydrothermal reaction of the metal with the zeolite. This method allows obtaining zeolite with a structure and with control of the metal location.

Abstract: The present disclosure relates to a novel staged-synthesis method for introduction of various metals in the structure of zeolite frameworks by isomorphous substitution. This new method is based on a hydrothermal synthesis in which the metal addition to the precursor suspensions (gel) is delayed. This so-called “staged-synthesis method” allows to obtain nanosized silanol highly homo- geneous crystalline zeolite structures with a control of the metal location.

Abstract: The present disclosure relates to a novel method for introducing various metals in the structure of zeolite frameworks by isomorphous substitution. This new method is based on a hydrothermal reaction of the metal with the zeolite. This method allows obtaining zeolite with a structure and with control of the metal location.

Abstract: The present disclosure relates to an RHO-type zeolite comprising caesium and M1 wherein M1 is selected from Na and/or Li remarkable in that it has a Si/Al molar ratio comprised between 1.2 and 3.0 as determined by 29Si magic angle spinning nuclear magnetic resonance, in that the RHO-type zeolite has a specific surface area comprised between 40 m2g?1 and 250 m2g?1 as determined by N2 adsorption measurements, in that the RHO-type zeolite being in the form of one or more nanoparticles with an average crystal size comprised between 10 nm and 400 nm as determined by scanning electron microscopy wherein said nanoparticles form monodispersed nanocrystals or form aggregates of nanocrystals having an average size ranging from 100 nm to 500 nm, as determined by scanning electron microscopy.

Abstract: The present disclosure relates to a chabazite-type zeolite, comprising at least two cages composed of 4- and 8-membered rings connected by one 6-membered double ring, remarkable in that it has a Si/Al molar ratio comprised between 1 and 15, in that it comprises caesium and potassium with a Cs/K molar ratio of at most 5.0 and in that it forms nanoparticles with an average crystal size comprised between 5 nm and 250 nm and with a specific surface area comprised between 50 m2g?1 and 200 m2g?1. Amorphous precursors, devoid of an organic structure-directing agent, as well as a method for preparation of these amorphous precursors in the absence of such organic structure-directing agent and method for preparation of the chabazite-type zeolite, are also described. Finally, the use of the chabazite-type zeolite as a sorbent for carbon dioxide is also demonstrated.

Abstract: A catalyst which comprises an amorphous support based on alumina, a C1-C4 dialkyl succinate, citric acid and optionally acetic acid, phosphorus and a hydrodehydrogenating function comprising at least one element from group VIII and at least one element from group VIB; the most intense bands comprised in the Raman spectrum of the catalyst are characteristic of Keggin heteropolyanions (974 and/or 990 cm?1), C1-C4 dialkyl succinate and citric acid (in particular 785 and 956 cm?1). Also a process for preparing said catalyst in which a catalytic precursor in the dried, calcined or regenerated state containing the elements of the hydrodehydrogenating function, and optionally phosphorus, is impregnated with an impregnation solution comprising at least one C1-C4 dialkyl succinate, citric acid and optionally at least one compound of phosphorus and optionally acetic acid, and is then dried. Further, the use of said catalyst in any hydrotreatment process.

Abstract: Polymer composition obtained from polymerization of C5 olefin composition, use for making an adhesive, and article or composite containing it.

Abstract: Polymer composition obtained from polymerization of C5 olefin composition, use for making an adhesive, and article or composite containing it.

Abstract: A process for the preparation of a catalyst from a catalytic precursor comprising a support based on alumina and/or silica-alumina and/or zeolite and comprising at least one element of group VIB and optionally at least one element of group VIII, by impregnation of said precursor with a solution of a C1-C4 dialkyl succinate. An impregnation step for impregnation of said precursor which is dried, calcined or regenerated, with at least one solution containing at least one carboxylic acid other than acetic acid, then maturing and drying at a temperature less than or equal to 200° C., optionally a heat treatment at a temperature lower than 350° C., followed by an impregnation step with a solution containing at least one C1-C4 dialkyl succinate followed by maturing and drying at a temperature less than 200° C. without subsequent calcination step. The catalyst is used in hydrotreatment and/or hydroconversion.

Abstract: A process for dearomatization of a petroleum cut produces a dearomatized hydrocarbon-containing fluid with a sulphur content less than or equal to 5 ppm and a content of aromatic compounds less than or equal to 300 ppm, the hydrocarbon-containing fluid has a boiling point between 100 and 400° C. according to the standard ASTM D-86 and a distillation range defined by the difference between the Initial Boiling Point (IBP) and the Final Boiling Point (FBP) determined by the standard ASTM D-86 not exceeding 80° C. The process includes at least one dearomatization cycle utilizing a mixture of the petroleum cut with one or more inert and light diluents having a distillation range not exceeding 80° C.