Abstract: The present invention relates to a method for capturing carbon oxides, in particular for recovering carbon oxides from an industrial facility, and specifically to a method for capturing CO2 contained in a gas flow with a view to storing said CO2, said method including placing said gas flow in contact with a solvent including an organometallic compound, such that said solvent captures said carbon oxides to form an enriched solvent. The present invention relates in particular to the use of said capture method in post-combustion or pre-combustion processes.

Abstract: The present invention relates to a hydrogenation catalyst, particularly useful for the hydrogenation of carbon disulphide (CS2) to form methyl mercaptan (CH3SH), and to a preparation method thereof. The present invention also relates to a method for continuously preparing methyl mercaptan by the catalytic hydrogenation of carbon disulphide, with a carbon disulphide conversion rate of 100%, and a methyl mercaptan selectivity of 100%.

Abstract: One subject of the invention is a dimethyl disulphide in which the content of biocarbon is at least 1%. Another subject of the invention is processes for preparing this dimethyl disulphide. Yet another subject of the invention is the use of such a dimethyl disulphide for the manufacture of methanesulphonic acid.

Abstract: The present invention relates to a sulphiding agent for a hydrotreating catalyst which makes possible faster sulphiding of the catalyst but which also makes possible to very significantly limit solid deposits, in particular of sulphur. The sulphiding agent according to the invention is essentially composed of diethyl disulphide (DEDS) or dipropyl disulphide(s) (DPDS) or dibutyl disulphide(s) (DBDS) and can be employed in “in situ” and “ex situ” presulphidation processes.

Abstract: A radical polymerization process for the in which a tert-dodecyl mercaptan prepared by reaction of hydrogen sulfide with tri(n-butene) in the presence of a catalyst as chain-transfer agent.

Abstract: The invention relates to a hydrocarbon hydroconversion catalyst comprising a carrier based on refractory oxide, a metal of the group VIII, and a metal of the group VIB. Said catalyst is characterised in that it also comprises at least one organic compound selected from the alkene diols of formula (I) wherein R1 represents a C2-10 alkenylene group, preferably C2-4 alkenylene, a C6-18 arylene group, or a C7-18 alkylene-arylene group, and each R2 independently represents a hydrogen atom or a C1-18 alkyl group, a C1-18 alkenyl group, a C6-18 aryl group, a C3-8 cycloalkyl group, or a C7-20 alkylaryl or arylalkyl group, or the two groups R2 together form a divalent C2-18 group, the carbonated chain of the R2 groups containing or carrying at least one heteroatom selected from S, N and O. The invention also relates to a method for preparing one such catalyst, and to the use of said catalyst for hydrotreatment or hydroconversion.

Abstract: The present invention concerns an additive for reducing the formation of coke and/or carbon monoxide in thermal hydrocarbon cracking units and/or of other organic compounds in heat exchangers. The additive according to the invention is essentially composed of diethyl disulphide (DEDS) or dipropyl disulphide(s) (DPDS) or dibutyl disulphide(s) (DBDS) and can be used on the metal walls of a cracking reactor and on the metal walls of a heat exchanger placed downstream from the cracking reactor, and during the process of cracking hydrocarbons and/or other organic compounds.

Abstract: The invention relates to a catalyst for hydroconversion of hydrocarbons, comprising a support made from at least one refractory oxide, at least one group VIII metal and at least one group VIB metal, characterised in further comprising at least one organic compound with at least two thiol functions separated by at least one oxygenated group of formula (I): HS—CxHyOz-SH (I), where x=1 to 20, preferably 2 to 9 and for example x=6, y=2 to 60, preferably 4 to 12 and z=1 to 10, preferably 1 to 6. The invention further relates to a method for preparation, a method for activation of said catalyst and use of the catalyst for the hydrotreatment and/or hydrocracking of hydrocarbons.

Abstract: In the photochemical synthetic process in semi-continuous mode according to the invention, a reactor comprising two zones is used, the radiating portion of the lamp(s) being totally immersed in a first zone which is completely filled with reaction medium and spills off via an overflow into a second zone whose volume is sufficient to contain the volume of reaction medium originating from the first zone and corresponding substantially to the volume of the reagent(s) gradually introduced.

Abstract: The present invention relates to a sulphiding agent for a hydrotreating catalyst which makes possible faster sulphiding of the catalyst but which also makes possible to very significantly limit solid deposits, in particular of sulphur. The sulphiding agent according to the invention is essentially composed of diethyl disulphide (DEDS) or dipropyl disulphide(s) (DPDS) or dibutyl disulphide(s) (DBDS) and can be employed in “in situ” and “ex situ” presulphidation processes.

Abstract: The invention relates to a hydrocarbon hydroprocessing catalyst comprising a support based on at least one refractory oxide, at least one metal from group VIII and at least one metal from group VIB. The inventive catalyst is characterised in that it also comprises at least one organic compound having formula (I) or (II) in which each R1 represents independently an alkyl group at C1-18, an alkenyl group at C2-18, an aryl group at C6-18, a cycloalkyl group at C3-8, an alkylaryl or arylalkyl group at C7-20, or the two R1 groups together form a divalent group at C2-18, and R2 represents an alkylene group at C1-18, an arylene group at C6-18, a cycloalkylene group at C3-7, or a combination of same. The invention also relates to a method of preparing one such catalyst and to the use thereof for hydroprocessing or hydrocracking.

Abstract: The invention relates to a hydrocarbon hydroconversion catalyst comprising a carrier based on refractory oxide, a metal of the group VIII, and a metal of the group VIB. Said catalyst is characterised in that it also comprises at least one organic compound selected from the alkene diols of formula (I) wherein R1 represents a C2-10 alkenylene group, preferably C2-4 alkenylene, a C6-18 arylene group, or a C7-18 alkylene-arylene group, and each R2 independently represents a hydrogen atom or a C1-18 alkyl group, a C1-18 alkenyl group, a C6-18 aryl group, a C3-8 cycloalkyl group, or a C7-20 alkylaryl or arylalkyl group, or the two groups R2 together form a divalent C2-18 group, the carbonated chain of the R2 groups containing or carrying at least one heteroatom selected from S, N and O. The invention also relates to a method for preparing one such catalyst, and to the use of said catalyst for hydrotreatment or hydroconversion.

Abstract: The process for preparing a mercaptan from an olefin and hydrogen sulphide is carried out in the presence of hydrogen and a catalyst composition comprising a strong acid, such as a heteropolyacid, and at least one metal belonging to group VIII of the Periodic Table.

Abstract: Process for the preparation of tert-dodecyl mercaptan by reaction of hydrogen sulfide with tri(n-butene) in the presence of a catalyst. tert-Dodecyl mercaptan thus prepared and its use as chain-transfer agent in radical (co)polymerization reactions.

Abstract: Process for the impregnation of a metal hydrotreating catalyst in the oxide form with at least one orthophthalate optionally dissolved or dispersed in a liquid. Process for the sulphidation of a metal hydrotreating catalyst in oxide form, comprising: a) a stage of impregnation according to the said process, followed by b) a stage of bringing the catalyst thus treated into contact with a sulphidation agent, and by c) a stage of bringing into contact with hydrogen; stage b) being followed by stage c) or else stages b) and c) being carried out simultaneously.

Abstract: The process for preparing a mercaptan from an olefin and hydrogen sulphide is carried out in the presence of hydrogen and a catalyst composition comprising a strong acid, such as a heteropolyacid, and at least one metal belonging to group VIII of the Periodic Table.

Abstract: The process for preparing a mercaptan from a thioether and hydrogen sulphide is carried out in the presence of hydrogen and a catalyst composition comprising a strong acid, such as a heteropolyacid, and at least one metal belonging to group VIII of the Periodic Table.

Abstract: The invention concerns a method for sulphurizing catalysts for hydrotreating of hydrocarbon feedstocks. The invention is characterised in that it consists in sulphurizing the catalyst in two steps: the first step consisting in sulphurization with tertiary mercaptan in the absence of hydrogen, and the second step, carried out consecutively in the same reactor, consisting of sulphurization with another sulphurizing agent in the presence of hydrogen. The catalysts thus sulphurized prove to be more active than those sulphurized by only the second step.

Abstract: In the photochemical synthetic process in semi-continuous mode according to the invention, a reactor comprising two zones is used, the radiating portion of the lamp(s) being totally immersed in a first zone which is completely filled with reaction medium and spills off via an overflow into a second zone whose volume is sufficient to contain the volume of reaction medium originating from the first zone and corresponding substantially to the volume of the reagent(s) gradually introduced.

Abstract: The invention concerns a method for sulphurizing catalysts for hydrotreating of hydrocarbon feedstocks. The invention is characterised in that it consists in sulphurizing the catalyst in two steps: the first step consisting in sulphurization with tertiary mercaptan in the absence of hydrogen, and the second step, carried out consecutively in the same reactor, consisting of sulphurization with another sulphurizing agent in the presence of hydrogen. The catalysts thus sulphurized prove to be more active than those sulphurized by only the second step.