Abstract: The present invention relates to a process for the rapid synthesis of an AFX-structure zeolite comprising at least: i) mixing, in an aqueous medium, a FAU-structure zeolite having an SiO2 (FAU)/Al2O3 (FAU) molar ratio of between 2.00 and 100, a nitrogen-containing organic compound R, at least one source of at least one alkali and/or alkaline-earth metal M of valence n, with the following molar composition: (SiO2 (FAU))/(Al2O3 (FAU)) between 2.00 and 100, H2O/(SiO2 (FAU)) between 1 and 100, R/(SiO2 (FAU)) between 0.01 and 0.6, M2/nO/(SiO2(FAU)) between 0.005 and 0.45, wherein SiO2 (FAU) denotes the amount of SiO2 provided by the FAU zeolite and Al2O3 (FAU) denotes the amount of Al2O3 provided by the FAU zeolite, until a homogeneous precursor gel is obtained; ii) hydrothermally treating said precursor gel obtained at the end of step i) under autogenous pressure at a temperature of between 120° C. and 250° C., for 4 to 12 hours.

Abstract: The invention relates to a catalyst comprising a mixture of AFX-structure and BEA-structure zeolites and at least one additional transition metal, to the process for preparing same and to the use thereof for the selective catalytic reduction of NOx in the presence of a reducing agent such as NH3 or H2.

Abstract: The invention relates to a process for preparing an AFX-structure zeolite comprising at least the following steps: i) mixing, in an aqueous medium, an FAU-structure zeolite having an SiO2 (FAU)/Al2O3 (FAU) molar ratio of between 2.00 (limit included) and 6.00 (limit excluded), an organic nitrogenous compound R, at least one source of at least one alkali and/or alkaline-earth metal M, the reaction mixture having the following molar composition: (SiO2 (FAU))/(Al2O3 (FAU)) between 2.00 (limit included) and 6.00 (limit excluded), H2O/(SiO2 (FAU)) between 1 and 100, R/(SiO2 (FAU)) between 0.01 and 0.6, M2/nO/(SiO2 (FAU)) between 0.005 and 0.7, limits included, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel obtained on conclusion of step i) at a temperature of between 120° C. and 220° C., for a time of between 12 hours and 15 days.

Abstract: The invention relates to a process for preparing a catalyst based on an AFX zeolite exchanged with at least one transition metal, comprising at least the following steps: i) mixing, in an aqueous medium, of at least one source of silicon (Si) in SiO2 oxide form, at least one source of aluminum (Al) in Al2O3 oxide form, 1,6-bis(methylpiperidinium)hexane dihydroxide, and at least one source of at least one alkali metal, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment at a temperature between 75° C. and 95° C., limits included; iii) at least one ion exchange with a solution comprising at least one species capable of releasing a transition metal, iv) heat treatment by drying followed by at least one calcination under a stream of air at a temperature between 400 and 700° C. The invention also relates to the catalyst obtained and to the use thereof for the selective reduction of NOx.

Abstract: The invention relates to a process for synthesizing a high-purity AFX zeolite, comprising at least the following steps: i) mixing, in an aqueous medium, of at least one source of silicon (Si) in SiO2 oxide form, at least one source of aluminum (Al) in Al2O3 oxide form, a nitrogenous organic compound of 1,6-bis(methylpiperidinium)hexane dihydroxide type, and at least one source of at least one alkali metal chosen from lithium, potassium or sodium, and the mixture of at least two of these metals, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel obtained at the end of step i) at a temperature of between 75° C. and 95° C., limits included, for a period of between 40 and 100 hours, limits included, to obtain a solid AFX-structure crystalline phase, termed “AFX zeolite”. The invention also relates to the high-purity AFX zeolite obtained.

Abstract: The present invention relates to a process for the rapid synthesis of an AFX-structure zeolite comprising at least: i) mixing, in an aqueous medium, a FAU-structure zeolite having an SiO2 (FAU)/Al2O3 (FAU) molar ratio of between 2.00 and 100, a nitrogen-containing organic compound R, at least one source of at least one alkali and/or alkaline-earth metal M of valence n, with the following molar composition: (SiO2 (FAU))/(Al2O3 (FAU)) between 2.00 and 100, H2O/(SiO2 (FAU)) between 1 and 100, R/(SiO2 (FAU)) between 0.01 and 0.6, M2/nO/(SiO2(FAU)) between 0.005 and 0.45, wherein SiO2 (FAU) denotes the amount of SiO2 provided by the FAU zeolite and Al2O3(FAU) denotes the amount of Al2O3 provided by the FAU zeolite, until a homogeneous precursor gel is obtained; ii) hydrothermally treating said precursor gel obtained at the end of step i) under autogenous pressure at a temperature of between 120° C. and 250° C., for 4 to 12 hours.

Abstract: The invention concerns a process for preparing a copper-comprising SAPO material with AFX structure, comprising at least the steps of mixing, in an aqueous medium, at least one aluminum source, at least one silicon source, at least one copper source, at least one phosphorus source, a TETA complexing agent and a TMHD structuring agent, in order to obtain a gel, and hydrothermal treatment of said gel with a shear rate of less than 50 s?1 in order to obtain crystallization of said copper-comprising SAPO material with AFX structure.

Abstract: The invention relates to a process for preparing an AFX-structure zeolite comprising at least the following steps: i) mixing, in an aqueous medium, an FAU-structure zeolite having an SiO2 (FAU)/Al2O3 (FAU) molar ratio of between 2.00 (limit included) and 6.00 (limit excluded), an organic nitrogenous compound R, at least one source of at least one alkali and/or alkaline-earth metal M, the reaction mixture having the following molar composition: (SiO2 (FAU))/(Al2O3 (FAU)) between 2.00 (limit included) and 6.00 (limit excluded), H2O/(SiO2 (FAU)) between 1 and 100, R/(SiO2 (FAU)) between 0.01 and 0.6, M2/nO/(SiO2 (FAU)) between 0.005 and 0.7, limits included, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel obtained on conclusion of step i) at a temperature of between 120° C. and 220° C., for a time of between 12 hours and 15 days.

Abstract: The invention relates to a catalyst comprising a mixture of AFX-structure and BEA-structure zeolites and at least one additional transition metal, to the process for preparing same and to the use thereof for the selective catalytic reduction of NOx in the presence of a reducing agent such as NH3 or H2.

Abstract: The invention concerns a process for preparing a copper-comprising microporous aluminosilicate material with AFX structure, comprising at least the steps of mixing, in an aqueous medium, at least one aluminum source, at least one silicon source, at least one copper source, a TETA or TEPA organic complexing agent and a DABCO-C4 structuring agent, in order to obtain a gel, and hydrothermal treatment of said gel with stirring in order to obtain crystallization of said copper-comprising microporous aluminosilicate material with AFX structure.

Abstract: The invention concerns a process for preparing a copper-comprising microporous aluminosilicate material with AFX structure, comprising at least the steps of mixing, in an aqueous medium, at least one aluminum source, at least one silicon source, at least one copper source, a TETA or TEPA organic complexing agent and a DABCO-C4 structuring agent, in order to obtain a gel, and hydrothermal treatment of said gel with stirring in order to obtain crystallization of said copper-comprising microporous aluminosilicate material with AFX structure.

Abstract: The invention concerns a process for preparing a copper-comprising SAPO material with AFX structure, comprising at least the steps of mixing, in an aqueous medium, at least one aluminum source, at least one silicon source, at least one copper source, at least one phosphorus source, a TETA complexing agent and a TMHD structuring agent, in order to obtain a gel, and hydrothermal treatment of said gel with a shear rate of less than 50 s?1 in order to obtain crystallization of said copper-comprising SAPO material with AFX structure.

Abstract: An olefin oligomerization process employs a particular silica-alumina catalyst which comprises a non zeolitic support based on silica-alumina containing a quantity of more than 5% by weight and 95% by weight or less of silica (SiO2) and has the following characteristics: a mean pore diameter, measured by mercury porosimetry, in the range 20 to 140 ?; a total pore volume, measured by mercury porosimetry, in the range 0.1 ml/g to 0.6 ml/g; a total pore volume, measured by nitrogen porosimetry, in the range 0.1 ml/g to 0.6 ml/g; a BET specific surface area in the range 100 to 550 m2/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 140 ?, of less than 0.1 ml/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 160 ?, of less than 0.1 ml/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 200 ?, of less than 0.

Abstract: The invention relates to a method for formulation of a synthetic gas oil or an additive for gas oil in which an alkyl-aromatic compound or a mixture of alkyl-aromatic compounds is selected based on at least one parameter that is selected from the group that consists of the number of cycles of the aromatic core, the number of alkyl chains that are grafted to the aromatic cycle, the length of the alkyl chain or chains, the position of the aromatic cycle or cycles on the alkyl chain or chains of said alkyl-aromatic compound or compounds such that the cetane number of the synthetic gas oil or the additive for gas oil is greater than 30. The invention also relates to a process for the production of alkyl-aromatic compounds for use as a gas oil or additive.

Abstract: A process is described for transforming an initial hydrocarbon feed containing 4 to 15 carbon atoms, limits included, into a hydrocarbon fraction having an improved octane number and a hydrocarbon fraction with a high cetane number.

Abstract: A process is described for the valorization of a charge of hydrocarbons and for reducing the vapour pressure of said charge, comprising three steps: a step a) consisting of separating said charge of hydrocarbons into a fraction (O1) comprising essentially compounds containing 5 carbon atoms, including at least 2% by weight of pentenes, a step b) consisting of placing said fraction (O1) in contact with a cut of hydrocarbons (O2) at least partly comprising hydrocarbons having a number of carbon atoms between 6 and 10, including at least 2% by weight of olefins, and a step c) consisting of separating the effluents originating from step b) into a gasoline cut (?) the upper distillation point of which is less than 100° C. and a kerosene cut (?) having a distillation range between 100° C. and 300° C.

Abstract: A process is described in which an unsaturated fat is reacted with ethylene in a metathesis reaction in the presence of at least one non-aqueous ionic liquid to produce both an olefinic fraction and a composition of monoalcohol or polyol esters. Particular application to an oleic sunflower seed oil, an oleic rapeseed oil or to a mixture of monoalcohol esters of said oils, the process producing both an olefinic fraction and a monoalcohol or glycerol esters composition generally having more than half of its chains constituted by unsaturated C10 chains.

Abstract: An olefin oligomerization process employs a particular silica-alumina catalyst which comprises a non zeolitic support based on silica-alumina containing a quantity of more than 5% by weight and 95% by weight or less of silica (SiO2) and has the following characteristics: a mean pore diameter, measured by mercury porosimetry, in the range 20 to 140 ?; a total pore volume, measured by mercury porosimetry, in the range 0.1 ml/g to 0.6 ml/g; a total pore volume, measured by nitrogen porosimetry, in the range 0.1 ml/g to 0.6 ml/g; a BET specific surface area in the range 100 to 550 m2/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 140 ?, of less than 0.1 ml/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 160 ?, of less than 0.1 ml/g; a pore volume, measured by mercury porosimetry, included in pores with a diameter of more than 200 ?, of less than 0.

Abstract: The desulfurization of a hydrocarbon-containing fraction, e.g. kerosene or gas oil that comprises at least one stage of treatment of said fraction with an oxidizing agent in the presence of a catalyst of said oxidation, in which said catalyst comprises at least one oxide of chemical formula MxOy, whereby M is an element that is selected from the group that consists of the elements of groups IV-B, V-B or VI-B of the periodic table.

Abstract: A process is described for the valorization of a charge of hydrocarbons and for reducing the vapour pressure of said charge, comprising three steps: a step a) consisting of separating said charge of hydrocarbons into a fraction (O1) comprising essentially compounds containing 5 carbon atoms, including at least 2% by weight of pentenes, a step b) consisting of placing said fraction (O1) in contact with a cut of hydrocarbons (O2) at least partly comprising hydrocarbons having a number of carbon atoms between 6 and 10, including at least 2% by weight of olefins, and a step c) consisting of separating the effluents originating from step b) into a gasoline cut (?) the upper distillation point of which is less than 100° C. and a kerosene cut (?) having a distillation range between 100° C. and 300° C.