Abstract: Process for the production of hydrogen and the co-production of carbon dioxide in separate streams comprising the following operations: feeding of a solid to a first reaction zone (R1) in which a liquid or gaseous hydrocarbon, preferably natural gas or methane, is also fed, which reacts with the solid fed at its maximum oxidation degree (over-oxidized form), leading to the formation of the combustion products carbon dioxide and water and the solid at its minimum oxidation degree (reduced form); feeding of the solid in reduced form to a second reaction zone (R2) into which water is also fed, which reacts with the reduced form of the solid, producing hydrogen, steam and the solid at an intermediate oxidation degree (oxidized form); feeding of the solid in oxidized form to a third reaction zone (R3) into which air is also fed, obtaining, from the further oxidation of the solid, heat and the solid in over-oxidized form to be recycled to the first reaction zone (R1), wherein the solid contains at least one element

Abstract: Partial oxidation process of liquid fuels, selected from hydrocarbon and/or oxygenated compounds, together with gaseous fuels, selected from hydrocarbon compounds, natural gas and LPG, by means of a suitable catalytic system comprising the following steps: premixing the reagents and possibly heating them to temperatures ranging from 25 to 400° C., said reagents consisting of said liquid fuels, said gaseous fuels and oxygen or air or oxygen enriched air, optionally in the presence of vapor and/or CO2; reacting the mixture of reagents in the catalytic zone, at inlet temperatures ranging from 50 to 500° C. and space velocities ranging from 1,000 to 1,000,000 Nl reagents/L cat×h, reaching temperatures ranging from 450 to 1350° C.

Abstract: A process is described for the upgrading of distillates having a boiling point ranging from 100 to 450° C., which comprises the opening of the ring of the naphthene compounds contained in these distillates to obtain paraffinic compounds, rich in branched paraffins, having for the most part the same number of carbon atoms as the starting naphthene. The process is carried out in the presence of a bifunctional catalytic system comprising one or more metals selected from Pt, Pd, Ir, Ru, Rh and Re, and a silico-aluminate of an acidic nature, selected from a micromesoporous silico-alumina and a zeolite belonging to the MTW group.

Abstract: Process for the removal/reduction of the hydrogen sulfide contained in natural gas which comprises: a) feeding natural gas and water to a reaction vessel maintained under thermodynamic conditions favourable for the formation of H2S hydrates and substantially at the production pressure of natural gas; b) discharging the H2S hydrates, from the bottom of the reaction vessel; c) optionally melting the hydrates and re-injecting water and/or gas comprising hydrogen sulfide and/or the hydrates as such into the same production field or into a geologically equivalent structure; and d) optionally feeding the remaining natural gas to a conventional softening process.

Abstract: The invention concerns a process for producing middle distillates from effluents obtained from the Fischer-Tropsch process, comprising separating a heavy cut with an initial boiling point of 120-200° C., hydrotreating said cut and fractionating the hydrotreated cut to obtain at least one intermediate fraction and at least one fraction that is heavier than the intermediate fraction. The intermediate fraction boils between T1 and T2, T1 being in the range 120-200° C. and T2 being in the range 300-410° C. The heavy and intermediate fractions are treated over a hydrocracking/hydroisomerisation catalyst and the effluents obtained are distilled. The invention also concerns a unit.

Abstract: Process for the preparation of polyalkenyl acylating agents which comprises: a. reacting at a temperature higher than 180° C. a reactive polyalkene, having a number average molecular weight Mn ranging from 500 to 5000 and having a content of terminal vinylidene groups greater than or equal to 30%, with an enophile; b. thermally carrying out the reaction for a time sufficient for having a conversion of the terminal vinylidene groups higher than 15%; c. completing the reaction always under heat in the presence of a reaction accelerator consisting of a Lewis acid selected from a tin, zinc, aluminum or titanium halide.

Abstract: A process for reducing the restart pressure of streams selected from waxy crude oils, water-in-crude emulsions and dispersions of hydrocarbon hydrates, at least partially structured. A mechanic disturbance is applied, in flow-stop conditions, on the streams, having: temperatures lower than the WAT (Wax Appearance Temperature) for the waxy crude oils and water-in-crude emulsions; temperatures lower than the forming temperatures of the hydrates and pressures higher than the forming pressure of the hydrates, for the dispersions of hydrocarbon hydrates.

Abstract: Process for the disposal of sulfur which comprises melting the sulfur, optionally in the presence of hydrogen sulfide, and injecting the molten sulfur into geological structures having a temperature ranging from 90 to 160° C.

Abstract: A method and apparatus for controlling a power supply. The system includes a power supply and a controller for outputting a command signal to regulate the operation of the power supply. The controller determines the command signal based on at least one error signal which is selected from a plurality of error signals based on a selection criterion.

Abstract: Equipment for the atomisation of a liquid stream by means of a dispersing gaseous stream and for mixing the atomised product with a further suitable gaseous stream, characterized in that it comprises: a feeding zone (A) equipped with means suitable for feeding the liquid stream, the gaseous dispersing stream and further gaseous stream; one or more two-stage atomisation zones (N) of the liquid stream by means of the gaseous dispersing stream; a distribution zone (D) of the further gaseous stream; the first stage of the atomisation zone (N1) essentially consisting of a tubular core (2), through which the liquid stream passes, equipped with an appropriate series of nozzles (5), situated at the same height, and an outer jacket (4) coaxial to said core, through which the gaseous dispersing stream passes, wherein said nozzles (5) allow the gaseous dispersing stream to enter the tubular core, perpendicularly to the axis of said tubular core (2), effecting a first atomisation of the liquid stream, the second stage of

Abstract: The present invention relates to a new zeolite having a beta-type crystalline structure, characterized by a distribution of the Lewis acid sites and Brønsted acid sites corresponding to a molar ratio [Lewis sites] [Brønsted sites] equal to or higher than 1.5. This new zeolite is useful in preparation processes of alkylated aromatic hydrocarbons through the alkylation and/or transalkylation of aromatic compounds. The preparation method of the new zeolite is also object of the present invention.

Abstract: Process for the production of hydrogen and the co-production of carbon dioxide in separate streams comprising the following operations: feeding of a solid to a first reaction zone (R1) in which a liquid or gaseous hydrocarbon, preferably natural gas or methane, is also fed, which reacts with the solid fed at its maximum oxidation degree (over-oxidized form), leading to the formation of the combustion products carbon dioxide and water and the solid at its minimum oxidation degree (reduced form); feeding of the solid in reduced form to a second reaction zone (R2) into which water is also fed, which reacts with the reduced form of the solid, producing hydrogen, steam and the solid at an intermediate oxidation degree (oxidized form); feeding of the solid in oxidized form to a third reaction zone (R3) into which air is also fed, obtaining, from the further oxidation of the solid, heat and the solid in over-oxidized form to be recycled to the first reaction zone (R1), wherein the solid contains at least en one elem

Abstract: A process is described for improving the quality as a fuel of hydrotreated hydrocarbon blends by reaction with hydrogen in the presence of a bifunctional catalytic system comprising one or more metals selected from Pt, Pd, Ir, Ru, Rh and Re, and a silico-aluminate of an acidic nature, selected from a micro-mesoporous silico-alumina and a zeolite belonging to the MTW family. The process of the invention produces an increase in the cetane index and a decrease in the density and T95.

Abstract: Process for selectively removing molybdenum from liquid mixtures containing it, in a quantity greater than (200) mg/l, together with vanadium characterized in that it comprises the following steps: bringing the liquid mixture to a pH of less than (3); adding a solution of an alkaline xanthate to the solution so that the molar ratio molybdenum/alkaline xanthate ranges from (¼) to (?), maintaining the pH constant by means of the addition of an inorganic acid; stirring the mixture causing the precipitation of the molybdenum present in the mixture.

Abstract: Hydrogen sulfide is oxidized to sulfur by means of treatment with an aqueous acid solution containing trivalent iron and a hetero polyacid having formula (I): HnXVyM(12-y)O40; or a sole hetero polyacid having formula (II): HnMeM12O40; wherein the symbols X, M Me n and y are specified in the text. At the end of the oxidation, the solution is treated with gas containing oxygen to re-oxidize the reduced metal.

Abstract: Process for the production of sulfur, obtained in pure form, and possibly easily disposable even at ambient tem-perature, starting from hydrogen sulphide contained in natural gas, which includes: a) oxidizing a portion of hydrogen sulphide to sulfur dioxide; b) dissolving in water the sulfur dioxide obtained in step (a); c) carrying out the reaction (I): 2H2S+SO2?3S+2H20 (I) making the remaining hydrogen sulphide to react with the solution prepared in step (b); and d) using the thus obtained sulfur suspension for the production sulfur or, alternatively, to use it for the disposal of the sulfur itself in a site reserved for such purpose.

Abstract: A process is described for synthesising hydrocarbons from a mixture comprising carbon monoxide and hydrogen and possibly carbon dioxide CO2, in the presence of a supported catalyst comprising at least one group VIII metal. The support comprises zirconia or a mixed zirconia-alumina oxide and the zirconia is present in the quadratic and/or amorphous form. Said catalyst is used in a liquid phase in a three-phase reactor.

Abstract: The present invention deals with a method which allows to determine the wall friction profile along pipes transporting liquids, particularly petroleum industry liquids, by measuring the pressure transients induced by fast changes in the flow rate. This method is applicable to pipes in which the discharge pressure is greater then the bubble point of the transported liquid and, in any case, when free gas is absent in the pipe.

Abstract: A highly selective process is described for preparing 2,6-dimethylnaphthalene which comprises reacting a naphthalene hydrocarbon selected from naphthalene, methylnaphthalenes, dimethylnaphthalenes, trimethylnaphthalenes, polymethylnaphthalenes, and/or their mixtures with one or more benzene hydrocarbons selected from benzene, toluene, xylenes, trimethylbenzenes, tetramethylbenzenes, pentamethylbenzene and/or hexamethylbenzene, under at least partially liquid phase conditions and in the presence of a catalytic composition comprising a zeolite belonging to the MTW structural type and at least one element selected from P, B and Si. The process is preferably carried out in the presence of a methylating agent.

Abstract: Integrated process for the conversion of feedstocks containing coal into liquid products by the joint use of at least the following seven process units: coal liquefaction (CL), flash or distillation of the product obtained from the liquefaction (F), extraction with a solvent to remove the ashes (SDAsh), distillation to separate the solvent (RS), hydroconversion with catalysts in slurry phase (HT), distillation or flash of the product obtained from the hydroconversion (D), deasphalting with a solvent (SDA).