In accordance with the present invention, there is provided a process for producing hydrogen and graphitic carbon from a hydrocarbon gas comprising: contacting at a temperature between 600° C. and 1000° C. the catalyst with the hydrocarbon gas to catalytically convert at least a portion of the hydrocarbon gas to hydrogen and graphitic carbon, wherein the catalyst is a low grade iron oxide.

A circular carbon process involves: a) reacting hydrogen and carbon monoxide to produce methane and water, b) decomposing methane into carbon and hydrogen, and c) using carbon as reducing agent and/or using carbon in a carbon-containing material as reducing agent, in a chemical process to produce carbon monoxide and a reduced substance. The methane produced in a) is used in b), the carbon produced in b) is used in c), and carbon monoxide produced in c) is used in a).

An integrated reformer includes an outer chamber, a first inlet, a second inlet, and a cooling unit associated with the outer chamber. The first inlet is configured to obtain a first gas stream into a first space in the outer chamber. The second inlet is configured to obtain a second gas stream into the first space in the outer chamber. The cooling unit is configured to absorb thermal energy from the first gas stream.

Provided are a method for producing a fluoroethane, which is the desired product, with high selectivity; and a method for producing a fluoroolefin. The production method according to the present disclosure comprises obtaining a product comprising a fluoroethane represented by CX.sup.1X.sup.2FCX.sup.3X.sup.4X.sup.5 (wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 are the same or different and each represents a hydrogen atom, a fluorine atom, or a chlorine atom; and at least one of X.sup.1, X.sup.2, X.sup.3, X.sup.4, and X.sup.5 represents a hydrogen atom) from a fluoroethylene by a reaction in the presence of at least one catalyst in at least one reactor. The reaction is performed by introducing a starting material gas comprising the fluoroethylene into the reactor, and the water content in the starting material gas is 150 ppm by mass or less based on the total mass of the starting material gas.

Device and process for converting a feedstock of aromatic compounds, in which the feedstock is notably treated using a fractionation train (4-7), a xylenes separating unit (10) and an isomerization unit (11), and in which a pyrolysis unit (13) treats a second hydrocarbon-based feedstock, produces a pyrolysis effluent feeding the feedstock, and produces a pyrolysis gas comprising CO, CO2 and H2; a WGS water gas shift reaction section (50) suitable for treating the pyrolysis gas and for producing a WGS gas enriched in CO2 and in hydrogen; a CO2 aromatization reaction section (52) suitable for: at least partly treating the WGS gas to produce a hydrocarbon effluent comprising aromatic compounds, and feeding the feedstock with the hydrocarbon effluent.

A method can be employed to regulate and stably operate a steam reforming system that is operated by steam reforming, that has a capacity utilization level that can be regulated, and that comprises a steam reformer, a hydrogenating and desulfurizing unit that is positioned upstream of the steam reformer and is configured for feedstock desulfurization, and a firing unit of the steam reformer. According to the method, a mandated capacity utilization level for the steam reforming system is established with automated regulation of the following continuously monitored parameter ratios: a hydrogen-to-feedstock ratio in the hydrogenating and desulfurizing unit, a steam-to-carbon ratio in the steam reformer, and a fuel-to-air ratio in the firing unit of the steam reformer.

Described herein are two-stage catalytic heating systems and methods of operating thereof. A system comprises a first-stage catalytic reactor and a second-stage catalytic reactor, configured to operate in sequence and at different operating conditions, For example, the first-stage catalytic reactor is supplied with fuel and oxidant at fuel-rich conditions. The first-stage catalytic reactor generates syngas. The syngas is flown into the second-stage catalytic reactor together with some additional oxidant. The second-stage catalytic reactor operates at fuel-lean conditions and generates exhaust. Splitting the overall fuel oxidation process between the two catalytic reactors allows operating these reactors away from the stoichiometric fuel-oxidant ratio and avoiding excessive temperatures in these reactors. As a result, fewer pollutants are generated during the operation of two-stage catalytic heating systems. For example, the temperatures are maintained below 1.000° C. at all oxidation stages.

A microwave-plasma system for generating fixed-nitrogen products comprises a microwave generator operably coupled with a gas chamber where the microwave generator provides microwave power to the gas chamber. The system further includes a source of gas, which may be for example oxygen, nitrogen and/or air, operably coupled with the plasma chamber. The microwave power produces a plasma of the gas within the chamber. The system further includes an absorber unit fluidically connected to the gas chamber to capture product from the plasma in the gas chamber. The captured product may include fixed nitrogen gaseous products.

Processes herein may be used to thermally crack various hydrocarbon feeds, and may eliminate the refinery altogether while making the crude to chemicals process very flexible in terms of crude. In embodiments herein, crude is progressively separated into at least light and heavy fractions. Depending on the quality of the light and heavy fractions, these are routed to one of three upgrading operations, including a fixed bed hydroconversion unit, a fluidized catalytic conversion unit, or a residue hydrocracking unit that may utilize an ebullated bed reactor. Products from the upgrading operations may be used as feed to a steam cracker.

A method for revamping an ammonia-urea plant wherein: the ammonia section is modernized to produce an extra amount of low pressure steam; condensation stage of the high-pressure urea synthesis loop is modified to use part of the condensation heat of the urea stripper vapours to produce medium-pressure steam, said medium-pressure steam is fed to one or more steam users of the urea section, particularly for carbamate decomposition, the input of low-pressure steam to the urea section is balanced by importing the extra low-pressure steam produced in the ammonia section.