Proposed is a carbon dioxide reforming (CDR) reactor having a multilayered catalyst layer arrangement for preventing catalyst deactivation, wherein, in the reactor in which a CDR reaction for reacting methane (CH.sub.4) with carbon dioxide (CO.sub.2) to reform the methane into a synthesis gas including carbon monoxide (CO) and hydrogen (H.sub.2) is performed, in order to prevent a case where an endothermic reaction between a catalyst and heated reactant gas supplied to the reactor gradually causes the temperature of the reactant gas to decrease and the catalyst is deactivated by cokes generated due to the decrease in temperature of the reactant gas, CDR catalysts in the reactor are arranged in multiple layers in a multilayered structure to allow the reactant gas temperature that has decreased due to the endothermic reaction to be restored in spaces between the catalyst layers.

Apparatuses for gasifying glycerol using solar energy, system including the apparatuses, and methods of using the apparatuses are provided. The apparatuses may include a concentrated solar dish comprising an opening and a gasifying reactor comprising a chamber. An entrance of the chamber may be aligned to the opening. The apparatuses may also include a thermal insulator disposed on outer surfaces of the concentrated solar dish and the gasifying reactor and a pipe in the thermal insulator. The pipe may be configured to deliver glycerol into the chamber of the gasifying reactor in the form of atomized mist. The glycerol may be delivered to a portion of the chamber adjacent the opening.

A reactor system, which is active in pyrolyzing methane at effective conditions, comprising a molten salt medium and a reaction vessel, the molten salt being contained within the reaction vessel using various methods of catalyst distribution within the vessel such that when methane passes through the vessel, it comes into contact with said catalyst causing a pyrolysis reaction thereby producing molecular hydrogen with reduced carbon dioxide emissions. The catalyst may be placed within the reaction vessel either as suspended particles or in a structured packed form.

Provided is a catalyst structure for a liquid organic hydrogen carrier (LOHC) dehydrogenation reactor, including a support, a plurality of channels formed on the support in such a manner that the LOHC may flow therethrough, and an LOHC dehydrogenation catalyst that is coated on the inner surfaces of the channels and is in contact with the LOHC to carry out LOHC dehydrogenation, wherein the hydrogen gas generated from the dehydrogenation is discharged along the channels so that the contact area between the LOHC and the LOHC dehydrogenation catalyst may be increased.

Carbon capture of carbon dioxide (CO.sub.2) gives an extracted CO.sub.2 stream that is reacted with hydrogen to produce methanol (MeOH), which can in turn be fed to catalytic production of olefins such as ethylene and propylene to give an integrated process.

Systems and methods are provided for conversion of methane and/or other hydrocarbons to hydrogen by pyrolysis while reducing or minimizing production of carbon oxides. The conversion of hydrocarbons to hydrogen is performed in one or more pyrolysis or conversion reactors that contain a plurality of sequential fluidized beds. The fluidized beds are arranged so that the coke particles forming the fluidized bed move in a counter-current direction relative to the gas phase flow of feed (e.g., methane) and/or product (H.sub.2) in the fluidized beds. By using a plurality of sequential fluidized beds, the heat transfer and management benefits of fluidized beds can be realized while also at least partially achieving the improved reaction rates that are associated with a plug flow or moving bed reactor.

The present disclosure provide for methods of reforming a hydrocarbon such as methane. In an aspect, when the method is driven via renewable energy (e.g., use of solar energy, wind energy, or other renewable energy) and coupled with zero-energy input product gas separation, this enables the capture of pure CO.sub.2 (i.e., carbon sequestration) and carbon-neutral utilization of methane can be achieved. As a result, the present disclosure can provide for a method to reform methane with zero-energy input product gas separation.

Moulded insulation bodies, processes for the production thereof and use thereof consisting essentially of ceramic material comprising SiO.sub.2 fibers and Al.sub.2O.sub.3 fibers which has been produced using Al.sub.2O.sub.3 sol as a binder and kilned at a temperature of above 800° C. for insulation of the ends of cracking tubes of a tubular reactor for performing a steam reforming process for generating synthesis gas which project out of the reactor heating space.

A method for producing elemental carbon and hydrogen gas directly from a hydrocarbon (for example, natural gas or methane) using a chemical reaction or series of reactions. In an aspect, other materials involved such as, for example, elemental magnesium, remain unchanged and function as a catalyst.

An integrated refinery process for the disposal of metal-containing spent coked catalyst from hydrotreating and/or hydrocracking unit operations includes introducing the spent coked catalyst into a membrane wall gasification reactor in the form of flowable particles along with predetermined amounts of oxygen and steam based upon an analysis of the hydrocarbon content of the coke, and optionally, a liquid hydrocarbon; gasifying the feed to produce synthesis gas and a slag material; recovering and subjecting the slag material to further processes in preparation for a leaching step to solubilize and form one or more active phase metal compounds that are recovered from the leaching solution, either separately by sequential processing, or together. The recovered active metal compounds can be used, e.g., in preparing fresh catalyst for use in the refinery's hydroprocessing units.