The present invention is generally directed to a reactor for the production of low-carbon syngas from captured carbon dioxide and renewable hydrogen. The hydrogen is generated from water using an electrolyzer powered by renewable electricity or from any other method of low-carbon hydrogen production. The improved catalytic reactor is energy efficient and robust when operating at temperatures up to 1800° F. Carbon dioxide conversion efficiencies are greater than 75% with carbon monoxide selectivity of greater than 98%. The catalytic reactor is constructed of materials that are physically and chemically robust up to 1800° F. As a result, these materials are not reactive with the mixture of hydrogen and carbon dioxide or the carbon monoxide and steam products. The reactor materials do not have catalytic activity or modify the physical and chemical composition of the conversion catalyst. Electrical resistive heating elements are integrated into the catalytic bed of the reactor so that the internal temperature decreases by no more than 100° F. from the entrance at any point within the reactor. The catalytic process exhibits a reduction in performance of less than 0.5% per 1000 operational hours.

A process and device for reducing the environmental contaminants in a ISO 8217 compliant Feedstock Heavy Marine Fuel Oil, the process involving: mixing a quantity of the Feedstock Heavy Marine Fuel Oil with a quantity of Activating Gas mixture to give a feedstock mixture; contacting the feedstock mixture with one or more catalysts to form a Process Mixture from the feedstock mixture; separating the Product Heavy Marine Fuel Oil liquid components of the Process Mixture from the gaseous components and by-product hydrocarbon components of the Process Mixture and, discharging the Product Heavy Marine Fuel Oil. The Product Heavy Marine Fuel Oil is compliant with ISO 821 7 for residual marine fuel oils and has a sulfur level has a maximum sulfur content (ISO 14596 or ISO 8754) between the range of 0.05% wt. to 0.5% wt. The Product Heavy Marine Fuel Oil can be used as or as a blending stock for an ISO 8217 compliant, IMO MARPOL Annex VI (revised) compliant low sulfur or ultralow sulfur heavy marine fuel oil.

A fluidized catalytic reactor utilizes an ascending temperature profile. The apparatus and process deliver cooler spent catalyst to a first catalyst distributor and a hotter regenerated catalyst to a second catalyst distributor that are spaced apart from each other. The reactant stream first encounters the first stream of catalyst and then encounters the second stream of catalyst. The process and apparatus stage the addition of hot catalyst to the reactant stream. The process and apparatus may be particularly advantageous in an endothermic reaction because the hotter catalyst will encounter reactants that have cooled due to the progression of endothermic reactions.

A method for analyzing a catalyst in a catalytic reactor that operates under non-isothermal conditions includes the steps of: positioning a catalyst basket within a catalyst bed within the catalytic reactor, the catalyst basket containing catalyst material the forms the catalyst bed; operating the catalytic reactor, the catalyst basket having dimensions such that a temperature difference (ΔT) along an axial direction (height) of the catalyst basket is non-isothermal; and analyzing the catalyst material contained within the catalyst basket. The temperature difference (ΔT) is, in one embodiment, within a range of 1° C. to 40° C. and preferably, within a range of 5° C. to 25° C.

A graphene manufacturing device using Joule heating includes: a chamber having a space provided therein so as to synthesize graphene; and a first roller portion and a second roller portion disposed inside the chamber to be spaced from each other such that same support a catalyst metal penetrating the interior of the chamber and are supplied with an electric current for graphene synthesis, thereby Joule-heating the catalyst metal. In order to compensate for a temperature deviation of the catalyst metal passing between the first roller portion and the second roller portion, a first area of the catalyst metal, which is close to the first roller portion, and a second area of the catalyst metal, which is close to the second roller portion, are disposed to have movement paths facing each other.

The machinery and methods disclosed herein are based on the use of a specialized extruder configured to continuously convey and plasticize/moltenize selected lignocellulosic biomass and/or waste plastic materials into a novel variable volume tubular reactor, wherein the plasticized/moltenized material undergoes reaction with circumferentially injected supercritical water—thereby yielding valuable simple sugar solutions and/or liquid hydrocarbon mixtures (e.g., “neodiesel”), both of which are key chemical commodity products. The reaction time may be adjusted by changing the reactor volume. The machinery includes four zones: (1) a feedstock conveyance and plasticization/moltenization zone; (2) a steam generation and manifold distribution zone; (3) a central supercritical water reaction zone; and (4) a pressure let-down and reaction product separation zone. The machinery and methods minimize water usage—thereby enabling the economic utilization of abundant biomass and waste plastics as viable renewable feedstocks for subsequent conversion into alternative liquid transportation fuels and valuable green-chemical products.

The present invention relates to a device for efficiently preparing magnesium hydroxide, comprising a material mixing tank, a coordinated pressure control unit I, a reactor, a coordinated pressure control unit II, a condenser, a three-way valve, a material storage tank, a coordinated pressure control unit III and a steam generator. A outlet of the material mixing tank is connected with one end of the coordinated pressure control unit I by a pump; the other end of the coordinated pressure control unit I is connected with an inlet of the reactor; the outlet of the reactor is connected with one end of the coordinated pressure control unit II; the other end of the coordinated pressure control unit II is connected with one end of the condenser; the other end of the condenser is connected with a first port of the three-way valve; a second port of the three-way valve is connected with a material inlet of the material mixing tank; a third port of the three-way valve is connected with the material storage tank; a steam inlet of the reactor is connected with one end of the coordinated pressure control unit III; and the other end of the coordinated pressure control unit III is connected with the steam generator.

Methods of preparing dispersions of carbon-based materials are disclosed herein. In some embodiments, a method comprises exposing the carbon-based material to an atmosphere comprising between about 0.5% v/v and about 5.0% v/v of oxygen for a selected time at an oxidation temperature to obtain a thermally oxidized material; and dispersing the thermally oxidized material in a liquid medium.

Reactor for catalytic chemical reactions comprising a catalyst bed with an annular-cylindrical form crossed by a radial flow or mixed axial-radial flow, wherein the bed is delimited by cylindrical walls made gas-permeable by means of slits and the catalyst bed is formed by particles of catalyst with a nominal minimum size such that: the ratio between a transverse dimension of the slits and the nominal minimum size of the particles of catalyst is smaller than or equal to 0.6; the catalyst bed contains no more than 3% by weight of particles with an actual size smaller than said nominal size.

A device D accommodated in a reactor R and containing a gas- and/or liquid-permeable bottom B, in the peripheral region of which is arranged a lateral boundary W which completely surrounds the bottom B and forms a volume V which is partially or completely filled with catalytic and/or non-catalytic moldings, there optionally being located on the side facing the bottom B in the upstream direction at least one noble metal and/or non-noble metal fabric, wherein a thermal insulation layer S is located on at least part of the surface of the inner side of the lateral boundary W of the device D, the material for the thermal insulation layer S being selected from the group consisting of ceramic material, microporous material and silicate fibers.