A system for the pyrolysis of a pyrolysis feedstock utilizes a pyrolysis reactor for producing pyrolysis products from the pyrolysis feedstock to be pyrolyzed. An eductor condenser unit in fluid communication with the pyrolysis reactor is used to condense pyrolysis gases. The eductor condenser unit has an eductor assembly having an eductor body that defines a first flow path with a venturi restriction disposed therein for receiving a pressurized coolant fluid and a second flow path for receiving pyrolysis gases from the pyrolysis reactor The second flow path intersects the first flow path so that the received pyrolysis gases are combined with the coolant fluid. The eductor body has a discharge to allow the combined coolant fluid and pyrolysis gases to be discharged together from the eductor. A mixing chamber in fluid communication with the discharge of the eductor to facilitates mixing of the combined coolant fluid and pyrolysis gases, wherein at least a portion of the pyrolysis gases are condensed within the mixing chamber.

Methods for producing ethylene using nanowires as heterogeneous catalysts are provided. The method includes, for example, an oxidative coupling of methane catalyzed by nanowires to provide ethylene.

A method (10) of synthesising Fischer-Tropsch products (20) includes feeding a synthesis gas (30) to a moving-bed Fischer-Tropsch synthesis reactor (16) containing a Fischer-Tropsch catalyst in a moving catalyst bed and catalytically converting at least a portion of the synthesis gas (30) in the moving catalyst bed to Fischer-Tropsch products (20). The Fischer-Tropsch products (20) are removed from the moving-bed Fischer-Tropsch synthesis reactor (16). The method (10) further includes, while the moving-bed Fisher-Tropsch synthesis reactor (16) is on-line, withdrawing a portion (50) of the Fischer-Tropsch catalyst from the moving-bed Fischer-Tropsch synthesis reactor (16), adding a reactivated Fischer-Tropsch catalyst (57, 58) to the moving-bed Fischer-Tropsch synthesis reactor (16), and adding a fresh Fischer-Tropsch catalyst (60,58), in addition to the reactivated catalyst (57,58), to the moving-bed Fischer-Tropsch synthesis reactor (16).

A system and method for converting (dry reforming) natural gas (methane) and carbon dioxide via reformer catalyst in a dry reformer into syngas including carbon monoxide and hydrogen, and discharging the syngas to a Fischer-Tropsch (FT) reactor. Supplemental hydrogen is generated via water electrolysis and added to the syngas in route to the FT reactor to increase the molar ratio of hydrogen to carbon monoxide in the syngas. The syngas may be converted via FT catalyst in the FT reactor into FT waxes.

In a broad form the present disclosure relates to a stabilized catalyst support comprising in oxide form; aluminum, zirconium, and one or more lanthanoid elements taken from the lanthanoid group of the periodic system characterized in that at least a part of the aluminum is present as transition alumina such as χ, κ, γ, δ, η, ρ and θ-alumina, characterized in the concentration of zirconium being at least 1.5 wt %, 5 wt % or 10 wt %, the concentration of lanthanoid being at least 0.5 wt %, 1.0 wt %, 2 wt % or 4 wt % and the combined concentration of zirconium and lanthanoid being at least 4 wt %, 7 wt % or 10 wt %, with the associated benefit of a support comprising transition alumina being a high surface area due to the small crystallites typical for transition alumina, and the benefit of the combined presence of oxides of zirconium and lanthanoid in the stated amounts being that at these levels these oxides stabilize the structure of the transition alumina.

Provided is a conversion process for an organic oil, relating to the field of biomass utilization, energy and chemical industry. The conversion process is carried out in presence of an aqueous slurry and a catalyst selected from the group consisting of an iron oxide compound, a waste agent resulting from use of an iron oxide compound as desulfurizer, and a regeneration product of the waste agent, under a controlled molar ratio of iron element to sulfur element. It is found that free radical condensation polymerization of organic oil during cracking process can be blocked effectively by using carbonylation, and hydrogenation is achieved with active hydrogen produced from the conversion of CO and water. In the conversion process, organic material, especially biomass solid, can be directly converted without dehydration, and water can be additionally added to the biomass liquid or the mineral oil.

Provided is a method for producing organic molecules having at least two carbon atoms chained together by the reaction of a hydrogen-containing source, a carbon-containing source and an optional nitrogen-containing source in the presence of a nanostructure or nanostructures, wherein the reaction is initiated by heat.

A process for preparing C.sub.2 to C.sub.3 hydrocarbons may include introducing a feed stream including hydrogen gas and a carbon-containing gas comprising carbon monoxide, carbon dioxide, and mixtures thereof into a reaction zone of a reactor, and converting the feed stream into a product stream comprising C.sub.2 to C.sub.3 hydrocarbons in the reaction zone in the presence of a hybrid catalyst. The hybrid catalyst may include a metal oxide catalyst component and a microporous catalyst component comprising 8-MR pore openings and may be derived from a natural mineral, the product stream comprises a combined C.sub.2 and C.sub.3 selectivity greater than 40 carbon mol%.

A modified catalyst support is described in the form of titan ia particles with a volume-median diameter in the range 100 to 1000 μm modified with one or more refractory oxides of metals selected from the group consisting of zirconium, lanthanum, cerium, yttrium and neodymium, wherein the total refractory oxide content of the modified catalyst support is in the range of 0.1 to 15% by weight, and the modified catalyst support has a pore volume in the range of 0.2 to 0.6 cm.sup.3/g and an average pore diameter in the range of 30 to 60 nm. The modified catalyst support may be used to prepare cobalt Fischer-Tropsch catalysts suitable for use in fixed bed processes.

Structures, catalysts, and reactors suitable for use for a variety of applications, including gas-to-liquid and coal-to-liquid processes and methods of forming the structures, catalysts, and reactors are disclosed. The catalyst material can be deposited onto an inner wall of a microtubular reactor and/or onto porous support structures using atomic layer deposition techniques.