A multi-stage process for transforming a high sulfur ISO 8217 compliant Feedstock Heavy Marine Fuel Oil involving a core desulfurizing process that produces a Product Heavy Marine Fuel Oil that can be used as a feedstock for subsequent refinery process such as anode grade coking, needle coking and fluid catalytic cracking. The Product Heavy Marine Fuel Oil exhibits multiple properties desirable as a feedstock for those processes including a sulfur level has a maximum sulfur content (ISO 14596 or ISO 8754) between the range of 0.05 mass % to 1.0 mass. A process plant for conducting the process is also disclosed.

A method of producing bimodal ethylene-based polymer includes reacting ethylene monomer and C.sub.3-C.sub.12 α-olefin comonomer in the presence of a first catalyst in an agitated reactor to produce a first polymer fraction, and outputting effluent from the agitated reactor. A second catalyst is added to the effluent downstream of the agitated reactor and upstream from a non-agitated reactor, the second catalyst facilitates production of a second polymer fraction having a density and melt index (I.sub.2) different from the first polymer fraction. The second catalyst and effluent are mixed in at least one mixer. The second catalyst, second polymer fraction, and the first polymer fraction are passed to the non-agitated reactor; and additional ethylene monomer, additional C.sub.3-C.sub.12 α-olefin comonomer, and solvent are passed to the non-agitated reactor to produce more second polymer fraction and thereby the bimodal ethylene-based polymer.

A reactor may have a catalyst bed for the catalytic treatment of a gas stream, with the catalyst bed extending substantially over a cross section of the reactor. Gas to be treated may axially fly through the catalyst bed. A carrier structure for the catalyst bed that is at least partly floatingly mounted in the reactor may include a sieve element and, radially outwardly, carrier elements fixedly joined to the reactor wall below the sieve element. The sieve element provides a resting surface for the catalyst bed. The sieve element terminates, radially outwardly, at a distance from the reactor wall. The carrier structure also includes support elements for the sieve element that are floatingly mounted in the reactor. An improved floating mounting is thus provided where not only the sieve element itself but also further parts of the carrier structure are mounted to prevent stresses due to thermal expansion.

A mixing device for mixing at least two particulate materials has a first riser used for loading first particles and a second riser surrounding and being coaxial with the riser and used for loading second particles. The upper part of the first riser extending beyond the top of the second riser. At least a part of the upper part of the first riser and at least a part of the upper part of the second riser being located inside a mixing zone container, such that the first and second particles are delivered to the inside of the mixing zone container by means of the first and second risers respectively and mixed.

Disclosed herein are methane conversion devices that achieve autothermal conditions and related methods using the methane conversion devices.

A process and system for maintaining optimum polymerization production in a loop polymerization reactor by continuously and periodically obtaining polymerization results, such as melt index (MI), production rate and ash content of the polymer produced, determining whether each of the results is within desired ranges, storing and averaging recently obtained results in a database within a reaction rate controller program, and when one of the results is out of the desired range modifying at least one reaction parameter set-point such as monomer concentration, catalyst feed rate and reactor temperature to drive any out-of-range polymerization result(s) toward the desired range for that result.

A device for mixing at least two granular materials has a first lifting tube used for loading first particles and a second lifting tube surrounding and coaxial to the first lifting tube and used for loading second particles. The upper part of said first lifting tube extends beyond the top of said second lifting tube, and at least part of the upper part of the first lifting tube and at least part of the upper part of the second lift tube are located inside a fast bed precipitator, allowing the first and second particles to be transported by means of the first and second lifting tubes to the interior of said fast bed precipitator and mixed.

Disclosed is an apparatus, system, and method, by which a plentiful supply of carbon dioxide may be provided to a fuel-conversion process operated in the deep sea far from shore thereby permitting a conversion of electrolysis-generated hydrogen gas into a carbonaceous liquid fuel. Because the cost and complexity of storing and transporting liquid fuels by ship is substantially simpler and less costly than is transporting gases, the present invention is expected to promote the extraction and distribution of energy harvested from the deep sea by permitting it to be accomplished with reasonable logistical complexity and at a reasonable and low cost.

The present specification relates to a method comprising: (A) mixing a ferrite-based catalyst molded article with diluent material particles; and (B) adding the mixture to a catalyst reactor, and a method for preparing butadiene using the same.

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.