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.

In an aspect, the present disclosure provides a method for the oxidative coupling of methane to generate hydrocarbon compounds containing at least two carbon atoms (C.sub.2+ compounds). The method can include mixing a first gas stream comprising methane with a second gas stream comprising oxygen to form a third gas stream comprising methane and oxygen and performing an oxidative coupling of methane (OCM) reaction using the third gas stream to produce a product stream comprising one or more C.sub.2+ compounds.

A multi-stage process for reducing the environmental contaminants in a ISO8217 compliant Feedstock Heavy Marine Fuel Oil involving a core desulfurizing process and an Oxidative desulfurizing process as either a pre-treating step or post-treating step to the core process. The Product Heavy Marine Fuel Oil is compliant with ISO 8217A 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. A process plant for conducting the process is also disclosed.

A process for reducing the environmental contaminants in a ISO8217 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 8217A 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 0.50% 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 device for conducting the process is also disclosed.

A method for producing metal chloride Mx+Clx? includes reacting metal carbonate in solid form using phosgene, diphosgene and/or triphosgene to form metal chloride Mx+Clx?, wherein the metal M is selected from the group containing alkali metals, alkaline earth metals, Al and Zn, Li and Mg, or Li, for example, and x corresponds to the valency of the metal cations. An apparatus for performing such method is also disclosed.

A method and device for producing ammonia from a syngas in a heterogeneous gas catalysis process in at least two reaction devices connected in series. Each reaction device includes at least two catalyst beds through which the syngas is conducted and in which an at least partial conversion of the syngas into the product gas is carried out. At least one first heat exchanger is provided in the first reaction device, and the fresh syngas is pre-heated in the first heat exchanger. The syngas exiting the first catalyst bed and which includes the product and non-converted reactants is cooled before entering the second catalyst bed. According to an embodiment of the invention, the pre-heating process is carried out in a first heat exchanger arranged between the first and the second catalyst bed. Thus, synthesis conversion can be increased without substantially increasing the process gas quantity.

Systems and methods are provided for conversion of light paraffinic gases to form liquid products in a process performed in a fixed bed radial-flow reactor. The light paraffins can correspond to C.sub.3+ paraffins. Examples of liquid products that can be formed include C.sub.6-C.sub.12 aromatics, such as benzene, toluene, and xylene. The fixed bed radial-flow reactor can allow for improved control over the reaction conditions for paraffin conversion in spite of the fixed bed nature of the reactor. This can allow the process to operate with improved efficiency while reducing or minimizing the complexity of operation relative to non-fixed bed reactor systems.

Systems for reforming a hydrocarbon feedstock, where the system is operable to selectively reform different sub-components of the hydrocarbon feedstock using at least two structurally-distinct reforming catalysts. Advantages may include a decreased rate of reforming catalyst deactivation and an increased yield of a liquid hydrocarbon reformate product that is characterized by at least one of an increased octane rating and a decreased vapor pressure compared to the liquid hydrocarbon reformate product of conventional one-step reforming systems.

The present invention relates to the field of biological and chemical transformation as well as physical and chemical trapping. More specifically, the invention relates to a new reactor arrangement for performing, by means of at least one solid reaction member, biological or chemical transformation, or physical or chemical trapping from or release of agents to, a fluidic medium. The reactor arrangement is comprised of an auxiliary reactor having a transformation device and a main reactor. The invention also provides an auxiliary reactor adapted for being connected to a main reactor, a method of using such a reactor arrangement, as well as a process involving the reactor arrangement.

The present invention relates to a process for converting a feed comprising C2-C4 alkanes to higher hydrocarbon(s) including aromatic hydrocarbon(s) in n reaction zones operated in series, wherein m reaction zones are not participating in the conversion process and only (n-m) reaction zones are operated under reaction conditions sufficient to convert at least a portion of said a feed comprising C2-C4 alkanes to an effluent having said higher hydrocarbon(s). An object of the present invention is to provide a process for converting LPG to higher hydrocarbon(s) including aromatic hydrocarbon(s) wherein a high reactant, i.e. ethane, propane and/or butane, conversion can be achieved.