A method and a system for converting ethane to ethylene are provided. An exemplary method includes providing a feed stream including the ethane and oxygen to an oxidative dehydrogenation reactor and converting at least a portion of the ethane to ethylene in the oxidative dehydrogenation reactor to provide a reactor effluent stream including ethane, ethylene, and oxygen, acetylene, or both. The method includes cooling the reactor effluent stream to form a cooled effluent stream and providing the cooled effluent stream to an oxygen removal reactor including an ODH catalyst bed. A deoxygenation stream including water and an alcohol is provided to the oxygen removal reactor to form a deoxygenated effluent.

The present invention describes a process for the simultaneous removal of arsenic and sulphur compounds from hydrocarbon streams of fossil origin, wherein hydrocarbon streams of fossil origin resulting from the retorting process of schist are purified by direct contact with hydrated iron oxide, such as goethite (-FeOOH) in its raw natural form (limonite ore particles).

A method of removing oxygenates from a hydrocarbon stream comprises passing a hydrocarbon stream to a caustic tower having a plurality of loops, contacting the hydrocarbon stream with a sulfided catalyst between a first loop of the plurality of loops and a second loop of the plurality of loops to produce a reaction product, passing the reaction product to the second loop, removing at least a portion of the hydrogen sulfide in the second loop of the caustic tower to produce a product stream, and separating the product stream into a plurality of hydrocarbon streams in a separation zone located downstream of the caustic tower. The hydrocarbon stream comprises hydrocarbons, oxygen containing components, and sulfur containing compounds. At least a portion of the sulfur compounds react in the presence of the sulfided catalyst to produce hydrogen sulfide in the reaction product.

Disclosed are methods and systems for removing a highly reactive polymer precursor such as acetaldehyde and acetone from a hydrocarbon gas stream. Embodiments may disclose a method for removal of carbonyls comprising providing a hydrocarbon gas stream comprising a carbonyl, providing a liquid bisulfite stream, and contacting the hydrocarbon gas stream and liquid bisulfite stream in a mass transfer device wherein at least a portion of the carbonyl reacts with the bisulfite to form a solid adduct that is soluble in the liquid bisulfite stream.

Disclosed are methods and systems for removing a highly reactive polymer precursor such as acetaldehyde and acetone from a hydrocarbon gas stream. Embodiments may disclose a method for removal of carbonyls comprising providing a hydrocarbon gas stream comprising a carbonyl, providing a liquid bisulfite stream, and contacting the hydrocarbon gas stream and liquid bisulfite stream in a mass transfer device wherein at least a portion of the carbonyl reacts with the bisulfite to form a solid adduct that is soluble in the liquid bisulfite stream.

Disclosed are methods and systems for removing a highly reactive polymer precursor such as acetaldehyde and acetone from a hydrocarbon gas stream. Embodiments may disclose a method for removal of carbonyls comprising providing a hydrocarbon gas stream comprising a carbonyl, providing a liquid bisulfite stream, and contacting the hydrocarbon gas stream and liquid bisulfite stream in a mass transfer device wherein at least a portion of the carbonyl reacts with the bisulfite to form a solid adduct that is soluble in the liquid bisulfite stream.

Hydroprocessing facilities may operate for extended periods of time before detection of mercury in the inlet facilities, as mercury adsorbs onto the metallic pipelines used to transport the hydrocarbon fluids, e.g., gas, produced waters, from the wells to processing facilities (flowlines). Once the pipelines become saturated with mercury, mercury will breakthrough and be detected at the inlet facilities. A mercury management/control scheme is disclosed wherein a chemical treatment step using aqueous sulfidic solution is integrated into a progressive pigging plan to clean the pipeline, managing mercury accumulation in the pipeline for a reduced mercury concentration in the fluid exiting the flowlines.

A composition useful in oxidative desulphurization of gaseous hydrocarbons is described. It comprises a CuZnAlO mixed oxide, and an H form of a zeolite. The mixed oxide can contain one or more metal oxide promoters. The H form of the zeolite can be desilicated, and can also contain one or more transition metals.

Disclosed is method for removing carbonyl sulphide and/or carbon disulphide from a sour gas stream. The method comprises subjecting the gas stream to simultaneous contact with an absorption liquid, such as an aqueous amine solution, and with a catalyst suitable for hydrolyzing carbonyl sulphide and/or carbon disulphide. To this end, the invention also provides a reactor system wherein both an absorption liquid and a catalyst are present. In a preferred embodiment, the catalyst is a heterogeneous catalyst present on or in an absorption column, either coated on the trays of a column with trays, or contained in the packing of a packed column.

The invention relates to a method for producing hydrocarbon products which comprises preparing a hydrocarbon stream (C4) which predominantly comprises branched and unbranched hydrocarbons each having four carbon atoms. A first and a second partial stream (i-C4, n-C4) are obtained from this stream (C4), the first partial stream (i-C4) predominantly comprising branched hydrocarbons with four carbon atoms and the second partial stream (n-C4) predominantly comprising unbranched hydrocarbons with four carbon atoms. The method further comprises the steam cracking of at least part of the first partial stream (i-C4) at a first, higher cracking severity and at least part of the second partial stream (n-C4), at a second, lower, cracking severity.