The present invention integrates adsorption and liquefaction techniques to separate hydrocarbon feed mixtures into light and heavy components. A feed is partially liquefied in two or more stages. A first stage occurs at higher pressure. A second stage occurs at lower pressure. At each stage, gas and liquid components are separated. The separated heavy components resulting from liquefaction provide a purified natural gas liquid product. The separated gas components may be further processed and/or handled to provide purified natural gas. Heavy streams resulting from the further processing of the separated gas streams may be recycled and incorporated into the feed mixture. By using separate liquefaction stages at different pressures to favor C1 and then C2 separation from the heavy stream, a natural gas liquid product with high C3+ purity results.

The present invention provides strategies to integrate adsorption and liquefaction techniques to separate hydrocarbon feed mixtures into purified light and heavy components, respectively. Initially, the hydrocarbon stream is separated into a light and heavy stream. The light stream can be integrated into a natural gas product. The heavy stream is partially liquefied. A first gas liquid separation of the partially liquefied heavy stream at an elevated pressure separates the liquid heavy stream from a methane-containing gas. The rejected methane component, which generally will include some rejected C2 and C3+ material, can be recycled to be combined with the feed mixture for re-processing. A further aspect of the strategy is then to practice at least one additional gas-liquid separation of the separated liquid heavy stream at a lower pressure effective to help further resolve the liquid heavy stream from C2-containing gas. The rejected C2 component, which generally will include some rejected C1 and C3+ material, can then be recycled back into the feed mixture for reprocessing or used as all or a portion of a light hydrocarbon product.

The method includes the introduction of a feed flow into a first flask, the dynamic; expansion of the gaseous flow issuing from the flask in a turbine, then its introduction into a first purification column. It comprises the production at the head of the first column of a purified gas and the recovery at the bottom of the first column of a liquefied bottom gas, which is introduced, after expansion, into a second column for elimination of the C.sub.5.sup.+ hydrocarbons. The purified head natural gas issuing from the first column is heated in a first heat exchanger by thermal exchange with a feed gas. The method includes the compression of the gaseous head flow of the second column in a compressor before its introduction into a second separator flask.

A process is provided for removing contaminants from olefin containing C.sub.4 streams. The streams are contacted with an X based zeolite adsorbent comprising greater than 88% X zeolite at a SiO.sub.2/Al.sub.2O.sub.3 ratio of less than 2.5 and an alkali metal salt present in excess of an amount required to achieve full exchange of cation sites on the X based zeolite. The resulting alkali oxide on a volatile free basis is less than 1% (by mass) of the X based adsorbent. The contaminants that are removed include sulfur, oxygenate, and nitrogen based contaminants.

Provided are systems and methods for obtaining ethylene and propylene products from, for example, shale gas and shale gas condensate feedstocks. These systems and method operate by utilizing a hydrocracker train to crack C4 and C5 hydrocarbons to a product stream of propane and ethane or using a hydrogenolysis train to process C4 and C5 hydrocarbons to a product stream of propane and ethane that is provided to a cracker for an efficient conversion to ethylene and propylene. The disclosed systems are configured to reduce the amount of offsite hydrogen needed and also provide product streams that include a well-defined set of products as compared to existing approaches.

A process and system for recovering natural gas liquids (NGL) using a combination of J-T cooling and membrane separation. The process involves compressing, separating, and cooling a flare gas stream comprising at least methane and C.sub.3+ hydrocarbons prior to being introduced to a J-T valve. The cooled stream exiting the J-T valve is further separated, producing a NGL product stream and an uncondensed gas stream. The uncondensed gas stream is directed to a membrane separation step, which results in a C.sub.3+ hydrocarbon enriched stream and a C.sub.3+ hydrocarbon depleted stream. The C.sub.3+ hydrocarbon enriched stream may be recycled back to the process to recover more NGL.

Processes for converting methane and/or other hydrocarbons to synthesis gas (i.e., a gaseous mixture comprising H.sub.2 and CO) are disclosed, in which at least a portion of the hydrocarbon(s) is reacted with CO.sub.2. At least a second portion of the methane may be reacted with H.sub.2O (steam), thereby improving overall thermodynamics of the process, in terms of reducing endothermicity (H) and the required energy input, compared to pure dry reforming in which no H.sub.2O is present. Such dry reforming (reaction with CO.sub.2 only) or CO.sub.2-steam reforming (reaction with both CO.sub.2 and steam) processes are advantageously integrated with Fischer-Tropsch synthesis to yield liquid hydrocarbon fuels. Further integration may involve the use of a downstream finishing stage involving hydroisomerization to remove FT wax. Yet other integration options involve the use of combined CO.sub.2-steam reforming and FT synthesis stages (optionally with finishing) for producing liquid fuels from gas streams generated in a number of possible processes, including the hydropyrolysis of biomass.

Copper sulfide of the formula Cu.sub.xS.sub.y, wherein x and y are integer or non-integer values, wherein (i) the copper sulfide has a sulfur 2p XPS spectrum with peaks at 162.3 eV (1 ev), 163.8 eV (1 ev) and 68.5 eV (1 ev), characterised in that the peak at 168.5 eV has a lower value of counts per second (CPS) than both the peak at 162.3 eV and the peak at 163.8 eV; and (ii) the copper sulfide has a copper 2p XPS spectrum with peaks at 932.0 eV (2ev) and 933.6 eV (3eV) and characterised in that the XPS spectrum does not comprise identifiable satellite peaks at 939.8 eV and 943.1 eV (3 eV).

The invention includes a gas processing system for transforming a hydrocarbon-containing inflow gas into outflow gas products, where the system includes a gas delivery subsystem, a plasma reaction chamber, and a microwave subsystem, with the gas delivery subsystem in fluid communication with the plasma reaction chamber, so that the gas delivery subsystem directs the hydrocarbon-containing inflow gas into the plasma reaction chamber, and the microwave subsystem directs microwave energy into the plasma reaction chamber to energize the hydrocarbon-containing inflow gas, thereby forming a plasma in the plasma reaction chamber, which plasma effects the transformation of a hydrocarbon in the hydrocarbon-containing inflow gas into the outflow gas products, which comprise acetylene and hydrogen. The invention also includes methods for the use of the gas processing system.

The Fischer-Tropsch process can be used for the conversion of hydrocarbonaceous feed stocks into normally liquid and/or solid hydrocarbons (i.e. measured at 0 C., 1 bar). The feed stock (e.g. natural gas, associated gas, coal-bed methane, residual oil fractions, biomass and/or coal) is converted in a first step into a mixture of hydrogen and carbon monoxide. This mixture is often referred to as synthesis gas or syngas. The present invention relates to process for preparing a paraffin product from a carbonaceous feedstock and a system for preparing a paraffin product from a carbonaceous feedstock.