A plant comprises a feed gas source, H2S removal unit, first absorber and a second, pressure reduction stages, first and second heat exchangers, stripping unit, and a conduit. The H2S removal unit selectively removes H2S from a feed gas from the feed gas source to produce an H2S depleted feed gas. The first absorber and the second absorber remove CO2 from the H2S depleted feed gas using a semi-lean and an ultralean solvent to produce a product gas and a rich solvent. The plurality of pressure reduction stages generates a cooled flashed solvent. The first heat exchanger and the second heat exchanger use the cooled flashed solvent to cool the H2S depleted feed gas and the semi-lean solvent. The stripping unit strips the flashed solvent with dried air to produce the ultralean solvent, and the conduit combines a portion of the ultralean solvent with the H2S depleted feed gas.

A process for cleaning and beneficiating biomass is described which may allow removal of entrained salts and light volatiles from biomass materials. The process may also minimize energy use through capturing steam and flue gases for re-use. The process may generally comprise the following steps: prewashing and/or preheating a biomass, pressurizing the biomass in a steam explosion vessel, rapidly depressurizing the steam explosion vessel, releasing the steam from the steam explosion vessel entrained with fine lignin-enriched particles into a cyclone-type gas expansion vessel, routing the steam from the gas expansion vessel to the input hopper, subjecting the biomass to a second washing step, mechanically removing a portion of the water from the biomass, and evaporatively heating the biomass.

A process for cleaning and beneficiating biomass is described which may allow removal of entrained salts and light volatiles from biomass materials. The process may also minimize energy use through capturing steam and flue gases for re-use. The process may generally comprise the following steps: prewashing and/or preheating a biomass, pressurizing the biomass in a steam explosion vessel, rapidly depressurizing the steam explosion vessel, releasing the steam from the steam explosion vessel entrained with fine lignin-enriched particles into a cyclone-type gas expansion vessel, routing the steam from the gas expansion vessel to the input hopper, subjecting the biomass to a second washing step, mechanically removing a portion of the water from the biomass. After the biomass has been steam-exploded, it may be washed and used as an engineered soil.

Provided are a reusable polymeric material for removing siloxane compounds in biogas, a method for removing siloxane using the same, and an apparatus therefor, and more particularly, a polyacrylate-based polymer absorbent for removing siloxane compounds in biogas and a method for removing siloxane compounds in biogas. The method for removing siloxane compounds in biogas includes (a) providing the biogas, and b) absorbing the siloxane compounds in a polymer absorbent by passing the biogas through the polymer absorbent according to any one of claims 1 to 5.

A system for recovering natural gas liquid from a gas source, comprising compression means (206) for increasing the temperature and pressure of the fluid from the gas source, cooling means (230) for cooling the fluid from the compression means, a gas/gas heat exchanger (204), fluid from the gas source flowing from a first inlet to a first outlet; at least one separator (208) for receiving the fluid from the first outlet of the gas/gas heat exchanger (204) and separating liquid from the gas, the gas from the separator being directed to expansion means (206) for reducing the temperature and pressure of the gas, the aqueous part of the liquid from the separator and/or the gas from the expansion means being directed to the gas/gas heat exchanger (204) where it flows therethrough from a second inlet to a second outlet for cooling the fluid flowing between the first inlet and first outlet, wherein injection means are provided between the cooling means and the gas/gas heat exchanger for saturating the gas with a liquid agent, wherein the liquid agent comprises an evaporant and an antifreeze agent; and a recovery vessel (240) is provided downstream of the second outlet, the antifreeze agent being recovered therein for injection into the fluid from the gas source upstream of the first inlet.

A method for removing heavy hydrocarbons from a feed gas by: feeding, into an absorber, a top reflux stream and a second reflux stream below the top reflux stream, wherein the absorber produces an absorber bottom product stream and an absorber overhead product stream; depressurizing and feeding the absorber bottom product stream to a stripper to produce a stripper bottom product stream and a stripper overhead product stream; cooling and feeding a portion of the absorber overhead product stream back to the absorber as the top reflux stream; and pressurizing and feeding the stripper overhead stream back to the absorber as the second reflux stream. A system for carrying out the method is also provided.

Implementations described and claimed herein provide systems and methods for processing liquefied natural gas (LNG). In one implementation, a solvent is injected into a feed of natural gas at a solvent injection point. A mixed feed is produced from a dispersal of the solvent into the feed of natural gas. The mixed feed contains heavy components. A chilled feed is produced by chilling the mixed feed. The chilled feed includes a vapor and a condensed liquid. The condensed liquid contains a fouling portion of the heavy components condensed by the solvent during chilling. The liquid containing the fouling portion of the heavy components is separated from the vapor. The vapor is directed into a feed chiller heat exchanger following separation of the liquid containing the fouling portion of the heavy components from the vapor, such that the vapor being directed into feed chiller heat exchanger is free of freezing components.

A process for the separation of a natural gas stream is provided. The process includes receiving an effluent gas flow from a first fractionator operating at a first pressure, splitting the effluent gas flow into a first stream and a second stream, and passing the first stream through a heat exchanger thereby causing a phase change of at least a portion of the first stream from a gaseous state to a liquid state. The process includes inserting the first stream into an upper portion of a second fractionator operating at a second pressure. The second pressure is lower than the first pressure. The process includes inserting the second stream into a lower portion of the second fractionator, and diverting liquids from a lower portion of the second fractionator to the first fractionator.

Systems and methods that utilize feed gases that are supplied in a wide range of compositions and pressure to provide highly efficient recovery of NGL products, such as propane, utilizing isenthalpic expansion, propane refrigeration, and shell and tube exchangers are described. Plants utilizing such systems and methods can be readily reconfigured between propane recovery and ethane recovery.

During hydrothermal carbonization, biomass is converted to biocoal. The reaction yield depends on the reaction conditions, including duration of the carbonization reaction or time period within which the slurry composed of water and biomass remains in the reaction tank and is exposed to pressure and temperature. These conditions should be selected so that the greatest possible dry residue of carbonized material remains in the slurry. It has been shown that the dry residue amount changes during the carbonization reaction with a curve that is similar, to a great extent, to that of the slurry pH value. Because determining the dry residue is difficult during the ongoing reaction, but determining the pH value can be easy during the entire reaction period, the reaction is terminated at a maximum of the pH value corresponding to a maximum of the biocoal dry residue, to the greatest possible extent.