The process of the present invention provides high recovery and low capital cost giving it an economic advantage over previously known purification processes. The present process has particular applicability to the purification of synthesis gases comprising at least hydrogen (H.sub.2), carbon monoxide (CO), methane (CH.sub.4), CO.sub.2, and H.sub.2O to obtain a gas stream including at least H.sub.2, CO, and CH.sub.4, that is substantially free of H.sub.2O and CO.sub.2. The process also has applicability to the purification of natural gases inclusive of at least CH.sub.4, N.sub.2, CO.sub.2, and H.sub.2O to produce a gas stream including at least CH.sub.4 and N.sub.2, but which is substantially free of H.sub.2O and CO.sub.2.

Disclosed are a facility and a method using the facility for treating a feed gas stream comprising at least methane and carbon dioxide by membrane permeation, the facility comprising: —a first membrane separation unit capable of receiving the feed gas stream and providing a first permeate and a first retentate, —a second membrane separation unit capable of receiving the first retentate and providing a second permeate and a second retentate, —a compressor for compressing the first permeate to a pressure of between 17 bar and 25 bar, —a means for cooling the first compressed permeate to a temperature lower than −40° C., —a distillation column for separating the first cooled permeate into a gas stream and a liquid stream, —at least one means for recycling the gas stream exiting the distillation column to the inlet of the first membrane separation unit, —a means for measuring the concentration of methane and/or carbon dioxide in the gas stream exiting the distillation column, —a means for comparing the concentration of methane and/or carbon dioxide measured by the measurement means with a target value, and —a means for adjusting the pressure and/or the temperature of the first permeate depending on the comparison carried out by the comparison means.

This disclosure relates to CO.sub.2-philic crosslinked polyethylene glycol membranes useful for natural gas purification processes. Also provided are methods of using the membranes to remove CO.sub.2 and H.sub.2S from natural gas.

Methods of designing zeolite materials for adsorption of CO.sub.2. Zeolite materials and processes for CO.sub.2 adsorption using zeolite materials.

The present disclosure is directed to a potassium-form MER framework type zeolite, a MER framework type zeolite having a stick-like morphology, wherein the potassium is present as K.sup.+ in extra-framework locations. The zeolite is essentially free of an extra-framework cation other than potassium.

An integrated amine and redox gas treatment system is configured to treat an influent hydrocarbon containing stream. The system includes a reduction oxidation unit connected directly downstream of an amine unit. The amine unit is configured to separate the influent fluid stream into a first amine effluent stream including hydrocarbons and a second amine effluent stream including a connection pressure and comprising CO.sub.2. The reduction oxidation unit is configured to receive the second amine effluent stream from the amine unit and operate at the connection pressure while releasing a reduction oxidation effluent stream including purified CO.sub.2 The connection pressure includes a single pressure or a plurality of pressures at which both the amine unit and the reduction oxidation unit are configured to operate.

A system including biogas purification and provides biogas as feedstock to a solid oxide fuel cell. The biogas purification treatment process provides a polished biogas that is substantially free of carbonyl sulfides and hydrogen sulfide. The system uses a biogas treatment apparatus, that includes apparatus such as a packed columns, comprising copper oxide or potassium permanganate packing material, and an activated carbon component configured to treat the biogas by polishing it to remove carbonyl sulfides and deleterious trace residues, such as hydrogen sulfide, that were not removed by any prior bulk H2S removal steps. In addition, an oil removal device is used to remove any entrained fine oil droplets in the biogas. A polished biogas having in the range of 60% methane is charged to the fuel cell. Electricity generated may be fed into a grid or used directly as energy to charge electrical-powered vehicles, for example. Energy credits are tracked in real time and are appropriately assigned.

Capturing mercury or arsenic heavy metal from a moist gas containing water vapour, by: a) cooling the moist gas by heat exchange with a heat transfer fluid produced in e) in order to obtain a gas cooled to a temperature Tf, vaporizing the heat transfer fluid; b) separating condensed water and condensates contained in the cooled gas obtained in a) obtaining a gas depleted in water and a liquid stream containing water; c) compressing vaporized heat transfer fluid obtained from a) obtaining compressed heat transfer fluid; d) heating water-depleted gas by heat exchange with compressed heat transfer fluid obtained in c) obtaining a cooled heat transfer fluid and a gas reheated to a temperature Tc; e) decompressing cooled heat transfer fluid obtained in d), recycling heat transfer fluid to a); f) contacting reheated gas obtained in d) with a capture mass for said heavy metal.

A method and apparatus for continuously treating acid gases including recovering absorbent chemicals by introducing streams leaving a regenerator and/or leaving an absorber into a static mixing zone wherein supplemental washing water is added to recover absorbent chemicals. Improvements to the prior art methods are provided where one or more absorbent chemical recovery units are included to increase the amount of recovered absorbent chemicals exiting the regenerator and/or exiting the absorber are increased and/or maximized. Absorbent chemical recovery units can include mixing units where liquid is added to the stream of sour gas and absorbent chemical to mix with and absorb the absorbent chemical from the stream.

An adsorption material is disclosed that comprises a metal-organic framework and a plurality of ligands. The metal-organic framework comprising a plurality of metal ions. Each respective ligand in the plurality of ligands is amine appended to a respective metal ion in the plurality of metal ions of the metal-organic framework. Each respective ligand in the plurality of ligands comprises a substituted 1,3-propanediamine. The adsorbent has a CO.sub.2 adsorption capacity of greater than 2.50 mmol/g at 150 mbar CO.sub.2 at 40° C. Moreover, the adsorbent is configured to regenerate at less than 120° C. An example ligand is diamine 2,2-dimethyl-1,3-propanediamine. An example of the metal-organic framework is Mg.sub.2(dobpdc), where dobpdc.sup.4− is 4,4′-dioxidobiphenyl-3,3′-dicarboxylate. Example applications for the adsorption material are removal of carbon dioxide from flue gas and biogasses.