Provided herein are metal organic frameworks comprising metal nodes and N-donor organic ligands which have high selectivity and stability in the present of gases and vapors including H.sub.2S, H.sub.2O, and CO.sub.2. Methods include capturing one or more of H.sub.2S, H.sub.2O, and CO.sub.2 from fluid compositions, such as natural gas.

Disclosed herein are processes and systems for removing heavy C5+ hydrocarbon components from a natural gas feed gas by subjecting the natural gas feed gas stream to an adsorber. The adsorber in the processes and systems described herein operating at a pressure that may be associated with improved adsorption capacity and longer breakthrough time.

A method for recovering paraxylene from a mixture of aromatic hydrocarbons. The process uses a pressure swing adsorption zone followed by a paraxylene recovery zone. The invention provides for lower throughput through the paraxylene recovery zone, resulting in lower capital costs and operating costs.

Systems for and methods of treating a fluid containing siloxanes, silanes and/or other silicon compounds. A hot box is configured to receive an initial flow of the fluid, react the flow with water at a temperature and pressure suitable for hydrolysis to generate a first treated flow, in which at least a portion is hydrolyzed to produce silicon dioxide and methane, and discharge the first treated flow. A solid removal mechanism can be configured to receive the first treated flow, separate at least a portion of the silicon dioxide as solid material, and discharge the remaining components as a second treated flow. Techniques of the present disclosure can lead to very low siloxane levels.

A system and method for sulfur recovery, including hydrogenating Claus tail gas, quenching the hydrogenated gas, adsorbing water and hydrogen sulfide from the quenched gas, and regenerating adsorbent with carbon dioxide and/or nitrogen and heating the adsorbent in a regeneration temperature ramp to desorb primarily hydrogen sulfide in a first part of the temperature ramp.

It is provided a water-saturated carbon molecular sieve membrane obtainable by a) providing a hydrophilic carbon molecular sieve membrane (CMSM) comprising pores of a pore size from 0.25 nm to 0.55 nm for molecular sieving, pores of a pore size from 0.55 nm to 0.90 nm for adsorption diffusion and a negligible amount of pores larger than 0.90 nm such that a plot of N.sub.2 permeance versus pressure of permeation at room temperature and at a pressure from 1 to 4 bar has zero or negative slope; and b) humidifying the membrane until obtaining a water-saturated carbon molecular sieve membrane. It is also provided a process for the separation of a gas from a gas mixture with such a water-saturated membrane, and its use for solvent dehydration, and as a membrane reactor.

Devices suitable for use in an advanced oxidation method for organic and inorganic pollutants deploying OH* radicals and ozone is disclosed. Optionally, a first discharge device, providing OH* radicals and second discharge device providing ozone, are combined to provide desirable chemical and biocidal characteristics. Further, efficient mixing systems for transferring the radicals to the target fluid are disclosed.

Processes, systems, and associated control methodologies are disclosed that control the flow of biogas during the biogas cleanup process to create a more consistent flow of biogas through the digester, while also optimizing the output and efficiency of the overall renewable natural gas facility. In representative embodiments, a biogas buffer storage system may be used during the cleanup process to control the pressure and flow rate of biogas. The biogas buffer storage system may monitor and control the biogas flow rate to either bring down or increase the digester pressure, thereby maintaining a normalized biogas flow rate.

The present invention generally relates to a pressure swing adsorption process for separating an adsorbate impurity from a feed stream comprising product gas, said process comprising feeding the feed stream to an adsorbent bed at a pressure of from about 60 psig to 2000 psig, wherein said adsorbent bed comprises adsorbent having: An isosteric heat of adsorption of from about 5 kJ/mol to about 30 kJ/mol, as determined by the LRC method, for the adsorbate, and an equivalent 65 kJ/mol or less isosteric heat of adsorption for the product,
wherein the adsorbent has a rate of adsorption for the adsorbate impurity that is at least 10 times greater than the rate of adsorption for the product gas as determined by the TGA method and recovering said product gas with a reduced a level of said adsorbate impurity. The invention also related to an adsorbent useful in PSA separations, particularly separating N.sub.2 from methane, CO.sub.2 from methane O.sub.2 from N.sub.2 and the like.

An object of the present invention is to provide a gas refining apparatus which can produce a product gas with high purity and high yield at low cost and can produce a plurality of types of gas as a product gas without changing an adsorbent, and the present invention provides a gas refining apparatus (10) including a first derivation line (L3) connected to the second adsorption towers (2a, 2b) and through which the first gas flows, a second derivation line (L4) connected to the second adsorption towers (2a and 2b) and through which the second gas flows, a regeneration line (L5) connected to the first adsorption towers (1a, 1b), through which a regeneration gas for regenerating a first adsorbent in the first adsorption towers (1a, 1b) flows, and a pump (P) provided in the second derivation line (L4) and configured to desorb the second gas from a second adsorbent in the second adsorption towers (2a and 2b), and the regeneration line (L5) is connected to each of the first derivation line (L3) and the second derivation line (L4).