Disclosed herein are a catalyst composition, catalyst devices, and methods for removing formaldehyde, volatile organic compounds, and other pollutants from an air flow stream. The catalyst composition including manganese oxide, optionally one or more of alkali metals, alkaline earth metals, zinc, iron, binder, an inorganic oxide, or carbon.

The present invention relates to an intensified 5-bed and 6-bed PSA process cycles features, as well as fast rate adsorbents that enable the intensified PSA system to meet cost and performance target are identified. The proposed capital efficient H.sub.2PSA system offers opportunity to reduce PSA capital expenditure by ten percent (10%).

The invention relates to a process and apparatus for separation of gas mixtures with reduced maintenance costs. The process and the apparatus consist of a feed stream separation stage (1), and a retentate separation stage (2), of which both are membrane separation stages, wherein the first retentate stream (7) is heated to temperature higher than the temperature of the feed stream (5), before it is introduced to the retentate separation stage (2), and the total capacity of the membranes used in the retentate separation stage (2) is higher than the total capacity of the membranes used in the feed stream stage (1).

In a process for the separation of a mixture containing hydrogen and carbon monoxide to produce gaseous hydrogen, the mixture is cooled down to a temperature below −180° C. and then separated at a temperature below −100° C. to produce a gas enriched in hydrogen and a fluid enriched in carbon monoxide, at least a part of the gas enriched in hydrogen is sent to a pressure swing adsorption separation apparatus operating at a temperature above 0° C. to produce a gas rich in hydrogen at a pressure of at least 20 bars, and at least a part of the gas rich in hydrogen is cooled in the heat exchanger down to a temperature below −100° C., reduced in pressure in a turbine down to a pressure of at least 8 bars and reheated in the heat exchanger to constitute a product rich in hydrogen at a pressure of at least 8 bars.

Deleterious gas is captured from atmospheric air using capture units dispersed across a geographic region. Each unit has a filter that is capable of capturing compounds from the gas from air when air is passed through the filter by fans. The units additionally include a sensor for sensing a level of the gas in the air. An electronic processor controls the fan, and communicates data from the sensor to other units and/or a central electronic processor. The electronic processors of the units or the central processor controls the fan speed of units in areas of higher concentration of the gas, selecting which units to become active based upon a proximity of each unit to the gas concentration, as well as a direction of movement of the concentration. A communicated presence of errors or a low battery state of a unit, is used by the processor to select other units nearby for operation instead of the affected unit.

The present disclosure relates to systems and methods useful for power production. In particular, a power production cycle utilizing CO.sub.2 as a working fluid may be configured for simultaneous hydrogen production. Beneficially, substantially all carbon arising from combustion in power production and hydrogen production is captured in the form of carbon dioxide. Further, produced hydrogen (optionally mixed with nitrogen received from an air separation unit) can be input as fuel in a gas turbine combined cycle unit for additional power production therein without any atmospheric CO.sub.2 discharge.

Embodiments of the present disclosure provide a metal-organic framework composition including a metal-organic framework having an ana topology, the metal-organic framework including one or more metals connected to one or more organic linkers. Embodiments of the present disclosure further provide a method of separating chemical species including contacting a metal-organic framework having an ana topology with a flow of paraffins and separating the paraffins.

A process for the production of a hydrogen gas stream having a CO content of less than 1 ppm having a production cycle comprising two phases: phase 1 includes a) purifying a synthesis gas in a PSA unit, b) recovering a hydrogen gas stream comprising a CO content of greater than 1 ppm, c) purifying the gas stream by adsorption in a TSA unit, and recovery a hydrogen gas stream exhibiting a CO content of less than 1 ppm, and phase 2 includes e) purifying the synthesis gas in a PSA unit, f) recovering a hydrogen gas stream having a CO content of less than 1 ppm, where throughout steps e) and f), the TSA unit is bypassed by the hydrogen gas stream and is regenerated.

A system and method of pre-purification of a feed gas stream is provided that is particularly suitable for pre-purification of a feed air stream in cryogenic air separation unit. The disclosed pre-purification systems and methods are configured to remove substantially all of the hydrogen, carbon monoxide, water, and carbon dioxide impurities from a feed air stream and is particularly suitable for use in a high purity or ultra-high purity nitrogen plant. The pre-purification systems and methods preferably employ two or more separate layers of hopcalite catalyst with the successive layers of the hopcalite separated by a zeolite adsorbent layer that removes water and carbon dioxide produced in the hopcalite layers.

The invention relates to the intensification of hydrogen PSA processes through utilization of specifically engineered core-shell composite adsorbents. Different embodiments of core-shell adsorbents can be used with either high or low heat capacity cores, and different adsorbent shells (e.g. activated carbon, zeolite, silica gel, alumina etc.) resulting in higher mass transfer rates and hence sharper mass transfer fronts during the PSA process. The location of the limiting impurity front determines the product purity. Therefore, with sharper impurity fronts, lower height of adsorbent bed is required, and cycle time can be proportionally reduced. Also, thermal swing during the PSA can be reduced by use of such adsorbents. The use of a high heat capacity core to reduce the thermal swing, leads to higher overall working capacity of the adsorbent bed.