A material for removing a contaminant, the material including an adsorption material for adsorption of a contaminant and a decomposition material for decomposition of a contaminant, wherein the adsorption material and the decomposition material are complexed with each other, and a contaminant decomposition onset temperature of the decomposition material is equal to or lower than a contaminant desorption onset temperature of the adsorption material.

The present invention describes an improved catalytic reactor system with an improved catalyst that transforms CO.sub.2 and low carbon H.sub.2 into low-carbon syngas with greater than an 80% CO.sub.2 conversion efficiency, resulting in the reduction of plant capital and operating costs compared to processes described in the current art. The inside surface of the adiabatic catalytic reactors is lined with an insulating, non-reactive surface which does not react with the syngas and effect catalyst performance. The improved catalyst is robust, has a high CO.sub.2 conversion efficiency, and exhibits little or no degradation in performance over long periods of operation. The low-carbon syngas is used to produce low-carbon fuels (e.g., diesel fuel, jet fuel, gasoline, kerosene, others), chemicals, and other products resulting in a significant reduction in greenhouse gas emissions compared to fossil fuel derived products.

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

A method and apparatus for cleaning and recycling stack gas from coal-fired power plants, from natural or propane burning heating plants, or from cement kilns by using renewable catalysts of zeolite to separate pollutants into recyclable and reusable materials. The method reduces from the stack gas carbon monoxide (CO), carbon dioxide (CO.sub.2), nitrogen oxide (NOx), sulfur oxide (SOx) as well as halogens such as chloride and fluorides and trace metals particularly, mercury, lead, and zinc. The method and apparatus also result in production of fertilizer products by purging with gaseous or liquid nitrogen the zeolite beds through which the stack gas flows. The oxygen generated may be recycled to the burners in the plant.

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

A material for removing a contaminant, a filter for removing a contaminant including the material, and a device for removing a contaminant including the filter, the material including an adsorption material for adsorption of a contaminant and a decomposition material for decomposition of a contaminant, wherein the adsorption material and the decomposition material are complexed with each other, and a contaminant decomposition onset temperature of the decomposition material is equal to or lower than a contaminant desorption onset temperature of the adsorption material.

A system for oxidizing nitrogen monoxide (NO) contained in exhaust gas injects a liquid oxidizing agent into the exhaust gas and simultaneously removes nitrogen oxides and sulfur oxides from exhaust gas using an organic catalyst. The system includes an absorption tank for storing an absorption solution containing an organic catalyst, the absorption tank communicating with an oxygen supply pipe for supplying oxygen-containing gas to the absorption tank; an absorption tower, extending upward from the absorption tank, through which the exhaust gas flows from an exhaust gas inlet duct to an exhaust gas outlet; a first injection unit to inject the absorption solution into the absorption tower; a second injection unit to inject an oxidizing agent solution into at least one of the inlet duct and the absorption tower; and an oxidizing agent supply unit for supplying the oxidizing agent solution to the second injection unit.

Certain embodiments of the invention are directed to nitrogen rich three dimensional C.sub.3N.sub.4+ mesoporous graphitic carbon nitride (gMCN) material formed from diaminoguanidine precursors, the gMCN having a spherical morphology and an average monomodal pore diameter between 6.5 to 9.5 nm.

There is provided a process and a system for producing CO and H.sub.2 (syngas) from a CO.sub.2-containing gas. The process includes a step of contacting a CO.sub.2-containing gas with an aqueous absorption solution to produce a bicarbonate loaded stream and a CO.sub.2-depleted gas, followed by a step of subjecting the bicarbonate loaded stream to an electrochemical conversion to generate a gaseous stream including CO and H.sub.2. The system includes an absorption unit wherein the CO.sub.2-containing gas is contacted with the absorption solution to produce the bicarbonate loaded stream and the CO.sub.2-depleted gas and a conversion unit including an electrolytic cell for electrochemically converting bicarbonate ions in the bicarbonate loaded stream into the gaseous stream including CO and H.sub.2 and a bicarbonate depleted stream. In some embodiments, an enzyme such as a carbonic anhydrase can be used to catalyze the conversion of the CO.sub.2-containing gas into the bicarbonate loaded stream.

The present invention solves the existing problem of using very expensive oxidation reagents, such as H.sub.2O.sub.2 and ozone, in removal of NO.sub.x and SO.sub.x from flue gases, by performing simultaneous oxidation of NO.sub.x and SO.sub.x with atmospheric oxygen in a combined system for catalytic oxidation and wet-scrubbing of both NO.sub.x and SO.sub.x from a flue gas and manufacturing fertilisers. Two major configurations of the oxidation system are disclosed in the present invention. The first configuration operates on oxygen-enriched air to increase efficiency of the oxidation reaction and requires an additional oxygen concentrator unit. The second configuration operates on atmospheric air at ambient conditions and requires an additional catalyst activation unit. In the second configuration, the efficient oxidation process is carried out at low temperatures of about 30-90 C. in the presence of recovered and re-activated catalyst. This temperature is a result of the exothermic character of the reaction, and therefore, no heating is required in the process.