The present disclosure provides a desulfurization and sulfur recovery method for sulfur dioxide flue gas, and belongs to the technical field of non-ferrous metal smelting. The method includes the following steps: desulfurizing the sulfur dioxide flue gas by taking slagging flux limestone or quicklime for smelting or converting process as a desulfurizer, and adsorbing SO.sub.2 in the gas to obtain gypsum residue, calcium sulfite, and the desulfurized flue gas, where SO.sub.2 in the sulfur dioxide flue gas before desulfurization is less than 1 vol %; and recycling the gypsum residue and the calcium sulfite to the smelting or converting furnace for slagging, resolving the SO.sub.2 into smelting off-gas, producing sulfuric acid in acid plant.

Atmospheric moisture harvester systems include two beds with water capture material, such as metal-organic framework (MOF), a heater, two fans, and a condenser having two sides, operatively configured into adsorption and desorption modes, wherein the MOF beds are interchangeable to cycle between the desorption and water adsorption modes. The systems may further include a photovoltaic panel powering the fans and condenser.

The present technology relates generally to parallel passage contactors having active layers and methods for its use. Particularly, the present technology relates to parallel passage contactors having active layers with sorbents and/or catalysts and methods of use in sorptive gas separation and/or catalytic reactions.

The present disclosure relates to systems and methods of making ammonia using stable ammonia absorbents. The system and method for producing ammonia, comprises a reactor comprising a catalyst that converts at least a portion of nitrogen feed gas and at least a portion of hydrogen feed gas to ammonia (NH3) forming a reaction mixture comprising the ammonia, unreacted nitrogen, and unreacted hydrogen. An absorber configured to selectively absorb ammonia from the reaction mixture at a temperature of about 180 deg. C. to 330 deg. C. and a pressure of about 1-20 bar, the absorber comprising a solid absorbent. Preferably the solid absorbent is at least one metal halide and a solid support. The unabsorbed ammonium, the unreacted nitrogen, and unreacted hydrogen gas are recycled to the reactor.

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.

Method and systems are disclosed for selectively removing naturally-occurring sugars in beverages in an effective, affordable and scalable manner.

A method for capturing CO.sub.2 from a gas stream using a metal organic framework (MOF) based physisorbent CO.sub.2 concentrator is provided. In the method, MOF material is pretreated, a gas stream is then introduced into the CO.sub.2 concentrator which comprises the pretreated MOF material. CO.sub.2 from the gas stream is captured with the CO.sub.2 concentrator to generate a CO.sub.2-free stream, which is discharged the from the CO.sub.2 concentrator into the atmosphere. Introduction of the gas stream into the CO.sub.2 concentrator is stopped when the pretreated MOF material becomes saturated with CO.sub.2. The CO.sub.2 concentrator with the saturated MOF material is then regenerated by introducing hot air, hot nitrogen, vacuum, or a combination thereof into the CO.sub.2 concentrator thereby generating a CO.sub.2-rich stream. The CO.sub.2-rich stream is diverted for purification and the regenerated CO.sub.2 concentrator is recycled for future capture of CO.sub.2.

An adsorbate-selective metal organic framework includes a transition metal; and a plurality of organic molecules coordinated to the transition metal so as to preserve open coordination sites for selectively adsorbing molecules that have low-lying π* orbitals. The transition metal has a lowest energy spin state in the presence of the selectively adsorbed molecules that are strongly bonding to the transition metal through π-donating interactions which is different than the lowest energy spin state in the absence of these adsorbed molecules. The transition metal has also a lowest energy spin state in the presence of non-selected molecules that are weakly bonding to the transition metal through σ- and/or π-accepting and/or donating interactions.

Disclosed are air-stable small-molecule adsorbents trimeric [Cu—Br].sub.3 and [Cu—H].sub.3 that undergo a reversible solid-state molecular rearrangements to [Cu—Br.(alkene)].sub.2 and [Cu—H.(alkene)].sub.2 dimers. The reversible solid-state rearrangement allows one to break adsorbent design trade-offs and achieve low heat of adsorption while retaining high selectivity and uptake.

A method for the regeneration of effluent from an absorber capturing emissions of carbon dioxide (CO2) from industrial sources. Reducing CO2 emissions from all sources is a key objective of most nations, and every industrial source of CO2 emissions has received extensive scrutiny.

The method involves designing and installing on a source a proprietary thermal regeneration system for a sorbent used in the CO2 capture equipment system, which recirculates the sorbent liquid through an absorption column (absorber). Because sorbents used in these systems are expensive, it would be useful if the spent sorbent following absorption of CO2 is regenerated for re-use in the absorber. The present invention's regeneration method uses thermal swing (changes in temperature of the spent sorbent), and describes the integration of a waste heat recovery process into the thermal swing method. In particular, the method uses a heat transfer agent in a sealed loop circulating the heat transfer agent through a hot industrial source producing the CO2 stream.