A method of exhaust gas scrubbing includes providing recycled concrete fines as a waste material rich in carbonatable Ca and/or Mg phases and with d.sub.90≤1000 μm and a Rosin-Rammler slope n from 0.6 to 1.4 , injecting the waste material into an exhaust gas stream containing CO.sub.2 and/or SO.sub.x for reaction with CO.sub.2 and/or SO.sub.x at a relative humidity of 50 to 100 Vol.-% and a temperature from 40 to 130° C. in an amount of dry waste material ranging from 5 to 30 kg/m.sup.3, withdrawing a partly carbonated and/or sulphurized waste material and purified exhaust gas, and recycling a part of the partly carbonated and sulphurized waste material while the remainder is discharged, as well as use of a waste material slurry for exhaust gas cleaning of CO.sub.2 and/or SO.sub.x.

The present invention relates to a device for absorbing water using a liquid desiccant and the regeneration of said liquid desiccant by evaporating the absorbed water. The device may further be used in an air cooler. The invention also relates to a method for controlling a device for absorbing water.

The invention pertains to methods of reducing dissolved elements such as arsenic, selenium and mercury in aqueous solutions using, for example, various barium compounds to partition said elements to a solid phase. Such methods are particularly useful for reducing such elements at various points in coal and oil-fired power plants prior to final waste water treatment.

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.

A system for producing gas streams for use in synthetic fuel production through CO2 capture and water splitting is disclosed. The system includes a CO2 capture device configured to receive a CO2-containing stream and including an aqueous alkaline solution. The alkaline solution includes hydroxide and/or carbonate ions. The CO2 capture device generates a carbon-rich solution when the alkaline solution absorbs CO2. The carbon-rich solution includes carbonate and/or bicarbonate ions. The system also includes an electrolyzer fluidically coupled to the CO2 capture device, and defining a volume including an anode region having an anode, and a cathode region having a cathode. The volume includes an electrolyte solution having a pH gradient generated by an electric current, causing the electrolyte solution to be acidic in the anode region and alkaline in the cathode region. The carbon-rich solution is received into the electrolyzer. The electrolyzer generates hydrogen, oxygen, and CO2 streams.

This disclosure provides a method for treating natural gas comprising causing at least some of a sour natural gas stream comprising hydrocarbon gas and hydrogen sulfide to contact an amine or pass through a separation system. A sweet natural gas stream comprising hydrocarbon gas and a waste gas stream comprising hydrogen sulfide are formed by contacting the sour natural gas with an amine or by passing it though a separation device. At least some of the hydrogen sulfide in the waste gas stream is oxidized, forming an exhaust gas stream comprising sulfur dioxide, which is then contacted with water or reactant and water solution or slurry to destroy or convert SO.sub.2 into a less environmentally harmful compound.

Methods of sequestering carbon dioxide (CO.sub.2) are provided. Aspects of the methods include contacting a CO.sub.2 containing gaseous stream with an aqueous medium under conditions sufficient to produce a bicarbonate rich product. The resultant bicarbonate rich product (or a component thereof) is then combined with a cation source under conditions sufficient to produce a solid carbonate composition and product CO.sub.2 gas, followed by injection of the product CO.sub.2 gas into a subsurface geological location to sequester CO.sub.2. Also provided are systems configured for carrying out the methods.

A method for simultaneously removing high-load sulfur dioxide and nitrogen oxide in waste gas, relating to the technical field of industrial waste gas purification by biological methods. According to the method, the waste gas is led into a simultaneous desulfurization and denitrification packing tower and removed, microbial floras for simultaneously removing the sulfur dioxide and the nitrogen oxide are loaded on fillers of the packing tower, and the molar concentration ratio of the sulfur dioxide to the nitrogen oxide in the waste gas is (0.76˜1.06):1.

The present invention can provide a new method for fixing carbon dioxide. The method for fixing carbon dioxide of the present invention includes a contact step of bringing a mixed liquid containing sodium hydroxide and further containing at least one of a chloride of a Group 2 element or a chloride of a divalent metal element into contact with a gas containing carbon dioxide, wherein in the contact step, the mixed liquid and the gas are brought into contact with each other by feeding the gas into the mixed liquid.

The present invention provides a new method for fixing carbon dioxide. The method for fixing carbon dioxide of the present invention includes: a first contact step of bringing a solution containing sodium hydroxide into contact with a gas containing carbon dioxide; and a second contact step of adding at least one of a chloride of a Group 2 element or a chloride of a divalent metal element to the solution after the first contact step.