An ozone purification catalyst, and a preparation method therefor and an application thereof are provided. The catalyst coating uses macroporous, high specific surface and CeO.sub.2 and/or La.sub.2O.sub.3 modified Al.sub.2O.sub.3 as the carrier material, and Mn and/or Pd as the active component. The preparation method is to prepare the Al.sub.2O.sub.3-based material by a sol-gel method, and then to load the active components on the carrier material, and to dry, calcinate and solidify to obtain the ozone purification catalyst. The catalysts as prepared shows a fast and efficient purification of ozone. The complete conversion temperature covers a wide range of temperature. The catalyst has excellent texture performance, high specific surface area and large pore volume, which is beneficial to ozone purification when the car is running at high speed. The particle sizes and colors of the catalyst can be modified according to various requirements. According to the actual application, it can be coated on the radiator fins of automobile water tanks, and any place where coating is allowed in public areas such as urban bus stations, stop signs, kiosks, roadside guardrails, or exterior walls of buildings that is in contact with outdoor air.

The invention relates to an aerogel concrete mixture containing a photocatalyst, a photocatalytically active high-performance aerogel concrete obtainable therefrom and a method for producing same.

A method of applying a NOx degrading composition on a concrete element, including providing a concrete element having a surface, and applying a composition including photocatalytic titanium dioxide particles dispersed in a continuous phase on the surface of said concrete element. Also, a concrete element having NOx degrading properties. Also, a concrete element having photocatalytic titanium dioxide particles dispersed thereon.

An article of manufacture for providing an O.sub.2 Tree for removing CO.sub.2 gas from the atmosphere according to the present invention is disclosed.

The application provides an oxide layer material capable of adsorbing and degrading methane gas, which is obtained by a method comprising the steps of: 1) subjecting a cracked household refuse to aerobic biological pretreatment; 2) subjecting the material which has been subjected to the aerobic biological pretreatment to biological stabilizing treatment; and 3) adding copper chloride, potassium sulfate, magnesium oxide, and a composite bacterial agent for oxidizing methane gas to the material which has been subjected to the biological stabilizing treatment to obtain the oxide layer material capable of adsorbing and degrading methane gas. This disclosure further discloses a method for preparing the oxide layer material capable of adsorbing and degrading methane gas described above.

Methods of producing solid CO.sub.2 sequestering carbonate materials are provided. Aspects of the methods include introducing a divalent cation source into a flowing aqueous liquid (e.g., a bicarbonate rich product containing liquid) under conditions sufficient such that a non-slurry solid phase CO.sub.2 sequestering carbonate material is produced. Also provided are systems configured for carrying out the methods.

A synthetic fuel production system and related techniques are disclosed. In accordance with some embodiments, the disclosed system may be configured to produce a liquid fuel using carbon dioxide extracted from the air and hydrogen generated from aqueous solutions by electrochemical means (e.g., water electrolysis). In production of the fuel, the disclosed system may be configured, in accordance with some embodiments, to react the carbon dioxide and hydrogen, for example, to form methanol. The disclosed system also may be configured, in accordance with some embodiments, to utilize one or more subsequent reaction steps to produce a given targeted set of hydrocarbons and partially oxidized hydrocarbons. For example, the disclosed system may be used to produce any one (or combination) of: ethanol; dimethyl ether; formic acid; formaldehyde; alkanes of various chain length; olefines; aliphatic and aromatic carbon compounds; and mixtures thereof, such as gasoline fuels, diesel fuels, and jet fuels.

Provided is an unsaturated double bond-containing compound capable of sufficiently advancing a crosslinking reaction or a curing reaction when used for a coating material or the like and having oxygen absorption performance. The present invention also provides an oxygen absorbent containing the unsaturated double bond-containing compound and a resin composition containing the same. Provided are an unsaturated double bond-containing compound represented by general formula (I), an oxygen absorbent containing the same, and a resin composition.

An air mover for forcing air through the system, a pre-treating stage with a particulate filter for removing larger contaminants from the air and an antimicrobial (e.g., copper and silver) filter for killing or damaging microorganisms, a UV chamber including an ultraviolet lamp that emits radiation and a catalytic (e.g., TiO.sub.2-coated) device and a reflective (e.g., mirror-finish anodized aluminum) lining for amplifying the UV radiation for killing microorganisms, a post-UV stage including a VOC-reducing (e.g., activated-charcoal) filter for removing odors and VOCs from the air, and optionally a supply of a surface disinfectant (e.g., ClO.sub.2). In example embodiments, the UV lamps and VOC filters are selected and configured for controlling microbial pathogens, and in other example embodiments they are selected and configured for removing ethylene from the air.

Methods of producing solid CO.sub.2 sequestering carbonate materials are provided. Aspects of the methods include introducing a divalent cation source into a flowing aqueous liquid (e.g., a bicarbonate rich product containing liquid) under conditions sufficient such that a non-slurry solid phase CO.sub.2 sequestering carbonate material is produced. Also provided are systems configured for carrying out the methods.