Provided are: a hydrocarbon adsorbent capable of adsorbing hydrocarbons, storing the adsorbed hydrocarbons up to a relatively high temperature, and desorbing the adsorbed and stored hydrocarbons at a relatively high temperature; an exhaust gas purifying catalyst composition using the same; an exhaust gas purifying catalyst; and a method for treating an exhaust gas. The hydrocarbon adsorbent comprises a zeolite having an MRT-type framework structure. The hydrocarbon adsorbent comprises a small-pore zeolite having a total desorption amount ZD.sub.1 of propylene desorbed at 50° C. or higher and lower than 300° C. being 3.5 mmol/g or less and a total desorption amount ZD.sub.2 of propylene desorbed at 300° C. or higher and 500° C. or lower being 0.5 mmol/g or more, per 1 g by mass of the small-pore zeolite, when adsorbing propylene at 50° C. and then heating from 50° C. to 500° C. under the condition of 10° C./min by a temperature-programmed desorption method.

A combination of bismuth oxyhalides is provided, which is a photooxidant, antibacterial and antiviral. The combination of bismuth oxyhalides is added to a filter medium (e.g., a multistage filter) to decompose VOCs and/or eliminate bacteria and/or viruses. Suitable designs of multistage filters are also provided.

A light shield structure is disposed between an ultraviolet lamp and a filter screen of an air purifier, and comprises a first light shield element and a second light shield element. The first light shield element is disposed on an inner wall of the second light shield element. The second light shield element is provided with air inlets, and the first light shield element is staggered with the second light shield element, so that the air inlets are completely blocked by the first light shield element in a radial direction. An air inlet channel is formed between the first light shield element and the second light shield element. Under the precondition that the air inlet channel is formed by the first light shield element and the second light shield element, ultraviolet light can be completely shielded, so that the service life of the filter screen is prolonged.

A packaging film is described comprising at least one polymer film layer in which particles of a small-pore or a medium-pore palladium-doped zeolite are dispersed. Such films are of particular utility for the adsorption of volatile organic compounds, such as those originating from organic matter.

Provided is a method for desulphurizating and denitrating a flue gas in an integrated manner based on low-temperature adsorption. The method includes: decreasing a temperature of the flue gas below a room temperature by using a flue gas cooling system; removing moisture in the flue gas by using a dehumidification system; sending the flue gas to a SO.sub.2 and NO.sub.x adsorbing column system; and simultaneously adsorbing SO.sub.2 and NO.sub.x of the flue gas with a material of activated coke, activated carbon, a molecular sieve or diatom mud in the SO.sub.2 and NO.sub.x adsorbing column system to implement an integration of desulphurization and denitration of the flue gas based on the low-temperature adsorption. With the present method, SO.sub.2 and NO.sub.x of the flue gas can be adsorbed simultaneously in an environment having a temperature below the room temperature.

A post-treatment system includes two SCRs, a second SCR is connected to a booster in parallel, and a three-way valve is arranged before the second SCR and the booster, such that whether an exhaust gas flows through the second SCR or the booster is controlled by means of controlling the three-way valve. In the case of a low temperature, the three-way valve is controlled to close a branch of the booster, such that the exhaust gas flows through the second SCR and a first SCR that are connected in series, thereby reducing the energy loss caused by the exhaust gas flowing through the booster, and improving the NO.sub.x conversion efficiency in the case of a low temperature. In a case of a high temperature, the three-way valve is controlled to close a by-pass line, such that the exhaust gas flows through the booster and the first SCR.

An air conditioner unit may include a housing, an outdoor heat exchanger assembly, an indoor heat exchanger assembly, a compressor, and a sterilization light assembly. The housing may define an indoor portion and an outdoor portion. The housing may further define an exhaust outlet downstream from the indoor portion to exhaust air therefrom. The sterilization light assembly may be disposed within the housing to transmit an ultraviolet light emission thereto. The sterilization light assembly may include a support board, an ultraviolet C (UVC) light source, and a lens casing. The UVC light source may be mounted to the support board and configured to emit radiation between 200 to 280 nanometers. The lens casing may be disposed over the support board and seal the UVC light source to prevent moisture from contacting the UVC light source.

The present disclosure provides an exhaust gas purification catalyst having an improved Rh activation, which comprises a substrate and a catalyst coat layer formed on the substrate, the catalyst coat layer having a two-layer structure, wherein the catalyst coat layer includes an upstream portion on an upstream side and a downstream portion on a downstream side in an exhaust gas flow direction, and a part or all of the upstream portion is formed on a part of the downstream portion, wherein the upstream portion contains Rh fine particles and Pt, wherein the Rh fine particles have an average particle size measured by a transmission electron microscope observation of 1.0 nm or more to 2.0 nm or less, and a standard deviation σ of the particle size of 0.8 nm or less, and wherein the downstream portion contains Rh.

Embodiments described herein provide for the flameless premixed combustion of the pyrolysis gases of a milligram-sized sample of solid material in a microscale fire calorimeter (MFC) at high temperatures of combustion and under precisely controlled fuel-to-oxygen ratios. The microscale fire calorimeter (MFC) device and techniques set out herein provide for the generation of fuel gases from solids and the mixing of those fuel gases with oxygen under controlled conditions to obtain precise fuel/oxygen ratios during combustion. Combustion is conducted under flameless, premixed conditions in a rapid test that can generate soot and other products of incomplete combustion, which may then be analyzed to determine their type and nature. This allows for microscale, accurate, and convenient techniques for the generation and determination of the type and nature of combustion species produced over the full range of fire stages from early stage (over-ventilated) fires to late-stage (under-ventilated/high-toxicity) fires.

Methods of sequestering CO.sub.2 from a gaseous source of CO.sub.2 are provided. Aspects of the methods include employing an alkali enrichment protocol, such as a membrane mediated alkali enrichment protocol, in a CO.sub.2 sequestration protocol. Also provided are systems for practicing the methods.