There is provided an exhaust gas processing apparatus which improves the removal rate of harmful substances and also achieves a compact size. An exhaust gas processing apparatus (10) absorbing gas by creating contact between gas and liquid includes: an absorbing tower main body (11) in which an internal space is formed; a spray apparatus (12) which sprays liquid in a prescribed region in an up/down direction of the internal space; and a gas supply apparatus (13) which introduces gas into the absorbing tower main body (11), wherein the spray apparatus (12) includes: a trunk pipe (12b) which extends in the up/down direction in the prescribed region of the internal space; branch pipes (12c) which are connected to the trunk pipe (12b) and extend towards the inner wall of the absorbing tower main body (11); and spray nozzles (12d) which spray liquid supplied from the branch pipes (12c), wherein the spray nozzles (12d) are installed such that an angle formed between the center line of the spraying region of the spray nozzle (12d), and the lengthwise direction of the branch pipe (12c) is an acute angle.

Multi-fiber, fiber optic cable assemblies may be configured so that the terminal ends of the cables have pre-assembled back-post assemblies that include pre-assembled ferrules, such as MPO ferrules that meet the requisite tolerances needed for fiber optic transmissions. To protect the pre-assembled components from damage prior to and during installation, pre-assembled components may be enclosed within a protective housing. The housing with pre-assembled components may be of a size smaller than fully assembled connectors so as to be sized to fit through a conduit. The remaining connector housing components for the multi-fiber connectors may be provided separately and may be configured to be attached to the back-post assembly after installation of the cable.

A method and composition of matter for detecting and decontaminating hazardous chemicals, the composition of matter including: a magnetic material for any of chemisorbing, molecularly dissociating, or decomposing a hazardous chemical, wherein the magnetic material changes its magnetic moment upon any of chemisorption, decomposition, and molecular dissociation of the hazardous chemical and the change in magnetic moment is used to detect the presence of the hazardous chemical, and wherein the hazardous chemical includes any of toxic industrial chemicals, chemical warfare agents, and chemical warfare agent related compounds.

Provided is a method of manufacturing a metal catalyst support including: transferring a plate member of the same size along a transfer unit; aligning the plate member so that a front portion of the plate member is located at a start point when the plate member reaches a set position; forming a corrugated plate by alternately forming a first corrugated portion and a second corrugated portion on the plate member which is aligned at the start point; and laminating the fabricated corrugated plates and the flat plates alternately in a case.

A rechargeable battery assembly for a vehicle has a housing and at least one metal-air rechargeable battery arranged in the housing. A filter device is arranged in the housing and conditions the inlet air of the at least one metal-air rechargeable battery such that the inlet air exhibits a predetermined air humidity.

A flow deflecting device is provided that deflects the inlet air in the housing such that the filter device can be regenerated by waste heat of the at least one metal-air rechargeable battery.

A catalyst system comprising a combination of: 1) one or more catalyst compounds comprising at least one nitrogen linkage; 2) a support comprising an organosilica material, which is a mesoporous organosilica material; and 3) an optional activator. Useful catalysts include pyridyldiamido transition metal complexes, HN5 compounds, and bis(imino)pyridyl complexes. The organosilica material is a polymer of at least one monomer of Formula [Z.sup.1OZ.sup.2SiCH.sub.2].sub.3(1), where Z.sup.1 represents a hydrogen atom, a C.sub.1-C.sub.4alkyl group, or a bond to a silicon atom of another monomer and Z.sup.2 represents a hydroxyl group, a C1-C.sub.4alkoxy group, a C.sub.1-C.sub.6 alkyl group, or an oxygen atom bonded to a silicon atom of another monomer. This invention further relates to processes to polymerize olefins comprising contacting one or more olefins with the above catalyst system.

Provided are mixed metal oxy-hydroxides that serve as reactive media to bind, sequester, or alter one or more toxic chemicals such as sulfur dioxide (SO.sub.2), hydrogen cyanide (HCN), and others. A reactive media includes: a porous metal oxy-hydroxide including at least one first transition metal that is optionally one or more of copper, zinc, or iron; a second transition metal linked to the first transition metal by a bond that includes an oxygen, the second transition metal selected optionally being one or more of magnesium, calcium, cobalt, titanium, zirconium, aluminum, and silicon; and the metal oxy-hydroxide terminated by at least one hydroxyl group. The resulting media provides for excellent porosity and reactivity for removal of toxic chemicals from the environment or a sample.

Industrial waste derived adsorbents were obtained by pyrolysis of sewage sludge, metal sludge, waste oil sludge and tobacco waste in some combination. The materials were used as media to remove hydrogen sulfide at room temperature in the presence of moisture. The initial and exhausted adsorbents after the breakthrough tests were characterized using sorption of nitrogen, thermal analysis, XRD, ICP, and surface pH measurements. Mixing tobacco and sludges result in a strong synergy enhancing the catalytic properties of adsorbents. During pyrolysis new mineral phases are formed as a result of solid state reaction between the components of the sludges. High temperature of pyrolysis is beneficial for the adsorbents due to the enhanced activation of carbonaceous phase and chemical stabilization of inorganic phase. Samples obtained at low temperature are sensitive to water, which deactivates their catalytic centers.

A system for absorbing and separating acid gases may include an absorbing tower in which a gas containing an acid gas is supplied, a recycling tower that is disposed close to the absorbing tower, an absorbent that absorbs an acid gas in the absorbing tower and discharges the acid gas back to the recycling tower while circulating through the absorbing tower and the recycling tower, and a condenser that is connected to the recycling tower and condenses an acid gas produced in the recycling tower, wherein a centrifugal separator that separates the absorbent, using a centrifugal force, is disposed at a lower portion in the absorbing tower.

Methods for treating an industrial byproduct, such as spent, granular, activated carbon, dredge spoils, or contaminated soils involve integrated steps to clean, concentrate, separate and/or otherwise collect hazardous and/or desired materials from such industrial byproducts. The cleaned, concentrated, separated, or collected materials may involve sufficient quantities to be useful to subsequent processors, raw materials, additives, and the like. Other treatment methods involve retaining the clean material stream at sufficient temperatures for sufficient time to separate and concentrate desired material for recovery therefrom, such as precious metals and rare earth elements.