The present invention relates to single thread composite fibers comprising at least one binder and at least one active catalyst for the capture and degradation of chemical threats such as chemical warfare agents (CWA), biological warfare agents, and toxic industrial chemicals (TIC) and a method for producing the same. The invention fibers are applicable to the fields of protective garments, filtration materials, and decontamination materials.

Disclosed herein are monolith oxidation catalysts for the destruction of CO and volatile organic compounds (VOC) chemical emissions, in particular, the destruction of light alkane organic compounds. The catalysts contain high surface area refractory oxides of silica- and hafnia-doped zirconia and silica, or tin oxide or stabilized alumina; and at least one platinum group metals, in particular platinum metal, or a combination of platinum and palladium.

The present disclosure provides an exhaust gas purification material and an exhaust gas purification device that can efficiently remove harmful components even after being exposed to high temperature. Such exhaust gas purification material comprises metal oxide particles and noble metal particles supported on the metal oxide particles. The noble metal particles have a particle size distribution with a mean of 1.5 nm and 18 nm and a standard deviation of less than 1.6 nm.

The present invention relates to a process for the production of butadiene by condensation of ethanol using a catalyst containing sillica-supported elements from group 3A and group 4B of the periodic table. The catalyst of the present invention has high activity and selectivity to butadiene in the synthesis reaction of said olefin from ethanol.

The present invention relates to a catalyst comprising two layers on an inert catalyst carrier, wherein a layer A lying directly on the catalyst carrier contains at least one platinum group metal and one cerium/zirconium/SE mixed oxide, and a layer B, applied on layer A and in direct contact with the flow of exhaust gas, contains at least one platinum group metal and a cerium/zirconium/SE mixed oxide, wherein SE stands for a rare earth metal other than from cerium, characterized in that the fraction of SE oxide in the cerium/zirconium/SE mixed oxide of layer A is less than the fraction of SE oxide in the cerium/zirconium/SE mixed oxide of layer B.

A method for producing an organohalosilane, the method comprising: reacting an organic compound comprising a halogen-substituted or unsubstituted aromatic compound with a hydridohalosilane mixture comprising at least two different hydridohalosilanes of formula (I) R.sub.nSiH.sub.mX.sub.4-m-n, where each R is independently C.sub.1-C.sub.14 hydrocarbyl or C.sub.1-C.sub.14 hologen-substituted hydrocarbyl, X is fluoro, chloro, bromo, or iodo, n is 0, 1, or 2, m is 1, 2, or 3 and m+n is 1, 2, or 3, in the presence of a catalyst comprising one or more of the elements Sc, Y, Ti, Zr, Hf, Nb, B, Al, Ga, In, C, Si, Ge, Sn, or Pb, at a temperature greater than 100° C., and at a pressure of at least 690 kPa, to produce a crude reaction product comprising the organohalosilane, provided that when the at least two different hydridohalosilane comprise a hydridohalosilane of formula (I) where n=0 and m=1 and a hydridohalosilane of formula (I) where n=0 and m=2, the catalyst is a heterogeneous catalyst comprising an oxide of one or more of the elements Sc, Y, Ti, Zr, Hf, B, Al, Ga, In, C, Si, Ge, Sn, or Pb.

A real-time measuring device of oxygen concentration in a droplet environment, comprising: a measurement pipeline, a gas-liquid separation structure installed inside a side of the gas inlet of the measurement pipeline, a pressure sensor, a zirconia oxygen concentration sensor with a builtin thermal resistor, a digital signal converter, a signal amplifier and a signal processing unit sequentially installed at the gas outlet of the measurement pipeline, wherein the pressure sensor, the thermal resistor and the zirconia oxygen concentration sensor are connected to the digital signal converter and the signal amplifier, respectively, and the signal processing unit obtains the amplified and AD converted zirconia oxygen concentration sensing signal, pressure sensing signal and the temperature sensing signal and calculates real-time oxygen concentration.

Systems for preparing butenes are provided. The systems can include a reactor inlet coupled to both a reactor and at least one reactant reservoir; at least one of the reactant reservoirs containing one or both of an aldehyde and/or ethanol; a catalyst within the reactor, the catalyst comprising a metal component and an acidic support material; and a reactor outlet operationally configured to convey a butene-rich reaction product to a product reservoir. Methods for preparing butenes are also provided. The methods can include exposing one or both of ethanol and/or an aldehyde to a catalyst comprising a metal component and an acidic support to form a butene-rich product that comprises one or both of 1-butene and/or 2-butene.

An object of the present invention is to provide a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature, and the present invention provides a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, including: a carrier that contains α-alumina; and a supported components that are supported on the carrier, wherein the supported components includes at least one platinum group element, a Ce oxide, and a Zr oxide.

This disclosure features a urea conversion catalyst located within a urea decomposition reactor (e.g., a urea decomposition pipe) of a diesel exhaust aftertreatment system. The urea conversion catalyst includes a refractory metal oxide and a cationic dopant. The urea conversion catalyst can decrease the temperature at which urea converts to ammonia, can increase the urea conversion yield, and can decrease the likelihood of incomplete urea conversion.