A method of fabricating composite filaments is provided. An initial composite filament including a core and a cladding (such as a Pt-group metal) is cut into smaller pieces (or is first mechanically reduced and then cut into smaller pieces). The smaller pieces of the filaments are inserted into a metal matrix, and the entire structure is then further reduced mechanically in a series of reduction steps. The process can be repeated until the desired cross sectional dimension of the filaments is achieved. The matrix can then be chemically removed to isolate the final composite filaments with the cladding thickness down to the nanometer range. The process allows the organization and integration of filaments of different sizes, compositions, and functionalities into arrays suitable for various applications. Materials and components made from such composite filaments and arrays of composite filaments are also disclosed.

Provided is a method for producing an aliphatic alcohol having 8 or more and 22 or less carbon atoms through hydrogenation of a fatty acid or a fatty acid ester using a catalyst, wherein the catalyst carries a catalyst metal on a support, (a) the catalyst contains one or more elements selected from Co and Cu as the catalyst metal, (b) the total pore volume of the catalyst is 0.05 mL/g or more, and (c) the volume of pores with a pore size of 0.1 m or more and 500 m or less is 50% or more of the total pore volume of the catalyst.

The invention is concerned with catalysts for heterogeneous hydrogenation of oxo process aldehydes. The problem addressed by the invention is that of developing a catalyst containing neither chromium nor nickel. In addition, it is to enable the economically viable hydrogenation of aldehyde mixtures originating from industrial oxo processes on the industrial scale. For this purpose, the catalyst should not be reliant on costly precious metals such as Ru, Pd or Pt. This problem was solved by omitting the chromium and nickel in the preparation of a conventional Cu/Ni/Cr system, such that a catalyst wherein only copper occurs as hydrogenation-active component on the support material thereof, and not chromium or nickel, is obtained. What is surprising here is that a functioning catalyst for the purpose intended still arises at all even though two of three hydrogenation-active metals are omitted. However, this requires as necessary conditions that support material used is silicon dioxide and that the content of Cu and SiO.sub.2 in the active catalyst is set accurately within very tight limits.

A catalytic structure has a substrate and a plurality of high-entropy alloy (HEA) nanoparticles. At least a surface layer of the substrate is formed of a metal oxide. The HEA nanoparticles can be formed on the surface layer. Each HEA nanoparticle can comprise a homogeneous mixture of at least four different elements forming a single-phase solid-solution alloy. The catalytic structures can be used to catalyze a chemical reaction, such as an ammonia oxidation reaction, an ammonia synthesis reaction, or an ammonia decomposition reaction.

The present invention relates to catalysts of iron and chromium with a platinum promoter for use in water-gas shift reactions, both at low temperatures (LTS) and at high temperatures (HTS). Their characteristics of higher activity due to the addition of Pt compared to the conventional catalysts make them superior to the commercial catalysts in the same operating conditions. Because precursors of the active phase (Fe.sub.3O.sub.4) are obtained in greater quantity per unit area, it was possible to prepare catalysts that are more promising with a smaller surface area.

Disclosed is a system for managing wireless transmitting devices in which a wireless transmission from a transmission device is detected within or about a set area and an allowability of the transmission device to continue transmitting is based on an identification information, of the device, a location of the device and a number being called by the device.

The present invention relates to a high-performance polyoxometalate catalyst and a method of preparing the same. More particularly, the present invention provides a high-performance polyoxometalate catalyst, the activity and selectivity of which may be improved by controlling the content of vanadium and the like and which has superior reproducibility and may unsaturated carboxylic acid from unsaturated aldehyde in a high yield for a long time, a method of preparing the same, and the like.

A catalyst comprising a Group IIIA metal, a Group VIII noble metal, and an optional promoter metal, on a support selected from silica, alumina, silica-alumina compositions, rare earth modified alumina, and combinations thereof, doped with iron, a Group VIB metal, a Group VB metal, or a combination thereof, offers decreased reactivation time under air soak in comparison with otherwise identical catalysts. Reducing reactivation time may, in turn, reduce costs, both in inventory and capital.

An exhaust gas-purifying catalyst includes a support and a catalytic metal as one or more precious metals supported by the support. The support includes a composite oxide having a composition represented by a general formula AB.sub.C.sub.O.sub.3, wherein A represents one or more elements selected from the group consisting of lanthanum, neodymium, and yttrium, B represents iron or a combination of iron and aluminum, C represents one or more elements selected from the group consisting of iridium, ruthenium, tantalum, niobium, molybdenum, and tungsten, and each represents a numerical value within a range of more than 0 and less than 1, and and satisfy relational formulae of > and +1.

The present invention relates to a process for preparing aldehydes and ketones by carbon-carbon bond cleavage of alkenes, wherein the process is catalysed by first row transition metal nitro coordinated polyoxometalate catalyst. The catalyst can be prepared by pre-treatment of aqua coordinated polyoxometalates with NO.sub.2, or they are formed in situ when the reactions are carried in nitroalkanes under aerobic conditions, or they are formed in situ from nitrosyl (NO) compounds in the presence of O.sub.2.