Described herein are heterogeneous materials comprising a mixture of a first n-type semiconductor and a second n-type semiconductor. The first n-type semiconductor may be a single or plural phase TiO.sub.2 material. The second n-type semiconductor includes a metal titanate and/or a noble metal. Upon activation with ultraviolet light, the photocatalytic material mixtures described herein efficiently decompose volatile chemical compounds. Furthermore, the photocatalytic materials disclosed herein are observably more stable, relative to known semiconductor materials, to inactivation by deposition.

The present invention provides a method of producing a honeycomb structured body having excellent mechanical strength. The present invention relates to a method of producing a honeycomb structured body including a honeycomb fired body in which multiple through-holes are arranged longitudinally in parallel with one another with a partition wall therebetween, the method including: a raw material mixing step of preparing a raw material paste containing ceria-zirconia composite oxide particles, alumina particles, an inorganic binder, and alumina fibers; a molding step of molding the raw material paste into a honeycomb molded body in which multiple through-holes are arranged longitudinally in parallel with one another with a partition wall therebetween; a drying step of drying the honeycomb molded body obtained in the molding step; and a firing step of firing the honeycomb molded body dried in the drying step into a honeycomb fired body, wherein the percentage of amorphous alumina fibers in the alumina fibers for use in the raw material mixing step is 50 to 100 wt %.

The present invention provides a method of producing a honeycomb structured body having excellent mechanical strength. The present invention relates to a method of producing a honeycomb structured body including a honeycomb fired body in which multiple through-holes are arranged longitudinally in parallel with one another with a partition wall therebetween, the method including: a raw material mixing step of preparing a raw material paste containing ceria-zirconia composite oxide particles, alumina particles, an inorganic binder, and inorganic fibers; a molding step of molding the raw material paste into a honeycomb molded body in which multiple through-holes are arranged longitudinally in parallel with one another with a partition wall therebetween; a drying step of drying the honeycomb molded body obtained in the molding step; and a firing step of firing the honeycomb molded body dried in the drying step into a honeycomb fired body, wherein the raw material mixing step includes pre-mixing of the inorganic binder and the inorganic fibers.

A LED ultraviolet germicidal lamp includes a bracket, a power box, a driving light source, a heat sink, an ultraviolet light source, a lampshade, a quartz glass, a catalyst gauze, and a lamp frame. The bracket is connected to the heat sink, and the power box and the driving light source are provided in the bracket in sequence from outside to inside. The driving light source is provided in the power box and is connected to the power box by bolts. The heat sink is connected to the power box and is provided at a lower end of the power box. Titanium dioxide is used as the catalyst and is catalyzed by the UVC light source. Hydroxyl radicals produced when nanoscale titanium dioxide catalyst gauze is exposed to the UVC light source destroy bacteria and viruses.

The present invention relates to a method for producing a support at least micrometric in size, photocatalytically active and at least in the visible range, containing nanocrystals each composed of from 80 to 100 mol % of TiO.sub.2 and from 0 to 20 mol % of at least one other metal or semi-metallic oxide, comprising the following steps, from an acidic aqueous reaction medium, at a heating temperature of between 20 and 60° C.: a step of adding the titanium oxide precursor, or a mixture of the titanium oxide precursor and the precursor of the other oxide, in the acidic aqueous reaction medium, and a condensation step on or inside the support, by spraying onto the support or immersing the support in the aqueous reaction medium, for a specific period of condensation, a heating step, the support allowing the nanocrystals to be crystallized, without using surfactant, in the aqueous reaction medium, a step of rinsing with water and a recovery step on the one hand of the support on which the crystallization took place, these nanocrystals being attached by covalent bonds to the support, and on the other hand of a residual solution.

The present disclosure relates to an isomerization method of a cyclohexane dicarboxylic acid (CHDA) and, more specifically, to a method for preparing a trans-cyclohexane dicarboxylic acid (t-CHDA) from a cis-cyclohexane dicarboxylic acid (c-CHDA) by means of catalytic isomerization.

Particularly, an embodiment of the present disclosure provides a method for preparing, in high efficiency and high yield and at a low cost, a CHDA having a high t-CHDA content from a CHDA mainly containing c-CHDA, by using an isomerization catalyst containing zirconia and having a BET specific surface area of 50 m.sup.2/g or more.

An electronic device includes a first image sensor, a second image sensor, one or more image processing modules, and a display. The first image sensor generates first image data. The second image sensor generates second image data. The one or more image processing modules process one or more image data among the first image and the second image data. The display displays the one or more image data among the first image data or second image data processed by the one or more image processing modules. The thumbnail generation module generates thumbnail data using the one or more image data among the first image data and second image data processed by the one or more image processing modules. A method includes converting the plurality of image data into a format displayable on a display, and generating thumbnail data using the image data of the displayable format.

A photo catalytic filter is configured such that a plurality of plate-shaped members on which a photocatalyst is carried face each other with a gap therebetween, and the gaps form an air flow path. Each plate-shaped member has end surfaces respectively on an air entrance side and an air exit side of the gap. A UV irradiation unit faces the end surfaces on at least one of the air entrance side and the air exit side of the plate-shaped members, and is a predetermined distance away from those end surfaces. An air supply path for taking air from a lateral direction substantially parallel to the end surfaces, and supplying the air to the flow path, or an air discharge path for discharging the air exiting the flow path to a lateral direction substantially parallel to the end surfaces, is formed between the UV irradiation unit and the end surfaces of the plate-shaped members.

The present invention provides an exhaust gas purification catalyst including an alkaline earth metal supported in a highly dispersed state on a porous carrier. A catalyst layer of the exhaust gas purification catalyst provided by the invention has an alkaline earth metal-supporting region including a porous carrier, a catalyst metal belonging to the platinum group, and a sulfate of at least one type of alkali earth metal supported on the porous carrier. In a cross-section of this region, a Pearson correlation coefficient R.sub.Ae/M is at least 0.5 as calculated using α and β for each pixel obtained by carrying out area analysis by FE-EPMA under conditions of pixel size of 0.34 μm×0.34 μm, and measured pixel number 256×256, and by measuring the characteristic X-ray intensity (α:cps) of the alkaline earth metal element (Ae) and the characteristic X-ray intensity (β:cps) of the main constituent element of the inorganic compound constituting the porous carrier for each pixel.

Embodiments of the present disclosure are directed to a process for modifying catalysts comprising introducing a precursor agent and hydrogen gas to a conversion reactor; contacting the precursor agent with a conversion catalyst in the conversion reactor, thereby producing an active agent; introducing the active agent to a production reactor; and contacting the active agent with a hydroprocessing catalyst in the production reactor, thereby producing a modified hydroprocessing catalyst.