A porous carbon material composite formed of a porous carbon material and a functional material and equipped with high functionality. The porous carbon material composite is formed of (A) a porous carbon material obtainable from a plant-derived material having a silicon (Si) content of 5 wt % or higher as a raw material; and (B) a functional material adhered on the porous carbon material, and has a specific surface area of 10 m.sup.2/g or greater as determined by the nitrogen BET method and a pore volume of 0.1 cm.sup.3/g or greater as determined by the BJH method and MP method.

Provided are catalyst particles for treating vehicle exhaust gas, containing semiconductor nanoparticles supported by noble metals.

The inventive concepts disclosed relate to the production of green and blue hydrogen from hydrocarbons using visible light (from a laser, lamp or sun) and defect-engineered boron-rich photocatalysts. We demonstrate that the environment of the B atoms in the lattice can be tuned to favor the dehydrogenation of desired hydrocarbons on reaction sites under visible light. In addition to the hydrogen produced in gas form, carbon atoms are captured by the catalyst and form structures of potential higher value for future applications. Further study of the dark carbonaceous product revealed a graphitic aspect of the material. These findings highlight a new functionality of 2D materials for visible light-assisted capture and conversion of hydrocarbons, with great potential for green hydrogen production—i.e, hydrogen produced from renewable energy and without the release of CO or CO.sub.2.

A lanthanum molybdenum composite oxide is provided. The lanthanum molybdenum composite oxide has a primary crystal phase formed of La.sub.2Mo.sub.2O.sub.9. The lanthanum molybdenum composite oxide also has a secondary crystal phase formed of a lanthanum molybdenum composite oxide species other than La.sub.2Mo.sub.2O.sub.9. The secondary crystal phase may contain at least one species selected from a group consisting of La.sub.2Mo.sub.3O.sub.12, La.sub.6MoO.sub.12, La.sub.7Mo.sub.7O.sub.30, La.sub.2Mo.sub.4O.sub.15, La.sub.2MoO.sub.6, La.sub.4MoO.sub.9, and LaMo.sub.2O.sub.5.

An air sanitizer unit that includes a housing, a substrate, and a light source. The substrate is provided in an interior space of the housing and includes at least one photocatalytic coating on at least one surface that extends along a flow path of airflow through the air sanitizer unit. The light source is disposed within the interior space of the housing in a way such that light produced by the light source activates the at least one photocatalytic coating to purify the airflow. Further, the substrate includes channels for allowing airflow there through, in which a substrate structure defining the channels include the photocatalytic coating and the substrate structure defining the channels is configured such that microbes in the airflow are captured on the least one photocatalytic coating at low airflow rates, in which the low airflow rates are airflow rates less than 20 air changes per hour.

Water purification particles have porous particles and photocatalyst particles formed of titanium-based compound particles that are supported on the porous particles, have absorption at a wavelength of 500 nm in a visible absorption spectrum, and have an absorption peak at 2,700 cm.sup.−1 to 3,000 cm.sup.−1 in an infrared absorption spectrum, and a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom.

Disclosed herein is a method of treating an aqueous solution containing impurities including a perfluoroalkyl substance and/or a polyfluoroalkyl substance, comprising introducing the aqueous solution into a batch or semi-batch photocatalytic reactor with a microparticulate catalyst configured to reduce chain length of the perfluoroalkyl substance and/or polyfluoroalkyl substance, forming a treated aqueous stream, the reactor including a catalyst flow controller configured to automatically increase the catalyst concentration in the reactor while agitating the catalyst-containing solution during reaction, and removing catalyst particles from the treated aqueous stream to form a purified aqueous stream. In some cases, the feed to the reactor is atomized. Corresponding systems also are disclosed.

In a photocatalytic device, a photocatalytic filter is formed of a corrugated member and a gas is allowed to flow over front and rear surfaces of the filter from one end toward the other end thereof along a direction in which ridges and valleys extend, and a gas inflow part and a gas outflow part are provided at both end positions of a photocatalytic filter instead of providing a gas inlet-side flow channel and a gas output-side flow channel at positions facing filter surfaces. Thus, a contact area between a gas and the filter surfaces can be maintained, and miniaturization of the device such as reduction in the thickness or diameter can be realized without increasing gas circulation resistance. In addition, enhanced light irradiation efficiency, simplified structure, energy saving, and cost reduction can be realized. Moreover, the problem of heat can be solved.

A plasmonic nanoparticle catalyst for producing hydrocarbon molecules by light irradiation, which comprises at least one plasmonic provider and at least one catalytic property provider, wherein the plasmonic provider and the catalytic property provider are in contact with each other or have distance less than 200 nm, and molecular composition of the hydrocarbon molecules produced by light irradiation is temperature-dependent. And a method for producing hydrocarbon molecules by light irradiation utilizing the plasmonic nanoparticle catalyst.

Provided is a titanium oxide particle dispersion liquid with an inhibited photocatalytic activity and a low level of coloration. Titanium oxide particles in this dispersion liquid contain:

(1) a tin component; and

(2) a manganese component and/or a cobalt component,

wherein only the tin component is solid-dissolved in the titanium oxide particles, and the manganese component and/or the cobalt component are each contained by an amount of 5 to 5,000 in terms of a molar ratio to titanium (Ti/Mn and/or Ti/Co).