A photoreactor having computer actuated input/output ports is operated by introducing reactant through an input port and collecting product through an output port, and upon closure of the input and output ports, treating photocatalyst within the photoreactor to remove intermediates limiting performance of the photocatalyst. Once the photocatalyst is regenerated, introduction of reactant to the photoreactor through the input port and collection of product from the output port can be resumed. The automated process does not require removal of catalyst from the photoreactor and significantly improves process economics.

A filtering system includes a catalyst filter including a plurality of channels through which air is introduced, and a light-emitting device arranged to irradiate light to the catalyst filter for catalyst activation, where the light-emitting device includes a light source array including a plurality of first light sources corresponding one-to-one with the plurality of channels. Each of the plurality of first light sources may include a substrate, a first light-emitting device on the substrate, and a capsule which seals the first light-emitting device on the substrate. Only one first light-emitting device is provided in the capsule, or a second light-emitting device is further provided together with the first light-emitting device in the capsule.

Embodiments of the present invention include a filter element for decomposing contaminants including a substrate, and a photocatalytic composition comprising at least a photocatalyst and a co-catalyst. The embodiments of the present invention also includes a system for decomposing contaminants including a substrate, and a photocatalytic composition comprising at least a photocatalyst and a co-catalyst; and a method using the system.

Use of Keplerate type polyoxomolybdates of the general structure Mo.sub.72M.sub.30, wherein M is selected from the group consisting of Fe, Cr, V or Mo.sub.2, for decontaminating aqueous media (water) from inorganic and organic pollutants.

The system includes a robot multi-jet system having a spray section, a drier section, and a catalyst section. The drier section includes a warm air blower, the catalyst section includes a photocatalyst tank, and the spray section includes a plurality of jet extensions. A first jet extension connected to the photocatalyst tank sprays a uniform layer of a photocatalyst through a first set of jets, and a second jet extension that is mechanically connected to the drier section and in fluid communication with the warm air blower is configured to spray a gas onto an inner surface of the glass tube with a second set of jets. Both the drier section and the catalyst section are mounted on wheels to move the system on the inner surface of the glass tube. A motor is electrically connected to a battery mounted within the robot and mounted to the wheels.

Described herein are covalent organic frameworks. The covalent organic frameworks have unique structural and physical properties, which lends them to be versatile in a number of different applications and uses. In one aspect, the covalent organic frameworks are composed of a plurality of fused aromatic groups and electron-deficient chromophores. The covalent organic frameworks are useful as photocatalysts in a number of different applications.

A composition for coating an overhead conductor is disclosed comprising: (i) a reflective agent; (ii) a photocatalytic 0 agent comprising ≥70 wt % anatase titanium dioxide (TiO.sub.2) having an average particle size (“aps”)≤100 nm; (iii) a polyorganosiloxane binder; and (iv) a superhydrophobic agent comprising either: surface functionalised silica nanoparticles, a functional polysiloxane or a polymethylsilsesquioxane.

An embodiment of the present invention provides a MXene nanodot core-carbon shell multifunctional catalyst including a MXene nanodot core and a carbon shell surrounding the MXene nanodot core. By introducing the carbon shell surrounding the nanodot core, the stability of the catalyst is ensured, thereby providing effects in that the catalyst may function under various conditions.

Provided is a p-type TiO.sub.2/n-type WO.sub.3 heterojunction catalyst and a preparation method and use thereof. The catalyst comprises p-type TiO.sub.2 and n-type WO.sub.3 supported on a surface of the p-type TiO.sub.2.

The present disclosure provides a quantum-dot ligand, a quantum-dot catalyst and a quantum-dot device. The quantum-dot ligand includes: a first ligand having a first group and a second group and a second ligand having an inorganic ion, in which a coordination bond is formed between the first group and a surface of a quantum dot, a hydrogen bond is formed between the second group and a hydroxyl group; and a coordination bond is formed between the inorganic ion and the surface of the quantum dot. The quantum-dot catalyst of the present disclosure can enhance a catalytic activity of the quantum dots and improve the catalytic performance.