Provided are a superatomic material, as well as a sol, a preparation method therefor, and application thereof. The superatomic material comprises a carrier and superatoms doped in the carrier, the superatoms being one or more of silver, copper, zinc superatoms and rare earth element superatoms, the scale of superatoms being 100-3000 pm, and the carrier being an inorganic carrier. The superatomic material and the sol have superior antimicrobial and antiviral properties, have a long service life, and are environmentally friendly.

Provided are a superatomic material, as well as a sol, a preparation method therefor, and application thereof. The superatomic material comprises a carrier and superatoms doped in the carrier, the superatoms being one or more of silver, copper, zinc superatoms and rare earth element superatoms, the scale of superatoms being 100-3000 pm, and the carrier being an inorganic carrier. The superatomic material and the sol have superior antimicrobial and antiviral properties, have a long service life, and are environmentally friendly.

An oxidation catalyst composition is provided, the composition including a plurality of platinum group metal particles having a multi-modal distribution of particle sizes. The plurality of platinum group metal particles includes a first population of platinum group metal particles having a range of particle sizes of from about 0.5 nm to about 3 nm, and a second population of platinum group metal particles having a range of particle sizes of from about 4 nm to about 15 nm. Methods for the preparation and use of the catalyst composition are also provided, as well as catalyst articles and emission gas treatment systems employing such catalyst articles. The catalyst exhibits enhanced stability with respect to oxidation performance after degreening and/or aging, as compared to conventional oxidation catalysts, in particular less loss of NOx oxidation performance.

A method of manufacturing a catalyst article, the method comprising: providing a complex of a humic acid or derivative thereof, and a PGM; providing a support material; applying the complex to the support material to form a loaded support material; disposing the loaded support material on a substrate; and heating the loaded support material to form nanoparticles of the PGM on the support material.

The devices, systems and techniques disclosed in this patent document include photocatalytic filter devices and can be used to provide a method for manufacturing a photocatalytic filter with improved adhesion. In addition, the present disclosure of this patent document includes technology to provide a method for reactivating a photocatalytic filter. Using the disclosed techniques, even if a photocatalytic filter is contaminated, the contaminated photocatalytic filter is easily reactivated while maintaining improved adhesion.

A process for preparing a titanic acid salt, titanic acid, and titanium oxide having a controllable particle size and a hierarchical structure, wherein the process includes the steps of: preparing a titanium-containing peroxo-complex solution; adding a basic metal compound to the titanium-containing peroxo-complex solution to form a mixture solution; adding one of polyvinyl alcohol, hydroxypropyl methyl cellulose, and polyethylene glycol to the mixture solution to form a precursor dispersion; and subjecting the precursor dispersion to a solvothermal reaction to obtain the titanic acid salt having a hierarchical structure. The process for preparing a titanic acid salt, titanic acid, and titanium oxide having a controllable particle size and a hierarchical structure, can not only realize the regulation of morphology and particle diameter of constituent units in the hierarchical structure, but also can achieve the regulation of particle size in the hierarchical structure.

The present invention relates to a catalytic material for the preparation of one or more of 4,4′-methylenedianiline, 2,2′-methylenedianiline, 2,4′-methylenedianiline, and oligomers of two or more thereof, the catalytic material comprising an oxidic support, wherein the oxidic support comprises an element E.sub.OS1 selected from the group consisting of Ti, Zr, Al, Si, and mixtures of two or more thereof, and further comprising a supported material supported on the oxidic support, wherein the supported material comprises an element E.sub.SM1 selected from the group consisting of Ti, Zr, V, Nb, Ta, Mo, W, Ge, Sn, Sc, Y, La, Ce, Nd, Pr, Hf, Cr, Fe, Co, Ni, Cu Zn, Pb and mixtures of two or more thereof. Further, the present invention relates in particular to a process for the preparation of a catalytic material and to a process for the preparation of one or more of 4,4′-methylenedianiline, 2,2′-methylenedianiline, 2,4′-methylenedianiline and oligomers of two or more thereof.

Provided are self-binding suspensions and coated substrates prepared using self-binding suspensions. Also provided are methods of preparing self-binding suspensions. Methods may include preparing a binder solution; preparing a titanium dioxide-zinc oxide suspension using ultrasonication; mixing the binder solution with the titanium dioxide-zinc oxide suspension and a surfactant to form a self-binding suspension composition; and coating a glass substrate with the self-binding suspension composition to form a coated glass substrate.

The invention refers to a method for manufacturing a catalytic device, with the steps: a) providing a first catalyst having photocatalytic activity, a second catalyst, which is a different molecule than the first catalyst, and an adsorbent, each in a powdered state, b) mingling the first catalyst, the second catalyst and the adsorbent to form a catalytic composition and suspending them in a suspension liquid to form a slurry, and c) repeatedly coating the slurry onto a solid grid-like carrier having a plurality of through holes, configured to allow a gas to flow through the carrier, and evaporating the suspension liquid.

Disclosed herein is a fungicide, including a porous carbon material and a silver member adhered to the porous carbon material, wherein a value of a specific surface area based on a nitrogen BET, namely Brunauer, Emmett, and Teller method is equal to or larger than 10 m.sup.2/g, and a volume of a fine pore based on a BJH, namely Barrett, Joyner, and Halenda method and an MP, namely Micro Pore method is equal to or larger than 0.1 cm.sup.3/g.