An iron-containing Chevrel phase material, contains iron and Mo.sub.6S.sub.8 clusters, in particular an iron-containing Chevrel phase material having a formula Fe.sub.xMo.sub.6S.sub.8, wherein 2≤x≤4. The iron-containing Chevrel phase provides an efficient catalyst for the electrochemical production of ammonia from water and nitrogen gas.

A method for preparing a powder comprising an intimate mixture of U.sub.3O.sub.8 particles and PuO.sub.2 particles and which may further comprise particles of ThO.sub.2 or NpO.sub.2. The method comprises: preparing, via oxalic precipitations, an aqueous suspension S.sub.1 of particles of uranium(IV) oxalate and an aqueous suspension S.sub.2 of particles of plutonium(IV) oxalate; mixing the aqueous suspension S.sub.1 with the aqueous suspension S.sub.2 to obtain an aqueous suspension S.sub.1+2; separating the aqueous suspension S.sub.1+2 into an aqueous phase and a solid phase comprising the particles of uranium(IV) oxalate and the particles of plutonium(IV) oxalate; and calcining the solid phase to convert (1) the particles of uranium(IV) oxalate to particles of triuranium octoxide and (2) the particles of plutonium(IV) oxalate to particles of plutonium(IV) dioxide, whereby the powder is obtained.

A hydrotalcite is represented by formula (1):
(M.sup.2+).sub.1-X(M.sup.3+).sub.X(OH).sub.2(A.sup.n−).sub.X/n.Math.mH.sub.2O  (1), wherein M.sup.2+ indicates a divalent metal, M.sup.3+ indicates a trivalent metal, A.sup.n− indicates an n-valent anion, n indicates an integer of 1 to 6, 0.17≤x≤0.36, and 0≤m≤10. The hydrotalcite has (A) a lattice strain in the <003> direction is 3×10.sup.−3 or less as measured using an X-ray diffraction method; (B) primary particles with an average width between 5 nm and 200 nm inclusive per a SEM method; and (C) a degree of monodispersity of 50% or greater (degree of monodispersity (%)=(average width of primary particles as measured using the SEM method/average width of secondary particles as measured using a dynamic light scattering method)×100). A resin containing the hydrotalcite, a suspension containing the hydrotalcite and a method for producing the hydrotalcite are disclosed.

The present disclosure relates to a method for producing metal oxide nanoparticles includes a first step of preparing a reaction solution containing a metal complex, an alcohol, and water; a second step of heating the reaction solution for phase-separation under a hermetically sealed atmosphere where the volumetric expansion ratio of the reaction solution reaches 5 to 15%; a third step of holding the reaction solution heated in the second step for 30 minutes or more for dehydrating the metal complex to precipitate the metal oxide nanoparticles; and a fourth step of collecting the metal oxide nanoparticles after the metal oxide nanoparticles are cooled.

A porous carbon material, wherein a half width (2θ) of a diffraction peak (10×) (38° to 49°) by X-ray diffraction is 4.2° or less, and wherein a ratio (mesopore volume/micropore volume) of a mesopore volume (cm.sup.3/g) measured by a BJH method to a micropore volume (cm.sup.3/g) measured by a HK method is 1.20 or more.

Disclosed are apparatus and method for preparing carbon black, in which the carbon black may be continuously formed and activated. In one embodiment, carbon black powders formed in a combustion reactor are converted into a slurry which in turn is refluxed to the combustion reactor in a repeated manner, thereby to allow successive activation treatments. In this way, a sufficient residence time for the activation of the carbon black may be secured.

The present invention is characterized by including an aromatic vinyl-based copolymer, glass fiber, and zinc oxide, wherein the zinc oxide has an average particle size (D50) of about 0.5 to 3 μm as measured by a particle size analyzer, and a size ratio (B/A) of peak B, spanning the range of 450 to 600 nm, to peak A, spanning the range of 370 to 390 nm, of about 0.01 to 1.0 when measuring photoluminescence. The thermoplastic resin composition exhibits excellent rigidity, antibacterial properties, weather resistance, external appearance and the like.

This present invention provides a microporous carbon nanospheres, method for synthesizing and activating thereof, the method comprising: adding and mixing well deionized water, absolute ethanol, triblock copolymer, ammonia solution, resorcinol and formaldehyde solution; separating solid and liquid of the mixture solution, then drying the separated solid substrate to have a dried solid substrate; sintering the dried solid substrate surrounding by nitrogen twice and collecting microporous carbon nanospheres after cooling down. Further sintering to activate these microporous carbon nanospheres surrounding by carbon dioxide, and collecting activated microporous carbon nanospheres after cooling down. Microporous carbon nanospheres and activated microporous carbon nanospheres synthesized by this present invention have spherical structure, small size and high the specific surface area, and the process is simplified, cost-effective and environment-friendly.

A silicon material can include a silicon aggregate comprising a plurality of porous silicon nanoparticles welded together. The silicon aggregate can optionally have a polyhedral morphology. A method can include: receiving a plurality of porous silicon nanoparticles and cold welding the plurality of porous silicon nanoparticles into an aggregated silicon particle.

Nitric oxide (NO) generating compositions can include a nitrite component, an acidifying component, and a support material configured to carry one of the nitrite component and the acidifying agent. In some examples, the support material can minimize NO generation prior to addition of an activating amount of a suitable solvent.