A composite comprising a MXene and a post-transition metal wherein the post-transition metal is at least partially encapsulated by from 1 to 4 layers of the MXene. Methods of making such a composite are also disclosed.

A thermal interface material for transferring heat by interposing between two materials may include a graphite film. The graphite film may have a thickness of 1 μm to 50 μm, a density of 1.40 g/cm.sup.3 to 2.26 g/cm.sup.3, a thermal conductivity of 500 W/mK to 2000 W/mK in a film plane direction, and an arithmetic average roughness Ra of 0.1 μm to 10 μm on a surface of the graphite film.

The present invention relates to a particulate porous carbon material having a continuous porous structure, the particulate porous carbon material satisfying the following A to C: A: branch portions forming the continuous porous structure have an aspect ratio of 3 or higher; B: the branch portions have aggregated through joints interposed therebetween, the number of the aggregated branch portions (N) being 3 or larger; C: a ratio of the number of the aggregated branch portions (N) to the number of the joints (n), N/n, is 1.2 or larger.

Aluminum chlorohydrate salts having an amount of Peak 1 material relative based on a total of Peaks 3, 4, and 5 of at least 20% as measured by size exclusion chromatography, together with water treatment compositions, antiperspirant compositions, and oral care compositions, comprising the same, and methods for making and using the same.

A process of preparing precipitated silica is disclosed. Said process comprises of reacting an aqueous solution of a metal silicate with a mineral acid in the presence of a surfactant solution comprising gelatin and C8-C20 sulfosuccinate blend, at a reaction temperature in a range of about 70 to 100° C. with constant stirring such that a reaction mixture having a pH of about 10.Math.0.3 is obtained; optionally, allowing the reaction mixture to age at a temperature in a range of about 70 to 100° C. for a time period in range of 10 to 100 minutes; adjusting the pH of the reaction mixture to about 4, followed by aging said mixture at a temperature in a range of about 70 to 100° C. for a time period in a range of 10 minutes to 2 hours; and recovering the precipitated silica from the reaction mixture.

A method is provided for producing an article which is transparent to IR wavelength in the region of 4 μm to 9 μm. The method includes the steps of (a) Producing ultra-fine powders of ZnS, (b) followed by pretreatment of the ultra-fine powders under reduced gas conditions including H2, H2S, N2, Ar and mixtures there of (c) followed by vacuum (3×10.sup.−6 torr) treatment to remove oxygen and sulfates adsorbed to the surface disposing a plurality of nano-particles on a substrate, wherein said nanoparticles comprise ZnS with ultra-high purity of cubic phase; (b) subjecting the nano-particles to spark plasma sintering thereby producing a sintered ZnS product with IR transmission reaching 75% in the wavelength range of 4 μm to 9 μm.

Provided is hexagonal strontium ferrite powder for magnetic recording, in which an activation volume is 800 to 1,500 nm.sup.3, a content of rare earth atom with respect to 100 atom % of iron atom is 0.5 to 5.0 atom %, and a rare earth atom surface portion uneven distribution is provided.

A formulation for use in the preferential formation of thin films of a perovskite material AMX 3 with a certain required crystalline structure, wherein said formulation comprises two or more compounds which between them comprise one or more first organic cations A; one or more metalcations M; one or more second cations A′; one or more first anions X and one or more second anions X′.

The invention relates to a novel method of preparing silicas and to highly-structured silicas having the following characteristics: a specific surface area CTAB (S.sub.CTAB) of between 40 and 525 m.sup.2/g; a specific surface area BET (S.sub.BET) of between 45 and 550 m.sup.2/g; an object size distribution width Ld ((d84−D16)/d50), which is measured by XDC particle size analysis after deagglomeration with ultrasound, of at least 0.91; and a pore-size distribution such that ratio V(d5−d50)/V(d5−d100) is at least 0.66. The invention also relates to the use of said silicas as polymer reinforcing fillers.

A high-quality nitride crystal can be produced efficiently by charging a nitride crystal starting material that contains tertiary particles having a maximum diameter of from 1 to 120 mm and formed through aggregation of secondary particles having a maximum diameter of from 100 to 1000 μm, in the starting material charging region of a reactor, followed by crystal growth in the presence of a solvent in a supercritical state and/or a subcritical state in the reactor, wherein the nitride crystal starting material is charged in the starting material charging region in a bulk density of from 0.7 to 4.5 g/cm.sup.3 for the intended crystal growth.