Polysilocarb formulations, cured and pyrolized materials, was well as articles and use for this material. In particular pyrolized polysilocarb ceramic materials and articles contain these materials where, the ceramic has from about 30 weight % to about 60 weight % silicon, from about 5 weight % to about 40 weight % oxygen, and from about 3 weight % to about 35 weight % carbon, and wherein 20 weight % to 80 weight % of the carbon is silicon-bound-carbon and 80 weight % to about 20 weight % of the carbon is free carbon.

Nanocomposite silicon and carbon compositions. These compositions can be made from polymer derived ceramics, and in particular, polysilocarb precursors. The nanocomposite can have non-voids or be nano-void free and can form larger macro-structures and macro-composite structures. The nanocomposite can contain free carbon domains in an amorphous SiOC matrix.

Nanocomposite silicon and carbon compositions. These compositions can be made from polymer derived ceramics, and in particular, polysilocarb precursors. The nanocomposite can have non-voids or be nano-void free and can form larger macro-structures and macro-composite structures. The nanocomposite can contain free carbon domains in an amorphous SiOC matrix.

The present invention relates to a 2-dimensional MXene particle surface-modified with a functional group comprising a saturated or unsaturated hydrocarbon, a preparation method thereof, and a use thereof (e.g., a conductive film).

The present invention relates to a 2-dimensional MXene particle surface-modified with a functional group comprising a saturated or unsaturated hydrocarbon, a preparation method thereof, and a use thereof (e.g., a conductive film).

A dielectric welding film capable of achieving a tight welding through a short period of dielectric heating, and a welding method using the dielectric welding film are provided. The dielectric welding film is configured to weld a pair of adherends of the same material or different materials through dielectric heating, the dielectric welding film including a thermoplastic resin as an A component and a dielectric filler as a B component and satisfying the conditions (i) and (ii): (i) a melting point or softening point measured in accordance with JIS K 7121 (1987) is in a range from 80 to 200 degrees C.; and (ii) heat of fusion measured in accordance with JIS K 7121 (1987) is in a range from 1 to 80 J/g.

A problem to be solved by the present invention is that there is no method for forming a dense structure on a porous structure at low cost. In addition, another object is to provide a high quality and inexpensive structure of a brittle material and a laminate thereof as an intermediate layer for facilitating formation of a dense structure on a porous structure. A structure is provided having a brittle particle assembly having a plurality of brittle particles, wherein the brittle particle assemblies are arranged adjacently to each other, and the brittle particles having a brittle material region in the periphery are crosslinked (connected) by the brittle material region to bond the brittle particles to each other, and thereby form a brittle material crosslinked structure region preventing the mobility of the brittle particles.

A problem to be solved by the present invention is that there is no method for forming a dense structure on a porous structure at low cost. In addition, another object is to provide a high quality and inexpensive structure of a brittle material and a laminate thereof as an intermediate layer for facilitating formation of a dense structure on a porous structure. A structure is provided having a brittle particle assembly having a plurality of brittle particles, wherein the brittle particle assemblies are arranged adjacently to each other, and the brittle particles having a brittle material region in the periphery are crosslinked (connected) by the brittle material region to bond the brittle particles to each other, and thereby form a brittle material crosslinked structure region preventing the mobility of the brittle particles.

A vulcanizing agent-modified graphene prepared through an in-situ chemical deposition process and a controllable crosslinked natural rubber composite containing the same. In the preparation of the vulcanizing agent-modified graphene, graphene oxide is coated on a spherical thermal-conductive functional particle through the chemical bonding to obtain a 3D graphene particle; and a vulcanizing agent is adsorbed on the 3D graphene particle through π-π conjugation by an in-situ chemical deposition process to obtain a vulcanizing agent-modified graphene particle. Further, the vulcanizing agent-modified graphene particle is mixed with natural rubber latex, and undergoes synergistic coagulation in water to form a graphene masterbatch, which is further processed into the controllable crosslinked natural rubber composite by adding a certain amount of natural rubber block, rubber additive and reinforcing filler.

A vulcanizing agent-modified graphene prepared through an in-situ chemical deposition process and a controllable crosslinked natural rubber composite containing the same. In the preparation of the vulcanizing agent-modified graphene, graphene oxide is coated on a spherical thermal-conductive functional particle through the chemical bonding to obtain a 3D graphene particle; and a vulcanizing agent is adsorbed on the 3D graphene particle through π-π conjugation by an in-situ chemical deposition process to obtain a vulcanizing agent-modified graphene particle. Further, the vulcanizing agent-modified graphene particle is mixed with natural rubber latex, and undergoes synergistic coagulation in water to form a graphene masterbatch, which is further processed into the controllable crosslinked natural rubber composite by adding a certain amount of natural rubber block, rubber additive and reinforcing filler.