A method for producing silicon carbide directly from comminuted coal and a silicon precursor is described. The process includes coating comminuted coal with a silicon precursor and heating the silicon precursor coated comminuted coal to initially form polymerized preceramic silicon-carbon foam and then further heating to form silicon carbide foam.

A method for producing silicon carbide directly from comminuted coal and a silicon precursor is described. The process includes coating comminuted coal with a silicon precursor and heating the silicon precursor coated comminuted coal to initially form polymerized preceramic silicon-carbon foam and then further heating to form silicon carbide foam.

A method for producing a siliconized carbon foam with regions of silicon carbide directly from comminuted coal and particulate silicone resin precursor is described. The process includes blending a comminuted coal and particulate silicone resin and heating the blended mixture to form a siliconized carbon foam and then further heating to form regions of silicon carbide.

A method for producing a siliconized carbon foam with regions of silicon carbide directly from comminuted coal and particulate silicone resin precursor is described. The process includes blending a comminuted coal and particulate silicone resin and heating the blended mixture to form a siliconized carbon foam and then further heating to form regions of silicon carbide.

The invention relates to processes for making improved ultra-high performance concrete with plasma-treated inclusions and articles made from the same. The invention includes a process for producing silicon carbide and multiwalled carbon nanotubes by heating agricultural waste husks in an inert atmosphere to a temperature higher than 1300 degrees C. to obtain a mixture containing silicon carbide and MWCNTs, and treating the mixture to extract the silicon carbide and MWCNTs for use as microinclusions in ultra high performance concrete.

Organosilicon chemistry, polymer derived ceramic materials, and methods. Such materials and methods for making polysilocarb (SiOC) and Silicon Carbide (SiC) materials having 3-nines, 4-nines, 6-nines and greater purity. Processes and articles utilizing such high purity SiOC and SiC.

Organosilicon chemistry, polymer derived ceramic materials, and methods. Such materials and methods for making polysilocarb (SiOC) and Silicon Carbide (SiC) materials having 3-nines, 4-nines, 6-nines and greater purity. Processes and articles utilizing such high purity SiOC and SiC.

Organosilicon chemistry, polymer derived ceramic materials, and methods. Such materials and methods for making polysilocarb (SiOC) and Silicon Carbide (SiC) materials having 3-nines, 4-nines, 6-nines and greater purity. Processes and articles utilizing such high purity SiOC and SiC.

Organosilicon chemistry, polymer derived ceramic materials, and methods. Such materials and methods for making polysilocarb (SiOC) and Silicon Carbide (SiC) materials having 3-nines, 4-nines, 6-nines and greater purity. Processes and articles utilizing such high purity SiOC and SiC.

The present invention relates to an intermediate for preparing porous silicon oxycarbide, a method of preparing the same, and a lithium secondary battery including porous silicon oxycarbide prepared from the same as a negative electrode active material. According to the present invention, since an intermediate prepared by adding a polyhedral oligomeric silsesquioxane (POSS) to a reaction mixture for preparing silicon oxycarbide, which is composed of a polysiloxane polymer and an aromatic compound, is pyrolyzed to prepare porous silicon oxycarbide (SiOC), although the content of a free carbon region is lower compared to conventional silicon oxycarbide, the cage structure of the POSS is maintained in the pyrolysis to form many pores uniformly distributed in the SiOC matrix, and thus rapid diffusion of electrolyte ions is possible, and because the contents of SiO.sub.3C and SiO.sub.2C.sub.2 in the SiOC matrix are increased, a reversible capacity in the Si—O—C phase can be enhanced.