The present invention provides: a fibrous carbon characterized in that the average effective fiber length is 1-100 μm, and the crystallite length (La) measured using X-ray diffraction is 100-500 nm; an electrode mixture layer for a non-aqueous-electrolyte secondary cell, said mixture comprising an electrode active material and a carbon-based electroconductive auxiliary agent containing said fibrous carbon; an electrode for a non-aqueous-electrolyte secondary cell, the electrode comprising a collector and said electrode mixture layer for a non-aqueous-electrolyte secondary cell, the electrode mixture layer being laminated on the collector; and a non-aqueous-electrolyte secondary cell having said electrode for a non-aqueous-electrolyte secondary cell.

A method of forming high molecular weight (“HMW”) coal tar can include combining supercritical carbon dioxide (sCO.sub.2) and an amount of coal tar, and fractionating the amount of coal tar to form the HMW coal tar. The method can further include forming the amount of coal tar from coal. Forming the amount of coal tar from coal can include extracting the coal tar from an amount of coal using sCO.sub.2.

The present disclosure relates to a process for preparing carbon fibers. The process involves blending a carbon nano-material with a carbon material to obtain a homogenous blend, heating the homogenous blend to obtain mesophase pitch having particles with reduced mesophase sphere size followed by spinning the mesophase pitch to obtain the pitch fibers. The pitch fibers are then carbonized to obtain the carbon fibers. The carbon fibers prepared by the process of the present disclosure have improved tensile properties as compared to the conventional pitch based carbon fibers.

The present disclosure relates to a process for preparing carbon fibers. The process involves blending a carbon nano-material with a carbon material to obtain a homogenous blend, heating the homogenous blend to obtain mesophase pitch having particles with reduced mesophase sphere size followed by spinning the mesophase pitch to obtain the pitch fibers. The pitch fibers are then carbonized to obtain the carbon fibers. The carbon fibers prepared by the process of the present disclosure have improved tensile properties as compared to the conventional pitch based carbon fibers.

A method for forming mesophase pitch can include applying a stimulus to a first amount of coal tar to form a first amount of mesophase pitch. The stimulus can include one or more of an electromagnetic field (“EMF”) or a magnetic field. The method can further include evaluating a characteristic of the first amount of mesophase pitch, changing a parameter of the stimulus in response to evaluating the characteristic of the first amount of mesophase pitch, and applying the stimulus exhibiting the changed parameters to a second amount of coal tar to form mesophase pitch.

A method of forming high molecular weight (“HMW”) coal tar can include combining supercritical carbon dioxide (sCO.sub.2) and an amount of coal tar, and fractionating the amount of coal tar to form the HMW coal tar. The method can further include forming the amount of coal tar from coal. Forming the amount of coal tar from coal can include extracting the coal tar from an amount of coal using sCO.sub.2.

A method of producing advanced carbon materials can include providing coal to a processing facility, beneficiating the coal to remove impurities from the coal, processing the beneficiated coal to produce a pitch, and treating the pitch to produce an advanced carbon material such as carbon fibers, carbon nanotubes, graphene, resins, polymers, biomaterials, or other carbon materials.

A method of producing advanced carbon materials can include providing coal to a processing facility, beneficiating the coal to remove impurities from the coal, processing the beneficiated coal to produce a pitch, and treating the pitch to produce an advanced carbon material such as carbon fibers, carbon nanotubes, graphene, resins, polymers, biomaterials, or other carbon materials.

Disclosed are a method of preparing polyaromatic oxide and polyaromatic oxide prepared thereby, wherein the method includes (a) placing a plurality of kinds of polyaromatic hydrocarbons and water in a reactor and then stirring them; (b) increasing the temperature inside the reactor to 150 to 300° C. and then feeding a gas containing 10 wt % or more of oxygen into the reactor to increase the partial pressure of oxygen inside the reactor to 2 to 30 bar; and (c) reacting the plurality of kinds of polyaromatic hydrocarbons with oxygen to oxidize the plurality of kinds of polyaromatic hydrocarbons.

Disclosed are a method of preparing polyaromatic oxide and polyaromatic oxide prepared thereby, wherein the method includes (a) placing a plurality of kinds of polyaromatic hydrocarbons and water in a reactor and then stirring them; (b) increasing the temperature inside the reactor to 150 to 300° C. and then feeding a gas containing 10 wt % or more of oxygen into the reactor to increase the partial pressure of oxygen inside the reactor to 2 to 30 bar; and (c) reacting the plurality of kinds of polyaromatic hydrocarbons with oxygen to oxidize the plurality of kinds of polyaromatic hydrocarbons.