Provided are: a material having high thermal conductivity that includes an alumina fiber sheet and a resin, wherein the material having high thermal conductivity includes 20-90% by mass of the alumina fiber sheet; and a method for producing a material having high thermal conductivity, the method including (1) a step for preparing a fiber sheet that includes an alumina source by electrostatic spinning or dry spinning in which a dispersion including an alumina source and a water-soluble polymer is used as a spinning material, (2) a step for firing the fiber sheet including an alumina source to prepare an alumina fiber sheet, and (3) a step for impregnating the alumina fiber sheet with a resin solution having a resin concentration of 10% by weight or less.

Disclosed are an inorganic nanofiber characterized in that the average fiber diameter is 2 m or less, the average fiber length is 200 m or less, and the CV value of the fiber length is 0.7 or less; and a method of manufacturing the same. In the manufacturing method, an inorganic nanofiber sheet consisting of inorganic nanofibers having an average fiber diameter of 2 m or less is formed by electrospinning, and then, the inorganic nanofiber sheet is pressed using a press machine and crushed so that the average fiber length becomes 200 m or less, and the CV value of the fiber length becomes 0.7 or less.

The invention relates to sintered abrasive particles of which the chemical composition comprises the weight concentration ranges indicated in the table, to give a total of 100%.

TABLE-US-00001 % Fe.sub.2O.sub.3 % TiO.sub.2 % CaO % MgO % SiO.sub.2 % Al.sub.2O.sub.3 0.5-2.5% 0-2% 0.5-2.5% 0.5-3% 0.5-3% 93-96.5%

A part made of oxide/oxide composite material includes fiber reinforcement constituted by a plurality of warp yarn layers and of weft yarn layers interlinked by three-dimensional weaving, with the spaces present between the reinforcing yarns being filled with a refractory oxide matrix. The fiber reinforcement presents a weave selected from the following weaves: interlock; multi-plain; multi-satin; and multi-serge, with warp and weft thread counts lying in the range 4 yarns/cm to 20 yarns/cm. The fiber reinforcement also presents a fiber volume fraction lying in the range 40% to 51%.

Disclosed are an inorganic nanofiber characterized in that the average fiber diameter is 2 m or less, the average fiber length is 200 m or less, and the CV value of the fiber length is 0.7 or less; and a method of manufacturing the same. In the manufacturing method, an inorganic nanofiber sheet consisting of inorganic nanofibers having an average fiber diameter of 2 m or less is formed by electrospinning, and then, the inorganic nanofiber sheet is pressed using a press machine and crushed so that the average fiber length becomes 200 m or less, and the CV value of the fiber length becomes 0.7 or less.

Provided herein are nanofibers and processes of preparing nanofibers. In some instances, the nanofibers are metal and/or ceramic nanofibers. In some embodiments, the nanofibers are high quality, high performance nanofibers, highly coherent nanofibers, highly continuous nanofibers, or the like. In some embodiments, the nanofibers have increased coherence, increased length, few voids and/or defects, and/or other advantageous characteristics. In some instances, the nanofibers are produced by electrospinning a fluid stock having a high loading of nanofiber precursor in the fluid stock. In some instances, the fluid stock comprises well mixed and/or uniformly distributed precursor in the fluid stock. In some instances, the fluid stock is converted into a nanofiber comprising few voids, few defects, long or tunable length, and the like.

A method of making a ceramic fiber tow and the system regarding the same may be included. The method may include commingling a plurality of ceramic fibers with a fugitive fiber to form a single ceramic fiber tow. The fugitive fiber may be positioned between at least two ceramic fibers included in the single ceramic fiber tow. The method may further include forming a porous ceramic preform including at least the single ceramic fiber tow. The method may further include removing the fugitive fiber from the ceramic fiber tow leaving a space between at least two ceramic fibers of the single ceramic fiber tow. The method may further include replacing the spaces between ceramic fibers included in the ceramic fiber tows with a ceramic matrix.

Provided herein are nanofibers and processes of preparing nanofibers. In some instances, the nanofibers are metal and/or ceramic nanofibers. In some embodiments, the nanofibers are high quality, high performance nanofibers, highly coherent nanofibers, highly continuous nanofibers, or the like. In some embodiments, the nanofibers have increased coherence, increased length, few voids and/or defects, and/or other advantageous characteristics. In some instances, the nanofibers are produced by electrospinning a fluid stock having a high loading of nanofiber precursor in the fluid stock. In some instances, the fluid stock comprises well mixed and/or uniformly distributed precursor in the fluid stock. In some instances, the fluid stock is converted into a nanofiber comprising few voids, few defects, long or tunable length, and the like.

An alumina fiber aggregate that is formed of alumina short fibers and has been subjected to needling treatment, wherein the alumina short fibers have an average fiber diameter of 6.0 m or more and 10.0 m or less and a specific surface area of 0.2 m.sup.2/g or more and 1.0 m.sup.2/g or less, and a residual percentage (%) of high-temperature-cycle opened gap pressure of the alumina fiber aggregate is 45% or more. A value obtained by subtracting twice the standard error of a length-weighted geometric mean diameter of fiber diameters of the alumina short fibers from the length-weighted geometric mean diameter is 6.0 m or more. A proportion of alumina short fibers having a fiber diameter of more than 10.0 m is preferably 5.0% or less on a number basis.

We provide methods and apparatus for preparing crystalline-clad and crystalline core optical fibers with minimal or no breakage by minimizing the influence of thermal stress during a liquid phase epitaxy (LPE) process as well as the fiber with precisely controlled number of modes propagated in the crystalline cladding and crystalline core fiber via precisely controlling the diameter of crystalline fiber core with under-saturated LPE flux. The resulting crystalline cladding and crystalline core optical fibers are also reported.