Spherical ceramic-glass nanocomposite dielectrics made from ceramics and glasses that are separately pre-milled by mechanical ball milling using selected ball-to-powder weight ratios and combined to form a mixture that is ball milled. A stable liquid suspension of the milled mixture including an added dispersant such as polyacrylic acid to improve uniformity is spray dried through a nozzle and recovered product is annealed. The novel dielectrics have a microstructure where ceramic primary particles are uniformly distributed and fully embedded in a glass matrix. The dielectrics have a mean particle size of about 1-20 um and a sphericity of about 0.8 or higher which are suitable for fabricating multilayer ceramic capacitors for high temperature applications. The novel dielectrics afford decreased sintering temperature, enhanced breakdown strength, lower dielectric lose tangent, and lower costs. Calcium titanate zirconate with manganese-doping-based or barium titanate-based dielectric ceramics and alkali-free borosilicate glass produce superior nanocomposite dielectrics.

There is disclosed herein processes and systems for forming fiber-reinforced ceramic composite structures which, contrary to conventional methods, directly deposit a ceramic fiber composite on a working surface. The processes and systems enable the printing of ceramic fiber composite structures having complex shapes and allow for multiple fiber-matrix material combinationsso far not possible with conventional approaches. In addition, the systems and process described herein enable the printing of ceramic fiber composites on complex 3D surfaces, such as gas turbine components.

A method of producing a ceramic matrix composite material component is provided. The method includes that steps of: a) producing a preform having one or more ceramic constituents, the preform being porous with internal voids; and b) applying at least one layer of a first material to the preform using an atomic layer deposition (ALD) process to decrease a porosity of the preform.

A metal oxide macroscopic fiber and a preparation method thereof, the method including: adding, as a spinning dope, an anionic metal oxide aqueous colloidal solution into wet spinning equipment, extruding the spinning dope from the spinning equipment into a thread, injecting the extruded thread into a coagulating bath containing a flocculating agent to obtain as-spun fiber, and repeatedly washing the resulted as-spun fiber with deionized water and drying same, thereby obtaining a metal oxide fiber. Said method makes the process simple and controllable, being adaptable to production on a large scale. The prepared metal oxide fiber having special physical and chemical properties is widely applicable in terms of intelligent spinning, biomedicine, energy recycling and conversion, and the field of microelectronic devices and the like.

A preparation method for an yttrium aluminum garnet continuous fiber. The method prepares a spinnable precursor sol by utilizing an Al.sub.13 colloidal particles contained alumina sol, -AIOOH nano-dispersion, yttria sol, glacial acetic acid and polyvinylpyrrolidone, then prepares a gel continuous fiber by adopting a dry spinning technique, and carries out a heat treatment to obtain the yttrium aluminum garnet continuous fiber.

The invention relates to a method for preparing a composite metal oxide hollow fibre. A certain stoichiometry of composite metal oxide raw material and a polymer binding agent are added to an organic solvent, and mixed mechanically to obtain an evenly dispersed spinning solution having a suitable viscosity. After defoaming treatment, the spinning solution is extruded through a spinneret and, after undergoing a certain dry spinning process, enters an external coagulation bath; during this period, a phase inversion process occurs and composite metal oxide hollow fibre blanks are formed. The blanks are immersed in the external coagulation bath and the organic solvent is displaced; after natural drying, the blanks undergo a heat treatment process; during this period, polymer burn off, in situ reaction, and in situ sintering processes occur to obtain the composite metal oxide hollow fibre.

Disclosed are a member for a gas sensor, a gas sensor using the member, and a method of fabricating the same. Specifically, disclosed are a member for a gas sensor using a metal oxide nanofiber material in which nanocatalysts have been uniformly bound and functionalized using chitosans with which nanoparticle catalysts have been combined, a gas sensor using the member, and a method of fabricating the same.

A filament containing a core material (CM) coated with a layer of shell material (SM), wherein the (CM) contains the components a) to c): a) 30 to 80% by volume, based on the total volume of the C) of at least one inorganic powder (IP), b) 20 to 70% by volume, based on the total volume of the CM of at least one binder (B) comprising component b1) b1) at least one polymer (P) and c) optionally at least one additive, wherein the at least one polymer (P) is a polyoxymethylene (POM) homopolymer, a POM copolymer or POM terpolymer and wherein at least some of the OH-end groups of the PO) homopolymer are capped, and the SM contains the components d) to f): d) 75 to 100% by volume, based on the total volume of the SM of at least one thermoplastic polymer, e) optionally at least one inorganic powder (IP), and f) optionally at least one additive, wherein the thickness of the layer of shell material is 0.05 to 0.5 mm.

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.

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.