A negative electrode active material includes a carbon material, where the carbon material has a specific degree of graphitization and aspect ratio distribution. A degree of graphitization Gr of the carbon material measured by an X-ray diffraction analysis method is 0.82 to 0.92, and based on a total quantity of particles of the carbon material, a proportion of particles with an aspect ratio greater than 3.3 in the carbon material is less than 10%. The negative electrode active material helps to improve cycle performance of the electrochemical apparatus. FIG. 1.

The present invention provides a silicon-silicon composite oxide-carbon composite, a method for preparing same, and a negative electrode active material for a lithium secondary battery, comprising same. More particularly, the silicon-silicon composite oxide-carbon composite of the present invention has a core-shell structure wherein the core comprises silicon, a silicon oxide compound, and magnesium silicate, and the shell comprises a carbon layer. In addition, by having a specific range of span values through the adjustment of particle size distribution of the composite, when used as a negative electrode active material of a secondary battery, the composite can improve not only the capacity of the secondary battery but also the cycle characteristics and initial efficiency thereof.

A carbonate apatite highly containing carbonate groups, having excellent heavy metal adsorption capacity is provided. The carbonate apatite contains not less than 15.6% by weight carbonate groups, preferably contains at least one of copper (Cu), zinc (Zn), strontium (Sr), magnesium (Mg), potassium (K), iron (Fe), and sodium (Na), and preferably has a Ca/P molar ratio of not less than 1.5.

A method of producing ceria nanocrystals is provided. The method includes providing a gas that includes ozone to a solution that includes a cerium salt, and obtaining ceria nanocrystals from the solution after the gas is provided to the first solution. A method of producing nanoparticles is provided. The method includes providing a gas that includes ozone to a solution that includes a metal salt that includes at least one of a transition metal or a lanthanide, and producing at least one of metal oxide nanoparticles, metal oxynitrate nanoparticles, or metal oxyhydroxide nanoparticles from the solution after the gas is provided to the solution.

A zirconium nitride powder which has a specific surface area of 20 to 90 m.sup.2/g as measured by a BET method, has a peak corresponding to zirconium nitride but does not have a peak corresponding to zirconium dioxide, a peak for lower zirconium oxide or a peak corresponding to lower zirconium oxynitride in an X-ray diffraction profile, and the light transmittance X at 370 nm is at least 18%, the light transmittance Y at 550 nm is 12% or less and the ratio (X/Y) of the light transmittance X at 370 nm to the light transmittance Y at 550 nm is 2.5 or more in the transmission spectra of a dispersion that contains the powder at a concentration of 50 ppm.

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework including a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework includes at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to bridging oxygen atoms. The organometallic moieties include a hafnium atom. The hafnium atom is bonded to a bridging oxygen atom, and bridging oxygen atom bridges the hafnium atom of the organometallic moiety and a silicon atom of the microporous framework.

A phosphor contains a crystal phase having a chemical composition Ce.sub.xM.sub.3-x-yβ.sub.6γ.sub.11-z. M is one or more elements selected from the group consisting of Sc, Y, La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu. β contains Si in an amount of 50 mol % or more of a total mol of β. γcontains N in an amount of 80 mol % or more N of a total mol of γ. x satisfies 0<x≦0.6. y satisfies 0≦y≦1.0. z satisfies 0≦z≦1.0. The phosphor shows a maximum peak of an emission spectrum in a wavelength range of 600 nm or more and 800 nm or less and a first peak of an excitation spectrum in a wavelength range of 500 nm or more and 600 nm or less.

A composite nanomaterial of ZnO impregnated by, e.g., a green copper phthalocyanine compound (CuPc) can be an efficient solar light photocatalyst for water remediation. The composite may include hollow shell microspheres and hollow nanospheres of CuPc-ZnO. CuPc may function as a templating and/or structure modifying agent, e.g., for forming hollow microspheres and/or nanospheres of ZnO particles. The composite can photocatalyze the degradation of organic pollutants such as crystal violet (CV) and 2,4-dichlorophenoxyacetic acid as well as microbes in water under solar light irradiation. The ZnO-CuPc composite can be stable and recyclable under solar irradiation.

The present invention relates to a carbon nanotube composition including entangled-type carbon nanotubes and bundle-type carbon nanotubes, wherein the carbon nanotube composition has a specific surface area of 190 m.sup.2/g to 240 m.sup.2/g and a ratio of specific surface area to bulk density of 0.1 to 5.29.

An object of the present invention is to provide composite particles capable of suppressing oxidation over time of a Si—C composite material. Composite particles (B) of the present invention contains composite particles (A) containing carbon and silicon; and amorphous layers coating surfaces thereof, where the composite particles (B) have I.sub.Si/I.sub.G of 0.10 or more and 0.65 or less, and have R value (I.sub.D/I.sub.G) of 1.00 or more and 1.30 or less, when a peak due to silicon is present at 450 to 495 cm.sup.−1, an intensity of the peak is defined as I.sub.Si, an intensity of a G band (peak intensity in the vicinity of 1600 cm.sup.−1) is defined as I.sub.G, and an intensity of a D band (peak intensity in the vicinity of 1360 cm.sup.−1) is defined as I.sub.D in a Raman spectrum, and where the composite particles (B) have a full width at half maximum of a peak of a 111 plane of Si of 3.0 deg. or more using a Cu-Kα ray in an XRD pattern.