A novel salt composition and a corresponding method of manufacture are described herein. The salt composition is formed from a plurality of salt crystals with a surface area of at least 0.19-0.23 m.sup.2/g and a Hall density of less than 0.8 g/cm.sup.3. In some embodiments, at least a portion of the salt composition has a hopper cube morphology.

The present invention relates to zeolite containing Cu2+ () and Cu2+ () having different NO adsorption capacities loaded at a specific ratio, wherein the zeolite is chabazite (CHA)-type zeolite, particularly chabazite (CHA)-type zeolite loaded with divalent copper ions in which the NO adsorption area ratio of Cu2+ ()/Cu2+ () after exposure to NO (nitrogen oxide) for 180 sec is 80% or more. In addition, the present invention relates to a method of preparing zeolite that is ion-exchanged in a slurry state and to a catalyst including the specified chabazite (CHA)-type zeolite.

A novel salt composition and a corresponding method of manufacture are described herein. The salt composition is formed from a plurality of salt crystals with a surface area of at least 0.19-0.23 m.sup.2/g and a Hall density of less than 0.8 g/cm.sup.3. In some embodiments, at least a portion of the salt composition has a hopper cube morphology.

The present application relates to a porous material and preparation methods thereof, and anodes and devices including the same. The porous material provided by the present application includes a material of the formula Si.sub.aM.sub.bO.sub.x, wherein the ratio of x to a is about 0.6 to about 1.5, and the ratio of a to b is about 8 to about 10,000, wherein M includes at least one selected from the group consisting of Al, Si, P, Mg, Ti and Zr. The anode and an electrochemical device including the porous material exhibit higher rate performance, higher first coulombic efficiency, higher cycle stability and lower cycle expansion ratio.

Further described herein are extensions to the basic concept of LHs as electrode materials, include both new materials for use with LHs and higher order poly-layer hydroxides (PLHs) as well as methods for synthesizing improved LH material such as with conductive supports or through the use of cross-linking. Finally, also described herein are embodiments enabling the use of LHs as flow electrodes as well as the use of 2-d LH materials for surface redox reactions.

This invention discloses a lithium metal oxide powder for a cathode material in a rechargeable battery, consisting of a core and a surface layer, the core having a layered crystal structure comprising the elements Li, M and oxygen, wherein M has the formula M=(Ni.sub.z(Ni.sub.1/2Mn.sub.1/2).sub.yCo.sub.x).sub.1-kA.sub.k, with 0.15x0.30, 0.20z0.55, x+y+z=1 and 0k0.1, wherein A is a dopant, wherein the Li content is stoichiometrically controlled with a molar ratio 0.95Li:M1.10; and wherein the surface layer comprises the elements Li, M and oxygen, wherein M has the formula M=(Ni.sub.z(Ni.sub.1/2Mn.sub.1/2).sub.yCo.sub.x).sub.1-kA.sub.k, with x+y+z=1 and 0k0.1, and wherein y/(y+2z)1.1*[y/(y+2z)]. The surface layer may also comprise at least 3 mol % Al, the Al content in the surface layer 10 being determined by XPS.

Provided is alumina material comprising alumina and zirconium, wherein in a radial distribution function obtained by Fourier-transforming an extended X-ray absorption fine structure (EXAFS) spectrum of a K absorption edge of the zirconium in the alumina material, the value of I.sub.B/I.sub.A is 0.5 or less where I.sub.A is a maximum intensity among the intensities of peaks present at 0.1 nm to 0.2 nm, and I.sub.B is a maximum intensity among the intensities of peaks present at 0.28 nm to 0.35 nm.

To provide a silver-coated graphite mixed powder including: silver-coated graphite particles each including a graphite particle and silver coated on a surface of the graphite particle, where when a solution obtained by dissolving the silver-coated graphite mixed powder in nitric acid is analyzed through inductively coupled plasma (ICP) emission spectrometry, an amount of silver is 5% by mass or more but 90% by mass or less, an amount of tin is 0.01% by mass or more but 5% by mass or less, and an amount of zinc is 0.002% by mass or more but 1% by mass or less.

Provided is an orientation agent for NMR spectroscopy containing a nanosheet which is easy to prepare, excellent in handleability, economic efficiency and versatility, and is capable of being stably aligned to the magnetic field. The nanosheet is coated with a compound having a molecular weight of 1,500 or more and containing 35 or more functional groups per molecule, said functional groups being composed of at least one selected from a hydroxy group, an amino group, an amide group, a carbonyl group, a carboxyl group, a sulfo group, a phosphate group, an imidazole group and a guanidine group.

A gallium-containing nitride crystals are disclosed, comprising: a top surface having a crystallographic orientation within about 5 degrees of a plane selected from a (0001) +c-plane and a (000-1) c-plane; a substantially wurtzite structure; n-type electronic properties; an impurity concentration of hydrogen greater than about 510.sup.17 cm.sup.3, an impurity concentration of oxygen between about 210.sup.17 cm.sup.3 and about 110.sup.20 cm.sup.3, an [H]/[O] ratio of at least 0.3; an impurity concentration of at least one of Li, Na, K, Rb, Cs, Ca, F, and Cl greater than about 110.sup.16 cm.sup.3, a compensation ratio between about 1.0 and about 4.0; an absorbance per unit thickness of at least 0.01 cm.sup.1 at wavenumbers of approximately 3175 cm.sup.1, 3164 cm.sup.1, and 3150 cm.sup.1, and wherein, at wavenumbers between about 3200 cm.sup.1 and about 3400 cm.sup.1 and between about 3075 cm.sup.1 and about 3125 cm.sup.1, said gallium-containing nitride crystal is essentially free of infrared absorption peaks having an absorbance per unit thickness greater than 10% of the absorbance per unit thickness at 3175 cm.