A mesoporous ozonation catalyst including a cerium-titanium-zirconium composite oxide. The catalyst is in the form of a solid spherical particle having a diameter of between 0.7 and 1.2 mm. The solid spherical particle exhibits lattice fringes under transmission electron microscope, and the lattice fringes have a spacing between 0.332 and 0.339 nm.

A lithium-ion battery cathode material and a method for preparing the same are disclosed. The lithium-ion battery cathode material includes a layered cathode material matrix and a defect layer. The layered cathode material matrix includes body layers and lithium layers, and the body layer includes a transition metal layer and a lithium layer. The defect layer includes atoms with a periodic arrangement different from that of atoms in the matrix or with content different from that of an element in the matrix. The defect layer is parallel to a 003 crystal plane of the layered cathode material matrix, and dimensions of the defect layer are 0.1 nm to 50 nm in at least one direction and 10 nm to 5000 nm in at least another direction.

A positive electrode active material powder suitable for lithium-ion batteries, comprising lithium transition metal-based oxide particles, said particles comprising a core and a surface layer, said surface layer being on top of said core, said particles comprising the elements: Li, a metal M′ and oxygen, wherein the metal M′ has a formula: M′=(Ni.sub.z(Ni.sub.0.5Mn.sub.0.5).sub.yCo.sub.x).sub.1-kA.sub.k, wherein A is a dopant, 0.60≤z≤0.86, 0.05≤y≤0.20, 0.05≤x≤0.20, x+y+z+k=1, and k≤0.01, said positive electrode active material powder having a median particle size D50 ranging from 5 μm to 15 μm and a surface layer thickness ranging from 10 nm to 200 nm,

said surface layer comprising: sulfur in a content superior or equal to 0.150 wt % and inferior or equal to 0.375 wt % with respect to the total weight of the positive electrode active material powder, and aluminum in a content superior or equal to 0.05 wt % and inferior or equal to 0.15 wt % with respect to the total weight of the positive electrode active material powder,
said surface layer of lithium transition metal-based oxide particles comprising a LiAlO.sub.2 phase and an LiM″.sub.1-aAl.sub.aO.sub.2 phase with M″ comprising: Ni, Mn, and Co, said LiAlO.sub.2 phase being present in the surface layer in a content superior or equal to 0.10 at % and inferior or equal to 0.30 at % with respect to the total atomic content of M′ in the positive electrode active material powder, said LiM″.sub.1-aAl.sub.aO.sub.2 phase being present in the surface layer in a content inferior to 0.14 at % with respect to the total atomic content of M′ in the positive electrode active material powder.

1. A positive electrode active material powder suitable for lithium-ion batteries, comprising lithium transition metal-based oxide particles, said particles comprising a core and a surface layer, said surface layer being on top of said core, said particles comprising the elements: Li, M′ and oxygen, wherein M′ has a formula: M′=Ni.sub.zMn.sub.yCo.sub.xA.sub.k, wherein A is a dopant, 0.60≤z≤0.89, 0.05≤y≤0.20, 0.05≤x≤0.20, x+y+z+k=1, and k≤0.01, said positive electrode active material powder having a median particle size D50 ranging from 5 μm to 15 μm, a span ranging from 0.25 to 0.90, and a surface layer thickness ranging from 10 nm to 200 nm, said surface layer comprising: sulfur in a content superior or equal to 0.150 wt % and inferior or equal to 0.375 wt % with respect to the total weight of the positive electrode active material powder, and aluminum in a content superior or equal to 0.05 wt % and inferior or equal to 0.15 wt % with respect to the total weight of the positive electrode active material powder,

A positive electrode active material powder suitable for lithium-ion batteries, comprising lithium transition metal-based oxide particles, said particles comprising a core and a surface layer, said surface layer being on top of said core, said particles comprising the elements: Li, M′ and oxygen, wherein M′ has a formula: M′=Ni.sub.zMn.sub.yCo.sub.xA.sub.k, wherein A is a dopant, 0.60≤z≤0.90, 0.05≤y≤0.20, 0.05≤x≤0.20, x+y+z+k=1, and k≥0.01, said positive electrode active material powder having a median particle size D50 ranging from 5 μm to 15 μm, a span ranging from 0.25 to 0.90, and a surface layer thickness ranging from 10 nm to 200 nm, said surface layer comprising: sulfur in a content superior or equal to 0.150 wt % and inferior or equal to 0.375 wt % with respect to the total weight of the positive electrode active material powder, and sulfate ion (SO.sub.4.sup.2−) in a content superior or equal to 4500 ppm and inferior or equal to 11250 ppm.

A positive electrode active material powder suitable for lithium-ion batteries, comprising lithium transition metal-based oxide particles, said particles comprising a core and a surface layer, said surface layer being on top of said core, said particle comprising the elements: Li, M′ and oxygen, wherein M′ has a formula: M′=Ni.sub.zMn.sub.yCo.sub.xA.sub.k, wherein A is a dopant, 0.80≤z≤0.90, 0.05≤y≤0.20, 0.05≤x≤0.20, x+y+z+k=1, and 0≤k≤0.01, said positive electrode active material powder having a median particle size D50 ranging from 5 μm to 15 μm and a surface layer thickness ranging from 10 nm to 200 nm, said surface layer comprising sulfate ion (SO.sub.4.sup.2−) in a content superior or equal to 6.78.Math.z−4.83 wt % and inferior or equal to 6.78.Math.z−4.33 wt % with respect to the total weight of the positive electrode active material.

The present invention generally relates to a method for preparing metal oxide nanosheets. In a preferred embodiment, graphene oxide (GO) or graphite oxide is employed as a template or structure directing agent for the formation of the metal oxide nanosheets, wherein the template is mixed with metal oxide precursor to form a metal oxide precursor-bonded template. Subsequently, the metal oxide precursor-bonded template is calcined to form the metal oxide nanosheets. The present invention also relates to a lithium-ion battery anode comprising the metal oxide nanosheets. In a further preferred embodiment, the battery anode may comprising reduced template, which is reduced graphene oxide (rGO) or reduced graphite oxide.

The invention relates to a process for the preparation of a citrate-coated amorphous calcium phosphate nanoparticle which comprises the following steps: 1) providing a first solution of a salt of calcium and a citrate salt wherein the molar ratio of citrate ion to calcium ion is in the range from 1 to 2 thus obtaining a clear first solution; 2) providing a second solution of a salt capable to give phosphate anion and a carbonate salt; 3) mixing together the first and the second solution at a pH in the range from 8 to 11; 4) precipitating the nanoparticle; and 5) drying the nanoparticle obtained from step 4). Preferably and advantageously the invention provides for the addition of a fluoride compound in step 2) for obtaining a fluorine-doped citrate-coated calcium phosphate nanoparticle or a nanoparticle agglomerate. The nanoparticle/nanoparticle agglomerate of the invention has a peculiar superficial area and a diameter that allow to use it as a biomaterial for dentistry application.

Described is a method for extracting lithium from salt lake brine and simultaneously preparing aluminum hydroxide. This method includes a. adding an aluminum salt to the brine, adding an alkali solution, then subjecting to crystallization reaction and solid-liquid separation to obtain lithium-containing brine; b. evaporating and concentrating the lithium-containing brine, adding an aluminum salt, adding an alkali solution dropwise to perform a co-precipitation reaction and solid-liquid separation to obtain a lithium-containing layered material filter cake, wherein in steps a and b, the alkali solution is an alkali solution free of carbonate ion; c. dispersing the lithium-containing layered material filter cake in deionized water to form a suspension slurry, then adjusting the pH value of the suspension slurry so as to carry out a lithium deintercalation reaction; d. filtering to obtain aluminum hydroxide filter cake; e. washing the aluminum hydroxide filter cake with deionized water and drying.

The present disclosure relates to an RHO-type zeolite comprising caesium and M.sup.1 .sub.wherein M.sup.1 is selected from Na and/or Li remarkable in that it has a Si/Al molar ratio comprised between 1.2 and 3.0 as determined by .sup.29Si magic angle spinning nuclear magnetic resonance, in that the RHO-type zeolite has a specific surface area comprised between 40 m.sup.2g.sup.−1 and 250 m.sup.2g.sup.−1 as determined by N.sub.2 adsorption measurements, in that the RHO-type zeolite being in the form of one or more nanoparticles with an average crystal size comprised between 10 nm and 400 nm as determined by scanning electron microscopy wherein said nanoparticles form monodispersed nanocrystals or form aggregates of nanocrystals having an average size ranging from 100 nm to 500 nm, as determined by scanning electron microscopy. Amorphous precursors, devoid of an organic structure-directing agent, as well as a method for preparation of these amorphous precursors in the absence of such organic structure-directing agent and method for preparation of the RHO-type zeolites, are alos described. Finally, the use of the RHO-type zeolite as a sorbent for carbon dioxide is also demonstrated.