Provided are a 2-dimensional microporous graphene and a method for preparing the same. The 2-dimensional microporous graphene has an average pore size of about 0.1 nm to about 2 nm, interpore spacing of about 0.3 nm to about 10 nm, and a standard deviation of the interpore spacing of less than or equal to about 5 nm.

The present exemplary embodiments relate to a cathode active material, a manufacturing method thereof, and a lithium secondary battery including the same. A cathode active material according to an exemplary embodiment is a lithium metal oxide particle in the form of a secondary particle including a primary particle, a coating layer including a boron compound is positioned on at least a portion of a surface of the primary particle, and the boron compound includes an amorphous structure.

A zirconia powder in which when a stabilizer is Y.sub.2O.sub.3, a content thereof is 1.4 mol % or more and less than 2.0 mol %; when the stabilizer is Er.sub.2O.sub.3, a content thereof is 1.4 mol % or more and 1.8 mol % or less; when the stabilizer is Yb.sub.2O.sub.3, a content thereof is 1.4 mol % or more and 1.8 mol % or less; and when the stabilizer is CaO, a content thereof is 3.5 mol % or more and 4.5 mol % or less; and in a range of 10 nm or more and 200 nm or less in a pore distribution, a peak top diameter of a pore volume distribution is 20 nm or more and 120 nm or less, a pore volume is 0.2 ml/g or more and less than 0.5 ml/g, and a pore distribution width is 30 nm or more and 170 nm or less.

According to an embodiment, there is provided an electrode including an active material-containing layer. A logarithmic differential pore volume distribution curve of the active material-containing layer by a mercury intrusion method includes first and second peaks. The first peak is a local maximum value in a range where a pore size is from 0.1 μm or more to 0.5 μm or less. The second peak is a local maximum value in a range where the pore size is from 0.5 μm or more to 1.0 μm or less. An intensity A1 of the first peak and an intensity A2 of the second peak satisfy 0.1≤A2/A1≤0.3. A density of the active material-containing layer is from 2.9 g/cm.sup.3 or more to 3.3 g/cm.sup.3 or less.

The present technology provides an adsorbent material that includes a silicate composition, wherein the silicate composition includes a crystalline phase; wherein the silicate composition may have an interconnected porous scaffold having a total mercury (Hg) pore volume of about 0.005 cc/g to about 0.25 cc/g for pores having a diameter of about 20-10,000 Å and a total nitrogen (N) pore volume of about 0.02 cc/g to about 0.1 cc/g for pores having a diameter of about 20-600 Å.

Provided is halloysite powder having a small b value. The halloysite powder is powder including a granule in which halloysite including halloysite nanotubes is aggregated, the granule has a first pore deriving from a tube hole of the halloysite nanotubes and a second pore different from the first pore, and the Fe.sub.2O.sub.3 content is not more than 2.00 mass %.

Disclosed is a method of decontamination by exposing a zirconium oxy(hydroxide) aerogel to a liquid, vapor, or gaseous sample suspected of containing a phosphonate compound. The aerogel may be doped with Fe.sup.3+ ions, Ce.sup.3+ ions, or SO.sub.4.sup.2− ions. The aerogel may be made by: providing a solution of ZrCl.sub.4; FeCl.sub.3, CeCl.sub.3, or Zr(SO.sub.4).sub.2; and a solvent; adding a cyclic ether to the solution to form a gel; infiltrating the gel with liquid carbon dioxide; applying a temperature and pressure to form supercritical fluid carbon dioxide; and removing the carbon dioxide for form an aerogel.

A method for producing mesoporous magnesium hydroxide nanoplates involving solvothermal treatment of a solution of a magnesium salt, a base, a glycol, and water is disclosed. The method does not use a surfactant or template in the solvothermal treatment. The method yields mesoporous nanoparticles of magnesium hydroxide having a plate-like morphology with a diameter of 20 nm to 100 nm, a mean pore diameter of 2 to 10 nm, a surface area of 50 to 70 m.sup.2/g, and a type-III nitrogen adsorption-desorption BET isotherm with a H3 hysteresis loop. An antibacterial composition containing the mesoporous magnesium hydroxide nanoplates is also disclosed. A method for reducing nitroaromatic compounds with a reducing agent and the mesoporous magnesium hydroxide nanoplates as a catalyst is also disclosed.

A method of preparing a mesoporous Fe—Cu—SSZ-13 molecular sieve includes activating an aluminum source, a silicon source, an iron source and a copper source respectively; mixing the activated minerals with sodium hydroxide, water and a seed crystal at 25-90° C., while controlling feeding amounts of respective raw materials so that molar ratios of respective materials in a synthesis system are as follows: SiO.sub.2/Al.sub.2O.sub.3=10-100, SiO.sub.2/Fe.sub.2O.sub.3=30-3000, SiO.sub.2/CuO=1-100, Na.sub.2O/SiO.sub.2=0.1-0.5, H.sub.2O/SiO.sub.2=10-50, template/SiO.sub.2=0.01-0.5; adding an acid source to adjust pH of the system for first aging; and adding the acid source again to adjust the pH of the system for second aging to obtain aged gel; pouring an aged mixture into a kettle; cooling a crystallized product and filtering to remove a liquor; washing a filter cake; drying to obtain a solid; performing ion exchange; and filtering, washing and drying the solid to obtain powder; and placing the powder in a muffle furnace.

The present invention concerns a material with a non-stoichiometric spinel-type crystalline structure based on cobalt oxide doped with alkaline elements, its production process for obtaining it by precipitation with controlled washing, and its particular use as a highly active catalyst in the N.sub.2O decomposition reaction. Therefore, we understand that the present invention is in the area of green industry aimed at reducing N.sub.2O emissions into the atmosphere.