Disclosed are a multi-wall carbon nanotube (MWCNT) formed using arc discharge and a method for manufacturing the same. The carbon source of the anode and boron that is the doping source, are evaporated through arc discharge and then deposited on the surface of the cathode to form MWCNTs, and boron is evenly distributed in the multi-walls of the MWCNTs. Therefore, the outer diameter of the MWCNT is reduced, high thermal stability is secured, and the effect of improving the field emission characteristics can be obtained.

The present invention provides a nanostructured titanic acid salt and a preparation process and use thereof. The process comprises preparing a dispersion containing titanium peroxy complex; slowly adding a metal compound to the dispersion containing the titanium peroxy complex to form a solution; adding an alcohol to the solution under normal temperature and normal pressure to produce the nanostructured titanic acid salt precursor precipitate in the solution, and separating the precipitate to obtain the titanic acid salt precursor; drying the precursor, and then heat treating it to obtain the nanostructured titanic acid salt product. The present invention provides a process for preparing a titanic acid salt with simple preparation process, easy control for process parameters and easy large-scale industrial production.

Provided is a method for producing a silica aerogel blanket and an apparatus for producing the same, which are capable of easily controlling the physical properties of a silica aerogel blanket by separately injecting silica sol and a gelation catalyst to control gelation time, improving aerogel pore structure to be uniform and improving thermal insulation performance by sufficiently and uniformly impregnating the silica sol and the gelation catalyst into a blanket, reducing the loss of silica sol and gelation catalyst by allowing the silica sol and the gelation catalyst to pass on an ascending slope before gelation to remove any excessive silica sol and gelation catalyst exceeding an appropriate impregnation amount, and providing a silica aerogel blanket having less process trouble, and less dust.

The present invention refers to a mineral matter powder preparation by wet process without acrylic additive or other grinding aid additives and to the use of said mineral matter after an optional hydrophobic treatment. Said mineral material having superior dispersing properties.

A CaTiO.sub.3-based oxide thermoelectric material and a preparation method thereof are disclosed. The CaTiO.sub.3-based oxide thermoelectric material has a chemical formula of Ca.sub.1-xLa.sub.xTiO.sub.3, where 0<x≤0.4. The present disclosure makes it possible to prepare a CaTiO.sub.3-based thermoelectric material with properties comparable to n-type ZnO, CaTiO.sub.3, SrTiO.sub.3 and other oxide thermoelectric materials. Among them, the La15 sample has a power factor reaching up to 8.2 μWcm.sup.−1K.sup.−2 (at about 1000 K), and a power factor reaching up to 9.2 μWcm.sup.−1K.sup.−2 at room temperature (about 300 K); and a conductivity reaching up to 2015 Scm.sup.−1 (at 300 K). The CaTiO.sub.3-based oxide thermoelectric material exhibits the best thermoelectric performance among calcium titanate ceramics. The method for preparing the CaTiO.sub.3-based oxide thermoelectric material of the present disclosure is simple in process, convenient in operation, low in cost, and makes it possible to prepare a CaTiO.sub.3-based ceramic sheet with high thermoelectric performance.

The present disclosure provides a cathode material and a method for preparing the cathode material, a cathode, a lithium ion battery and a vehicle. The cathode material comprises a matrix particle, wherein the matrix particle is a monocrystal particle comprising nickel lithium manganate and nickel cobalt lithium manganate. A position in the matrix particle close to a surface layer is provided with a buffer layer. A content of at least one of elements Ni, Co and Mn in the buffer layer is lower than contents thereof in other positions of the matrix particle. The cathode material has at least one of advantages of relatively high specific capacity, cycling stability, better safety performance and the like, and the buffer layer can alleviate erosion by an electrolyte and inhibit separation of active oxygen.

The invention described herein provides a dry graphene powder composition comprising pristine graphene flakes, wherein the pristine graphene flakes are non-covalently functionalised with polymeric amphiphilic molecules and wherein the dry graphene powder composition is capable of forming a stable homogeneous dispersion in aqueous or alcoholic media, in the absence of free dispersants or stabilizers, as well as methods for producing same, and the use thereof in graphene inks, for 2D and 3D printing, for production of flexible circuits, electrodes, electrocatalysts, for fabrication of nanocomposites and for wet-spinning of pristine graphene fibers.

Preparing MAX phase structures includes forming a gel including a transition metal M, a Group 3A or Group 4A metal or semimetal A, and an acidic chelating agent or gelling agent X. X includes one or both of carbon and nitrogen. Preparing the MAX phase structures further includes shaping the gel to yield a shaped gel and heating the shaped gel to yield carbonaceous MAX phase structures with a composition represented by M.sub.n+1AX.sub.n, wherein n is 1, 2, 3, or 4. The MAX phase structures can be thick films, microspheres, or microwires.

Embodiments of the present disclosure generally relate to carbon materials for battery electrodes and methods for preparing such carbon materials. More specifically, embodiments relate to methods for coating a carbon film onto nano-ordered carbon particles to produce carbon-coated particles which can be used as an anode material within a battery, such as a lithium-ion battery, a sodium-ion battery, other types of batteries. In one or more embodiments, a method for producing carbon-coated particles is provided and includes positioning nano-ordered carbon particles within a processing region of a processing chamber, purging the processing region containing the nano-ordered carbon particles with an inert gas, heating the nano-ordered carbon particles to a temperature of about 700° C. or greater during an annealing process, and depositing a carbon film on the nano-ordered carbon particles to produce carbon-coated particles during a vapor deposition process.

There are provided a new type of crystal laminate of an alkaline earth metal titanate having improved catalytic activity, and a method for producing the same. The crystal laminate is provided having a crystal of the alkaline earth metal titanate as a constitutional unit, wherein the crystal being the constitutional unit is a cubic crystal, a tetragonal crystal or an orthorhombic crystal; the crystal being the constitutional unit has a primary particle diameter of 500 nm or less; and the crystal is layered with an orientation in a {100} plane direction thereof.