Disclosed are a transition metal precursor for preparation of a lithium transition metal oxide, in which a ratio of tap density of the precursor to average particle diameter D50 of the precursor satisfies the condition represented by Equation 1 below, and a lithium transition metal oxide prepared using the same. $\begin{array}{cc}0<\frac{\mathrm{Tap}\mathrm{density}}{\begin{array}{c}\mathrm{Average}\mathrm{particle}\mathrm{diameter}D50\\ \mathrm{of}\mathrm{transition}\mathrm{of}\mathrm{metal}\mathrm{precursor}\end{array}}<3500\left(g/\mathrm{cc}.Math.\mathrm{cm}\right)& \left(1\right)\end{array}$

A production method is provided in which submicronic particles containing silicon are incorporated into a matrix, wherein, during the incorporation of the particles, the particles are in a compacted state with a bulk density of more than 0.10 grams per cubic centimeter, and the compacted particles have a specific surface area at least 70% of that of the particles considered separately without contact between each other.

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.

A precipitated silica suitable for thermal insulation applications and a process for its manufacture.

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 present invention relates to a method of preparing a hydrophobic metal oxide-silica composite aerogel having a high specific surface area and a low tap density and a hydrophobic metal oxide-silica composite aerogel prepared thereby. Thus, the preparation method may not only have excellent productivity and economic efficiency due to a relatively simpler preparation process and shorter preparation time than the related art, but may also prepare a hydrophobic metal oxide-silica composite aerogel having a high specific surface area and a low tap density.

A solidified porous carbon material uses a plant-derived material as a raw material, a bulk density of the solidified porous carbon material is in the range of 0.2 to 0.4 grams/cm.sup.3, preferably, 0.3 to 0.4 grams/cm.sup.3. A value of a cumulative pore volume in the range of 0.05 to 5 μm in pore size based on a mercury press-in method is in the range of 0.4 to 1.2 cm.sup.3, preferably, 0.5 to 1.0 cm.sup.3 per 1 gram of the solidified porous carbon material.

The present application discloses a composite graphite material, a secondary battery, an apparatus and a preparation method thereof. The composite graphite material includes a core material and a coating layer coating at least a part of the surface of the core material, the core material including graphite; wherein the absolute value K of zeta potential of the composite graphite material in deionized water with a pH of 7 is at least 20 mV. The use of the composite graphite material provided by the present application can improve the cohesion and bonding force of the negative electrode plate, thereby reducing the cyclic expansion of the secondary battery.

The present invention relates to a positive electrode active material containing a spinel composite solid solution oxide, a method for manufacturing same, and a lithium secondary battery including the same. The spinel composite solid solution oxide contains cubic (P4.sub.332) and face-centered cubic (Fd-3m) in an optimized solid solution ratio in the crystal, and a low content of lithium nickel oxide (Li.sub.zNi.sub.1−zO) is combined. A positive electrode active material containing the spinel composite solid solution oxide provides excellent output characteristics while having stable cycle-life characteristics according to the type and content of doping elements replacing transition metals, the synthesis temperature, and the amount of impurities generated.

Silica-based hydrophobic granular material with an increased polarity Silica-based granular material, comprising silica and at least one IR-opacifier, hydrophobized with a surface treatment agent comprising a silicon atom, wherein the granular material has: a) a cumulative pore volume of pores>4 nm of more than 2.5 cm.sup.3/g, as determined by the mercury intrusion method according to DIN ISO 15901-1; b) a tamped density of 140 g/L to 290 g/L; c) a number of silanol groups relative to BET surface area d.sub.SiOH of at least 0.5 SiOH/nm.sup.2, as determined by reaction with lithium aluminium hydride. d) a number of silicon atoms in the surface treatment agent relative to BET surface area d.sub.[Si] of at least 1.0 [Si atoms]/nm.sup.2.