A method for the large-scale synthesis of a zeolite-templated carbon (ZTC). The method includes the steps of: introducing a bed material comprising a zeolite to a fluidized bed reactor and heating the bed material to a temperature between 550° C. and 800° C.; fluidizing the bed material with a fluidizing gas and maintaining the temperature of the bed material between 550° C. and 800° C.; introducing an organic carbon precursor while fluidizing the zeolite for a period of time such that carbon is deposited on the zeolite by chemical vapor deposition to produce a zeolite-carbon composite; and treating the zeolite-carbon composite with an acid solution such that the zeolite template is dissolved and the ZTC is obtained.

A titanium oxide powder of the present invention contains a polyhedral-shaped titanium oxide particles, in which each particle of the polyhedral-shaped titanium oxide particles has eight or more faces and an average primary particle diameter is 300 nm or higher and 1000 nm or lower, and a crystallinity is 0.95 or higher.

The present invention relates to a positive electrode active material and a lithium secondary battery including the same, and more particularly, to a bimodal-type positive electrode active material that includes a first lithium composite oxide which is a small particle and a second lithium composite oxide which is a large particle, which have different average particle diameters, thereby improving an increasing deviation of an average particle diameter and degraded impedance and lifetime characteristics due to excessive calcination for any one of the small and large particles during simultaneous calcination, a positive electrode including the same, and a lithium secondary battery using the same.

Precipitated silica having large median particle size for use as reinforcing filler in elastomeric compositions as well as its method of manufacture. In particular, a precipitated silica characterised by a CTAB surface area S.sub.CTAB in the range from 70 to 350 m.sup.2/g; an amount W.sub.M of at least one metal M selected from elements of groups 3, 4 and 5 of at least 0.1 mol %; and a median particle size d50, measured by centrifugal sedimentation, such that: |d50|≥183×|R.sub.ION|×|W.sub.M|−0.67×|S.sub.CTAB|+233 (I) wherein |d50| represents the numerical value of median particle size d50 measured by centrifugal sedimentation and expressed in nm; |R.sub.ION|, the numerical value of the ionic radius of metal M expressed in nm; |S.sub.CTAB|, the numerical value of the CTAB surface area S.sub.CTAB expressed in m.sup.2/g; and |W.sub.M|, the numerical value of the percentage molar amount of the metal W.sub.M.

A thermal sensing bulb (102) for an expansion valve (104) in a refrigerant system, the bulb containing a ballast material (108), the ballast material including alumina. More particularly, the ballast material (108) includes alpha alumina, which may be in the form of a plurality of discrete particles having a desired surface area, particle size, and/or particle size distribution.

A precipitated silica having large particle size for use in tire applications. In particular, a precipitated silica characterised by a CTAB surface area S.sub.CTAB equal to or greater than 160 m.sup.2/g; a median particle size d50, measured by centrifugal sedimentation, such that

|d50|>25000/|S.sub.CTAB|  (I)

wherein |d50| represents the numerical value of the median particle size d50 measured by centrifugal sedimentation and expressed in nm and |S.sub.CTAB| represents the numerical value of the CTAB surface area S.sub.CTAB expressed in m.sup.2/g; and
an aluminium content not exceeding 4500 ppm.

A large-particle spherical salt with a particle size of 400-950 μm and a sphericity of 0.5-1.0 is disclosed, which overcomes the existing difficulty in this field for larger particle size as well as higher sphericity. A preparation method of the large-particle spherical salt is also disclosed, wherein in one preparation process, 2% of gum arabic (based on the mass percentage of solute sodium chloride in a sodium chloride saturated solution) is added, and under conditions of an evaporating temperature of 60° C. a stirring rate of 350 rpm, and an evaporating time of 8 hours, a large-particle spherical salt with a particle size of 921.593 μm and an average sphericity of 0.904 is successfully prepared. The large-particle spherical salt prepared by the method has a uniform particle size distribution and good appearance, can be combined with other substances, adding some extra value to the salt. Meanwhile, the large-particle spherical salt prepared by the method has a high safety grade (e.g.: food grade) and can be used as edible salt, nutrient salt or foot bath salt.

The present invention relates to a silicon oxide composite for a lithium secondary battery anode material and a method for manufacturing same and, more specifically, to a silicon oxide composite for a lithium secondary battery anode material and a method for manufacturing same, wherein the silicon oxide composite comprises a Si cluster and MgxSiOy(0≤x≤3, 0≤y≤5) formed on a peripheral portion of the Si cluster.

Provided are a manufacturing method of a positive electrode active material for a lithium secondary battery including: a first step of dry-mixing a transition metal hydroxide and an anhydrous lithium raw material; a second step of subjecting the mixture of the transition metal hydroxide and the anhydrous lithium raw material to primarily firing; and a third step of finely pulverizing and mixing the primarily fired material and performing secondary firing, and thus obtaining a lithium transition metal oxide, wherein, in the first step, the anhydrous lithium raw material is mixed at 40 parts by weight or less based on 100 parts by weight of the transition metal hydroxide, and a positive electrode for a lithium secondary battery including a positive electrode active material manufactured by the above-described manufacturing method, and a lithium secondary battery.

The present invention relates to a technology for producing a black pearlescent pigment for cosmetics which is a human-friendly and nature-friendly by using a pigment including natural charcoal powder. The production method of the pearlescent pigment using natural charcoal according to the present invention includes (a) milling natural charcoal to produce a pigment including natural charcoal powder; and (b) coating a flake substrate with the produced pigment including the natural charcoal powder, wherein the milling is performed at 20 to 40 Hz for 24 to 72 hours, and an average particle size of the pigment including the natural charcoal powder is 100 to 300 nm.