C01B25/16

Carbonate apatite with high carbonate content

A carbonate apatite highly containing carbonate groups, having excellent heavy metal adsorption capacity is provided. The carbonate apatite contains not less than 15.6% by weight carbonate groups, preferably contains at least one of copper (Cu), zinc (Zn), strontium (Sr), magnesium (Mg), potassium (K), iron (Fe), and sodium (Na), and preferably has a Ca/P molar ratio of not less than 1.5.

Carbonate apatite with high carbonate content

A carbonate apatite highly containing carbonate groups, having excellent heavy metal adsorption capacity is provided. The carbonate apatite contains not less than 15.6% by weight carbonate groups, preferably contains at least one of copper (Cu), zinc (Zn), strontium (Sr), magnesium (Mg), potassium (K), iron (Fe), and sodium (Na), and preferably has a Ca/P molar ratio of not less than 1.5.

HYDROGENATION CATALYST AND PREPARATION METHOD THEREFOR AND USE THEREOF

A catalyst has a carrier and a hydrogenation active metal component supported on the carrier. The hydrogenation active metal component contains at least one Group VIB metal component and at least one Group VIII metal component, and the carrier is composed of phosphorus-containing alumina. When the hydrogenation catalyst is measured using a hydrogen temperature programmed reduction method (H.sub.2-TPR), the ratio of the peak height of the low-temperature reduction peak, P.sub.low-temp peak, at a temperature of 300-500° C. to the peak height of the high-temperature reduction peak, P.sub.hi-temp peak, at a temperature of 650-850° C., i.e. S=P.sub.low-temp peak/P.sub.hi-temp peak, is 0.5-2.0; preferably 0.7-1.9, and more preferably 0.8-1.8. The hydrogenation catalyst shows excellent heteroatom removal effect and excellent stability when used in hydrotreatment.

Process for producing carbonate apatite

An efficient method of producing a carbonate apatite is provided. The method comprises: a first step of calcining animal bone; and a second step of reacting a bone calcined product obtained in the first step with a basic carbonate compound.

Process for producing carbonate apatite

An efficient method of producing a carbonate apatite is provided. The method comprises: a first step of calcining animal bone; and a second step of reacting a bone calcined product obtained in the first step with a basic carbonate compound.

Cathode active material for lithium secondary battery and lithium secondary battery comprising the same

The present invention relates to an anode active material for lithium secondary battery and a lithium secondary battery including the same, and more specifically it relates to an anode active material for lithium secondary battery in which the a lithium ion diffusion path in the primary particles is formed to exhibit specific directivity, and a lithium secondary battery including the same. The cathode active material for lithium secondary battery of the present invention has a lithium ion diffusion path exhibiting specific directivity in the primary particles and the secondary particles, thus not only the conduction velocity of the lithium ion is fast and the lithium ion conductivity is high but also the cycle characteristics are improved as the crystal structure hardly collapses despite repeated charging and discharging.

Cathode active material for lithium secondary battery and lithium secondary battery comprising the same

The present invention relates to an anode active material for lithium secondary battery and a lithium secondary battery including the same, and more specifically it relates to an anode active material for lithium secondary battery in which the a lithium ion diffusion path in the primary particles is formed to exhibit specific directivity, and a lithium secondary battery including the same. The cathode active material for lithium secondary battery of the present invention has a lithium ion diffusion path exhibiting specific directivity in the primary particles and the secondary particles, thus not only the conduction velocity of the lithium ion is fast and the lithium ion conductivity is high but also the cycle characteristics are improved as the crystal structure hardly collapses despite repeated charging and discharging.

Apparatus for preparing phosphoric acid from fume exiting the kiln in a kiln phosphoric acid process

Disclosed is an apparatus for preparing phosphoric acid from a fume exiting the kiln in a kiln phosphoric acid process, the apparatus comprises a hydration tower and an acid solution cyclical spraying system, a fume inlet of the fume exiting the kiln is disposed at a lower portion of the hydration tower, a fume outlet after hydration and absorption is disposed at the top, a spraying device is disposed in a cavity of the hydration tower above the fume inlet, a liquid inlet of the acid solution cyclical spraying system is disposed on a bottom of the hydration tower, a liquid outlet of the acid solution cyclical spraying system is connected to a liquid intake pipe of the spraying device. The present invention has the advantages of simple structure, reasonable layout, strong adaptability, high raw material utilization rate, reduced contaminant emissions, and high recovery rate of phosphoric acid etc.

Solid electrolyte battery

There is provided a solid electrolyte including at least one layer with no nitrogen and which includes Li.sub.xPO.sub.yS.sub.z, with 0<z≤3, 2.1≤x≤2.4, and 1≤y≤4. A battery including the electrolyte, and a method for producing the electrolyte, are also provided.

Solid electrolyte battery

There is provided a solid electrolyte including at least one layer with no nitrogen and which includes Li.sub.xPO.sub.yS.sub.z, with 0<z≤3, 2.1≤x≤2.4, and 1≤y≤4. A battery including the electrolyte, and a method for producing the electrolyte, are also provided.