The present invention relates to a method for producing lithium phosphate, comprising: passing a lithium-containing solution through an aluminum-based adsorbent to adsorb lithium on the aluminum-based adsorbent, passing the distilled water or an aqueous solution having a lower lithium concentration than the lithium-containing solution through the aluminum-based adsorbent on which the lithium is adsorbed to obtain a lithium-containing desorption solution, and putting a phosphorous supplying material in the lithium-containing desorption solution to obtain lithium phosphate.

The present invention relates to a method for producing lithium phosphate, comprising: passing a lithium-containing solution through an aluminum-based adsorbent to adsorb lithium on the aluminum-based adsorbent, passing the distilled water or an aqueous solution having a lower lithium concentration than the lithium-containing solution through the aluminum-based adsorbent on which the lithium is adsorbed to obtain a lithium-containing desorption solution, and putting a phosphorous supplying material in the lithium-containing desorption solution to obtain lithium phosphate.

An anode active material for batteries includes anode active substance particles. The anode active substance particles include silicon oxide compound particles including nano-silicon grains and lithium; and a composite oxide coating layer partially or entirely covering the silicon oxide compound particles and containing a composite oxide of a metal M and phosphorus, where the metal M includes lithium and a non-lithium metal. The anode active material has good water tolerance. A battery prepared from the anode active material has at least the advantages of good cycle performance, high energy density, high coulombic efficiency, good rate performance, and the like.

A process of preparing a lithium metal phosphate includes contacting a water-soluble metal precursor, a water-insoluble metal precursor, and a phosphate precursor in an acidic aqueous medium; to form a reaction mixture; precipitating from the reaction mixture a metal phosphate; collecting the metal phosphate; combining the metal phosphate with a lithium precursor; and calcining the combined metal phosphate and lithium precursor at elevated temperature to form a lithium metal phosphate; wherein a mol ratio of water-soluble metal precursor to water-insoluble metal precursor is from 0.5:99.5 to 99.5:0.5.

An improved method of lithium recovery from borax dilute solution is provided. In this method, boron in the borax dilute solution is removed from the medium as borax decahydrate and while this removal process is carried out, liquid-liquid extraction with organic sedimentary chemicals or ion exchange resins are not used.

An iron manganese phosphate precursor, a lithium iron manganese phosphate positive electrode material and a method for preparation thereof, an electrode material, an electrode, and a lithium-ion battery are disclosed. The lithium iron manganese phosphate precursor is represented by (NH.sub.4)Mn.sub.1-x-yFe.sub.xM.sub.yPO.sub.4H.sub.2O/C, wherein 0.1<x≤0.6 and 0≤y≤0.04, and M is selected from at least one of Mg, Co, Ni, Cu, Zn, and Ti. Lithium iron manganese phosphate positive electrode material prepared from the precursor is uniform in carbon coating, has a dense secondary spherical morphology, is high in compaction density, can improve the electrochemical performance of the lithium-ion battery when applied to the lithium-ion battery, is high in specific capacity and good in cycle performance.

The present invention discloses a preparation method for water-soluble potassium polymetaphosphate, and relates to the technical field of potassium polymetaphosphate production and preparation. In the present invention, potassium dihydrogen phosphate is mixed with a divalent cationic metal oxide at a mixing mass ratio of 70-90:5-18 to obtained a mixture, wherein the divalent cationic metal oxide is one or more of calcia, magnesia and zinc oxide in the field of food processing; then the mixture is heated and melted, and the temperature is kept constant for 1-3 h at a temperature of 600-700° C.; and after temperature keeping, the melted mixture is cooled naturally to obtain a product. The water-soluble potassium polymetaphosphate prepared by the present invention has a high water solubility and effectively solves the application defect of a traditional potassium polymetaphosphate product which is insoluble in water.

The present invention relates to a method for producing lithium hydroxide, and provides a method for producing lithium hydroxide, the method comprising the steps of: preparing lithium carbonate and calcium hydroxide; and reacting the lithium carbonate and the calcium hydroxide in a solvent to obtain an aqueous solution of lithium hydroxide, wherein in the step of reacting the lithium carbonate and the calcium hydroxide in a solvent to obtain an aqueous solution of lithium hydroxide, the concentration of lithium carbonate in the solvent is 110 g/L or less.

A method of making a proppant-gel matrix comprising: a) hydrating a gelling agent to form a hydrated gelling agent; b) adding a basic compound to the hydrated gelling agent to form a basic hydrated gelling agent having a pH in the range of 11.5 to 14.0; c) mixing the basic hydrated gelling agent and a proppant to form a basic hydrated gelling system; and d) adding a crosslinking agent to the basic hydrated gelling system to form the proppant-gel matrix, is disclosed. The proppant-gel matrix can then be used as a fracturing fluid in a hydraulic fracturing process.

A method of making a proppant-gel matrix comprising: a) hydrating a gelling agent to form a hydrated gelling agent; b) adding a basic compound to the hydrated gelling agent to form a basic hydrated gelling agent having a pH in the range of 11.5 to 14.0; c) mixing the basic hydrated gelling agent and a proppant to form a basic hydrated gelling system; and d) adding a crosslinking agent to the basic hydrated gelling system to form the proppant-gel matrix, is disclosed. The proppant-gel matrix can then be used as a fracturing fluid in a hydraulic fracturing process.