1650 results about "Lithium chloride" patented technology

The present invention relates to adsorption process of extracting lithium from salt lake brine, and the process is suitable for producing lithium carbonate and lithium chloride with lithium-containing Qinghai saline lake brine, including concentrated lithium-containing Qinghai saline lake brine. The process includes sun shining saline lake brine to obtain concentrated lithium containing brine, adsorption of lithium ion with aluminum salt adsorbent, eluting adsorbed lithium ion with water, and refining and concentrating the elutriant to obtain material for preparing lithium carbonate and lithium chloride.

The nanofiltration process is suitable for Mg-Li separation and Li enriching of Li containing bittern or Li containing solution from salt lake to prepare lithium carbonate or lithium chloride with the Li enriching bittern. Nanofiltration membrane is used in separating and enriching lithium from lithium containing bittern, which contains Mg, Ca and other cations and sulfate radical and other anions and has Li ion concentration of 0.1-11.5 g/L and Mg/Li ion weight ratio 1-200, to obtain lithium enriched bittern suitable for preparing lithium carbonate or lithium chloride. The said process is effective, and can obtain lithium enriched bittern with Mg/Li ion weight ratio 0.6-5 and Li ion content of 0.6-20 g/L.

The invention discloses a dehumidizer for air dehumidification. The dehumidizer provided by the invention is an ionic liquid solution formed by dissolving an ionic liquid in water, wherein the ionic liquid is formed by organic positive ions and inorganic negative ions, and the melting point of the ionic liquid is close to or is lower than room temperature. In addition, the invention further discloses a method and a device for air dehumidification by the adoption of the above dehumidizer. In comparison with traditional salting liquids (lithium bromide, lithium chloride and calcium chloride aqueous solutions and the like), the dehumidizer provided by the invention has the following advantages: 1) the applied ionic liquid solution is in the liquid state at normal temperature, is intermiscible with water, and will not be crystallized during operation, so as to guarantee the reliable operation of a system; 2) the applied ionic liquid solution has similar or lower water vapor pressure than a traditional dehumidifying salting liquid so as to raise the dehumidifying efficiency; 3) the applied ionic liquid solution will not corrode metal equipment such as steel equipment such that the equipment has low cost and long service life; 4) the dehumidizer has nonvolatility so as to reduce the environmental pollution.

Lithium cobaltate forming the positive electrode of a lithium secondary battery is subjected together with lithium metal to reducing reaction in molten lithium chloride to produce lithium oxide and to precipitate and separate cobalt or cobalt oxide. The lithium oxide is subjected to electro-deposition in molten lithium chloride contained in a lithium electro-deposition tank provided with an anode and a cathode to recover lithium metal deposited on the cathode.

A remote humidity monitor system for detecting a targeted object utilizes a humidity sensor to detect humidity and sends a result to a reader via the wireless communication device; a server can execute monitor management. The humidity sensor can be a mass hygrometer, an optical condensation dew-point hygrometer, a psychrometer (wet-and-dry bulb thermometer), a hair hygrometer, an electrolysis humidity sensor, a lithium chloride humidity sensor, an aluminum oxide humidity sensor, a high polymer humidity sensor, or an infrared hygrometer.

The invention discloses a method for extracting ultrahigh-purity lithium carbonate from chloride brine with a high magnesium-lithium ratio. The method comprises the following steps of: preparing a lithium chloride concentrated solution by an adsorption, desorption and evaporation concentration process; purifying, and precipitating lithium carbonate by using ammonium bicarbonate pulp; and converting into a lithium bicarbonate solution, filtering, and decarburizing. By improving steps and parameters of the conventional process, the purity of a product is more than 99.99 weight percent and the total amount of major impurities is not more than 0.002 weight percent without the introduction of additional high-cost purification steps such as ion exchange resin/membranes; and additional sodium ions are not introduced in the production process, byproducts at all stages can be recycled, and only an extremely small amount of waste solution is generated.

The invention discloses a solid phase synthesis method of carbetocin. The technical proposal comprises the following steps of: obtaining Fmoc-Gly-amino resin by reaction of Fmoc-Gly-OH and amino resin with the substitutability being 0.2 mmol/g-0.9 mmol/g; sequentially connecting amino acids with Fmoc protecting groups by the solid phase synthesis method to obtain carbetocin precursor peptide I-amino resin; stripping off cysteine side chain protecting groups to obtain carbetocin precursor peptide II-amino resin; adding organic alkali and lithium chloride in solvent for cyclization to obtain carbetocin-amino resin; cracking to obtain carbetocin crude peptide; and purifying and freeze-drying to obtain the carbetocin. The method adopts the amino resin to synthesize carbetocin by the solid phase cyclization technology. The process is characterized by simple operation, easy post-treatment, high yield, low cost, and the like, and has considerable economical and practical value and broad application prospect.

The present invention is manganese dioxide process of extracting lithium from salt lake brine, and the process is suitable for producing lithium carbonate and lithium chloride with lithium-containing Qinghai saline lake brine, including concentrated lithium-containing Qinghai saline lake brine. The process includes sun shining saline lake brine to obtain concentrated lithium containing brine, selective adsorption of lithium ion with MnO2 adsorbent, eluting adsorbed lithium ion with hydrochloric acid solution, and refining and concentrating the elutriant to obtain material for preparing lithium carbonate and lithium chloride.

The invention relates to a separation and recovery method for n-methylpyrrolidone (NMP) and a lithium chloride catalyst during polyphenylene sulfide producing. The method is characterized by: directly carrying out vacuum distillation for a polyphenylene sulfide polycondensation mother liquid until the polyphenylene sulfide polycondensation mother liquid is dried to recover a solvent of the NMP, wherein the NMP can be used in the next recycling production; adding water to the distilled residues, then heating to a temperature of 40 DEG C, carrying out stirring and completely dissolving the distilled residues, carrying out filtering and washing the filter residues, mixing the resulting filtrate and the washing solution, and analyzing lithium content in the mixed solution; adding the mixed solution to a phosphoric acid solution or a sodium aluminate solution, wherein the phosphoric acid solution or the sodium aluminate solution has a lithium reaction equivalent of 105-115%, then completely stirring to enable lithium phosphate or lithium aluminate to be precipitated completely, then carrying out steps of filtering, washing, drying for the lithium phosphate or the lithium aluminate to recover the lithium salt having a purity more than 97%. According to the present invention, the operation of the method is simple; the cost is low; the recovered NMP and the recovered lithium salt havehigh purities.

The invention relates to a method for preparing high-purity lithium carbonate and other available byproducts from salt lake brine. The method comprises the following steps: (1) separating potassium and sodium by exposing salt in a salt field, (2) separating boron by an acidification method, (3) separating magnesium by a sedimentation method, (4) separating calcium by the sedimentation method, (5) preparing lithium chloride, and (6) preparing the lithium carbonate. The preparation method of the invention can purify the potassium, sodium, boron, magnesium and calcium ions respectively besides obtaining the lithium carbonate product of which the purity is over 99.5 percent so as to fully utilize the salt lake brine resource.

The invention relates to a method for preparing an aramid IIII fiber, which comprises the following steps of: (1) synthesizing a spinning stock solution, carrying out low-temperature copolymerization by adopting three monomers of p-phenylenediamine, paraphthaloyl chloride and 5(6)-amido-2-(4-amidophenyl)benzimidazole as raw materials and adopting dimethylacetylamide/lithium chloride as a solvent; (2) spinning by adopting a dry method spinning process, i.e. leading the spinning stock solution obtained in the previous step to pass through a spinneret and directly enter a hot inert gas channel and evaporating and removing the solvent in the spinning stock solution by utilizing a hot inert gas to obtain cured raw yarn; and (3) carrying out water washing and heat treatment on the raw yarn and winding to obtain the aramid IIII fiber. The method has high solid content of the spinning stock solution, high spinning speed, great improvement of spinning efficiency, obvious reduction of fiber manufacturing cost, improved mechanical performance of the manufactured aramid IIII fiber and wide application prospect.

The invention relates to a method for recycling lithium chloride from waste lithium iron phosphate, belongs to the technical field of waste and old lithium ion battery recycle, and solves the technical problem that the method for recycling lithium chloride from the waste lithium iron phosphate is provided. The method comprises the following steps of: roasting the waste lithium iron phosphate for 1-4hours under the temperature of 500-800 DEG C; leaching the materials after roasting by using hydrochloric acid, wherein the pH value is controlled to be within 0.5-1 during leaching; filtering so as to obtain a mixing liquid of lithium phosphate, iron phosphate and ferric chloride; heating the obtained mixing liquid to be at 80-100 DEG C; adjusting the pH value to be 2-2.5; reacting for 1-4hours; filtering; washing; drying so as to obtain the iron phosphate; adjusting the pH value of obtained filtrate to be 6-7; adding calcium chloride to perform phosphorous removal; and filtering; evaporating, concentrating, crystallizing, washing and drying the obtained filtrate to obtain lithium chloride.

The invention discloses an active agent and a method for carrying out surface treatment on materials to be welded of aluminium and aluminium alloys so as to improve the energy utilization rate of the aluminium and the aluminium alloys, deepen the fusion depth of welding seams and further obtain higher welding quality. The active agent for laser welding consists of a chloride and a fluoride, wherein the mass ratio of the chloride to the fluoride is (1-2): (1-4); the chloride is at least one of lithium chloride, sodium chloride, potassium chloride, zinc chloride, magnesium chloride, aluminium chloride, calcium chloride or tin chloride; and the fluoride is at least one of lithium fluoride, sodium fluoride, magnesium fluoride or calcium fluoride. When the surface treatment is carried out, firstly the fluoride and the chloride are mixed fully and uniformly, water is added to form a supersaturated solution, then the supersaturated solution is coated on the surface of a welded test piece as a coating agent, then drying is carried out, and finally laser welding is carried out under the condition of gas protection.

The invention discloses humidity conditioning building material which can automatically condition indoor humidity; the components of raw material and weight percentages of the building material are as follows: 60-80 percent of building gypsum, 8-15 percent of plant fiber, 5-15 percent of lithium chloride sol, 3-8 percent of gypsum retarder and 4-9 percent of white cement. The building material has strong humidity conditioning ability, obvious humidity releasing effect, low construction cost and easy-obtained raw materials.

This invention discloses a method for preparing anhydrous LiCl. The method comprises: (1) adding CaCl2 to Li2SO4 solution to obtain LiCl and CaSO4; (2) filtering and washing to remove CaSO4 and obtain LiCl solution; (3) concentrating, adding BaCl2 solution, reacting, filtering and washing to remove SO42-; (4) adding LiCO3 solution, reacting, filtering and washing to remove Ba2+ and Ca2+; (5) concentrating, cooling, crystallizing, separating and drying to obtain anhydrous LiCl. The method has such advantages as simple process, easy operation, low energy and water consumption, low Li loss, and high LiCl yield.

The invention relates to a solvent and catalyst recovery technology in polyphenyl thioether production, which comprises the steps of: after polycondensation reaction is finished, firstly adding 1-3mol/mol Na2S and fresh NMP (N-methyl pyrrolidone) solvent as a diluting agent, diluting the reaction system with NMP to obtain another mixture, and further treating the mixture by filtering, extraction, evaporation and spiral evaporator to respectively obtain a mixed solution containing NMP and water and a powder mixture containing a cosolvent and byproducts; and evaporating the mixed solution containing NMP and water to remove water to obtain NMP solvent containing certain impurities, further rectifying and purifying the NMP solvent by a rectifying tower to obtain NMP solvent with the purity of 99.98% and the recovery rate of 96-98%to be recycled for polyphenyl thioether resin synthesis, and treating the powder mixture containing the cosolvent and byproducts to obtain catalyst lithium chloride with the purity of 99.95-99.98% and the recovery rate of 98-99%.

The invention provides a sulfide solid electrolyte based on oxygen doping. The sulfide solid electrolyte is prepared from the chemical ingredients, in percentage by mass: 36-60% of lithium sulfide orlithium selenide, 18-48% of phosphorus pentasulfide or phosphorus selenide, 1-23% of metal oxide or specific nonmetallic oxide and 8-37% of lithium chloride, lithium bromide or lithium iodide. The preparation method of the sulfide solid electrolyte mainly comprises the steps that the raw materials are sufficiently blended and subjected to tabletting, then placed in a quartz tube to be burned and sealed, the product is placed in a muffle furnace and heated to be 400-600 DEG C at a slow heating rate, the optimal heating rate is 0.3 DEG C/minute, heat preservation is conducted for 12-48 hours, and then the product is cooled to reach the room temperature; and the product is ground to be powder, and the sulfide solid electrolyte based on oxygen doping is prepared. The sulfide solid electrolyteis easy to prepare and high in repeatability, the prepared solid electrolyte has the high ionic conductivity and good stability to the air and positive and negative electrodes.