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51results about How to "Less impurity ions" patented technology

Gas-sensor nanometer sensitive material, slurry with gas-sensor nanometer sensitive material, preparing method of gas-sensor nanometer sensitive material, preparing method of slurry and application of gas-sensor nanometer sensitive material

The invention relates to a gas-sensor nanometer sensitive material, slurry with the gas-sensor nanometer sensitive material, preparing of the gas-sensor nanometer sensitive material, preparing of the slurry and an application of the gas-sensor nanometer sensitive material. A preparing method of the gas-sensor nanometer sensitive material includes the following steps that 1, stannate is added into ultrapure water and subjected to ultrasonic dispersion, a stannate solution is obtained, a urea ethanol solution is added, ultrasonic processing continues, an obtained mixed solution is transferred into a hydrothermal reaction kettle, after reaction is completed, cooling is carried out, and bottom precipitate is collected, centrifugally washed, arranged in a dryer and dried; 2, nanometer SnO2 hollow sphere powder obtained after drying is added into distilled water to be subjected to ultrasonic dispersion, a Pd(NO3)2 solution is dropwise added under the stirring condition, ammonium hydroxide is added till the pH of the mixed solution ranges from 9 to 12, the mixture is stirred at the indoor temperature, bottom precipitate is centrifugally collected, washed to be neutral and dried, and finally Pd-doping nanometer SnO2 hollow spheres are obtained. The gas-sensor nanometer sensitive material, the slurry, the preparing and the application have the advantages that the preparing methods are simple, the quantity of introduced foreign ions is small, the yield is high, volume production is facilitated, the specific area of the material is large, dispersity is good, and high sensitivity and short response recovery time are achieved.
Owner:WUHAN INSTITUTE OF TECHNOLOGY

Method for producing water-soluble potassium ammonium phosphate from wet-process phosphoric acid

The invention relates to a method for producing water-soluble potassium ammonium phosphate from wet-process phosphoric acid. According to the method, a monoammonium phosphate solution is prepared from low-cost wet-process phosphoric acid as the raw material by the steps of desulfuration and defluorination and neutralization with ammonia; then the replacement reaction of the monoammonium phosphate solution and potassium chloride and the crystallization are carried out to obtain a water-soluble fertilizer which contains potassium dihydrogen phosphate as a main component and adopts ammonium dihydrogen phosphate as an auxiliary component, wherein the content of chlorine is smaller than 2%; and excess potassium chloride and nitrogen produce a by-product such as nitrogen phosphorus and potassium chloride water soluble compound fertilizer. Meanwhile, the by-product in the production process can be directly used as a citric acid soluble phosphatic fertilizer. The method has simple processes, and the prepared water-soluble ammonium potassium dihydrogen phosphate is high in purity, nutrient and potassium content. No waste residues are discharged in the whole process, so that the method is environment-friendly and has better social and economical benefits.
Owner:KINGENTA ECOLOGICAL ENG GRP

Method for preparing iron p-toluenesulfonate and solution thereof

The invention discloses a method for preparing iron p-toluenesulfonate and a solution thereof. The method for preparing the iron p-toluenesulfonate includes the steps that (1) a sodium hydroxide solution and an ammonium ferric sulfate solution are prepared; (2) the sodium hydroxide solution is added in the ammonium ferric sulfate solution, the final potential of hydrogen (pH) value of reaction is 7.0 to 9.0, and iron hydroxide precipitation is obtained; (3) the iron hydroxide precipitation is washed, placed in a filter bag and suspended to be dried at room temperature until the iron hydroxide precipitation which is colloid and contains a small amount of water is formed; (4) iron hydroxide which is suspended to be dried is reacted with a p-toluene sulfonic acid to generate an iron p-toluenesulfonate solution; (5) the iron p-toluenesulfonate solution is filtered and concentrated to be viscous, and discharging-cooling and crystallization are performed; and (6) crystals are crushed and dried to obtain the product. The method for preparing the iron p-toluenesulfonate and the solution thereof has the advantages that the activity of the reaction intermediate iron hydroxide is good, the reaction with the p-toluene sulfonic acid is complete, the process is simple, the energy consumption and the cost are low, and the environmental pollution is small.
Owner:广州化学试剂厂

Method for co-production of industrial grade ammonium dihydrogen phosphate and feed grade calcium phosphate by using defluorinated phosphoric acid

The invention relates to a method for co-production of industrial grade ammonium dihydrogen phosphate and feed grade calcium phosphate by using defluorinated phosphoric acid, belonging to the technical field of chemical industry production. The invention aims at solving a technical problem of providing a method for co-production of industrial grade ammonium dihydrogen phosphate and feed grade calcium phosphate by using defluorinated phosphoric acid. The method comprises the following steps: neutralizing the defluorinated phosphoric acid and a primary neutralizer, performing solid-liquid separation to obtain a filtrate A and a filter cake A, neutralizing the filtrate A and a secondary neutralizer to make pH of reaction liquid reach 3.0-5.0, and performing solid-liquid separation to obtain a filtrate B and a filter cake B; concentrating, crystallizing, filtering and drying the filtrate B; or directly performing spray drying at 60-200 DEG C on the filtrate B to obtain the industrial grade ammonium dihydrogen phosphate; and drying the filter cake A and the filter cake B in combination to obtain the feed grade calcium phosphate. According to the method provided by the invention, the technology is simple, generation of waste residue is avoided, raw materials are fully used, and purity of the produced products is high, so that the method has better social benefit and economic benefit.
Owner:SINOCHEM YUNLONG +1

Production method of ore brine crystal salt

The invention provides a production method of an ore brine crystal salt. In the method, ore brine is used as raw brine, wind and sunlight are used as energy sources, and a shoal pool is used as a crystallization pool. The production method is characterized by comprising the following steps: after exploiting the ore brine, firstly passing the exploited ore brine through a pipeline and then weighing with a pump station, respectively storing the weighed ore brine crystallization salt in a brine hoarding table, pouring to a crystallization pool from the brine hoarding table, and evaporating and crystallizing through the wind and sunlight in the crystallization pool; and controlling the concentration and depth of the brine, properly adding or replacing novel brine, mastering the depth and market demand of the crystal salt, discharging the brine and recovering the salt timely, and recycling the old brine. According to the invention, energy consumption is low, 0.18 ton of coal and 50-60kw.h of electricity are consumed for producing every ton of ore salt, and the electricity consumption of every ton of salt is about 5kw.h in the invention; large land area is saved and accounts for 1 / 20 of that of sea salt; the method is environmentally-friendly, and zero emission is basically achieved; and the produced ore brine crystal salt has high quality, meets a GB / T5 462-2003 prior industrial salt standard, has extremely less impurity ions and large crystalline particles, and is especially suitable for a chlor-alkali industry.
Owner:江苏省东泰盐业投资管理有限公司

Heterojunction solar cell taking silicon nanorod array as substrate and fabrication method of heterojunction solar cell

The invention discloses a heterojunction solar cell taking a silicon nanorod array as a substrate and a fabrication method of the heterojunction solar cell. The solar cell uses a silicon nanorod array with a large depth-width ratio as the substrate, and other thin film materials are wrapped by a magnetron sputtering method to form a heterojunction structure. The fabrication method comprises the following steps of fabricating the silicon nanorod array with the large depth-width ratio on a surface of a P-type silicon wafer by a self-assembly method of a cesium chloride nanometer island; fabricating an aluminum back filed on a back surface; wrapping a surface of the silicon nanorod array with an N-type material layer such as zinc oxide and cadmium sulfide by the magnetron sputtering method; covering a surface of the N-type material layer with an ITO transparent conductive layer; and fabricating a titanium-silver electrode on an upper surface. The solar cell taking the silicon nanorod array with the large depth-width ratio as the substrate has the advantages that 1, the surface ratio of the substrate can be effectively increased, the effective area of a heterojunction is expanded, and absorption to incident light is improved; and 2, by means of a favorable light trapping effect, reflection can be reduced, and the performance of the heterojunction cell is improved.
Owner:INST OF HIGH ENERGY PHYSICS CHINESE ACAD OF SCI

Method for efficiently removing fluorine ions in manganese sulfate solution

InactiveCN108118152AWith physical adsorptionEasy to separateProcess efficiency improvementIon contentSulfate
The invention provides a method for efficiently removing fluorine ions in a manganese sulfate solution. The method is characterized in that a certain quantity of to-be-processed manganese sulfate solution is added into reaction equipment, the content of the fluorine ions in the solution is measured, solid cerium hydroxide with a certain fluorine ion content proportion is added under the conditionsthat the temperature is 30-50 DEG C and the pH value is 2-6, the material is stirred for 8-12 h at the rotational speed of 150-350 r / min, then stirring is stopped, the material is left to stand for 12-18 h and then transferred into filtering equipment for filtration, the filtrate is a fluorine-removed qualified manganese sulfate solution, filter cake is added into reverse osmosis water at a solid-liquid mass ratio of 1:(1-6), stirring and washing are performed for 0.5 h, and filtering is performed to obtain fluorine-containing cerium hydroxide which is then fed into a regeneration procedure.According to the method, lots of residual fluorine ions in a manganese sulfate solution system can be removed, the content of a fluoride in the processed solution can be reduced to 100 ppm or below, and the fluorine removal agent cerium hydroxide can be recycled after being regenerated, so that the production cost is greatly lowered.
Owner:GUANGDONG GUANGHUA SCI TECH

Production device and production method of lithium hexafluorophosphate

The invention relates to a production device and a production method of lithium hexafluorophosphate, and the method comprises the following steps: introducing phosphorus pentachloride and anhydrous hydrogen fluoride into a replacement reaction tank for reaction, and introducing the generated phosphorus pentafluoride into a synthesis reaction kettle; introducing anhydrous hydrogen fluoride and lithium carbonate into an acidification pool to prepare a hydrogen fluoride and lithium fluoride mixed solution; and feeding the phosphorus pentafluoride and the mixed solution into a circular reaction kettle for reaction, feeding excessive hydrogen fluoride and lithium fluoride into a synthesis reaction kettle for synthesis of lithium hexafluorophosphate, and feeding the generated product liquid into a crystallization tank for crystallization. And returning the rest mother liquor to a rectification refining section through a pump to participate in the reaction again. The hydrogen chloride gas generated by the circular reaction kettle can be absorbed to prepare industrial hydrochloric acid. The purity of the lithium hexafluorophosphate crystal produced by the system reaches 99% or above, and the moisture (mass fraction) can be controlled to be 5 * 10 <-6 > or below.
Owner:BEIJING UNIV OF CHEM TECH

Method for preparing high-purity manganese sulfate and high-purity manganese carbonate by reduction leaching of pyrolusite through scrap iron

The invention discloses a method for preparing high-purity manganese sulfate and high-purity manganese carbonate by reduction leaching of pyrolusite through scrap iron. The method comprises the following steps of: performing reduction leaching on the pyrolusite with the scrap iron in a sulfuric acid medium to obtain manganese, regulating the pH value to be 5-6 by using a neutralization method, hydrolyzing ferric iron in the solution into an iron hydroxide precipitate, and filtering to obtain primary filtrate of manganese sulfate and filter residue; adding a vulcanizing agent into the primary filtrate for vulcanization to remove heavy metal ions, adding a fluorinating agent for removing calcium, magnesium and other ions in the solution, standing the solution and removing sediments; and concentrating and crystallizing the purified solution to prepare the high-purity manganese sulfate, or adding ammonium carbonate to prepare high-purity manganese carbonate, concentrating the filtrate andrecovering the ammonium carbonate, wherein the filter residue in the first step is leached by solution of dilute sulfuric acid, and the filtrate after filtration is subjected to calcium removal, standing and concentration to form polyferric sulfate. The method is low in cost and investment, is suitable for comprehensive exploitation and utilization of different grades of pyrolusite, can effectively utilize natural resources and also can create obvious economic benefit.
Owner:HUNAN UNIV OF SCI & TECH

Method for producing water-soluble potassium ammonium phosphate from wet-process phosphoric acid

The invention relates to a method for producing water-soluble potassium ammonium phosphate from wet-process phosphoric acid. According to the method, a monoammonium phosphate solution is prepared from low-cost wet-process phosphoric acid as the raw material by the steps of desulfuration and defluorination and neutralization with ammonia; then the replacement reaction of the monoammonium phosphate solution and potassium chloride and the crystallization are carried out to obtain a water-soluble fertilizer which contains potassium dihydrogen phosphate as a main component and adopts ammonium dihydrogen phosphate as an auxiliary component, wherein the content of chlorine is smaller than 2%; and excess potassium chloride and nitrogen produce a by-product such as nitrogen phosphorus and potassium chloride water soluble compound fertilizer. Meanwhile, the by-product in the production process can be directly used as a citric acid soluble phosphatic fertilizer. The method has simple processes, and the prepared water-soluble ammonium potassium dihydrogen phosphate is high in purity, nutrient and potassium content. No waste residues are discharged in the whole process, so that the method is environment-friendly and has better social and economical benefits.
Owner:KINGENTA ECOLOGICAL ENG GRP

Method for preparing large-particle lithium carbonate from salt lake lithium-rich brine

The invention discloses a method for preparing large-particle lithium carbonate from salt lake lithium-rich brine. The method comprises the following steps: step 1, heating the salt lake lithium-richbrine to 70-85 DEG C, after heating is completed, maintaining the temperature and adding a surfactant into the salt lake lithium-rich brine; step 2, maintaining the temperature in the step 1, adding acarbonate solution into the pre-treated salt lake lithium-rich brine, and performing a reaction for 1-3 h to obtain reaction product slurry; and step 3, allowing the reaction product slurry to standfor 10-20 h, performing solid-liquid separation, washing the obtained solid particles, and performing drying to obtain the large-particle lithium carbonate. According to the method provided by the invention, the certain surfactant is added into the reaction system, so that a particle size of the lithium carbonate is increased in the precipitation process, and the obtained lithium carbonate has a particle size d(0.9) of 300-600 [mu]m; and meanwhile impurity ions adsorbed at the surface of the lithium carbonate product are reduced, and purity and a yield of a primary product are improved, wherein the purity of the primary product is >=95%.
Owner:QINGHAI INST OF SALT LAKES OF CHINESE ACAD OF SCI

Method for recovering copper and iron from etching waste liquid

The invention discloses a method for recovering copper and iron from etching waste liquid. The method comprises the following steps: oxidizing the etching waste liquid containing copper and iron elements into a ferric trichloride solution containing the copper element, adding industrial hydrochloric acid and butyl acetate for extraction, standing for layering, taking an organic phase, adding an iron-containing and acid-containing washing solution for washing the organic phase, and adding a stripping agent into the organic phase for stripping, to obtain ultralow-impurity ferric trichloride, and evaporating and concentrating to remove organic matters to obtain the high-purity ferric trichloride. The organic phase can be recycled, a water phase is extracted for multiple times until no ferric trichloride exists, a high-purity copper plate can be obtained through an electrolytic copper extraction process, and a low-copper electrolyte can be electrolyzed again through evaporation and concentration or can be used as hydrochloric acid required by extraction. The copper content of the high-purity ferric trichloride product produced by the process is lower than 5 ppm, and the high-purity ferric trichloride product can be applied to the fields of drinking water treatment, medical intermediates, analysis and testing, precise etching and the like; and the copper plate obtained by electrolysis has high purity and high value.
Owner:3R ENVIRONMENTAL TECH CO LTD

Method for recovering vanadium by virtue of magnesiation and roasting of stone coal

The invention belongs to the technical field of mineral processing and particularly relates to a method for recovering vanadium by virtue of magnesiation and roasting of stone coal. The technical scheme is as follows: decarburizing stone coal ores, then adding MgSO4, performing fine grinding until the granularity is not greater than 100 meshes, performing fluosolid roasting, and performing water leaching on the roasted sample at a certain temperature, thereby obtaining vanadium-containing leachate; leaching the water leaching dregs with sulphuric acid, washing the leaching dregs with water, mixing acid leaching liquor with a washing solution so as to obtain a mixture used for leaching roasting dregs during water leaching, drying washed residues, mixing the dried washed residues with the decarburized stone coal ore, and performing ore grinding; and performing extraction and impurity removal on the obtained vanadium-containing leachate, then adding an NH4Cl solution for molybdenum precipitation, and incinerating the precipitate to obtain V2O5. The method is used for processing stone coal vanadium ore with vanadium content of no less than 0.80%; the recovery rate of vanadium in the obtained leachate is no less than 75%. According to the method, less harmful gases are discharged in a roasting process, the water consumption and the acid consumption are less, the production cost is low, solids and liquids can be recycled, and the application potential is great, so that the method is an economical and effective vanadium recovery method.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

A kind of red fluorescent powder for near ultraviolet light excitation and preparation method thereof

The invention discloses a red fluorescent powder for near-ultraviolet light excitation and a preparation method thereof. According to the stoichiometric ratio 2:(1-x):x, respectively take Li 2 MoO 4 Powder, La(No 3 ) 3 ·nH 2 O powder and Eu(NO 3 ) 3 The solution is used as raw material, where x=0~1.0; hydrothermal reaction at 240°C for 24h, then the precursor is centrifuged and dried at 525~550°C for 3~4h, and finally taken out and ground to obtain the target product La 1.0‑x Mo 2 o 9 :xEu 3+ Red fluorescent powder; using hydrothermal method to form a pure phase structure phosphor, the cost is low, after the hydrothermal reaction, the overall process is simple; the raw materials are lithium molybdate, hydrated lanthanum nitrate, europium nitrate and lithium hydroxide, and Compared with the target product, the amount of introduced impurity ions is small, which can improve the purity of the product; the doping method of the present invention helps crystallization, Li + The addition of ions promotes the formation of crystals; the phosphor has a strong charge transfer band, which has the highest intensity under the excitation of near-ultraviolet light from 335nm to 350nm, and its color coordinates are similar to standard red light, with high color purity and luminous intensity. Excellent performance.
Owner:SHAANXI UNIV OF SCI & TECH
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