Abstract: The present invention provides methods for preparing trimanganese tetroxide with low BET specific surface area and methods for controlling particle size of trimanganese tetroxide and trimanganese tetroxide product.

Abstract: Provided is a method for preparing barium titanate, which comprises: dissolving BaCl2.2H2O into TiCl4 solution to prepare Ba—Ti mixed solution with a Ba/Ti mol ratio of 1:1; adding ammonia and ammonium bicarbonate into deionized water to prepare synthetic agent with a NH4OH/NH4HCO3 mol ratio of 5:1; adding Ba—Ti mixed solution and synthesis agent into a reactor for synthesis to obtain a slurry; pressure filtering, thermal washing and then pressure filtering, to obtain a filter cake; calcining the filter cake for 1 hour at 590-610° C., followed by further calcining for 2 hours at 700-950° C.; crushing the obtained solid produced by a crusher, and thereby obtaining barium titanate. The obtained barium titanate is spherical, and has a narrower particle size distribution. The method reduces costs.

Abstract: The present invention provides methods for preparing trimanganese tetroxide with low BET specific surface area and methods for controlling particle size of trimanganese tetroxide and trimanganese tetroxide product.

Abstract: The present invention provides methods for preparing trimanganese tetroxide with low BET specific surface area and methods for controlling particle size of trimanganese tetroxide and trimanganese tetroxide product.

Abstract: A method for preparing manganese sulfate monohydrate by desulfurizing fume with middle-low grade manganese dioxide ore, which includes: preparing a slurry by using middle-low grade manganese dioxide ore powder, putting sulfur-containing fume in an absorbing device and controlling gas velocity and gas-liquid ratio, and then adding manganese dioxide slurry and controlling the slurry to backwards flow relative to the sulfur-containing fume, discharging the desulfurized fume from the absorbing device, pressure-filtering and separating the slurry discharged from the absorbing device, recycling the mother liquor to the absorbing device, and continuing the recycling operation until the manganese sulfate in the mother liquor is >=200 g/l, the obtained filter cake at 60-70° C., adjusting pH value of the clear solution obtained to 2-4, adding manganese sulfide under agitation at 25-95° C.

Abstract: Provided is a method for preparing manganese sulfate monohydrate, which comprises the following steps: (1) reacting MnO with (NH4)2SO4 solution under heat, and separating solid from liquid after reaction 2) determining the concentration of MnSO4 in the resulting solution of step 1), adding equimolar ammonium sulfide solution thereto to carry out reaction under agitation, separating solid from liquid after reaction, and then washing solid phase: 3) dissolving the solid phase with concentrated sulfuric acid, adding hydrogen peroxide to the obtained solution, heating to boiling, adjusting the pH value of the solution to 5-6, removing the solid phase through precise filtration, evaporating and oven drying the filtrate to obtain MnSO4.H2O product. The impurities are separated away and the amount of byproducts is reduced by this method, and the yield of manganese sulfate monohydrate is improved.

Abstract: The present invention provides methods for preparing trimanganese tetroxide with low BET specific surface area and methods for controlling particle size of trimanganese tetroxide and trimanganese tetroxide product.

Abstract: The present invention relates to a method for preparing barium carbonate and the barium carbonate product obtained by the method. The method for preparing barium carbonate comprises: (1) Adding barium hydroxide octahydrate crystal into the ice-water bath and mixing them, and controlling the temperature to be within 0˜5° C.; (2) Introducing carbon dioxide into the mixture obtained from the step (1), till pH value of the reaction solution reaches 6.0-7.0; (3) Carrying out solid-liquid separation for the solid-liquid mixture obtained from the step (2), drying the obtained solid so as to obtain barium carbonate product. The present invention method solves the problem in the prior art that the character of low strontium and the character of large specific surface area can not co-exist, which makes the property of barium carbonate product can not affect the sintering temperature, and thus the property material is improved.

Abstract: High-purity barium chloride (99.60% or more) is produced having low strontium (lower than 10 ppm) by using barium carbonate or a clear barium chloride filtration and hydrochloric acid mixed under agitation at a maintained temperature and pH. The barium chloride is obtained as liquid phase and then crystallized through further processes.

Abstract: Provided is a method for preparing manganese sulfate monohydrate, which comprises the following steps: (1) adding equimolar BaS or SrS solution into manganese sulfate solution to carry out reaction fully, and separating and washing the obtained solid; (2) mixing the solid with deionized water to prepare a slurry, dissolving the slurry with concentrated sulfuric acid, and separating solid from liquid to obtain MnSO4 solution; (3) adding proper amount of hydrogen peroxide to the MnSO4 solution, heating to boiling, adjusting the pH value of the solution within 5-6, evaporation the filtrate after a precise filtration, and crystallizing and drying to obtain MnSO4 H2O product. Manganese sulfate monohydrate can be produced at high yield in a cost-efficient manner by this method.

Abstract: An innovative end cap for IC trays includes a bottom and side walls. The side walls extend upwardly from the bottom and form a tray-accommodating space. The innovative end cap includes a plurality of buffering ribs and buffering grooves on its surfaces. The buffering ribs and buffering grooves arranged on the end cap can fully absorb, disperse and transfer the impact energy generated during testing, storage, collision and shock of the trays which accommodate the precision semiconductor components therein, and increase impact strength and anti-dropping damage ability of the end cap. Therefore, the innovative end cap with the buffering ribs and buffering grooves can not only protect the trays and extend the service lifetime of the trays, but also give better protection to the precision semiconductor components such as Chips, IC etc in the trays.

Abstract: An intelligent tray for chips includes a main body having a readable and writable memory unit thereon. The readable and writable memory unit has parameters related to the intelligent tray written therein. The parameters written in the readable and writable memory unit can be read out automatically by a machine, and no need to be manually checked one by one. This helps to automate production, improve production efficiency and shorten production cycle.

Abstract: A method for preparing manganese sulfate monohydrate by desulfurizing fume with middle-low grade manganese dioxide ore, which includes: preparing a slurry by using middle-low grade manganese dioxide ore powder, putting sulfur-containing fume in an absorbing device and controlling gas velocity and gas-liquid ratio, and then adding manganese dioxide slurry and controlling the slurry to backwards flow relative to the sulfur-containing fume, discharging the desulfurized fume from the absorbing device, pressure-filtering and separating the slurry discharged from the absorbing device, recycling the mother liquor to the absorbing device, and continuing the recycling operation until the manganese sulfate in the mother liquor is >=200 g/l, the obtained filter cake at 60-70° C., adjusting pH value of the clear solution obtained to 2-4, adding manganese sulfide under agitation at 25-95° C.

Abstract: Provided is a method for preparing manganese sulfate monohydrate, which comprises the following steps: (1) adding equimolar BaS or SrS solution into manganese sulfate solution to carry out reaction fully, and separating and washing the obtained solid; (2) mixing the solid with deionized water to prepare a slurry, dissolving the slurry with concentrated sulfuric acid, and separating solid from liquid to obtain MnSO4 solution; (3) adding proper amount of hydrogen peroxide to the MnSO4 solution, heating to boiling, adjusting the pH value of the solution within 5-6, evaporation the filtrate after a precise filtration, and crystallizing and drying to obtain MnSO4 H2O product. Manganese sulfate monohydrate can be produced at high yield in a cost-efficient manner by this method.

Abstract: Provided is a method for preparing manganese sulfate monohydrate, which comprises the following steps: (1) reacting MnO with (NH4)2SO4 solution under heat, and separating solid from liquid after reaction; 2) determining the concentration of MnSO4 in the resulting solution of step 1), adding equimolar ammonium sulfide solution thereto to carry out reaction under agitation, separating solid from liquid after reaction, and then washing solid phase; 3) dissolving the solid phase with concentrated sulfuric acid, adding hydrogen peroxide to the obtained solution, heating to boiling, adjusting the pH value of the solution to 5-6, removing the solid phase through precise filtration, evaporating and oven drying the filtrate to obtain MnSO4.H2O product. The impurities are separated away and the amount of byproducts is reduced by this method, and the yield of manganese sulfate monohydrate is improved.

Abstract: Provided is a method for preparing barium titanate, which comprises: dissolving BaCl2.2H2O into TiCl4 solution to prepare Ba—Ti mixed solution with a Ba/Ti mol ratio of 1:1; adding ammonia and ammonium bicarbonate into deionized water to prepare synthetic agent with a NH4OH/NH4HCO3 mol ratio of 5:1; adding Ba—Ti mixed solution and synthesis agent into a reactor for synthesis to obtain a slurry; pressure filtering, thermal washing and then pressure filtering, to obtain a filter cake; calcining the filter cake for 1 hour at 590-610° C., followed by further calcining for 2 hours at 700-950° C.; crushing the obtained solid produced by a crusher, and thereby obtaining barium titanate. The obtained barium titanate is spherical, and has a narrower particle size distribution. The method reduces costs.