,;where CF is mass fraction of fluorides, %; mF is weight of produced lead fluorochloride precipitate, g; mnF is weight of sample of electrolyte taken during analysis for fluoride content, g; 0.0726 is conversion factor of lead fluorochloride weight per weight of fluoride; 200 – capacity of volumetric flask with electrolyte solution, cm3; 100 is volume of aliquot of electrolyte solution, cm3. In the absence of an aluminum-containing thickener in the electrolyte, the mass fraction of fluorides is determined by potentiometric titration with a fluoride-selective electrode. For this purpose, a portion of the ground sample is dissolved in a diluted HCl solution, into which a fluoride-selective and auxiliary electrodes are placed, and while continuously stirring on a magnetic mixer, titration of fluorides from the glass buret is carried out with a solution of lanthanum nitrate to an equivalence point according to a pH meter-ionomer; mass fraction of fluorides is calculated by formula: ; ,;where CF is weight fraction of fluorides, %; VLa is volume of nitrate lanthanum solution, consumed for titration, cm3; mnF is weight of sample of electrolyte taken during analysis for content of fluorides in absence of aluminum, g; TLa-F is mass concentration of lanthanum nitrate solution by fluoride, mg/cm3. To determine weight fraction of bromides in electrolyte water solution of ground sample of solid lithium electrolyte is prepared with addition of concentrated sulfuric acid (H2SO4) with subsequent addition of solution with mixture of potassium iodate and sodium thiosulphate. Reaction of lithium bromide with potassium iodide results in production of bromine, its removal by boiling and titration of excess potassium iodide to determine mass fraction of bromides by iodometric method by formula:; ,;where CBr is mass fraction of bromides in electrolyte, %; 10 is volume of iodine nitrate solution added in excess of potassium iodate, cm3; mnBr is weight of sample of electrolyte, taken during analysis for content of bromides, g; CK-Br is mass concentration of potassium iodate solution in terms of bromide, mg/cm3. To determine weight ratio of chlorides in electrolyte, difference is determined between total value of weight fractions of bromides and chlorides determined by mercurimetric titration in acid medium with indicator diphenylcarbazone, and preset mass fraction of bromides in sample, which is installed during titration of mercury (I) with nitric-acid. Then, volume difference of mercury (I) nitric-acid for titration of chlorides is calculated from difference of volumes and mass fraction of chlorides in lithium electrolyte corresponding to this value is calculated by formula:; ,;where CCl is weight fraction of chlorides in electrolyte, %; is volume of solution of mercury (I) nitric-acid, consumed for titration of sum of chlorides and bromides, cm3; – volume of mercury (I) nitric-acid solution, consumed for bromides titration, cm3:; ; – mass concentration of nitric acid solution of mercury chloride and bromide, mg/cm3; is mass fraction of bromides in electrolyte, %; mnCl is a charge of electrolyte taken during determination of chlorides, g.;EFFECT: invention provides high accuracy of determining individual concentrations of lithium halides in the presence of aluminum salts in solid lithium electrolyte.;1 cl, 7 tbl, 2 ex"/> METHOD OF QUANTITATIVE DETERMINATION OF LITHIUM HALIDES IN LITHIUM ELECTROLYTE FOR THERMAL CHEMICAL SOURCES OF CURRENT
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METHOD OF QUANTITATIVE DETERMINATION OF LITHIUM HALIDES IN LITHIUM ELECTROLYTE FOR THERMAL CHEMICAL SOURCES OF CURRENT

机译:电流热化学源中锂电解液中卤化锂的定量测定方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to analytical chemistry, specifically to methods of determining concentration of electrolyte components for thermal chemical current sources (TCCS), and can be used for determination of halogenides of alkali metals at their joint presence in solid lithium electrolytes. For this purpose grinding of solid sample of electrolyte is preliminary grinding, then taken and ground samples of solid lithium electrolyte are directed to separate stages of consecutive determination of fluorides, bromides and chlorides. To determine mass fraction of fluorides gravimetric method is used after preliminary fusion of ground sample with complex reagent from carbonate salts of potassium and sodium and further leaching mixture with hot distilled water. Precipitate of aluminum and silicon impurities is separated and neutralized with hydrochloric acid (HCl), then with nitric acid (HNO3) at temperature not exceeding 40 °C. Fluorides are concentrated by precipitation with lead acetate solution, lead fluorochloride is washed at pH 3.5–4.6, then dried and weight fraction of fluorides is determined by formula: ; ,;where CF is mass fraction of fluorides, %; mF is weight of produced lead fluorochloride precipitate, g; mnF is weight of sample of electrolyte taken during analysis for fluoride content, g; 0.0726 is conversion factor of lead fluorochloride weight per weight of fluoride; 200 – capacity of volumetric flask with electrolyte solution, cm3; 100 is volume of aliquot of electrolyte solution, cm3. In the absence of an aluminum-containing thickener in the electrolyte, the mass fraction of fluorides is determined by potentiometric titration with a fluoride-selective electrode. For this purpose, a portion of the ground sample is dissolved in a diluted HCl solution, into which a fluoride-selective and auxiliary electrodes are placed, and while continuously stirring on a magnetic mixer, titration of fluorides from the glass buret is carried out with a solution of lanthanum nitrate to an equivalence point according to a pH meter-ionomer; mass fraction of fluorides is calculated by formula: ; ,;where CF is weight fraction of fluorides, %; VLa is volume of nitrate lanthanum solution, consumed for titration, cm3; mnF is weight of sample of electrolyte taken during analysis for content of fluorides in absence of aluminum, g; TLa-F is mass concentration of lanthanum nitrate solution by fluoride, mg/cm3. To determine weight fraction of bromides in electrolyte water solution of ground sample of solid lithium electrolyte is prepared with addition of concentrated sulfuric acid (H2SO4) with subsequent addition of solution with mixture of potassium iodate and sodium thiosulphate. Reaction of lithium bromide with potassium iodide results in production of bromine, its removal by boiling and titration of excess potassium iodide to determine mass fraction of bromides by iodometric method by formula:; ,;where CBr is mass fraction of bromides in electrolyte, %; 10 is volume of iodine nitrate solution added in excess of potassium iodate, cm3; mnBr is weight of sample of electrolyte, taken during analysis for content of bromides, g; CK-Br is mass concentration of potassium iodate solution in terms of bromide, mg/cm3. To determine weight ratio of chlorides in electrolyte, difference is determined between total value of weight fractions of bromides and chlorides determined by mercurimetric titration in acid medium with indicator diphenylcarbazone, and preset mass fraction of bromides in sample, which is installed during titration of mercury (I) with nitric-acid. Then, volume difference of mercury (I) nitric-acid for titration of chlorides is calculated from difference of volumes and mass fraction of chlorides in lithium electrolyte corresponding to this value is calculated by formula:; ,;where CCl is weight fraction of chlorides in electrolyte, %; is volume of solution of mercury (I) nitric-acid, consumed for titration of sum of chlorides and bromides, cm3; – volume of mercury (I) nitric-acid solution, consumed for bromides titration, cm3:; ; – mass concentration of nitric acid solution of mercury chloride and bromide, mg/cm3; is mass fraction of bromides in electrolyte, %; mnCl is a charge of electrolyte taken during determination of chlorides, g.;EFFECT: invention provides high accuracy of determining individual concentrations of lithium halides in the presence of aluminum salts in solid lithium electrolyte.;1 cl, 7 tbl, 2 ex
机译:技术领域本发明涉及分析化学,尤其涉及确定用于热化学电流源(TCCS)的电解质组分的浓度的方法,并且可以用于在固体锂电解质中联合存在时测定碱金属的卤化物。 。为此目的,将固体电解质样品的研磨先进行初步研磨,然后将固体锂电解质的样品研磨后,分别引导至依次测定氟化物,溴化物和氯化物的单独阶段。为了测定氟化物的质量分数,在将磨碎的样品与钾和钠的碳酸盐形成的复杂试剂进行初步融合后,再用热蒸馏水浸出混合物,然后采用重量分析法。分离出铝和硅杂质的沉淀并先用盐酸(HCl)中和,然后再用硝酸(HNO 3 )在不超过40°C的温度下中和。氟化物通过用乙酸铅溶液沉淀而浓缩,氟氯化铅在pH 3.5–4.6洗涤,然后干燥,氟化物的重量分数由下式确定: ,其中C F 是氟化物的质量分数,% ; m F 是所产生的氟氯化铅沉淀的重量,g; m nF 是分析氟化物含量时所取电解质样品的重量,g; 0.0726是氟氯化铅重量/氟化物重量的换算系数; 200 –带电解液的容量瓶的容量,cm 3 ; 100是电解质溶液的等分体积,cm 3 。在电解质中不存在含铝增稠剂的情况下,氟化物的质量分数通过用氟化物选择电极的电位滴定法确定。为此,将一部分磨碎的样品溶解在稀盐酸溶液中,并在其中放置了氟化物选择电极和辅助电极,并在磁力搅拌器上连续搅拌的同时,用滴定管从玻璃滴定管中滴定氟化物。根据pH计离聚物,将硝酸镧溶液溶解至当量点;氟化物的质量分数由下式计算: ,其中C F 是氟化物的重量分数,% ; V La 为硝酸镧溶液的体积,用于滴定消耗,cm 3 ; m nF 是在不存在铝的情况下分析氟化物含量时获取的电解质样品的重量,g; T La-F 是氟化镧硝酸镧溶液的质量浓度,mg / cm 3 。为了确定溴化锂在电解液水溶液中的重量分数,准备了固体锂电解质研磨样品,方法是加入浓硫酸(H 2 SO 4 ),然后再加入溶液与碘酸钾和硫代硫酸钠的混合物。溴化锂与碘化钾的反应产生溴,通过沸腾除去溴并滴定过量的碘化钾,通过碘量法通过以下公式确定溴化物的质量分数: ,其中C Br 是电解质中溴化物的质量分数,%; 10是加入过量碘酸钾cm 3 的硝酸碘溶液的体积; m nBr 是在分析溴化物含量时所获取的电解质样品的重量g; C K-Br 是以溴化物计的碘酸钾溶液的质量浓度,mg / cm 3 。为了确定电解质中氯化物的重量比,需要确定溴化物的重量分数与通过在指示剂二苯基卡巴zone在酸性介质中进行滴定滴定而确定的氯化物的总重量与样品中预先设置的溴化物的质量分数之间的差,该质量分数在汞滴定过程中安装( I)用硝酸。然后,由锂电解液中氯化物的体积差和质量分数计算出用于滴定氯化物的硝酸汞(I)的体积差。 ,其中C Cl 是电解质中氯化物的重量分数,%; 是汞(I)硝酸溶液的体积,用于滴定总和氯化物和溴化物,cm 3 ; –溴化滴定法消耗的硝酸汞溶液的体积,cm 3 :; ; <图像文件=“ 00000070.JPG” he =“ 6” imgContent =“未定义” imgFormat =“ JPEG” wi =“ 20” /> –氯化汞和溴化物的硝酸溶液的质量浓度,mg / cm 3 ; 是电解质中溴化物的质量分数,%; m nCl 是在氯化物的测定过程中获取的电解质电荷,g;效果:本发明提供了在固体锂电解质中存在铝盐的情况下测定卤化锂的各个浓度的高精度。 ,7汤匙,2前

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