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首页> 外文期刊>Accreditation and Quality Assurance: Journal for Quality, Comparability and Reliability in Chemical Measurement >Investigation on drying conditions and assays of amidosulfuric acid and sodium carbonate by acidimetric coulometric titration and gravimetric titration
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Investigation on drying conditions and assays of amidosulfuric acid and sodium carbonate by acidimetric coulometric titration and gravimetric titration

机译:酸式库仑滴定和重量滴定法研究氨基硫酸和碳酸钠的干燥条件和测定方法

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Amidosulfuric acid and sodium carbonate as standards for acid–base titrimetry were assayed by coulometric titration and gravimetric titration. Amidosulfuric acid was directly assayed by coulometric titration with electrogenerated hydroxide ions, and sodium carbonate was assayed by gravimetric back-titration. For sodium carbonate, excess amount of sulfuric acid, whose concentration was determined by coulometric titration, was added to sodium carbonate, and then gravimetrically back-titrated using a sodium hydroxide solution whose concentration was determined by gravimetric titration using the sulfuric acid. The accuracy of the coulometric titration for amidosulfuric acid and sulfuric acid was evaluated by examining the current efficiency of pulse electrolysis, the amount of the electrolysis current used, and the time spent for a titration. In addition, the drying conditions for high purity primary standards have a significant effect on the titration results due to changes in the acid–base assay. The suitable drying conditions for amidosulfuric acid and sodium carbonate were evaluated by mass-change measurements, coulometric titration and gravimetric titration. The measurement uncertainties were estimated from the uncertainties on the titration processes. Finally, the assays of amidosulfuric acid and sodium carbonate were 99.986% ± 0.010% (k = 2) after drying at 50 °C for 2 h, and 99.970% ± 0.016% (k = 2) after drying at 280 °C for 4 h, respectively. In addition, the international consistency was confirmed by measuring certified reference materials (CRMs) available from different National Metrology Institutes, and the compatibility of values among CRMs was experimentally ascertained.
机译:通过库仑滴定和重量滴定法测定了氨基磺酸和碳酸钠作为酸碱滴定的标准。用电生氢氧根离子通过库仑滴定法直接测定酰胺基硫酸,而重量比重滴定法测定碳酸钠。对于碳酸钠,将过量的硫酸(其浓度通过电量滴定法确定)添加到碳酸钠中,然后使用氢氧化钠溶液进行重量分析反滴定,该氢氧化钠溶液的浓度通过使用硫酸的重量滴定法确定。通过检查脉冲电解的电流效率,所用电解电流的量以及滴定所花费的时间来评估库仑滴定法对氨基硫酸和硫酸的准确性。此外,由于酸碱法的变化,高纯度一级标准品的干燥条件对滴定结果有重要影响。通过质量变化测量,电量滴定和重量滴定评估了氨基硫酸和碳酸钠的合适干燥条件。测量不确定度是根据滴定过程的不确定度估算的。最后,在50°C下干燥2小时后,氨基磺酸和碳酸钠的含量分别为99.986%±0.010%(k = 2),在280°C下干燥4之后为99.970%±0.016%(k = 2) h,分别。此外,通过测量可从不同国家计量学会获得的认证参考材料(CRM)来确认国际一致性,并通过实验确定CRM值之间的兼容性。

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