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Evaluation of slurry preparation procedures for the determination of mercury by axial view inductively coupled plasma optical emission spectrometry using on-line cold vapor generation

机译:使用在线冷蒸气发生的轴向观察电感耦合等离子体发射光谱法评估浆料制备方法测定汞的方法

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Five different slurry preparation procedures were tested,after grinding the solid samples to a particle size <=53 mum:(1) using aqua regia plus HF,30 min of sonication,standing time of 24 h followed by another 30 min of sonication;(2) same as the previous one,except that the standing time and the second ultrasound treatment were omitted;(3) same as the previous one,except that HF was not used;(4) same as the previous one,except that the aqua regia was replaced by nitric acid;(5) same as the previous one,except that the acid nitric was replaced by tetramethylammonium hydroxide (TMAH).The Hg vapor was generated on-line,and the emission signal intensity measured at 253.652 nm by axial view inductively coupled plasma optical emission spectrometry.Initially,four experimental conditions were optimized using a multivariate factorial analysis:the concentrations of HC1 and of the reducing agent,NaBH_4,used in the cold vapor generation,and two instrumental parameters,the plasma radiofrequency power and the carrier gas flow rate.The radiofrequency power was statistically significant,but limited to 1.2 kW for practical reasons.The procedures were applied to 11 biological and environmental materials.Both,the slurries and the filtrates were analyzed,using calibration solutions in the same medium as in the slurries.The first three procedures produced results in agreement with the certified values.The two last procedures,using nitric acid or TMHA could not be used for quantitative analysis.For practical reasons,Procedure 3,with a detection limit (3s,n=10) of 0.06 mug g~(-1) for a sample mass of 20 mg in a final volume of 15 mL is recommended.The relative standard deviations for mercury in the investigated materials,using the recommended procedure,were lower than 12.5%,indicating a good precision for slurry sampling.The recommended procedure is simple,rapid and robust.
机译:测试了五种不同的浆料制备程序,将固体样品研磨至粒径小于等于53微米:(1)使用王水加HF进行30分钟的超声处理,静置24小时,然后再进行30分钟的超声处理;( 2)与上一个相同,只是省去了站立时间和第二次超声处理;(3)与上一个相同,除了不使用HF;(4)与上一个相同,除了浅绿色将regia替换为硝酸;(5)与上一个相同,只是将酸性硝酸替换为四甲基氢氧化铵(TMAH).Hg蒸汽在线产生,并且在253.652 nm处通过轴向测量发射信号强度最初,使用多因素分析优化了四个实验条件:冷蒸气产生中使用的HC1和还原剂的浓度NaBH_4,以及两个仪器参数,即等离子体射频功率射频功率具有统计学意义,但出于实际原因限制为1.2 kW。该程序适用于11种生物和环境材料。在实验室中使用校准溶液对浆液和滤液进行了分析。前三种方法产生的结果与认证值相符。后两种方法使用硝酸或TMHA不能进行定量分析。由于实际原因,方法3的检出限为(对于20 mg的样品质量,最终体积为15 mL,建议使用0.06马克杯g((-1)的3s,n = 10)。最终样品中汞的相对标准偏差(使用推荐的程序)要低一些小于12.5%,表明泥浆采样具有良好的精度。推荐的过程简单,快速且可靠。

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