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Chemical amplification method for the polarographic determination of trace amounts of Boron

机译:化学放大法极谱法测定痕量硼

摘要

It is shown that boron can be estimated by dc polarography at mu g/ ml level by using two chemical amplification reactions in sequence. In this method, boron is converted into molybdotungstoboric acid by its reaction with ammonium molybdate and sodium tungstate under suitable conditions and is separated by solvent extraction. Determination of molybdenum in the organic extract gives an indirect estimation of boron with an enhancement factor of 6. A further enhancement by a factor of 40 is achieved by determining molybdenum through catalytic dc polarography in nitrate medium. With the overall enhancement factor of 240 and with the use of charging current compensation to minimize the background, the detection limit for boron is 0. 25 mu g/ml and the relative standard deviation is 5% (at 20 mu g level).
机译:结果表明,通过依次使用两个化学扩增反应,可以通过直流极谱法以μg / ml的水平估算硼。在这种方法中,硼通过在适当的条件下与钼酸铵和钨酸钠反应而转化为钼酸钨硼酸,并通过溶剂萃取进行分离。测定有机萃取物中的钼可以间接估算出硼,其增强因子为6。通过在硝酸盐介质中通过催化dc极谱法测定钼,可以进一步提高40倍。在总增强因子为240的情况下,并通过使用充电电流补偿来最小化背景,硼的检出限为0. 25μg / ml,相对标准偏差为5%(在20μg水平)。

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