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首页> 外文期刊>鉄と鋼/Journal of the Iron and Steel Institute of Japan. >Multi-elemental determination of trace amounts impurities in iron ores by atomic absorption spectrometry using iron excluding method by means of 4-methyl 2-pentanone extraction
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Multi-elemental determination of trace amounts impurities in iron ores by atomic absorption spectrometry using iron excluding method by means of 4-methyl 2-pentanone extraction

机译:通过4-甲基2-戊酮提取方法,通过原子吸收光谱法测定铁矿中痕量痕量的多元素测定铁矿石中的杂质

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摘要

In recent year, the high quality steel products were developed by decrease of impurity elements in the steel. Generally speaking the determination of impurity elements of iron ore were performed by JIS (Japanese Industrial Standard) Method. Butthese JIS method (published in 1983) were specified that the determination limit of impurity elements in iron ores were ranged from 0.01% to 0.003%. To be suited to control of the steel production process, the determination limit of impurity elements were required to 0.001% contents level. At the same time the establishment of multi-elemental determination of impurity elements were required to the time saving on the analytical procedures.Analytical precision on the iron excluding atomic absorption method was significantly improved than the direct atomic absorption method. The determination limit at 0.001% contents level were obtained by the iron excluding atomic absorption method. Sulfate ion interfered in the atomic absorption by the molecular absorption from 200 nm to 300 nm. Therefore in the case of the pretreatment of analytical samples for the trace amounts determination the use of the sulfate reagents must be avoided in the atomicabsorption method. The improvements of the accuracy of the calibration were obtained that the standard addition method was applied to compensate of the effect on the residual iron amounts. The multi-elemental determination can be applied to the samepretreatment solution in this method.
机译:近年来,高品质的钢铁产品是通过钢中杂质元素的降低而开发的。一般而言,通过JIS(日本工业标准)方法进行铁矿石的杂质元素的测定。 Butthese JIS方法(于1983年发布)指定铁矿石中杂质元素的测定极限范围为0.01%至0.003%。为了适合控制钢铁生产过程,需要杂质元素的测定极限为0.001%的含量水平。同时,需要建立杂质元素的多元素测定,以节省分析程序的时间。不包括原子吸收法的铁上的分析精度显着改善了直接原子吸收法。通过不包括原子吸收法获得0.001%含量水平的测定极限。通过200nm至300nm的分子吸收,硫酸根离子干扰原子吸收。因此,在对痕量的分析样品的预处理的情况下,必须在原子吸附方法中避免使用硫酸盐试剂的用途。获得了校准精度的改进,施加标准添加方法以补偿对残留的铁量的影响。在该方法中可以应用多元素确定。

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