鋳鉄および銑鉄中の微量の銅および鉛の定量
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Quantitative determination of 0.0050.02% copper and 0.00020.002% lead in pig iron and cast iron was made by means of S. W. polarograph.<BR>The sample (1g) is dissolved by heating in a mixture of 15 m<I>l</I> hydrochloric acid, 5 m<I>l</I> nitric acid and 5 m<I>l</I> water, it is evaporated to dryness, the residue is taken up in 6<I>N</I> hydrochloric acid, the precipitate is filtered off and the filtrate is transferred into a separatory funnel. This is shaken with 30 m<I>l</I> methyl isobutyl ketone to separate iron. The aqueous layer is transferred into another separatory funnel and one more extraction is repeated. The aqueous layper is concentrated to about 2 m<I>l</I>, and is heated with nitric acid for the decomposition of organic compounds by oxidation. It is further concentrated, 2.5 m<I>l</I> hydrochloric acid added, made up to 25 m<I>l</I> with water and the polarogram is taken.<BR>By use of 1g sample containing 1% each of manganese and chromium, and 0.1% arsenic, the estimation of copper and lead of the above content was possible. Quantitative determination of lead was possible for a sample containing 0.0005% lead and 0.1% copper.<BR>The time required for the estimation of copper and lead was about 40 min.
- 社団法人 日本分析化学会の論文
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