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作 者:韦小玲[1] 潘雪珍[1] 韦湫阳[1] 龚琦[1] 朱薇[1]
出 处:《冶金分析》2010年第3期45-49,共5页Metallurgical Analysis
基 金:广西自然科学基金资助(No.0832111)
摘 要:针对锌焙砂酸浸液中高浓度Fe^3+和Zn^2+对微量In^3+的光谱测定存在严重的基体干扰,提出一种铟与锌、铁粗分离,并使铟得以富集的还原一共沉淀前处理方法。用Na2SO3溶液将锌焙砂酸浸液中大量Fe^3+还原成Fe^2+,调节溶液pH值为4.0~4.5,溶液中少量未被还原的Fe^3+形成Fe(OH)3沉淀,In^2+也以In(OH)3形式共沉淀而得到富集,大量Zn^2+和Fe^2+则留在溶液中。富集铟的滤泥用酸溶解,以原子吸收光谱法测定铟。该方法对铟富集率达到98%以上,锌和铁的去除率分别达到90%以上,基本满足铟光谱测定的要求。In view of the serious matrix interference brought high concentration of Fe^3+ and Zn^2+ in acidic leaching solution of zinc calcine in the spectrometric determination of trace indium, a reduction-co precipitation pre-treatment method was proposed. By this method, indium could be enriched while being roughly separated from Zn and Fe. After most Fe^3+ was reduced to Fe^2+ by Na2SO3, the leaching solution was adjusted to pH 4.0-4.5, so that the residual Fe^3+ was precipitated into Fe(OH)3 and In^3+ was enriched in the form of In(OH)3 through precipitation while Fe^2+ and Zn^2+ were left in the liquid solution. The filter mud for enriching indium was dissolved in hydrochloride before atomic absorption spectrometric determination. Through the method, 98 % indium could be enriched while 90 % Zn and Fe could be removed, which basically met the requirements of spectrometric determination.
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