Donaldson E M
Mineral Sciences Laboratories, Canada Centre for Mineral and Energy Technology, Department of Energy, Mines and Resources, Ottawa, Canada.
Talanta. 1989 May;36(5):543-8. doi: 10.1016/0039-9140(89)80121-3.
A method for determining approximately 0.5, mug/g or more of cobalt, nickel and lead and approximately 3 mug/g or more of bismuth and indium in ores, soils and related materials is described. After sample decomposition and dissolution of the salts in dilute hydrochloric-tartaric acid solution, iron(III) is reduced with ascorbic acid and the resultant iron(II) is complexed with ammonium fluoride. Cobalt, nickel, lead, bismuth and indium are subsequently separated from iron, aluminium, zinc and other matrix elements by a triple chloroform extraction of their xanthate complexes at pH 2.00 +/- 0.05. After the removal of chloroform by evaporation and the destruction of the xanthates with nitric and perchloric acids, the solution is evaporated to dryness and the individual elements are ultimately determined in a 20% v/v hydrochloric acid medium containing 1000 mug/ml potassium by atomic-absorption spectrometry with an air-acetylene flame. Co-extraction of arsenic and antimony is avoided by volatilizing them as the bromides during the decomposition step. Small amounts of co-extracted molybdenum, iron and copper do not interfere.
描述了一种测定矿石、土壤及相关材料中钴、镍、铅含量约0.5μg/g及以上,铋和铟含量约3μg/g及以上的方法。样品分解并将盐溶解于稀盐酸 - 酒石酸溶液后,用抗坏血酸将铁(III)还原,所得的铁(II)与氟化铵络合。随后在pH 2.00±0.05条件下,通过对其黄原酸盐络合物进行三次氯仿萃取,将钴、镍、铅、铋和铟与铁、铝、锌及其他基体元素分离。通过蒸发除去氯仿并用硝酸和高氯酸破坏黄原酸盐后,将溶液蒸发至干,最终在含1000μg/ml钾的20% v/v盐酸介质中,用空气 - 乙炔火焰原子吸收光谱法测定各元素。在分解步骤中,通过将砷和锑以溴化物形式挥发来避免它们的共萃取。少量共萃取的钼、铁和铜不产生干扰。