首页> 外文期刊>Atomic Spectroscopy >Determination of Au, Pd, Pt, and Rh inks, ores, concentrates, and sulfide float samples by ICP-OES/FAAS after reductive coprecipitation using Se as collector
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Determination of Au, Pd, Pt, and Rh inks, ores, concentrates, and sulfide float samples by ICP-OES/FAAS after reductive coprecipitation using Se as collector

机译:硒作捕收剂还原共沉淀后,通过ICP-OES / FAAS测定Au,Pd,Pt和Rh油墨,矿石,精矿和硫化物浮标

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A method is described for the determination of gold, palladium, platinum, and rhodium inks, ores, and concentrates, including sulfide float samples, by inductively coupled plasma optical emission spectrometry (ICP-OES) and flame atomic absorption spectroscopy (FAAS). The samples were analyzed after decomposition with a mixture of hydrofluoric acid aqua regia and hydrochloric acid potassium chlorate for sulfide matrix samples. Fusion was used for any insoluble residue with sodium peroxide and the analytes were collected using selenium as the collector and stannous chloride as the reductant. The method was tested for Au, Pd, Pt, and Rh with three Canadian certified reference standards, MA-lb, PTC-1, and PTM-l, and one National Institute of Metallurgical Standard from South Africa, SARM-7, and then applied to the determination of these elements in some ore samples and sulfide-rich flotation products from the Jaduguda Uranium deposits in Singhbhum (Bihar, India). The results obtained by this method compare favorably with the certified values. The gold and palladium values obtained in sulfide float samples are discussed and compared with the values obtained by the ICP-MS methods. Detailed studies were carried out to precipitate gold and platinum- group elements (PGEs) using different precipitating agents such as H sub 2 S, Na sub 2 S in the presence of various carrier elements. Investigations were also carried out using Se as the collector and various reducing agents such as sulfurous acid (SO sub 2 ), hypophosphorous acid (H sub 3 PO sub 2 ), ammonium formate (HCOO NH sub 4 ), hydroquinone [C sub 6 H sub 4 (OH) sub 2 ], and hydroxyl ammonium chloride (NH sub 2 OH HCl). The recoveries of Au, Pd, and other PGEs are discussed. The relative error for one sulfide float sample was established to be within plus/minus1.0 to 1.5% RSD for both Au and Pd values using the proposed method.
机译:描述了一种通过电感耦合等离子体发射光谱法(ICP-OES)和火焰原子吸收光谱法(FAAS)测定金,钯,铂和铑油墨,矿石和精矿(包括硫化物浮标)的方法。用氢氟酸王水和盐酸氯酸钾的混合物分解后分析样品,得到硫化物基质样品。用过氧化钠对任何不溶残留物进行融合,并使用硒作为收集剂和氯化亚锡作为还原剂收集分析物。使用三种加拿大认证参考标准,MA-1b,PTC-1和PTM-1和南非国家冶金标准学会的SARM-7对方法进行了Au,Pd,Pt和Rh的测试。应用于确定来自Singhbhum(印度比哈尔)的Jaduguda铀矿床的一些矿石样品和富含硫化物的浮选产品中的这些元素。通过这种方法获得的结果与认证值相比具有优势。讨论了硫化物浮子样品中获得的金和钯值,并将其与通过ICP-MS方法获得的值进行了比较。在各种载体元素存在下,使用不同的沉淀剂(例如H sub 2 S,Na sub 2 S)进行了详细的研究,以沉淀金和铂族元素(PGE)。还使用硒作为收集剂和各种还原剂,例如亚硫酸(SO sub 2),次磷酸(H sub 3 PO sub 2),甲酸铵(HCOO NH sub 4),氢醌[C sub 6 H sub 4(OH)sub 2]和羟基氯化铵(NH sub 2 OH HCl)。讨论了金,钯和其他PGE的回收率。使用建议的方法,对于Au和Pd值,将一个硫化物浮标的相对误差确定为在±1.0-1.5%RSD之内。

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