Ana Carolina de Souza, Luiz Rogério Pinho de Andrade Lima
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Chemical and mineralogical characterizations were accomplished on the products of this process and the results indicated that the initial concentrate is rich in light rare earths, the alkaline fusion product is predominantly composed of rare earth hydroxides and free of NaOH. The acid leaching tailings showed to be rich in zirconite, indicating that the dissolution of the rare earth hydroxides formed in the previous step was complete. Spectral interferences in the lines of the predominant elements were considered in the ICP-OES analysis using individual patterns of these elements. The following lines were defined for the predominant elements: Ce 456.236 nm, Th 283.730 nm, La 384.902 nm, Nd 430.058 nm, Pr 390.844 nm, and Sm 428,079 nm. The leachate obtained after acid leaching of rare earth hydroxides was analyzed by this method and the concentrations of the predominant elements (in g/L) were: Ce 32.81, Th 14.76, La 8.58, Nd 3.35, Pr 3.02, and Sm 1.28","PeriodicalId":53327,"journal":{"name":"Tecnologia em Metalurgia Materiais e Mineracao","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tratamento térmico para desfosfatização de monazita e recuperação dos elementos das terras raras\",\"authors\":\"Ana Carolina de Souza, Luiz Rogério Pinho de Andrade Lima\",\"doi\":\"10.4322/2176-1523.20222637\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Brazil has the second largest reserve of monazite, which is one of the three main minerals bearing of rare earth elements. 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Spectral interferences in the lines of the predominant elements were considered in the ICP-OES analysis using individual patterns of these elements. The following lines were defined for the predominant elements: Ce 456.236 nm, Th 283.730 nm, La 384.902 nm, Nd 430.058 nm, Pr 390.844 nm, and Sm 428,079 nm. 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引用次数: 0
摘要
独居石是三种主要含稀土元素的矿物之一,巴西的独居石储量居世界第二位。在这项研究中,使用了一种从巴伊亚州和Espírito桑托斯州沿海地带的重矿物中提取的独居石精矿。对ICP-OES分析富稀土水溶液的最佳方法进行了评价。在这项工作中,从独居石精矿中获得富含稀土的水溶液的步骤包括以下步骤:向精矿中加入NaOH,在400℃下加热3小时,用水洗涤,随后用HCl浸出剩余的固相。对该工艺产物进行了化学和矿物学表征,结果表明:初始精矿富含轻稀土,碱性熔融产物以稀土氢氧化物为主,不含NaOH。酸浸尾矿中锆英石含量丰富,说明前一步形成的稀土氢氧化物溶解完成。在ICP-OES分析中,利用这些元素的单个模式考虑了主要元素谱线的光谱干扰。主要元素为Ce 456.236 nm, Th 283.730 nm, La 384.902 nm, Nd 430.058 nm, Pr 390.844 nm, Sm 428,079 nm。对稀土氢氧化物酸浸后的渗滤液进行了分析,其优势元素浓度(g/L)为:Ce 32.81, Th 14.76, La 8.58, Nd 3.35, Pr 3.02, Sm 1.28
Tratamento térmico para desfosfatização de monazita e recuperação dos elementos das terras raras
Brazil has the second largest reserve of monazite, which is one of the three main minerals bearing of rare earth elements. In this study, a monazite concentrate, derived from the occurrence of heavy minerals in the coastal strips of the states of Bahia and Espírito Santos, was used. The best way to analyze aqueous solutions rich in rare earths by ICP-OES was also evaluated. In this work, the steps used to obtain an aqueous solution rich in rare earths from the monazite concentrate involved the following steps: addition of NaOH to the concentrate, heating at 400 ºC for 3 hours, washing with water and subsequent leaching of the remaining solid phase with HCl. Chemical and mineralogical characterizations were accomplished on the products of this process and the results indicated that the initial concentrate is rich in light rare earths, the alkaline fusion product is predominantly composed of rare earth hydroxides and free of NaOH. The acid leaching tailings showed to be rich in zirconite, indicating that the dissolution of the rare earth hydroxides formed in the previous step was complete. Spectral interferences in the lines of the predominant elements were considered in the ICP-OES analysis using individual patterns of these elements. The following lines were defined for the predominant elements: Ce 456.236 nm, Th 283.730 nm, La 384.902 nm, Nd 430.058 nm, Pr 390.844 nm, and Sm 428,079 nm. The leachate obtained after acid leaching of rare earth hydroxides was analyzed by this method and the concentrations of the predominant elements (in g/L) were: Ce 32.81, Th 14.76, La 8.58, Nd 3.35, Pr 3.02, and Sm 1.28