{"title":"HLLME预富集法和ICP-MS法测定精矿样品加工过程中轻稀土元素钐","authors":"A. Dehghan, S. Veyseh, Shabnam Najafi Aslipashaki","doi":"10.3390/iecms2021-09339","DOIUrl":null,"url":null,"abstract":"Abstract:\nIn this study, a method based on flotation assistance of homogeneous liquid-liquid microextraction (FA-HLLME) combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed for the measurement of trace Samarium in Mineral concentrate samples. As one of the miniaturized separation and extraction techniques, homogenous liquid-liquid microextraction (HLLME) has been widely applied in the field of Mineral processing. PAN (1-(2-Pyridylazo)-2-naphthol) was used as the complexing agent and 1-Dodecanol and Acetone were selected as extraction and homogeneous solvents, respectively. The factors that influenced the extraction efficiency for Samarium measurement (including pH, extraction, and homogeneous solvents, the concentration of PAN and NaCl, extraction time) were studied statistically. Under the optimum conditions (pH=8.0, 140µL 1-Dodecanol, 1.2 mL Tetrahydrofuran, 3.045×10-4 mol L-1PAN, 2.5mol L-1 NaCl, and 120 sec of extraction time), the linear dynamic range for Samarium determination was 10.0 - 220.0 ng L-1 (R2=0.9862) with a limit of detection (LOD) for Samarium was 2.91 ng L-1. The relative standard deviation (R.S.D.) (C=40 ng L-1, n=7) was 2.1% and the enrichment factor of 250 for Samarium extraction. The proposed method was successfully applied to the measurement of Samarium in different Mineral concentrate samples.","PeriodicalId":118040,"journal":{"name":"Proceedings of The 2nd International Electronic Conference on Mineral Science","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Measurement of Light Rare Earth element of Samarium in the Processing of Mineral Concentrate Samples by HLLME Pre-concentration Method and ICP-MS\",\"authors\":\"A. Dehghan, S. Veyseh, Shabnam Najafi Aslipashaki\",\"doi\":\"10.3390/iecms2021-09339\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract:\\nIn this study, a method based on flotation assistance of homogeneous liquid-liquid microextraction (FA-HLLME) combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed for the measurement of trace Samarium in Mineral concentrate samples. As one of the miniaturized separation and extraction techniques, homogenous liquid-liquid microextraction (HLLME) has been widely applied in the field of Mineral processing. PAN (1-(2-Pyridylazo)-2-naphthol) was used as the complexing agent and 1-Dodecanol and Acetone were selected as extraction and homogeneous solvents, respectively. The factors that influenced the extraction efficiency for Samarium measurement (including pH, extraction, and homogeneous solvents, the concentration of PAN and NaCl, extraction time) were studied statistically. Under the optimum conditions (pH=8.0, 140µL 1-Dodecanol, 1.2 mL Tetrahydrofuran, 3.045×10-4 mol L-1PAN, 2.5mol L-1 NaCl, and 120 sec of extraction time), the linear dynamic range for Samarium determination was 10.0 - 220.0 ng L-1 (R2=0.9862) with a limit of detection (LOD) for Samarium was 2.91 ng L-1. The relative standard deviation (R.S.D.) (C=40 ng L-1, n=7) was 2.1% and the enrichment factor of 250 for Samarium extraction. The proposed method was successfully applied to the measurement of Samarium in different Mineral concentrate samples.\",\"PeriodicalId\":118040,\"journal\":{\"name\":\"Proceedings of The 2nd International Electronic Conference on Mineral Science\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of The 2nd International Electronic Conference on Mineral Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/iecms2021-09339\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of The 2nd International Electronic Conference on Mineral Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/iecms2021-09339","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
摘要:本研究提出了一种基于均相液液微萃取(FA-HLLME)辅助浮选结合电感耦合等离子体质谱(ICP-MS)测定矿物精矿样品中痕量钐的方法。均相液液微萃取作为一种小型化的分离萃取技术,在选矿领域得到了广泛的应用。以PAN(1-(2-吡啶偶氮)-2-萘酚)为络合剂,以1-十二醇和丙酮分别作为萃取溶剂和均相溶剂。统计研究了pH、萃取剂、均相溶剂、PAN和NaCl浓度、萃取时间等因素对钐测定萃取效率的影响。在最佳提取条件(pH=8.0, 1-十二醇140µL,四氢呋喃1.2 mL, 3.045×10-4 mol L- 1pan, 2.5mol L-1 NaCl,提取时间120秒)下,钐的线性动态范围为10.0 ~ 220.0 ng L-1 (R2=0.9862),检出限为2.91 ng L-1。相对标准偏差(rsd) (C=40 ng L-1, n=7)为2.1%,富集系数为250。该方法成功地应用于不同矿物精矿样品中钐的测定。
Measurement of Light Rare Earth element of Samarium in the Processing of Mineral Concentrate Samples by HLLME Pre-concentration Method and ICP-MS
Abstract:
In this study, a method based on flotation assistance of homogeneous liquid-liquid microextraction (FA-HLLME) combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed for the measurement of trace Samarium in Mineral concentrate samples. As one of the miniaturized separation and extraction techniques, homogenous liquid-liquid microextraction (HLLME) has been widely applied in the field of Mineral processing. PAN (1-(2-Pyridylazo)-2-naphthol) was used as the complexing agent and 1-Dodecanol and Acetone were selected as extraction and homogeneous solvents, respectively. The factors that influenced the extraction efficiency for Samarium measurement (including pH, extraction, and homogeneous solvents, the concentration of PAN and NaCl, extraction time) were studied statistically. Under the optimum conditions (pH=8.0, 140µL 1-Dodecanol, 1.2 mL Tetrahydrofuran, 3.045×10-4 mol L-1PAN, 2.5mol L-1 NaCl, and 120 sec of extraction time), the linear dynamic range for Samarium determination was 10.0 - 220.0 ng L-1 (R2=0.9862) with a limit of detection (LOD) for Samarium was 2.91 ng L-1. The relative standard deviation (R.S.D.) (C=40 ng L-1, n=7) was 2.1% and the enrichment factor of 250 for Samarium extraction. The proposed method was successfully applied to the measurement of Samarium in different Mineral concentrate samples.