{"title":"电热汽化多收集器电感耦合等离子体质谱法分析Cd同位素。","authors":"Linjie Chen, Xing Liu, Zhe Zhang, Miaomiao Jiang, Yuzhe Wang, Yu Li, Wenkai Zhang, Zhenli Zhu","doi":"10.1007/s00216-025-06026-4","DOIUrl":null,"url":null,"abstract":"<p><p>A fast and highly sensitive method for cadmium (Cd) isotopic analysis was developed by coupling electrothermal vaporization (ETV) with multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS). In this approach, a 5 μL Cd sample was dropped onto the W-coil ETV, followed by sequential drying and vaporization. The vaporized analyte was then swept into the MC-ICPMS for isotopic analysis, and the whole analysis process took only 3 min. This system exhibited exceptional sampling efficiency, achieving > 99% Cd vaporization and reducing sample consumption to only 2 ng per analysis, representing a 20-fold improvement over conventional pneumatic nebulization (PN). The ETV transient signals were recorded in time resolved analysis (TRA) mode, and the isotope ratio processing was calculated using the linear regression slope (LRS) method. These ratios were further corrected for instrumental mass bias using a combination of double spike (DS) and standard-sample bracketing (SSB), ensuring high precision and accuracy. Repeated analyses of NIST 3108 and GBW 08612 (in-house standard) yielded δ<sup>114/110</sup>Cd values of 0.00 ± 0.05‰ (2SD, n = 12) and - 0.96 ± 0.05‰ (2SD, n = 12), respectively. Tests on standard samples purified once and twice showed no significant differences, indicating better matrix tolerance over the conventional PN method. This method enables high-throughput Cd isotopic analysis of trace-level environmental samples, facilitating investigations into biogeochemical cycling at low Cd concentrations and pollution source tracing.</p>","PeriodicalId":462,"journal":{"name":"Analytical and Bioanalytical Chemistry","volume":" ","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sensitive Cd isotopic analysis by multi-collector inductively coupled plasma mass spectrometry using electrothermal vaporization.\",\"authors\":\"Linjie Chen, Xing Liu, Zhe Zhang, Miaomiao Jiang, Yuzhe Wang, Yu Li, Wenkai Zhang, Zhenli Zhu\",\"doi\":\"10.1007/s00216-025-06026-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A fast and highly sensitive method for cadmium (Cd) isotopic analysis was developed by coupling electrothermal vaporization (ETV) with multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS). In this approach, a 5 μL Cd sample was dropped onto the W-coil ETV, followed by sequential drying and vaporization. The vaporized analyte was then swept into the MC-ICPMS for isotopic analysis, and the whole analysis process took only 3 min. This system exhibited exceptional sampling efficiency, achieving > 99% Cd vaporization and reducing sample consumption to only 2 ng per analysis, representing a 20-fold improvement over conventional pneumatic nebulization (PN). The ETV transient signals were recorded in time resolved analysis (TRA) mode, and the isotope ratio processing was calculated using the linear regression slope (LRS) method. These ratios were further corrected for instrumental mass bias using a combination of double spike (DS) and standard-sample bracketing (SSB), ensuring high precision and accuracy. Repeated analyses of NIST 3108 and GBW 08612 (in-house standard) yielded δ<sup>114/110</sup>Cd values of 0.00 ± 0.05‰ (2SD, n = 12) and - 0.96 ± 0.05‰ (2SD, n = 12), respectively. Tests on standard samples purified once and twice showed no significant differences, indicating better matrix tolerance over the conventional PN method. This method enables high-throughput Cd isotopic analysis of trace-level environmental samples, facilitating investigations into biogeochemical cycling at low Cd concentrations and pollution source tracing.</p>\",\"PeriodicalId\":462,\"journal\":{\"name\":\"Analytical and Bioanalytical Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-07-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical and Bioanalytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s00216-025-06026-4\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical and Bioanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s00216-025-06026-4","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
摘要
建立了电热汽化(ETV)与多集热器电感耦合等离子体质谱(MC-ICPMS)耦合分析镉(Cd)同位素的快速、高灵敏度方法。在该方法中,将5 μL的Cd样品滴入w线圈ETV,然后依次干燥和汽化。然后将蒸发的分析物扫入MC-ICPMS进行同位素分析,整个分析过程仅需3分钟。该系统具有出色的采样效率,实现了> 99%的Cd汽化,每次分析的样品消耗仅为2 ng,比传统的气动雾化(PN)提高了20倍。采用时间分辨分析(TRA)模式记录ETV瞬态信号,采用线性回归斜率法(LRS)计算同位素比值处理。这些比率使用双尖峰(DS)和标准样品括号(SSB)的组合进一步校正仪器质量偏差,确保高精度和准确性。NIST 3108和GBW 08612(内部标准)的δ114/110Cd值分别为0.00±0.05‰(2SD, n = 12)和- 0.96±0.05‰(2SD, n = 12)。对纯化一次和两次的标准样品的测试没有显着差异,表明比传统的PN方法更好的基质耐受性。该方法可实现痕量环境样品的高通量Cd同位素分析,有利于低Cd浓度下生物地球化学循环研究和污染源追踪。
Sensitive Cd isotopic analysis by multi-collector inductively coupled plasma mass spectrometry using electrothermal vaporization.
A fast and highly sensitive method for cadmium (Cd) isotopic analysis was developed by coupling electrothermal vaporization (ETV) with multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS). In this approach, a 5 μL Cd sample was dropped onto the W-coil ETV, followed by sequential drying and vaporization. The vaporized analyte was then swept into the MC-ICPMS for isotopic analysis, and the whole analysis process took only 3 min. This system exhibited exceptional sampling efficiency, achieving > 99% Cd vaporization and reducing sample consumption to only 2 ng per analysis, representing a 20-fold improvement over conventional pneumatic nebulization (PN). The ETV transient signals were recorded in time resolved analysis (TRA) mode, and the isotope ratio processing was calculated using the linear regression slope (LRS) method. These ratios were further corrected for instrumental mass bias using a combination of double spike (DS) and standard-sample bracketing (SSB), ensuring high precision and accuracy. Repeated analyses of NIST 3108 and GBW 08612 (in-house standard) yielded δ114/110Cd values of 0.00 ± 0.05‰ (2SD, n = 12) and - 0.96 ± 0.05‰ (2SD, n = 12), respectively. Tests on standard samples purified once and twice showed no significant differences, indicating better matrix tolerance over the conventional PN method. This method enables high-throughput Cd isotopic analysis of trace-level environmental samples, facilitating investigations into biogeochemical cycling at low Cd concentrations and pollution source tracing.
期刊介绍:
Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.