{"title":"利用气相色谱-质谱法分析衍生化后土壤中的无机砷和甲基砷。","authors":"Wenzhi Zhao, Yuan Yang, Jintao Zhang, Tao Liu","doi":"10.1371/journal.pone.0313924","DOIUrl":null,"url":null,"abstract":"<p><p>Gas chromatography-mass spectrometry (GC-MS) has been applied to the analysis of arsenic forms in water, plants, and other samples; however, it has not been used to determine the form of arsenic in soil due to the complex soil matrix. The purpose of this study was to develop an analytical method for the simultaneous determination of inorganic arsenic species (As (III) and As (V)) and monomethylarsonic acid (MMA) in soil using GC-MS. The arsenic compounds were subjected to derivatization with 2,3-dimercapto-1-propanol (BAL) and subsequently analyzed using GC-MS. The BAL volume, derivatization reaction time, and temperature were optimized using standard added soil extracts. A reaction with 150 μL of BAL at 40°C for 30 min was selected as the optimal condition for quantitative derivatization of both inorganic arsenic (iAs) and MMA. The calibration curves exhibited linearity within the range of 5-100 ng/mL for each arsenic species, with correlation coefficients exceeding 0.997. The limits of detection for each arsenic species were determined to be 0.24 ng/mL and 1.31 ng/mL, respectively. The accuracy of the method was verified by the recovery of reference samples. The recovery experiments for reference samples showed that the recovery rates for As (III), As (V), and MMA were 89.5-93.7%, 88.5-105.6%, and 90.2-95.8% respectively, with precision ranging from 4.6 to 6.5%, 2.3 to 3.8%, and 2.4 to 6.3%. These results indicate good accuracy and precision. The accuracy of this method is not significantly different from that of liquid chromatography-inductively coupled plasma mass spectrometry (p = 0.05). The optimized method was sensitive, convenient and reliable for the extraction and analysis of different arsenic species in soil samples.</p>","PeriodicalId":20189,"journal":{"name":"PLoS ONE","volume":"19 11","pages":"e0313924"},"PeriodicalIF":2.9000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of inorganic arsenic and methylarsenic in soil after derivatization by gas chromatography-mass spectrometry.\",\"authors\":\"Wenzhi Zhao, Yuan Yang, Jintao Zhang, Tao Liu\",\"doi\":\"10.1371/journal.pone.0313924\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Gas chromatography-mass spectrometry (GC-MS) has been applied to the analysis of arsenic forms in water, plants, and other samples; however, it has not been used to determine the form of arsenic in soil due to the complex soil matrix. The purpose of this study was to develop an analytical method for the simultaneous determination of inorganic arsenic species (As (III) and As (V)) and monomethylarsonic acid (MMA) in soil using GC-MS. The arsenic compounds were subjected to derivatization with 2,3-dimercapto-1-propanol (BAL) and subsequently analyzed using GC-MS. The BAL volume, derivatization reaction time, and temperature were optimized using standard added soil extracts. A reaction with 150 μL of BAL at 40°C for 30 min was selected as the optimal condition for quantitative derivatization of both inorganic arsenic (iAs) and MMA. The calibration curves exhibited linearity within the range of 5-100 ng/mL for each arsenic species, with correlation coefficients exceeding 0.997. The limits of detection for each arsenic species were determined to be 0.24 ng/mL and 1.31 ng/mL, respectively. The accuracy of the method was verified by the recovery of reference samples. The recovery experiments for reference samples showed that the recovery rates for As (III), As (V), and MMA were 89.5-93.7%, 88.5-105.6%, and 90.2-95.8% respectively, with precision ranging from 4.6 to 6.5%, 2.3 to 3.8%, and 2.4 to 6.3%. These results indicate good accuracy and precision. The accuracy of this method is not significantly different from that of liquid chromatography-inductively coupled plasma mass spectrometry (p = 0.05). 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引用次数: 0
摘要
气相色谱-质谱法(GC-MS)已被用于分析水、植物和其他样品中的砷形态,但由于土壤基质复杂,尚未用于测定土壤中的砷形态。本研究旨在开发一种利用气相色谱-质谱法同时测定土壤中无机砷(As (III)和 As (V))和一甲基胂酸(MMA)的分析方法。砷化合物用 2,3-二巯基-1-丙醇(BAL)进行衍生,然后用气相色谱-质谱法进行分析。使用标准添加的土壤提取物对 BAL 体积、衍生反应时间和温度进行了优化。150 μL BAL 在 40°C 下反应 30 分钟被选为对无机砷(iAs)和 MMA 进行定量衍生的最佳条件。每种砷的校准曲线在 5-100 纳克/毫升范围内呈线性关系,相关系数超过 0.997。每种砷的检测限分别为 0.24 纳克/毫升和 1.31 纳克/毫升。参考样品的回收率验证了该方法的准确性。参考样品的回收实验表明,As (III)、As (V)和MMA的回收率分别为89.5-93.7%、88.5-105.6%和90.2-95.8%,精密度分别为4.6-6.5%、2.3-3.8%和2.4-6.3%。这些结果表明该方法具有良好的准确度和精密度。该方法的准确度与液相色谱-电感耦合等离子体质谱法的准确度无明显差异(p = 0.05)。优化后的方法灵敏、简便、可靠,可用于土壤样品中不同砷种类的提取和分析。
Analysis of inorganic arsenic and methylarsenic in soil after derivatization by gas chromatography-mass spectrometry.
Gas chromatography-mass spectrometry (GC-MS) has been applied to the analysis of arsenic forms in water, plants, and other samples; however, it has not been used to determine the form of arsenic in soil due to the complex soil matrix. The purpose of this study was to develop an analytical method for the simultaneous determination of inorganic arsenic species (As (III) and As (V)) and monomethylarsonic acid (MMA) in soil using GC-MS. The arsenic compounds were subjected to derivatization with 2,3-dimercapto-1-propanol (BAL) and subsequently analyzed using GC-MS. The BAL volume, derivatization reaction time, and temperature were optimized using standard added soil extracts. A reaction with 150 μL of BAL at 40°C for 30 min was selected as the optimal condition for quantitative derivatization of both inorganic arsenic (iAs) and MMA. The calibration curves exhibited linearity within the range of 5-100 ng/mL for each arsenic species, with correlation coefficients exceeding 0.997. The limits of detection for each arsenic species were determined to be 0.24 ng/mL and 1.31 ng/mL, respectively. The accuracy of the method was verified by the recovery of reference samples. The recovery experiments for reference samples showed that the recovery rates for As (III), As (V), and MMA were 89.5-93.7%, 88.5-105.6%, and 90.2-95.8% respectively, with precision ranging from 4.6 to 6.5%, 2.3 to 3.8%, and 2.4 to 6.3%. These results indicate good accuracy and precision. The accuracy of this method is not significantly different from that of liquid chromatography-inductively coupled plasma mass spectrometry (p = 0.05). The optimized method was sensitive, convenient and reliable for the extraction and analysis of different arsenic species in soil samples.
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