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利用便携式 RGB 颜色传感器快速评估野外土壤可利用的六价铬。

Rapid assessment of soil accessible Cr(Ⅵ) in the field by a portable RGB color sensor.

机构信息

State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, P.O. Box 821, Nanjing, China; College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.

State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, P.O. Box 821, Nanjing, China.

出版信息

Ecotoxicol Environ Saf. 2024 Mar 15;273:116117. doi: 10.1016/j.ecoenv.2024.116117. Epub 2024 Feb 19.

Abstract

Field rapid determination of soil accessible Cr(Ⅵ) is of great significance for on-site assessment and decision-making about the health risks of contaminated sites. When the thickness of solutions with various concentrations of Cr(Ⅵ) is constant, there would be a quantitative relationship between the chromogenic difference of Cr(Ⅵ) solutions and the concentration of Cr(Ⅵ). The chromogenic difference could be described by Red (R), Green (G), Blue (B) values. Based on the chromogenic reaction between 1,5-diphenylcarbazide and Cr(Ⅵ), this study first established the calibration curve between the chromogenic difference and the concentration of Cr(Ⅵ) in standard solution with or without 0.01 M CaCl, using an RGB color sensor. This is the subsequent determination basis of the method for rapidly assessing accessible Cr(Ⅵ) in the field (M-RGB). Then, the concentration of accessible Cr(Ⅵ) of contaminated soil with "hand-shaking + standing" field extraction method was compared with "end-over-end shaking" laboratory extraction method. Finally, the accessible Cr(Ⅵ) of contaminated soil extractants was determined via M-RGB integrating the field extraction method. Results indicated there was a highly significant linear relationship between colorimetric difference value (∆E) and Cr(Ⅵ) concentration in the range of 0.1-3 mg/L (R > 0.99, P < 0.01), based on the Euclidean formula for calculating ∆E. The "hand-shaking + standing" field extraction method was effective in obtaining accessible Cr(Ⅵ) extractants with or without 0.01 M CaCl, with the high extraction efficiency within 100±1%. The concentrations of accessible Cr(Ⅵ) in various polluted soils determined by M-RGB were consistent with that determined by the ultraviolet-visible spectrophotometry, with the relative error within ±5%, and the relative standard deviation ≤ 20%. The spiked recovery experiments showed that the recovery of M-RGB was between 95% and 105%, which means M-RGB could realize the trace analysis for accessible Cr(Ⅵ) in the field.

摘要

现场快速测定土壤可利用态六价铬对于污染场地的现场评估和健康风险决策具有重要意义。当不同浓度的铬(VI)溶液的厚度保持恒定时,铬(VI)溶液的显色差异与铬(VI)的浓度之间存在定量关系。显色差异可以用红(R)、绿(G)、蓝(B)值来描述。本研究基于 1,5-二苯卡巴肼与 Cr(VI)的显色反应,首次利用 RGB 颜色传感器建立了标准溶液中显色差异与 Cr(VI)浓度在有无 0.01 M CaCl 条件下的校准曲线,这是随后快速评估现场可利用态六价铬的方法(M-RGB)的后续测定依据。然后,采用“手动摇动+静置”野外提取法与“颠倒混合”实验室提取法比较了污染土壤中可利用态六价铬的浓度。最后,采用 M-RGB 法结合野外提取法测定了污染土壤浸提剂的可利用态六价铬。结果表明,基于计算 ∆E 的欧几里得公式,在 0.1-3 mg/L 范围内,比色差值(∆E)与 Cr(VI)浓度之间存在高度显著的线性关系(R > 0.99,P < 0.01)。“手动摇动+静置”野外提取法在有无 0.01 M CaCl 条件下均能有效提取可利用态六价铬浸提剂,提取效率在 100±1%范围内较高。M-RGB 法测定的各种污染土壤中可利用态六价铬的浓度与紫外可见分光光度法测定的浓度一致,相对误差在±5%以内,相对标准偏差≤20%。加标回收实验表明,M-RGB 的回收率在 95%-105%之间,这意味着 M-RGB 可以实现现场可利用态六价铬的痕量分析。

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