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首页> 外文期刊>Chromatographia >Synthesis and Characterization of Fluorocarbon from Rice Husk and its Application as an Efficient Sorbent for Micro-Solid-Phase Extraction of N-Nitrosamines in Desalinated Water Samples
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Synthesis and Characterization of Fluorocarbon from Rice Husk and its Application as an Efficient Sorbent for Micro-Solid-Phase Extraction of N-Nitrosamines in Desalinated Water Samples

机译:稻壳中氟碳的合成与表征及其作为脱盐水样中N-亚硝胺微固相萃取的高效吸附剂

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摘要

Fluorocarbon derived from rice husk was synthesized and utilized as an efficient sorbent for micro-solid-phase extraction to determine N-nitrosamines in desalinated water samples. Three different sorbents from pure rice husk (rice husk ash, sulfonated rice husk, and fluorocarbon) were synthesized. Various techniques were used to characterize the physicochemical properties of the sorbents. N-Nitrosamine mixtures (N-nitrosodimethylamine, N-nitrosodi-n-propylamine, and N-nitrosodiphenylamine) were used as target analytes for micro-solid-phase extraction. The factors influencing the performance of micro-solid-phase extraction, such as the selection of suitable sorbent, desorption solvent, desorption time, sample pH, and extraction time, were optimized. Under the optimized conditions, the newly improved micro-solid-phase extraction method provided a linear range between 1.0 and 50 mu g/L with R-2 value ranges from 0.9916 to 0.9998. The limit of quantification ranges between 0.01 and 0.004 mu g/L with satisfactory intraday and interday precision ranging from 3.9 to 5.1% and 4.7 to 7.5%, respectively. Recovery experiments evaluated the accuracy of the micro-solid-phase extraction; the recoveries were in the range of 85.6-102.4%. The micro-solid-phase extraction method was successfully utilized for the sensitive, accurate, and precise trace-level detection of N-nitrosamines in desalinated water samples with satisfactory results.
机译:合成衍生自水稻壳的氟碳化合成并用作微固相萃取的有效吸附剂,以确定脱盐水样中的N-亚硝胺。合成了来自纯稻壳(稻壳灰,磺化稻壳和氟碳)的三种不同吸附剂。各种技术用于表征吸附剂的物理化学性质。使用N-亚硝基胺混合物(N-硝基二甲胺,N-硝基二甲胺,N-亚硝膦嘧啶胺)作为微固相萃取的靶分析物。优化影响微固相提取性能的因素,例如选择合适的吸附剂,解吸溶剂,解吸时间,样品pH和提取时间。在优化的条件下,新改进的微固相提取方法提供了1.0至50μg/ L的线性范围,R-2值范围为0.9916至0.9998。定量极限范围为0.01和0.004μg/ l,令人满意的盘中和白天精度分别为3.9%至5.1%和4.7%至7.5%。回收实验评估了微固相提取的准确性;回收率在85.6-102.4%的范围内。经过令人满意的结果,成功地利用了微固相萃取方法的裂解,准确,精确的甲状腺胺的敏感,准确,精确的痕量检测。

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