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Fenton reaction-triggered colorimetric detection of phenols in water samples using unmodified gold nanoparticles

机译:使用Fenton反应触发的比色法检测未改性金纳米颗粒中水样中的酚

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This work demonstrates a rapid and sensitive colorimetric detection of phenols by using single-stranded DNA (ssDNA)-regulated gold nanoparticles (AuNPs) as indicators.AuNPs can be stabilized in the presence of ssDNA through electrostatic repulsion,which prevents the salt-induced aggregation of AuNPs in solution.However,hydroxyl radicals (· OH) generated by the Fenton reaction can cleave the ssDNA on the nanoparticle surface into mono-or oligonucleotide fragments,disrupting AuNPs stability.Phenolic compounds are known to be capable of being degraded or oxidized by.OH produced by Fenton reaction.Thus,phenols can effectively scavenge· OH to avoid ssDNA cleavage,protecting AuNPs from salt-induced aggregation.The ability of phenols to scavenge.OH provides a quantitative basis for phenol sensing.In this study,catechol and hydroquinone were selected as analytes and detected using the proposed ssDNA-AuNPs colorimetric probe.The detection sensitivities of the colorimetric sensor are 0.2-7.0 μM for catechol and 2.7-19 μM for hydroquinone.The proposed bioassay eliminates tedious sample pretreatment and offers favorable sensitivity and selectivity for targets in the presence of other investigated metal ions and organic molecules.The detection limits are 0.11μM for catechol and1.6 μM for hydroquinone,with relative standard deviations of 3.7% for catechol and 4.8% for hydroquinone.The recovery rote of catechol in real water samples ranges from 95% to 116%,confirming the application potential of the method to measure phenols in real samples.
机译:这项工作证明了使用单链DNA(ssDNA)调节的金纳米颗粒(AuNPs)作为指示剂的酚的快速灵敏检测.ausNPs可以通过静电排斥在ssDNA存在的情况下稳定,从而防止盐诱导的聚集Fenton反应产生的羟基自由基(·OH)可以将纳米颗粒表面上的ssDNA裂解为单核苷酸或寡核苷酸片段,破坏AuNPs的稳定性。已知酚类化合物能够被以下物质降解或氧化Fenton反应产生的.OH。因此,酚能够有效清除OH,避免ssDNA裂解,保护AuNPs免受盐诱导的聚集。酚的清除能力。OH为酚感测提供了定量基础。选择对苯二酚作为分析物并使用拟议的ssDNA-AuNPs比色探针进行检测。比色传感器的检测灵敏度为0.2-7.0μM邻苯二酚的检出限为2.7-19μM,对苯二酚的检定限为2.7-19μM。在其他被研究的金属离子和有机分子存在的情况下,该生物测定消除了繁琐的样品前处理,并为目标提供了有利的灵敏度和选择性。对苯二酚,邻苯二酚的相对标准偏差为3.7%,对苯二酚的相对标准偏差为4.8%。实际水样中邻苯二酚的回收率在95%至116%之间,这证明了该方法在实际样品中测定酚的应用潜力。

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