Advancing on ametrine pesticide detection through surface-enhanced Raman spectroscopy and Ag colloid: Understanding the pH effect and the adsorption mechanism supported by theoretical calculation

IF 2.4 3区 化学 Q2 SPECTROSCOPY
Rafael Jesus Gonçalves Rubira, Leonardo Negri Furini, Maria Eugenia Tuttolomondo, Carlos José Leopoldo Constantino, Santiago Sanchez-Cortes
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引用次数: 0

Abstract

The excessive use of pesticides has detrimental effects on the ecosystem, leading to soil contamination and the spread of pollution beyond the targeted areas. Concerns arise regarding the permissible limits of pesticides, typically around 10−8 mol/L. In this study, we employed surface-enhanced Raman spectroscopy (SERS), a highly sensitive and selective technique, to investigate the behavior of the pesticide ametrine (AMT) on silver colloids. The Ag nanoparticles (AgNPs) exhibited an average size of (26 ± 2) nm and a zeta potential of (−30 ± 1) mV in the absence of AMT, which decreased to (−24 ± 1) mV in the presence of AMT, resulting in mild AgNPs aggregation, with the average diameter of AgNPs increasing to approximately 300 nm. This aggregation is advantageous, as they provide active sites for pesticide detection. Besides, the purification method employed ensured that AMT remained undegraded, and various conformations of AMT were simulated using Ag clusters to study the SERS effect. Comparison with the experimental spectra indicated that the SERS-4 conformer closely resembled the experimental spectrum, suggesting simultaneous interaction between the Ag surface and the sulfur (S) and nitrogen (N) atoms of the AMT triazine ring. Notably, changes in the AMT molecule were observed with pH variations: at pH below 5, hydroxylation occurred, resulting in an Ag–Cl stretching at 241 cm−1 in the SERS spectra. Conversely, at pH above 5 (pH 6–13), the presence of bands at 230 and 219 cm−1 in the SERS spectra indicate the formation of Ag–N and Ag–S bonds, respectively, between the AMT and the AgNPs. Furthermore, the study successfully detected AMT at pH 7, establishing a limit of detection (LOD) of 1.36 × 10−8 mol/L (3 ppb) based on the SERS spectra. These findings underscore the applicability of the SERS technique in the sensitive and selective detection of AMT, offering a promising approach for monitoring the presence of this pesticide in environmental samples.

Abstract Image

通过表面增强拉曼光谱和银胶体推进阿米替林农药检测:通过理论计算理解pH值效应和吸附机理
过量使用杀虫剂会对生态系统造成有害影响,导致土壤污染,并使污染扩散到目标区域之外。人们对农药的允许极限(通常约为 10-8 mol/L)表示担忧。在这项研究中,我们采用了表面增强拉曼光谱(SERS)这一高灵敏度和高选择性的技术,来研究杀虫剂阿米替林(AMT)在银胶体上的行为。银纳米粒子(AgNPs)的平均尺寸为 (26 ± 2) nm,在没有 AMT 的情况下,zeta 电位为 (-30 ± 1) mV,在有 AMT 的情况下,zeta 电位降至 (-24 ± 1) mV,从而导致 AgNPs 轻度聚集,AgNPs 的平均直径增至约 300 nm。这种聚集是有利的,因为它们为农药检测提供了活性位点。此外,所采用的纯化方法确保了 AMT 不降解,并利用银簇模拟了 AMT 的各种构象,以研究 SERS 效果。与实验光谱比较表明,SERS-4 构象与实验光谱非常相似,这表明银表面与 AMT 三嗪环的硫(S)和氮(N)原子之间同时存在相互作用。值得注意的是,随着 pH 值的变化,AMT 分子也发生了变化:当 pH 值低于 5 时,AMT 分子发生羟基化,导致 SERS 光谱中 241 cm-1 处出现 Ag-Cl 伸展。相反,当 pH 值高于 5 时(pH 值为 6-13),SERS 光谱中出现的 230 和 219 cm-1 带分别表明 AMT 和 AgNPs 之间形成了 Ag-N 和 Ag-S 键。此外,该研究还成功地在 pH 值为 7 的条件下检测到了 AMT,根据 SERS 光谱确定的检测限(LOD)为 1.36 × 10-8 mol/L(3 ppb)。这些发现强调了 SERS 技术在灵敏和选择性检测 AMT 方面的适用性,为监测环境样本中是否存在这种农药提供了一种前景广阔的方法。
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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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