Sustainable PVP-capped gold nanoparticles synthesis “green” chemistry plasma-liquid method and colorimetric activity for water pollutant chromium ion (Cr(VI))

IF 1.5 4区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Margarita Skiba, Viktoria Vorobyova
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引用次数: 0

Abstract

Gold nanoparticles (AuNPs) are widely utilized in colorimetric sensing, leveraging their optical characteristics to identify variables through noticeable color alterations. Polymer (PVP)-functionalized gold nanoparticles were successfully prepared in a single step by the induced plasma-under-liquid process. We will evaluate plasma-liquid method synthesis by GREEnness calculator. The effects of different concentrations of PVP on the synthesis and characteristics of the AuNPs, such as size distributions, hydrodynamic diameters, polydispersity indices (PDI), absorbance intensity, and LSPR, were characterized and investigated. The as-synthesized PVP-AuNPs were characterized by SEM, DLS, and UV–visible spectroscopy. Spherical AuNPs were generated, displaying a maximal absorption peak at around 530–560 nm and a size range of 30–50 nm, which can be adjustable depending on the initial concentration precursor and capping agent used in the synthesis process. Polyvinylpyrrolidone-coated gold nanoparticles (PVP-AuNPs) were employed as a colorimetric probe for the quick, easy, sensitive, and selective measurement of chromium ion (Cr(VI)) contamination in water. In fact, chromium ion (Cr(VI)) caused the colloidal solution’s hue to change from red to blue by forcing PVP-AuNPs to aggregate with PVP on the surface of AuNPs. It was established that size and polydispersity affect the colorimetric properties of functionalized nanoparticles during colorimetric detection of the analyte. Optimizing the experimental parameters (volume/concentration AuNPs, the dependence of limit of quantification (LOQ), limit of detection (LOD) at temperature) revealed a good linear connection between the concentration of chromium ion (Cr(VI)) and the absorption ratio (A690/A530-560) in the range of 0.1–3.0 µM with a detection Limit of 0.072–0.1 µM. The selectivity of the developed colorimetric nanoprobe was evaluated by testing its response to various common heavy metal ions. The analytical GREEnness calculator, a comprehensive assessment approach to this method, uses 12 principles of green analytical chemistry which transformed into a unified 0–1 scale. Potential use of methods in quality control laboratories is valuable for the pharmaceutical sector.

可持续pvp包盖金纳米颗粒合成“绿色”化学等离子体-液相法及其对水污染物铬离子(Cr(VI))的比色活性
金纳米颗粒(AuNPs)广泛应用于比色传感,利用其光学特性通过明显的颜色变化来识别变量。采用诱导等离子体液下工艺一步成功制备了聚合物(PVP)功能化金纳米颗粒。我们将用GREEnness计算器对等离子液法合成进行评价。研究了不同浓度PVP对AuNPs合成及其粒径分布、水动力直径、PDI、吸光度、LSPR等性能的影响。通过SEM、DLS和紫外可见光谱对合成的PVP-AuNPs进行了表征。制备出球形AuNPs,其最大吸收峰在530 - 560nm左右,尺寸范围为30 - 50nm,可根据合成过程中使用的前驱体和封盖剂的初始浓度进行调节。采用聚乙烯吡咯烷酮包覆金纳米颗粒(PVP-AuNPs)作为比色探针,快速、简便、灵敏、选择性地测定水中铬离子(Cr(VI))污染。实际上,铬离子(Cr(VI))通过迫使PVP-AuNPs与PVP在AuNPs表面聚集,使胶体溶液的色调由红色变为蓝色。在分析物的比色检测中,确定了尺寸和多分散性对功能化纳米颗粒比色性能的影响。通过优化实验参数(体积/浓度AuNPs、定量限(LOQ)、温度下检出限(LOD)的依赖关系),发现铬离子(Cr(VI))浓度与吸收比(A690/A530-560)在0.1 ~ 3.0µM范围内呈良好的线性关系,检出限为0.072 ~ 0.1µM。通过测定纳米比色探针对多种常见重金属离子的响应,评价了其选择性。分析性绿色计算器是该方法的一种综合评估方法,它使用了绿色分析化学的12个原则,这些原则转化为统一的0-1刻度。这些方法在质量控制实验室的潜在应用对制药部门是有价值的。
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来源期刊
Gold Bulletin
Gold Bulletin Chemistry-Inorganic Chemistry
CiteScore
3.70
自引率
4.50%
发文量
21
期刊介绍: Gold Bulletin is the premier international peer reviewed journal on the latest science, technology and applications of gold. It includes papers on the latest research advances, state-of-the-art reviews, conference reports, book reviews and highlights of patents and scientific literature. Gold Bulletin does not publish manuscripts covering the snthesis of Gold nanoparticles in the presence of plant extracts or other nature-derived extracts. Gold Bulletin has been published over 40 years as a multidisciplinary journal read by chemists, physicists, engineers, metallurgists, materials scientists, biotechnologists, surface scientists, and nanotechnologists amongst others, both within industry and academia. Gold Bulletin is published in Association with the World Gold Council.
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