作为膳食补充剂中三价铬离子双模传感器的光学银纳米粒子封端碳点的合成与应用

Ratchadaporn Seedad , Pornpimol Prayongpan , Wutthikrai Busayaporn , Kriangsak Songsrirote
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引用次数: 0

摘要

利用光学银纳米粒子封端碳点(Ag@CDs)开发了一种测定三价铬(Cr3+)离子的简便方法。检测了 Ag@CDs 在 Cr3+ 离子存在下的吸收和荧光响应。该纳米复合材料的最大吸收波长为 406.0 nm,而在 406.0 nm 处激发时的发射波长为 526.0 nm。Ag@CDs 对 Cr3+ 离子的最佳检测条件为 pH 值为 6,Ag@CDs 与 Cr3+ 离子的体积比为 1.0:4.0,反应时间为 20 分钟。检测线性范围为 0.1-10.0 mg/L。在吸收模式下,检出限(LOD)和定量限(LOQ)分别为 0.10 mg/L 和 0.31 mg/L。荧光检测模式的检测限和定量限分别为 0.06 mg/L 和 0.18 mg/L。由于 Cr3+ 是人体必需的微量营养元素,被广泛应用于补充剂产品中,因此该双模式传感器被用于膳食补充剂样品中 Cr3+ 离子的定量分析。加标样品提取物的回收率为 96.86-103.05%。该结果与传统原子发射光谱法的结果一致。纳米复合材料的光学变化机理可通过 Ag@CDs 向 Cr3+ 的电子转移来解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis and application of optical silver nanoparticles capped carbon dots as dual-mode sensors for trivalent chromium ions in dietary supplements

Synthesis and application of optical silver nanoparticles capped carbon dots as dual-mode sensors for trivalent chromium ions in dietary supplements

A facile method for trivalent chromium (Cr3+) ion determination using optical silver nanoparticles capped carbon dots (Ag@CDs) was developed. The optical responses via absorption and fluorescence of Ag@CDs in the presence of Cr3+ ion were detected. The nanocomposite showed maximum absorption wavelength at 406.0 nm, while emission wavelength appeared at 526.0 nm when excited at 406.0 nm. Optimal conditions for the Ag@CDs activity on Cr3+ ion detection were at pH 6, volume ratio between Ag@CDs and Cr3+ ion of 1.0:4.0, and reaction time of 20 min. The linearity range of the detection was 0.1–10.0 mg/L. In the absorption mode, the limit of detection (LOD) and limit of quantification (LOQ) were 0.10 mg/L and 0.31 mg/L, respectively. The fluorescence mode of detection showed LOD and LOQ of 0.06 mg/L and 0.18 mg/L, respectively. The dual-mode sensor was applied for Cr3+ ion quantification in dietary supplement samples because it is an essential micronutrient and widely used as supplement products. The recovery study of the spiked sample extracts was in the range of 96.86–103.05 %. The results showed good agreement with those from a conventional method of atomic emission spectrometry. The optical changing mechanism of the nanocomposite could be explained by the electron transfer from Ag@CDs to Cr3+.

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