Hyder Ali, Ali Akbar, Buledi Jamil Ahmed, Memon Roomia, Al-Anzi Bader S, Memon Ayaz Ali, Kazi Mohsin, Solangi Amber Rehana, Yang Jun, Thebo Khalid Hussain
National Centre of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080, Pakistan.
State Key Laboratory of Multi-phase Complex Systems, Institute of Process Engineering (IPE), Chinese Academy of Sciences, Beijing 100F190, China.
Phys Chem Chem Phys. 2024 Apr 3;26(14):10940-10950. doi: 10.1039/d4cp00138a.
Herein, NiO nanoparticles (NPs) functionalized with a -hexanitrocalix[6]arene derivative (-HNC6/NiO) were synthesized by using a facile method and applied as a selective electrochemical sensor for the determination of bisphenol S (BPS) in real samples. Moreover, the functional interactions, phase purities, surface morphologies and elemental compositions of the synthesized -HNC6/NiO NPs were investigated advanced analytical tools, such as Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). Additionally, the synthesized -HNC6/NiO NPs were cast on the surface of a bare glassy carbon electrode (GCE) a drop casting method, which resulted in uniform deposition of -HNC6/NiO/GCE over the surface of the GCE. Additionally, the developed -HNC6/NiO/GCE sensor demonstrated an outstanding electrochemical response to BPS under optimized conditions, including a supporting electrolyte, a Briton-Robinson buffer electrolyte at pH 4, a scan rate of 110 mV s and a potential window of between -0.2 and 1.0 V. The wide linear dynamic range was optimized to 0.8-70 μM to obtain a brilliant linear calibration curve for BPS. The limit of detection (LOD) and limit of quantification (LOQ) of the developed sensor were estimated to be 0.0059 and 0.019 μM, respectively, which are lower than those of reported sensors for BPS. The feasibility of the developed method was successfully assessed by analyzing the content of BPS in waste water samples, and good recoveries were achieved.
在此,通过一种简便的方法合成了用α-六硝基杯[6]芳烃衍生物(α-HNC6)功能化的氧化镍纳米颗粒(NPs)(α-HNC6/NiO),并将其用作选择性电化学传感器,用于测定实际样品中的双酚S(BPS)。此外,使用傅里叶变换红外(FT-IR)光谱、X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和能量色散X射线光谱(EDX)等先进分析工具,研究了合成的α-HNC6/NiO NPs的功能相互作用、相纯度、表面形态和元素组成。此外,通过滴铸法将合成的α-HNC6/NiO NPs浇铸在裸玻碳电极(GCE)表面,使得α-HNC6/NiO/GCE在GCE表面均匀沉积。此外,所开发的α-HNC6/NiO/GCE传感器在优化条件下对BPS表现出出色的电化学响应,包括支持电解质、pH为4的Briton-Robinson缓冲电解质、110 mV s的扫描速率和-0.2至1.0 V的电位窗口。宽线性动态范围优化为0.8 - 70 μM,以获得BPS的出色线性校准曲线。所开发传感器的检测限(LOD)和定量限(LOQ)分别估计为0.0059和0.019 μM,低于报道的用于BPS的传感器。通过分析废水样品中BPS的含量,成功评估了所开发方法的可行性,并实现了良好的回收率。