Graphene and gold nanoparticle-based bionanocomposite for the voltammetric determination of bisphenol A in (micro)plastics

双酚A 双酚 石墨烯 双酚S 材料科学 玻璃碳 检出限 胶体金 纳米颗粒 化学工程 电极 电化学 核化学 纳米技术 化学 循环伏安法 复合材料 色谱法 环氧树脂 物理化学 工程类
作者
Luan Gabriel Baumgarten,Aline Alves Freitas,Edson Roberto Santana,João Paulo Winiarski,Juliana Priscila Dreyer,Iolanda Cruz Vieira
出处
期刊:Chemosphere [Elsevier]
卷期号:334: 139016-139016 被引量:15
标识
DOI:10.1016/j.chemosphere.2023.139016
摘要

The monitoring of endocrine disruptors in the environment is one of the main strategies in the investigation of potential risks associated with exposure to these chemicals. Bisphenol A is one of the most prevalent endocrine-disrupting compounds and is prone to leaching out from polycarbonate plastic in both freshwater and marine environments. Additionally, microplastics also can leach out bisphenol A during their fragmentation in the water environment. In the quest for a highly sensitive sensor to determine bisphenol A in different matrices, an innovative bionanocomposite material has been achieved. This material is composed of gold nanoparticles and graphene, and was synthesized using a green approach that utilized guava (Psidium guajava) extract for reduction, stabilization, and dispersion purposes. Transmission electron microscopy images revealed well-spread gold nanoparticles with an average diameter of 31 nm on laminated graphene sheets in the composite material. An electrochemical sensor was developed by depositing the bionanocomposite onto a glassy carbon surface, which displayed remarkable responsiveness towards bisphenol A. Experimental conditions such as the amount of graphene, extract: water ratio of bionanocomposite and pH of the supporting electrolyte were optimized to improve the electrochemical performance. The modified electrode displayed a marked improvement in current responses for the oxidation of bisphenol A as compared to the uncovered glassy carbon electrode. A calibration plot was established for bisphenol A in 0.1 mol L−1 Britton-Robinson buffer (pH 4.0), and the detection limit was determined to equal to 15.0 nmol L−1. Recovery data from 92 to 109% were obtained in (micro)plastics samples using the electrochemical sensor and were compared with UV–vis spectrometry, demonstrating its successful application with accurate responses.
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