4.7 Article

An ultra-sensitive molecularly imprinted polymer (MIP) and gold nanostars (AuNS) modified voltammetric sensor for facile detection of perfluorooctance sulfonate (PFOS) in drinking water

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 352, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.131055

关键词

Perfluorooctance sulfonate (PFOS); Molecularly imprinted polymer (MIP); Gold nanostar (AuNS); Electropolymerization optimization; Differential pulse voltammetry (DPV)

资金

  1. Natural Science Foundation of Zhejiang Province, CN [Q22B051349, LY21E090004]
  2. Key Research and Development Program of Zhejiang Province, CN [2020C03082]
  3. National Natural Science Foundation of China [52070103]
  4. Public Welfare Science and Technology Plan Project of Ningbo [202002N3052]
  5. U.S. National Science Foundation [1952147]
  6. Direct For Computer & Info Scie & Enginr
  7. Division Of Computer and Network Systems [1952147] Funding Source: National Science Foundation

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A highly sensitive voltammetric sensor for PFOS detection in tap water was developed using AuNS and MIP modification on a glassy carbon electrode. The sensor showed comparable analytical performance to the EPA method and minor interference from common interferents in drinking water sources.
Perfluorooctance sulfonate (PFOS) is one of the most studied Per-and-polyfluoroalkyl substances (PFAS) due to its relatively high environmental ubiquity and toxicity. This study presented an ultra-sensitive voltammetric sensor for the detection of PFOS in tap water based on a glassy carbon electrode (GCE) modified with a thin coating of gold nanostar (AuNS) and electropolymerized molecularly imprinted polymer (MIP). The AuNS coating helps to enhance the voltammetric response of blank signal intensity regarding the Fe2+ oxidation of the selected ferrocenecarboxylic acid (FcCOOH) redox probe; meanwhile, the statistical optimization of the MIP layer offers a higher peak change. Analytical results indicated the sensor could detect PFOS with an LoD and LoQ of 0.015 and 0.041 nM (i.e., 7.5 and 20.5 ppt), respectively. Moreover, it showed comparable analytical performance in tap water with the U.S. Environmental Protection Agency (EPA) method (i.e., Method 537.1). Interfering effects of approximately 10% underestimation were observed when samples contained equimolar perfluorobutanoic Acid (PFBA) or perfluorobutanesulfonic acid (PFBS). Additionally, common interferents in drinking water sources, such as humic acid and chloride ion, showed minor influence in the voltammetric response in terms of accuracy and reproducibility.

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