4.7 Article

A high-performance electrochemical sensor based on a mesoporous silica/titania material and cobalt(II) phthalocyanine for sensitive pentachlorophenol determination

期刊

MICROCHIMICA ACTA
卷 189, 期 8, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-022-05360-z

关键词

Hybrid materials; Mixed oxide; Mesoporous materials; Persistent organic pollutant; Electroanalytical method; Differential pulse voltammetry; Environmental monitoring

资金

  1. Coordination for the Improvement of Higher Education Personnel (CAPES Foundation, Brazil) [001]
  2. National Council for Scientific and Technological Development (CNPq, Brazil) [446757/2014-4]

向作者/读者索取更多资源

The synthesis and characterization of a novel titania/silica hybrid xerogel subsequently modified with 4-methylpyridine (4-Pic), named TiSi4Pic(+)Cl(-), is reported. Anchoring cobalt(II) phthalocyanine (CoTsPc) in TiSi4Pic(+)Cl(-) showed greater electroanalytical sensitivity over other sensors built with these materials. A novel electroanalytical method was developed to quantify the noxious biocide pentachlorophenol (PCP) for environmental monitoring, which exhibited high accuracy.
The synthesis and characterization of a novel titania/silica hybrid xerogel subsequently modified with 4-methylpyridine (4-Pic), named TiSi4Pic(+)Cl(-) is reported. The physicochemical, structural and thermal properties of TiSi4Pic(+)Cl(-) were characterized using several techniques. Anchoring cobalt(II) phthalocyanine (CoTsPc) in TiSi4Pic(+)Cl(-) showed greater electroanalytical sensitivity over other sensors built with these materials. A novel electroanalytical method was developed to quantify the noxious biocide pentachlorophenol (PCP) for environmental monitoring. The peak current intensity increased linearly with the analyte concentration in the range between 0.99 and 4.21 mu mol L-1, based on the oxidation process (at + 0.81 V, vs. Ag/AgCl) of differential pulse voltammetry (DPV). The estimated limit of detection (LOD) was 29 nmol L-1. Recovery tests in environmental samples showed a PCP concentration of 2.05 +/- 0.03 mu mol L-1 (n = 3). The method was statistically validated by comparing the PCP concentrations with those obtained by molecular absorption spectrometry and high-performance liquid chromatography-diode array detection (HPLC-DAD). At a 95% confidence level, no difference between the results was found, therefore confirming the excellent accuracy of the proposed method.

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