TY - JOUR
T1 - Bar adsorptive microextraction coated with carbonbased phase mixtures for performance-enhancement to monitor selected benzotriazoles, benzothiazoles, and benzenesulfonamides in environmental water matrices
AU - Ahmad, Samir M.
AU - Calado, Bruno B.C.
AU - Oliveira, Mariana N.
AU - Neng, Nuno R.
AU - Nogueira, J. M.F.
N1 - Publisher Copyright:
© 2020 by the authors.
PY - 2020/5
Y1 - 2020/5
N2 - In the present work we propose, for the first time, bar adsorptive microextraction coated with carbon-based phase mixtures, followed by microliquid desorption and high performance liquid chromatography-diode array detection (BAμE-μLD/HPLC-DAD) analysis, to enhance the performance of the determination of traces of benzotriazoles (BTRs), benzothiazoles (BTs), and benzenesulfonamide derivatives (BSDs) in environmental water matrices. Assessing six carbonbased sorbents (CA1, CN1, B test EUR, SX PLUS, SX 1, and R) with different selectivity properties allowed us to tailor the best phase mixture (R, 12.5%/CN1, 87.5%) that has convenient porosity, texture, and surface chemistry (pHPZC,mix ∼6.5) for trace analysis of benzenesulfonamide, 1- hydroxybenzotriazole, 1H-benzotriazole, 5-methyl-1H-benzotriazole, benzothiazole, and 1,3- benzothiazol-2-ol chemicals in aqueous media. Optimized experimental conditions provided average recoveries ranging from 37.9% to 59.2%, appropriate linear dynamic ranges (5.0 to 120.0 μg L-1; r2 ≥ 0.9964), limits of detection between 1.0 and 1.4 μg L-1, and good precisions (relative standard deviation (RSD) ≤9.3%). The proposed methodology (BAμE(R, 12.5%/CN1, 87.5%)-μLD/HPLCDAD) also proved to be a suitable sorption-based static microextraction alternative to monitor traces of BTRs, BTs, and BSDs in rain, waste, tap, and estuarine water samples. From the data obtained, the proposed approach showed that the BAμE technique with the addition of lab-made devices allows users to adapt the technique to use sorbents or mixtures of sorbents with the best selectivity characteristics whenever distinct classes of target analytes occur simultaneously in the same application.
AB - In the present work we propose, for the first time, bar adsorptive microextraction coated with carbon-based phase mixtures, followed by microliquid desorption and high performance liquid chromatography-diode array detection (BAμE-μLD/HPLC-DAD) analysis, to enhance the performance of the determination of traces of benzotriazoles (BTRs), benzothiazoles (BTs), and benzenesulfonamide derivatives (BSDs) in environmental water matrices. Assessing six carbonbased sorbents (CA1, CN1, B test EUR, SX PLUS, SX 1, and R) with different selectivity properties allowed us to tailor the best phase mixture (R, 12.5%/CN1, 87.5%) that has convenient porosity, texture, and surface chemistry (pHPZC,mix ∼6.5) for trace analysis of benzenesulfonamide, 1- hydroxybenzotriazole, 1H-benzotriazole, 5-methyl-1H-benzotriazole, benzothiazole, and 1,3- benzothiazol-2-ol chemicals in aqueous media. Optimized experimental conditions provided average recoveries ranging from 37.9% to 59.2%, appropriate linear dynamic ranges (5.0 to 120.0 μg L-1; r2 ≥ 0.9964), limits of detection between 1.0 and 1.4 μg L-1, and good precisions (relative standard deviation (RSD) ≤9.3%). The proposed methodology (BAμE(R, 12.5%/CN1, 87.5%)-μLD/HPLCDAD) also proved to be a suitable sorption-based static microextraction alternative to monitor traces of BTRs, BTs, and BSDs in rain, waste, tap, and estuarine water samples. From the data obtained, the proposed approach showed that the BAμE technique with the addition of lab-made devices allows users to adapt the technique to use sorbents or mixtures of sorbents with the best selectivity characteristics whenever distinct classes of target analytes occur simultaneously in the same application.
KW - BAμE
KW - Benzenesulfonamides
KW - Benzothiazoles
KW - Benzotriazoles
KW - Carbon-based sorbents
KW - Environmental water matrices
KW - HPLC-DAD
KW - Phase mixtures
UR - http://www.scopus.com/inward/record.url?scp=85084328399&partnerID=8YFLogxK
U2 - 10.3390/molecules25092133
DO - 10.3390/molecules25092133
M3 - Article
C2 - 32370134
AN - SCOPUS:85084328399
SN - 1420-3049
VL - 25
JO - Molecules
JF - Molecules
IS - 9
M1 - molecules25092133
ER -