Facile Preparation of Tannic Acid-Gold Nanoparticles for Catalytic and Selective Detection of Mercury(II) and Iron(II) Ions in the Environmental Water Samples and Commercial Iron Supplement

被引:0
|
作者
Sun, Kun-Yu [1 ]
Chueh, Chen-Yu [1 ]
Wu, Mei-Yao [2 ]
Wu, Tsunghsueh [3 ]
Lin, Yang-Wei [1 ]
机构
[1] Natl Changhua Univ Educ, Dept Chem, Changhua 50007, Taiwan
[2] China Med Univ, Sch Postbaccalaureate Chinese Med, Taichung 40424, Taiwan
[3] Univ Wisconsin, Dept Chem, Platteville, WI 53818 USA
来源
ACS OMEGA | 2024年 / 9卷 / 40期
关键词
COLORIMETRIC SENSOR; FE2+;
D O I
10.1021/acsomega.4c05167
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tannic acid (TA), a plant-derived polyphenol rich in hydroxyl groups, serves as both a reducing agent and stabilizer for synthesizing gold nanoparticles (TA-AuNPs). This study presents a groundbreaking method that utilizes TA to fabricate TA-AuNPs and develop two distinct colorimetric detection systems for mercury (Hg2+) and iron (Fe2+) ions. The first detection system leverages the interaction between TA-AuNPs and Hg2+ to enhance the peroxidase-like activity of TA-AuNPs, facilitating the production of hydroxyl radicals upon reaction with hydrogen peroxide, which subsequently oxidizes 3,3 ',5,5 '-tetramethylbenzidine (TMB) into a blue-colored product (ox-TMB). The second system capitalizes on TA-AuNPs to catalyze the Fenton reaction between Fe2+ and hydrogen peroxide in the presence of 2, 6-pyridinedicarboxylic acid, boosting the generation of hydroxyl radicals that oxidize TMB into a blue-colored ox-TMB. Absorbance measurements at 650 nm display a linear relationship with Hg2+ concentrations ranging from 0.40 to 0.60 mu M (R-2 = 0.99) and Fe2+ concentrations from 0.25 to 2.0 mu M (R-2 = 0.98). The established detection limits for Hg2+ and Fe2+ are 18 nM and 96 nM, respectively. Applications to real-world samples achieved an excellent spiked recovery, spanning 101.6% to 108.0% for Hg2+ and 90.0% to 112.5% for Fe2+, demonstrating the method's superior simplicity, speed, and cost-effectiveness for environmental monitoring of these ions compared to existing techniques.
引用
收藏
页码:41521 / 41531
页数:11
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