Ultrasensitive fluorescence-quenched chemosensor for Hg(II) in aqueous solution based on mercaptothiadiazole capped silver nanoparticles

被引:60
作者
Vasimalai, N. [1 ]
Sheeba, G. [1 ]
John, S. Abraham [1 ]
机构
[1] Gandhigram Rural Inst, Dept Chem, Dindigul 624302, Tamil Nadu, India
关键词
Chemosensor; Mercuric ions; 2,5-Dimercapto-1,3,4-thiadiazole; Silver nanoparticles; Water samples; LIGAND-EXCHANGE REACTION; GOLD NANOPARTICLES; LUMINESCENT CHEMOSENSORS; COLORIMETRIC DETECTION; MERCURY; HG2+; SENSOR; NANOCLUSTERS; MECHANISMS; CHEMISTRY;
D O I
10.1016/j.jhazmat.2012.01.079
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This manuscript describes a highly selective and ultra sensitive determination of Hg(II) in aqueous solution using functionalized mercaptothiadiazole capped silver nanoparticles (AgNPs) by spectrofluorimetry. We have synthesized 2,5-dimercapto-1,3,4-thiadiazole (DMT), 2-mercapto-5-methyl-1,3,4-thiadiazole (MMT) and 2-mercapto-5-amino-1,3,4-thiadiazole (AMT) capped AgNPs by wet chemical method. Among these AgNPs, DMT capped AgNPs (DMT-AgNPs) were more stable and highly fluorescent than the other two AgNPs. DMT-AgNPs show the emission maximum at 677 nm while exciting at 400 nm. After the addition of Hg(II), the emission intensity was decreased at 677 nm. The observed decreased emission intensity was ascribed to the aggregation of AgNPs and it was confirmed by TEM. Based on the decrease in emission intensity, the concentration of Hg(II) was determined. The lowest detection limit (LOD = 3 S/m) of 1.0 pg L-1 was achieved for the first time using DMT-AgNPs by spectrofluorimetry. The quantum yield (phi(F)). Stern-Volmer constant (K-SV), Gibbs free energy changes (Delta G degrees), association constant (K-f) were calculated and the quenching mechanism also was discussed. Finally, the proposed method was successfully utilized for the determination of Hg(II) in river water, industrial effluent water and tap water samples. The obtained results were fairly matches with the ICP-AES method. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:193 / 199
页数:7
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