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Picomolar-level detection of mercury within non-biological/biological aqueous media using ultra-sensitive polyaniline-Fe3O4-silver diethyldithiocarbamate nanostructure
Mercury as the 3rd most toxic, non-biodegradable, and carcinogenic pollutant can adversely affect the ecosystem and health of living species through its bioaccumulation within the nature that can affect the top consumer in the food chain; therefore, it is vital to sense/remove Hg 2+ within/from aque...
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Published in: | Analytical and bioanalytical chemistry 2020-09, Vol.412 (22), p.5353-5365 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Mercury as the 3rd most toxic, non-biodegradable, and carcinogenic pollutant can adversely affect the ecosystem and health of living species through its bioaccumulation within the nature that can affect the top consumer in the food chain; therefore, it is vital to sense/remove Hg
2+
within/from aqueous media using practical approaches. To address this matter, we modified the glassy carbon electrode (GCE) with ultra-sensitive, interconnected, sulfurized, and porous nanostructure consisted of polyaniline-Fe
3
O
4
-silver diethyldithiocarbamate (PANi-F-S) to enhance the sensitivity, selectivity, and limit of detection (LOD) of the sensor. Obtained results showed that at optimum conditions (i.e., pH value of 7, deposition potential of − 0.8 V, and accumulation time of 120 s), for Hg
2+
concentration ranging from 0.4 to 60 nM, the modified electrode showing linear relative coefficient of 0.9983, LOD of 0.051 nM, LOQ of 0.14 nM, and sensitivity of 1618.86 μA μM
−1
cm
−2
highlights superior sensitivity of the developed platform until picomolar level. Additionally, the modified electrode showed ideal repeatability, stability, reproducibility, and selectivity (by considering Zn
2+
, Cd
2+
Pb
2+
, Cu
2+
, Ni
2+
, and Co
2+
as metal interferences) and recovered more than 99% of the Hg
2+
ions within non-biological (mineral, tap, and industrial waters) and biological (blood plasma sample) fluids.
Graphical abstract |
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ISSN: | 1618-2642 1618-2650 |
DOI: | 10.1007/s00216-020-02750-1 |