Publication: Chromatic analysis by monitoring unmodified silver nanoparticles reduction on double layer microfluidic paper-based analytical devices for selective and sensitive determination of mercury(II)
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Issued Date
2016-08-01
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00399140
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2-s2.0-84964869857
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Mahidol University
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SCOPUS
Bibliographic Citation
Talanta. Vol.155, (2016), 193-201
Suggested Citation
Rattapol Meelapsom, Purim Jarujamrus, Maliwan Amatatongchai, Sanoe Chairam, Chadin Kulsing, Wei Shen Chromatic analysis by monitoring unmodified silver nanoparticles reduction on double layer microfluidic paper-based analytical devices for selective and sensitive determination of mercury(II). Talanta. Vol.155, (2016), 193-201. doi:10.1016/j.talanta.2016.04.037 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/42982
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Title
Chromatic analysis by monitoring unmodified silver nanoparticles reduction on double layer microfluidic paper-based analytical devices for selective and sensitive determination of mercury(II)
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Abstract
© 2016 Elsevier B.V. All rights reserved. This study demonstrates chromatic analysis based on a simple red green blue (RGB) color model for sensitive and selective determination of mercury(II). The analysis was performed by monitoring the color change of a microfluidic Paper-based Analytical Device (μPAD). The device was fabricated by using alkyl ketene dimer (AKD)-inkjet printing and doped with unmodified silver nanoparticles (AgNPs) which were disintegrated when being exposed to mercury(II). The color intensity was detected by using an apparatus consisting of a digital camera and a homemade light box generating constant light intensity. A progressive increase in color intensity of the tested area on the μPAD (3.0 mm) was observed with increasing mercury(II) concentration. The developed system enabled quantification of mercury(II) at low concentration with the detection limit of 0.001 mg L-1 (3 SD blank/slope of the calibration curve) and small sample volume uptake (2 μL). The linearity range of the calibration curve in this technique was demonstrated from 0.05 to 7 mg L-1 (r2=0.998) with good precision (RSD less than 4.1%). Greater selectivity towards mercury(II) compared with potential interference ions was also observed. Furthermore, the percentage recoveries of spiked water samples were in an acceptable range which was in agreement with the values obtained from the conventional method utilizing cold vapor atomic absorption spectrometer (CVAAS). The proposed technique allows a rapid, simple, sensitive and selective analysis of trace mercury(II) in water samples.