Issue 5, 2016

Functionalization of silver nanoparticles with 5-sulfoanthranilic acid dithiocarbamate for selective colorimetric detection of Mn2+ and Cd2+ ions

Abstract

In this work, we have described the use of sulfoanthranilic acid dithiocarbamate functionalized silver nanoparticles as a probe for simple, rapid and simultaneous colorimetric detection of Mn2+ and Cd2+ ions. The Mn2+ and Cd2+ ions induce the aggregation of sulfoanthranilic acid dithiocarbamate functionalized silver nanoparticles, resulting in a color change from yellow to orange associated with a red-shift in their surface plasmon resonance peak from 395 to 580 and 535 nm for Mn2+ and Cd2+ ions, respectively. Moreover, the aggregation of sulfoanthranilic acid dithiocarbamate functionalized silver nanoparticles induced by Mn2+ and Cd2+ ions was confirmed by dynamic light scattering and transmission electron microscopy. The Mn2+ and Cd2+ ion detection method based on their surface plasmon resonance peak using UV-visible spectrophotometry offers wide linear detection ranges from 5 to 50 μM and 10 to 100 μM with detection limits of 1.7 and 5.8 μM for Mn2+ and Cd2+ ions, respectively. The sulfoanthranilic acid dithiocarbamate functionalized silver nanoparticles act as a simple colorimetric probe for the simultaneous detection of Mn2+ and Cd2+ ions in various environmental water samples (drinking, tap, canal and river water) with good recovery values at minimal volumes of samples.

Graphical abstract: Functionalization of silver nanoparticles with 5-sulfoanthranilic acid dithiocarbamate for selective colorimetric detection of Mn2+ and Cd2+ ions

Supplementary files

Article information

Article type
Paper
Submitted
05 Dec 2015
Accepted
07 Mar 2016
First published
08 Mar 2016

New J. Chem., 2016,40, 4566-4574

Author version available

Functionalization of silver nanoparticles with 5-sulfoanthranilic acid dithiocarbamate for selective colorimetric detection of Mn2+ and Cd2+ ions

V. N. Mehta, J. V. Rohit and S. K. Kailasa, New J. Chem., 2016, 40, 4566 DOI: 10.1039/C5NJ03454J

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