113
Views
4
CrossRef citations to date
0
Altmetric
PRECONCENTRATION TECHNIQUES

Immobilization of Guanazyl Functional Groups on Silica for Solid-Phase Extraction of Metal Ions

, , , &
Pages 2665-2681 | Received 12 Dec 2013, Accepted 13 Apr 2014, Published online: 30 Aug 2014
 

Abstract

Guanazyl groups were grafted on silica gel by 4-nitrobenzoyl chloride acylation, sodium dithionite reduction, diazotation, and reaction with 2-benzylidenehydrazinecarboximidamide. The modified silica gel was used for separation and preconcentration of Cu(II), Ni(II), Cd(II), and Co(II). Quantitative extraction of the ions was achieved after 30 min and at the optimal pH of 7.5–8 at an initial concentration of 2 mg L−1. Analysis of metal sorption isotherms allowed estimation of the sorbent's interaction efficacy under static conditions at optimal pH. Distribution coefficients were determined to be 3 ± 0.3 L g−1 for Ni(II), 3 ± 0.3 L g−1 for Co(II), 1.6 ± 0.2 L g−1 for Cd(II), and 4.6 ± 0.4 L g−1 for Cu(II) at 20–60 µg analyte. The applicability of pseudo-second order kinetic equations for metal sorption kinetics description was investigated. Chemically modified silica was used for solid-phase extraction of the metal ions to improve the detection limit using X-ray fluorescence spectrometry. The method was employed for the determination of Cu(II) in water with a low limit of detection, high accuracy, and good precision.

Notes

BDL, below the detection limit.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.