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 Removal of mercury (II) by dithiocarbamate surface functionalized magnetite particles: application to synthetic and natural spiked waters
Please use this identifier to cite or link to this item http://hdl.handle.net/10773/6301

title: Removal of mercury (II) by dithiocarbamate surface functionalized magnetite particles: application to synthetic and natural spiked waters
authors: Figueira, P.
Lopes, C. B.
Daniel-da-Silva, A. L.
Pereira, E.
Duarte, A. C.
Trindade, T.
keywords: Mercury
Magnetite particles
Dithiocarbamate functionalization
Isotherms
Water remediation
issue date: Nov-2011
publisher: Elsevier
abstract: In order to take advantage of the high affinity between mercury and sulphur, magnetite (Fe3O4) particles functionalized with dithiocarbamate groups (CS 2 ), were synthesized to be used as a new type of sorbent to remove Hg (II) from synthetic and natural spiked waters. The effectiveness of this type of sorbent was studied, and its potential as cleanup agent for contaminated waters was assessed. Batch stirred tank experiments were carried out by contacting a volume of solution with known amounts of functionalized Fe3O4 particles, in order to study the effect of sorbent dose, salinity, and the kinetics and the equilibrium of this unit operation. A complete Hg (II) removal (ca. 99.8%) was attained with 6 mg/L of magnetic particles for an initial metal concentration of 50 mg/L. It was confirmed that highly complex matrices, such as seawater (ca. 99%) and river water (ca. 97%), do not affect the removal capacity of the functionalized magnetic particles. Concerning isotherms, no significant differences were observed between two- and three-parameter models (P ¼ 0.05%); however, Sips isotherm provided the lowest values of SS and Sx/y, predicting a maximum sorption capacity of 206 mg/g, in the range of experimental conditions under study. The solid loadings measured in this essay surmount the majority of the values found in literature for other type of sorbents.
URI: http://hdl.handle.net/10773/6301
ISSN: 0043-1354
publisher version/DOI: dx.doi.org/10.1016/j.watres.2011.08.057
source: Water Research
appears in collectionsDQ - Artigos

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