Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/45614
Title: Chemical and structural characterization of copper adsorbed on mosses (Bryophyta)
Authors: González, Aridane G. 
Jimenez-Villacorta, Felix
Reski, Ralf
Adamo, Paola
Pokrovsky, Oleg S.
Beike, Anna K.
UNESCO Clasification: 2301 química analítica
Keywords: Copper
Adsorption
XAS
XANES
Biomonitoring
Issue Date: 2016
Project: Changes in carbon uptake and emissions by oceans in a changing climate ItemCrisRefDisplayStrategy.project.deleted.icon
Journal: Journal of Hazardous Materials 
Abstract: The adsorption of copper on passive biomonitors (devitalized mosses Hypnum sp., Sphagnum denticulatum, Pseudoscleropodium purum and Brachythecium rutabulum) was studied under different experimental conditions such as a function of pH and Cu concentration in solution. Cu assimilation by living Physcomitrella patents was also investigated. Molecular structure of surface adsorbed and incorporated Cu was studied by X-ray Absorption Spectroscopy (XAS). Devitalized mosses exhibited the universal adsorption pattern of Cu as a function of pH, with a total binding sites number 0.05–0.06 mmolgdry−1 and a maximal adsorption capacity of 0.93–1.25 mmolgdry−1 for these devitalized species. The Extended X-ray Absorption Fine Structure (EXAFS) fit of the first neighbor demonstrated that for all studied mosses there are ∼4.5 O/N atoms around Cu at ∼1.95 Å likely in a pseudo-square geometry. The X-ray Absorption Near Edge Structure (XANES) analysis demonstrated that Cu(II)-cellulose (representing carboxylate groups) and Cu(II)-phosphate are the main moss surface binding moieties, and the percentage of these sites varies as a function of solution pH. P. patens exposed during one month to Cu2+ yielded ∼20% of Cu(I) in the form of Cu–S(CN) complexes, suggesting metabolically-controlled reduction of adsorbed and assimilated Cu2+.
URI: http://hdl.handle.net/10553/45614
ISSN: 0304-3894
DOI: 10.1016/j.jhazmat.2016.01.060
Source: Journal of Hazardous Materials [ISSN 0304-3894], v. 308, p. 343-354
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