Humic-rich hydrocolloids and their metal species (e.g., Al, Fe, Ca, Cu, Fe, Mg, Mn, Pb, Zn) in selected bogwaters of German origin (Black Forest (HO), Muensterland (VM), Arnsberger Wald (AW)) were size classified in the subparticulate and macromolecular range by on-site multistage ultrafiltration (MST-UF). For this purpose two MST-UF cascades, equipped with up to eight conventional flat membranes (0.45, 0.22, 0.1 micron (Millipore); 100, 50, 10, 5, 3, and/or 1 kDa (Gelman PallFiltron OMEGA), were coupled and used for an online fractionation of hydrocolloidal matter immediately after water sample collection. Quantification of dissolved organic carbon (DOC) and metals was carried out off-site by conventional laboratory methods (carbon analyzer, atomic spectrometry). The size distribution of some humic-rich hydrocolloids (e.g. in HO) was exhibited to be surprisingly stable even over storage periods of 1-4 weeks. On the other side, their size distribution (e.g. in VM) considerably varied during the collection period. The natural metal loadings (e.g. Al, Fe, Mn, Zn) of hydrocolloids showed characteristic size distributions and, mostly, strong metal enrichment in subparticulate and macromolecular fractions. Further results of on-site classification of hydrocolloids, obtained by parallel single-stage ultrafiltration (P-UF) with the same membranes, were only comparable to those of MST-UF in the case of low DOC concentration.
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J Hazard Mater
June 2024
GRIL, Département de sciences biologiques, Complexe des Sciences, Université de Montréal, Québec, Canada; Centre d'Études Nordiques, Québec, Canada. Electronic address:
The emergence of mining projects for rare earth elements (REEs) in response to rising global demand and geopolitical factors introduces environmental concerns, such as the suspected release of anthropogenic REEs to aquatic systems and the coexistence of radionuclides (U, Th). Northern regions confront heightened challenges from limited research and accelerated climate change. Drivers of REEs in surface waters (including George and Koroc rivers, their tributaries, and thermokarst lakes) were studied (2017-2023) in subarctic Canada within a climate transition zone, near a prospective REE mine.
View Article and Find Full Text PDFJ Colloid Interface Sci
July 2011
CNRS-UMR 6118, Géosciences Rennes, University of Rennes 1, Avenue du Général Leclerc, 35042 Rennes Cedex, France.
Few studies have so far examined the kinetics and extent of the formation of Fe-colloids in the presence of natural organic ligands. The present study used an experimental approach to investigate the rate and amount of colloidal Fe formed in presence of humic substances, by gradually oxidizing Fe(II) at pH 6.5 with or without humic substances (HS) (in this case, humic acid--HA and fulvic acid--FA).
View Article and Find Full Text PDFEnviron Sci Technol
November 2010
Environmental Research Institute, Thurso, Caithness KW14 7JD, UK.
This study investigated the physicochemical forms of dissolved iron in the coastal plume (salinity = 28-35) of a small river draining a peat-rich catchment. Speciation information was obtained through a combination of fractionation by crossflow filtration (CFF) along with voltammetric detection of either naturally occurring iron-humic complexes (July survey) or known, synthetic complexes (September survey) formed by titrating the samples with the competing ligand 2-(2-thiazolylazo)-p-cresol (TAC). The majority of colloidal iron (>5000 Da) was present as iron-humic complexes supplied by the river and showing uniform conditional stability constants throughout the plume (log K′(Fe′HS) = 11.
View Article and Find Full Text PDFAnal Bioanal Chem
May 2010
Departamento de Engenharia Ambiental, UNESP - Universidade Estadual Paulista, 18087-180, Sorocaba, SP, Brazil.
This paper deals with the development and optimization of an analytical procedure using ultrafiltration and a flow-injection system, and its application in in-situ experiments to characterize the lability and availability of metal species in humic-rich hydrocolloids. The on-line system consists of a tangential flow ultrafiltration device equipped with a 3-kDa filtration membrane. The concentration of free ions in the filtrate was determined by atomic-absorption spectrometry, assuming that metals not complexed by aquatic humic substances (AHS) were separated from the complexed species (M-AHS) retained by the membrane.
View Article and Find Full Text PDFAnal Bioanal Chem
August 2005
ISAS, Institute for Analytical Sciences, Bunsen-Kirchhoff-Str. 11, 44139 Dortmund, Germany.
The separation behavior of the frequently administered pharmaceuticals sulfamethoxazol (Sulfa), carbamazepine (Carba), diclofenac (Diclo), and ibuprofen (Ibu) on different natural and synthetic ultrafiltration membranes was studied. Commercially available cattle intestine natural membranes (NM), polyethersulfone (PES), and regenerated cellulose-based (RC) flat membranes (nominal cut-off 1 kDa) have been investigated as ultrafiltration membranes in a small tangential-flow ultrafiltration unit (TF-UF). First, the nominal cut-off of the NM membranes under study was assessed at approximately 5 kDa, by using polystyrenesulfonate standards for pore-size classification at low TF-UF pressure (0.
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