Interference by organic complexation of Fe and A1 on the SO2-4 adsorption in Spodic B horizons in Sweden

1993 ◽  
Vol 44 (4) ◽  
pp. 625-632 ◽  
Author(s):  
E. KARLTUN ◽  
J. P. GUSTAFSSON
Keyword(s):  
1995 ◽  
Vol 50 (1-4) ◽  
pp. 139-157 ◽  
Author(s):  
Constant M.G. van den Berg
Keyword(s):  

2018 ◽  
Vol 204 ◽  
pp. 144-151 ◽  
Author(s):  
Kuo Hong Wong ◽  
Hajime Obata ◽  
Taejin Kim ◽  
Asami Suzuki Mashio ◽  
Hideki Fukuda ◽  
...  

2011 ◽  
Vol 8 (5) ◽  
pp. 485 ◽  
Author(s):  
Jon Petter Gustafsson ◽  
Charlotta Tiberg ◽  
Abubaker Edkymish ◽  
Dan Berggren Kleja

Environmental contextLead(II) is a toxic metal pollutant with many anthropogenic sources. We show that lead(II) is bound more strongly to soil surfaces than previously understood. This knowledge may lead to better models for lead(II) dissolution from the soils, which will improve risk assessments for this metal. AbstractLead(II) adsorption to soil organic matter and iron (hydr)oxides is strong, and may control the geochemical behaviour of this metal. Here, we report the adsorption of Pb2+ (i) to 2-line ferrihydrite, and (ii) to a mor layer. The results showed that ferrihydrite has heterogeneous Pb2+ binding. Use of a surface complexation model indicated that ~1 % of the surface sites adsorbed Pb2+ more strongly than the remaining 99 %. Although only one surface complexation reaction was used (a bidentate complex of the composition (≡FeOH)2Pb+), three classes of sites with different affinity for Pb2+ were needed to simulate Pb2+ binding correctly over all Pb/Fe ratios analysed. For the mor layer, Pb2+ sorption was much stronger than current models for organic complexation suggest. The results could be described by the Stockholm Humic Model when the binding heterogeneity was increased, and when it was assumed that 0.2 % of the binding sites were specific for Pb. Use of revised model parameters for nine Vietnamese soils suggest that lead(II) binding was more correctly simulated than before. Thus, underestimation of lead(II) sorption to both (hydr)oxide surfaces and organic matter may explain the failure of previous geochemical modelling attempts for lead(II).


1992 ◽  
Vol 26 (6) ◽  
pp. 1248-1250 ◽  
Author(s):  
Jeffrey Gaffney ◽  
Namcy Marley ◽  
Kent Orlandini

2007 ◽  
Vol 4 (2) ◽  
pp. 81 ◽  
Author(s):  
Sylvia G. Sander ◽  
Andrea Koschinsky ◽  
Gary Massoth ◽  
Matthew Stott ◽  
Keith A. Hunter

Environmental context. Deep-sea hydrothermal vents represent a natural habitat for many extremophile organisms able to cope with extreme physical and chemical conditions, including high loads of heavy metals and reduced gases. To date, no information is available on the level and role of organic complexation of metals in these systems, which will have consequences on the bioavailability and precipitation or mineralisation of metals. In this work, we give evidence for the presence of organic molecules, including thiols, capable of forming complexes with copper strong enough to compete against sulfide present at high levels in hydrothermal systems. Abstract. Here we report, for the first time, that strong organic complexation plays an important role in the chemical speciation of copper in hydrothermal vent systems including medium temperature outlets, diffuse vents with an adjacent hydrothermal biocommunity, and local mixing zone with seawater. Samples from three deep-sea hydrothermal vent areas show a wide concentration range of organic copper-binding ligands, up to 4000 nM, with very high conditional stability constants (log K′Cu′L = 12.48 to 13.46). Measurements were usually made using voltammetric methods after removal of sulfide species under ambient seawater conditions (pH 7.8), but binding still occurs at pH 4.5 and 2.1. The voltammetric behaviour of our hydrothermal samples is compared with that of glutathione (GSH) a known strong Cu-binding ligand, as a representative of an organic thiol. Our results provide compelling evidence for the presence of organic ligands, including thiols, which form complexes strong enough to play an important role in controlling the bioavailability and geochemical behaviour of metal ions around hydrothermal vents.


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