Donnan membrane speciation of Al, Fe, trace metals and REEs in coastal lowland acid sulfate soil-impacted drainage waters
Creators
- 1. School of Civil and Environmental Engineering, University of New South Wales, Sydney, NSW 2052 (Australia)
- 2. Institute for Environmental Research (IER), Australian Nuclear Science and Technology Organisation (ANSTO), Lucas Heights, NSW 2234 (Australia)
Description
Donnan dialysis has been applied to forty filtered drainage waters collected from five coastal lowland acid sulfate soil (CLASS) catchments across north-eastern NSW, Australia. Despite having average pH values < 3.9, 78 and 58% of Al and total Fe, respectively, were present as neutral or negatively-charged species. Complementary isotope dilution experiments with 55Fe and 26Al demonstrated that only soluble (i.e. no colloidal) species were present. Trivalent rare earth elements (REEs) were also mainly present (> 70%) as negatively-charged complexes. In contrast, the speciation of the divalent trace metals Co, Mn, Ni and Zn was dominated by positively-charged complexes and was strongly correlated with the alkaline earth metals Ca and Mg. Thermodynamic equilibrium speciation calculations indicated that natural organic matter (NOM) complexes dominated Fe(III) speciation in agreement with that obtained by Donnan dialysis. In the case of Fe(II), however, the free cation was predicted to dominate under thermodynamic equilibrium, whilst our results indicated that Fe(II) was mainly present as neutral or negatively-charged complexes (most likely with sulfate). For all other divalent metals thermodynamic equilibrium speciation calculations agreed well with the Donnan dialysis results. The proportion of Al and REEs predicted to be negatively-charged was also grossly underestimated, relative to the experimental results, highlighting possible inaccuracies in the stability constants developed for these trivalent Me(SO4)2− and/or Me–NOM complexes and difficulties in modeling complex environmental samples. These results will help improve metal mobility and toxicity models developed for CLASS-affected environments, and also demonstrate that Australian CLASS environments can discharge REEs at concentrations an order of magnitude greater than previously reported. - Highlights: • CLASS discharge large amounts of metals and their speciation is poorly understood. • Metal speciation determined using Donnan dialysis — a first for acid sulfate soils. • Divalent metals largely present as free cations or neutral sulfate complexes. • Trivalent metal species mostly present as negative or neutral in/organic complexes. • Stability constants of trivalent metal disulfate and NOM complexes need revisiting.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2016.01.024Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2016.01.024;
- PII
- S0048-9697(16)30024-9;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 547
- Journal Page Range
- p. 104-113
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48011107
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ACID SULFATES; ALKALINE EARTH METALS; ALUMINIUM 26; ALUMINIUM SULFATES; AUSTRALIA; CATIONS; CONCENTRATION RATIO; DIALYSIS; DRAINAGE; ECOLOGICAL CONCENTRATION; ENVIRONMENT; ENVIRONMENTAL MATERIALS; IRON; IRON 55; MEMBRANES; ORGANIC MATTER; PH VALUE; RARE EARTHS; SOILS; TOXICITY
- Descriptors DEC
- ALUMINIUM COMPOUNDS; ALUMINIUM ISOTOPES; AUSTRALASIA; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; CHARGED PARTICLES; DEVELOPED COUNTRIES; DIMENSIONLESS NUMBERS; ELECTRON CAPTURE RADIOISOTOPES; ELEMENTS; EVEN-ODD NUCLEI; INTERMEDIATE MASS NUCLEI; IONS; IRON ISOTOPES; ISOTOPES; LIGHT NUCLEI; MATERIALS; MATTER; METALS; NUCLEI; ODD-ODD NUCLEI; OXYGEN COMPOUNDS; RADIOISOTOPES; SECONDS LIVING RADIOISOTOPES; SEPARATION PROCESSES; SULFATES; SULFUR COMPOUNDS; TRANSITION ELEMENTS; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.