| 1. |
- Pedersen, Kristine B., et al.
(författare)
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Impacts of climate change on metal leaching and partitioning for submarine mine tailings disposal
- 2022
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Ingår i: Marine Pollution Bulletin. - : Elsevier Ltd. - 0025-326X .- 1879-3363. ; 184
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Tidskriftsartikel (refereegranskat)abstract
- At present, there are no standardised tests to assess metal leaching during submarine tailings discharge. In this study the influence of variables known to affect metal mobility and availability (dissolved organic carbon (DOC), pH, salinity, temperature, aerated/anoxic conditions) along with variables affected by the discharge conditions (flocculant concentration, suspension) were studied in bench-scale experiments. The leaching tests were developed based on the case of a copper mine by Repparfjorden, northern Norway, which is planned to re-open in 2022.The experiments, which had three week duration, revealed low (<6 %) leaching of metals. Multivariate analysis showed that all variables, apart from DOC, highly influenced leaching and partitioning of at least one metal (Ba, Cr, Cu, and/or Mn). The high quantity of the planned annual discharge of mine tailings to the fjord (1–2 million tonnes) warranted estimation of the leached quantity of metals. Multivariate models, using present-day conditions in the fjord, estimated leaching of up to 124 kg Ba, 154 kg Cu and 2400 kg Mn per year during discharge of tailings. Future changes in the fjord conditions caused by climate change (decreased pH, increased temperature) was predicted by the multivariate models to increase the leaching up to 55 %, by the year 2065.The bench-scale experiments demonstrated the importance of including relevant variables (such as pH, salinity, and temperature) for metal leaching and -partitioning in leaching tests. The results showed that metal leaching during discharge is expected and will increase in the future due to the changed conditions caused by the foreseen climate change, and thereby underline the importance of monitoring metal concentrations in water during operations to determine the fate of metals in the fjord.
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| 2. |
- Pedersen, Kristine B., et al.
(författare)
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Tailored Leaching Tests as a Tool for Environmental Management of Mine Tailings Disposal at Sea
- 2022
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Ingår i: Journal of Marine Science and Engineering. - : MDPI. - 2077-1312. ; 10:3
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Tidskriftsartikel (refereegranskat)abstract
- The expanding human activities in coastal areas increase the need for developing solutions to limit impacts on the marine environment. Sea disposal affects the marine environment, but despite the growing knowledge of potential impacts, there are still no standardized leaching tests for sea disposal. The aim of this study was to contribute to the development of leaching tests, exemplified using mine tailings, planned for submarine disposal in the Repparfjord, Norway. The mine tailings had elevated concentrations of Ba, Cr, Cu, Mn and Ni compared to background concentrations in the Repparfjord. Variables known to affect metal leaching in marine environments (DOC, pH, salinity, temperature, aerated/anoxic) were studied, as was the effect of flocculant (Magnafloc10), planned to be added prior to discharge. Stirred/non-stirred setups simulated the resuspension and disposal phases. Leaching of metals was below 2% in all experiments, with the highest rate observed for Cu and Mn. Multivariate analysis revealed a different variable importance for metals depending on their association with minerals. Higher leaching during resuspension than disposal, and lower leaching with the addition of Magnafloc10, especially for Cu and Mn, was observed. The leaching tests performed in this study are transferable to other materials for sea disposal.
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| 3. |
- Pour, Fatemeh Shouli, et al.
(författare)
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Comparison of 2- and 3-Compartment Electrodialytic Remediation Cells for Oil Polluted Soil from Northwest Russia
- 2021
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Ingår i: Environmental technology. - : Taylor & Francis. - 0959-3330 .- 1479-487X. ; 42:25, s. 3900-3906
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Tidskriftsartikel (refereegranskat)abstract
- Electrodialytic remediation is a method based on electrokinetics, in which an electric field of low intensity increases the availability of pollutants in solid waste materials. The electric field induces processes that mobilize and transport inorganic and organic pollutants. The transport of ions in the electrodialytic cell is controlled by employing ion-exchange membranes, allowing separation of the electrodes from the solids. In this study, using a two cell design, electrodialytic experiments were conducted to compare remediation of a heavily oil-polluted soil from Arkhangelsk, Russia. The 2-compartment cell has not previously been employed for electrodialytic removal of organic pollutants and was tested along with the traditional 3-compartment design. The influence of experimental variables (current density, remediation time, stirring and light) and settings on the two cell designs was investigated. The highest removal (77%) of total hydrocarbons (THC) was observed in the 3-compartment cell at high current density (0.68 mA/cm2), longer remediation time (28 days), stirring and exposure to daylight. High current density and stirring increased the removal efficiencies in both cell designs. Within the studied experimental domain, the removal efficiencies in the 3-compartment cell (10-77%) were however, higher than those observed in the 2-compartment cell (0-38%).
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| 4. |
- Ren, Zhongfei, et al.
(författare)
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Combination of adsorption/desorption and photocatalytic reduction processes for PFOA removal from water by using an aminated biosorbent and a UV/sulfite system
- 2023
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Ingår i: Environmental Research. - : Elsevier. - 0013-9351 .- 1096-0953. ; 228
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Tidskriftsartikel (refereegranskat)abstract
- Per- and polyfluoroalkyl substances (PFAS) are stable organic chemicals, which have been used globally since the 1940s and have caused PFAS contamination around the world. This study explores perfluorooctanoic acid (PFOA) enrichment and destruction by a combined method of sorption/desorption and photocatalytic reduction. A novel biosorbent (PG-PB) was developed from raw pine bark by grafting amine groups and quaternary ammonium groups onto the surface of bark particles. The results of PFOA adsorption at low concentration suggest that PG-PB has excellent removal efficiency (94.8%–99.1%, PG-PB dosage: 0.4 g/L) to PFOA in the concentration range of 10 μg/L to 2 mg/L. The PG-PB exhibited high adsorption efficiency regarding PFOA, being 456.0 mg/g at pH 3.3 and 258.0 mg/g at pH 7 with an initial concentration of 200 mg/L. The groundwater treatment reduced the total concentration of 28 PFAS from 18 000 ng/L to 9900 ng/L with 0.8 g/L of PG-PB. Desorption experiments examined 18 types of desorption solutions, and the results showed that 0.05% NaOH and a mixture of 0.05% NaOH + 20% methanol were efficient for PFOA desorption from the spent PG-PB. More than 70% (>70 mg/L in 50 mL) and 85% (>85 mg/L in 50 mL) of PFOA were recovered from the first and second desorption processes, respectively. Since high pH promotes PFOA degradation, the desorption eluents with NaOH were directly treated with a UV/sulfite system without further adjustment. The final PFOA degradation and defluorination efficiency in the desorption eluents with 0.05% NaOH + 20% methanol reached 100% and 83.1% after 24 h reaction. This study proved that the combination of adsorption/desorption and a UV/sulfite system for PFAS removal is a feasible solution for environmental remediation.
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| 5. |
- Uwayezu, Jean Noel, et al.
(författare)
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Combination of separation and degradation methods after PFAS soil washing
- 2023
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Ingår i: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 907
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Tidskriftsartikel (refereegranskat)abstract
- The current study evaluated a three-stage treatment to remediate PFAS-contaminated soil. The treatment consisted of soil washing, foam fractionation (FF), and electrochemical oxidation (EO). The possibility of replacing the third stage, i.e., EO, with an adsorption process was also assessed. The contamination in the studied soils was dominated by perfluorooctane sulfonate (PFOS), with a concentration of 760 and 19 μg kg−1 in soil I and in soil II, accounting for 97 % and 70 % of all detected per-and polyfluoroalkyl substances (PFAS). Before applying a pilot treatment of soil, soil washing was performed on a laboratory scale, to evaluate the effect of soil particle size, initial pH and a liquid-to-soil ratio (L/S) on the leachability of PFAS. A pilot washing system generated soil leachate that was subsequently treated using FF and EO (or adsorption) and then reused for soil washing. The results indicated that the leaching of PFAS occurred easier in 0.063–1 mm particles than in the soil particles having a size below 0.063 mm. Both alkaline conditions and a continual replacement of the leaching solution increased the leachability of PFAS. The analysis using one-way ANOVA showed no statistical difference in means of PFOS washed out in laboratory and pilot scales. This allowed estimating twenty washing cycles using 120 L water to reach 95 % PFOS removal in 60 kg soil. The aeration process removed 95–99 % PFOS in every washing cycle. The EO and adsorption processes achieved similar results removing up to 97 % PFOS in concentrated soil leachate. The current study demonstrated a multi-stage treatment as an effective and cost-efficient method to permanently clean up PFAS-contaminated soil.
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| 6. |
- Uwayezu, Jean Noel, et al.
(författare)
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Electrochemical degradation of per- and poly-fluoroalkyl substances using boron-doped diamond electrodes
- 2021
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Ingår i: Journal of Environmental Management. - : Elsevier. - 0301-4797 .- 1095-8630. ; 290
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical degradation using boron-doped diamond (BDD) electrodes has been proven to be a promising technique for the treatment of water contaminated with per- and poly-fluoroalkyl substances (PFAS). Various studies have demonstrated that the extent of PFAS degradation is influenced by the composition of samples and electrochemical conditions. This study evaluated the significance of several factors, such as the current density, initial concentration of PFAS, concentration of electrolyte, treatment time, and their interactions on the degradation of PFAS. A 24 factorial design was applied to determine the effects of the investigated factors on the degradation of perfluorooctanoic acid (PFOA) and generation of fluoride in spiked water. The best-performing conditions were then applied to the degradation of PFAS in wastewater samples. The results revealed that current density and time were the most important factors for PFOA degradation. In contrast, a high initial concentration of electrolyte had no significant impact on the degradation of PFOA, whereas it decreased the generation of F−. The experimental design model indicated that the treatment of spiked water under a current density higher than 14 mA cm−2 for 3–4 h could degrade PFOA with an efficiency of up to 100% and generate an F− fraction of approximately 40–50%. The observed high PFOA degradation and a low concentration of PFAS degradation products indicated that the mineralization of PFOA was effective. Under the obtained best conditions, the degradation of PFOA in wastewater samples was 44–70%. The degradation efficiency for other PFAS in these samples was 65–80% for perfluorooctane sulfonic acid (PFOS) and 42–52% for 6–2 fluorotelomer sulfonate (6-2 FTSA). The presence of high total organic carbon (TOC) and chloride contents was found to be an important factor affecting the efficiency of PFAS electrochemical degradation in wastewater samples. The current study indicates that the tested method can effectively degrade PFAS in both water and wastewater and suggests that increasing the treatment time is needed to account for the presence of other oxidizable matrices.
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| 7. |
- Våbenø, Jon, et al.
(författare)
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Conformational restrictions in ligand binding to the human intestinal di-/tripeptide transporter: implications for design of hPEPT1 targeted prodrugs.
- 2005
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Ingår i: Bioorganic & medicinal chemistry. - : Elsevier BV. - 0968-0896. ; 13:6, s. 1977-88
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Tidskriftsartikel (refereegranskat)abstract
- The aim of the present study was to develop a computational method aiding the design of dipeptidomimetic pro-moieties targeting the human intestinal di-/tripeptide transporter hPEPT1. First, the conformation in which substrates bind to hPEPT1 (the bioactive conformation) was identified by conformational analysis and 2D dihedral driving analysis of 15 hPEPT1 substrates, which suggested that psi(1) approximately 165 degrees , omega(1) approximately 180 degrees , and phi(2) approximately 280 degrees were descriptive of the bioactive conformation. Subsequently, the conformational energy required to change the peptide backbone conformation (DeltaE(bbone)) from the global energy minimum conformation to the identified bioactive conformation was calculated for 20 hPEPT1 targeted model prodrugs with known K(i) values. Quantitatively, an inverse linear relationship (r(2)=0.81, q(2)=0.80) was obtained between DeltaE(bbone) and log1/K(i), showing that DeltaE(bbone) contributes significantly to the experimentally observed affinity for hPEPT1 ligands. Qualitatively, the results revealed that compounds classified as high affinity ligands (K(i)<0.5 mM) all have a calculated DeltaE(bbone)<1 kcal/mol, whereas medium and low-affinity compounds (0.5 mM
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| 8. |
- Våbenø, Jon, et al.
(författare)
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Dipeptidomimetic ketomethylene isosteres as pro-moieties for drug transport via the human intestinal di-/tripeptide transporter hPEPT1: design, synthesis, stability, and biological investigations.
- 2004
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Ingår i: Journal of medicinal chemistry. - : American Chemical Society (ACS). - 0022-2623 .- 1520-4804. ; 47:19, s. 4755-65
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Tidskriftsartikel (refereegranskat)abstract
- Five dipeptidomimetic-based model prodrugs containing ketomethylene amide bond replacements were synthesized from readily available alpha,beta-unsaturated gamma-ketoesters. The model drug (BnOH) was attached to the C-terminus or to one of the side chain positions of the dipeptidomimetic. The stability, the affinity for the di-/tripeptide transporter hPEPT1, and the transepithelial transport properties of the model prodrugs were investigated. ValPsi[COCH(2)]Asp(OBn) was the compound with highest chemical stability in buffers at pH 6.0 and 7.4, with half-lives of 190 and 43 h, respectively. All five compounds showed high affinity for hPEPT1 (K(i) values < 1 mM), and PhePsi[COCH(2)]Asp(OBn) and ValPsi[COCH(2)]Asp(OBn) had the highest affinities with K(i) values of 68 and 19 microM, respectively. An hPEPT1-mediated transport component was demonstrated for the transepithelial transport of three compounds, a finding that was corroborated by hPEPT1-mediated intracellular uptake. The results indicate that the stabilized Phe-Asp and Val-Asp derivatives are promising pro-moieties in a prodrug approach targeting hPEPT1.
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| 9. |
- Våbenø, Jon, et al.
(författare)
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Phe-Gly dipeptidomimetics designed for the di-/tripeptide transporters PEPT1 and PEPT2: synthesis and biological investigations.
- 2004
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Ingår i: Journal of medicinal chemistry. - : American Chemical Society (ACS). - 0022-2623 .- 1520-4804. ; 47:4, s. 1060-9
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Tidskriftsartikel (refereegranskat)abstract
- A series of five Phe-Gly dipeptidomimetics containing different amide bond replacements have been synthesized in a facile way from the readily available unsaturated ketoester 1, and their affinities for the di-/tripeptide transporters hPEPT1 (Caco-2 cells) and rPEPT2 (SKPT cells) were tested. The compounds contained the amide bond isosteres ketomethylene (2a), (R)- and (S)-hydroxyethylidene (3a and 4a), and (R)- and (S)-hydroxyethylene (5a and 6a) to provide information on the conformational and stereochemical requirements for hPEPT1 and rPEPT2 affinity. The affinity studies showed that for rPEPT2 there is no significant difference in affinity between the ketomethylene isostere 2a and the natural substrate Phe-Gly (K(i) values of 18.8 and 14.6 microM, respectively). Also the affinities for hPEPT1 are in the same range (K(i) values of 0.40 and 0.20 mM, respectively). This corroborates earlier findings that the amide bond as such is not essential for binding to PEPTX, but the results also reveal possible differences in the binding of ketomethylene isosteres to hPEPT1 and rPEPT2. The trans-hydroxyethylidene and hydroxyethylene isosteres proved to be poor substrates for PEPTX. These results provide new information about the importance of flexibility and of the stereochemistry at the C(4)-position for this class of compounds. Furthermore, the intracellular uptake of 2a-4a in Caco-2 cells was investigated, showing a 3-fold reduction of the uptake of 2a in the presence of the competetive inhibitor Gly-Pro, indicating contribution from an active transport component. No active uptake of 3a and 4a was observed. Transepithelial transport studies also indicated active transport of 2a across Caco-2 monolayers.
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