| 1. |
- Kendir Cakmak, Ece, et al.
(författare)
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How to develop a bio-based phosphorus mining strategy for eutrophic marine sediments: Unlocking native microbial processes for anaerobic phosphorus release
- 2024
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Ingår i: Chemosphere. - : Elsevier BV. - 0045-6535 .- 1879-1298. ; 358
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Tidskriftsartikel (refereegranskat)abstract
- This study examined the anaerobic release of phosphorus (P) from two different Baltic Sea sediments (B and F), focusing on the impact of initial concentration of externally introduced waste-derived volatile fatty acids (VFA) as the carbon source, temperature, pH, and mixing conditions. The first batch bioreactor set was operated to demonstrate the effect of VFA on anaerobic P release at different concentrations (1000–10000 mg/L as COD) at 20 °C. A notable P release of up to 15.85 mg/L PO4–P was observed for Sediment B at an initial carbon concentration of 10000 mg COD/L. However, VFA consumption in the bioreactors was minimal or no subsequent. The second batch bioreactor set was carried out to investigate the effect of temperature (20 °C-35 °C), pH (5.5, 7.0 and 8.5) and mixing conditions on P release by introducing lower initial carbon concentration (1000 mg COD/L) considering the potential risk for VFA accumulation in the bioreactors. Maximum P releases of 4.4 mg/L and 3.5 mg/L were for Sediment B and Sediment F, respectively. Two-way ANOVA tests revealed that the operation time and pH and their interactions were statistically significant (p < 0.05) for both sediments while the effect of mixing was not statistically significant. Most of the sulfate was reduced during batch bioreactor operation and Desulfomicobiaceae became dominant among other sulfate-reducing bacteria (SRB) possibly shows the importance of SRB in terms of anaerobic P release. This study gives an insight into future implementations of phosphorus mining from eutrophic environment under anaerobic conditions.
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| 2. |
- Liu, Yujie, 1995-, et al.
(författare)
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Voltammetric Ion-Selective Electrodes in Thin-Layer Samples : Absolute Detection of Ions Using Ultrathin Membranes
- 2024
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Ingår i: Analytical Chemistry. - : American Chemical Society (ACS). - 0003-2700 .- 1520-6882. ; 96:3, s. 1147-1155
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Tidskriftsartikel (refereegranskat)abstract
- Calibration-free sensors are generally understood as analytical tools with no need for calibration apart from the initial one (i.e., after its fabrication). However, an "ideal" and therefore "more restricted" definition of the concept considers that no calibration is necessary at all, with the sensor being capable of directly providing the analyte concentration in the sample. In the electroanalysis field, investigations have been directed to charge-based readouts (i.e., coulometry) that allow for concentration calculation via the Faraday Law: The sample volume must be precisely defined and the absoluteness of the electrochemical process in which the analyte is involved must be ensured (i.e., the analyte in the sample is similar to 100% converted/transported). Herein, we report on the realization of calibration-free coulometric ISEs based on ultrathin ion-selective membranes, which is demonstrated for the detection of potassium ions (K+). In essence, the K+ transfer at the membrane-sample interface is modulated by the oxidation state of the conducting polymer underlying the membrane. The accumulation/release of K+ to/from the membrane is an absolute process owing to the confinement of the sample to a thin-layer domain (thickness of <100 mu m). The capacity of the membrane expressed in charge is fixed to ca. 18 mu C, and this dictates the detection of micromolar levels of K+ present in ca. 5 mu L sample volume. The system is interrogated with cyclic voltammetry to obtain peaks related to the K+ transfer that can be treated charge-wise. The conceptual and technical innovative steps developed here made the calibration-free detection of K+ possible in artificial and real samples with acceptable accuracy (<10% difference compared with the results obtained from a current-based calibration and ion chromatography). The charge-based analysis does not depend on temperature and appeared to be repetitive, reproducible, and reversible in the concentration range from 1 to 37.5 mu M, with an average coulometry efficiency of 96%.
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| 3. |
- Molina Osorio, Andres, et al.
(författare)
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Evidence of transient potentials in ion-selective electrodes based on thin-layer ion-exchange membranes
- 2024
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Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686 .- 1873-3859. ; 484
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Tidskriftsartikel (refereegranskat)abstract
- Polymeric membranes with ion-exchange properties have found numerous applications in water treatment, dialysis, energy storage, chemical sensors, and bio-interfaces, among others. Notably, it is common to operate under non-equilibrium conditions while pursuing specific features (e.g., current generation) through an electron-to-ion mechanism. To maximize the final performance, it is crucial to understand the role of each interface within the system, which becomes complex when the device is tailored with several materials and films. This is the case for ion sensors based on thin membranes in backside contact with a redox active conducting polymer. Herein, we investigate such a system operating under a charge transfer mechanism, which features electroneutrality maintenance as the main driving force upon application of a linear sweep potential. This potential is modeled as being unequally distributed among the various system interfaces. Our results demonstrate and quantify the existence of a transient membrane potential at the membrane-electrolyte interface, owing to the implementation of a strategical measurement point on the buried membrane side and connected to a built-in electrometer for the exclusive acquisition of the potential difference at such an interface. The transient membrane potential was found to be <1 % of the total applied potential, meaning that the ion-transfer process at the electrolyte-membrane interface is less energetically costly that the electron transfer and doping processes occurring at the conducting polymer side. This small contribution can be potentiated by increasing the ion-exchange capacity of the membrane, which indirectly enlarges the system current and serves as a strategy for increasing the efficiency of the device.
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