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result(s) for
"Nagode, Klara"
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Multi-Isotope Characterization of Water in the Water Supply System of the City of Ljubljana, Slovenia
2022
Urban water supply systems (WSS) are complex and challenging to manage since the properties of water in the WSS change from source to the end user over time. However, understanding these changes requires a more profound knowledge of the WSS. This study describes the urban water cycle within the WSS of Ljubljana, Slovenia, where different water parameters such as temperature, electrical conductivity, total alkalinity, δ2H, δ18O, and δ13CDIC were monitored from September to November 2018. Altogether 108 samples were collected, including from the source (3) and at different levels of the WSS: wells (41), joint exits from water pumping stations (7), reservoirs (22), water treatment locations (2), drinking fountains (13), taps (19) and wastewater system (1). The data show that although the ranges of δ2H and δ18O values were small, each well is represented by a unique fingerprint when considering additional parameters. A statistically significant difference was observed between sampling months, and temperature and most parameters showed higher variability within the wells than across the WSS, suggesting a more unified WSS. Finally, based on δ13CDIC values, a distinction could be made between river/groundwater interactions within the WSS and between shallower and deeper wells and their distance from the river bank.
Journal Article
Daily Fluctuations in the Isotope and Elemental Composition of Tap Water in Ljubljana, Slovenia
2021
The isotope and elemental composition of tap water reflects its multiple distinct inputs and provides a link between infrastructure and the environment over a range of scales. For example, on a local scale, they can be helpful in understanding the geological, hydrogeological, and hydrological conditions and monitor the proper functioning of the water supply system (WSS). However, despite this, studies examining the urban water system remain limited. This study sought to address this knowledge gap by performing a 24 h multiparameter analysis of tap water extracted from a region where the mixing of groundwater between two recharge areas occurs. This work included measurements of temperature and electrical conductivity, as well as pH, δ2H, δ18O, d, δ13CDIC, and 87Sr/86Sr ratios and major and trace elements at hourly intervals over a 24 h period. Although the data show only slight variations in the measured parameters, four groups were distinguishable using visual grouping, and multivariate analysis (Spearman correlation coefficient analysis, hierarchical cluster analysis, and principal components analysis). Finally, changes in the mixing ratios of the two sources were estimated using a linear mixing model. The results confirm that the relative contribution from each source varied considerably over 24 h.
Journal Article
Effect of the Cooling Regime on the Mineralogy and Reactivity of Belite-Sulfoaluminate Clinkers
2020
This study investigated the influence of different cooling regimes on the microstructure and consequent reactivity of belite-sulfoaluminate clinkers. The cement clinkers were synthesized by incorporating secondary raw materials, such as titanogypsum and bottom ash, to the natural raw materials. Clinker phases were determined by Rietveld quantitative phase analysis, while the distribution morphology and the incorporation of substitute ions in the phases were characterized by scanning electron microscopy using energy-dispersive X-ray spectroscopy (SEM/EDS). Clinker reactivity was studied using isothermal calorimetry and was additionally investigated through compressive strength, which was determined for the cement prepared from the synthesized clinkers. X-ray diffraction analysis showed that, as well as the three main phases (belite, calcium sulfoaluminate, and ferrite), the clinkers contained additional minor phases (mayenite, gehlenite, arkanite, periclase, and perovskite), the ratios of which varied according to the cooling regime utilized. Microscopic observations indicated that the cooling regime also influenced the crystal size and morphology of the main phases, which consequently affected clinker reactivity. Furthermore, a smaller amount of substitute elements was incorporated in the main phases when cooling was slowed. Results showed that, in comparison to clinkers cooled at slower rates, air quenched clinkers reacted faster and exhibited a higher compressive strength at 7 days.
Journal Article