Abstract. This study aims to characterise the rainfall exceptionality and the meteorological context of the 20 February 2010 flash-floods in Madeira (Portugal). Daily and hourly precipitation records from the available rain-gauge station networks are evaluated in order to reconstitute the temporal evolution of the rainstorm, as its geographic incidence, contributing to understand the flash-flood dynamics and the type and spatial distribution of the associated impacts. The exceptionality of the rainstorm is further confirmed by the return period associated with the daily precipitation registered at the two long-term record stations, with 146.9 mm observed in the city of Funchal and 333.8 mm on the mountain top, corresponding to an estimated return period of approximately 290 yr and 90 yr, respectively. Furthermore, the synoptic associated situation responsible for the flash-floods is analysed using different sources of information, e.g., weather charts, reanalysis data, Meteosat images and radiosounding data, with the focus on two main issues: (1) the dynamical conditions that promoted such anomalous humidity availability over the Madeira region on 20 February 2010 and (2) the uplift mechanism that induced deep convection activity.

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Highlights• Self-produced H2 from electrodialytic treatment of environmental matrices collected • Collected H2 average purity (% mol/mol) of ≈ 98%• A fuel cell used to produce electricity from the self-produced H2 (~1 V)• Experimental self-generated energy promotes savings on electroremediation (≈ 7%) AbstractElectrodialytic technologies are clean-up processes based on the application of a low-level electrical current to produce electrolysis reactions and the consequent electrochemically-induced transport of contaminants. These treatments inherently produce electrolytic hydrogen, an energy carrier, at the cathode compartment, in addition to other cathode reactions. However, exploring this by-product for self-energy generation in electroremediation has never been researched. In this work we present the study of hydrogen production during the electrodialytic treatment of three different environmental matrices (briny water, effluent and mine tailings), at two current intensities (50 and 100 mA). In all cases, hydrogen gas was produced with purities between 73% to 98%, decreasing the electrical costs of the electrodialytic treatment up to ≈ 7%. A protonexchange membrane fuel cell was used to evaluate the possibility to generate electrical energy from the hydrogen production at the cathode, showing a stable output (~1 V) and demonstrating the proof of concept of the process.

Degradation technologies applied to emerging organic contaminants from human activities are one of the major water challenges in the contamination legacy. Triclosan is an emerging contaminant, commonly used as antibacterial agent in personal care products. Triclosan is stable, lipophilic and it is proved to have ecotoxicology effects in organics. This induces great concern since its elimination in wastewater treatment plants is not efficient and its by-products (e.g. methyl-triclosan, 2,4dichlorophenol or 2,4,6-trichlorophenol) are even more hazardous to several environmental compartments. This work provides understanding of two different electrochemical reactors for the degradation of triclosan and its derivative by-products in effluent. A batch reactor and a flow reactor (mimicking a secondary settling tank in a wastewater treatment plant) were tested with two different working anodes: Ti/MMO and Nb/BDD. The degradation efficiency and kinetics were evaluated to find the best combination of current density, electrodes and set-up design. For both reactors the best electrode combination was achieved with Ti/MMO as anode. The batch reactor at 7 mA/cm2 during 4 h attained degradation rates below the detection limit for triclosan and 2,4,6-trichlorophenol and, 94% and 43% for 2,4-dichlorophenol and methyl triclosan, respectively. The flow reactor obtained, in approximately 1 h, degradation efficiencies between 41% and 87% for the four contaminants under study. This study suggests an alternative technology for emergent organic contaminants degradation, since the combination of a low current density with the flow and matrix induced disturbance increases and speeds up the compounds' elimination in a real environmental matrix.

Emerging organic contaminants (EOC) are synthetic or naturally occurring chemicals that have the potential to enter the environment and cause known or suspected adverse ecological and human health effects. Despite not being commonly monitored, EOC are often detected in effluents and water bodies because of their inefficient removal in conventional wastewater treatment plants. There is a growing concern about the presence and impact of EOC as well as the need for reliable and effective water monitoring using sensors capable of detecting the target molecules in complex media. Due to their specificities, such as fast response times, low cost, portability and user-friendly operation, electronic tongue (e-tongue) systems present some advantages over the traditional analytical techniques (e.g., chromatographic systems) used for environmental monitoring. We reviewed e-tongue sensors, focusing on their ability for real-time environmental monitoring. A bibliometric evaluation was carried out, along with a study of the status of the existing e-tongue systems, how they worked, and their applications in different fields. The potential of e-tongue sensors to detect organic contaminants in aqueous environmental matrices is discussed, with a particular focus on EOC.

Triclosan (TCS) is a bacteriostatic used in household items that promotes antimicrobial resistance and endocrine disruption effects both to humans and biota, raising health concerns. In this sense, new devices for its continuous monitoring in complex matrices are needed. In this work, sensors, based on polyelectrolyte layer-by-layer (LbL) films prepared onto gold interdigitated electrodes (IDE), were studied. An electronic tongue array, composed of (polyethyleneimine (PEI)/polysodium 4-styrenesulfonate (PSS))5 and (poly(allylamine hydrochloride/graphene oxide)5 LbL films together with gold IDE without coating were used to detect TCS concentrations (10−15–10−5 M). Electrical impedance spectroscopy was used as means of transduction and the obtained data was analyzed by principal component analysis (PCA). The electronic tongue was tested in deionized water, mineral water and wastewater matrices showing its ability to (1) distinguish between TCS doped and non-doped solutions and (2) sort out the TCS range of concentrations. Regarding film stability, strong polyelectrolytes, as (PEI/PSS)n, presented more firmness and no significant desorption when immersed in wastewater. Finally, the PCA data of gold IDE and (PEI/PSS)5 sensors, for the mineral water and wastewater matrices, respectively, showed the ability to distinguish both matrices. A sensitivity value of 0.19 ± 0.02 per decade to TCS concentration and a resolution of 0.13 pM were found through the PCA second principal component.

Large forest fires have repeatedly affected Europe, in particular the Mediterranean countries. It is now crucial to continue the effort to feed the several layers of prediction models and understand how wildfire spreads in order to develop modern preventative and mitigation methods. The present study evaluates the performance of Sentinel 5-P TROPOMI for the monitoring of carbon monoxide (CO) and methane (CH4) during extreme fire events in Portugal, focusing on the Monchique (2018) and Vila de Rei/Mação (2019) wildfires, which devastated 27,154 ha and 9249 ha, respectively. The spatial distribution and trend of CO and CH4 prior to, during, and following the fire event were accessed and linked with in situ data in a qualitative and quantitative exploration. Large CO plumes were observed with CO columns exceeding 4.5 × 1018 and 6 × 1018 molecules/cm2 on 21 July 2019, and 7 August 2018, respectively. CO distribution profiles after consecutive digital processing steps showed the ability to follow CO fluctuations according to the fire spread. Furthermore, statistically significant differences were found between CO emissions inside and outside the burning area in both fire events. Finally, the CO2 estimated through CO column data presented an emission of 7.6 × 1019 molecules/cm2 for the uppermost emission day on 7 August 2018. Although CH4 monitoring is still unwavering to draw exact conclusions, the CO patterns during extreme fire events show promising and consistent data when compared with in situ data.

Triclosan, which is a bacteriostatic used in household items, has raised health concerns, because it might lead to antimicrobial resistance and endocrine disorders in organisms. The detection, identification, and monitoring of triclosan and its by-products (methyl triclosan, 2,4-Dichlorophenol and 2,4,6-Trichlorophenol) are a growing need in order to update current water treatments and enable the continuous supervision of the contamination plume. This work presents a customized electronic tongue prototype coupled to an electrochemical flow reactor, which aims to access the monitoring of triclosan and its derivative by-products in a real secondary effluent. An electronic tongue device, based on impedance measurements and polyethylenimine/poly(sodium 4-styrenesulfonate) layer-by-layer and TiO2, ZnO and TiO2/ZnO sputtering thin films, was developed and tested to track analyte degradation and allow for analyte detection and semi-quantification. A degradation pathway trend was observable by means of principal component analysis, being the sample separation, according to sampling time, explained by 77% the total variance in the first two components. A semi-quantitative electronic tongue was attained for triclosan and methyl-triclosan. For 2,4-Dichlorophenol and 2,4,6-Trichlorophenol, the best results were achieved with only a single sensor. Finally, working as multi-analyte quantification devices, the electronic tongues could provide information regarding the degradation kinetic and concentrations ranges in a dynamic removal treatment.