Cyanobacteria, particularly thermophilic strains, represent an important potential source of EPSs, harboring structural complexity that predicts diverse and specific bioactive potential. The thermophilic cyanobacteria Gloeocapsa gelatinosa, isolated from a natural hot source in Ain Echfa (Tunisia), was cultivated in a cylindrical reactor, and the production of biomass and EPSs was investigated. Results revealed that the strain is amongst the most efficient EPSs producers (0.89 g L⁻¹) and that EPSs production was not correlated with the growth phase. EPSs were sulfated heteropolysaccharides containing carbohydrates (70%) based on nine different monosaccharides, mainly mannose (22%), and with the presence of two uronic acids. EPSs were formed by two polymers moieties with a molecular weight of 598.3 ± 7.2 and 67.2 ± 4.4 kDa. They are thermostable in temperatures exceeding 100 °C and have an anionic nature (zeta potential of −40 ± 2 mV). Atomic force microscopy showed that EPSs formed multimodal lumps with 88 nm maximum height. EPSs presented high water holding capacity (70.29 ± 2.36%) and solubility index (97.43 ± 1.24%), and a strong bivalent metal sorption capacity especially for Cu²⁺ (91.20 ± 1.25%) and Fe²⁺ (75.51 ± 0.71%). The antioxidant activity of G. gelatinosa EPSs was investigated using four methods: the β-carotene-bleaching activity, DPPH assays, iron-reducing activity, and metal-chelating activity. EPS has shown high potential as free radicals’ scavenger, with an IC₅₀ on DPPH (0.2 g L⁻¹) three-fold lower than ascorbic acid (0.6 g L ⁻¹) and as a metal chelating activity (IC₅₀ = 0.4 g L⁻¹) significantly lower than EDTA. The obtained results allow further exploration of the thermophilic G. gelatinosa for several biotechnological and industrial applications.

The present study aimed to develop and characterize new heavy metal sensors functionalized by extracellular polymeric substances (EPSs) isolated from a Tunisian thermophilic microalga strain Graesiella sp. The elaborated sensor showed a highly homogeneous character and revealed a microstructural lamellar arrangement, high crystalline nature, and several functional groups. Electrochemical impedance spectroscopy (EIS) and acoustic wave sensing were used as sensing techniques to explore the ability of microalgae-EPS-functionalized sensors to detect cadmium and mercury as heavy metals. For impedimetric measurements, a two-dipole circuit was adopted and showed good-fitted results with a low total error. The acoustic sensor platforms showed good compatibility with EPS in adjacent water. For both EPS-functionalized sensors, metal ions (Cd²⁺, Hg²⁺) were successfully detected in the concentration range from 10⁻¹⁰ M to 10⁻⁴ M. Impedimetric sensor was more sensitive to Cd²⁺ at low concentrations before saturation at 10⁻⁷ M, while the acoustic sensor exhibited more sensitivity to Hg²⁺ over the full range. The results highlight a new potential alternative to use microalgae EPSs as a sensitive coating material for the detection of heavy metals. However, its use in a real liquid medium requires further investigation of its selectivity in the presence of other compounds.

The findings presented in this paper demonstrate the effectiveness of a new method for analyzing the electroacoustic response of Love wave acoustic sensors to assess the mechanical and dielectric properties of liquid samples. The Love wave sensor was modified by applying a solution of extracellular polymeric substances (EPS) using a self-assembled monolayer technique. The mechanical parameters of the EPS-modified sensors, such as insertion losses and phase, were found to be slightly affected by turbidity, even at high levels, while allowing a chemical detection by mass loading effect. On the other hand, the sensor electrical parameters such as capacitance and resistance showed a positive correlation with increasing turbidity. The experimental chemical detection also showed changes in the mechanical parameters (wave amplitude and phase) of the EPS-modified sensor in response to different concentrations of mercury (Hg²⁺), ranging from 10E−10 M to 10E−2 M. Furthermore, the study utilized response surface methodology to analyze the nonlinear behavior of the sensor under combined factors of turbidity and mercury concentration. Through this approach, a mathematical model was developed to simulate measurements of capacitance and resistance, considering both turbidity and mercury concentration as variables. This study demonstrated that integrating an EPS-Love wave sensor enables the simultaneous detection of mercury concentration and assessment of water turbidity via changes in capacitance and resistance, underscoring the sensor’s promise for high-performance environmental monitoring.

Electrolyte degradation and trace water contamination critically affect the lifetime and safety of lithium-ion batteries. In organic-based electrolytes such as acetonitrile (MeCN), even small amounts of water can trigger ${\mathrm{PF}}_6^{-}$ hydrolysis, producing HF, POF₃, and related species that contribute to electrolyte ageing and alter interfacial reactions. This study explores the electrochemical signatures of ageing and moisture contamination in Bu₄NPF₆- and LiPF₆-based MeCN electrolytes through a systematic cyclic voltammetry protocol. Platinum electrodes with different surface morphologies—flat, Nafion-coated, and nanostructured—were compared to assess their sensitivity to water-induced degradation. Cathodic Faradaic currents appearing around −0.7 to −1.0 V vs. Ag/AgCl were attributed to the protonic species generated by ${\mathrm{PF}}_6^{-}$-induced hydrolysis. The presence of LiPF₆, commonly used in battery electrolytes, further increases the concentration of anions responsible for the protonic species, therefore contributing to the acceleration of the electrolyte degradation. Experiments using a Nafion proton-conductive membrane assess the protonic origin of these peaks. Meanwhile, nanostructured platinum exhibits approximately four times higher current responses and enhanced sensitivity to water additions, reflecting the influence of surface roughness and active area. Overall, the findings indicate that electrode morphology significantly influences the detectability of ageing- and water-driven reactions, supporting the potential of nanostructured Pt as a diagnostic material for in situ monitoring.