The corrosion within photovoltaic (PV) systems has become a critical challenge to address, significantly affecting the efficiency of solar-to-electric energy conversion, longevity, and economic viability. This review provides a comprehensive analysis of electrochemical corrosion mechanisms affecting solar panels and environmental factors that accelerate material degradation, including (i) humidity, (ii) temperature fluctuations, (iii) ultraviolet radiation, and (iv) exposure to saline environments, leading to reduced performance and premature failures. The role of encapsulation materials, solder interconnections, and conductive coatings in the corrosion formation process is examined. Various electrochemical and surface characterization techniques provide insights into material degradation and corrosion mechanisms within panels. Essential parameters are presented and discussed, including materials used, geographical location of analysis, environmental considerations, and corrosion characterization techniques, to enhance the assessment of solar panels. This review emphasizes the importance of corrosion management for sustainable PV systems and proposes future research directions for developing more durable materials and advanced coatings.

In this work a Metal–Organic Framework (MOF) was prepared using a solvothermal method, taking as precursors 1. 2-di-(4-pyridyl)-ethylene, 1.2.4.5-benzenetetracarboxylic acid and Co(No₃)₂-6H₂O. This MOF was called UV-11 and was evaluated using microscopic, spectroscopic and electrochemical techniques. According to the obtained results, the melting point of the compound is located in a higher interval than its precursors. Stereoscopic microscopy analysis shows the presence of pink crystals in the form of needles. MEB technique displays a laminar morphology as well as crystals with approximate sizes (36 mm wide and 150 mm long). EDS analysis corroborated the presence of precursor elements such as cobalt, carbon and oxygen. Furthermore, the XRD technique shows the cobalt-related phases in the sample, which is cobalt bis (pyridine-6-carboxylic-2-carboxylate). A modified carbon paste electrode was prepared using MOF UV-11 and by cyclic voltammetry electrochemical technique, semi-reversible redox processes are identified, as well as thermodynamic and kinetic parameters were obtained with the Laviron equation, and electrochemical performance properties from the cyclic voltammetry experimental data.

The growing demand for chicken meat products has increased the amount of wastewater associated with their production; their treatment has increased the generation of sludge and oils trapped in the trap process treatment. This work presents a process for the valorization of this residual oil recovered through the production of biodiesel. An oil degumming process was applied, and the quality of the treated oil was evaluated. This was transesterified with alkaline conditions and a homogeneous catalyst (KOH); a 3^k experimental design was applied with two factors: the temperature at 50, 60, and 70 °C and the molar ratios of 5, 6, and 7 moles of methanol per mole of recovered chicken oil. The biodiesel quality parameters were evaluated based on the ASTM standard. The process achieved a yield of 90.2%. The biodiesel obtained met all the quality parameters; however, only the process conditions with a molar ratio of 6:1 and a temperature of 60 °C achieved a kinematic viscosity of 5.64 ± 0.15 mm² s⁻¹, meeting the limits of 1.9–6.0 mm² s⁻¹ of the ASTM regulation. The fluidity of this biodiesel in mixtures of 25, 50, and 75% v with petroleum diesel was also evaluated, and a better adjustment of the Bingham mixing rule model and rheological analysis revealed that the mixtures did not lose their Newtonian behavior. This allows for the application of this biodiesel in internal combustion engines, achieving the valorization of residual oil.