The strawberry has a very short postharvest life due to its fast softening and decomposition. The goal of this research is to see how well a starch-silver nanoparticle (St-AgNPs) coating affects the physical, chemical, and microbiological qualities of strawberries during postharvest life. Additionally, the effect of washing with running water on silver concentration in coated strawberry fruit was studied by an inductively coupled plasma-optical emission spectrometer (ICP-OES). Furthermore, the shelf-life period was calculated in relation to the temperature of storage. Fourier transform infrared-attenuated total reflectance (FTIR-ATR), UV-Visible, and Transmission Electron Microscopic (TEM) were used to investigate the structure of starch-silver materials, the size and shape of AgNPs, respectively. The AgNPs were spherical, with an average size range of 12.7 nm. The coated samples had the lowest weight loss, decay, and microbial counts as compared to the uncoated sample. They had higher total acidity and anthocyanin contents as well. The washing process led to the almost complete removal of silver particles by rates ranging from 98.86 to 99.10%. Finally, the coating maintained strawberry qualities and lengthened their shelf-life from 2 to 6 days at room storage and from 8 to 16 days in cold storage.

The effect of microstructure and chemistry on the kinetics of passive layer growth and passivity breakdown of some Ti-based alloys, namely Ti-6Al-4V, Ti-6Al-7Nb and TC21 alloys, was studied. The rate of pitting corrosion was evaluated using cyclic polarization measurements. Chronoamperometry was applied to assess the passive layer growth kinetics and breakdown. Microstructure influence on the uniform corrosion rate of these alloys was also investigated employing dynamic electrochemical impedance spectroscopy (DEIS). Corrosion studies were performed in 0.9% NaCl solution at 37 °C, and the obtained results were compared with ultrapure Ti (99.99%). The different phases of the microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Chemical composition and chemistry of the corroded surfaces were studied using X-ray photoelectron spectroscopy (XPS) analysis. For all studied alloys, the microstructure consisted of α matrix, which was strengthened by β phase. The highest and the lowest values of the β phase’s volume fraction were recorded for TC21 and Ti-Al-Nb alloys, respectively. The susceptibility of the investigated alloys toward pitting corrosion was enhanced following the sequence: Ti-6Al-7Nb < Ti-6Al-4V << TC21. Ti-6Al-7Nb alloy recorded the lowest pitting corrosion resistance (R_pit) among studied alloys, approaching that of pure Ti. The obvious changes in the microstructure of these alloys, together with XPS findings, were adopted to interpret the pronounced variation in the corrosion behavior of these materials.

In this work, PdO/TiO₂ and Eu₂O₃/TiO₂ nanocomposites (NCs) were synthesized using a new facile, template‐free, and one‐step solvothermal approach and characterized by several instrumentation techniques. X‐ray photoelectron spectroscopy studies revealed the presence of oxidized form of the Pd and Eu nanoparticles within the NC materials (PdO and Eu₂O₃). The two catalysts exhibited remarkable activity for the hydrogen evaluation reaction (HER) in a strong alkaline solution (4.0 M NaOH) with PdO/TiO₂ catalyst being the best, which recorded an exchange current density (j_o) of 0.26 mA cm⁻² and a Tafel slope (β_c) of 125 mV dec⁻¹. Such parameters are not far from those recorded for a commercial Pt/C catalyst (0.71 mA cm⁻² and 120 mV dec⁻¹) performed here under the same operating conditions. Eu₂O₃/TiO₂ catalyst recorded j_o and β_c values of 0.05 mA cm⁻² and 135 mV dec⁻¹. The Tafel slopes 125 and 135 mV dec⁻¹ calculated on the PdO/TiO₂ and Eu₂O₃/TiO₂ catalysts suggest a HER kinetics controlled by the Volmer step. PdO/TiO₂ catalyzed the HER with a high turnover frequency of 2.3 H₂/s at 0.2 V versus the reversible hydrogen electrode, while Eu₂O₃/TiO₂ catalyst only measured a turnover frequency value of 1.25 H₂/s at the same overpotential. The two catalysts exhibited excellent stability and durability after 10 000 cycles and 72 hours of controlled potential electrolysis at a high cathodic overpotential, reflecting their practical applicability. Scanning electron microscope and X‐ray photoelectron spectroscopy examinations revealed that the morphology and chemistry of both catalysts were not altered as a result of the performed long‐term stability and durability tests.