The incorporation of a recycled concrete aggregate (RCA) as a replacement of natural aggregates (NA) in road construction has been the subject of recent research. This tendency promotes sustainability, but its use depends mainly on the final product’s properties, such as chemical stability. This study evaluates the physical and chemical properties of RCAs from two different sources in comparison with the performance of NA. One RCA was obtained from the demolition of a building (recycled concrete aggregate of a building—RCAB) and another RCA from the rehabilitation of a Portland cement concrete pavement (recycled concrete aggregate from a pavement—RCAP). Characterization techniques such as X-ray fluorescence (XRF), X-ray diffraction (XRD), UV spectroscopy, and atomic absorption spectrometry were used to evaluate the RCAs’ coarse fractions for chemical potential effects on asphalt mixtures. NA was replaced with RCA at 15%, 30%, and 45% for each size of the coarse fractions (retained 19.0, 12.5, 9.5, and 4.75 sieves in mm). The mineralogical characterization results indicated the presence of quartz (SiO₂) and calcite (CaCO₃) as the most significant constituents of the aggregates. XFR showed that RCAs have lower levels of CaO and Al₂O₃ concerning NA. Potential reactions in asphalt mixtures by nitration, sulfonation, amination of organic compounds, and reactions by alkaline activation in the aggregates were discarded due to the minimum concentration of components such as NO₂, (–SO₃H), (–SO₂Cl), and (Na) in the aggregates. Finally, this research concludes that studied RCAs might be used as replacements of coarse aggregate in asphalt mixtures since chemical properties do not affect the overall chemical stability of the asphalt mixture.

This study evaluates the potential of Chlorella vulgaris sp. extracts as eco-friendly corrosion inhibitors for API 5L 42 Steel in a 1M HCl acidic environment, offering sustainable alternatives for industrial applications. Two corrosion inhibitors were obtained through solvent extraction methods: M1 (methanol) and M2 (methanol/chloroform). The extracts were characterized using infrared spectroscopy, the analysis revealed hydroxyl, methyl and vinyl groups as the most representative. The effect of corrosion inhibition was study by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. The results show significant reductions in corrosion current density and increases in charge transfer resistance, with M2 achieving the highest protection efficiency of 91.20 % and a charge transfer resistance of 501.80 Ω at a 120 ppm concentration, while M1 reached 88.22 % efficiency with a charge transfer resistance of 102.30 Ω. Uv–Vis measurements were performed to determine the electronic transitions of the metal-inhibitor system for each of the extracts. ANOVA highlighted the significant influence of biomass concentration on corrosion resistance. The adsorption of M1 and M2 extracts on the carbon steel surface obeyed the Langmuir isotherm and Gibbs free energy calculations indicated a physisorption mechanism for both extracts. Surface morphology analysis by Scanning electron microscope (SEM) revealed less pitting and reduced surface roughness as inhibitor concentration increased. These findings underscore the potential of Chlorella vulgaris extracts, particularly M2 at 120 ppm, as effective and sustainable corrosion inhibitors for steel in acidic environments.

Industrial wastewater from petrochemical processes is an essential source of the synthetic phenolic phosphite antioxidant (Irgafos P-168), which negatively affects the environment. For the determination and analysis of Irgafos P-168, DSC, HPLC-MS, and FTIR methodologies were used. Solid phase extraction (SPE) proved to be the best technique for extracting Irgafos from wastewater. HPLC-MS and SPE determined the repeatability, reproducibility, and linearity of the method and the SPE of the standards and samples. The relative standard deviations, errors, and correlation coefficients for the repeatability and reproducibility of the calibration curves were less than 4.4% and 4.2% and greater than 0.99955, respectively. The analysis of variance (ANOVA), using the Fisher method with confidence in 95% of the data, did not reveal significant differences between the mentioned parameters. The removal of the antioxidant from the wastewater by SPE showed recovery percentages higher than 91.03%, and the chemical characterization of this antioxidant by FTIR spectroscopy, DSC, TGA, and MS showed it to be structurally the same as the Irgafos P-168 molecule. The recovered Irgafos was added to the polypropylene matrix, significantly improving its oxidation times. An OIT analysis, performed using DSC, showed that the recovered Irgafos-blended polypropylene (PP) demonstrated oxidative degradation at 8 min. With the addition of the Irgafos, the oxidation time was 13 min. This increases the polypropylene’s useful life and minimizes the environmental impact of the wastewater.

Magnesium alloys have been extensively studied as degradable biomaterials for clinical applications due to their biocompatibility and mechanical properties. However, their poor corrosion resistance can lead to issues such as osteolysis and the release of gaseous hydrogen. This study investigated the influence of the activation time of magnesium surfaces in a sodium hydroxide (NaOH) solution on the concentration of active hydroxyl groups and corrosion resistance. The results indicated that immersion time significantly influences the formation of a corrosion-resistant film and the distribution of surface hydroxyl groups. Specifically, specimens treated for 7.5 h exhibited the highest concentration of hydroxyl groups and the most uniform oxide film distribution. Electrochemical tests demonstrated capacitive behavior and passive surface formation for all evaluated times, with the 7.5-h immersion in NaOH yielding superior corrosion resistance, lower current density, and a more efficient and thicker protective film. SEM and EDS analyses confirmed increased formation of Mg(OH)₂ for samples treated for 5 and 7.5 h, while a 10-h treatment resulted in a brittle, porous layer prone to degradation. Statistical analysis using ANOVA and Fisher's LSD test corroborated these findings. The optimal 7.5-h alkali treatment enhanced magnesium's corrosion resistance and surface properties, making it a promising candidate for orthopedic implants. However, further studies are necessary to assess biocompatibility and physiological responses before clinical implementation.

This study presents a comprehensive framework for designing eco-friendly corrosion inhibitors from Spirulina platensis. Biomass production was optimized for yield and quality, followed by selective extraction using ultrasound-assisted and orbital-shaking methods applied to wet and dry biomass. Extracts were chemically characterized and tested via potentiodynamic polarization and electrochemical impedance spectroscopy. The dry-biomass ultrasound-assisted extract (D1) showed the highest inhibition efficiency (90%–92%) and achieved a corrosion rate of ∼1.41 mm year−1 at 1,000 ppm, maintaining ∼77% efficiency over 72 h. Statistical analysis confirmed that the presence of Spirulina extracts significantly improved corrosion resistance, with extract type, concentration, and immersion time identified as key variables. This work validates the potential of microalgal formulations as effective green inhibitors and offers a reproducible methodology for the long-term evaluation of bio-based corrosion protection strategies relevant to sustainable materials engineering.

**Abstract Body** Corrosion in acidic environments, common in the hydrocarbon industry, poses serious economic and environmental challenges. Conv | ORAL