José Alberto Andraca-Adame

Self-healing materials have garnered significant interest in the industry due to their potential for various applications, particularly in the automotive sector, including exterior parts and interior components

Tomatoes are among the most widely consumed and economically significant fruits in the world. However, the extensive use of pesticides in their cultivation has led to the contamination of the peels, posing potential health risks to consumers. As one of the top global producers, consumers, and exporters of tomatoes, Mexico requires rapid, non-destructive, and real-time methods for pesticide monitoring. In this study, a detailed characterization of six pesticides using Raman and Fourier Transform Infrared (FT-IR) spectroscopies was carried out to identify their characteristic vibrational modes. The pesticides examined included different chemical classes commonly used in tomato cultivation: organophosphorus (dichlorvos and methamidophos), pyrethroids (lambda-cyhalothrin and cypermethrin), and carbamates (methomyl and benomyl). Tomato peel samples were examined both before and after pesticide application. Prior to treatment, the peel exhibited a well-organized polygonal structure and showed the presence of carotenoid compounds. After pesticide application, no visible structural damage was observed; however, distinct vibrational bands enabled the detection of each pesticide. Organophosphorus pesticides could be identified through vibrational bands associated with P-O and C-S bonds. Pyrethroid detection was facilitated by benzene ring breathing modes and C=C stretching vibrations, while carbamates were identified through C-N stretching contributions. Phytotoxicity testing in the presence of pesticides indicates no significant damage during the germination of tomatoes.

The extensive use of pesticides has led to the contamination of natural resources, sometimes causing significant and irreversible damage to the environment and human health. Even though the use of many pesticides is banned, these compounds are still being found in rivers worldwide. In this review, 205 documents have been selected to provide an overview of pesticide contamination in rivers over the last 10 years (2014–2024). After these documents were examined, information of 47 river systems was organized according to the types of pesticides most frequently detected, including organochloride, organophosphorus, and pyrethroid compounds. A total of 156 compounds were classified, showing that 46% of these rivers contain organochlorine compounds, while 40% exhibit organophosphorus pesticides. Aldrin, hexachlorocyclohexane, and endosulfan were the predominant organochlorine pesticides with concentration values between 0.4 and 37 × 10⁵ ng L⁻¹. Chlorpyrifos, malathion, and diazinon were the main organophosphorus pesticides with concentrations between 1 and 11 × 10⁵ ng L⁻¹. Comparing the pesticide concentrations with standard guidelines, we found that the Ganga River in India (90 ng L⁻¹), the Owan and Okura Rivers in Nigeria (210 and 9 × 10³ ng L⁻¹), and the Dong Nai River in Vietnam (68 ng L⁻¹) exceed the permissible levels of aldrin (30 ng L⁻¹).

In recent years, advances in materials engineering based on adaptive electronics have found a new paradigm to optimize drawbacks in signal processing. A two-layer MnO/ZnO:Zn heterostructure envisioned for frequency adaptive electronic signal processing is synthesized by sputtering, where the use of internal states allows reconfigurability to obtain new operating modes at different frequency input signals. X-ray diffraction (XRD) analysis is performed on each layer, revealing a cubic structure for MnO and a hexagonal structure for ZnO:Zn with preferential growth in [111] and [002] directions, respectively. Scanning electron microscope (SEM) micrographs show that the surface of both materials is homogeneous and smooth. The thickness for each layer is determined to be approximately 106.3 nm for MnO, 119.3 nm for ZnO:Zn and 224.1 nm for the MnO/ZnO:Zn structure. An electrical characterisation with an oscilloscope and signal generator was carried out to obtain the time-response signals and current-voltage (I–V) curves, where no degradation is detected when changing frequencies within the range of 100 Hz to 1 MHz. An equivalent circuit is proposed to explain the effects in the interface. Measurements of switching speeds from high resistance state (HRS) to low resistance state (LRS) at approximately 17 ns, highlight the device’s rapid adaptability, and an estimated switching ratio of approximately 2 × 10⁴ indicates its efficiency as a memristive component. Finally, the MnO/ZnO:Zn heterojunction delivers states that are stable, repeatable, and reproducible, demonstrating how the interaction of the materials can be utilised in adaptive device applications by applying frequencies and internal states to create new and innovative design schematics, thus reducing the number of components/connections in a system for future sustainable electronics.

In the last years, advances in materials engineering based on adaptive electronics have found a new paradigm to optimize drawbacks in signal processing. A two-layer MnO/ZnO:Zn heterostructure envisioned for frequency adaptive electronic signal processing is synthesized by sputtering where the use of internal states allows reconfigurability to obtain new operating modes at different frequency input signals. An X-Ray Diffraction (XRD) is performed on each layer, MnO:Mn had a cubic and ZnO:Zn a hexagonal structure with preferential growth in [111] and [002] directions respectively. It is determined that the coupling in this heterojunction is compatible with a mismatch less 1 % due texture in each layer which implies a low number of defects. An electrical characterisation with an oscilloscope and signal generator was carried out to obtain the time-response signals and current-voltage (I-V) curves where no degradation is detected when changing from a range of frequencies (100 Hz – 1 MHz). An equivalent circuit is proposed to explain the effects in the interface. Finally, the MnO/ZnO:Zn heterojunction delivers states that are stable, repeatable, and reproducible and it demonstrates how the interaction of the materials can be used in adaptive device applications applying frequencies and internal states as to create new and innovative design schematics, reducing the numbers of components/connections in a system for future sustainable electronics.

Las reacciones fotocatalíticas son una propuesta amigable con el medio ambiente para la degradación de compuestos tóxicos en aguas contaminadas. En este trabajo, catalizadores de cobre soportados en TiO2-P25 para la fotodegradación catalítica de pesticidas en agua fueron sintetizados. Para ello, tres diferentes tipos de pesticidas altamente tóxicos; diclorvos, cipermetrina y carbofurán fueron caracterizados por espectroscopía Raman. Los fotocatalizadores de CuO soportados en TiO2-P25 sintetizados fueron caracterizados fisicoquímicamente por espectroscopías de reflectancia difusa UV-vis y Raman después de cada una de las etapas de su preparación, es decir, después del secado (120 °C, 4 h) y después de la calcinación (300 °C, 4 h). Los resultados muestran que los catalizadores sintetizados pueden ser una alternativa viable para la fotodegradación de pesticidas en agua.

In this study, composite material films of pyridine-based polymer and metal oxides (ZnO and TiO₂) were successfully deposited by spin coating method for environmental remediation. Firstly, the polymers poly(2-vinylpyridine) P(2-VP), and poly(4-vinylpyridine) P(4-VP) were synthesized via solution polymerization. The analysis by grazing incidence X-ray diffraction (GIXRD) reveals semicrystalline nature and scanning electron microscopy (SEM) indicates that the poly(vinylpyridines) clusters of particles were observed on the surface of the films. It was also shown that the morphology of composite materials is completely dependent on the chemical nature of the oxide. In the case of P(2-VP)-TiO₂ and P(4-VP)-TiO₂, some channels or pathways of TiO₂ on the surface of films were observed. However, the surface morphology of the polymer composites formulated with ZnO shows a homogeneous distribution in P(2-VP) and P(4-VP) matrix. The effectiveness of the composite materials in the photodegradation of methyl orange (MO) was evaluated by photocatalysis. According to the results, the P(4-VP)-ZnO composite exhibited the highest photodegradation of MO, allowing the separation of photogenerated species required for the photocatalytic reaction. The P(4-VP)-ZnO composite was also tested in benzoic acid (BA) photodegradation in water. The presence of some scavengers in the reaction system reveals that hydroxyl radicals (OH•), superoxide radicals (O₂-•) and holes (h+) are responsible for the BA reduction by photocatalysis.

The photoluminescence characteristics of films consisting of Si nanocrystals either coated with or embedded into Spin on Glass (SOG) were studied. Si nanocrystals showing red or blue luminescence when suspended in alcohol solution were obtained from porous silicon films. These were then either deposited in Si substrates and coated with SOG, or mixed in an SOG solution that was later spun on Si substrates. Both types of films were thermally annealed at 1100 °C for three hours in N₂ atmosphere. Transmission electron microscopy measurements showed a mean diameter of 2.5 nm for the Si nanocrystals, as well as the presence of polycrystalline Si nanoagglomerates. These results were confirmed by X-ray diffraction studies, which revealed the (111), (220) and (311) Bragg peaks in Si nanocrystals. Fourier transform infrared spectroscopy studies showed that the coated films present higher chemical reactivity, promoting the formation of non-stoichiometric SiO₂, while the embedded films behave as a stoichiometric SiO₂ after the thermal annealing. The PL (photoluminescence) characterization showed that both embedded and coated films present emission dominated by the Quantum Confinement Effect before undergoing any thermal treatment. After annealing, the spectra were found to be modified only in the case of the coated films, due to the formation of defects in the nanocrystals/SiO₂ interface.

Thick and homogeneous hybrid film systems based on poly(methyl methacrylate) (PMMA) and CeO₂ nanoparticles were synthesized using the melt compounding method to improve thermal stability, mechanical and UV-shielding properties, as well as to propose them for use in the multifunctional materials industry. The effect of the inorganic phase on these properties was assessed by using two different weight percentages of synthesized CeO₂ nanoparticles (0.5 and 1.0 wt %) with the sol–gel method and thermal treatment at different temperatures (120, 235, 400, 600 and 800 °C). Thereafter, the nanoceria powders were added to the polymer matrix by single screw extrusion. The absorption in the UV region was increased with the crystallite size of the CeO₂ nanoparticles and the PMMA/CeO₂ weight ratio. Due to the crystallinity of CeO₂ nanoparticles, the thermal, mechanical and UV-shielding properties of the PMMA matrix were improved. The presence of CeO₂ nanostructures exerts an influence on the mobility of PMMA chain segments, leading to a different glass transition temperature.