Alma Berenice Jasso-Salcedo

The atypical proliferation of Sargassum (Sargassum spp.) in the tropical Atlantic and the Caribbean Sea over the past decade has triggered an unprecedented environmental and socioeconomic crisis along the Mexican coastline. Continuous beaching events of this macroalga on the Riviera Maya have caused coastal ecosystem degradation, severe impacts on the tourism sector, toxic gas emissions during decomposition, and high cleanup costs. To address this challenge, the valorization of Sargassum as a raw material for synthesizing functional materials represents a sustainable management strategy. In this study, a superabsorbent hydrogel was developed from Sargassum biomass (collected in Cancún, Quintana Roo, in 2025) using an innovative process that bypasses the conventional cellulose isolation step. The biomass was subjected to high-energy milling (15 and 30 min) to prepare Sargassum powder, which was subsequently carboxymethylated using monochloroacetic acid. This modified biomass was then crosslinked with citric acid, a process evaluated at three different citric acid/carboxymethylated Sargassum mass ratios. The hydrogel synthesized with the lowest crosslinking agent ratio achieved a maximum water absorption capacity of 1160 wt%, a value that exceeds the typical absorption capacities of 700–900% for biopolymer hydrogels. Successful material formation was confirmed by Fourier transform infrared spectroscopy (FTIR), which revealed the characteristic functional groups of CMC and the ester bonds formed during crosslinking. Additionally, scanning electron microscopy (SEM) analysis showed a well-defined porous structure with pore sizes ranging from 8.5 to 19.5 µm, which is essential for its high absorption performance. This study demonstrates the feasibility of producing high performance hydrogels from Sargassum through a simplified, cost-effective, and environmentally friendly process. These findings open a promising avenue for the integrated management of this problematic biomass, transforming it into value-added materials with potential applications in agriculture, hygiene, and environmental remediation.

Synthèse et mise en oeuvre de nanocomposites à base d’oxyde de zinc utilisés pour le traitement photocatalytique de l’eau contaminée par des disrupteurs endocriniens: Le présent travail porte sur la photodégradation de polluants aqueux utilisant des catalyseurs à base de ZnO. La première étape a consisté à fonctionnaliser ZnO avec des nanoparticules d'argent. Deux méthodes ont été utilisées : la photodéposition et l'imprégnation des particules d'argent sur ZnO. L’activité des catalyseurs obtenus vis-à-vis de la dégradation du bisphenol-A, du triclosan et de la rhodamine-B a été ensuite étudiée. L'effet du pH, des concentrations du photocatalyseur et du polluant et de la longueur d'onde sur la dégradation du bisphenol-A a été analysée et la constante cinétique déterminée. L'optimisation a montré qu'une teneur faible en argent et un pH alcalin, tant pour la fonctionnalisation de ZnO que pour la photodégradation, maximisent la constante cinétique de dégradation du bisphenol-A. Un modèle a également prédit que le système obtenu par photodéposition présente une activité photocatalytique supérieure à celle de celui obtenu par imprégnation. D'autre part, pour surmonter des problèmes d'agrégation, les particules d’Ag/ZnO ont été immobilisées grâce à leur incorporation dans une matrice d'acide polyacrylique réticulé. La surface des particules de catalyseur a, au préalable, été modifiée grâce à un agent de couplage silané qui a permis (i) la dispersion et l'ancrage par estérification des nanoparticules sur la matrice polyacrylique (ii) de promouvoir la cristallisation du polymère. Les composites obtenus ont été testés avec succès sous rayonnement UV avec une efficacité comparable à celle des particules non-immobilisées. L'immobilisation permet par ailleurs d'empêcher la photocorrosion du catalyseur et d'utiliser ces composites en mode continu

This study presents a novel, circular-economy-driven strategy for valorizing post-consumer denim waste into high-performance hydrogels through a fully integrated and eco-friendly process. Unlike conventional approaches that rely on virgin cellulose or harsh chemical treatments, our method uniquely combines high-energy mechanochemical pretreatment, in situ carboxymethylation to produce carboxymethylcellulose (CMC), and citric acid/urea-based crosslinking, all using recycled denim as the sole cellulose source. High-energy milling effectively reduced particle size and lowered the crystallinity index (CI) from 75.7% to 66.1%, transforming the fibrous structure into a more reactive substrate for etherification. Successful CMC synthesis was confirmed by FTIR (COO⁻ stretch at 1587 cm⁻¹), while citric acid crosslinking generated ester bonds (C=O at ~1724 cm⁻¹), forming a 3D network further tailored by urea, acting as a green porogen. The resulting hydrogels exhibited enhanced thermal stability (TGA) and a tunable porous morphology (SEM), with pore sizes reaching up to 147 µm as the urea content increased. Notably, the hydrogel Hy/CMC/U2/CA achieved an exceptional swelling capacity of 1900%, which is among the highest reported for denim-derived or citric acid-crosslinked systems. The objective of this work is to demonstrate, for the first time, the feasibility of converting waste denim directly into functional hydrogels without intermediate purification steps, offering a scalable and sustainable route for agricultural applications, such as soil water retention, controlled nutrient release, or environmental remediation, within a true circular economy framework.

This study investigates a novel approach to moderate-temperature carbon capture by examining the enhanced performance of thermally pre-treated dolomite. To obtain mixed oxides, dolomite samples were prepared via calcination in a quartz cylindrical furnace under an ambient atmosphere at 900 °C, and subsequently thermally pre-treated under an inert (argon) stream at 650 °C. Characterization of the as-prepared samples involved morphological, structural, textural, and optical features examined through XRD, BET, SEM-EDS, FT-IR, and RAMAN, XPS, and UV-vis spectroscopy, whereas TGA and subsequent multicyclic tests were used to study the CO₂ sorption. The dolomite sample calcined at 900 °C for 60 min, and after being activated under an inert atmosphere (argon), labeled PCD60Act, exhibited the highest CO₂ uptake of 0.477 g_CO2/g_sorbent; after 15 sorption–regeneration cycles, it still retained a CO₂ uptake of 0.38 g_CO2/g_sorbent at 650 °C, and it was also successfully regenerated at this moderate temperature, demonstrating 84% capture capacity retention. These remarkable results are explained by the crystalline defects generated during the thermal pre-treatments of the dolomite. This research offers valuable perspectives on the viability of employing thermally pre-treated dolomite as an inexpensive, thermally stable, and moderate-temperature regenerable CaO-based sorbent for applications in CO₂ removal in the context of integrated carbon capture and conversion (ICCC) for the production of high-purity hydrogen.

Achieving net-zero carbon emissions, this study introduces a sustainable pathway for reducing strontium sulfate (SrSO₄) and celestite ore to strontium sulfide (SrS) using biofuels (biomethane, bioethanol) derived from agro-industrial waste and green hydrogen. Traditional SrSO₄ reduction methods, which rely on fossil-derived reductants like coal and operate at energy-intensive temperatures (1100–1200 °C), generate significant greenhouse gases and toxic byproducts, highlighting the need for eco-friendly alternatives. Experimental results demonstrate that bioethanol outperformed other reductants, achieving 97% conversion of synthetic SrSO₄ at 950 °C within 24 min and 74% conversion of natural celestite ore over 6 h. Remarkably, this bioethanol-driven process matches the energy efficiency of the conventional black ash method while enabling carbon neutrality through renewable feedstock utilization, reducing CO₂ emissions by 30–50%. By valorizing agro-industrial waste streams, this strategy advances circular economy principles and aligns with Mexico’s national agenda for sustainable industrial practices, including its commitment to decarbonizing heavy industries. This study contributes to sustainable development goals and offers a scalable solution for decarbonizing strontium compound production in the chemical industry.

Nanocellulose (NC)-based materials constitute a new class of bio-based building blocks that are inspiring advances for the next generation of high-performance sustainable materials. However, NC exhibits important drawbacks which limit its applications, such as its inherent interaction with bacteria and proteins, low conductivity, poor thermal stability, high water absorption (leading to, among other things, loss of structural integrity), etc. An efficient strategy to improve this, besides the possibility of introducing further properties, is through mineralization by in situ growing inorganic subcomponents to form NC-based hybrids. Following the example of nature which has been mineralizing biopolymers from the beginning of life to create complex structures (forming protective shields or structural supports), mineralization can be adopted in different (2D/3D) configurations, for instance, membranes, scaffolds, sponges, and monoliths (as per requirements), by in situ growing multiple subcomponents such as metal oxides, silicates, and metal–organic frameworks. The components act synergistically complementing each other, thus providing new functionalities that the components individually do not possess. For instance, it is possible to introduce properties such as self-healing behavior, magnetic character, antimicrobial properties, electrical and thermal conductivity, etc., which opens a wide range of opportunities in a variety of fields (e.g., energy, printed electronics, biomedicine, water/gas purification, etc.) of current interest and requirements. The present review paper summarizes and discusses the advanced applications of thus-formed nanocellulose hybrids, along with a general overview of the synthesis protocol and advanced characterization tools used to analyze these complex materials.