• Energy Research

Oxytetracycline is one of the antibiotics most frequently used in the Shrimp Industry during the control of bacterial diseases. These emerging pollutants, which appear in low concentrations, are persistent and alternative treatments and are required for their elimination. The degradation of oxytetracycline was evaluated in an aqueous solution by applying homogeneous (UV/H2O2 and photo-Fenton) and heterogeneous (UV/TiO2/H2O2) advanced oxidative processes (AOPs). The studies were carried out using a bench reactor with short-wave ultraviolet lamps (UV-C). We quantified the extent to which the degradation of the drug had been efficient by employing highly efficient liquid chromatography (HPLC) and a PDA detector with a wavelength of 354 nm and a C18 column. The best results were obtained when applying the UV/H2O2 treatment, which attained a degradation of 97% under the initial conditions of a dose of 8 µL of H2O2 and 120 min of radiation. The pseudo-first order kinetic model proposed by Chan and Chu showed that the experimental results had an adequate fit, with values greater than R2 ≥ 0.95. Toxicity tests were applied to verify the effect of AOPs employed, when the drug was present in low concentrations. The test results demonstrated a decrease in the root growth of the species Lactuca sativa and Daucus carota.

The management and final disposal of agro-industrial wastes are one of the main environmental problems. Due to the presence of silica in some agricultural by-products, it is possible to convert waste into materials with advanced properties. This contribution was aimed to extract and characterize silica materials from various feedstocks including sugarcane bagasse (SCB), corn stalk (CS), and rice husk (RH). Silica yields of 17.91%, 9.39%, and 3.25% were obtained for RH, CS, and SCB. On the other hand, the textural properties show that the siliceous materials exhibited mesoporous structures, with high silica composition in the materials due to the formation of crystalline SiO2 for SCB and CS and amorphous for RH. XPS spectra demonstrate the presence of Si4+ species in RH, and Si3+/Si4+ tetrahedra in SCB and CS.

This study provides a full characterization of ashes generated from the combustion of bagasse at two different sugarcane ethanol plants, one in the state of Pernambuco, Brazil (SBA1), and the other in Villa Clara, Cuba (SBA2), with a view to examining their usage as adsorbing agents for the removal of heavy metals and various organic impurities. The ash samples were analyzed for both chemical composition and for structural features that would aid their use. Chemical characterization was done spectrally, through the examination of X-ray fluorescence and diffraction, Fourier transform infrared spectroscopy, and thermally, through thermogravimetric and differential thermal analysis. Structural and surface characterization was carried out by examining N2-physisorption, helium pycnometry, and scanning electron microscopy. The results of each analysis were compared to those of recognized or potential adsorbent materials. Both ashes have structural similarities, heterogeneous morphologies, irregular surfaces, and a prevalence of superficial polar groups (carbonyl, carboxyl, and hydroxyl). Based on their physical and chemical characteristics, ashes could be used as adsorbent for both, organic (e.g., dyes, phenols, etc.) and inorganic (e.g., heavy metals) compounds.

Tagua shell is a material generated in the handcrafted jewelry industry, which is discarded since it does not have a specific use. The present study evaluates this material as an adsorbent for the removal of lead (II) in aqueous media. The adsorbent was characterized through the point of zero charge technique, X-ray microanalysis, scanning electron microscopy, and Fourier-transform infrared spectroscopy. Tests were carried out in a static system using a lead (II) solution of 100 mg·L−1 to establish the process conditions, setting a pH of 5, an adsorbent dose of 1.8 g/100 mL, and a contact time of 60 min. The kinetic study performed showed that the experimental data had a better fit with the pseudo-second order model. The experimental equilibrium data were correlated using the Langmuir, Freundlich, Toth, Redlich–Peterson, and Sips models, of which the Langmuir and Sips models proved to be the best to represent the adsorption process due to the high coefficient of determination they presented at the different temperatures, being between 0.9629–0.9899 and 0.9819–0.9900, respectively. The maximum amount of lead adsorbed was 22.0348 mg·g−1 at a temperature of 298 K. Finally, the thermodynamics study indicated that the process is endothermic, spontaneous, and thermodynamically stable.

The use of food additives (such as dyes, which improve the appearance of the products) has become more prominent, due to the rapid population growth and the increase in demand for beverages and processed foods. The dyes are usually found in effluents that are discharged into the environment without previous treatment; this promotes mass contamination and alters the aquatic environment. In recent years, advanced oxidation processes (AOPs) have proven to be effective technologies used for wastewater treatment through the destruction of the total organic content of toxic contaminants, including food dyes. Studies have shown that the introduction of catalysts in AOPs improve treatment efficiency (i.e., complete decomposition without secondary contamination). The present review offers a quick reference for researchers, regarding the treatment of wastewater containing food dyes and the different types of AOPs, with different catalyst and nanocatalyst materials obtained from traditional and green chemical syntheses.

The integration of layered double hydroxides (LDHs) into hybrid catalysts markedly enhances the efficiency of overall water splitting, thereby advancing the potential for large-scale hydrogen production. This review elucidates the advantages of combining LDHs with various materials, including metal-organic frameworks (MOFs), MXenes, and carbonaceous substrates, to augment electrical conductivity and catalytic activity, particularly in the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Recent investigations have demonstrated the efficacy of LDH-based materials in catalyzing water-splitting reactions, underscoring their role in energy production. The unique properties of LDHs, characterized by a two-dimensional layered structure and exceptional physicochemical characteristics, render them suitable candidates for such applications. Moreover, this review discusses innovative design strategies for LDHs, encompassing nanostructuring, hybridization with conductive materials, partial cation substitution, interlayer anion exchange, and vacancy creation. Variations in metal composition within LDHs are also examined to elucidate their impact on OER and HER performances. Through a comprehensive analysis of the promising applications of LDHs as catalysts for hydrogen production, this article highlights significant advancements and delineates critical areas for future research, thereby contributing to the ongoing discourse in the field of electrocatalysis.

MOF@Biomass layered hybrids were designed through in situ growth from rice husk (RH) and microwave-assisted synthesized MIL-53(Al) particles that enable the reduction of reaction times. The synthesis process included steps to pretreat RH, Al adsorption on RH, and then MIL-53(Al) in-situ growth reaction at 125 °C for 60 min and 200 W irradiation power. The resulting hybrid (MIL-53(Al)@RH) and its parent separate materials were characterized using TGA, SEM, FTIR, XRD, among others. MIL-53(Al)@RH showed high crystallinity in the hybridized MOF particles, thermal decomposition phases, and functional groups (Al-O, O-H, CO, and CC). The hybrid particles allow an easy separation during heterogeneous processing due to their 400 times larger size compared to MIL-53(Al) crystals. The properties of the layered hybrids for removal of Oxytetracycline (OTC), Diclofenac (DCL), and Glyphosate (GLY) in aqueous solutions, were tested by adsorption (ADS) and advanced oxidation processes (AOP). The high ADS capacities (162 mg g-1 GLY, 139 mg g-1 OTC, 93 mg g-1 DCL) and % removal in AOP (97% GLY, 91% OTC, 80% DCL) demonstrated that MIL-53(Al) maintained its properties after hybridization.

This contribution aims to demonstrate the scope of new hybrids between biomass and metal-organic frameworks (MOF@biomass) used in the adsorption process of pollutants. After a brief presentation of the use of the main series of MOFs as efficient adsorbents for different types of pollutants, the limitations of these structures related to particle size and hydrodynamic problems during their application are highlighted. Lignocellulosic biomasses are also recognized as an alternative adsorbent, mainly due to their high natural abundance and their low environmental impact during and after their application. The limited capacity of bioadsorbents becomes important in this research. Consequently, the largest amount of information existing in the last ten years on MOF-Biomass functionalization as a hybrid and improvement technology for adsorption processes is compiled, analyzed, compared and contrasted. So far, there is no evidence of works that exploit the concept of functionalization of adsorbents of different nature to give rise to new hybrid materials. Through this review it was found that the hybrids obtained show a higher adsorption capacity (Qe) compared to their precursors, due to the increase of organic functional groups provided by the biomass. Thus, for heavy metals, dyes, Arsenium anions and other organic and pharmaceutical compounds, there are increases in Qe of about 100 mg g-1. The possibility of the new hybrid being studied for desorption and reuse processes is also raised, resulting in a new line of research that is attractive for the industry from an economic and environmental point of view. The functionalization methods and techniques used in the studies cited in this article are outlined. In conclusion, this research brings a new horizon of study in the field of adsorption and mentions the main future challenges related to new sustainable applications.