María Emma Borges

Direct air capture (DAC) of CO₂ via temperature-swing adsorption (TSA) can support sustainable carbon dioxide removal, but only if sorbents regenerate with low energy demand and maintain performance under humid ambient air. In this paper, we evaluate three commercial molecular sieves (JLPM3, 13X, and 4A) in packed-bed tests using humid ambient air. We compared 40 g samples as received with 200 g samples conditioned for 12 days at 100 °C to emulate prolonged exposure to regeneration temperature (the cumulative effect of many heating/desorption cycles); all cycle-stabilized uptake values are reported from the conditioned materials. JLPM3 delivered the highest stabilized CO₂ uptake (0.24 ± 0.01 mmol·g⁻¹), consistent with a combined physisorption/chemisorption mechanism. Its higher total porosity (26.190%) and smaller mesopores (7.569 nm width) promoted rapid mass transfer and site accessibility, while slightly greater micropore area (710.285 m²·g⁻¹) and volume (0.267 cm³·g⁻¹) than 13X supported its marginally higher capacity. Evidence of partial structural degradation under mechanical and thermal stress indicates that minimizing strain during cycling will be important for scale-up and for reducing sorbent replacement. Conditioning at 100 °C activated additional chemisorption sites across all sieves but reduced physisorption capacity. Importantly, a ~100 °C desorption step fully regenerated physisorbed CO₂ while purging moisture from zeolite pores, indicating that low-temperature TSA (compatible with low-grade or waste heat) can replace harsher 300 °C regeneration and lower energy demand. CO₂–H₂O competition experiments confirmed substantial site occupancy by water vapor, which limits capture under humid conditions and motivates water management strategies. Overall, maximizing DAC performance requires tailoring pore structure and operating conditions while preserving sorbent integrity; JLPM3 emerges as a promising candidate for more energy- and resource-efficient DAC.

Direct air capture (DAC) of CO2 via temperature-swing adsorption (TSA) can support sustainable carbon dioxide removal, but only if sorbents regenerate with low energy demand and maintain performance under humid ambient air. Here, we evaluate three commercial molecular sieves (JLPM3, 13X and 4A) in packed-bed tests using humid ambient air. We compared 40 g samples as received with 200 g samples conditioned for 12 days at 100 °C to emulate prolonged exposure to regeneration temperature (the cumulative effect of many heating/desorption cycles); all cycle-stabilized uptake values are reported from the conditioned materials. JLPM3 delivered the highest stabilized CO2 uptake (0.24 ± 0.01 mmol·g-1), consistent with a combined physisorption/chemisorption mechanism. Its higher total porosity and smaller mesopores promoted rapid mass transfer and site accessibility, while slightly greater micropore area and volume than 13X supported its marginally higher capacity. Evidence of partial structural degradation under mechanical and thermal stress indicates that minimizing strain during cycling will be important for scale-up and for reducing sorbent replacement. Conditioning at 100 °C activated additional chemisorption sites across all sieves but reduced physisorption capacity. Importantly, a ~100 °C desorption step fully regenerated physisorbed CO2 while purging moisture from zeolite pores, indicating that low-temperature TSA (compatible with low-grade or waste heat) can replace harsher 300 °C regeneration and lower energy demand. CO2–H2O competition experiments confirmed substantial site occupancy by water vapor, which limits capture under humid conditions and motivates water-management strategies. Overall, maximizing DAC performance requires tailoring pore structure and operating conditions while preserving sorbent integrity; JLPM3 emerges as a promising candidate for more energy- and resource-efficient DAC.

Municipal solid waste management (MSWM) on islands involves several challenges relating to politics, society, the environment, and technology. This paper addresses the potential for producing biogas and biomethane from food waste on Tenerife, including waste from households, with the aim of reducing landfill and primary fossil energy consumption. The study also introduces the European and Regional policy framework and requirements. Effective microorganisms have been studied as proposals to stabilise the food waste from households, avoiding odours and decomposition during storage. The trials show positive results in terms of the preservation of organic matter until the food waste is transported to the biogas plant. In addition, a new concept for a small biogas plant made of textile materials, which are suited to the municipalities of Tenerife, is presented to provide an easy-to-build solution, with ranges of up to 75 kW in electrical power. With a theoretical potential of 299,012 tons of food waste being available per year (based on 2022), preliminary laboratory experiments with real samples of the island showed a theoretical potential of 28.97 × 10⁶ Nm³ for biogas and 264,612 tons for digestate, which can be used as fertilisers, with potential savings of 18.15 × 10⁶ L of gasoline and 42.66 × 10³ equivalent CO₂ tons.

In small German farms, there is a technically usable potential of cattle manure and pig manure ranging from 153 to 187 million tons of fresh matter per year. Since 2021 and 2023, new incentives under the Renewable Energy Sources Act (EEG) have been promoting biogas production in small farms. These incentives, applicable to biogas plants up to 150 kWel, include direct compensations for plants up to 100 kWel and market premiums for those up to 150 kWel. A small biogas plant made of textile materials was designed for both pilot and full-scale applications. Compared to conventional concrete biogas reactors, these textile-based reactors offer a simplified construction and operation, eliminating the need for specialized civil engineering. The primary objective of this research is to demonstrate the process engineering feasibility of biogas reactors based on textile materials for small farm biogas plants (30 to 75 kWel). Another goal is to design the construction method in such a way that this type of system can be built by farmers themselves after type testing on site. Operational insights were gathered from the laboratory plant with a 300-L digester volume, using cattle manure and clover grass silage. To adapt the system to the biogas reactor made of textile materials, the reactor was designed without a stirrer. These insights were considered in the design and approval procedure of the full-sized demonstration biogas plant made of textile materials. The full-size demonstration plant digesters underwent an approval procedure from local authorities, featuring treatment volumes of 120 m³ for the main biogas reactor and 550 m³ for the digestate reactor in an earth basin style. This new type of biogas plant could be built in small farms for self-sufficiency in electrical and thermal energy or for treating sewage sludge in small-scale communal wastewater treatment and biogas plants.

Photocatalysis is an advanced oxidation process that is an environmentally friendly option and one of the most critical technologies in green chemistry today. This work studied the upscaling of photocatalysis as a suitable process for wastewater treatment to remove emerging pollutants. For this purpose, unsupported and supported TiO₂ photocatalysts were tested in the photodegradation of ciprofloxacin as a model molecule of an emerging wastewater component, using visible, UV radiation, and solar light. The suitability of TiO₂ as a photocatalyst to decompose ciprofloxacin was confirmed in batch photoreactor under Visible and UV radiation, with degradation rates up to 90% after 30 min of irradiation and low adsorption values. TiO₂ as a photocatalyst coated in glass support material at the packed bed photoreactor showed good photoactivity for emergent contaminants degradation (95%) under solar radiation. It has been possible to verify that the photocatalytic reactor system constitutes a viable process for eliminating emerging contaminants through environmentally sustainable treatments. Our results corroborate the possibility of degrading emerging contaminants by solar radiation using a packed bed photoreactor, providing a more effective option from a practical and economical point of view for wastewater effluent treatments.

Cattle manure usually contains a proportion of carbohydrates in the form of organic residues from incompletely digested feed and farm husbandry practices. These are not usually available for biogas production due to the long fermentation time. This paper investigates the optimal application of alkali, NaOH and KOH and mechanical pre-treatments to improve the degradation of the lignocellulosic content and the potential biogas yields from a local farm in Bavaria, Germany. Parameters such as temperature, pH, soluble chemical oxygen demand, organic acids, dry matter and volatile solids were analysed for this purpose. Alkali pre-treatments in 0.2, 0.1 and 0.05 M NaOH concentrations were tested in single mode and combined with shredding in batch experiments. The maximum increment of the soluble chemical oxygen demand during the pre-treatments took place during the first 50 h of experimentation, and it showed an improvement of 10,060.0 ± 8% mg/L s COD after the application of 0.2 M NaOH compared to the untreated substrate, which had an initial value of 2145.0 ± 8% mg/L s COD. Pre-treatments with 0.1 and 0.05 M NaOH concentrations showed similar s COD increments, with an additional 6860.0 ± 8% mg/L s COD and 8505.0 ± 8% mg/L s COD, respectively. The pH values varied strongly after the addition of the pre-treatment chemicals, with a continuous pH of 12 by 0.2 M NaOH during the 7 days of pre-treatment. Batch biogas experiments were done by applying 0.05 M NaOH and 0.05 M KOH pre-treatments in single mode and combined with shredding. The chemically pre-treated substrates showed a faster biogas production with an advantage of 18 days in comparison to the untreated cattle manure by a biogas yield of 350.0 NL/kg VS. All experiments were done under mesophilic conditions.

Brewing beer is one of the most popular food processes in the current society, and it has been widely used as a learning course at many universities. However, most laboratory experiences take a very long time for development. In this work, we discuss the brewing process from malt extract as an intelligent way to reduce the timing for implementation by simplifying some of its stages, such as malting or mashing, but remaining the same core process. During brewing with malt extract, the students deal with this multidisciplinary process, enhancing primary learning outcomes related to the unit operations of chemical engineering applied to the food industry. At the university level, the addition of brewing as a laboratory experiment might directly affect the productive fabric of the area through the development of new beer-related businesses.

Recently, photocatalysis has been demonstrated as a solid approach for efficient wastewater cleaning. Using natural materials as photocatalysts means a promising solution to develop green catalysts for environmental purposes. This work aimed to study the suitability of a natural volcanic material (La Gomera, Canary Islands, Spain) as a photocatalytic material for the degradation of pollutants in wastewater with solar energy. After analysing the properties of the natural material (BET surface 0.188 m²/g and band-gap of 3 eV), the photocatalytic activity was evaluated at laboratory and pilot plant scale for the degradation of methylene blue (MB) in water (50 mg L⁻¹), at 20 °C, during a period of 4 h, under UV/Vis light and solar irradiation. Photolytic and adsorption studies were developed to distinguish the photocatalytic contribution to the wastewater decontamination process by photocatalysis. Our results enable us to determine the viability of black sand as a photocatalytic material activated by solar irradiation (photodegradation of MB up to 100% by using solar energy), developing a natural and green photocatalytic system with significantly high potential for application in a sustainable wastewater cleaning process.

As consequence of the digital transformation, e-learning methodologies have become an inseparable part of the standard classes in schools and universities, assuming an increasingly significant role in compensating for the difficulties resulting from the COVID-19 pandemic. Numerous pedagogical methodologies and strategies can be easily implemented in high education, promoting students’ motivation and interest in learning. This research study analyses the implementation of gamification pedagogical strategy on 50-60 undergraduate chemical engineering students at the university, by evaluating its effect on the success rate on a specific topic of Chemical Reactions Engineering subject and the motivation effect for the following topics. Our results show a significant positive effect of the gamification strategy on university lectures, increasing up to 25-30 % of the success ratio with an apparent motivation effect. During the subsequent years, the changes in the lifestyle of study also play a role in students’ performance. Therefore, it is necessary to evaluate case studies such as the one presented here to understand better the use of these pedagogical methods and strategies in high education, especially in technical subjects described in this paper.

This work reports initial results on the effect of low concentrations (ppm level) of a stabilizing agent (2,6-di-tert-butyl-4-methylphenol, BHT) present in an off-the-shelf solvent on the catalyst performance for the hydrogenolysis of γ-butyrolactone over Cu–ZnO-based catalysts. Tetrahydrofuran (THF) was employed as an alternative solvent in the hydrogenolysis of γ-butyrolactone. It was found that the Cu–ZnO catalyst performance using a reference solvent (1,4-dioxane) was good, meaning that the equilibrium conversion was achieved in 240 min, while a zero conversion was found when employing tetrahydrofuran. The deactivation was studied in more detail, arriving at the preliminary conclusion that one phenomenon seems to play a role: the poisoning effect of a solvent additive present at the ppm level (BHT) that appears to inhibit the reaction completely over a Cu–ZnO catalyst. The BHT effect was also visible over a commercial Cu–ZnO–MgO–Al₂O₃ catalyst but less severe than that over the Cu–ZnO catalyst. Hence, the commercial catalyst is more tolerant to the solvent additive, probably due to the higher surface area. The study illustrates the importance of solvent choice and purification for applications such as three-phase-catalyzed reactions to achieve optimal performance.