The photocatalytic degradation of methylene blue (MB) dye has been performed under UV irradiation in aqueous suspension, employing photocatalysts based on Au (1.5 wt %) and AuCu (Au/Cu = 1, 2.0 wt %), and supported on SBA-15-ordered mesoporous silica, with and without titania (Si/Ti = 3), in order to evaluate the versatility of this mesoporous support in this type of reaction of great impact from the environmental point of view. Samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N₂ adsorption-desorption at −196 °C, and X-ray photoelectron spectroscopy (XPS), so as to study their structural, optical, and chemical properties. All the prepared catalysts were found to be active in the test reaction. The bimetallic AuCu-based catalysts attained very high MB degradation values, in particular AuCu/SBA-15 titania-silica sample reached 100% of dye oxidation after the monitored reaction period (120 min).

The global demand for energy and industrial growth has generated an exponential use of fossil fuels in recent years. It is well known that carbon dioxide (CO₂) is mainly produced, but not only from fuels, which has a negative impact on the environment, such as the increasing emission of greenhouse gases. Thus, thinking about reducing this problem, this study analyzes microwave irradiation as an alternative to conventional heating to optimize zeolite A synthesis conditions for CO₂ capture. Synthesis reaction parameters such as different temperatures (60–150 °C) and different time durations (1–6 h) were evaluated. The CO₂ adsorption capacity was evaluated by CO₂ adsorption–desorption isotherms at 25 °C and atmospheric pressure. The results showed that the synthesis of zeolite A by microwave irradiation was successfully obtained from natural kaolinite (via metakaolinization), reducing both temperature and time. Adsorption isotherms show that the most promising adsorbent for CO₂ capture is a zeolite synthesized at 100 °C for 4 h, which reached an adsorption capacity of 2.2 mmol/g.

The effect of adding iron, cobalt or nickel to a prepared niobium-supported catalyst using mesoporous silica SBA-15 as a support was evaluated in the hydrodeoxygenation (HDO) reaction of anisole, chosen as a model compound in lignocellulosic biomass derived bio-oil. HDO activity as well as selectivity toward O-free products were highly dependent on the catalyst formulation: Ni incorporation showed the highest anisole conversion and selectivity to deoxygenated products, followed by Co and Fe counterparts. The activity was explained in terms of acidity, metal surface exposure and reducibility as a function of the interaction between the phases present. Regarding the characterization results, the better performance of NiNb/SBA-15 was associated with its lower acidity, higher Nb/Si surface exposure, NbO₂/Nb₂O₅ ratio and better interaction between Ni and Nb species.

The adsorption of greenhouse gases (GHG) as a method to reduce their emissions into the atmosphere is an alternative that is easier to implement industrially and cheaper than other existing technologies, such as chemical capture, cryogenic separation, or membrane separation. The vast majority of works found in the literature have focused their efforts on capturing CO₂ as it is the largest GHG. However, although N₂O emissions are not as large as CO₂, the impact that N₂O has on the stratosphere and climate is much larger in proportion, despite which there is not much research on N₂O capture. Since both gases are usually emitted into the atmosphere together (along with other gases), it is necessary to design selective adsorbents capable of capturing and separating these gases from each other and from other gases, to mitigate the effects of climate change. This review aims to compile the existing information to date on porous adsorbents, the characteristics of the N₂O adsorption processes and, above all, aims to focus the reader’s gaze on the importance of designing selective adsorbents for greenhouse gas mixtures.

The climate situation that the planet is experiencing, mainly due to the emission of greenhouse gases, poses great challenges to mitigate it. Since CO₂ is the most abundant greenhouse gas, it is essential to reduce its emissions or, failing that, to use it to obtain chemicals of industrial interest. In recent years, much research have focused on the use of CO₂ to obtain methanol, which is a raw material for the synthesis of several important chemicals, and dimethyl ether, which is advertised as the cleanest and highest efficiency diesel substitute fuel. Given that the bibliography on these catalytic reactions is already beginning to be extensive, and due to the great variety of catalysts studied by the different research groups, this review aims to expose the most important catalytic characteristics to take into account in the design of silica-based catalysts for the conversion of carbon dioxide to methanol and dimethyl ether.

Three chitosans with different morphologies have been used (commercial chitosan powder, chitosan in film form and chitosan in globular form synthesized by the freeze-dried method) for the synthesis of biochars. The pyrolytic treatment has revealed that the biochar synthesized from the chitosan formed by the freeze-dried method reaches the highest CO₂-adsorption capacity (4.11 mmol/g at 0 °C and a pressure of 1 bar) due to this adsorbent is highly microporous. Moreover, this biochar is more resistant to the pyrolytic treatment in comparison to the biochars obtained from the commercial chitosan and chitosan in the form of film. CO₂-adsorption studies at different temperatures have also shown that the adsorption capacity diminishes as the adsorption temperature increases, thus suggesting that the adsorption takes place by a physical process.