Zeolites have a well-ordered crystalline network with pores controlled in the synthesis process. Their composition comprises silicon and aluminum, so industrial residues with this composition can be used for the synthesis of zeolites. The use of zeolites for CO₂ adsorption is feasible due to the characteristics that these materials have; in particular, zeolites with a low Si/Al ratio have greater gas adsorption capacities. In this work, the synthesis of LTA (Linde Type A) zeolites from silica fumes obtained from the industrial LIASA process and light coal ash is presented. We explore three different synthesis routes, where the synthesized materials undergo cation exchange and are applied in CO₂ adsorption processes. Studying the synthesis processes, it is observed that all materials present characteristic diffractions for the LTA zeolite, as well as presenting specific areas between 6 and 19 m²/g and average pore distributions of 0.50 nm; however, the silica fume yielded better synthesis results, due to its lower impurity content compared to the light coal ash (which contains impurities such as quartz present in the zeolite). When applied for CO₂ adsorption, the standard materials after cation exchange showed greater adsorption capacities, followed by the zeolites synthesized from silica fume and, finally, the zeolites synthesized from coal ash. By analyzing the selectivity of the materials for CO₂/N₂, it is observed that the materials in sodium form present greater selectivity when compared to the calcium-based materials.

Emissions caused by polluting gases, such as carbon dioxide, are one of the main contributors to the generation of the greenhouse effect that leads to global warming, responsible for climate change. An alternative to mitigating these emissions is the use of adsorbents capable of capturing CO₂. Zeolites are considered one of the most effective adsorbents in gas adsorption and separation technologies due to their high specific area and pore size and, consequently, greater adsorption capacity when compared to other commonly used materials. Despite this, reagents used in syntheses as the source of silica often make obtaining these materials more expensive. Seeking to overcome this limitation, in this work, materials (for CO₂ capture) were developed with a zeolitic structure using a low-cost alternative source of silica from beach sand called MPI silica to make the synthesis process eco-friendly. The crystallization time of the materials was studied, obtaining an LTA zeolite with MPI silica in a period of 1 h (ZAM 1 h), with a relative crystallinity of 74.26%. The materials obtained were characterized using the techniques of X-ray diffraction (XRD), X-ray fluorescence (XRF), absorption spectroscopy in the infrared region with Fourier transform (FTIR), scanning electron microscopy (SEM), and thermal analysis. The evaluation of the experimental adsorption isotherms showed that the zeolite LTA Aerosil^®200 (standard zeolite) and MP had adsorption capacities of 5.25 mmol/g and 4.83 mmol/g of CO₂, respectively. The evaluation of mathematical models indicated that the LTA zeolites fit the Temkin model best and had the same trend, with calculated adsorption capacities of 3.97 mmol/g and 3.75 mmol/g, respectively.

In recent years, climate change has attracted the attention of the scientific community. These changes are attributed to human action, which is responsible for the emission of polluting gases, mainly through the burning of fossil fuels, deforestation, and industrial processes that are responsible for the greenhouse effect. Post-combustion CO₂ capture using solid adsorbents is a technology that is currently gaining prominence as an alternative and viable form of capture to other industrial processes used. Zeolites are adsorbents capable of capturing CO₂ selectively due to their properties such as textural properties, high surface area, and active sites. In this context, this work developed materials with a zeolite structure with an alternative low-cost silica source from beach sand, called MPI silica, to make the process eco-friendly. Crystallization time studies were carried out for materials containing MFI-type zeolites with MPI silica with a time of 15 h (ZM 15 h) and 3 days (SM 3 d), with relative crystallinities of 92.90% and 111.90%, respectively. The synthesized materials were characterized by several techniques such as X-ray diffraction (XRD), X-ray fluorescence (XRF), the textural analysis of N₂ adsorption/desorption isotherms, absorption spectroscopy in the infrared region with Fourier transform (FTIR), scanning electron microscopy (SEM), and thermal analysis. The evaluation of the experimental adsorption isotherms showed that the best results were for the zeolites synthesized in the basic medium, namely ZMP 3 d, ZM 10.5 h, and ZM 15 h, with capacities of 3.72, 3.10, and 3.22 mmol/g of CO₂, respectively, and in the hydrofluoric medium, namely SP 9 d, SM 3 d, and SM 6 d, with capacities of 3.94, 3.78, and 3.60 mmol/g of CO₂, respectively. The evaluation of the mathematical models indicated that the zeolites in the basic medium best fitted the Freündlich model, namely ZMP 3 d, ZM 10.5 h, and ZM 15 h, with capacities of 2.56, 1.68, and 1.87 mmol/g of CO₂, respectively. The zeolites in the hydrofluoric medium are adjusted to the Langmuir model (SP 9 d and SM 3 d) and Temkin model (SM 6 d), with capacities of 3.79, 2.23, and 2.11 mmol/g of CO₂, respectively.

Anais do SIAMQUI: Simpósio Amazônico de Química (978-85-5722-288-5) - Avaliação De Fatores Que Influenciam O Crescimento Da Saccharomyces Cerevisiae Na Fermentação Do Melaço