In the present work, modifications were made in the typical synthesis of KIT-6 mesoporous material. The molar ratio of P123 and its dissolution time, the type of alcohol, the aging time, and the heat treatment time were varied. The materials obtained were characterized by X-ray diffraction (XRD), thermogravimetry and differential thermogravimetry (TG/DTG), Fourier-transform infrared spectroscopy (FTIR), adsorption and desorption of N₂ and transmission electron microscopy (TEM). It was observed that the modifications interfered directly in the ordered structure of materials, displaying materials with cubic structures Ia3d (KIT-6 mesoporous material) and hexagonal structures P6mm, (SBA-15 mesoporous material). The type of alcohol probably acts on generation of the micelle, influencing the formation of the porous system and ordered structure. The results obtained indicate that the cubic structure of KIT-6 can be formed with a reduction of 30% in the P123 concentration, and decreases of 2, 6 and 12 h in times of P123 dissolution, aging and heat treatment, respectively. The modifications carried out in the synthesis procedure have resulted in ir being possible to employ materials with different characteristics, such as mesoscopic ordering and textural properties, in applications in the areas of catalysis and adsorption.

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.

Herein, ordered mesoporous materials like SBA-15 and Al/SBA-15 were prepared using the pH adjustment method. Thus, these materials were developed in different pH of synthesis, from the pH adjustment method using a KCl/HCl solution and varying the Si/Al molar ratio (5, 25, and 75). All the ordered mesoporous materials were characterized by FRX, ²⁷Al NMR, SEM, XRD, N₂ adsorption/desorption, and CO₂ adsorption. From the applied method, it was possible to obtain SBA-15 and Al/SBA-15 with high mesoscopic ordering based on the XRD patterns, independent of the pH employed. From the chemical composition, the insertion of higher amounts of Al into the synthesis caused a progressive improvement in the structural and textural properties of the ordered mesoporous materials. Thus, the chosen synthesis conditions can lead to different aluminum coordination (tetrahedral and octahedral), which gives these materials a greater potential to be applied. The presence of Al in high amounts provides material with the ability to form micropores. Finally, the proposed method proved to be innovative; low-cost; less aggressive to the environment, with efficient insertion of aluminum in the framework of SBA-15 mesoporous material; and practical, based on only one step.

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.

Cementing operations are among the most critical steps in oil-well construction. When performed improperly, the integrity and useful life of the well can be significantly compromised. Light cement pastes are used to cement formations with a low fracture gradient to ensure zonal isolation and maintain the integrity of the casing. Extenders are additives used to reduce the density of cement pastes, ensuring that the paste has desirable properties before and after setting. This work aimed to evaluate the application of palygorskite clay as an additive in lightweight cement pastes for oil wells, highlighting how its fibrous morphology influences the microstructure and enhances the macroscopic properties of the hardened cement matrix. For this, the clay sample was initially characterized regarding its physicochemical properties using X-ray diffraction (XRD), X-ray fluorescence (XRF), thermogravimetry (TG), textural analysis (BET/N₂), and scanning electron microscopy (SEM). Lightweight pastes (1.56 g/cm³) were then formulated, varying the clay concentration by 1%, 3%, and 6% of the total mass. Cement pastes using bentonite were also formulated for comparison. Technological tests of atmospheric consistency, rheological behavior, free water, and stability were applied. It can be noted that the pastes formulated with palygorskite had lower viscosity, reflected in the reduced plastic viscosity and yield stress values, indicating easier flow behavior when compared with bentonite-based pastes. The pastes formulated with 6% palygorskite and 3% bentonite showed satisfactory stability and drawdown results. Therefore, applying palygorskite satisfies the minimum requirements for acting as an extending agent for lightweight cement pastes and is an option for application in oil-well cementing operations.

A necessidade de se desenvolver novas fontes de energias menos poluentes e de menor custo, tem gerado um incentivo na produção do biodiesel por ser uma fonte ...