The Al incorporation on SBA-15 type material and the effects of pH adjusting and presence of NaF were studied. The direct synthesis method was performed for comparison. The following parameters were evaluated: the Si/Al ratio, pH increase, and amount of NaF added. These parameters have a great influence on the synthesis of the mesoporous Al/SBA-15 type, but the pH the most influential parameter for the incorporation of Al into the SBA-15 structure. The formation of the SBA-15 structure was observed through the direct synthesis method. However, aluminum is not present in the material. The increase in pH contributed to the formation of a disorganized material. By EDX, it was observed that synthesis with a Si/Al = 5 ratio and pH approximately 4 provides materials containing aluminum. When the amount of aluminum during the synthesis is lower, a pH of approximately 8 is required to incorporate aluminum into the final material. The Al-NMR analysis showed that it was possible to insert aluminum in the structure of SBA-15, but with the presence of aluminum hexa and pentacoordinated. In the catalytic test of the dehydration reaction of ethanol, the samples with higher aluminum contents showed better catalytic performance due to its higher acidity.

The NaOH/metakaolin ratio and crystallization time were studied for the synthesis of zeolite NaA from a sample of kaolin from a Capim mine. The tests were carried out by using statistical design with axial points and replication of the central point. The samples obtained were characterized by X-ray diffraction (DRX), scanning electron microscopy and chemical analysis using a microprobe EPMA. The results showed that there is a relationship between the amount of NaOH added and crystallization time. The tests carried out using the lowest NaOH/metakaolin ratio (0.5) and the shortest time (4 h) produced a non-crystalline material. On the other hand, increasing the NaOH/metakaolin ratio and the crystallization time led to the formation of a NaA phase with a high structural level, but with the presence of a sodalite phase as an impurity.

In this work, the synthesis of zeolites using 1-butyl-3-methylimidazolium chloride [C4MI]Cl as a structure-directing agent was investigated. The organic cation shows effectiveness and selectivity for the syntheses of TON zeolites under different reaction conditions compared to the traditional structure-directing agent, 1,8-diaminooctane. The 1-butyl-3-methylimidazolium cation lead to highly crystalline materials and its role as OSDA in our synthesis conditions has been confirmed by characterization techniques. ICP-OES confirms the presence of Al in the samples and 27Al MAS NMR analysis indicated that aluminum atoms were incorporated in tetrahedral coordination. Scanning electron microscopy indicated that changing the crystallization condition (static or stirring), zeolites with different crystal size were obtained, which consequently affects the textural properties of the zeolites. Moreover, varying some synthesis parameters MFI zeolite can also be obtained.

Zeolite A was synthesized using the coal ash from Siderópolis/RS - Brazil. The synthesis was based on a standard IZA synthesis using coal ash as the Si and Al source. XRF analysis showed that the coal ash has a Si/Al ratio of 1.52, which is close to the Si/Al ratio required to produce zeolite A (1.0). The synthesized materials were analyzed by XRD, SEM and N2 adsorption. More crystalline materials were obtained during synthesis when an additional treatment was applied at a temperature of 353 K at the dissolution of NaOH step. The product formed after 4 hours was the most crystalline, but even the product formed after 1 hour proved to be better than that formed using the standard 4 hours IZA synthesis. The zeolites synthesized by this method had an adsorption capacity of 120 mg.g-1 for Ca2+, half the capacity of commercial zeolite A (300 mg.g-1). It was not possible to obtain blue or green pigments using the synthesized zeolite A.

Montmorillonite clay from Brazil was pillared with aluminium polyhydroxications. The influence of aging of the pillaring solution and the concentration of the clay suspension on the properties of the prepared materials was studied. The materials were characterized by chemical analysis, XRD and pore analysis by N2 adsorption. The catalytic properties were evaluated in the cumene cracking reaction. Results showed that the pillarization process increases the basal spaces of natural clay from 9.7 to 18.5 Å and the surface area from 41 to 300 m²/g.

This work presents a proposal for the management of residues from teaching laboratories. The main goals of the proposal are: scale reduction of experiments, reuse of residues as raw materials for new experiments and appropriate treatment and storage of residues. The methodology includes standardized labels for residue classification and registration of experimental classes and their residues in files. The management seemed to be efficient, resulting in a reduction of the amount of reagents utilized and residues generated, and an increase of reutilization of residues. A considerable decrease of needed storage space and suitable methods for correct residue disposal were achieved. We expect that all laboratories, including those exclusively for research activities, become involved, in a near future, in the Residue Management Project of URI - Campus Erechim.

Direct decomposition of NO on copper supported on zeolite catalysts such as MCM-22 and Beta was compared with that on the thoroughly studied Cu-ZSM-5. The catalysts were prepared by ion-exchange in basic media. They were characterized by atomic absorption, surface area, nitrogen adsorption at 77K, X-ray diffraction and temperature programmed reduction. The products of the reaction were analyzed by Fourier transform infrared spectroscopy using a gas cell. Catalytic activity tests indicated that zeolite catalysts, like Beta and MCM-22, lead to NO conversion values comparable to ZSM-5.