LEANDRO GOULART DE ARAUJO

LEANDRO GOULART DE ARAUJO

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TiO2 P25 and Kronos vlp 7000 materials activated by simulated solar light for atrazine degradation
2023 - MOYA, MURILO T.M.; ARAUJO, LEANDRO G. de; LOPES, FERNANDO S.; TEIXEIRA, ANTONIO C.S.C.
Photocatalysis-based technologies have been proposed for the treatment of wastewater containing atrazine (ATZ), a persistent and recalcitrant pollutant. This study aims to evaluate and compare the efficiency of TiO2 P25 and TiO2 modified with carbon (C–TiO2 Kronos vlp 7000) in the photocatalytic degradation of ATZ in aqueous systems. The experiments were performed in a tubular photochemical reactor equipped with a compound parabolic collector (CPC) irradiated by simulated solar light. The materials were characterized by X-ray diffraction, infrared spectroscopy, BET specific surface area, and diffuse reflectance spectroscopy. For TiO2 P25, ATZ removals varied in the range 86–100 % after 120 min of irradiation, although the total organic carbon (TOC) analyses indicated that no significant ATZ mineralization occurred (<20 %). C–TiO2 Kronos vlp 7000, on the other hand, was not able to completely remove ATZ after 120 min of irradiation. In this case, pesticide removals were 37–45 % over 120 min, while C–TiO2 performed better with regard to ATZ mineralization, with 38 % TOC removal. Given the low mineralization of atrazine, the intermediate compounds formed were identified for each photocatalytic material.
An adsorption agent based on chitosan–zeolite composite
2023 - ARAUJO, LEANDRO G. de; MEDEIROS, VINICIUS L.; GUARNIERI, GUILHERME de P.; SILVA, DANILO A. da; WATANABE, TAMIRES; MARUMO, JULIO T.; NERY, JOSE G.
In this article, we present a chitosan–zeolite composite, which was synthesized and used as an adsorbent material for caesium (Cs) removal from aqueous media and real liquid radioactive organic waste (LROW). The compound was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy techniques. The physicochemical characterization indicates the production of a composite. Adsorption experiments were first performed using the prepared solutions contaminated with Cs using full factorial design with two variables of interest: initial Cs concentration (Cs0) and adsorbent dosage (mg L−1 ). The results indicated a high caesium removal rate with removal values above 93% and adsorption capacity of up to 10 mg g−1 . With the best experimental conditions according to our experimental domain, time was evaluated and equilibrium was reached in 180 min. Finally, the adsorbent material was tested as an adsorbent for Cs, Am, and U from LROW. When in contact with LORW, the removal rates (%) were 21.51 (137Cs), 26.39 (241Am), and 20.26 (U (total)). Although lower, this material indicated that it has the potential to be used for multi-elemental adsorption.
Physicochemical modifications and decolorization of textile wastewater by ozonation
2023 - PRADO, E.S.P.; MIRANDA, F.S.; ARAUJO, L.G. de; FERNANDES, G.L.; PEREIRA, A.L.J.; GOMES, M.C.; SILVA SOBRINHO, A.S. da; BALDAN, M.R.; PETRACONI, G.
This is an experimental study on the decolorization efficiency and the degradation of organic compounds from textile wastewater by the ozonation process in a batch system. The effects of different sample volumes of textile wastewater over time were investigated. The experiments were performed in a 1 L glass reactor with a magnetic stirrer and a bubble diffuser at the bottom to feed the ozone. The applied cumulative ozone dosage varied at 120 gO3 L−1, 60 gO3 L−1, and 30 gO3 L−1, and the total interaction time for each test was 1 h. To investigate the physicochemical properties of the textile wastewater (solid and liquid phases) before and after the treatment, multiple analytical characterization methods were used: Thermal Gravimetric Analysis, Scanning Electron Microscopy coupled with Energy-Dispersive X-ray Spectroscopy, X-ray diffraction, Fourier Transform Infrared spectroscopy, and Spectrophotometer. The most perceptive change was observed in the color of the liquid medium, which turned from black to transparent, and a visual color number indicator known as DurchsichtFarbZahl (DFZ) was used for the evaluation of this process. Absorbance values decreased about 3.5 times after 5 min of treatment with a 0.15 L sample volume, and these values differed for tests with larger sample volumes. FTIR spectroscopy demonstrated that the bands’ intensities associated with the C − H, C − N, and C − O decrease during treatment. On the other hand, it was possible to conclude that combining treatment methods to improve the degradation of persistent compounds after the ozonation process is necessary. Finally, the ozonation of the textile wastewater proved to be effective at removing color due to its high reaction capacity.
Experimental study on treatment of simulated radioactive waste by thermal plasma
2021 - PRADO, E.S.P.; MIRANDA, F.S.; ARAUJO, L.G.; PETRACONI, G.; BALDAN, M.R.; ESSIPTCHOUK, A.; POTIENS JUNIOR, A.J.
Thermal plasma technology is a process that demonstrates high performance for the processing of different types of waste. This technology can also be applied in the treatment of radioactive wastes, which requires special care. Beyond that, volumetric reduction, inertization, as well as a cheap and efficient process are necessary. In this context, the purpose of this paper is to demonstrate the application of thermal plasma technology for the treatment of solid radioactive waste. For this, stable Co and Cs were used to simulate compactable and non-compactable radioactive waste; about 0.8 g Co and 0.6 g Cs were added in each experimental test. The experimental tests were conducted using plasma of transferred arc electric discharge generated by the graphite electrode inside the process reactor. The behavior and distribution of the radionuclides present in the waste were assessed during the plasma process. The results show that the significant amounts of Co and Cs leave the melt by volatilization and are transferred to the gas phase with a small portion retained in the molten slag. The retention rate of Co in the slag phase is about 0.03% and 0.30% for compactable and non-compactable waste, respectively. On the other hand, Cs is completely transferred to the gas phase when added to the compactable waste. Conversely, when in the non-compactable waste, only 1.4% Cs is retained.
Synthesis and physicochemical characterization of a novel adsorbent based on yttrium silicate
2020 - MEDEIROS, VINICIUS L.; ARAUJO, LEANDRO G. de; RATERO, DAVI R.; PAULA, ALEX S.; MOLINA, EDUARDO F.; JAEGER, CHRISTIAN; MARUMO, JULIO T.; NERY, JOSE G.
A new metallosilicate based on yttrium was synthesized and characterized by XRD, FT-IR, 29Si MAS-NMR, and 89Y MAS-NMR. The mixed framework of the material was confirmed by the detection of distinct chemical shift groups using 29Si MAS-NMR (at -82 to -87 ppm, -91 to -94 ppm, -96 to -102 ppm, and -105 to -108 ppm), as well as four distinct chemical shifts in the 89Y MAS-NMR spectrum (at -89, -142, -160, and -220 ppm). Adsorption and kinetic analyses indicated the potential of the new material for the removal of lead and cadmium from aqueous media. The adsorption results for lead indicated that dynamic equilibrium was reached after five hours, with total lead removal of around 94 %, while for cadmium it was reached in the first hour, with total cadmium removal of around 74 %. The adsorptions of lead and cadmium were modeled using pseudo-first order (PFO) and pseudo-second order (PSO) kinetic models. Although both models provided high R2 values (0.9903 and 0.9980, respectively), the PSO model presented a much lower χ2 red value (4.41×10−4), compared to the PFO model (2.12×10−3), which indicated that the rate-limiting step was probably due to the chemisorption of lead from the solution onto the yttrium-based metallosilicate.