LEANDRO GOULART DE ARAUJO
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Artigo IPEN-doc 29048 Uranium biosorption by hydroxyapatite and bone meal2022 - WATANABE, TAMIRES; GUILHEN, SABINE N.; MARUMO, JULIO T.; SOUZA, RODRIGO P. de; ARAUJO, LEANDRO G. deBiosorption has been examined for the treatment of aqueous solutions containing uranium, a radiotoxic pollutant. Nevertheless, the evaluation of the role of process variables by experimental design on the use of hydroxyapatite and bone meal as biosorbents for uranium has not yet been previously addressed. In this study, the effects of adsorbent dosage (M), initial uranium concentrations ([U]0), and solution pH were investigated, using a two-level factorial design and response surface analysis. The experiments were performed in batch, with [U]0 of 100 and 500 mg L−1, pH 3 and 5, and adsorbent/uranium solution ratios of 5 and 15 g L−1. Contact time was fixed at 24 h. Removal rates were higher than 88%, with a maximum of 99% in optimized conditions. [U]0 and M were found to be the most influential variables in U removal in terms of adsorption capacity (q). The experiments revealed that bone meal holds higher adsorption capacity (49.87 mg g−1) and achieved the highest uranium removal (~ 100%) when compared to hydroxyapatite (q = 49.20 mg g−1, removal = 98.5%). The highest value of q for both biomaterials was obtained for [U]0 = 500 mg L−1, pH 3, and M = 5 g L−1. Concerning the removal percentage, bone meal achieved the best performance for [U]0 = 500 mg L−1, pH 3, and M = 15 g L−1. Further experiments were made with real radioactive waste, resulting in a high uranium adsorption capacity for both materials, with 22.11 mg g−1 for hydroxyapatite and 22.08 mg g−1 for bone meal, achieving uranium removal efficiencies higher than 99%.Artigo IPEN-doc 28879 Biosorption of uranium from aqueous solutions by Azolla sp. and Limnobium laevigatum2022 - ARAUJO, LEANDRO G. de; VIEIRA, LUDMILA C.; CANEVESI, RAFAEL L.S.; SILVA, EDSON A. da; WATANABE, TAMIRES; FERREIRA, RAFAEL V. de P.; MARUMO, JULIO T.The main goal of this study was to assess alternatives to the current challenges on environmental quality and circular economy. The former is here addressed by the treatment of radioactively contaminated solutions, and the latter by using abundant and low-cost biomass. In this paper, we examine the biosorption of hexavalent uranium (U(VI)) in a batch system using the macrophytes Limnobium laevigatum and Azolla sp. by three operational parameters: biomass dose, metal ion concentration, and contact time. Simulated solutions were firstly addressed with two biomasses, followed by studies with real liquid organic radioactive waste (LORW) with Azolla sp. The batch experiments were carried out by mixing 0.20 g biomass in 10 mL of the prepared solution or LORW. The total contact time employed for the determination of the equilibrium times was 240 min, and the initial U(VI) concentration was 0.63 mmol L−1. The equilibrium times were 15 min for L. laevigatum and 30 min for Azolla sp. respectively. A wide range of initial U(VI) concentrations (0.25–36 mmol L−1) was then used to assess the adsorption capacity of each macrophyte. Isotherm models validated the adsorption performance of the biosorption process. Azolla sp. presented a much higher U(VI) uptake (0.474 mmol g−1) compared to L. laevigatum (0.026 mmol g−1). When in contact with LORW, Azolla sp. removed much less uranium, indicating an adsorption capacity of 0.010 mmol g−1. In conclusion, both biomasses, especially Azolla sp., can be used in the treatment of uranium-contaminated solutions.Artigo IPEN-doc 27250 Synthesis and physicochemical characterization of a novel adsorbent based on yttrium silicate2020 - 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.Artigo IPEN-doc 27144 Physicochemical modifications of radioactive oil sludge by ozone treatment2020 - ARAUJO, LEANDRO G. de; PRADO, EDUARDO S.P.; MIRANDA, FELIPE de S.; VICENTE, ROBERTO; SILVA SOBRINHO, ARGEMIRO S. da; PETRACONI FILHO, GILBERTO; MARUMO, JULIO T.An experimental study on the degradation of organic compounds from radioactive oil sludge by the ozonation process is presented. The effects of different concentrations of ozone in the oil sludge degradation over time were investigated. The experiments were performed in a 0.125 L glass reactor with magnetic stirring and a diffuser plate at the bottom to feed the ozone. The ozone concentration varied from 13 to 53 mg L−1 and the total interaction time was 1 h. To investigate the physicochemical properties of the oil sludge (solid and liquid components) prior to and after the treatment, multiple analytical characterization methods were used: Thermal Gravimetric Analysis, X-ray diffraction, Scanning Electron Microscopy coupled with Energy-Dispersive X-ray Spectroscopy, Fourier Transform Infrared spectroscopy, Spectrophotometer, and Residual Gas Analyzer. The most perceptive change is in the color of the liquid medium turned from dark brown to light yellow, especially under ozone concentrations higher than 33 mg L−1. Absorbance values decreased about 3.5 times after 30 min of treatment with [O3] =53 mg L−1. FTIR spectroscopy showed that the bands associated with the CH3 and CeH in CH2 disappeared during treatment. On the other hand, a greater presence of C]C aromatics was observed. By residual gas analysis, various organic and inorganic gases were identified during the treatment, such as CH4, H2, CO2, and H2S. Finally, the ozonation of the oil sludge proved to be effective, due to its high reaction capacity.