SABINE NEUSATZ GUILHEN

Resumo

Possui graduação em Química com atribuições Tecnológicas e Biotecnológicas pelo Instituto de Química da Universidade de São Paulo (2005), mestrado (2009) e doutorado (2018) em Tecnologia Nuclear (Materiais) pelo Instituto de Pesquisas Energéticas e Nucleares (IPEN), Universidade de São Paulo. Tem experiência em Química Analítica com ênfase em Análise de Traços, atuando principalmente no desenvolvimento de métodos analíticos empregando técnicas espectrofotométricas (AAS, ICP OES e ICP-MS) para caracterização de amostras ambientais, arqueológicas, biológicas, forenses e nucleares. Atualmente, ocupa o cargo de Tecnologista em "Caracterização Química" no Centro de Química e Meio Ambiente (CQMA) do IPEN (CNEN/SP), onde desempenha atividades de pesquisa e desenvolvimento tecnológico em atendimento às demandas institucionais ligadas ao Ciclo do Combustível Nuclear e aos Programas de Pesquisa de caráter multidisciplinar, em apoio a projetos de Inovação Tecnológica e ao Programa de Pós-Graduação do IPEN/USP. Além disso, atua na geração de produtos tecnológicos e no desenvolvimento de materiais adsorventes de baixo custo e alto valor agregado visando o aproveitamento de materiais e resíduos naturais e/ou renováveis no tratamento de efluentes e rejeitos. (Texto extraído do Currículo Lattes em 4 maio 2023)

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  • Artigo IPEN-doc 27702
    Uranium removal from aqueous solution using macauba endocarp-derived biochar
    2021 - GUILHEN, SABINE N.; ROVANI, SUZIMARA; ARAUJO, LEANDRO G. de; TENORIO, JORGE A.S.; MASEK, ONDREJ
    The main aim of this study was to evaluate options for addressing two pressing challenges related to environmental quality and circular economy stemming from wastage or underutilization of abundant biomass residue resources and contamination of water by industrial effluents. In this study we focused on residues (endocarp) from Macaúba palm (Acrocomia aculeata) used for oil production, its conversion to activated biochar, and its potential use in uranium (U) removal from aqueous solutions. Batch adsorption experiments showed a much higher uranyl ions (U(VI)) removal efficiency of activated biochar compared to untreated biochar. As a result of activation, an increase in removal efficiency from 80.5% (untreated biochar) to 99.2% (after activation) was observed for a 5 mg L 1 initial U(VI) concentration solution adjusted to pH 3 using a 10 g L 1 adsorbent dosage. The BET surface area increased from 0.83 to 643 m2 g 1 with activation. Surface topography of the activated biochar showed a very characteristic morphology with high porosity. Activation significantly affected chemical surface of the biochar. FTIR analysis indicated that U(VI) was removed by physisorption from the aqueous solution. The adsorbed U(VI) was detected by micro X-ray fluorescence technique. Adsorption isotherms were employed to represent the results of the U adsorption onto the activated biochar. An estimation of the best fit was performed by calculating different deviation equations, also called error functions. The Redlich-Peterson isotherm model was the most appropriate for fitting the experimental data, suggesting heterogeneity of adsorption sites with different affinities for uranium setting up as a hybrid adsorption. These results demonstrated that physical activation significantly increases the adsorption capacity of macauba endocarp-derived biochar for uranium in aqueous solutions, and therefore open up a potential new application for this type of waste-derived biochar.