Use este identificador para citar ou linkar para este item: http://www.repositorio.ufop.br/jspui/handle/123456789/17834
Título: A hybrid molecularly imprinted polymer for selective adsorption of urinary S-Phenylmercapturic Acid.
Autor(es): Gomes, Rafaela de Paiva
Tonucci, Marina Caldeira
Prete, Maiyara Carolyne
Tarley, César Ricardo Teixeira
Baeta, Bruno Eduardo Lobo
Afonso, Robson José de Cássia Franco
Palavras-chave: Benzene
S-phenylmercapturic acid
Hybrid molecular imprinted polymer
4-vinylpyridine
Tetraethyl orthosilicate
Data do documento: 2023
Referência: GOMES, R. P. et al. A hybrid molecularly imprinted polymer for selective adsorption of urinary S-Phenylmercapturic Acid. Journal of the Brazilian Chemical Society, v. 34, n. 8, p. 1197-1207, 2023. Disponível em: <https://www.scielo.br/j/jbchs/a/g7jWWKYz8WqrkMgfMVD9ZZh/>. Acesso em: 01 ago. 2023.
Resumo: A hybrid molecular imprinted polymer (HMIP) obtained by the organic monomer 4-vinylpyridine (4-VP) and the inorganic precursor tetraethyl orthosilicate (TEOS) was synthesized for the selective extraction of urinary S-phenylmercapturic acid (u-SPMA), a biomarker of benzene exposure. The chemical and structural characterization of the synthetic adsorbent was performed by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and textural analysis employing N2 adsorption-desorption isotherms. Selective and adsorptive performance of the imprinted polymers were evaluated by kinetic, isothermal, thermodynamic, and selectivity studies. The kinetic data were well adjusted to pseudo-second order and intraparticle diffusion models, leading to selectivity coefficient (K) value of 0.03 g mg-1 min-1 for HMIP. In addition, the adsorption isotherms were better described by the Sip model achieving a maximum adsorption capacity of 284.81 μg g-1 (at 288.15 K).
URI: http://www.repositorio.ufop.br/jspui/handle/123456789/17834
DOI: https://doi.org/10.21577/0103-5053.20230032
ISSN: 1678-4790
Licença: This is an open-access article distributed under the terms of the Creative Commons Attribution License. Fonte: PDF do artigo.
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