Use este identificador para citar ou linkar para este item: https://locus.ufv.br//handle/123456789/19905
Tipo: Artigo
Título: Synthesis and application of a new carboxylated cellulose derivative. Part III: Removal of auramine-O and safranin-T from mono- and bi-component spiked aqueous solutions
Autor(es): Teodoro, Filipe Simões
Elias, Megg Madonyk Cota
Ferreira, Gabriel Max Dias
Adarme, Oscar Fernando Herrera
Savedra, Ranylson Marcello Leal
Siqueira, Melissa Fabíola
Silva, Luis Henrique Mendes da
Gil, Laurent Frédéric
Gurgel, Leandro Vinícius Alves
Abstract: In the third part of this series of studies, the adsorption of the basic textile dyes auramine-O (AO) and safranin-T (ST) on a carboxylated cellulose derivative (CTA) were evaluated in mono- and bi-component spiked aqueous solutions. Adsorption studies were developed as a function of solution pH, contact time, and initial dye concentration. Adsorption kinetic data were modeled by monocomponent kinetic models of pseudo-first- (PFO), pseudo-second-order (PSO), intraparticle diffusion, and Boyd, while the competitive kinetic model of Corsel was used to model bicomponent kinetic data. Monocomponent adsorption equilibrium data were modeled by the Langmuir, Sips, Fowler-Guggenhein, Hill de-Boer, and Konda models, while the IAST and RAST models were used to model bicomponent equilibrium data. Monocomponent maximum adsorption capacities for AO and ST at pH 4.5 were 2.841 and 3.691 mmol g−1, and at pH 7.0 were 5.443 and 4.074 mmol g−1, respectively. Bicomponent maximum adsorption capacities for AO and ST at pH 7.0 were 1.230 and 3.728 mmol g−1. Adsorption enthalpy changes (ΔadsH) were obtained using isothermal titration calorimetry. The values of ΔadsH ranged from −18.83 to −5.60 kJ mol−1, suggesting that physisorption controlled the adsorption process. Desorption and re-adsorption of CTA was also evaluated.
Palavras-chave: Adsorption
Auramine-O
Safranin-T
Desorption
Isothermal titration calorimetry
Thermodynamics
Molecular quantum mechanics
Editor: Journal of Colloid and Interface Science
Tipo de Acesso: Elsevier Inc.
URI: https://doi.org/10.1016/j.jcis.2017.10.083
http://www.locus.ufv.br/handle/123456789/19905
Data do documento: 25-Out-2017
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