Use este identificador para citar ou linkar para este item: https://locus.ufv.br//handle/123456789/19167
Tipo: Artigo
Título: Regular article synthesis and application of a new carboxylated cellulose derivative. Part I: Removal of Co 2+ , Cu 2+ and Ni 2+ from monocomponent spiked aqueous solution
Autor(es): Ferreira, Gabriel Max Dias
Teodoro, Filipe Simões
Ramos, Stela Nhandeyara do Carmo
Elias, Megg Madonyk Cota
Mageste, Aparecida Barbosa
Silva, Luis Henrique Mendes da
Gil, Laurent Frédéric
Gurgel, Leandro Vinícius Alves
Abstract: A new carboxylated cellulose derivative (CTA) was prepared from the esterification of cellulose with 1,2,4- Benzenetricarboxylic anhydride. CTA was characterized by percent weight gain (pwg), amount of carboxylic acid groups (nCOOH), elemental analysis, FTIR, TGA, solid-state ^13C NMR, X-ray diffraction (DRX), specific surface area, pore size distribution, SEM and EDX. The best CTA synthesis condition yielded a pwg and nCOOH of 94.5% and 6.81 mmol g^−1, respectively. CTA was used as an adsorbent material to remove Co^2+, Cu^2+ and Ni^2+ from monocomponent spiked aqueous solution. Adsorption studies were developed as a function of the solution pH, contact time and initial adsorbate concentration. Langmuir model better fitted the experimental adsorption data and the maximum adsorption capacities estimated by this model were 0.749, 1.487 and 1.001 mmol g−1 for Co^2+, Cu^2+ and Ni^2+, respectively. The adsorption mechanism was investigated by using isothermal titration calorimetry. The values of ΔadsH° were in the range from 5.36 to 8.09 kJ mol^−1, suggesting that the mechanism controlling the phenomenon is physisorption. Desorption and re-adsorption studies were also performed. Desorption and re-adsorption efficiencies were closer to 100%, allowing the recovery of both metal ions and CTA adsorbent.
Palavras-chave: Carboxylated cellulose
1,2,4-Benzenetricarboxylic anhydride
Adsorption
Desorption
Isothermal titration calorimetry
Thermodynamics
Editor: Journal of Colloid and Interface Science
Tipo de Acesso: Elsevier Inc
URI: https://doi.org/10.1016/j.jcis.2016.08.004
http://www.locus.ufv.br/handle/123456789/19167
Data do documento: 2-Ago-2016
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