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Adsorption of red azo dyes on multi-walled carbon nanotubes and activated carbon: A thermodynamic study.

Authors :
Ferreira, Guilherme Max Dias
Ferreira, Gabriel Max Dias
Hespanhol, Maria C.
de Paula Rezende, Jaqueline
dos Santos Pires, Ana Clarissa
Gurgel, Leandro Vinícius Alves
da Silva, Luis Henrique Mendes
Source :
Colloids & Surfaces A: Physicochemical & Engineering Aspects. Sep2017, Vol. 529, p531-540. 10p.
Publication Year :
2017

Abstract

Carbonaceous materials have been extensively studied as highly efficient adsorbents for the removal of dyes from wastewater. However, investigations of thermodynamic aspects of the interactions between these materials and dyes remain scarce. This paper describes the thermodynamics of the interactions between the Ponceau 4R (PR), Congo Red (CR), and Allura Red (AR) dyes and multi-walled carbon nanotubes (MWCNTs). The interactions between the dyes and activated carbon (AC) were also evaluated for comparison. The investigation used a combination of adsorption isotherms and isothermal titration nanocalorimetry (ITC) measurements, and a thermodynamic approach provided full characterization of the adsorption process. For both MWCNT and AC, the amount of adsorbed dye ( Γ D ) increased in the order Γ D (PR) < Γ D (AR) < Γ D (CR), and the adsorption capacity normalized by the adsorbent specific area was up to 5.6 times higher for MWCNT. The maximum amount adsorbed ( Γ D,max ) reached values of up to 2.00 μmol m −2 for CR adsorption on MWCNT. For both adsorbents, the process of dye adsorption was enthalpically driven and entropically unfavorable. All the thermodynamic parameters depended on the surface coverage and the structures of both dye and adsorbent. The adsorption enthalpy change (Δ ads H ) and entropy change (TΔ ads S ref ) values were higher than −137.0 kJ mol −1 and −114.2 kJ mol −1 , respectively. In addition to the structural differences between MWCNT and AC, the ITC data suggested that the adsorption sites are heterogeneous and that the dyes preferentially adsorb on the more hydrophilic sites on the adsorbent surfaces. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09277757
Volume :
529
Database :
Academic Search Index
Journal :
Colloids & Surfaces A: Physicochemical & Engineering Aspects
Publication Type :
Academic Journal
Accession number :
124472189
Full Text :
https://doi.org/10.1016/j.colsurfa.2017.06.021