The influence of the pore size distribution of activated carbon on the adsorption of phenol from aqueous solutions was explored. Activated carbons with different porous structures were prepared by gasifying a bituminous coal char to different extents of burn-off. The results of adsorption experiment
Adsorption of phenol onto activated carbons having different textural and surface properties
✍ Scribed by V. Fierro; V. Torné-Fernández; D. Montané; A. Celzard
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 193 KB
- Volume
- 111
- Category
- Article
- ISSN
- 1387-1811
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✦ Synopsis
Adsorption of phenol in aqueous phase onto activated carbons (ACs) having different textural and surface properties has been considered. Six types of ACs were used: three were commercial, and three were obtained from Kraft lignin chemically activated with sodium hydroxide, potassium hydroxide or ortho-phosphoric acid. The apparent surface areas of the commercial ACs varied from 620 to 1320 m 2 /g, while ACs made from lignin presented surface areas as high as 1300 m 2 /g and 2900 m 2 /g when prepared with H 3 PO 4 and alkaline hydroxides, respectively; moreover, the highest proportion of microporosity was found for ACs derived from lignin. A kinetic study was carried out, showing that the phenol adsorption data may be correctly adjusted, for all the ACs tested, by an equation corresponding to a pseudo second-order chemical reaction. Freundlich, Langmuir and Tempkin equations were tested for modelling the adsorption isotherms at equilibrium, and it was concluded that Langmuir model fitted adequately the experimental data. However, Tempkin model fitted even better the adsorption data obtained with ACs derived from lignin activated with alkaline hydroxides, which are characterized by the highest number of surface groups. Remarkably high phenol adsorption capacities were found for the ACs prepared by activation of Kraft lignin with NaOH and KOH: 238 and 213 mg/g of AC, respectively. Finally, the adsorption of phenol was found to depend not only on the micropore volume, but also on the total amount of carbonyl and basic groups and on the ratio of acid to basic groups.
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