RESUMO

The importance of the textural and physicochemical characteristics upon the adsorption capacity of the commercial activated carbons (ACs) Coconut, Wood, Merck, Darco, and Norit towards ronidazole (RNZ) and diclofenac (DCF) from water solution was investigated thoroughly in this work. At pH = 7, Coconut AC and Wood AC presented the highest adsorption capacity towards RNZ (444 mg/g) and DCF (405 mg/g). The maximum mass of RNZ adsorbed onto Coconut AC was higher in this study than those outlined previously in other works. Besides, the maximum capacity of Wood AC for adsorbing DCF was comparable to those found for other ACs. The adsorption capacity of all the ACs was increased by surface area and was favored by incrementing the acidic site concentration. The π-π stacking interactions were the predominant adsorption mechanism for the RNZ and DCF adsorption on ACs, and the acidic sites favored the adsorption capacity by activating the π-π stacking. Electrostatic interactions did not influence the adsorption of RNZ on Coconut AC, but electrostatic repulsion decreased that of DCF on Wood AC. The adsorption of DCF on Wood AC was reversible but not that of RNZ on Coconut AC. Besides, the adsorption of RNZ and DCF on the Coconut and Wood ACs was endothermic in the range of 15-25 °C.

Assuntos

Carvão Vegetal , Poluentes Químicos da Água , Carvão Vegetal/química , Ronidazole , Diclofenaco/química , Adsorção , Água/química , Poluentes Químicos da Água/química , Concentração de Íons de Hidrogênio , Cinética

RESUMO

The effect of surface chemistry and morphology of carbon nanotubes (CNTs) on their adsorption capacity towards dimetridazole (DTZ) and metronidazole (MNZ) antibiotics from water solutions was investigated in this work. The CNTs studied were single-walled carbon nanotubes (SWCNTs), CNTs doped with nitrogen (N-CNTs), multiwalled CNTs (MWCNTs), and MWCNTs functionalized with carboxylic groups (MWCNT-COOH). The experimental adsorption equilibrium data were best interpreted with the Redlich-Peterson (R-P) isotherm model. At T of 25 °C and pH of 7, the capacities of adsorption decreased as follows: SWCNT > MWCNT > N-CNT ≈ MWCNT-COOH, and the maximum capacities of SWCNT towards MNZ and DTZ were 101 mg/g and 84 mg/g, correspondingly. The SWCNT had the highest adsorption capacity because SWCNT presented the largest surface area, and was the only nanomaterial with a basic surface. The adsorption of both antibiotics on the CNTs was predominantly ascribed to the π-π stacking. The basic groups promoted the π-π stacking interactions and favored the adsorption capacity towards MNZ and DTZ. The capacity of SWCNT for adsorbing MNZ was lessening substantially by reducing the pH from 11 to 2, and the electrostatic interactions caused this trend. The Sheindorf-Rebuhn-Sheintuch adsorption model interpreted the data for the competitive adsorption of DTZ and MNZ on SWCNT adequately.

Assuntos

Metronidazol , Nanotubos de Carbono , Adsorção , Antibacterianos , Dimetridazol

RESUMO

The competitive sorption of the antibiotics sulfamethoxazole (SMX) and trimethoprim (TMP) and SMX-Cd(II) on a hybrid clay nanosorbent (NanoSorb) was investigated in detail in this work. NanoSorb was synthesized by sorbing a surfactant on bentonite. Besides, the sorption of SMX on the NanoSorb was confirmed by FTIR analysis, and SMX was mainly sorbed on NanoSorb by a partition mechanism due to hydrophobic interactions. Otherwise, the single adsorption of Cd(II) and TMP onto NanoSorb were due to electrostatic interaction and hydrophobic partition, respectively. The capacity of NanoSorb for sorbing single SMX was very similar to that for single Cd(II), but more than 10 times higher than that for single TMP. The competitive sorption of SMX-TMP was antagonistic because the sorption of one antibiotic on NanoSorb was decreased by the presence of the other antibiotic. The uptake of SMX was reduced up to 43.4% by the presence of TMP, whereas the presence of SMX decreased the uptake of TMP up to 29.6%. The non-modified Langmuir multicomponent isotherm (NLMI) interpreted quite well the experimental competitive sorption data of SMX-TMP. On the other hand, the competitive sorption of SMX-Cd(II) on NanoSorb revealed that the sorption of SMX was non-interactive because it was not influenced by the presence of Cd(II). Whereas, the sorption of Cd(II) was synergistic or cooperative since the uptake of Cd(II) sorbed increased considerably with the uptake of SMX sorbed on NanoSorb. The two-site Langmuir model fitted the experimental competitive sorption data of Cd(II) on NanoSorb saturated with SMX. The application of this isotherm was based on the fact that Cd(II) sorbed on two types of sites: a) cationic sites of the NanoSorb and b) Pi-cation interactions between the aromatic ring of the SMX sorbed on NanoSorb and Cd2+.