A novel peroxo-functionalized Ti3C2Tx adsorbent with abundant surface termination groups was facilely prepared in situ to remove aqueous anionic and cationic dyes. The adsorption behavior of methylene blue on peroxo-functionalized Ti3C2Tx was systematically investigated by adsorption kinetics, isotherms, and thermodynamics. Compared with Ti3C2Tx, the adsorption capacities of peroxo-functionalized Ti3C2Tx for cationic dyes methylene blue (558.0 mg g-1), rhodamine B (524.6 mg g-1) and anionic dyes methyl orange (292.6 mg g-1), congo red (258.2 mg g-1) were increased at room temperature without adjustment of pH, background ions and humic acid, etc of the contaminant solution by 7.9, 5.3, 5.9 and 4.6 times, respectively. In addition, peroxo-functionalized Ti3C2Tx could well tolerate the effects of pH, ionic strength, and humic acid. As revealed by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy, the adsorption mechanism of peroxo-functionalized Ti3C2Tx for anionic and cationic dyes was mainly attributed to the electrostatic interaction, hydrogen bonding interaction, and noncovalent surface-π attraction interaction. This study demonstrates a facile modification strategy for Ti3C2Tx adsorbent materials and aims to provide insights for the development of excellent Ti3C2Tx-based adsorbent materials.
Keywords: Adsorption mechanism; Dyes; Oxygen-containing terminal groups; Peroxo-functionalized Ti(3)C(2)T(x); Ti(3)C(2)T(x).
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