The main objective of this study is to prepare and characterize two functionalizated carbon materials with enhanced adsorptive properties for Cu(II). Thus, two novel hybrid materials have been prepared by a non-covalent functionalization method based on the adsorption of a pyrimidine-desferrioxamine-B conjugate compound (H4L) on two activated carbons, ACs (labelled Merck and F). The adsorption of H4L on the ACs is pH-dependent and highly irreversible. This is due to strong pi-pi interactions between the arene centers of the ACs and the pyrimidine moiety of H4L. The textural characterization of the AC/H4L hybrids shows large decreases of their surface areas. Thus the values of Merck and F are 1031 and 1426 m(2)/g respectively, while these of Merck/H4L and F/H4L hybrids are 200 and 322 m(2)/g. An important decrease in the micropore volumes is also found, due to the blockage of narrow porosity produced by the adsorption of H4L molecules. The ACs/H4L hybrids show larger adsorption capacities for Cu(II) (0.105(4) and 0.13(2) mmol/g, at pH 2.0, and 0.20(3) and 0.242(9) mmol/g, at pH 5.5, for Merck/H4L and F/H4L, respectively) than those of the ACs (0.024(6) and 0.096(9) mmol/g, at pH 2.0, and 0.10(2) and 0.177(8) mmol/g, at pH 5.5, for Merck and F respectively), which is explained on the basis of the complexing ability of the trihydroxamic acid functions. The desorption of Cu(II) from the ACs/H4L/Cu(II) materials in acid solution allows the regeneration of most active sites (78.5% in the case of Merck/H4L/Cu(II) and 83.0% in the case of F/H4L/Cu(II)). (C) 2016 Elsevier B.V. All rights reserved.