Owing to the enormous threat from anthropogenic contamination in water resources, the effective control of heavy-metal pollution has become increasingly important. In this study, the combination of permanent magnetic anion exchange resin (MAER) and magnetic cation exchange resin (MCER) was employed to efficient removal of Cu(II) and citrate acid (CA). The removal mechanisms were systematically investigated by batch adsorption experiments, and also certificated by species distribution calculation, kinetic tests and solid-phase characterizations. The presence of CA markedly inhibited the adsorption of Cu(II) onto MCER, while the co-existing Cu(II) was beneficial for CA uptake onto MAER. With the increase of Cu(II) concentrations, the adsorption amount of CA onto MAER gradually increased and reached a plateau, with promotion rates ranging of 24.4%-47.9%. For combined magnetic resins treatment, as the MAER dosage increased from 0 to 1.50 g/L, the removal efficiencies of CA and Cu(II) were enhanced from 1.1% and 33.2% to 98.8% and 99.1%, respectively. The anionic [Cu-CA] complexes (mainly CuL-and a small fraction of Cu2L22-) in bi-solutes system possessed higher affinity than free-CA species towards MAER, resulting in a mutual enhancement of Cu(II) and CA uptake. Both decomplexing-adsorption of Cu(II) from neutral Cu species (CuHL0) by MCER and direct complex-adsorption of anionic complex species (CuL-and Cu2L22-) by MAER were proposed as the mechanisms for synergetic removal of CA and Cu(II) in combined processes. Furthermore, nanoscale Cu powders were recovered from the desorption liquid by chemical reduction. The combined magnetic resins exhibited superior reusability over five repeated cycles, indicating their great potential in treatment of complexing heavy metal-organic acid wastewaters.