1H-Benzo[d]imidazole (BMA) has been considered as an emerging pharmaceutical organic contaminant, leading to the increasing BMA detection in wastewaters and need to be removed from ecosystem. This study investigated a highly synergistic BMA chemisorption using a novel ternary cross-coupled nanohybrid [γ-APTES]-FeO@PAN@rGO. Magnetic nanoparticles (FeO) were in situ core-shell co-precipitated with polyacrylonitrile polymer (PAN). Then, the prepared FeO@PAN was decorated on hexagonal arrays of reduced graphene oxide (rGO) inside the framework of γ-aminopropyltriethoxysilane ([γ-APTES]). The final nanohybrid [γ-APTES]-FeO@PAN@rGO produced adjacent inter-fringe distances of 0.2-0.4 nm corresponded well to (111), (220), and (311) parallel sub-lattices with two oblique intersections at 90° right angle and 60° triangle. The BMA adsorption was favorable in neutral pH 7, aroused temperature (50 °C), and controlled by endothermic process. The identified maximum adsorption capacity of 221.73 mg g was 30% higher than the reported adsorbents. The adsorption mechanisms include ion exchange, hydrogen bond, dipole-dipole force, π-conjugation, electrostatic, and hydrophobic interaction. Graphical abstract The synthetic route of novel nanohybrid [γ-APTES]-FeO@PAN@rGO was investigated. After BMA adsorption, the adsorbent surface was entirely changed, thus an efficiently facile magnetic separation within 8s. [γ-APTES]-FeO@PAN@rGO formed different oblique intersections of 60° and 90° sub-lattices.
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