Department of Civil and Environmental Engineering, University of Ulsan, Ulsan, 44610, South Korea.
Environ Sci Pollut Res Int. 2018 Aug;25(22):21901-21914. doi: 10.1007/s11356-018-2297-3. Epub 2018 May 23.
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.
1H-苯并[d]咪唑(BMA)已被认为是一种新兴的药物有机污染物,导致废水中 BMA 的检测不断增加,需要从生态系统中去除。本研究采用新型三元交联纳米杂化[γ-APTES]-FeO@PAN@rGO 对 BMA 进行了高效协同化学吸附。磁性纳米颗粒(FeO)与聚丙烯腈聚合物(PAN)原位共沉淀形成核壳结构。然后,将制备的 FeO@PAN 修饰在γ-氨丙基三乙氧基硅烷([γ-APTES])框架内的还原氧化石墨烯(rGO)的六方阵列中。最终的纳米杂化[γ-APTES]-FeO@PAN@rGO 产生了相邻的干涉条纹间距为 0.2-0.4nm,与(111)、(220)和(311)平行亚晶格对应良好,两个斜交在 90°直角和 60°三角形处相交。BMA 的吸附在中性 pH7 下是有利的,引起温度(50°C)升高,并受吸热过程控制。鉴定的最大吸附容量为 221.73mg g,比报道的吸附剂高 30%。吸附机制包括离子交换、氢键、偶极-偶极相互作用、π-共轭、静电和疏水相互作用。