Abdel Salam Mohamed, Mokhtar Mohamed, Albukhari Soha M, Baamer Doaa F, Palmisano Leonardo, Jaremko Mariusz, Abukhadra Mostafa R
Department of Chemistry, Faculty of Science, King Abdulaziz University, P.O. Box 80200, Jeddah 21589, Saudi Arabia.
Schiavello-Grillone Photocatalysis Group, Dipartimento di Ingegneria, Università degli Studi di Palermo, Viale delle Scienze (Ed. 6), 90128 Palermo, Italy.
Polymers (Basel). 2022 Jun 9;14(12):2329. doi: 10.3390/polym14122329.
A green ZnO@polynaniline/bentonite composite (G.Zn@PN/BE) was synthesized as an enhanced adsorbent for As (V) ions. Its adsorption properties were assessed in comparison with the integrated components of bentonite (BE) and polyaniline/bentonite (PN/BE) composites. The G.Zn@PN/BE composite achieved an As (V) retention capacity (213 mg/g) higher than BE (72.7 mg/g) and PN/BE (119.8 mg/g). The enhanced capacity of G.Zn@PN/BE was studied using classic (Langmuir) and advanced equilibrium (monolayer model of one energy) models. Considering the steric properties, the structure of G.Zn@PN/BE demonstrated a higher density of active sites (Nm = 109.8 (20 °C), 108.9 (30 °C), and 67.8 mg/g (40 °C)) than BE and PN/BE. This declared the effect of the integration process in inducing the retention capacity by increasing the quantities of the active sites. The number of adsorbed As (V) ions per site (1.76 up to 2.13) signifies the retention of two or three ions per site by a multi-ionic mechanism. The adsorption energies (from -3.07 to -3.26 kJ/mol) suggested physical retention mechanisms (hydrogen bonding and dipole bonding forces). The adsorption energy, internal energy, and free enthalpy reflected the exothermic, feasible, and spontaneous nature of the retention process. The structure is of significant As (V) uptake capacity in the existence of competitive anions or metal ions.
合成了一种绿色的ZnO@聚苯胺/膨润土复合材料(G.Zn@PN/BE)作为吸附As(V)离子的增强吸附剂。与膨润土(BE)和聚苯胺/膨润土(PN/BE)复合材料的组成成分相比,评估了其吸附性能。G.Zn@PN/BE复合材料的As(V)保留容量(213 mg/g)高于BE(72.7 mg/g)和PN/BE(119.8 mg/g)。使用经典(Langmuir)模型和高级平衡(单能量单层模型)对G.Zn@PN/BE增强的容量进行了研究。考虑到空间特性,G.Zn@PN/BE的结构显示出比BE和PN/BE更高的活性位点密度(Nm = 109.8(20℃)、108.9(30℃)和67.8 mg/g(40℃))。这表明整合过程通过增加活性位点数量对保留容量产生影响。每个位点吸附的As(V)离子数量(1.76至2.13)表明通过多离子机制每个位点保留两到三个离子。吸附能(-3.07至-3.26 kJ/mol)表明为物理保留机制(氢键和偶极键力)。吸附能、内能和自由焓反映了保留过程的放热、可行和自发性质。该结构在存在竞争性阴离子或金属离子的情况下具有显著的As(V)吸收能力。