Vences-Alvarez Esmeralda, Chazaro-Ruiz Luis F, Rangel-Mendez J Rene
Environmental Sciences Division, Instituto Potosino de Investigación Científica y Tecnológica A. C., San Luis Potosí, S.L.P., 78216, Mexico.
Environmental Sciences Division, Instituto Potosino de Investigación Científica y Tecnológica A. C., San Luis Potosí, S.L.P., 78216, Mexico.
Chemosphere. 2022 Jun;297:134177. doi: 10.1016/j.chemosphere.2022.134177. Epub 2022 Mar 1.
Bimetallic oxy(hydroxides) have gain great interest in water treatment systems based on adsorption processes. Their high OH groups density, in addition to inheriting the oxides properties make them highly promising adsorbents of anions. In this work, highly affine and selective bimetallic oxyhydroxides of cerium and iron (Ce:Fe-P's) for arsenic(V) were synthesized by implementing an assisted microwave methodology. The Ce:Fe-P's were characterized by various techniques (SEM, FTIR, XRD and XPS) and the As(V) adsorption capacity and kinetics as well as the effect of pH and the presence of coexisting anions were determined. The results showed that Ce:Fe-P's have an outstanding As(V) adsorption capacity (179.8 mg g at C = 3 mg L) even at low concentrations (120 mg g at C = 37 μg L). Moreover, the adsorption equilibrium was reached very fast, just in 3 min, with an adsorption rate of 0.123 mg min, that is, 80% of the initial As(V) concentration of 5 mg L was removed in the first 3 min. The arsenic adsorption capacity decreased only up to 20% at pH above 7, attributed to electrostatic repulsions due to the adsorbent's pH, which was 6.8. On the other hand, the arsenic adsorption capacity of Ce:Fe-P's decreased just 21% in the presence of 10 mg L of each of the following competing anions: F, Cl, SO, NO, PO and CO, which usually coincide in contaminated water with As(V). Ce:Fe-P's has proven to be one of the most promising As(V) adsorbent materials reported so far in the literature, because it presented an outstanding adsorption capacity and at the same time a very fast adsorption speed. Furthermore, the pH and the concentration of coexisting anions caused little interference in the adsorption processes. Due to the above, the Ce:Fe-P's is already in the process of intellectual protection.
双金属羟基氧化物在基于吸附过程的水处理系统中引起了极大的关注。它们具有高OH基团密度,除继承氧化物的性质外,使其成为极具潜力的阴离子吸附剂。在本工作中,通过采用辅助微波方法合成了对砷(V)具有高度亲和性和选择性的铈铁双金属羟基氧化物(Ce:Fe-P's)。通过多种技术(扫描电子显微镜、傅里叶变换红外光谱、X射线衍射和X射线光电子能谱)对Ce:Fe-P's进行了表征,并测定了其对As(V)的吸附容量和动力学,以及pH值和共存阴离子的影响。结果表明,即使在低浓度下(C = 37 μg L时为120 mg g),Ce:Fe-P's仍具有出色的As(V)吸附容量(C = 3 mg L时为179.8 mg g)。此外,吸附平衡在3分钟内即可快速达到,吸附速率为0.123 mg min,即在最初3分钟内去除了初始浓度为5 mg L的As(V)的80%。在pH高于7时,砷吸附容量仅下降至20%,这归因于吸附剂pH值为6.8时的静电排斥作用。另一方面,在存在以下各10 mg L的竞争性阴离子(F、Cl、SO、NO、PO和CO,这些通常在受污染水中与As(V)共存)的情况下,Ce:Fe-P's的砷吸附容量仅下降21%。Ce:Fe-P's已被证明是迄今为止文献中报道的最有前景的As(V)吸附材料之一,因为它具有出色的吸附容量,同时吸附速度非常快。此外,pH值和共存阴离子的浓度对吸附过程的干扰很小。基于上述原因,Ce:Fe-P's已在进行知识产权保护。