Centro Universitario de los Lagos, Universidad de Guadalajara, Lagos de Moreno 47460, Jalisco, Mexico.
Department of Physical Chemistry and Materials Science, University of Szeged, Rerrich Béla tér 1, 6720 Szeged, Hungary.
Int J Environ Res Public Health. 2022 Mar 18;19(6):3640. doi: 10.3390/ijerph19063640.
Amino acid complexes of zirconia represent an entirely new class of materials that were synthesized and studied for the first time for the decontamination of fluoride ion containing aqueous solutions. Glutamic and aspartic acid complexes of zirconia assembled with thin carbon (stacked graphene oxide) platelets deriving from graphite oxide (GO) were synthesized by a two-step method to prepare adsorbents. The characterization of the complexes was carried out using infrared spectroscopy to determine the functional groups and the types of interaction between the composites and fluoride ions. To reveal the mechanisms and extent of adsorption, two types of batch adsorption measurements were performed: (i) varying equilibrium fluoride ion concentrations to construct adsorption isotherms at pH = 7 in the absence of added electrolytes and (ii) using fixed initial fluoride ion concentrations (10 mg/L) with a variation of either the pH or the concentration of a series of salts that potentially interfere with adsorption. The experimental adsorption isotherms were fitted by three different theoretical isotherm equations, and they are described most appropriately by the two-site Langmuir model for both adsorbents. The adsorption capacities of Zr-glutamic acid-graphite oxide and Zr-aspartic acid-graphite oxide are 105.3 and 101.0 mg/g, respectively. We found that two distinct binding modes are combined in the Zr-amino acid complexes: at low solution concentrations, F ions are preferentially adsorbed by coordinating to the surface Zr species up to a capacity of ca. 10 mg/g. At higher concentrations, however, large amounts of fluoride ions may undergo anion exchange processes and physisorption may occur on the positively charged ammonium moieties of the interfacially bound amino acid molecules. The high adsorption capacity and affinity of the studied dicarboxylate-type amino acids demonstrate that amino acid complexes of zirconia are highly variable materials for the safe and efficient capture of strong Lewis base-type ions such as fluoride.
氧化锆氨基酸配合物代表了一类全新的材料,它们是首次被合成并研究用于含氟离子水溶液的净化。通过两步法合成了由石墨氧化物 (GO) 衍生的薄碳 (堆叠氧化石墨烯) 片组装的氧化锆谷氨酸和天冬氨酸配合物,以制备吸附剂。使用红外光谱对配合物进行了表征,以确定官能团和复合材料与氟离子之间的相互作用类型。为了揭示吸附的机制和程度,进行了两种类型的批量吸附测量:(i) 改变平衡氟离子浓度,在没有添加电解质的情况下在 pH = 7 处构建吸附等温线,以及 (ii) 使用固定的初始氟离子浓度 (10 mg/L) ,改变一系列可能干扰吸附的盐的 pH 或浓度。实验吸附等温线由三种不同的理论等温线方程拟合,对于两种吸附剂,它们最适合由双位朗缪尔模型描述。Zr-谷氨酸-氧化石墨和 Zr-天冬氨酸-氧化石墨的吸附容量分别为 105.3 和 101.0 mg/g。我们发现,Zr-氨基酸配合物中结合了两种不同的结合模式:在低溶液浓度下,F 离子优先通过与表面 Zr 物种配位而被吸附,最大吸附容量约为 10 mg/g。然而,在较高浓度下,大量的氟离子可能经历阴离子交换过程,并且物理吸附可能发生在界面结合的氨基酸分子的带正电荷的铵部分上。所研究的二羧酸型氨基酸的高吸附容量和亲和力表明,氧化锆氨基酸配合物是用于安全高效捕获强路易斯碱型离子(如氟化物)的高度可变材料。