Group of Environmental Physical Chemistry, Department F.-A. Forel for Environmental and Aquatic Sciences, University of Geneva, Uni Carl Vogt, 66, boulevard Carl-Vogt, CH-1211 Geneva 4, Switzerland.
SIG, Industrial Boards of Geneva, Ch. du Château-Bloch, Le Lignon, 1211 Genève 2, Switzerland.
Sci Total Environ. 2021 Oct 15;791:148175. doi: 10.1016/j.scitotenv.2021.148175. Epub 2021 Jun 1.
In this study Granular Activated Carbon (GAC) used in drinking water treatment processes is evaluated for its capacity to adsorb and remove polystyrene (PS) nanoplastics. Batch experiments are conducted in ultrapure and surface water from Lake Geneva, currently used as drinking water resources. Equilibrium and kinetic studies are conducted to understand adsorption mechanisms and limiting factors. Our results show that in ultrapure water the adsorption and removal of PS nanoplastics are mainly due to electrostatic interactions between the positively charged nanoplastics and negatively charged GAC. It is found that the adsorption capacity increases with nanoplastic concentration with a maximum adsorption capacity of 2.20 mg/g. The adsorption kinetics follows a pseudo-second-order model and indicates that the intra-particle diffusion is not the only rate-controlling step. The Langmuir isotherm indicates that nanoplastics are adsorbed as a homogeneous monolayer onto the GAC surface with a maximum monolayer adsorption capacity of 2.15 mg/g in agreement with the experimental value. In Lake Geneva water the adsorption capacity and removal efficiency of PS nanoplastics are found three times higher than in ultrapure water and increase significantly with increasing PS nanoplastics concentration with a maximum adsorption capacity of 6.33 mg/g. This improvement in adsorption capacity is due to the presence of Dissolved Organic Matter (DOM), resulting in PS surface charge modification, presence of divalent ions making possible the adsorption of PS-DOM complexes, and, aggregation of PS nanoplastics. The kinetic pseudo-second-order and intra-particle diffusion provide a good correlation with the experimental data. In contrast, neither Langmuir nor Freundlich isotherms describe in a satisfactory way the adsorption of nanoplastics by GAC. This study reveals that GAC produced from renewable sources can be considered as a moderate adsorbent for the removal of PS nanoplastics in water treatment plants and that the presence of DOM and cationic species play a major role.
在这项研究中,评估了用于饮用水处理过程的颗粒状活性炭 (GAC) 去除和吸附聚苯乙烯 (PS) 纳米塑料的能力。在超纯水和日内瓦湖地表水中进行了批量实验,目前这些水被用作饮用水资源。进行了平衡和动力学研究,以了解吸附机制和限制因素。我们的研究结果表明,在超纯水中,PS 纳米塑料的吸附和去除主要是由于带正电荷的纳米塑料和带负电荷的 GAC 之间的静电相互作用。发现吸附容量随纳米塑料浓度的增加而增加,最大吸附容量为 2.20mg/g。吸附动力学符合准二级模型,表明内扩散不是唯一的速率控制步骤。Langmuir 等温线表明纳米塑料以均匀的单层形式被吸附到 GAC 表面上,最大单层吸附容量为 2.15mg/g,与实验值一致。在日内瓦湖水中,PS 纳米塑料的吸附容量和去除效率比超纯水中高三倍,且随着 PS 纳米塑料浓度的增加而显著增加,最大吸附容量为 6.33mg/g。这种吸附容量的提高是由于溶解有机物 (DOM) 的存在导致 PS 表面电荷发生变化、二价离子的存在使得 PS-DOM 配合物的吸附成为可能,以及 PS 纳米塑料的聚集。准二级动力学和内扩散能够很好地与实验数据相关联。相比之下,Langmuir 和 Freundlich 等温线都不能令人满意地描述 GAC 对纳米塑料的吸附。这项研究表明,可再生来源的 GAC 可被视为水处理厂中去除 PS 纳米塑料的中等吸附剂,并且 DOM 和阳离子的存在起着重要作用。