Li Junsuo, Li Xinying, Ma Shoucheng, Zhao Wei, Xie Wenming, Ma Jianqing, Yao Yijun, Wei Wei
School of Environment, Nanjing Normal University, Nanjing, 210023, China; Jiangsu Province Engineering Research Center of Environmental Risk Prevention and Emergency Response Technology, Jiangsu Engineering Lab of Water and Soil Eco-remediation, Nanjing, 210023, China; Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, Nanjing, 210023, China.
School of Environment, Nanjing Normal University, Nanjing, 210023, China; Jiangsu Province Engineering Research Center of Environmental Risk Prevention and Emergency Response Technology, Jiangsu Engineering Lab of Water and Soil Eco-remediation, Nanjing, 210023, China.
Chemosphere. 2022 Nov;307(Pt 1):135697. doi: 10.1016/j.chemosphere.2022.135697. Epub 2022 Jul 14.
Microplastics (MPs) can act as vectors for various contaminants in the aquatic environment. Although some research has investigated the adsorption characteristics and influencing factors of metals/organic molecules on MPs, the effects of dissolved organic matter (DOM) (which are ubiquitous active species in ecosystems) on metal oxyanions such as Cr(VI) capture by MPs are largely unknown. This study explored the adsorption behaviors and mechanisms of Cr(VI) oxyanions onto polystyrene (PS) MPs using batch adsorption experiments and multiple spectroscopic methods. The effects of representative DOM components (i.e., humic acid (HA), fulvic acid (FA) and tannic acid (TA)) on Cr(VI) capture by PS were particularly studied. Results revealed a significantly enhanced adsorption of Cr(VI) on PS in the presence of TA. The Cr(VI) adsorption capacity was increased from 2876 μg g to 4259 μg g and 5135 μg g when the TA concentrations raised from 0 to 10 and 20 mg L, respectively. Combined microscopic and spectroscopic investigations revealed that Cr(VI) was reduced to Cr(III) by TA and formed stable Cr(OH) colloids on PS surfaces. Contrarily, HA and FA inhibited Cr(VI) adsorption onto PS, especially at pH > 2.0 and higher DOM concentrations, due to site competition and electrostatic repulsion. Increase in pH was found to reduce zeta potentials of MPs, resulting in inhibited Cr(VI) adsorption. The adsorbed Cr(VI) declined with increasing ionic strength, implying that outer-sphere surface complexation affected the adsorption process in the presence of DOM. These new findings improved our fundamental understanding of the fate of Cr(VI) and MPs in DOM-rich environmental matrices.
微塑料(MPs)可作为水生环境中各种污染物的载体。尽管一些研究调查了金属/有机分子在微塑料上的吸附特性及影响因素,但溶解有机物(DOM,生态系统中普遍存在的活性物质)对微塑料捕获六价铬(Cr(VI))等金属氧阴离子的影响仍 largely 未知。本研究采用批量吸附实验和多种光谱方法,探究了 Cr(VI) 氧阴离子在聚苯乙烯(PS)微塑料上的吸附行为和机制。特别研究了代表性 DOM 成分(即腐殖酸(HA)、富里酸(FA)和单宁酸(TA))对 PS 捕获 Cr(VI) 的影响。结果表明,在 TA 存在下,Cr(VI) 在 PS 上的吸附显著增强。当 TA 浓度分别从 0 提高到 10 和 20 mg/L 时,Cr(VI) 的吸附容量从 2876 μg/g 增加到 4259 μg/g 和 5135 μg/g。结合微观和光谱研究表明,TA 将 Cr(VI) 还原为 Cr(III),并在 PS 表面形成稳定的 Cr(OH) 胶体。相反,HA 和 FA 抑制 Cr(VI) 在 PS 上的吸附,尤其是在 pH > 2.0 和较高 DOM 浓度下,这是由于位点竞争和静电排斥。发现 pH 升高会降低微塑料的 zeta 电位,从而抑制 Cr(VI) 的吸附。吸附的 Cr(VI) 随离子强度增加而下降,这意味着在 DOM 存在下,外层表面络合作用影响了吸附过程。这些新发现增进了我们对富 DOM 环境基质中 Cr(VI) 和微塑料归宿的基本理解。