College of Marine Ecology and Environment, Shanghai Ocean University, No 999, Huchenghuan Road, Shanghai, 201306, PR China.
College of Marine Ecology and Environment, Shanghai Ocean University, No 999, Huchenghuan Road, Shanghai, 201306, PR China.
Environ Res. 2022 Sep;212(Pt A):113132. doi: 10.1016/j.envres.2022.113132. Epub 2022 Mar 16.
With the progress of research on micro-nano plastics, the weathering degradation process in the natural environment has gradually become the focus of academic discussion. This study adopted the Fenton immersion method to accelerate the simulation of the weathering process of microplastics in nature, and explored the interface behavior of the weathered microplastics and hydrophilic antibiotics. It was found that the weathered polystyrene (PS) has a smaller crystallinity, increased oxygen-containing functional groups, and cracks appear on the surface, making it more likely to be weathered. At the same time, the rougher surface and stronger hydrophilicity of the weathered PS particles made it easier to adsorb hydrophilic antibiotics. Subsequent studies showed that the adsorption of ciprofloxacin (CIP·HCl) by weathered PS is much larger than that of original PS particles, whose maximum adsorption is 5.45 mg/g in the isotherm experiments. We found that the adsorption behavior of weathered PS particles with CIP in seawater would be weakened in the real seawater environment and humic acid, which might be due to the competitive adsorption of CIP by various ions. Further studies have shown that changes in the ionic strength and pH of the solution also affected the adsorption behavior to varying degrees. The results of dynamic adsorption were the same as the static adsorption, and the adsorption rate and capacity of weathered PS particles were enhanced compared with the original particles. The results of this article not only provided a data reference for studying the weathering process of microplastics but also helped to explore the ultimate fate of microplastics.
随着微纳米塑料研究的进展,自然环境中的风化降解过程逐渐成为学术讨论的焦点。本研究采用芬顿浸出法加速模拟微塑料在自然界中的风化过程,并探讨了风化微塑料与亲水性抗生素的界面行为。结果表明,风化聚苯乙烯(PS)的结晶度更小,含氧官能团增加,表面出现裂纹,更容易风化。同时,风化 PS 颗粒的表面更粗糙,亲水性更强,更容易吸附亲水性抗生素。随后的研究表明,风化 PS 对环丙沙星(CIP·HCl)的吸附量远大于原始 PS 颗粒,在等温实验中最大吸附量为 5.45mg/g。我们发现,在真实海水环境和腐殖酸中,风化 PS 颗粒与 CIP 的吸附行为会减弱,这可能是由于各种离子对 CIP 的竞争吸附所致。进一步的研究表明,溶液的离子强度和 pH 值的变化也会对吸附行为产生不同程度的影响。动态吸附的结果与静态吸附相同,风化 PS 颗粒的吸附速率和容量均比原始颗粒增强。本文的研究结果不仅为研究微塑料的风化过程提供了数据参考,还有助于探索微塑料的最终归宿。