Wang Lin, Wang Shu-Xin, Zeng Xiang-Ying, He Yang, Huang Wen, Zheng Shi-Jie, Zhang Jian-Qiang
Faculty of Geosciences and Environmental Engineering, Southwest Jiaotong University, Chengdu 611756, China.
Huan Jing Ke Xue. 2022 Oct 8;43(10):4511-4521. doi: 10.13227/j.hjkx.202112299.
As new pollutants, microplastics (MPs) can adsorb antibiotics in the water environment and migrate together as carriers. However, microplastics will age continuously in the environment, and their adsorption capacity and adsorption mechanism will change accordingly. With polyethylene (PE) and polystyrene (PS) as the target MPs, which were irradiated by ultraviolet (UV-254), the changes in the physical and chemical properties of MPs before and after aging, such as the color, surface morphology, and functional groups, were compared, and their effects on the adsorption of tetracycline (TC) as well as the related mechanism were explored. The results showed that the pseudo-second-order model could better fit the adsorption process, the adsorption equilibrium was reached within 24 hours, the adsorption capacity of aged MPs for TC was significantly higher than that of original MPs, and the adsorption capacity of PS was higher than that of PE. Langmuir and Freundlich isothermal adsorption equations could both describe the adsorption isothermal test data, and the adsorption of TC on MPs was a spontaneous and endothermic physical adsorption process, whereas aging had no obvious effect on the adsorption thermodynamic characteristics of MPs. With the increase in pH value, the adsorption capacity first increased and then decreased. The maximum adsorption capacity of MPs before and after aging was reached at pH=5. UV aging increased the specific surface area of MPs, generating oxygen-containing functional groups such as -C=O, -OH, and O=C=O, changing the physical and chemical properties of MPs, and thus changing the adsorption mechanism of MPs for TC. Compared with the original PE MPs, in addition to hydrophobic distribution, van der Waals forces, and electrostatic interactions, pore filling was also an important adsorption mechanism of aged PE. The main adsorption mechanisms of original PS microplastics were hydrophobic distribution, van der Waals forces, electrostatic interaction, and π-π interaction, whereas there was hydrogen bonding for aged PS.
作为新型污染物,微塑料(MPs)能够在水环境中吸附抗生素并作为载体共同迁移。然而,微塑料在环境中会不断老化,其吸附能力和吸附机制也会相应改变。以聚乙烯(PE)和聚苯乙烯(PS)作为目标微塑料,通过紫外线(UV - 254)进行辐照,比较老化前后微塑料的物理化学性质变化,如颜色、表面形态和官能团等,并探究其对四环素(TC)吸附的影响及相关机制。结果表明,准二级模型能更好地拟合吸附过程,24小时内达到吸附平衡,老化后的微塑料对TC的吸附量显著高于原始微塑料,且PS的吸附量高于PE。Langmuir和Freundlich等温吸附方程均可描述吸附等温试验数据,TC在微塑料上的吸附是一个自发的吸热物理吸附过程,而老化对微塑料的吸附热力学特性无明显影响。随着pH值升高,吸附量先增加后降低,老化前后微塑料在pH = 5时达到最大吸附量。紫外线老化增加了微塑料的比表面积,产生了如 -C=O、-OH和O=C=O等含氧官能团,改变了微塑料的物理化学性质,进而改变了微塑料对TC的吸附机制。与原始PE微塑料相比,除疏水分配、范德华力和静电相互作用外,孔隙填充也是老化PE的重要吸附机制。原始PS微塑料的主要吸附机制为疏水分配、范德华力、静电相互作用和π - π相互作用,而老化后的PS存在氢键作用。