Department of Municipal Engineering, School of Civil Engineering, Southeast University, Nanjing, 211189, China.
Jiangsu Environmental Engineering Technology Co., Ltd., Nanjing, 210019, China.
Environ Pollut. 2023 Apr 1;322:121231. doi: 10.1016/j.envpol.2023.121231. Epub 2023 Feb 6.
With continued exposure to CuO nanoparticles (NPs) which were toxic to organisms, the performance of wastewater treatment facility might be affected. In present study, the feasibility of constructed wetlands (CWs) for wastewater treatment containing CuO NPs and common pollutants was comprehensively explored. It was found that CWs removed 98.80-99.84% CuO NPs and 90.91-91.83% COD within 300 days. However, N and P removals were affected to varying degrees by CuO NPs. N removal was inhibited only by 0.5 mg/L CuO NPs with 19.75% decreases on the mean from day 200-300. P removal was reduced by 3.80-50.75% and 1.92-7.19% under exposure of 0.5 and 5 mg/L CuO NPs throughout the experiment. Moreover, CuO NPs changed the adsorption potential of P and ammonium-N on sand-biofilm. Cu concentrations in spatial distribution decreased, while they in temporal distribution increased from 36.94 to 97.78 μg/g and from 70.92 to 282.66 μg/g at middle sand layer exposed to 0.5 and 5 mg/L CuO NPs. Mass balance model showed that substrate-biofilm was main pollutant sink for CuO NPs, N, and P. The minor Cu was absorbed by plants exposed to 0.5 and 5 mg/L CuO NPs, which decreased N by 53.40% and 18.51%,and P by 52.35% and 21.62%. Sequencing analysis indicated that CuO NPs also altered spatial microbial community. N-degrading bacteria (Rhodanobacter, Thauera, Nitrospira) changed differently, while phosphate accumulation organisms (Acinetobacter, Pseudomonas, Microlunatus) reduced. Overall, the negative effects of CuO NPs on N and P removal should be noted when CWs as ecological technologies are used to treat CuO NPs-containing wastewater.
在持续接触氧化铜纳米颗粒(NPs)的情况下,这些物质对生物体有毒,废水处理设施的性能可能会受到影响。在本研究中,全面探索了构建湿地(CWs)处理含氧化铜 NPs 和常见污染物废水的可行性。结果发现,CWs 在 300 天内去除了 98.80-99.84%的氧化铜 NPs 和 90.91-91.83%的 COD。然而,N 和 P 的去除受到氧化铜 NPs 的不同程度影响。只有 0.5 mg/L 的氧化铜 NPs 会抑制 N 的去除,从第 200-300 天的平均值减少 19.75%。在暴露于 0.5 和 5 mg/L 的氧化铜 NPs 的整个实验过程中,P 的去除率分别降低了 3.80-50.75%和 1.92-7.19%。此外,氧化铜 NPs 改变了 P 和铵-N 在沙-生物膜上的吸附潜力。暴露于 0.5 和 5 mg/L 的氧化铜 NPs 的中层沙中,Cu 浓度在空间分布上减少,而在时间分布上从 36.94 增加到 97.78μg/g 和从 70.92 增加到 282.66μg/g。质量平衡模型表明,基质-生物膜是氧化铜 NPs、N 和 P 的主要污染物汇。暴露于 0.5 和 5 mg/L 的氧化铜 NPs 的植物吸收了少量的 Cu,导致 N 减少了 53.40%和 18.51%,P 减少了 52.35%和 21.62%。序列分析表明,氧化铜 NPs 还改变了空间微生物群落。N 降解细菌(Rhodanobacter、Thauera、Nitrospira)的变化不同,而聚磷菌(Acinetobacter、Pseudomonas、Microlunatus)减少。总的来说,在将 CWs 作为生态技术用于处理含氧化铜 NPs 的废水时,应注意氧化铜 NPs 对 N 和 P 去除的负面影响。