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高效利用微纳米臭氧气泡增强电过氧乙酸过程,快速去除医院废水中痕量药物污染物。

High-efficiently utilizing micro-nano ozone bubbles to enhance electro-peroxone process for rapid removal of trace pharmaceutical contaminants from hospital wastewater.

机构信息

Jiangsu Key Laboratory of Anaerobic Biotechnology, School of Environment and Ecology, Jiangnan University, Wuxi, Jiangsu, 214122, China.

Jiangsu Key Laboratory of Anaerobic Biotechnology, School of Environment and Ecology, Jiangnan University, Wuxi, Jiangsu, 214122, China.

出版信息

Water Res. 2024 Aug 1;259:121896. doi: 10.1016/j.watres.2024.121896. Epub 2024 Jun 5.

Abstract

The electro-peroxone (EP) process encounters two inherent challenges in wastewater treatment: sluggish O/O transfer and substantial ozone waste. To overcome these limitations, we introduced micro-nano bubbles (MNBs) aeration to enhance O/O dissolution and diffusion, ultimately aiming to improve the removal of trace pharmaceutical contaminants from hospital wastewater. In the MNBs aeration system, the ozone transfer coefficient ranging from 0.536 to 0.265 min, significantly surpassing that of conventional aeration (0.220 to 0.090 min) by approximately 2 to 4.5 times. Consequently, the EP process under MNBs aeration significantly enhanced ozone-resistant ibuprofen (IBU) removal, achieving a removal rate of 98.4 ± 1.5 %, far exceeding the 47.3 ± 4.7 % observed with conventional aeration. This significant improvement was attributed to the heightened production of hydroxyl radicals (•OH), reaching 0.97 × 10 M s, compared to only 0.28 × 10 M s in conventional aeration. The mechanism behind the enhanced •OH production in the MNBs-EP process relied primarily on two factors: improved O/O dissolution due to high internal pressure/large surface and enhanced O/HO activation from high collapse energy. These factors together contributed to the robust oxidation capability of the MNBs-EP system. As a result, over 97 % removal efficiency was achieved for five representative pharmaceutical pollutants (sulfamethoxazole, ribavirin, norfloxacin, tetracycline and ampicillin) in just 1 min. Furthermore, when applied to real hospital wastewater, the MNBs-O-E treatment system reduced all 15 detected trace pharmaceutical compounds to below 10 ng L and achieved 14 types of pollutants with removal rates of over 85 % within 15 min, resulting in an ultrahigh total removal rate of 98.6 %, from an initial total concentration of 2108 ng L to less than 30 ng L. Thus, micro-nano aeration endowed the EP process as a promising advanced oxidation system for rapid and highly-effective removal of trace pharmaceutical contaminants from hospital wastewater.

摘要

电过氧协同(EP)工艺在处理废水时面临两个固有挑战:O/O 转移缓慢和臭氧浪费严重。为了克服这些限制,我们引入了微纳米气泡(MNBs)曝气来增强 O/O 的溶解和扩散,最终旨在提高从医院废水中去除痕量药物污染物的效果。在 MNBs 曝气系统中,臭氧传质系数为 0.536 至 0.265 min,比传统曝气(0.220 至 0.090 min)高 2 至 4.5 倍。因此,MNBs 曝气下的 EP 工艺显著提高了对臭氧耐药的布洛芬(IBU)的去除率,达到了 98.4 ± 1.5%,远高于传统曝气下的 47.3 ± 4.7%。这种显著的改进归因于羟基自由基(•OH)的产生量增加,达到 0.97×10 M s,而传统曝气中只有 0.28×10 M s。MNBs-EP 工艺中•OH 产量增加的机制主要依赖于两个因素:由于高压/大表面积而提高的 O/O 溶解和由于高坍塌能而增强的 O/HO 激活。这些因素共同促成了 MNBs-EP 系统的强大氧化能力。结果,在仅仅 1 分钟内,5 种代表性药物污染物(磺胺甲恶唑、利巴韦林、诺氟沙星、四环素和氨苄西林)的去除效率超过 97%。此外,当应用于实际医院废水时,MNBs-O-E 处理系统将 15 种检测到的痕量药物化合物全部降低到 10 ng L 以下,并在 15 分钟内实现了 14 种污染物的去除率超过 85%,总去除率高达 98.6%,从初始总浓度 2108 ng L 降至 30 ng L 以下。因此,微纳米曝气使 EP 工艺成为一种有前途的高级氧化系统,可用于快速、高效地去除医院废水中的痕量药物污染物。

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