School of Environmental and Municipal Engineering, North China University of Water Resources and Electric Power, Zhengzhou 450046, China.
School of Water Conservancy & Environment, Zhengzhou University, Zhengzhou 450001, China.
Environ Pollut. 2020 Oct;265(Pt B):114597. doi: 10.1016/j.envpol.2020.114597. Epub 2020 Apr 22.
Composite magnetic oxide at cow dung ash, nano-FeO@cow dung ash (nano-FeO@CDA), was used as catalytic material for the degradation of 2, 2'-methylenebis (4-methyl-6-tert-butylphenol) (AO 2246) in real biologically pretreated landfill leachate. The FeO@CDA composite exhibited catalytic ozonation activity and allowed material separation and magnetic recovery. The effects of several operating parameters including O concentration, catalyst dosage, temperature and scavengers were evaluated in parallel. Over 70% of AO 2246 were removed by the nano-FeO@CDA/O system under optimum conditions within 120min reaction time. The EPR, GC-MS and free-radical quenching experiments expatiated the mechanism of this degradation process. It was confirmed that the AO 2246 was degraded efficiently in this catalytic micro-ozonation process, Additionally, GC-MS analysis state clearly that the 3,5-bis(1,1-dimethylethyl)phenol, 4-(1,5-dihydroxy-2,6,6-trimethylcyclohex-2-enyl)but-3-en-2-one, ethanone, 1-(1,4-dimethyl-3-cyclohexen-1-yl)-, 5-tert-butyl-6-3, 5-diene-2-one, 2-hydroxyhexanoic acid, 2-propenoic acid 1,1-dimethylethyl ester, butanoic acid, 2-methyl-, methyl ester and propanoic acid, 2, 2-dimethyl- were the dominant oxidation products (OPs) during the degradation of the AO 2246. The EPR results showed that the catalytic ozonation over FeO@CDA led to produce more hydroxyl radicals, which were in favor of AO 2246 degradation. The toxicity evolution was also performed through a QSAR analysis calculated by the ECOSAR program which further demonstrated the different responses toward the AO 2246 and its OPs.
以牛粪灰中的复合磁性氧化物、纳米-FeO@牛粪灰(nano-FeO@CDA)为催化剂,用于降解实际生物预处理垃圾渗滤液中的 2,2'-亚甲基双(4-甲基-6-叔丁基苯酚)(AO 2246)。FeO@CDA 复合材料表现出催化臭氧化活性,并允许材料分离和磁性回收。同时评估了几个操作参数的影响,包括 O 浓度、催化剂用量、温度和猝灭剂。在 120min 反应时间内,在最佳条件下,纳米-FeO@CDA/O 体系可去除超过 70%的 AO 2246。EPR、GC-MS 和自由基猝灭实验阐述了该降解过程的机理。实验证实,在这种催化微臭氧化过程中,AO 2246 被有效地降解。此外,GC-MS 分析清楚地表明,3,5-双(1,1-二甲基乙基)苯酚、4-(1,5-二羟基-2,6,6-三甲基环己-2-烯基)丁-3-烯-2-酮、乙酮、1-(1,4-二甲基-3-环己烯-1-基)-、5-叔丁基-6-3,5-二烯-2-酮、2-羟基己酸、2-丙烯酸 1,1-二甲基乙酯、丁酸、2-甲基-、甲酯和丙酸、2,2-二甲基是 AO 2246 降解过程中的主要氧化产物(OPs)。EPR 结果表明,FeO@CDA 上的催化臭氧化导致产生更多的羟基自由基,有利于 AO 2246 的降解。通过 ECOSAR 程序计算的 QSAR 分析也进行了毒性演变,进一步证明了 AO 2246 及其 OPs 的不同响应。