Oxidation of methylparaben (MeP) and p‑hydroxybenzoic acid (p-HBA) by manganese dioxide (MnO2) and effects of iodide: Efficiency, products, and toxicity
It is reported that methylparaben (MeP, a widely used phenolic preservative) and its major metabolite p‑hydroxybenzoic acid (p-HBA) display estrogenic activity and are frequently detected in various environmental settings. Naturally occurring manganese dioxide (MnO2) plays an important role in atten...
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| Published in | The Science of the total environment Vol. 661; pp. 670 - 677 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Netherlands
Elsevier B.V
15.04.2019
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| Abstract | It is reported that methylparaben (MeP, a widely used phenolic preservative) and its major metabolite p‑hydroxybenzoic acid (p-HBA) display estrogenic activity and are frequently detected in various environmental settings. Naturally occurring manganese dioxide (MnO2) plays an important role in attenuation of contaminants released into the environment, and the presence of iodide (I−) may affect these processes. In this work, it was found that both MeP and p-HBA displayed considerable reactivity towards MnO2 with their half-lives increased with decreasing MnO2 concentrations or increasing pH. The presence of I− obviously accelerated the transformation efficiency of MeP and p-HBA by MnO2 with stronger enhancement at higher I− concentrations or lower pH. Dimeric products (e.g., dimeric MeP or p-HBA) were generated from MeP/p-HBA treated by MnO2, and iodinated aromatic products (e.g., mono-/di-iodinated MeP/p-HBA) were additionally identified in the presence of I−. Higher concentrations of these iodinated aromatic products were generally formed at higher I− or lower MnO2 concentrations or lower pH. Ecotoxicity analysis showed that dimeric and iodinated aromatic products were more eco-toxic than parent MeP/p-HBA. This work shows that MnO2 may greatly affect the fate of MeP and p-HBA released into the environment, and the presence of I− can significantly affect these processes.
[Display omitted]
•MnO2 showed considerable reactivity towards MeP and p-HBA•Dimeric products were generated from both MeP and p-HBA oxidation by MnO2•Addition of I− significantly enhanced MeP and p-HBA transformation by MnO2 at pH ≤ 7•Iodinated aromatic products were detected in MnO2/MeP (p-HBA)/I− system•Dimeric and iodinated aromatic products were more toxic than parent MeP/p-HBA |
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| AbstractList | It is reported that methylparaben (MeP, a widely used phenolic preservative) and its major metabolite p‑hydroxybenzoic acid (p-HBA) display estrogenic activity and are frequently detected in various environmental settings. Naturally occurring manganese dioxide (MnO
) plays an important role in attenuation of contaminants released into the environment, and the presence of iodide (I
) may affect these processes. In this work, it was found that both MeP and p-HBA displayed considerable reactivity towards MnO
with their half-lives increased with decreasing MnO
concentrations or increasing pH. The presence of I
obviously accelerated the transformation efficiency of MeP and p-HBA by MnO
with stronger enhancement at higher I
concentrations or lower pH. Dimeric products (e.g., dimeric MeP or p-HBA) were generated from MeP/p-HBA treated by MnO
, and iodinated aromatic products (e.g., mono-/di-iodinated MeP/p-HBA) were additionally identified in the presence of I
. Higher concentrations of these iodinated aromatic products were generally formed at higher I
or lower MnO
concentrations or lower pH. Ecotoxicity analysis showed that dimeric and iodinated aromatic products were more eco-toxic than parent MeP/p-HBA. This work shows that MnO
may greatly affect the fate of MeP and p-HBA released into the environment, and the presence of I
can significantly affect these processes. It is reported that methylparaben (MeP, a widely used phenolic preservative) and its major metabolite p‑hydroxybenzoic acid (p-HBA) display estrogenic activity and are frequently detected in various environmental settings. Naturally occurring manganese dioxide (MnO2) plays an important role in attenuation of contaminants released into the environment, and the presence of iodide (I−) may affect these processes. In this work, it was found that both MeP and p-HBA displayed considerable reactivity towards MnO2 with their half-lives increased with decreasing MnO2 concentrations or increasing pH. The presence of I− obviously accelerated the transformation efficiency of MeP and p-HBA by MnO2 with stronger enhancement at higher I− concentrations or lower pH. Dimeric products (e.g., dimeric MeP or p-HBA) were generated from MeP/p-HBA treated by MnO2, and iodinated aromatic products (e.g., mono-/di-iodinated MeP/p-HBA) were additionally identified in the presence of I−. Higher concentrations of these iodinated aromatic products were generally formed at higher I− or lower MnO2 concentrations or lower pH. Ecotoxicity analysis showed that dimeric and iodinated aromatic products were more eco-toxic than parent MeP/p-HBA. This work shows that MnO2 may greatly affect the fate of MeP and p-HBA released into the environment, and the presence of I− can significantly affect these processes. [Display omitted] •MnO2 showed considerable reactivity towards MeP and p-HBA•Dimeric products were generated from both MeP and p-HBA oxidation by MnO2•Addition of I− significantly enhanced MeP and p-HBA transformation by MnO2 at pH ≤ 7•Iodinated aromatic products were detected in MnO2/MeP (p-HBA)/I− system•Dimeric and iodinated aromatic products were more toxic than parent MeP/p-HBA |
| Author | Gao, Yuan Pang, Su–Yan Zhou, Yang Wang, Lihong Wang, Zhen Li, Juan Jiang, Jin Sun, Shaofang |
| Author_xml | – sequence: 1 givenname: Juan surname: Li fullname: Li, Juan organization: Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China – sequence: 2 givenname: Jin surname: Jiang fullname: Jiang, Jin email: jiangjinhit@126.com organization: Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China – sequence: 3 givenname: Su–Yan surname: Pang fullname: Pang, Su–Yan organization: Key Laboratory of Songliao Aquatic Environment, Ministry of Education, School of Municipal and Environmental Engineering, Jilin Jianzhu University, Changchun 130118, China – sequence: 4 givenname: Shaofang surname: Sun fullname: Sun, Shaofang organization: School of Civil Engineering and Architecture, University of Jinan, Jinan 250022, China – sequence: 5 givenname: Lihong surname: Wang fullname: Wang, Lihong organization: State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin 150090, China – sequence: 6 givenname: Yang surname: Zhou fullname: Zhou, Yang organization: Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China – sequence: 7 givenname: Zhen surname: Wang fullname: Wang, Zhen organization: State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin 150090, China – sequence: 8 givenname: Yuan surname: Gao fullname: Gao, Yuan organization: Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou 510006, China |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30684835$$D View this record in MEDLINE/PubMed |
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| Keywords | p‑Hydroxybenzoic acid (p-HBA) Iodinated aromatic products Methylparaben (MeP) Iodide (I−) Manganese dioxide (MnO2) Iodide (I(−)) Manganese dioxide (MnO) |
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| SubjectTerms | Iodide (I−) Iodinated aromatic products Manganese dioxide (MnO2) Methylparaben (MeP) p‑Hydroxybenzoic acid (p-HBA) |
| Title | Oxidation of methylparaben (MeP) and p‑hydroxybenzoic acid (p-HBA) by manganese dioxide (MnO2) and effects of iodide: Efficiency, products, and toxicity |
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