4.7 Article

Bronsted-acid sites promoted degradation of phthalate esters over MnO2: Mineralization enhancement and aquatic toxicity assessment

期刊

CHEMOSPHERE
卷 291, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.132740

关键词

Manganese oxide; Advanced oxidation processes; Mineralization; Dimethyl phthalate; Zebrafish; Aquatic toxicity

资金

  1. National Natural Science Foundation of China [21403256, 21573261]
  2. Youth Innovation Promotion Association CAS [2018456]
  3. LICP Cooperation Foundation for Young Scholars [HZJJ20-10]
  4. Fundamental Research Funds for the Central Universities [lzujbky-2019-74]
  5. Double First-Class Research Start-up Funds of Lanzhou University [561119201]

向作者/读者索取更多资源

In this study, a manganese oxide nanomaterial with abundant acid sites was synthesized, and the catalytic performance for the degradation of phthalate esters was tested. The catalyst showed high efficiency in degrading and mineralizing the organic pollutants, and it could be reused for multiple cycles. Moreover, the catalyzed advanced oxidation processes significantly reduced the developmental toxicity of the wastewater on zebrafish.
Advanced oxidation processes (AOPs) are important technologies for aqueous organics removal. Despite organic pollutants can be degraded via AOPs generally, high mineralization of them is hard to achieve. Herein, we synthesized a manganese oxide nanomaterial (H2-OMS-2) with abundant Bronsted-acid sites via ion-exchange of cryptomelane-type MnO2 (OMS-2), and tested its catalytic performance for the degradation of phthalate esters via peroxymonosulfate (PMS) activation. About 99% of dimethyl phthalate (DMP) at a concentration of 20 mg/L could be degraded within 90 min and 82% of it could be mineralized within 180 min over 0.6 g/L of catalyst and 1.8 g/L of PMS. The catalyst could activate PMS to generate SO4-center dot and center dot OH as the dominant reactive oxygen species to reach complete degradation of DMP. Especially, the higher TOC removal rate was obtained due to the rich Bronsted-acid sites and surface oxygen vacancies on the catalyst. Kinetics and mechanism study showed that Mn-II/Mn-III might work as the active sites during the catalytic process with a lower reaction energy barrier of 55.61 kJ/mol. Furthermore, the catalyst could be reused for many times through the regeneration of the catalytic ability. The degradation and TOC removal efficiencies were still above 98% and 65% after seven consecutive cycles, respectively. Finally, H2-OMS-2-catalyzed AOPs significantly reduced the organismal developmental toxicity of the DMP wastewater through the investigation of zebrafish model system. The present work, for the first time, provides an idea for promoting the oxidative degradation and mineralization efficiencies of aqueous organic pollutants by surface acid-modification on the catalysts.

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