Next Article in Journal
Technical Note: A Device to Directly Measure Transpiration from Vegetation Grown in Containers
Previous Article in Journal
Implementation of Modified Acacia Tannin by Mannich Reaction for Removal of Heavy Metals (Cu, Cr and Hg)
Open AccessArticle

Effects of Persulfate Activation with Pyrite and Zero-Valent Iron for Phthalate Acid Ester Degradation

1
Beijing Key Laboratory of Water Resources & Environmental Engineering, China University of Geosciences (Beijing), Beijing 100083, China
2
School of Environmental Science & Engineering, Southern University of Science & Technology, Shenzhen 518055, China
*
Author to whom correspondence should be addressed.
Water 2020, 12(2), 354; https://doi.org/10.3390/w12020354
Received: 28 November 2019 / Revised: 23 January 2020 / Accepted: 24 January 2020 / Published: 28 January 2020
(This article belongs to the Section Wastewater Treatment and Reuse)
Phthalic acid esters (PAEs) are often detected in remediated groundwater using appropriate oxidant materials by in situ groundwater treatment. The study compares zero-valent iron–persulfate with a pyrite–persulfate system to degrade three PAEs—di(2-ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP), and dimethyl phthalate (DMP). Column experiments were conducted, and rapid oxidation occurred in a pyrite–persulfate system due to sulfate radical generation. DMP concentration was found at about 60.0% and 53.0% with zero-valent iron (ZVI) and pyrite activation of persulfate, respectively. DBP concentration was measured as 25.0–17.2% and 23.2–16.0% using ZVI–persulfate and pyrite–persulfate systems, respectively. However, DEHP was not detected. The total organic carbon concentration lagged behind the Ʃ3 PAEs. Persulfate consumption with ZVI activation was half of the consumption with pyrite activation. Both systems showed a steady release of iron ions. Overall, the oxidation–reduction potential was higher with pyrite activation. The surface morphologies of ZVI and pyrite were investigated using scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and XPS. Intensive corrosion occurs on the pyrite surface, whereas the ZVI surface is covered by a netting of iron oxides. The pyrite surface showed more oxidation and less passivation in comparison with ZVI, which results in more availability of Fe 2 + for persulfate activation. The pyrite–persulfate system is relatively preferred for rapid PAE degradation for contamination. View Full-Text
Keywords: PAEs; persulfate; zero-valent iron; pyrite; column experiment PAEs; persulfate; zero-valent iron; pyrite; column experiment
Show Figures

Graphical abstract

MDPI and ACS Style

Imran, M.A.; Tong, Y.; Hu, Q.; Liu, M.; Chen, H. Effects of Persulfate Activation with Pyrite and Zero-Valent Iron for Phthalate Acid Ester Degradation. Water 2020, 12, 354.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Search more from Scilit
 
Search
Back to TopTop