Efficient removal of naphthenic acids from real petroleum wastewater by natural pyrite activated persulfate system

Shuai Zhu; Zhuoyu Li; Meiqi Yu; Qinghong Wang; Chunmao Chen; Jun Ma

doi:10.1016/j.jenvman.2023.119239

Efficient removal of naphthenic acids from real petroleum wastewater by natural pyrite activated persulfate system

J Environ Manage. 2023 Dec 15:348:119239. doi: 10.1016/j.jenvman.2023.119239. Epub 2023 Oct 10.

Authors

Shuai Zhu¹, Zhuoyu Li², Meiqi Yu¹, Qinghong Wang¹, Chunmao Chen¹, Jun Ma³

Affiliations

¹ State Key Laboratory of Heavy Oil Processing, China University of Petroleum-Beijing, Beijing, 102249, PR China.
² State Key Laboratory of Heavy Oil Processing, China University of Petroleum-Beijing, Beijing, 102249, PR China. Electronic address: Lizyhit@163.com.
³ State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, PR China.

PMID: 37827079
DOI: 10.1016/j.jenvman.2023.119239

Abstract

The petroleum wastewater (PWW) contains a diverse range of recalcitrant organic contaminants. Of particular concern is the removal of naphthenic acids (NAs) due to the high toxicity and persistence. Persulfate (PS) based oxidation processes have shown promising in treating refractory wastewater, while the high costs of prepared catalysts limited their widespread implementation. This study aims to develop a cost-effective natural pyrite activated PS system for PWW treatment. The removal of NAs by pyrite/PS system was initially investigated. More than 90% of cyclohexanoic acid (CHA), a model NA, was removed in pyrite/PS system (2.0 g/L pyrite, 4.0 mM PS) at initial pH of 3-11. Scavenging experiments revealed that Fe(II) on pyrite surface was the reactive site for PS activation to generate reactive species, including sulfate radical (SO₄^·-), Fe(IV) and hydroxyl radical (·OH) for CHA degradation. Reactions of Fe(III) with S helped restore Fe(II) and enhance PS activation, resulting in the sustained catalytic activity of pyrites over five cycles. Cl^-, SO₄^2- and NO₃^- below 10 mM had minimal impact on CHA degradation in pyrite/PS system. However, over 1 mM of HCO₃^- inhibited 80% of CHA removal due to the buffer effect to maintain the high solution pH. Removing HCO₃^- from real PWW restored the removal of CHA and of total organic carbon (TOC) to over 90% and 71.3% in pyrite/PS system, respectively. Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) results indicated that O_2‒6 species including NAs were primarily eliminated through mineralization and oxygen addition. Besides, O₃-₅S, NO₃-₅S and N₃O_2‒4 species were the most susceptible to oxidation in PWW, resulting in the increase of the oxidation level (i.e., O/C_wa) from 0.41 to 0.56 after treatment. This study provides valuable insights into the treatment of NAs in real PWW, and potential application of natural minerals in the treatment of industrial wastewater.

Keywords: FT-ICR MS; Naphthenic acids; Persulfate oxidation; Petroleum wastewater; Pyrite.

MeSH terms

Ferric Compounds / chemistry
Ferrous Compounds
Petroleum* / analysis
Wastewater
Water Pollutants, Chemical* / chemistry

Substances

pyrite
Wastewater
Petroleum
Ferric Compounds
naphthenic acid
Water Pollutants, Chemical
Ferrous Compounds