Reductive degradation of chlorinated organophosphate esters by nanoscale zerovalent iron/cetyltrimethylammonium bromide composites: Reactivity, mechanism and new pathways

Dan Li, Yin Zhong, Xifen Zhu, Heli Wang, Weiqiang Yang, Yirong Deng, Weilin Huang, Ping'an Peng

Research output: Contribution to journalArticlepeer-review

Abstract

Chlorinated organophosphate esters (Cl-OPEs), e.g., tris(2-chloroethyl) phosphate (TCEP), tris(2-chloro-2-propyl) phosphate (TCPP) and tris(1,3-dichloro-2-propyl) phosphate (TDCPP), are widely used as additive flame retardants in commercial and building products. They have potential persistent organic pollutant properties and are frequently detected in various waters, especially in wastewaters. Nanoscale zerovalent iron (nZVI)-based method is an efficient reductive technology for treating waters polluted by halogenated organic pollutants (HOCs). Cetyltrimethylammonium bromide (CTAB) is a ubiquitous surfactant in wastewaters and can favorably affect the interaction between HOCs and nZVI. However, its effect on the Cl-OPEs removal by nZVI-based materials still remains unknown. Herein, the adsorption and degradation efficiencies of Cl-OPEs by nZVI and sulfidated nZVI (S-nZVI) in the presence or absence of CTAB were quantified based on the decreasing concentrations of Cl-OPEs in reaction systems. Our results showed that TDCPP and TCPP were adsorbed onto the nZVI or S-nZVI surface and subsequently degraded. In contrast, TCEP was just adsorbed onto the particle surface without further degradation. The addition of CTAB significantly enhanced the hydrophobic adsorption between Cl-OPEs and nZVI or S-nZVI, leading to increased degradation of Cl-OPEs (especially TCEP). CTAB adsorption isotherms indicated that S-nZVI had a higher adsorption capacity for CTAB than nZVI. The S-nZVI/CTAB composite exhibited a better performance than nZVI/CTAB composite. When S-nZVI was combined with 100.0 mg L−1 CTAB, 100% of TDCPP, TCPP and TCEP was degraded within 3 hours, 5 and 14 days, respectively. As the concentration of CTAB was increased up to 335.0 mg L−1, TCEP could be completely degraded within 3 days by S-nZVI. Five degradation products of TCEP were identified, of which O,O-di-(2-chloroethyl) O-ethyl phosphate (DCEEP) and ethane were reported for the first time. We propose that TCEP is dechlorinated by nZVI or S-nZVI through the electron attack at the ethyl-chlorine group to form bis(2-chloroethyl) phosphate, DCEEP, chloride, ethene and ethane, representing previously unknown degradation pathways.

Original languageEnglish (US)
Article number116447
JournalWater Research
Volume188
DOIs
StatePublished - Jan 1 2021

All Science Journal Classification (ASJC) codes

  • Ecological Modeling
  • Water Science and Technology
  • Waste Management and Disposal
  • Pollution

Keywords

  • ethane
  • hydrophobic adsorption
  • O,O-di-(2-chloroethyl)O-ethyl phosphate
  • S-nZVI/CTAB
  • TCEP

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