4.7 Article

Identification of emerging organic pollutants from solid waste incinerations by FT-ICR-MS and GC/Q-TOF-MS and their potential toxicities

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 428, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.128220

Keywords

Organic pollutants; Waste incineration; FT-ICR-MS; GC/Q-TOF-MS; ToxCast library

Funding

  1. National Natural Science Foundation of China [21936007, 91843301, 21906165, 21777172]
  2. National Key Research and Devel-opment Program of China [2019YFE0111100]
  3. Second Tibetan Plateau Scientific Expedition and Research Program (STEP) [2019 QZKK0605]
  4. CAS Interdisciplinary Innovation Team [JCTD-2019-03]
  5. Hebei Academy of Sciences [21109]
  6. Chinese Academy of Sciences [21109]

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Emissions from the incineration of solid waste contain previously unrecognized chemical compounds that pose a global public health concern. Assessing the toxicity and activity of these compounds can provide valuable information for regulating and controlling the emissions from waste incineration.
Emissions from the incineration of solid waste are a global public health concern, but little attention has been paid to previously unrecognized chemical compounds that are generated by waste incineration and released into the atmosphere. We conducted nontarget analysis of organic chemicals formed during waste incineration by Fourier-transform ion cyclotron resonance mass spectrometry and gas chromatography-quadrupole time-of-flight mass spectrometry. Using toxicity data in the ToxCast library and predicted toxicity data for traditional priority polycyclic aromatic hydrocarbons and 2,3,7,8-tetrachlorodibenzo-p-dioxin, we prioritized 13 compounds including hexachloro-1,3-butadiene, 9 of which are reported here for the first time as constituents of emissions from the incineration of solid waste and hexachloro-1,3-butadiene was included in the Stockholm Convention in 2017. The predicted activity of these pollutants to androgen receptors and to the aryl hydrocarbon receptor were comparable to, or higher than, the 2,3,7,8-tetrachlorodibenzo-p-dioxin and benzo [a]pyrene. In addition, some alkylated polycyclic aromatic hydrocarbons and heteroatom polycyclic aromatic hydrocarbons were also identified in solid waste incineration processes, peak areas of which were 1-2 orders of magnitude higher than di-oxins and 1-3 orders of magnitude lower than their parent polycyclic aromatic hydrocarbons. Our study can provide information for better recognizing and regulating the emissions of organic pollutants formed by the incineration of solid waste.

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