Elevated concentration and high Diversity of organophosphate esters (OPEs) were Discovered in Sediment from Industrial, and E-Waste Recycling Areas.

Aquatic environments in industrial, and e-waste recycling areas might undergo severe contamination; however, there are few studies comprehensively assessing the pollution status of organophosphate esters (OPEs) in these two areas. Here, we applied both atmospheric pressure chemical ionization (APCI) and electron spray ionization (ESI) sources in our target, suspect, and functional group-dependent screening strategy, which enhanced the confidence for confirmation on precursor ions of OPEs. Then, n=53 sediment samples (30 from the industrial area, and 23 from the e-waste recycling area) were analyzed. Twenty-three out of 30 target OPEs were quantifiable in these analyzed samples. Total OPE concentrations (ΣOPEs) in samples from e-waste recycling area range from 12.8 to 9250 ng/g dry weight (dw), that are statistically significantly greater (t-test, p < 0.001) than those from industrial area (25.1-5520 ng/g dw). ΣOPEs in the sediments from industrial, or e-waste recycling area are statistically significantly greater (one-way ANOVA, p < 0.001) as compared to those (32.0-369 ng/g dw) from Taihu Lake in our previous study. In sediment from three areas, suspect and non-target analysis fully or tentatively identified other 20 OPEs. Four of them have not been recorded or registered in any of online chemical databases, and they are tentatively named as ((methoxy(phenoxy)phosphoryl)oxy)phenyl diphenyl phosphate (mPPODP), (tert-butyl)phenyl (ethyne-oxidane) bis(2,4-di-tert-butylphenyl) phosphate (TPBDTP), bis(dichlorophenyl) propane-1,3-diyl bis(hexylated phosphate) (BDCBHP), and bis(2-hexadecoxyethyl) ethyl phosphate (BHEPP). Overall, this study provided new insights regarding both analytical methodology and pollution status of OPEs, and highlights that elevated concentrations and high diversity of OPEs exist in sediments from industrial, and e-waste recycling areas.