PMID- 38197207 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240113 IS - 1872-2059 (Electronic) IS - 1000-8713 (Print) IS - 1000-8713 (Linking) VI - 42 IP - 1 DP - 2024 Jan 8 TI - [Matrix solid-phase dispersion extraction of organophosphorus flame retardants in soil based on response surface methodology]. PG - 64-74 LID - 10.3724/SP.J.1123.2023.04018 [doi] AB - Organophosphorus flame retardants (OPFRs) are widely used in commercial products owing to their exceptional flame-retarding and plasticizing properties. However, OPFRs are also well recognized as emerging persistent organic pollutants (POPs) because of their environmental persistence, biological concentration, and potential toxicity. Thus, the accurate detection of OPFRs in environmental media is critical for analyzing their fate, transport, and ecological risk. However, very few OPFR detection methods are currently available, and the types of OPFRs detected may vary from site to site. In this study, matrix solid-phase dispersion extraction (MSPD), a simple, rapid, and versatile technique for preparing solid, semisolid, liquid, and viscous samples, was combined for the first time with gas chromatography-tandem mass spectrometry (GC-MS/MS) to analyze 10 OPFRs in soil, namely, tripropyl phosphate (TPrP), tri-n-butyl phosphate (TnBP), tri-iso-butyl phosphate (TiBP), tris(2-chloroisopropyl) phosphate (TCIPP), tris(2-chloroethyl) phosphate (TCEP), tris(1,3-dichloro-2-propyl) phosphate (TDCPP), triphenyl phosphate (TPHP), 2-ethylhexyl diphenyl phosphate (EHDPP), triphenylphosphine oxide (TPPO), and trimethylphenyl phosphate (TCP). The GC-MS/MS system was equipped with a Bruker-5MS capillary column coupled with a triple quadrupole mass spectrometer operated in multiple reaction monitoring (MRM) mode. Prior to detection, a mixed standard solution was fortified with 10 ng of(13)C-PCB208 as an internal standard. The optimal conditions under which MSPD could achieve high selectivity for OPFRs were determined. In addition, single-factor analysis was used to examine the influence of the sorbent (i. e., C18, PSA, Florisil, GCB, and multiwalled carbon nanotubes (MWCNTs)) as well as the dosage, type, and volume of the eluent on the extraction efficiency of the method for the 10 OPFRs. When GCB and ethyl acetate were used as the adsorbent and solvent, respectively, during elution, high extraction recoveries for the OPFRs were achieved. Optimization via response surface methodology (RSM) was adopted to further analyze the impact of three key factors, namely, the adsorbent dosage, eluent volume, and grinding time, as well as their interactions, on OPFR recoveries. Under the optimal conditions of 0.3 g of GCB as the adsorbent, 10 mL of ethyl acetate as the eluent, and 5 min of grinding time, the relative average recovery of the OPFRs was 87.5%. Furthermore, the 10 OPFRs showed good linear relationships under five concentration gradients, with correlation coefficients greater than 0.998. The limits of detection (LODs) and quantification (LOQs) were calculated as signal-to-noise ratios (S/N) of 3 and 10, respectively, and found to be in the ranges of 0.006-0.161 and 0.020-0.531 ng/g, respectively. The performance of the proposed method was verified by determining the recoveries and relative standard deviations (RSDs) of the OPFRs in soils spiked at low, medium, and high levels (10, 20, and 100 ng/g, respectively). The recoveries of the OPFRs ranged from 70.4% to 115.4%, with RSDs ranging from 0.7% to 6.7%. Compared with the conventional accelerated solvent extraction (ASE) method, MSPD presents higher efficiency, simpler operation, and less solvent requirements. The developed method was applied to determine OPFRs in soil samples collected from different sites in Suzhou, including an electronics factory, an auto-repair factory, a paddy field, and a school field. The results revealed that the contents of OPFRs in the soils from the electronics and auto-repair factories were significantly higher than those in the soils from the paddy and school fields. The main pollutants in the soil samples collected from the electronics and auto-repair factories were TCIPP, TPPO, TCEP, and TDCPP. Moreover, the contents of these compounds were 5.30, 4.44, 4.54, and 4.20 ng/g, in soils from the electronics factory and 2.70, 3.93, 7.60, and 5.04 ng/g, in soils from the auto-repair factory. To the best of our knowledge, this study is the first to determine high concentrations of TPPO in industrial soils. Thus, the combination of MSPD and GC-MS/MS adopted in this study can provide useful insights into the detection of the 10 OPFRs in soil. FAU - Wang, Junxia AU - Wang J AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. AD - Jiangsu Key Laboratory for Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Xu, Sijie AU - Xu S AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Sun, Yueying AU - Sun Y AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Lei, Huihui AU - Lei H AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Cheng, Yuanyuan AU - Cheng Y AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Wang, Xuedong AU - Wang X AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. FAU - Zhang, Zhan'en AU - Zhang Z AD - School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. AD - Jiangsu Key Laboratory for Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China. LA - chi PT - English Abstract PT - Journal Article PL - China TA - Se Pu JT - Se pu = Chinese journal of chromatography JID - 9424804 SB - IM PMC - PMC10782277 OTO - NOTNLM OT - gas chromatography-tandem mass spectrometry (GC-MS/MS) OT - matrix solid-phase dispersion extraction (MSPD) OT - organophosphorus flame retardants (OPFRs) OT - response surface methodology (RSM) OT - soil EDAT- 2024/01/10 06:41 MHDA- 2024/01/10 06:42 PMCR- 2024/01/08 CRDT- 2024/01/10 04:33 PHST- 2024/01/10 06:42 [medline] PHST- 2024/01/10 06:41 [pubmed] PHST- 2024/01/10 04:33 [entrez] PHST- 2024/01/08 00:00 [pmc-release] AID - 10.3724/SP.J.1123.2023.04018 [doi] PST - ppublish SO - Se Pu. 2024 Jan 8;42(1):64-74. doi: 10.3724/SP.J.1123.2023.04018.