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The development of highly selective and sensitive analytical methods for the nontarget screening of persistent organic pollutants such as halogenated compounds in environmental samples is a challenging task. Soft ionization mass spectrometry has emerged as a powerful technique for obtaining essential molecular information, and it is expected to reveal compounds that remain hidden with conventional fragmentation techniques such as electron ionization (EI). In this study, a soft ionization method based on electron capture negative ionization using an inert gas was developed for the nontarget screening of chlorinated aromatics in environmental samples and was applied to comprehensive two-dimensional gas chromatography-high-resolution time-of-flight mass spectrometry (GC × GC-HRToFMS). In particular, argon (Ar) and helium (He) were evaluated as inert moderating gases, and were compared against the conventional methane (CH 4 ). The optimal ionization conditions, including the flow rate and ion source temperature, were investigated based on the molecular ion intensities of highly chlorinated aromatics decachlorobiphenyl and octachlorodibenzofuran. Ar-mediated soft ionization provided the best sensitivity to molecular ions among the three gases at a low flow rate (0.1 mL min -1 ) and low ion source temperature, and more selective detection of molecular ions (i.e., less fragmentation) was obtained with the inert gases than with CH 4 . This method is also applicable to other chlorinated aromatics such as tetra- to nonachlorobiphenyls, tetra- to heptachlorinated dibenzofurans, pentachlorobenzene, and hexachlorobenzene. To demonstrate the applicability of the proposed method to a wide range of chlorinated aromatics in environmental samples, both Ar-mediated soft ionization and conventional EI were applied to GC × GC-HRToFMS for analysis of a crude extract of house dust. Soft ionization enabled the selective and sensitive detection of molecular ions for minor amounts of chlorinated aromatics, even in complex matrices. Furthermore, the extracted ion chromatograms of halide anions (Cl - or Br - ) were useful for screening other chlorinated or brominated compounds in the environmental samples. The results suggest that combining information on halide anions obtained by soft ionization and the structural information provided by EI would constitute a powerful approach for the comprehensive identification of chlorinated aromatics., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

As reproducible coating of stir bars with more polar phases was found to be very difficult, a supporting grid was used in the development of an ethyleneglycol-modified Silicone (EG Silicone) coated stir bar. This new polar coating showed good performance for the extraction of polar solutes, but long term use also showed degradation of the coating due to friction while stirring. In order to address the lower robustness of the EG Silicone stir bar which has a much softer coating compared to a conventional polydimethylsiloxane (PDMS) stir bar, a novel SBSE procedure termed multi-SBSE ((m)SBSE) was developed. (m)SBSE consists of the robust PDMS stir bar stirring at the bottom of the vial and the EG Silicone stir bar attached on the inner side wall of the vial (a magnetic clip is used for the set-up). After extraction, the two stir bars are placed in a single glass desorption liner and are simultaneously thermally desorbed. The desorbed compounds were analyzed by thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS). Compared to conventional SBSE, (m)SBSE provides more uniform enrichment of a wide range of odor compounds in aqueous sample since both stir bars can complement each other, while eliminating the damage of the EG Silicone phase during the extraction. The robustness of the EG Silicone stir bar was dramatically increased and more than 30 extraction and desorption cycles were possible without loss in performance. The recoveries for polar solutes such as 2-acetyl pyrrole (logKow: 0.55), benzyl alcohol (logKow: 1.08), guaiacol (logKow: 1.34), and indole (logKow: 2.05) were increased by a factor of about 2-7. The (m)SBSE-TD-GC-MS method showed good linearity (r(2)>0.9913) and high sensitivity (limit of detection: 0.011-0.071 ng mL(-1)) for the test compounds spiked in water. The feasibility and benefit of the method was demonstrated with analysis of odor compounds in roasted green tea. The normalized areas obtained from (m)SBSE showed the best enrichment for most of the selected compounds compared to conventional SBSE using the PDMS stir bar or the EG Silicone stir bar. Fifteen compounds were determined in the range of 0.15-210 ng mL(-1) (RSD<14%, n=6)., (Copyright © 2013 Elsevier B.V. All rights reserved.)

We developed a highly sensitive method for determination of polycyclic aromatic hydrocarbons (PAHs) and their derivatives (oxygenated, nitrated, and methylated PAHs) in trace particulate samples by using thermal desorption followed by comprehensive two-dimensional gas chromatography coupled with tandem mass spectrometry (TD-GC×GC-MS/MS) with a selected reaction monitoring mode. The sensitivity of TD-GC×GC-MS/MS was greater than that of TD-GC-HRMS and TD-GC×GC-QMS by one or two orders of magnitude. The instrumental detection limits were 0.03-0.3pg (PAHs), 0.04-0.2pg (oxygenated PAHs), 0.03-0.1pg (nitrated PAHs), and 0.01-0.08pg (methylated PAHs). For small amounts (10-20μg) of standard reference materials (SRMs 1649a and 1650b, urban dust and diesel exhaust particles, respectively), the values measured by using TD-GC×GC-MS/MS agreed with the certified or reference values within a factor of two. Major analytes were quantified successfully by TD-GC×GC-MS/MS from diesel exhaust nanoparticles (18-32nm) and accumulation-mode particles (100-180nm) from an 8-L diesel engine with no exhaust after-treatment system. The PAH profiles differed among driving conditions but they did not differ markedly among the particle sizes., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A method for the determination of ultra-trace amounts of organochlorine pesticides (OCPs) in river water was developed by using stir bar sorptive extraction (SBSE) followed by thermal desorption and comprehensive two-dimensional gas chromatography coupled to high-resolution time-of-flight mass spectrometry (SBSE-TD-GC×GC-HRTOF-MS). SBSE conditions such as extraction time profiles, phase ratio (β: sample volume/polydimethylsiloxane (PDMS) volume), and modifier addition, were examined. Fifty milli-liter sample including 10% acetone was extracted for 3 h using stir bars with a length of 20 mm and coated with a 0.5 mm layer of PDMS (PDMS volume, 47 μL). The stir bar was thermally desorbed and subsequently analyzed by GC×GC-HRTOF-MS. The method showed good linearity over the concentration range from 50 to 1000 pg L(-1) or 2000 pg L(-1) for all analytes, and the correlation coefficients (r(2)) were greater than 0.9903 (except for β-HCH, r(2)=0.9870). The limit of detection (LOD) ranged from 10 to 44 pg L(-1). The method was successfully applied to the determination of 16 OCPs at pg L(-1) to ng L(-1) in river water. The results agree fairly well with the values obtained by a conventional liquid-liquid extraction (LLE)-GC-HRMS (selected ion monitoring: SIM) method using large sample volume (20 L). The method also allows screening of non-target compounds, e.g. pesticides and their degradation products, polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and pharmaceuticals and personal care products (PPCPs) and metabolites in the same river water sample, by using full spectrum acquisition with accurate mass in GC×GC., (Copyright © 2011 Elsevier B.V. All rights reserved.)

We successfully detected halogenated compounds from several kinds of environmental samples by using a comprehensive two-dimensional gas chromatograph coupled with a tandem mass spectrometer (GC×GC-MS/MS). For the global detection of organohalogens, fly ash sample extracts were directly measured without any cleanup process. The global and selective detection of halogenated compounds was achieved by neutral loss scans of chlorine, bromine and/or fluorine using an MS/MS. It was also possible to search for and identify compounds using two-dimensional mass chromatograms and mass profiles obtained from measurements of the same sample with a GC×GC-high resolution time-of-flight mass spectrometer (HRTofMS) under the same conditions as those used for the GC×GC-MS/MS. In this study, novel software tools were also developed to help find target (halogenated) compounds in the data provided by a GC×GC-HRTofMS. As a result, many dioxin and polychlorinated biphenyl congeners and many other halogenated compounds were found in fly ash extract and sediment samples. By extracting the desired information, which concerned organohalogens in this study, from huge quantities of data with the GC×GC-HRTofMS, we reveal the possibility of realizing the total global detection of compounds with one GC measurement of a sample without any pre-treatment., (Copyright © 2011 Elsevier B.V. All rights reserved.)

A method for the analysis of chlorinated and brominated polycyclic aromatic hydrocarbon (Cl-/Br-PAHs) congeners in environmental samples, such as a soil extract, by comprehensive two-dimensional gas chromatography coupled to a high resolution time-of-flight mass spectrometry (GC×GC-HRTOF-MS) is described. The GC×GC-HRTOF-MS method allowed highly selective group type analysis in the two-dimensional (2D) mass chromatograms with a very narrow mass window (e.g. 0.02Da), accurate mass measurements for the full mass range (m/z 35-600) in GC×GC mode, and the calculation of the elemental composition for the detected Cl-/Br-PAH congeners in the real-world sample. Thirty Cl-/Br-PAHs including higher chlorinated 10 PAHs (e.g. penta, hexa and hepta substitution) and ClBr-PAHs (without analytical standards) were identified with high probability in the soil extract. To our knowledge, highly chlorinated PAHs, such as C(14)H(3)Cl(7) and C(16)H(3)Cl(7), and ClBr-PAHs, such as C(14)H(7)Cl(2)Br and C(16)H(8)ClBr, were found in the environmental samples for the first time. Other organohalogen compounds; e.g. polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs), and polychlorinated dibenzofurans (PCDFs) were also detected. This technique provides exhaustive analysis and powerful identification for the unknown and unconfirmed Cl-/Br-PAH congeners in environmental samples., (Copyright © 2011 Elsevier B.V. All rights reserved.)

A method is described for characterization of size-resolved particles including the nanoparticles fraction with a diameter of 29-58 nm in roadside atmosphere. The method is based on thermal desorption (TD) of a sample followed by comprehensive two-dimensional gas chromatography (GC x GC) with novel detection capabilities, including high resolution time-of-flight mass spectrometry (HRTOF-MS) and simultaneous detection with a nitrogen phosphorous detector (NPD) and a quadrupole mass spectrometer (qMS). Increased selectivity with the GC x GC-HRTOF-MS allows a group type separation of a selected chemical class, e.g. oxygenated polycyclic aromatic hydrocarbons (oxy-PAHs), using mass chromatography with a 0.05 Da wide window in the complex sample matrix. Also, exact mass measurements provide candidate elemental compositions as well as NIST library search results for tentative identifications of 50 compounds. Moreover, the simultaneous detection with the NPD and the qMS elucidate the presence of 15 nitrogen-containing compounds. Quantitative analysis of selected PAHs in several size-resolved particles was also performed by use of the TD-GC x GC-qMS with limited scan range. The method showed good linearity (r2>0.988) and high sensitivity (limit of quantification: <10 pg) for most of the target PAHs. The concentration of PAHs per particulate matter (PM) mass in nanoparticles was considerably higher than those of larger size of particles with a diameter of >102 nm.