Detection Of Persistent Organic Pollutants Research Articles

Porous rod-shaped Fe2O3/Ag/BP: a novel substrate for highly sensitive SERS detection of persistent organic pollutants

A surface enhanced Raman scattering (SERS) substrate of porous rod-shaped ferric oxide (Fe2O3) combined with silver nanoparticles (Ag NPs) and black phosphorus (Fe2O3/Ag/BP) was fabricated to detect the persistent organic pollutants (POPs) at low concentration. The organic pollutant Rhodamine 6G (R6G) was used as the probe molecule to study the performances of Fe2O3/Ag/BP, and 4-chlorobiphenyl (PCB-3) was the target of detection. The limit of detection (LOD) of R6G based on this novel SERS substrate Fe2O3/Ag/BP was as low as 1.0 × 10−15 M, which was five orders of magnitude lower than that of Fe2O3/Ag (10−10 M). The enhancement factor (EF) of Fe2O3/Ag/BP was 6.44 × 108, which was 3.1 times higher than that of porous rod-shaped Fe2O3/Ag (2.08 × 108). The Raman signal of R6G based on Fe2O3/Ag/BP had a good homogeneity, and the relative standard deviation (RSD) of Raman signal intensities of R6G at 1643 cm−1 was only 5.97%. Furthermore, the Fe2O3/Ag/BP substrate exhibited a recyclability through the photocatalytic degradation of R6G. The LOD of PCB-3 based on Fe2O3/Ag/BP was 10−9 M. Besides, Fe2O3/Ag/BP had a high SERS activity even it was kept in a centrifuge tube without requiring complicated treatment. These results highlight the potential application of Fe2O3/Ag/BP for ultra-trace detection of POPs in the environment.

Microextraction of electric fields and analytes by Janus hydrophobic/hydrophilic microfiber filter: Application in Raman detection of persistent organic pollutants in complex liquid environments

As one of the most pressing environmental issues, the prevention and control of persistent organic pollutants (POPs) continue to garner the attention of various fields. However, there is a lack of effective detection methods for trace amounts of POPs in sewage with a complex composition. To address this, a new Janus microextraction surface-enhanced Raman spectroscopy (SERS) strategy was explored in this study. By designing a Janus glass microfiber filter (GF) membrane structure with a superhydrophobic screening surface and a ZIF-8/Ag/GF detection surface, we demonstrated that POPs molecules in mixed sewage can be sensitively detected and specifically adsorbed and enriched. Thus, a concentration of p-aminothiophenol solution as low as 10−12 M was successfully detected with an enhancement factor as high as 5.16 × 109. Additionally, the collected Raman signal remained unimpeded by impurities such as dye molecules or sediment particles in sewage. Most importantly, the Janus GF substrate enabled the separation and detection of other POPs molecules such as PCB-77, perylene, and pyrene, indicating the immense potential of the Janus SERS strategy in the field of POPs detection.

Zr-MOF-Induced Smart Accumulation Enables Surface-Enhanced Raman Spectroscopic Detection of Dioxin at ppt Level in Food Samples.

The fast and economical detection of trace polychlorinated dibenzo-p-dioxins (PCDDs) in food samples by current mass spectrum-based methods is hindered by tedious sample preparation and bulky & expensive analytical instruments. Surface-enhanced Raman spectroscopy (SERS) successfully detects many organic pollutants in foods but not dioxins because the employed metal nanoparticles weakly adsorb hydrophobic PCDDs. Herein, we report the detection of PCDDs in milk with SERS for the first time using a bifunctional substrate consisting of Au nanoparticles embedded in a zirconium-based metal-organic framework shell (AuNP/Zr-MOF). 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD), as the most toxic PCDD, is detected as low as 1.2 parts per trillion (ppt) in real milk samples with massive interfering substances in 30 min, which is the lowest among all reported methods. The aromatic rings of Zr-MOF promote the smart accumulation of TCDD through π-π interactions, and Au-Cl interactions drive TCDD onto Au surfaces. Zr-MOF shells with pore sizes of 12.7 and 20 Å block the accessibility of larger interfering molecules. A one-step apparatus and protocol are established to be superior to traditional methods in terms of time and cost. This work provides new insight into a rational screening method for the detection of persistent organic pollutants in a real sample matrix.

Rapid on-site detection of persistent organic pollutants using multiwalled carbon nanotube-modified paper spray ionization and a miniature mass spectrometer.

Rapid on-site detection of persistent organic pollutants (POP) is highly desirable for environmental protection. Herein, a rapid on-site analytical workflow was developed for the investigation of polycyclic aromatic hydrocarbons and perfluorinated compounds using multiwalled carbon nanotube-modified paper spray ionization (PSI) coupled with a miniature ion trap mass spectrometer. Critical parameters regarding PSI and miniature mass spectrometry analysis were optimized. The analytical performance of the developed method was evaluated under optimized conditions, obtaining a short analysis duration of less than 1min, sufficient linearity with correlation coefficients greater than 0.99, acceptable recovery rates of 93.1%-105.8% with relative standard deviations of between 3.5% and 10.3%, and reasonable sensitivity with limits of detection and quantitation of 2-200 and 5-500 μg/L, respectively. Considering these aspects, it was concluded that the present approach demonstrated a promising solution for rapid on-site detection of emerging POPs.

Biomarkers of Oxidative Stress and Persistent Organic Pollutants in Plasma and Eggs of Chelonia mydas Nesting in the Southern Gulf of Mexico

AbstractThe major nesting sites for the endangered green turtle (Chelonia mydas) are in Campeche, Mexico: Carmen, Isla Aguada, and Sabancuy. Although they are in a natural reserve, these nesting sites are threatened by agricultural activities and oil extraction. This study aimed to determine the presence and concentration of organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in plasma and eggs and to assess the antioxidant response in plasma of nesting C. mydas from the southern Gulf of Mexico. Using censored statistics allowed us to do a realistic calculation incorporating the presence of non-detects in the analysis. A few contaminants (α+β+γ-HCH, trans-chlordane, 4,4′-DDE, 4,4′-DDT, methoxychlor, naphthalene, acenaphthylene, 2-Bromo naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, and dibenz[a,h]anthracene) were detected in plasma and their corresponding eggs, but correlations were not-significant. Spatial differences in concentrations of persistent organic pollutants (POPs) among nesting sites may reflect differences in foraging areas. Approximately 30% of the POPs in plasma and 60% of the POPs in eggs correlated with the biomarkers of oxidative stress. Detection of POPs in C. mydas indicated that plasma and eggs are suitable matrices to assess POPs concentrations.

Evaluation of sample preparation methods for suspect and non-target screening in water, sediment, and biota samples using gas chromatography coupled to high-resolution mass spectrometry

In this study, the sample preparation methods were proposed for the suspect and non-target screening (SNTS) using gas chromatography coupled to high-resolution mass spectrometry in the aquatic environment. The pretreatment methods were evaluated based on detection rates, recoveries, and screening detection limits (SDLs) for 316 substances spiked into surface water, sediment, and biota samples. The detection rates of the spiked compounds were 92.1 % and 98.7 % by the sample preparation methods for water (solid-phase extraction using HLB cartridge) and sediment (ultrasonic extraction (USE) with HLB cartridge clean-up), respectively. Similarly, USE with HLB cartridge clean-up gave the highest detection rate (87.9 %) for biota samples; however, additional pretreatment method using deactivated silica gel clean-up was necessary for the detection of persistent organic pollutants (POPs). The SDL ranges of spiked compounds by the suggested pretreatment methods were 0.01–23.5 ng/L for surface water, 0.02–37.5 ng/g dry weight for sediment, and 0.01–12.2 ng/g wet weight for biota. Although some pollutants, such as POPs had SDLs that were higher than the levels normally detected in the aquatic environment as reported in previous studies, the analytical methods suggested in the present study were satisfactory for the SNTS of most pollutants originated from anthropogenic sources.

Ultrahigh-permeance functionalized boron nitride membrane for nanoconfined heterogeneous catalysis

Practical applications of heterogeneous advanced oxidation processes for organic pollutant destruction remain elusive due to poor yield of reactive oxygen species (ROS) as well as their ultrashort lifetimes and mass transfer limitations. To address these issues, nanoconfined catalysis, whereby improved reaction efficiency is attained due to rapid mass transfer, has recently gained traction in environmental remediation. Here, we introduce a simple concept of functionalizing the boron nitride nanosheet (BNNS) membrane, involving nucleation of cobalt nanocatalysts within the membrane intralayer network of water transport nanochannels. Membrane-confined crystalline reactive species with multiple exposed active sites spontaneously activate peroxymonosulfate, producing ROS for ultrafast (∼80 ms) destruction of organic pollutants at a fast flow rate of 548 L m −2 h −1 . Co-BNNS membrane showed good stability and outperformed previously developed membrane-confined catalysis systems (up to 26-fold higher permeance). Co-BNNS membrane enabled ultrafast destruction of several organic pollutants, offering an attractive alternative for membrane-based catalysis applications. • Cobalt nanocatalysts are grown in boron nitride membrane for heterogeneous catalysis • Analyses confirmed the membrane-confined growth of α-Co(OH) 2 and Co 3 O 4 crystals • Catalysis performance of membrane is explained both theoretically and experimentally • Functionalized membrane can achieve rapid destruction of organic pollutants in 80 ms Water pollution is mainly caused by anthropogenic activities and could disrupt the smooth functioning of economic activities and human health. In this context, detection of persistent organic pollutants, such as pharmaceutical and pesticides, in freshwater bodies is alarming due to their well-documented harmful impacts on human health (e.g., genetic malformations) after prolonged exposure. Due to these severe consequences, clean water (SDG6) and good health (SDG3) are included in the UN sustainable development goals. Herein, we developed a compact platform by combining a membrane separation process and advanced oxidation process in a single step for nanoconfined heterogeneous catalysis of persistent organic pollutants to produce clean water. The in situ functionalization strategy presented here is convenient and allows nucleation of nanocatalysts within the water transport nanochannels of boron nitride membrane, opening a promising avenue for the construction of catalytic membranes. We present an in situ approach of functionalizing the intralayer nanochannels of 2D boron nitride membrane, which allows simultaneous confinement of nanocatalysts, ROS species, and fluids within the intralayer for ultrafast organic pollutant destruction. Compared with conventional AOP reactors, the functionalized boron nitride membrane can be operated in a continuous-flow mode at an ultrahigh water permeance, which would allow its widespread application in water treatment.

Preparation of MOF/Au composite nanoparticles and their SERS properties

Surface-enhanced Raman scattering (SERS) spectrum has the characteristics of fast-detection, high-sensitivity and low-requirements for sample pretreatment. It plays a more and more important role in the detection of organic pollutants. In this study, MIL-101 and Au nanoparticles were prepared by hydrothermal method and aqueous solution reduction method respectively, and MIL-101/Au composite nanoparticles were prepared by electrostatic interaction. The SERS properties of the composite substrate were optimized by adjusting the size of Au nanoparticles and the surface distribution density of MIL-101 nanoparticles. The detection limit of Rhodamine 6G (R6G) for the composite substrate with the optimal ratio was investigated, which was as low as 10–11 M. It is proved that MIL-101/Au composite nanoparticles have high sensitivity to probe molecules. When they are applied to the detection of persistent organic pollutants, the detection limit for fluoranthene can reach 10–9 M and for 3,3’,4,4’-tetrachlorobiphenyl (PCB-77) can reach 10–5 M.

Utilizing ion mobility spectrometry-mass spectrometry for the characterization and detection of persistent organic pollutants and their metabolites.

Persistent organic pollutants (POPs) are xenobiotic chemicals of global concern due to their long-range transport capabilities, persistence, ability to bioaccumulate, and potential to have negative effects on human health and the environment. Identifying POPs in both the environment and human body is therefore essential for assessing potential health risks, but their diverse range of chemical classes challengeanalytical techniques. Currently, platforms coupling chromatography approaches with mass spectrometry (MS) are the most common analytical methods employed to evaluate both parent POPs and their respective metabolites and/or degradants in samples ranging from d rinking water to biofluids. Unfortunately, different types of analyses are commonly needed to assess both theparent and metabolite/degradant POPs from thevarious chemicalclasses. Themultipletime-consuminganalyses necessary thus present a number of technical and logistical challenges when rapid evaluations are needed and sample volumes are limited. To address these challenges, we characterized 64 compounds including parent per- and polyfluoroalkyl substances (PFAS), pesticides, polychlorinated biphenyls (PCBs), industrial chemicals, and pharmaceuticals and personal care products (PPCPs), in addition to their metabolites and/or degradants, using ion mobility spectrometry coupled with MS (IMS-MS)as a potential rapid screening technique. Different ionization sources including electrospray ionization (ESI) and atmospheric pressure photoionization (APPI) were employed to determine optimal ionization for each chemical. Collectively, this study advances the field of exposure assessment by structurally characterizing the 64 important environmental pollutants, assessing their best ionization sources, and evaluating their rapid screening potential with IMS-MS.

Detection of Persistent Organic Pollutants in Omental Adipose Tissue from Patients with Diffuse-Gastric Cancer: A Pilot Study.

Simple SummaryThis pilot study reported the observation that great omentum could be analyzed to detect persistent organic pollutants (POPs). Diffuse gastric cancer is an increasing disease that could be associated with pollutants’ exposition. Here, we report a specific POP profile regarding a patient not affected by cancer, nor by diffuse gastric cancer or other abdominal cancers. The widespread presence of a substantial list of POPs (PCDDs/Fs, PCBs, and brominated flame retardants) was found in the omentum from patients with diffuse gastric cancer with minor presence of some organochlorine pesticides.The greater omentum represents a specific adipose tissue resected with gastric surgery for cancer. Diffuse gastric adenocarcinoma (diffuse-GC) is of major relevance among gastric cancers due to its unknown origin, aggressiveness, and metastasis in the peritoneal cavity. We postulated that persistent organic pollutants (POPs) could be detected in the greater omentum. Great omentum from patients with (i) diffuse-GC, or (ii) with other peritoneal metastatic cancer, and (iii) control group without cancer disease were analyzed for the distribution of a large panel of 96 POPs. POPs include polychlorinated dioxins/furans (PCDD/Fs), polychlorobiphenyls (PCBs), polybrominated diphenyl ethers (PBDE), polybrominated biphenyls (PBB), hexabromocyclododecanes, organochlorine pesticides, and polycyclic aromatic hydrocarbons (PAHs). The widespread presence of a substantial list of POPs (PCDDs/Fs, PCBs, and brominated flame retardants) was found in the omentum from patients with aggressive diffuse-GC, with minor presence of some organochlorine pesticides and PAHs at the low analyzed levels. Some chemicals appeared in larger concentrations in diffuse-GC or other cancer groups, including some PCDDs, PCB105, 123, 138, PBDE209, and PBB153. Overall, the present pilot study provides novel information regarding POPs levels in the omental fat, which is an understudied fat depot in terms of POPs load, and diffuse-GC association.

Distribution characteristics of persistent organic pollutants in water environment based on evolutionary stabilization strategy

In order to solve the problem of poor evaluation performance of pollution parameters in the detection of persistent organic pollutants in water environment, the distribution characteristics of persistent organic pollutants in water environment were studied based on an evolutionary stabilization strategy. The detection method of multi-index system and the regression analysis model of multiple pollution parameters are established. Combined with the method of sample statistical analysis, the statistical characteristics of persistent organic pollutants in water environment are analyzed. The simulation results show that the method can detect the characteristics of persistent organic pollutants in the effluent environment, and the evaluation performance of pollution parameters is good, which can effectively improve the detection ability.

Evaluation of public and animal health risks in case of a delayed post-mortem inspection in ungulates.

The potential effects of a 24 or 72‐h delay in post‐mortem inspection (PMI) of ungulates on public health and monitoring of animal health and welfare was evaluated. The assessment used a survey of meat inspectors, expert opinion, literature search and a stochastic model for Salmonella detection sensitivity. Disease detection sensitivity at a delayed PMI is expected to reduce detection sensitivity to a variable extent, depending on the hazard and on the signs/lesions and organs involved. No reduction is expected for Trichinella detection in meat from susceptible animal species and any decrease in detection of transmissible spongiform encephalopathies (TSEs) will not exceed the current tolerance for fallen stock. A 24‐h delay in PMI could result in a small reduction in sensitivity of detection for tuberculosis, echinococcosis and cysticercosis. A greater reduction is expected for the detection of pyaemia and Rift valley fever. For the detection of Salmonella, the median model estimates are a reduction of sensitivity of 66.5% (90% probability interval (PI) 0.08–99.75%) after 24‐h delay and 94% (90% PI 0.83–100%) after 72‐h delay of PMI. Laboratory testing for tuberculosis following a sampling delay of 24–72 h could result in no, or a moderate, decrease in detection depending on the method of confirmation used (PCR, culture, histopathology). For chemical contaminants, a delay in meat inspection of 24 or 72 h is expected to have no impact on the effectiveness of detection of persistent organic pollutants and metals. However, for certain pharmacologically active substances, there will be a reduced effectiveness to detect some of these substances due to potential degradation in the available matrices (tissues and organs) and the non‐availability of specific preferred matrices of choice.

One-Pot Synthesis of rGO Supported Nb2O5Nanospheres for Ultra-Selective Sensing of Bisphenol a and Hydrazine in Water Samples

Herein, we report a facile solvothermal assisted synthesis of reduced graphene oxide (rGO) supported niobium pentoxide (Nb <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> O <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">5</sub> ) nanosphere modified glassy carbon electrode (rGO-Nb <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> O <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">5</sub> /GCE) sensor for the detection of persistent organic pollutants (POPs) like bisphenol A (BPA) and hydrazine (Hy). The as-fabricated sensor exhibits high sensitivity, selectivity and a wide dynamic range of detection from 10 μM to 300 μM for BPA, at a low electro-oxidation potential of 0.3 V with a sensitivity of 0.153 μA/μM.cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sup> and limit of detection (LOD) of 0.295 μM. Similarly, the sensor exhibits a wide dynamic range of detection from 10 nM to 50 μM under a low electro-oxidation potential of 0.2 V with a low LOD of 2.709 nM and a sensitivity of 11.5 μA/μM.cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sup> for Hy. Additionally, the sensor is found successful in sensing the BPA and Hy in drinking water and tap water samples. The excellent performance of the rGO-Nb <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> O <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">5</sub> /GCE sensor can be attributed to the synergistic effect of rGO, providing excellent electrical conductivity and the Nb <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> O <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">5</sub> providing high electrostatic adsorption of the analyte via Nb <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">4+</sup> /Nb <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">5+</sup> redox couple favouring electrooxidation process at the surface of the electrode. This proves the as-fabricated sensor as an ideal platform for developing simple electrochemical sensors for numerous bioanalytical applications.

Determination of Persistent Organic Pollutants (POPs) in Propolis by Solid-Phase Extraction (SPE) and Gas Chromatography – Mass Spectrometry (GC-MS)

Bee products produced in environments with persistent organic pollutants (POPs) may be contaminated by these compounds. Propolis usually consists of beeswax, resins, water, inorganic and phenolic substances, and essential oils. Although there are some studies on the detection of POPs in honey and some bee products, these are quite limited. Because propolis is a botanical-based and highly complex matrix, and thus difficult to analyze, a reliable and selective method based on solid-phase extraction (SPE) combined with gas chromatography-mass spectrometry was developed for the determination of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in the propolis. All analytes were extracted with acetonitrile and centrifuged for 10 min at 4000 rpm and 6 °C in a refrigerated centrifuge. The samples were filtered using a homemade SPE cartridge containing C18, primary-secondary amine, and magnesium sulfate. The residue collected with acetonitrile was subsequently analyzed by gas chromatography – mass spectrometry (GC-MS). The proposed method was validated according to the Eurachem guidelines and applied directly to the collected propolis samples. The results show that the method may be used successfully in residue monitoring laboratories for the determination of OCPs, PCBs and PBDEs in propolis.

Ratiometric Sensing of Polycyclic Aromatic Hydrocarbons Using Capturing Ligand Functionalized Mesoporous Au Nanoparticles as a Surface-Enhanced Raman Scattering Substrate.

The absorption behavior between plasmonic nanostructures and a target molecule plays key roles in effective surface-enhanced Raman scattering (SERS) detection. However, for analytes with low surface affinity to the metallic surface, e.g., polycyclic aromatic hydrocarbons (PAHs), it remains challenging to observe the enhanced Raman signal. In this work, we reported a ratiometric SERS strategy for sensitive PAH detection through the surface functionalization of 3D ordered mesoporous Au nanoparticles (meso-Au NPs). By employing mono-6-thio-β-cyclodextrin (HS-β-CD) as capture ligands, the hydrophobic molecules, e.g., anthracene, could be effectively absorbed on the meso-Au NP surface via a host-guest interaction. Besides, a hydrophobic slippery surface is used as a concentrator to deliver and enrich the Au/analyte droplets into a small area. Consequently, the detection limits of anthracene and naphthalene are down to 1 and 10 ppb. The improved SERS enhancement is mainly ascribed to the host-guest effect of HS-β-CD ligands, large surface area and high-density of sub-10 nm mesopores of Au networks, as well as the enrichment effect of hydrophobic slippery surface. Moreover, the HS-β-CD (480 cm-1 band) could serve as an internal standard, leading to the ratiometric determination of anthracene ranging from 1 ppm to 1 ppb. The proposed surface modification strategy in combination with the hydrophobic slippery surface shows great potential for active capture and trace detection of persistent organic pollutants in real-world SERS applications.

QUICK: Quality and Usability Investigation and Control Kit for Mass Spectrometric Data from Detection of Persistent Organic Pollutants.

Persistent organic pollutants (POPs) cause a significant public and environmental health concern due to their toxicity, long-range transportability, persistence, and bioaccumulation. The US Food and Drug Administration (FDA) has a program to monitor POPs in human and animal foods at ultra-trace levels, using gas chromatography coupled with mass spectrometry (GC–MS). Stringent quality control procedures are practiced within this program, ensuring the reliability and accuracy of these POP results. Due to the complexity of this program’s quality control (QC), the decision-making process for data usability was very time-consuming, upward of three analyst hours for a batch of six extracts. We significantly reduced this time by developing a software kit, written in Python, to evaluate instrument and sample QC, along with data usability. A diverse set of 45 samples were tested using our software, QUICK (Quality and Usability Investigation and Control Kit), that resulted in equivalent results provided by a human reviewer. The software improved the efficiency of the analytical process by reducing the need for user intervention, while simultaneously recognizing a 95% decrease in data reduction time, from 3 hours to 10 minutes.

Monitoring of environmental persistent organic pollutants in hair samples collected from wild terrestrial mammals of Primorsky Krai, Russia.

Persistent organic pollutants (POPs) constitute a wide range of chemicals. Their release into the environment has raised great concern due to their potentially harmful impact in humans and wildlife species. The aim of this current study was to detect selected POPs in hair samples of wild terrestrial mammals from Primorsky Krai, Russia, so as to assess potential environmental exposure. The tested wild species were leopard cat, musk deer, wolf, amur hedgehog, and raccoon dog. The targeted organochlorines were hexachlorobenzene (HCB) and DDTs (opDDE, ppDDE, and opDDD), polychlorinated biphenyl (PCB) congeners (28, 52, 101, 118, 138, 153, and 180), and polycyclic aromatic hydrocarbons (PAHs) (acenaphylene (ACEN), fluorene (FLU), anthracene (ANTH) phenathrene (PHEN), and pyrene (PYR)). The detection of POPs was conducted in hair samples by a one-step hair extraction method, by using a headspace solid-phase microextraction technique (HS-SPME) and analyzed then by GC-MS. The majority of the wild animal hair samples were found positive in all tested pollutants. More specifically, the percentage of positive hair samples for HCB was 93.3% and for DDTs, PCBs, and PAHs, 20.0 to 100.0%, 6.7 to 100.0%, and 75.0 to 100.0%, respectively. DDT, PCB, and PAH detection ranged from 1.26 to 52.06pgmg-1, 0.73 to 31.34pgmg-1, and 2.59 to 35.00pgmg-1, respectively. The highest mean concentration levels of all tested pollutants were found for musk deer (PCBs 12.41pgmg-1, DDTs 21.87pgmg-1, PAHs 22.12pgmg-1) compared to the other wild species. To the best of our knowledge, this is the first study that provides results regarding contamination in different terrestrial mammals by POP exposure. The use of hair as a matrix is proven to be an effective tool for nondestructive biological monitoring of POP contamination in terrestrial ecosystems.

Electrochemical Sensing of Bisphenol A on Facet-Tailored TiO2 Single Crystals Engineered by Inorganic-Framework Molecular Imprinting Sites.

Noble metals, nanostructured carbon, and their hybrids are widely used for electrochemical detection of persistent organic pollutants. However, despite of the rapid detection process and high accuracy, these materials generally suffer from high costs, metallic impurity, heterogeneity, irreversible adsorption and poor sensitivity. Herein, the high-energy {001}-exposed TiO2 single crystals with specific inorganic-framework molecular recognition ability was prepared as the electrode material to detect bisphenol A (BPA), a typical and widely present organic pollutant in the environment. The oxidation peak current was linearly correlated to the BPA concentration from 10.0 nM to 20.0 μM ( R2 = 0.9987), with a low detection limit of 3.0 nM (S/N = 3). Furthermore, it exhibited excellent discriminating ability, high anti-interference capacity, and good long-term stability. Its good performance for BPA detection in real environmental samples, including tap water, lake and river waters, domestic wastewater, and municipal sludge, was also demonstrated. This work extends the applications of TiO2 semiconductor and suggests that this material could be used as a highly active, stable, low-cost, and environmentally benign electrode material for electrochemical sensing.

Thymine based copolymers: feasible sensors for the detection of persistent organic pollutants in water

A multidisciplinary approach for understanding properties of thymine-based copolymer sensors.

Detection of Persistent Organic Pollutants in Blood Serum of Electricians and Welders in Latvia

Abstract Persistent organic pollutants (POPs) are chemical substances that persist in the environment, bioaccumulate through the food web, and pose a risk of causing adverse effects to human health and the environment. The aim of the study was to assess the POP (polychlorinated biphenyls (PCBs), polybrominated diphenylethers (PBDEs), DDT and their derivatives) levels in blood serum to identify possible risk group workers. Blood serum samples (116 in total) were collected from two groups of employees — electricians, who can come in contact with PCB-containing transformer and capacitor oil, and welders, who were used as a control group. Sample purification was done by double solid phase extraction. The concentrations of POPs in blood serum were determined by gas chromatography with electron capture detector GC/ECD and recovery controlled by internal standard CB-174. None of the 116 samples contained the full range of tested POPs. However, all samples contained at least one of pesticides, and a marker PCB and mono-ortho PCB. Blood serum samples of 52% of electricians and 97.8% of welders contained non-ortho PCB compared to 84% and 74.7%, respectively, for PBDE’s. The concentrations of 18 detected PCBs, 4 detected PBDEs and 6 chlorinated pesticides and their metabolites varied in wide ranges and the differences in mean values between groups were not statistically significant (p &gt; 0.05). The estimated concentrations of POPs correspond to the lowest levels detected in other countries. Mean concentrations of low-chlorinated marker PCBs were higher in the electrician group, suggesting that the employment sites are contaminated with PCBs, or that employees have contact with PCB-containing items.