Nontarget and Comprehensive Analyses of Halogenated Organic Additives in Electrical Product Plastics by GC-NCI-Q-Orbitrap-HRMS and Cl/Br-Screening Algorithms.

Halogenated organic additives (HOAs) are used in plastic components of various electrical products, potentially causing detrimental effects on the eco-environment and humans. Besides reported HOAs, many unknown HOAs may be present in electrical product plastics and urgently require identification and characterization. This study performed nontarget analysis and comprehensive characterization of HOAs in three typical electrical product plastics by nontarget analysis using gas chromatography-negative chemical ionization-high-resolution mass spectrometry in association with in-house-developed chlorine/bromine-specific data-processing algorithms. A total of 674 formulas of HOAs were identified in the plastics dismantled from three electrical products, among which 166, 362, and 146 were organochlorines, organobromines, and mix-chlorinated/brominated organic compounds, respectively. The identified HOAs were semiquantified, and the total concentrations of HOAs in individual plastics were 445-1549 ng/g. Organobromines showed the most species and the highest abundances in all of the plastics, of which the abundances accounted for 86.6-98.0% of the total HOAs. Partial HOAs (209 formulas) were tentatively structurally elucidated, which were classified into 13 groups, i.e., halogenated alkyl phenoxyethyls (H-alkyl phenoxyethyls), H-alkylbenzenes, H-benzenes, H-bisphenol A (H-BPAs), H-dioxins, H-diphenyl ethers, H-biphenyls/terphenyls, H-polycyclic aromatic hydrocarbons, H-phenols, H-phenyl esters, H-phenyl-aldehydes/ketones, H-quinones, and an undefined group containing the HOAs such as dechlorane plus and chlordane. H-BPAs were the predominant HOAs in the plastics, showing relatively high concentrations (13-281 ng/g), and tetrabromobisphenol A was the most abundant H-BPA, with the concentrations of 9-196 ng/g. The comprehensive characterization results represent a holistic picture on the species features and abundance distributions of HOAs in electrical product plastics and provide an inventory of crucial HOAs worthy of concern. HOAs may migrate from plastics and release into the environment and are possibly an important source of halogenated organic pollutants in the environment, thus calling for further investigation and proper regulation.

High temperature resistant ultra-short DBR Yb-doped fiber laser.

We present a distributed Bragg reflector (DBR) Yb-doped fiber laser based on a pair of type IA fiber Bragg gratings (FBGs). The high temperature resistant gratings are fabricated in high absorption hydrogen loaded Yb-doped silica fiber by use of a 244 nm argon laser and phase mask method. The DBR laser, with only 10 mm cavity length, exhibits high signal-noise ratio (SNR) of over 50 dB and can survive at 450°C in a long term with stable output power and central wavelength. Besides, the laser has a relatively low temperature sensitivity of 8.9 pm/°C, which contributes to cross-sensitization of stress and temperature.

High-Temperature Sensor Based on Fabry-Perot Interferometer in Microfiber Tip.

A miniaturized tip Fabry-Perot interferometer (tip-FPI) is proposed for high-temperature sensing. It is simply fabricated for the first time by splicing a short length of microfiber (MF) to the cleaved end of a standard single mode fiber (SMF) with precise control of the relative cross section position. Such a MF acts as a Fabry-Perot (FP) cavity and serves as a tip sensor. A change in temperature modifies the length and refractive index of the FP cavity, and then a corresponding change in the reflected interference spectrum can be observed. High temperatures of up to 1000 °C are measured in the experiments, and a high sensitivity of 13.6 pm/°C is achieved. This compact sensor, with tip diameter and length both of tens of microns, is suitable for localized detection, especially in harsh environments.

Ultrasensitive Mach-Zehnder Interferometric Temperature Sensor Based on Liquid-Filled D-Shaped Fiber Cavity.

A liquid-filled D-shaped fiber (DF) cavity serving as an in-fiber Mach–Zehnder interferometer (MZI) has been proposed and experimentally demonstrated for temperature sensing with ultrahigh sensitivity. The miniature MZI is constructed by splicing a segment of DF between two single-mode fibers (SMFs) to form a microcavity (MC) for filling and replacement of various refractive index (RI) liquids. By adjusting the effective RI difference between the DF and MC (the two interference arms), experimental and calculated results indicate that the interference spectra show different degrees of temperature dependence. As the effective RI of the liquid-filled MC approaches that of the DF, temperature sensitivity up to −84.72 nm/°C with a linear correlation coefficient of 0.9953 has been experimentally achieved for a device with the MC length of 456 μm, filled with liquid RI of 1.482. Apart from ultrahigh sensitivity, the proposed MCMZI device possesses additional advantages of its miniature size and simple configuration; these features make it promising and competitive in various temperature sensing applications, such as consumer electronics, biological treatments, and medical diagnosis.

High power all-fiber amplifier with different seed power injection.

We report a high power all-fiber amplifier with suitable seed power injected by an all-fiber laser. Different seed powers were injected into the all-fiber amplifier during our amplification experiments, and we found the stimulated Raman scattering (SRS) threshold was inversely proportional to the injected seed power. More than 3 kW signal light with good beam quality (M2 = 1.28) has been obtained with a suitable seed power injected, and the slope efficiency of the all-fiber amplifier was about 84.4%.

Tissue Distribution, Growth Dilution, and Species-Specific Bioaccumulation of Organic Ultraviolet Absorbents in Wildlife Freshwater Fish in the Pearl River Catchment, China.

Tissue distributions and body-size dependent and species-specific bioaccumulation of 12 organic ultraviolet absorbents (UVAs) were investigated in 9 species of wildlife freshwater fish from the Pearl River catchment, South China. The concentrations of the 12 UVAs were from 109 to 2320 ng/g lipid weight in the fish tissue samples. The UVAs 2-hydroxy-4-methoxybenzophenone (BP-3), octocrylene (OCR), UV531, and 5 benzotriazole UV stabilizers (UVP, UV329, UV234, UV328, and UV327) were detected in more than half of the fish tissue samples. The UVA UV531 showed an obvious potential for bioaccumulation in the wild freshwater fish, with an estimated bioaccumulation factor (log BAF) and a biota-sediment accumulation factor (BSAF) of 4.54 ± 0.55 and 4.88 ± 6.78, respectively. Generally, liver (989 ± 464 ng/g lipid wt) contained the highest level of UVAs, followed in decreasing order by belly fat (599 ± 318 ng/g lipid wt), swimming bladder (494 ± 282 ng/g lipid wt), dorsal muscle (470 ± 240 ng/g lipid wt), and egg (442 ± 238 ng/g lipid wt). The bioaccumulation of UVAs in the freshwater wild fish was species specific and compound dependent. Bottom-dwelling detritus-ingesting omnivorous fish contained obviously higher UVA concentrations, suggesting that detritus/sediment ingestion is a significant pathway for exposure of the wild freshwater fish to the UVAs. The UVAs UV531 and BP-3 demonstrated a potential for growth dilution. Metabolism might play a significant role in elimination of the UVAs in the fish tissues, with the highest rate of metabolism in the liver. The UVAs did not demonstrate obvious trophic magnification in the freshwater ecosystem of the Pearl River catchment. More research is warranted to elucidate maternal transfer of the UVAs. Environ Toxicol Chem 2020;39:343-351. © 2019 SETAC.

Body size-dependent bioaccumulation, tissue distribution, and trophic and maternal transfer of phenolic endocrine-disrupting contaminants in a freshwater ecosystem.

Parabens, bisphenol A (BPA), triclosan, and triclocarban are recognized endocrine-disrupting contaminants (EDCs); and their occurrence in the environment has attracted increasing concern. Body size-dependent bioaccumulation, tissue distribution, trophic magnification, and maternal transfer of methyl-, ethyl-, propyl-, and butylparabens; 2-phenylphenol (PHP); BPA; triclosan; and triclocarban were investigated in freshwater fish of the Pearl River catchment, China. Most of the EDCs were detected in more than half of the biota samples, ranging from not detected to 6750 ng g-1 lipid weight, with median concentrations of 5 to 72 ng g-1 lipid weight. Livers generally contained the highest EDC levels (1609 ± 1860 ng g-1 lipid wt, mean ± standard deviation), followed in decreasing order by eggs (842 ± 1317 ng g-1 lipid wt), belly fats (488 ± 465 ng g-1 lipid wt), and dorsal muscles (240 ± 239 ng g-1 lipid wt) of the wildlife. Body size-dependent bioaccumulation of the EDCs was observed in the freshwater fish, which varied according to species, tissue, and compound. The concentrations of triclosan, PHP, and BPA usually showed decreasing trends, whereas parabens mostly demonstrated increasing tendency with increasing fish weights, indicating effects of growth dilution and bioaccumulation, respectively. Potential biomagnification was shown by triclosan with trophic magnification factors of 3.0, 4.3, and 4.0 in liver, belly fat, and dorsal muscle, respectively. In addition, the potential of maternal transfer in the fish was primarily revealed for methyl- and propylparabens, PHP, triclosan, and BPA. Presence of the EDCs in the freshwater organisms of the Pearl River catchment warrants more attention considering the potential of trophic magnification and maternal transfer. Environ Toxicol Chem 2018;37:1811-1823. © 2018 SETAC.

Bioaccumulation and biomagnification of ultraviolet absorbents in marine wildlife of the Pearl River Estuarine, South China Sea.

Bioaccumulation and trophic transfer in ecosystems is an important criterion for assessing environmental risks of contaminants. This study investigated bioaccumulation and biomagnification of 13 organic ultraviolet absorbents (UVAs) in marine wildlife organisms in the Pearl River Estuary, South China Sea. The UVAs could accumulate in the organisms with biota - sediment accumulation factors (BSAF) of 0.003-2.152. UV531 was the most abundant and showed the highest tendency to accumulate in the organisms with a median BSAF of 1.105. The UVAs demonstrated species - and compound-specific accumulation in the marine organism. Fishes showed significantly higher capability than the cephalopods and crustaceans in accumulation of the UVAs. Habitat did not demonstrate obvious impact on accumulation of the UVA. On the other hand, benzophenone-3, UV328, and UV234 showed significantly higher concentration in the detritus feeding fishes than carnivorous and planktivorous fishes, suggesting governing effect of dietary habits of the organisms on bioaccumulation of these UVAs. Direct uptake from growth media was a significant exposure pathway of the organisms to the UVAs. The estimated trophic magnification factors and biomagnification factors revealed that UV329, UV531, and octocrylene could potentially biomagnify in the marine food web.

Chlorine and bromine isotope fractionation of halogenated organic pollutants on gas chromatography columns.

Compound-specific chlorine/bromine isotope analysis (CSIA-Cl/Br) has become a powerful approach to investigate degradation pathways and apportion sources of halogenated organic pollutants (HOPs) in the environment. CSIA-Cl/Br is usually conducted by gas chromatography-mass spectrometry (GC-MS), which could be negatively impacted by isotope fractionation on GC columns. In this study, on-column Cl/Br isotope fractionation of 31 organochlorines and 4 organobromines was explored using GC-double focus magnetic-sector high resolution MS (GC-DFS-HRMS). Twenty-nine HOPs exhibited inverse Cl/Br isotope fractionation for which the heavier isotopologues eluted faster than the lighter ones on GC columns, and two polychlorinated biphenyls (PCB-138 and PCB-153) showed normal isotope fractionation, whereas the rest four HOPs did not show observable isotope fractionation. The isotope fractionation extents varied from -13.0‰ to 73.1‰. Mechanisms of the on-column Cl/Br isotope fractionation were tentatively elucidated with a modified two-film model. The results demonstrate that integrating peak area as complete as possible for separable chromatographic peaks and integrating the middle retention-time segments for the inseparable peaks are helpful to improve precision and accuracy of the CSIA-Cl/Br data. The findings of this study will shed light on development of CSIA-Cl/Br methods with respect to improving precision and accuracy.

Persistence, temporal and spatial profiles of ultraviolet absorbents and phenolic personal care products in riverine and estuarine sediment of the Pearl River catchment, China.

A variety of personal care products have been classified as emerging contaminants (ECs). Occurrence, fate, spatial and vertical profiles of 13 ultraviolet absorbents, triclocarban (TCC) and its dechlorinated products, triclosan (TCS), 2-phenylphenol and parabens were investigated in riverine and estuarine sediment of the Pearl River catchment, China. Bisphenol A (BPA), a widely applied plasticizer, was also investigated. The ECs were widely present in the bed sediment. TCC was the most abundant with a maximum concentration of 332ngg-1 dry weight. The other prominent ECs included BPA, TCS, octocrylene, and benzotriazole UV stabilizers UV326 and UV328. Treated wastewater effluent was the major source of the ECs in the riverine sediment. TCC, BPA, TCS, methyparaben, UV531, UV326, and UV328 were also detected throughout the estuarine sediment cores, indicating their persistence in the sediment. Temporal trends of the ECs in the sediment cores reflected a combined effect of industrial development, population growth, human life quality improvement, and waste treatment capacity in the Pearl River Delta over the last decades. TCC dechlorination products were frequently detected in the bed sediment with higher levels near treated effluent outlets but only occasionally observed in the sediment cores, suggesting insignificant in-situ TCC dechlorination in the sediment.