High concentrations of the main components in Scotchgard™ fabric protector products (pre-2002 and post-2002; side-chain fluorinated polymer surfactants, S1 and S2, respectively) were detected in biosolids samples from twenty pan-Canadian wastewater treatment plants (WWTPs). Based on mass spectrometric analysis, S1 and S2 can be named as side-chain perfluorooctane sulfonamide-urethane polymer and side-chain perfluorobutane sulfonamide-urethane polymer, respectively. S1 (with CF side-chain) concentrations ranged from 1.08-105 ng/g d.w. and S2 (with CF side-chain) concentrations ranged from 37.5-2051 ng/g d.w., which were much higher than that of other commonly monitored perfluoroalkyl substances (PFAS). S1 and S2 concentrations were significantly correlated (p < 0.001; r = 0.6142) indicating similar source origins. A negative linear correlation was observed (p < 0.05) between concentrations of S1 (or S2) with the volume of WWTP treated wastewater per day per person (m/person/day). The total concentration of 22 other PFAS ranged from 4.93 to 92.6 ng/g d.w., and approximately thirty times lower than S1 and S2 concentrations. The calculated elemental fluorine concentrations of ƩF were generally much higher than the sum of the other PFAS. PFAS concentrations in biosolids are likely underestimated without consideration of S1 and S2.
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http://dx.doi.org/10.1016/j.jhazmat.2020.122044 | DOI Listing |
J Am Chem Soc
January 2025
College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing 314001, China.
The ground-state charge generation (GSCG) in photoactive layers determines whether the photogenerated carriers occupy the deep trap energy levels, which, in turn, affects the device performance of organic solar cells (OSCs). In this work, charge-quadrupole electrostatic interactions are modulated to achieve GSCG through a molecular strategy of introducing different numbers of F atom substitutions on the BTA3 side chain. The results show that 8F substitution (BTA3-8F) and 16F substitution (BTA3-16F) lead to different patterns of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy level changes.
View Article and Find Full Text PDFThis paper explores optimization strategies for polymeric materials in organic solar cells (OSCs) with the focus on varying alkyl side chain, addition of fluorine atom, and thiophenated derivatives onto polymer. As such, it outlines the significance of renewable energy sources and the potential of photovoltaic technologies, particularly organic photovoltaics (OPVs). Objectives include factors affecting power conversion efficiency (PCE), open-circuit voltage (Voc), aggregation tendencies, and optoelectronic properties in OPVs.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
School of Textile Science and Engineering, Jiangnan University, Wuxi 214021, China. Electronic address:
Perfluoroalkyl and poly-fluoroalkyl substances (PFAS) release from textiles is a source of human exposure, but the mechanisms behind this release remain insufficiently studied. This research investigates the release and transport mechanisms of PFAS in outdoor jacket fabrics treated with a short side-chain fluorinated polymers (CF-SFPs) for durable water repellency (DWR). PA-based and PET-based fabrics were exposed to outdoor conditions and subjected to accelerated aging, followed by abrasion, washing, and drying experiments to simulate wear and degradation.
View Article and Find Full Text PDFChemistry
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Institute of Materials and Clean Energy, Shandong Provincial Key Laboratory of Clean Production of Fine Chemicals, Shandong Normal University, Jinan, 250014, P. R. China.
Non-fused electron acceptors have obtained increasing curiosity in organic solar cells (OSCs) thanks to simple synthetic route and versatile chemical modification capabilities. However, non-fused acceptors with varying quinoxaline core and as-cast device have rarely been explored, and the molecular structure-photovoltaic performance relationship of such acceptors remains unclear. Herein, two non-fused acceptors L19 and L21 with thienyl substituted non-fluorinated/fluorinated quinoxaline core were developed via five-step synthesis.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, 117997 Moscow, Russia.
Enveloped viruses, such as flaviviruses and coronaviruses, are pathogens of significant medical concern that cause severe infections in humans. Some photosensitizers are known to possess virucidal activity against enveloped viruses, targeting their lipid bilayer. Here we report a series of halogenated difluoroboron-dipyrromethene (BODIPYs) photosensitizers with strong virus-inactivating activity.
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