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The key components of aqueous film foaming foam extinguishing agents are fluorocarbon surfactants. Due to their toxicity and bioaccumulation, long-chain fluorocarbon surfactants have limited application prospects. Therefore, it is of great significance to study short-chain fluorocarbon surfactants as substitutes. In this work, three short-chain fluorocarbon surfactants with various hydrophilic groups and corresponding fire extinguishing agents were prepared. The physical and chemical properties of a single system and mixed system of fluorocarbon surfactants, including surface activity, spreading property, foaming property, 25% drainage time, and AFFF fire extinguishing property, were studied. For the results of the mixed systems, it was found that the critical micelle concentrations did not exceed 3.97 mmol/L and the minimum surface tension did not exceed 17.21 mN/m. Fluorocarbon surfactant solutions spread effectively on the surface of all fuels. The foam expansion is greater than 7.2, and the shortest of all 25% drainage times is 3.31 min. The extinguishing time of AFFFs on several fuel fires does not exceed 55 s, and the shortest burn-back time is 15.08 min. Anyways, these results indicate that the grafted hydrophilic short-chain fluorocarbon surfactants have significant application prospects in AFFFs.
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http://dx.doi.org/10.1021/acsomega.4c04414 | DOI Listing |
Langmuir
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, People's Republic of China.
The study of the self-assembly of surfactants in aqueous solutions, though a traditional field, remains fascinating and full of novelty. In this article, the anionic perfluorodecanoic acid surfactant (PFA) is separately complexed with three hydroxyalkylamines (monoethanolamine (MEA), diethylamine (DEA), and triethanolamine (TEA)) in aqueous solutions. The transformation of aggregate morphologies from spherical unilamellar to nanotubes and then to spherical bilamellar is observed at room temperature, which is confirmed by cryo-transmission electron microscopy (cryo-TEM).
View Article and Find Full Text PDFLab Chip
September 2025
Department of Biomedical Engineering, Faculty of Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
Block copolymer fluorosurfactants are frequently utilized to stabilize water-oil interfaces in droplet microfluidics, enabling parallel and compartmentalized biochemical reactions within individual droplets. Surfactants are able to self-assemble into inverse micelles with the concentration exceeding the critical micelle concentration (CMC), which has been identified as the main reason causing cross-contamination among droplets. This study explored the possibility to utilize the inverse micelles for passive cargo delivery from the fluorocarbon oil phase into the aqueous droplet interior, which has rarely been studied previously.
View Article and Find Full Text PDFAdv Mater Interfaces
February 2025
Department of Genetics, Stanford University, Stanford, CA 94305, USA; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA; Sarafan ChEM-H Institute, Stanford University, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
Biphasic environments can enable successful chemical reactions where any single solvent results in poor substrate solubility or poor catalyst reactivity. For screening biphasic reactions at high throughput, a platform based on microfluidic double emulsions can use widely available FACS (Fluorescence Activated Cell Sorting) machines to screen millions of picoliter reactors in a few hours. However, encapsulating biphasic reactions within double emulsions to form FACS-sortable droplet picoreactors requires optimized solvent phases and surfactants to produce triple emulsion droplets that are stable over multi-hour assays and compatible with desired reaction conditions.
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.
The temperature-dependent air-water partitioning behavior of a novel class of perfluoroalkyl and polyfluoroalkyl substances (PFAS) was assessed both experimentally and via prediction. These PFAS contain ether or thioether linkages and are transformation products of an alternative PFAS surfactant. A modified version of the static headspace method with variable headspace/solution ratios was used to determine the dimensionless air/water partition coefficients () over a wide range of temperatures (25-80 °C).
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
Department of Chemical & Environmental Engineering, University of Cincinnati, Cincinnati, Ohio 45221, United States.
Per- and polyfluoroalkyl substances (PFAS) present a major challenge in environmental remediation due to their extreme persistence and resistance to conventional chemical treatments. While recent advances in reductive approaches using hydrated electrons () have shown promise for C-F bond activation, most require high photosensitizer loadings, suffer from poor electron utilization, and lack compatibility with diverse PFAS structures. Here, we report a micellar photocatalytic system using the cationic surfactant cetyltrimethylammonium bromide (CTAB) under UV irradiation to enhance utilization for PFAS degradation.
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