Johanna Freilinger
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Johanna Freilinger has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Herwig Schottenberger
Faculty of Chemistry and Pharmacy, University of Innsbruck, Innsbruck, Austria
2 shared publications - Jan O. Back
Department of Environmental, Process & Energy Engineering, MCI - The Entrepreneurial School, Innsbruck, Austria
2 shared publications - Rania Bakry
Leopold-Franzens University
2 shared publications - Sven Nerdinger
Sandoz GmbH, Biochemiestr. 10, 6250 Kundl, Austria
2 shared publications Christian Huck
University of Innsbruck
1 shared publicationChristian W. Huck
1 shared publication
Latest Publications
- Open Access
Crystal Structure of [1046127-79-0], 3,3′-(n-Hexane-1,6-diyl)bis(1-vinylimidazolium) Bromide
Vinylimidazolium salts constitute a highly relevant class of polymerizable heterocycles, especially in the field of so-called polymer ionic liquids (PILs), and they are frequently used as components of polyelectrolytes. Therefore, crystallographic characterizations, in particular studies of charge distribution and conformational features, can provide fundamental insights concerning ion–ion and ion–dipole interactions. The structure of the title compound [1046127-79-0] has the space group symmetry P21/c. Its asymmetric unit contains one formula unit, consisting of two bromide anions and the halves of two cation moieties. The cation units possess inversion symmetry, and their C6H12 chains adopt an all-trans conformation.
Open AccessCrystal Structure of [1046127-79-0], 3,3′-(n-Hexane-1,6-diyl)bis(1-vinylimidazolium) Bromide
Vinylimidazolium salts constitute a highly relevant class of polymerizable heterocycles, especially in the field of so-called polymer ionic liquids (PILs), and they are frequently used as components of polyelectrolytes. Therefore, crystallographic characterizations, in particular studies of charge distribution and conformational features, can provide fundamental insights concerning ion–ion and ion–dipole interactions. The structure of the title compound [1046127-79-0] has the space group symmetry P21/c. Its asymmetric unit contains one formula unit, consisting of two bromide anions and the halves of two cation moieties. The cation units possess inversion symmetry, and their C6H12 chains adopt an all-trans conformation.
- Open Access
- 6 May 2025
- Published by Elsevier in Journal of Hazardous Materials Advances
- Vol. 18
Interactions between perfluorinated alkyl substances (PFAS) and microplastics (MPs): Findings from an extensive investigation
- 6 May 2025
- Published by Elsevier in Journal of Hazardous Materials Advances
- Vol. 18
Open AccessInteractions between perfluorinated alkyl substances (PFAS) and microplastics (MPs): Findings from an extensive investigation
- Open Access
- 4 April 2025
- Published by Elsevier in SSRN Electronic Journal
Development of a Fluorophilic Ion-Exchange Material with Dual Binding Mechanism for Solid-Phase Extraction of Pfas
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants, for which regulatory authorities worldwide have been compelled to impose limits in drinking water, groundwater, and surface water. This has created challenges in PFAS detection, and there is an urgent need for reliable and selective solid-phase extraction (SPE) materials for PFAS analysis. In addressing this demand, we have tailored highly crosslinked copolymers containing 3-(1H,1H,2H,2H-perfluorooctyl)-1-vinylimidazolium chloride as a comonomer with ethylene dimethacrylate in various molar ratios. For ionic fluorosurfactants, these copolymers feature a dual binding mechanism that synergistically combines fluorophilic interactions and electrostatic attraction, enhancing selectivity and binding efficiency. The adsorption behavior of short- and long-chain PFAS acids and their recoveries were evaluated and compared to those of commercial SPE cartridges. Characterization revealed the highest porosity and ion-exchange capacity (412.7±22 µeq g-1) for a monomer-to-crosslinker ratio of 2:1. Recovery experiments consistently demonstrated high PFAS recoveries (98.8%–121.6%), while PFAS enrichment studies from effluent wastewater further confirmed its robustness in complex environmental matrices (recoveries: 90.8%–99.2%). The findings underscore the potential of this innovative polyelectrolyte as a selective, regenerable, and efficient alternative to conventional SPE materials, qualifying it as a superior candidate for PFAS enrichment, detection and environmental remediation applications.
- 4 April 2025
- Published by Elsevier in SSRN Electronic Journal
Open AccessDevelopment of a Fluorophilic Ion-Exchange Material with Dual Binding Mechanism for Solid-Phase Extraction of Pfas
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants, for which regulatory authorities worldwide have been compelled to impose limits in drinking water, groundwater, and surface water. This has created challenges in PFAS detection, and there is an urgent need for reliable and selective solid-phase extraction (SPE) materials for PFAS analysis. In addressing this demand, we have tailored highly crosslinked copolymers containing 3-(1H,1H,2H,2H-perfluorooctyl)-1-vinylimidazolium chloride as a comonomer with ethylene dimethacrylate in various molar ratios. For ionic fluorosurfactants, these copolymers feature a dual binding mechanism that synergistically combines fluorophilic interactions and electrostatic attraction, enhancing selectivity and binding efficiency. The adsorption behavior of short- and long-chain PFAS acids and their recoveries were evaluated and compared to those of commercial SPE cartridges. Characterization revealed the highest porosity and ion-exchange capacity (412.7±22 µeq g-1) for a monomer-to-crosslinker ratio of 2:1. Recovery experiments consistently demonstrated high PFAS recoveries (98.8%–121.6%), while PFAS enrichment studies from effluent wastewater further confirmed its robustness in complex environmental matrices (recoveries: 90.8%–99.2%). The findings underscore the potential of this innovative polyelectrolyte as a selective, regenerable, and efficient alternative to conventional SPE materials, qualifying it as a superior candidate for PFAS enrichment, detection and environmental remediation applications.
- Open Access
- 25 December 2024
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1327
Ammonium 6:2 fluorotelomer sulfonate: crystal structure, thermal analysis and use as internal standard in PFAS analysis
- 25 December 2024
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1327
Open AccessAmmonium 6:2 fluorotelomer sulfonate: crystal structure, thermal analysis and use as internal standard in PFAS analysis