Regulating the Hydrophilicity of Hyper-Cross-Linked Polymers via Thermal Oxidation for Atmospheric Water Harvesting
Source abstract
Abstract
We explore the thermal oxidation of hyper-cross-linked polymers to enhance their hydrophilicity and efficacy in atmospheric water harvesting. Comprehensive chemical and physical characterizations are used to confirm the successful incorporation of polar oxygen moieties and the preservation of porosity upon thermal treatment. Newly introduced oxygen-based functional groups significantly improve water sorption properties, increasing total water uptake capacities by up to 400% and shifting water uptake onsets to significantly lower relative humidity. We also investigate the regeneration of oxidized hyper-cross-linked polymers after water sorption to probe their potential for multiple water harvesting cycles and reuse. Our findings outline a simple and cost-effective postsynthetic modification route for optimizing porous organic polymers for more sustainable and efficient atmospheric water harvesting.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Surface Modification and Superhydrophobicity · Membrane Separation Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Materials Chemistry and Research, Faculty of Chemistry, University of Vienna, Währinger Straße 42, 1090 Vienna, Austria
Vienna Doctoral School in Chemistry, University of Vienna, Währinger Straße 42, 1090 Vienna, Austria
Funding
Erasmus+ · ?sterreichische Forschungsf?rderungsgesellschaft · Universit?t Wien
References (29)
Show source-provided references
1. United Nations. Sustainable Development Goals Report, 2022, https://unstats.un.org/sdgs/report/2022/ (accessed June 12, 2024).
2. Gleick, P. Water in Crisis: A Guide to the World’s Fresh Water Resources; Oxford University Press: Oxford, 1993; pp 13–24.
3. 10.1016/j.eti.2020.10116910.1016/j.eti.2020.101169 ↗
4. 10.1016/j.atmosres.2016.07.02910.1016/j.atmosres.2016.07.029 ↗
5. 10.1039/D2EE03079A10.1039/D2EE03079A ↗
6. 10.1126/science.aam874310.1126/science.aam8743 ↗
7. 10.1038/s41565-020-0673-x10.1038/s41565-020-0673-x ↗
8. 10.1021/ja500330a10.1021/ja500330a ↗
9. 10.1021/cr500258910.1021/cr5002589 ↗
10. 10.1002/adma.20230001810.1002/adma.202300018 ↗
11. 10.1039/C5TA07998E10.1039/C5TA07998E ↗
12. 10.1002/cssc.20230190610.1002/cssc.202301906 ↗
13. 10.1021/acs.chemmater.5b0215110.1021/acs.chemmater.5b02151 ↗
14. 10.1021/jacs.3c0257210.1021/jacs.3c02572 ↗
15. 10.1021/acscentsci.2c0039810.1021/acscentsci.2c00398 ↗
16. 10.1021/cm070356a10.1021/cm070356a ↗
17. 10.1039/D0CC01002B10.1039/D0CC01002B ↗
18. 10.1021/ma200630s10.1021/ma200630s ↗
19. 10.1002/adfm.20200826510.1002/adfm.202008265 ↗
20. 10.1002/smll.20230456210.1002/smll.202304562 ↗
21. 10.1039/D2MA00379A10.1039/D2MA00379A ↗
22. 10.1002/anie.20180038010.1002/anie.201800380 ↗
23. 10.1016/j.reactfunctpolym.2024.10601410.1016/j.reactfunctpolym.2024.106014 ↗
24. 10.1002/chem.20190094010.1002/chem.201900940 ↗
25. 10.1016/0141-3910(92)90137-T10.1016/0141-3910(92)90137-T ↗
26. 10.1016/j.cej.2024.14892010.1016/j.cej.2024.148920 ↗
27. 10.1038/ncomms581310.1038/ncomms5813 ↗
28. 10.1515/pac-2014-111710.1515/pac-2014-1117 ↗
29. 10.1038/s41578-024-00665-210.1038/s41578-024-00665-2 ↗