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Autor(en) / Beteiligte
Titel
A robust and highly compressible polyacrylamide co-polymer hydrogel developed through g-C3N4 initiated photopolymerisation and its photocatalytic activity towards dye removal
Ist Teil von
  • New journal of chemistry, 2024-02, Vol.48 (9), p.3984-3997
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2024
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Photocatalytic hydrogels have drawn significant interest in many research fields, including energy conversion and wastewater treatment. However many synthesized hydrogels show mechanical brittleness, which limits their practical application. Here, we have developed a simple, cost-effective, and eco-friendly synthesis method for the photopolymerisation of g-C3N4/polyacrylamide co-polymer hydrogel under visible light irradiation. The developed hydrogel exhibits high compressibility up to a strain of 230% with a mechanical strength of 0.55 MPa. We have addressed the dual functions of g-C3N4 in the hydrogel. First, as a photoinitiator and reinforcing agent in the polymerisation of a photocatalytic hydrogel. Second, as a photocatalyst embedded in the hydrogel for the degradation of organic dye pollutants. The three-dimensional network of the hydrogel allows rapid permeation of the cationic dye molecules into the hydrogel matrix, thereby accelerating the photodegradation process. The applicability of the synthesized photocatalytic hydrogel towards the selective degradation of different cationic dyes over anionic dyes has been determined. In addition, the synthesized hydrogel demonstrates recyclability for up to 5 cycles, without losing its photocatalytic properties. Along with this, the hydrogel shows adsorption maxima of 72 mg g−1 towards CV dye. Thus, the simple and easy preparation of the g-C3N4 based hydrogel and its excellent photocatalytic and adsorption properties have proved it to be a potential photocatalytic material for green and sustainable water remediation techniques.
Sprache
Englisch
Identifikatoren
ISSN: 1144-0546
eISSN: 1369-9261
DOI: 10.1039/d3nj05474h
Titel-ID: cdi_proquest_journals_2931515012

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