Cargando…

Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials

In this study, the acidity of urazole (pKa 5–6) was exploited to fabricate a hydrogel in two simple and scalable steps. Commercially available poly(hexamethylene)diisocyanate was used as a precursor to synthesize an urazole containing gel. The formation of urazole was confirmed by FT-IR and (1)H-NMR...

Descripción completa

Detalles Bibliográficos
Autores principales: Hanay, Saltuk B., Fallah, Ali, Senturk, Efsun, Yetim, Zeliha, Afghah, Ferdows, Yilmaz, Hulya, Culha, Mustafa, Koc, Bahattin, Zarrabi, Ali, Varma, Rajender S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701905/
https://www.ncbi.nlm.nih.gov/pubmed/34940320
http://dx.doi.org/10.3390/gels7040261
Descripción
Sumario:In this study, the acidity of urazole (pKa 5–6) was exploited to fabricate a hydrogel in two simple and scalable steps. Commercially available poly(hexamethylene)diisocyanate was used as a precursor to synthesize an urazole containing gel. The formation of urazole was confirmed by FT-IR and (1)H-NMR spectroscopy. The hydrogel was characterized by microscopy imaging as well as spectroscopic and thermo-gravimetric analyses. Mechanical analysis and cell viability tests were performed for its initial biocompatibility evaluation. The prepared hydrogel is a highly porous hydrogel with a Young’s modulus of 0.91 MPa, has a swelling ratio of 87%, and is capable of exchanging ions in a medium. Finally, a general strategy was demonstrated to embed urazole groups directly into a crosslinked material.