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Al(3+) Modification of Graphene Oxide Membranes: Effect of Al Source

Graphene oxide (GO) membranes are promising materials for water filtration applications due to abundant nanochannels in the membrane structure. Because GO membranes are unstable in water, metal cations such as Al(3+) are often introduced to the membrane structure to promote cross-linking between ind...

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Detalles Bibliográficos
Autores principales: Robertson, Ellen J., Stehle, Yijing Y., Hu, Xiaoyu, Kilby, Luke, Olsson, Katelyn, Nguyen, Minh, Cortez, Rebecca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788489/
https://www.ncbi.nlm.nih.gov/pubmed/36557144
http://dx.doi.org/10.3390/membranes12121237
Descripción
Sumario:Graphene oxide (GO) membranes are promising materials for water filtration applications due to abundant nanochannels in the membrane structure. Because GO membranes are unstable in water, metal cations such as Al(3+) are often introduced to the membrane structure to promote cross-linking between individual GO sheets. Here, we describe a simple yet versatile method to incorporate Al(3+) into GO membranes formed via a slow self-assembly process. Specifically, we directly added aluminum to acidic GO sheet solutions from a variety of sources: Al(2)O(3), AlCl(3) and Al foil. Each species reacts differently with water, which can affect the GO solution pH and thus the density of carboxylate groups on the sheet edges available for cross-linking to the Al(3+) cations. We demonstrate through characterization of the GO sheet solutions as well as the as-formed membranes’ morphologies, hydrophobicities, and structures that the extent to which the Al(3+) cross-links to the GO sheet edges vs. the GO sheet basal planes is dependent on the Al source. Our results indicate that greatest enhancements in the membrane stability occur when electrostatic and coordination interactions between Al(3+) and the carboxylate groups on the GO sheet edges are more extensive than Al(3+)–π interactions between basal planes.