Digital Repository

Novel membranes for treatment of water: Graphene oxide membranes cross-linked with metal cations

Show simple item record

dc.contributor.author Bandara, W. R. N. M.
dc.contributor.author Liyanage, J. A.
dc.contributor.author Kumarasinghe, A. R.
dc.date.accessioned 2019-12-12T10:32:46Z
dc.date.available 2019-12-12T10:32:46Z
dc.date.issued 2019
dc.identifier.citation Bandara, W. R. N. M., Liyanage, J. A. and Kumarasinghe, A. R. (2019). Novel membranes for treatment of water: Graphene oxide membranes cross-linked with metal cations. 4th International Research Symposium on Pure and Applied Sciences, Faculty of Science, University of Kelaniya, Sri Lanka. p141 en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/20642
dc.description.abstract Declining of water resources and rapid expansion of the consumption of water worldwide have led to the search of novel water treatment technologies that can provide a safe water supply to the mankind. Graphene oxide (GO), which is an oxidative exfoliation product of graphite, is an ideal candidate to be used as a new material for this purpose. However, GO sheets gradually disintegrate in water because of electrostatic repulsions between ionized oxygen containing functional groups. This research work explores the ways in which impart physical properties needed for GO sheets to overcome their inherent dispensability in water environment and to enhance the necessary stability by cation cross-linking. GO membranes cross-linked with unit amount of Al3+, Zn2+ and K+ shows greater stability in water compared to the unmodified GO membranes. Energy Dispersive X-ray Absorption (EDXA) analysis proves the incorporation of metal ions into the GO membrane. Accordingly GO membrane cross-linked with Al3+, Zn2+and K+ (1000 mg mL-1, 300 μL) has caused a surface composition of 0.14%, 0.14% and 0.13% respectively by weight of particular metal cation. Scanning Electron Microscopy (SEM) images confirm the cation cross linking since cross-linked GO membranes have a wrinkled surface morphology compared to unmodified GO membranes. According to FTIR-ATR spectrums of GO membrane cross-linked with Al3+, Zn2+and K+ (1000 mg mL-1, 300 μL, 2000 μL, 3200 μL) intensity of carbonyl and epoxy peaks have been decreased and peak positions have been shifted to lower wave numbers with the increase of cation concentration compared to unmodified membrane since the amount of freely available functional groups decrease as the cross-linker concentration increase. Following cross-linking with Al3+, Zn2+and K+ (1000 mg mL-1, 300 μL) elastic modulus of GO membranes has been increased by 191%, 173% and 147% respectively. Hence tensile testing analysis confirms the cation cross-linking in the in-plane direction. Also tensile testing analysis represents the presence of a linear relationship between charge density of the cross-linker and enhancement of mechanical strength as the charge density of the cross-linker increased the enhancement in the mechanical strength has been increased. According to X ray diffraction (XRD) analysis, there is no significant change in the interlayer spacing of GO membranes with and without metal ion cross-linking. This may suggest that metal ion intercalation via the stacking direction has not been taken place or it is non-homogeneous. Studies are underway in order to further investigate the relationship between charge density of the cross-linker and the enhancement in mechanical strength and the aqueous stability caused due to cation cross-linking of GO membranes. en_US
dc.language.iso en en_US
dc.publisher 4th International Research Symposium on Pure and Applied Sciences, Faculty of Science, University of Kelaniya, Sri Lanka en_US
dc.subject Graphene oxide en_US
dc.subject Aqueous stability en_US
dc.subject Cross-linked GO en_US
dc.subject Mechanical strength en_US
dc.subject Charge density en_US
dc.title Novel membranes for treatment of water: Graphene oxide membranes cross-linked with metal cations en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search Digital Repository


Browse

My Account