Ojha, AbhijeetAbhijeetOjhaIbrahim, HelenHelenIbrahimAlyabyeva, NataliaNataliaAlyabyevaLazzari, RémiRémiLazzariGoldmann, MichelMichelGoldmannThareja, PrachiPrachiThareja2025-08-312025-08-312020-11-0110.1016/j.synthmet.2020.1164942-s2.0-85088899118https://d8.irins.org/handle/IITG2025/23954The variation of lateral dimensions of GO nanosheets by subjecting them to different ultrasonication time (t = 30, 60, and 120 min) influences the rheology, microstructure, and adsorption capacity of graphene oxide (GO) suspensions. The average storage modulus (G'<inf>p</inf>) of GO aqueous dispersions (volume fraction (ϕ<inf>GO</inf>) = 0.018) varies as GO-30 < GO-60 < GO-120, although the C/O of GO nanosheets does not change significantly with ultrasonication. Addition of 10⁻⁵ M – 10^-1 M NaCl and MgCl<inf>2</inf> lead to a rise in G'<inf>p</inf> as compared to electrolyte-free suspensions with the formation of liquid-like, fragile gels and solid gel-like samples. Independent of time of ultrasonication, solid gels are formed at 10^-1 M of electrolytes. The maximum G'<inf>p</inf> is observed in gels of GO-30 with 10^-1 M MgCl<inf>2</inf>. We hypothesize that an increase in ultrasonication time causes the formation of new nanosheets with un-functionalized edges. While Na⁺ screens the negative charge of GO causing aggregation, but Mg²⁺ not only screens but also interacts with carboxyl groups of GO nanosheets. Therefore, the degree of Mg²⁺ bridging the GO nanosheets is the lowest in GO-120 and the highest in GO-30 suspensions. The adsorption capacity of methylene blue (MB) on GO-120-electrolyte lyophilized gels is the smallest, in agreement with the weak cross-linking and mechanical strength of these gels.falseAdsorption | Gel | Graphene oxide | Microstructure | RheologyArticlehttps://hal.science/hal-02995172November 20209116494arJournal8WOS:000588106700002