2021
DOI: 10.1039/d1cp01734a
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Carboxyl groups do not play the major role in binding metal cations by graphene oxide

Abstract: In this study, we investigate chemical interactions of Mn2+ ions with graphene oxides, prepared by Hummers (HGO) and Brodie (BGO) methods in aqueous solutions by means of the NMR relaxation....

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Cited by 16 publications
(14 citation statements)
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“…Considering the first modification approach, small molecules or functional groups, the introduction of new functionality on the graphene backbone results in a decrease of thermal stability. Both HMDA and PB afforded similar results with a residual mass of over 65% at 900 • C. As expected, the oxidation of graphene resulted in the introduction of functional groups hydroxyl [34,35], carboxyl [34,36,37], and oxirane [38], but the registered weight loss is lower than that afforded by the graphene functionalized by the radical grafting of benzoyl peroxide radicals and HMDA addition. The TGA results for polymer functionalized graphene indicate a relatively low polymer to graphene ratio in the case of methyl methacrylate and hexyl methacrylate.…”
Section: Resultssupporting
confidence: 67%
“…Considering the first modification approach, small molecules or functional groups, the introduction of new functionality on the graphene backbone results in a decrease of thermal stability. Both HMDA and PB afforded similar results with a residual mass of over 65% at 900 • C. As expected, the oxidation of graphene resulted in the introduction of functional groups hydroxyl [34,35], carboxyl [34,36,37], and oxirane [38], but the registered weight loss is lower than that afforded by the graphene functionalized by the radical grafting of benzoyl peroxide radicals and HMDA addition. The TGA results for polymer functionalized graphene indicate a relatively low polymer to graphene ratio in the case of methyl methacrylate and hexyl methacrylate.…”
Section: Resultssupporting
confidence: 67%
“…Compared with manganese, the EDTA quantity was at a 400-fold excess. As well, for highly oxidized samples, 1 g GO contains 5 to 8 mmol of acidic groups [ 72 ], which correlates to the found sub-mmol/g quantity (1.4 ± 0.2 mmol/g), see the Supplementary Materials, Section S1.1 (Figure S5) ; it is much lower than the EDTA concentration (up to 500 times). Therefore, the thermodynamic equilibrium shifts towards a more stable EDTA complex.…”
Section: Discussionsupporting
confidence: 58%
“…We suggest that interlayer ions chelated with GO surface moieties, mainly carboxyl and hydroxyl functional groups, would provide competitive binding with excess EDTA and then released due to diffusion [ 71 ]. It is well-known that GO coordinate Mn 2+ preventing its hydrolysis [ 72 ]. It is impossible to unequivocally answer which form of the element is associated with EDTA; the speciation analysis [ 73 ] was beyond the scope of this work.…”
Section: Discussionmentioning
confidence: 99%
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“…18 More current work also strongly suggested a possibility that the other functional groups (not only carboxyl) have played a signicant role for binding to metal ions. 43 The as-formed enols as the product resulted from reorganization of GO structure might serve as a chelating agent for the metal cations. 3.3.2.…”
Section: Optical Properties Of Goqds and Their Nanocompositementioning
confidence: 99%