Graphene oxides : transformations in natural waters over a period of three months
Graphene oxide (GO), a derivative of graphene consisting of various oxygen moieties, has gained popularity owing to its excellent physiochemical properties and applicability in various fields. GO nanomaterials can be synthesized by using Hofmann (HO), Hummers (HU), and Staudenmaier (ST) methods of o...
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sg-ntu-dr.10356-1051962019-12-06T21:47:24Z Graphene oxides : transformations in natural waters over a period of three months Teo, Wei Zhe Pumera, Martin School of Physical and Mathematical Sciences DRNTU::Science::Chemistry Graphene oxide (GO), a derivative of graphene consisting of various oxygen moieties, has gained popularity owing to its excellent physiochemical properties and applicability in various fields. GO nanomaterials can be synthesized by using Hofmann (HO), Hummers (HU), and Staudenmaier (ST) methods of oxidative treatment of graphite to give GO-HO, GO-HU, and GO-ST, respectively. These GO nanomaterials were found to exhibit different degrees of cytotoxicity that were suggested to be dependent on the amount and type of the oxygen-containing functional group present in the nanomaterials. Therefore, in this study, the transformations of GO-HO, GO-HU, and GO-ST nanomaterials in three types of natural waters over time were investigated to determine whether the oxygen-containing functional groups present in these nanomaterials undergo any changes after residing in natural waters. Based on the data obtained from Raman spectroscopy and X-ray photoelectron spectroscopy, although the density of defects in the GO nanomaterials remained relatively similar (a slight increase was detected in the GO-HO nanomaterials) over the period of examination, changes in the oxygen content of the GO nanomaterials were observed in most of the GO suspensions, which suggests that interaction between the natural waters and the GO nanomaterials do occur. Cyclic voltammetry measurements revealed that the natural waters had opposing effects on the GO nanomaterials: the GO-HU nanomaterials suffered a reduction in the amount of electroactive oxygen-containing functional groups present, whereas an increase was observed in the GO-HO and GO-ST nanomaterials. In addition, it was proposed that some of the electroactive oxygen moieties were completely lost from the GO-ST nanomaterials after exposing them to the natural waters. More studies should be performed in the future to comprehend the underlying mechanism for the transformations observed in this study so that the fate, transport, and toxicity of GO nanomaterials in environmental waters can be better understood. 2014-09-15T03:24:43Z 2019-12-06T21:47:24Z 2014-09-15T03:24:43Z 2019-12-06T21:47:24Z 2014 2014 Journal Article Teo, W. Z., & Pumera, M. (2014). Graphene oxides : transformations in natural waters over a period of three months. ChemPlusChem, 79(6), 844-849. 2192-6506 https://hdl.handle.net/10356/105196 http://hdl.handle.net/10220/20686 http://dx.doi.org/10.1002/cplu.201400033 en ChemPlusChem © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
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DRNTU::Science::Chemistry Teo, Wei Zhe Pumera, Martin Graphene oxides : transformations in natural waters over a period of three months |
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Graphene oxide (GO), a derivative of graphene consisting of various oxygen moieties, has gained popularity owing to its excellent physiochemical properties and applicability in various fields. GO nanomaterials can be synthesized by using Hofmann (HO), Hummers (HU), and Staudenmaier (ST) methods of oxidative treatment of graphite to give GO-HO, GO-HU, and GO-ST, respectively. These GO nanomaterials were found to exhibit different degrees of cytotoxicity that were suggested to be dependent on the amount and type of the oxygen-containing functional group present in the nanomaterials. Therefore, in this study, the transformations of GO-HO, GO-HU, and GO-ST nanomaterials in three types of natural waters over time were investigated to determine whether the oxygen-containing functional groups present in these nanomaterials undergo any changes after residing in natural waters. Based on the data obtained from Raman spectroscopy and X-ray photoelectron spectroscopy, although the density of defects in the GO nanomaterials remained relatively similar (a slight increase was detected in the GO-HO nanomaterials) over the period of examination, changes in the oxygen content of the GO nanomaterials were observed in most of the GO suspensions, which suggests that interaction between the natural waters and the GO nanomaterials do occur. Cyclic voltammetry measurements revealed that the natural waters had opposing effects on the GO nanomaterials: the GO-HU nanomaterials suffered a reduction in the amount of electroactive oxygen-containing functional groups present, whereas an increase was observed in the GO-HO and GO-ST nanomaterials. In addition, it was proposed that some of the electroactive oxygen moieties were completely lost from the GO-ST nanomaterials after exposing them to the natural waters. More studies should be performed in the future to comprehend the underlying mechanism for the transformations observed in this study so that the fate, transport, and toxicity of GO nanomaterials in environmental waters can be better understood. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Teo, Wei Zhe Pumera, Martin |
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Article |
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Teo, Wei Zhe Pumera, Martin |
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Teo, Wei Zhe |
title |
Graphene oxides : transformations in natural waters over a period of three months |
title_short |
Graphene oxides : transformations in natural waters over a period of three months |
title_full |
Graphene oxides : transformations in natural waters over a period of three months |
title_fullStr |
Graphene oxides : transformations in natural waters over a period of three months |
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Graphene oxides : transformations in natural waters over a period of three months |
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graphene oxides : transformations in natural waters over a period of three months |
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2014 |
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https://hdl.handle.net/10356/105196 http://hdl.handle.net/10220/20686 http://dx.doi.org/10.1002/cplu.201400033 |
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