TY - JOUR
T1 - The contribution of indirect photolysis to the degradation of graphene oxide in sunlight
AU - Hou, Wen Che
AU - Henderson, W. Matthew
AU - Chowdhury, Indranil
AU - Goodwin, David G.
AU - Chang, Xiaojun
AU - Martin, Sharon
AU - Fairbrother, D. Howard
AU - Bouchard, Dermont
AU - Zepp, Richard G.
N1 - Funding Information:
This paper has been reviewed in accordance with the U.S. Environmental Protection Agency's (U. S. EPA) peer and administrative review policies and approved for publication. Mention of trade names or commercial products does not constitute an endorsement or recommendation for use by the U.S. EPA. Financial support provided by the Ministry of Science and Technology (MOST) of Taiwan (for Hou) under grant number MOST 103-2221-E-006-015-MY3 is acknowledged. D.H.F. acknowledges financial support by the U.S. EPA under grant R834858 . Goodwin acknowledges the Owens Fellowship at JHU for financial support.
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/12/1
Y1 - 2016/12/1
N2 - This paper probes the role of hydroxyl radicals (·OH) generated by H2O2 photolysis on graphene oxide (GO) phototransformation, under simulated sunlight. It focuses on comparing the photoreaction of GO with (indirect) and without (direct) added H2O2 under simulated sunlight conditions. The biomarker responses of fish epithelial cells in in vitro assays of parent GO and GO photoreacted with H2O2 and their interaction with model biomembranes are also compared. GO was found to be far more extensively photodecomposed in the presence of H2O2, with ∼85% of the initial carbon content converted to CO2 during 48 h of irradiation. Direct and indirect photoreactions occurred concurrently in GO samples containing H2O2, and indirect photoreaction accounted for ∼70% of GO conversion to CO2. Reaction with ·OH causes increases in the concentrations of carboxylic acid groups of photoreacted GO and low-molecular-weight (LMW) species as part of the intermediate photoproducts. Compared to parent GO, intermediate photoproducts exhibited reduced interaction with model cell membranes and altered biomarker responses. Kinetic analysis extrapolating our data to conditions prevalent in sunlit surface waters predicts that initial GO photoreaction is dominated by direct photolysis, while indirect photoreactions involving ·OH determine subsequent conversion of intermediate GO photoproducts to CO2.
AB - This paper probes the role of hydroxyl radicals (·OH) generated by H2O2 photolysis on graphene oxide (GO) phototransformation, under simulated sunlight. It focuses on comparing the photoreaction of GO with (indirect) and without (direct) added H2O2 under simulated sunlight conditions. The biomarker responses of fish epithelial cells in in vitro assays of parent GO and GO photoreacted with H2O2 and their interaction with model biomembranes are also compared. GO was found to be far more extensively photodecomposed in the presence of H2O2, with ∼85% of the initial carbon content converted to CO2 during 48 h of irradiation. Direct and indirect photoreactions occurred concurrently in GO samples containing H2O2, and indirect photoreaction accounted for ∼70% of GO conversion to CO2. Reaction with ·OH causes increases in the concentrations of carboxylic acid groups of photoreacted GO and low-molecular-weight (LMW) species as part of the intermediate photoproducts. Compared to parent GO, intermediate photoproducts exhibited reduced interaction with model cell membranes and altered biomarker responses. Kinetic analysis extrapolating our data to conditions prevalent in sunlit surface waters predicts that initial GO photoreaction is dominated by direct photolysis, while indirect photoreactions involving ·OH determine subsequent conversion of intermediate GO photoproducts to CO2.
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U2 - 10.1016/j.carbon.2016.09.013
DO - 10.1016/j.carbon.2016.09.013
M3 - Article
AN - SCOPUS:84988892673
SN - 0008-6223
VL - 110
SP - 426
EP - 437
JO - Carbon
JF - Carbon
ER -