Anodic production of hydrogen peroxide using commercial carbon materials

Author(s):  
Dhananjai Pangotra ◽  
Lénárd-István Csepei ◽  
Arne Roth ◽  
Carlos Ponce de León ◽  
Volker Sieber ◽  
...  
2016 ◽  
Vol 14 (4) ◽  
pp. 843-850 ◽  
Author(s):  
Orlando García-Rodríguez ◽  
Jennifer A. Bañuelos ◽  
Arturo Rico-Zavala ◽  
Luis A. Godínez ◽  
Francisco J. Rodríguez-Valadez

Abstract The in-situ generation of hydrogen peroxide in the electro-Fenton process is paramount. For this reason, in this research the electrocatalytic activity of three carbon materials was evaluated in the reaction of oxygen reduction via two electrons. Furthermore, in order to eliminate the use of iron salts in solution (homogeneous process), the iron was electrodeposited on the surface of the carbon material and was applied in a heterogeneous electro-Fenton process for the degradation of methyl orange dye. The largest amount of generated H2O2 was achieved with the Carbon Felt (CF) electrode (460 mg L−1) without iron after 60 minutes. The electrodes with electrodeposited iron were characterized by SEM and EDS, which showed that the surface of the Carbon Sponge (CS) electrode had the largest amount of iron (23.84 %). However, the CF electrode showed a greater and faster degradation of the dye (98 %) after 30 minutes of treatment. The CF material was the best and most-viable choice of material compared to the CS and Carbon Cloth (CC) for industrial application in electro-Fenton processes, due to its greater catalytic activity in the production of H2O2, uniform distribution of iron, more efficient TOC removal and lower cost per cm2 of material.


2020 ◽  
Vol 63 (9-10) ◽  
pp. 895-912
Author(s):  
Haiyan Song ◽  
Lishan Wei ◽  
Luning Chen ◽  
Han Zhang ◽  
Ji Su

2016 ◽  
Vol 88 (23) ◽  
pp. 11783-11790 ◽  
Author(s):  
Filipa R. F. Simoes ◽  
Nitin M. Batra ◽  
Bashir H. Warsama ◽  
Christian G. Canlas ◽  
Shashikant Patole ◽  
...  

iScience ◽  
2021 ◽  
Vol 24 (2) ◽  
pp. 102094
Author(s):  
Rusen Zou ◽  
Aliyeh Hasanzadeh ◽  
Alireza Khataee ◽  
Xiaoyong Yang ◽  
Mingyi Xu ◽  
...  

2004 ◽  
Vol 28 (12) ◽  
pp. 1431 ◽  
Author(s):  
Wei-Liang Feng ◽  
Yong Cao ◽  
Nan Yi ◽  
Wei-Lin Dai ◽  
Kang-Nian Fan

1987 ◽  
Vol 253 (4) ◽  
pp. C495-C499 ◽  
Author(s):  
P. D. Walker ◽  
S. V. Shah

Agents that affect mitochondrial respiration have been shown to enhance the generation of reactive oxygen metabolites. On the basis of the well-demonstrated ability of gentamicin to alter mitochondrial respiration (stimulation of state 4 and inhibition of state 3), it was postulated that gentamicin may enhance the generation of reactive oxygen metabolites by renal cortical mitochondria. The aim of this study was to examine the effect of gentamicin on the production of hydrogen peroxide (measured as the decrease in scopoletin fluorescence) in rat renal cortical mitochondria. The hydrogen peroxide generation by mitochondria was enhanced from 0.17 +/- 0.02 nmol . mg-1 . min-1 (n = 14) in the absence of gentamicin to 6.21 +/- 0.67 nmol . mg-1 . min-1 (n = 14) in the presence of 4 mM gentamicin. This response was dose dependent with a significant increase observed at even the lowest concentration of gentamicin tested, 0.01 mM. Production of hydrogen peroxide was not increased when gentamicin was added to incubation media in which mitochondria or substrate was omitted or heat-inactivated mitochondria were used. The gentamicin-induced change in fluorescence was completely inhibited by catalase (but not by heat-inactivated catalase), indicating that the decrease in fluorescence was due to hydrogen peroxide. Thus this study demonstrates that gentamicin enhances the production of hydrogen peroxide by mitochondria. Because of their well-documented cytotoxicity, reactive oxygen metabolites may play a critical role in gentamicin nephrotoxicity.


2010 ◽  
Vol 446 ◽  
pp. 23-31
Author(s):  
Anastasia Pikasi ◽  
Pantelitsa Georgiou ◽  
Johannis Simitzis

Carbonaceous materials have been obtained by pyrolysis of composites based on olive stones biomass, novolac resin as binding agent, with or without an aromatic compound (naphthalene). The pyrolysis residue at 1000 °C is 40 w% and its electrical conductivity, σ, is 0.13 S/cm. Small cylindrical specimens have been manufactured and pyrolyzed at 1000 °C in order to be used as electrodes. Platinum was electrodeposited by cyclic voltammetry on these specimens using them as working electrodes or on commercial carbon fibres, respectively, for correlating purposes. The morphology of both carbon materials, used as electrodes, was characterized by SEM images and the presence of Pt was determined based on EDS analysis. The crystallographic planes of Pt–carbon of Pt deposited on carbon materials were characterized with XRD. The oxidation of ethanol from a proper solution using the carbonaceous specimen and the carbon fibres as working electrodes was examined by cyclic voltammetry.


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