The influence of porosity and surface oxygen groups of peat-based activated carbons on benzene adsorption from dry and humid air

Carbon ◽  
2009 ◽  
Vol 47 (10) ◽  
pp. 2371-2378 ◽  
Author(s):  
Andrei Veksha ◽  
Eiji Sasaoka ◽  
Md. Azhar Uddin
Carbon ◽  
2001 ◽  
Vol 39 (2) ◽  
pp. 309-310 ◽  
Author(s):  
P Lodewyckx ◽  
D Van Rompaey ◽  
L Verhoeven ◽  
E.F Vansant

2018 ◽  
Vol 395 ◽  
pp. 271-279 ◽  
Author(s):  
Jocelyn E. Zuliani ◽  
Shitang Tong ◽  
Charles Q. Jia ◽  
Donald W. Kirk

2007 ◽  
Vol 331 ◽  
pp. 26-33 ◽  
Author(s):  
L.J. Lemus-Yegres ◽  
I. Such-Basáñez ◽  
M.C. Román-Martínez ◽  
C. Salinas-Martínez de Lecea

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Marina Maletić ◽  
Marija Vukčević ◽  
Ana Kalijadis ◽  
Zoran Laušević ◽  
Mila Laušević

The new and simple approach for deposition of catalytically active TiO2coating on carbon monolith (CM) carrier was presented. CM photocatalysts were impregnated with TiO2using titanium solution and thermal treatment, and their photocatalytic activity was investigated in the process of methylene blue (MB) photodegradation. For the purpose of comparison, CM composite photocatalysts were prepared by dip-coating method, which implies binder usage. The presence of TiO2on CM carrier was confirmed by Raman spectroscopy and scanning electron microscopy. The sorption characteristics of CM and the role of adsorption in the overall process of MB removal were evaluated through amount of surface oxygen groups obtained by temperature-programmed desorption and specific surface area determined by BET method. CM has shown good adsorption properties toward MB due to high amount of surface oxygen groups and relatively high specific surface area. It was concluded that photocatalytic activity increases with CM disc thickness due to increase of MB adsorption and amount of deposited TiO2. Good photocatalytic activity achieved for samples obtained by thermal treatment is the result of better accessibility of MB solution to the TiO2particles induced by binder absence.


2012 ◽  
Vol 15 (1) ◽  
pp. 10-13 ◽  
Author(s):  
Stefan Klink ◽  
Edgar Ventosa ◽  
Wei Xia ◽  
Fabio La Mantia ◽  
Martin Muhler ◽  
...  

Carbon ◽  
2014 ◽  
Vol 77 ◽  
pp. 89-98 ◽  
Author(s):  
Alba Anfruns ◽  
Eduardo J. García-Suárez ◽  
Miguel A. Montes-Morán ◽  
Rafael Gonzalez-Olmos ◽  
María J. Martin

Author(s):  
Hirokazu Ishitobi ◽  
Satoshi Sugawara ◽  
Kosuke Oba ◽  
Takumi Hirano ◽  
Honoka Doki ◽  
...  

Abstract Higher power output by a lower kinetic resistance of the vanadium redox flow battery is needed for its commercialization. In this study, we focused on the air oxidation conditions of carbon paper, which is the electrode material, to reduce the kinetic resistance. The air oxidation is considered to affect the number of surface oxygen groups such as the phenol-type hydroxyl group due to oxidation of the carbon fiber. The surface oxygen groups may correspond to the active sites for the charge/discharge reaction. We quantitatively evaluated the number of surface oxygen groups by temperature-programmed desorption. In addition, we measured the double-layer capacitances of the carbon papers, which may reflect the surface area of the carbon fiber. The single-cell performances, i.e., current–voltage curves and charge–discharge profile, of the electrodes were studied. The air oxidized carbon paper, heat-treated at 500 °C for 3 h (8.4% mass decrease from the pristine sample), showed the highest power density (960 mW cm−2) in this study with thin electrode material (ca., 0.2 mm for one sheet). The negative half-reaction was enhanced by air oxidation. This result could be explained by the reduction of the kinetic resistance by increasing the number of phenol groups, and this power output was relatively high as the vanadium redox flow battery by using a commercial carbon paper and the standard flow field.


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