Electrochemical oxidation of methyl orange azo dye at pilot flow plant using BDD technology

2013 ◽  
Vol 19 (2) ◽  
pp. 571-579 ◽  
Author(s):  
Cecilia Ramírez ◽  
Adriana Saldaña ◽  
Berenice Hernández ◽  
Roberto Acero ◽  
Ricardo Guerra ◽  
...  
2017 ◽  
Vol 244 ◽  
pp. 199-208 ◽  
Author(s):  
Eloy Isarain-Chávez ◽  
Maria Dolors Baró ◽  
Emma Rossinyol ◽  
Ulises Morales-Ortiz ◽  
Jordi Sort ◽  
...  

Author(s):  
Chunwei Yang ◽  
Dong Wang ◽  
Qian Tang ◽  
Yuwei Sun

AbstractA novel internal circulation batch reactor (ICBR) was utilized to treat an azo dye pollutant methyl orange (MO) solution by the Electro-Fenton process, with graphite rods as the anodes and metal processing waste iron shavings as the cathodes. The MO decoloration efficiency reached 98.6 % for 0.08 g L


Author(s):  
Ahmad Ali Pourbabaee ◽  
F. Malekzadeh ◽  
Mohamad N. Sarbolouki ◽  
Ali Mohajeri
Keyword(s):  

2015 ◽  
Vol 14 (3) ◽  
pp. 528-535 ◽  
Author(s):  
Zacharias Frontistis ◽  
Evroula Hapeshi ◽  
Despo Fatta-Kassinos ◽  
Dionissios Mantzavinos

In this work, the degradation of the azo dye methyl orange in model aqueous solutions by UVC light-induced persulfate oxidation was studied.


2013 ◽  
Vol 291-294 ◽  
pp. 602-605 ◽  
Author(s):  
Liang Liu ◽  
Wen Yi Zhang

In this study we investigated the use of a microbial fuel cell (MFC) to abioticlly cathodic decolorization of a model azo dye, Methyl Orange (MO). Experimental results showed that electricity could be continuously generated the MO-fed MFC and MO was successfully decolorized in the cathode. The decolorization rate was highly dependent on the catholyte pH. When pH was varied from 3.0 to 9.0, the k value in relation to MO degradation decreased from 0.298 to 0.016 μmol min-1, and the maximum power density decreased from 34.77 to 1.51 mW m-2. Sulfanilic acid and N,N-dimethyl-p-phenylenediamine were identified as the decolorization products of MO by HPLC-MS.


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