2001
DOI: 10.1002/jctb.524
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Electrochemical conversion of phenolic wastewater on carbon electrodes in the presence of NaCl

Abstract: The electrochemical conversion of highly concentrated synthetic phenolic wastewater was studied on carbon electrodes in a batch electrochemical reactor. The effects of reaction temperature, electrolyte concentration, current density and initial phenol concentration on phenol conversion were elucidated. The wastewater was synthetically prepared and used in reactions carried out generally at 25°C with an initial phenol concentration of 3500 mg dm À3. Although current density increased, phenol conversion% and ini… Show more

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Cited by 32 publications
(24 citation statements)
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“…Such polymeric derivatives were observed while subjecting phenolic wastewater to electro-chemical oxidation. 33 Anodic oxidation of phenol in the presence of NaCl has led to organochlorinated compounds, which were further oxidized to volatile CHCl 3 . Although chlorophenols are formed in the initial stages they were eventually converted to polymeric compounds free from chlorine.…”
Section: Catecholmentioning
confidence: 99%
“…Such polymeric derivatives were observed while subjecting phenolic wastewater to electro-chemical oxidation. 33 Anodic oxidation of phenol in the presence of NaCl has led to organochlorinated compounds, which were further oxidized to volatile CHCl 3 . Although chlorophenols are formed in the initial stages they were eventually converted to polymeric compounds free from chlorine.…”
Section: Catecholmentioning
confidence: 99%
“…Electrochemical oxidation of phenol has been studied by various workers at platinum [7][8][9], doped SnO 2 [8,9], PbO 2 [8,[12][13][14], Bi 2 O 5 -PbO 5 [14], IrO 2 [10], carbon [15] and borondoped diamond anodes [16]. Among these electrode materials, besides the diamond electrode, metal oxide electrodes, which are cheaper, are also preferred.…”
Section: Introductionmentioning
confidence: 99%
“…The catholyte was a solution of 0.1 M MA in 1.0 M H 2 SO 4 . The current density was 58 mA cm −2 (the cell voltage range was 3.80-4.10 V) and the teperature of the water bath was 60 • C, the same temperature as that used in several published works [36,37]. As shown in Table 1, the SA yield and the current efficiency using the Ti/Ce nano-TiO 2 electrode (Ce/Ti molar ratio = 0.003), 98% and 91% respectively, were higher than those obtained with the Ti/nano-TiO 2 electrode, 81% and 80%.…”
Section: Galvanostatic Electrolysismentioning
confidence: 99%