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Treatment of reverse-osmosis concentrate of printing and dyeing wastewater by electro-oxidation process with controlled oxidation-reduction potential (ORP).

Authors :
Wang, Jiade
Zhang, Tian
Mei, Yu
Pan, Bingjun
Source :
Chemosphere. Jun2018, Vol. 201, p621-626. 6p.
Publication Year :
2018

Abstract

Reverse osmosis concentrate (ROC) of printing and dyeing wastewater remains as a daunting environmental issue, which is characterized by high salinity, chemical oxygen demand (COD), chroma and low biodegradability. In this study electro-oxidation process (PbO 2 /Ti electrode) coupled with oxidation-reduction potential (ORP) online monitor was applied to treat such a ROC effluent. The results show that with the increase of specific electrical charge (Q sp ), the removal efficiencies of COD, TN and chroma increased significantly at the incipience and then reached a gentle stage; the optimal total current efficiency (12.04 kWh m −3 ) was obtained with the current density of 10 mA cm −2 (Q sp , 3.0 Ah L −1 ). Meanwhile, some inorganic ions can be simultaneously removed to varying degrees. FTIR analyses indicated that the macromolecular organics were decomposed into smaller molecules. A multi-parameter linear relationship between ORP and Q sp , COD and Cl − concentration was established, which can quantitatively reflect the effect of current density, chloride ion concentration, pollutants and reaction time on the performance of the electro-oxidation system. As compared to a traditional constant-current system, the constant-ORP system developed in this study (through the back-propagation neural network [BPN] model with ORP monitoring) approximately reduced the energy cost by 24–29%. The present work is expected to provide a potential alternative in optimizing the electro-oxidation process. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
201
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
128804514
Full Text :
https://doi.org/10.1016/j.chemosphere.2018.03.051