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Performance of electrochemical oxidation over BDD anode for the treatment of different industrial dye-containing wastewater effluents
Author(s) -
Arwa Abdelhay,
Inshad Jum’h,
Abeer Al Bsoul,
Dina Abu Arideh,
Bahaa Qatanani
Publication year - 2020
Publication title -
journal of water reuse and desalination
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.548
H-Index - 16
eISSN - 2408-9370
pISSN - 2220-1319
DOI - 10.2166/wrd.2020.064
Subject(s) - wastewater , chemical oxygen demand , turbidity , electrolysis , effluent , pulp and paper industry , chemistry , electrolyte , anode , supporting electrolyte , electrochemistry , nuclear chemistry , environmental engineering , electrode , environmental science , oceanography , engineering , geology
This paper presents the results of electrochemical oxidation of dye-containing wastewater over a BDD anode. Batch experiments were conducted at a fixed current density of 2.8 mA/cm2 to analyze the performance of the electrochemical process for the treatment of textile and paint wastewater utilizing different supporting electrolytes (Na2SO4 and NaCl). During electrolysis, emphasis was put on measuring different parameters such as chemical oxygen demand (COD), turbidity, conductivity, and color removal. The results revealed that BDD cell exhibited higher COD removal efficiency for textile wastewater than for paint wastewater. Adding supporting electrolytes had a positive effect on COD, turbidity, and color removal efficiencies for both textile and paint industry effluents. For textile wastewater, Na2SO4 and NaCl yielded a reduction in COD of 94% in 6 hours compared to 84% with no electrolyte added. The presence of Na2SO4 and NaCl in paint wastewater resulted in different COD removal percentages of 71 and 85% respectively with 21% in raw sample after 4 hours of treatment. The discoloration reached a percentage higher than 96% for both effluents and for both electrolytes. Under the same experimental conditions, all cases showed turbidity removal higher than 97%. The kinetic study showed that the reaction rate followed pseudo-first-order kinetics.

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