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Electrocoagulation of simulated reactive dyebath effluent with aluminum and stainless steel electrodes

Araştırma sonucu: Dergiye katkıMakalebilirkişi

80 Atıf (Scopus)

Özet

Reactive dyebath effluents are ideal candidates for electrocoagulation due to their intensive color, medium strength, recalcitrant COD and high electrolyte (NaCl) content. The present study focused on the treatability of simulated reactive dyebath effluent (CODo = 300 mg/L; color in terms of absorbance values Ao,436 = 0.532 cm-1, Ao,525 = 0.693 cm-1 and Ao,620 = 0.808 cm-1) employing electrocoagulation with aluminum and stainless steel electrodes. Optimization of critical operating parameters such as initial pH (pHo 3-11), applied current density (Jc = 22-87 mA/cm2) and electrolyte type (NaCl or Na2SO4) improved the overall treatment efficiencies resulting in effective decolorization (99% using stainless steel electrodes after 60 min, 95% using aluminum electrodes after 90 min electrocoagulation) and COD abatement (93% with stainless steel electrodes after 60 min, 86% with aluminum electrodes after 90 min of reaction time). Optimum electrocoagulation conditions were established as pHo 5 and Jc = 22 mA/cm2 for both electrode materials. The COD and color removal efficiencies also depended on the electrolyte type. No in situ, surplus adsorbable organically bound halogens (AOX) formation associated with the use of NaCl as the electrolyte during electrocoagulation was detected. An economical evaluation was also carried out within the frame of the study. It was demonstrated that electrocoagulation of reactive dyebath effluent with aluminum and stainless steel electrodes was a considerably less electrical energy-intensive, alternative treatment method as compared with advanced chemical oxidation techniques.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)1586-1594
Sayfa sayısı9
DergiJournal of Hazardous Materials
Hacim164
Basın numarası2-3
DOI'lar
Yayın durumuYayınlandı - 30 May 2009

Finansman

The authors thank Dr. Izzet Alaton for supplying the reactive dyestuffs and dye auxiliary chemicals. The present work was financially supported by TUBA (The Turkish Academy of Sciences) under the GEBIP Program and Istanbul Technical University Scientific Research Project Foundation.

Finansörler
TUBA
Türkiye Bilimler Akademisi
Istanbul Teknik Üniversitesi

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