4.6 Article

Efficient Removal of Azo Dye from Wastewater Using the Non-Toxic Potassium Ferrate Oxidation-Coagulation Process

Journal

APPLIED SCIENCES-BASEL
Volume 11, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/app11156825

Keywords

azo dye removal; potassium ferrate; coagulation; oxidation; textile wastewater

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2017R1A6A3A04004335]
  2. Brain Korea 21 FOUR Project in the Education and Research Center for Infrastructure of Smart Ocean City (i-SOC Center)
  3. Pusan National University
  4. National Research Foundation of Korea [2017R1A6A3A04004335] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study investigated the removal of azo dye from textile wastewater effluents using oxidation and coagulation processes. Potassium ferrate was found to be an effective oxidant and coagulant, achieving nearly 100% removal of azo dyes under optimized conditions. Despite its high efficiency, the removal performance decreased at higher pH levels.
The wastewater effluents from textile industries contain highly toxic metal complex dyes. For instance, azo dye has received significant attention owing to its toxicity and environmental stability. This study investigated the oxidation and coagulation processes to effectively remove azo dye from wastewater effluents. Potassium ferrate (K2FeO4) was selected as an oxidant because it has a high oxidation potential, is environmentally stable, and does not generate toxic byproducts. Moreover, it has a combination effect of coagulation and oxidation. Its performance was compared with a single oxidation process (using NaOCl) and a single coagulation process (using FeCl3 center dot 6H(2)O). Based on the jar test experiment, the optimized pH was estimated to be 3 and the optimal dosage was 56.4 mg/L for K2FeO4, and it removed nearly 100% of orange II azo dye (OD) and lissamine green B dye (LGB). However, its removal efficiency decreased when the pH increased to 12. In all processes, dye removal was completed in 5 min of the reaction. Overall, OD and LGB were effectively removed by K2FeO4, compared to the NaOCl and FeCl3 center dot 6H(2)O. This indicates that the combination of oxidation and coagulation of K2FeO4 outperformed the single treatment process without toxic byproduct production.

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