4.7 Article

Improving dewaterability of waste activated sludge by thermally-activated persulfate oxidation at mild temperature

Journal

JOURNAL OF ENVIRONMENTAL MANAGEMENT
Volume 281, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jenvman.2020.111899

Keywords

Thermally-activated persulfate; Waste activated sludge; Dewaterability; Sulfate radicals; Extracellular polymeric substances

Funding

  1. National Natural Science Foundation of China [51978618, 51508509, 51878582]
  2. Natural Science Foundation of Zhejiang Province [LY21E080018, LY18E080036]
  3. Foundation of Key Laboratory of Yangtze River Water Environment, Ministry of Education (Tongji University), China [YRWEF201901]

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The study utilized the thermally-activated sodium persulfate process to improve the dewaterability of waste activated sludge, where SPS decomposition at mild temperature generated radicals that oxidized EPS and facilitated solid-liquid separation, enhancing sludge dehydration.
The mass production of waste activated sludge in wastewater treatment plants may lead to environmental pollution and sludge dewatering is an essential process during its treatment. The oxidation of extracellular polymeric substances (EPS) was the core step to achieve deep sludge dewatering. In this study, thermally-activated sodium persulfate (SPS) process was managed to improve the dewaterability of waste activated sludge (WAS) and its internal mechanism was systematically elaborated. Experimental results showed that with 2.0 mmol/g VSS SPS at 80 degrees C, capillary suction time (CST) was roughly 59.74% of that in raw sludge. Under this condition, 14.66 +/- 0.10 x 10(11) kg/m of specific resistance to filtration (SRF) and 61.8% +/- 0.1% of water content (W-C) was determined, respectively. A solubilization/oxidation process was proposed to unravel the mechanism of the enhanced dewaterability of WAS in thermally-activated SPS process. Mild temperature efficiently disrupted the sludge flocs and broke cell walls, releasing large amounts of EPS into bulk phase. Meanwhile, mild temperature accelerated the decomposition of SPS to generate sulfate radicals (SO4 center dot-) and hydroxyl radicals (center dot OH) for oxidizing EPS, facilitating the conversion of bound hydrated water into free water and achieving solid-water separation. The higher reaction temperature favored sludge dewatering, whereas overdosing SPS posed no significant impact. Further analysis illustrated that tyrosine protein-like, tryptophan protein-like, fulvic acid-like and humic acid-like substances in various EPS fractions together exerted the influence on sludge dewatering. Furthermore, the synergy process could alter the secondary structure of protein, which caused a loose structure of EPS and the exposure of hydrophobic sites, facilitating the dehydration of sludge flocs. The details of how thermally-activated SPS process enhanced sludge dewaterability provided the theoretical and technical basis for the application of the process under a real-world situation.

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