Electrochemical valorization of waste activated sludge for short-chain fatty acids production.

Front Chem

Chemical and Electrochemical Technology and Innovation Laboratory, Department of Chemical Engineering, Edward E. Whitacre Jr. College of Engineering, Texas Tech University, Lubbock, TX, United States.

Published: August 2022

A tremendous amount of waste activated sludge (WAS) ends up in landfilling even after a substantial retention time during anaerobic digestion. This leftover activated sludge is an organic-rich material with the high potential to produce value-added chemicals such as short chain fatty acids (SCFAs). In the present study, a novel electrochemical conversion of activated sludge (E-WAS) was carried out on the surface of non-precious electrodes (nickel, stainless-steel and copper) in alkaline media at low applied potential and temperature. Cyclic voltammetry showed that Cu (II)/Cu (III) and Ni (II)/Ni(III) redox couple catalyzed the WAS oxidation reaction to produce SCFAs and hydrogen. The results revealed that Cu(II)/Cu(III) has higher catalytic oxidation capability towards SCFAs. Yields of 48.7, 21.4, and 14.6 mg SCFAs per g of volatile solids were achieved by using copper, nickel and stainless-steel as working electrodes, respectively. Post analysis characterization techniques indicate that copper oxide films lead to WAS oxidation. Total volatile solid removal of 30% was obtained at 35°C and 1.65 V in 0.2 M NaOH after 2 h of operation in an electrochemical digestor with copper electrodes which is more efficient than a conventional alkaline treatment (24 h, 55%, 1M NaOH). Ammonia was produced as the by-product of E-WAS oxidation. The highest amount of ammonia (250 mg L) was obtained by using nickel as the working electrode after 2 h operation at 35°C and 1.35 V applied potential. The change in WAS morphology revealed that the copper oxide film is an effective electrocatalyst for WAS disinfection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469876PMC
http://dx.doi.org/10.3389/fchem.2022.974223DOI Listing

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