New insight into waste activated sludge acetogenesis triggered by coupling sulfite/ferrate oxidation with sulfate reduction-mediated syntrophic consortia.

• Coupling SO 4 ∙‾ oxidation with io-SRB mediation enhanced acetogenesis from WAS. • SO 4 ∙‾ and ∙OH were the key radicals responsible for coupled Fe(VI)/S(IV) oxidation. • io-SRB mediation promoted the organics transformation on the basis of SO 4 ∙‾ oxidation. • SO 4 ∙‾/io-SRB altered the structure of WAS fermentative acidogenic microbiome. • Synergistic relationships among io-SRB, hydrolyzing bacteria and acidogens were revealed. Acetate (HAc) production via acetogenesis is a promising biorefinery approach for waste activated sludge (WAS); however, it is hampered by the thermodynamic constraints of the bioconversion of 3–5 carbon atom short-chain fatty acids (SCFAs). Sulfate radical (SO 4 ∙‾)-based advanced oxidation is regarded as an appropriate candidate for accelerating WAS fermentation. In this study, we enriched an incomplete-oxidative sulfate reducing bacteria (io-SRB), combined with SO 4 ∙‾ oxidation (generated by potassium ferrate (PF) and sodium sulfite (Na 2 SO 3)), to boost WAS acetogenesis. Generated sulfate during SO 4 ∙‾ oxidation served as the necessary substrates for io-SRB metabolism. A proof-of-concept based on experimental data for the whole process is presented. Results confirmed that the PF + Na 2 SO 3 + SRB test achieved the maximum SCFAs generation (4261 ± 210 mg COD/L with 60.9 ± 0.5% HAc) over the PF + Na 2 SO 3 test without io-SRB mediation (2521 ± 109 mg COD/L with 50.6 ± 0.3% HAc). Particle size analysis and fluorescence spectroscopy indicated that PF + Na 2 SO 3 oxidation had positive effects on accelerating soluble organics release. SO 4 ∙‾ was the key radical, playing the most important role, as indicated by electron paramagnetic resonance and radical scavenging analysis. X-ray photoelectron spectroscopy revealed that io-SRB mediation further promoted the transformation of polysaccharides and proteins into carboxylic acids, based on SO 4 ∙‾ oxidation. Moreover, 79% Fe(VI) was reduced to Fe(III), and most S(IV) was converted to SO 4 2−, approximately 40% of which was metabolized by io-SRB consortium. Clearly, SO 4 ∙‾ oxidation and io-SRB stimulation significantly altered the composition of the key microbiome, with fermentative acidogenic bacteria predominating. The possible synergistic relationships among io-SRB, hydrolyzing bacteria and acidogens were revealed by molecular ecological network analysis. This study provides new insights into the improvement of value-added bio-metabolite recovery from SO 4 ∙−-based WAS fermentation. [ABSTRACT FROM AUTHOR]