TY - JOUR
T1 - Electrochemical pretreatment for stabilization of waste activated sludge
T2 - Simultaneously enhancing dewaterability, inactivating pathogens and mitigating hydrogen sulfide
AU - Zeng, Qian
AU - Zan, Feixiang
AU - Hao, Tianwei
AU - Biswal, Basanta Kumar
AU - Lin, Sen
AU - van Loosdrecht, Mark C.M.
AU - Chen, Guanghao
PY - 2019
Y1 - 2019
N2 - Stabilization of waste activated sludge (WAS) is an essential step for the disposal or reuse. In this study, WAS stabilization via electrochemical pretreatment (EPT) at 0–15V was evaluated for simultaneous dewaterability enhancement, pathogen removal and H2S mitigation. The mechanism underlying EPT was investigated and discussed based on the changes in the physicochemical (e.g., particle size, zeta potential, hydrophobicity and extracellular polymeric substances) and biological characteristics (i.e. cell morphology, and distribution and percentages of live/dead cells) of WAS with different EPT voltages. The results revealed that EPT disintegrated WAS flocs and disrupted the cell walls leading to a reduction in particle size (by up to 50%), increased release of extracellular and intracellular substances (by up to 4 times) to facilitate WAS stabilization. With EPT at 15V, the capillary suction time of WAS decreased by 42%, and the concentrations of E. coli and indicator pathogens (Salmonella spp. and Streptococcus faecalis) fell by nearly 5 log10 reaching U.S. EPA hygienization levels. Furthermore, EPT at 12V or higher suppressed the amounts of dissolved sulfide and H2S(g) produced from the WAS under anaerobic conditions by over 99%. This study demonstrates the feasibility of EPT for simultaneous WAS dewaterability enhancement, pathogen inactivation and H2S mitigation, providing a one-step alternative for sludge stabilization.
AB - Stabilization of waste activated sludge (WAS) is an essential step for the disposal or reuse. In this study, WAS stabilization via electrochemical pretreatment (EPT) at 0–15V was evaluated for simultaneous dewaterability enhancement, pathogen removal and H2S mitigation. The mechanism underlying EPT was investigated and discussed based on the changes in the physicochemical (e.g., particle size, zeta potential, hydrophobicity and extracellular polymeric substances) and biological characteristics (i.e. cell morphology, and distribution and percentages of live/dead cells) of WAS with different EPT voltages. The results revealed that EPT disintegrated WAS flocs and disrupted the cell walls leading to a reduction in particle size (by up to 50%), increased release of extracellular and intracellular substances (by up to 4 times) to facilitate WAS stabilization. With EPT at 15V, the capillary suction time of WAS decreased by 42%, and the concentrations of E. coli and indicator pathogens (Salmonella spp. and Streptococcus faecalis) fell by nearly 5 log10 reaching U.S. EPA hygienization levels. Furthermore, EPT at 12V or higher suppressed the amounts of dissolved sulfide and H2S(g) produced from the WAS under anaerobic conditions by over 99%. This study demonstrates the feasibility of EPT for simultaneous WAS dewaterability enhancement, pathogen inactivation and H2S mitigation, providing a one-step alternative for sludge stabilization.
KW - Dewaterability enhancement
KW - Electrochemical pretreatment
KW - Pathogen inactivation
KW - Sludge stabilization
KW - Sulfide removal
UR - http://www.scopus.com/inward/record.url?scp=85071735891&partnerID=8YFLogxK
U2 - 10.1016/j.watres.2019.115035
DO - 10.1016/j.watres.2019.115035
M3 - Article
AN - SCOPUS:85071735891
SN - 0043-1354
VL - 166
JO - Water Research
JF - Water Research
M1 - 115035
ER -