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dc.contributor.authorKaterina Papp
dc.contributor.authorDuane Moser
dc.contributor.authorDaniel Gerrity
dc.date.accessioned2022-01-30T19:26:22Z
dc.date.available2022-01-30T19:26:22Z
dc.date.issued2020
dc.identifier.other%28ASCE%29EE.1943-7870.0001617.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4265301
dc.description.abstractThis study employed quantitative polymerase chain reaction (qPCR) to evaluate the occurrence and removal of five microbial surrogates at two water reuse facilities. The surrogates were (1) the 16S rRNA gene; (2) the AllBac assay for Bacteroides; (3) the Bacteroides bacteriophage ϕB124-14; (4) the Bacteroides bacteriophage ϕcrAssphage; and (5) the pepper mild mottle virus (PMMoV). Log removal values (LRVs) were quantified for a membrane bioreactor (MBR) and across a full advanced treatment (FAT) train. PMMoV, ϕB124-14, and ϕcrAssphage were detected in the MBR feed at concentrations of approximately 103  gene⁢  copies(gc)/mL, 105  gc/mL, and 106  gc/mL, respectively. Only PMMoV was above the limit of quantification (LoQ) in the MBR filtrate (25±8  gc/mL), resulting in a wide range of viral LRVs: 1.4±0.5 for PMMoV, >3.9±0.3 for ϕB124-14, and >6.2±0.3 for ϕcrAssphage. All molecular targets were above the LoQ in the biologically treated FAT feed, but only the bacterial 16S rRNA gene was >LoQ after ozonation and biological activated carbon (BAC) and in the reverse osmosis (RO) concentrate. The gene was <LoQ in the RO permeate and after the UV advanced oxidation process (AOP).
dc.publisherASCE
dc.titleViral Surrogates in Potable Reuse Applications: Evaluation of a Membrane Bioreactor and Full Advanced Treatment
dc.typeJournal Paper
dc.journal.volume146
dc.journal.issue2
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001617
dc.page04019103
dc.treeJournal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 002
dc.contenttypeFulltext


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