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dc.contributor.authorGillis, Joseph Daniel
dc.date.accessioned2011-09-06T14:03:42Z
dc.date.available2011-09-06T14:03:42Z
dc.date.issued2011-09-06
dc.identifier.urihttp://hdl.handle.net/10222/14188
dc.description.abstractThe application of municipal sewage biosolids to agricultural land is a common practice worldwide. Increasing attention is being directed at the presence of organic contaminants bound to the organic phase during wastewater treatment, which end up in the biosolids. The goal of this study was to investigate the decomposition of an alkaline-stabilized biosolid being used as an agricultural soil amendment containing unknown organic contaminants. A two year field trial and a 120 day laboratory soil incubation using increasing rates (0, 7, 14, 28, and 42 Mg ha-1) of an alkaline-stabilized biosolid (ASB) were set up to monitor biosolid decomposition and concentrations of selected contaminants over time. The seven contaminants selected for monitoring (p-cresol, indole, 4-t-octylphenol, phenanthrene, triclosan, carbamazepine, and benzo[a]pyrene) represent a wide range of physico-chemical properties and fall under several different chemical classes. The decomposition of ASB in soil was examined in the incubation study. Almost half of the CO2-C evolved from ASB amended soils occurred within the first 6 days, indicating that a relatively labile pool of carbon remains in ASB following the sewage treatment process. By day 121, between 71 to 78% of the total carbon added to soil had been evolved as CO2-C. A new model developed during this study to describe carbon mineralization, a first order plus logistic function (FLOG), performed better than other commonly used models. The method chosen to analyze organic contaminants in soil was only able to determine four out of seven compounds reliably, with recoveries greater than 50% for 4-t-octylphenol, phenanthrene, triclosan, and benzo[a]pyrene. In treated soils, only triclosan was able to be detected and quantified. Average triclosan concentration in the incubation study ranged from a high of 143 ng g-1 on day 3 to a low of 26 ng g-1 by day 121, representing an 81% decrease over a roughly 4 month period under idealized conditions. In the field, triclosan concentrations following a Fall biosolids application in Oct. 2008 increased to detectable levels (29 to 47 ng g-1) in all three plots measured in Nov. 2008, which remained elevated (29 to 66 ng g-1) over the winter period in two out of three plots when sampled in May 2009. Following the Spring application in June 2009, measured triclosan concentrations in July 2009 samples from these same two plots were lower than predicted (33 to 48 ng g-1) and eventually decreased to levels below the detection limit by the Oct. 2009 sampling.en_US
dc.language.isoenen_US
dc.subjectbiosoliden_US
dc.subjectsewage sludgeen_US
dc.subjectcarbon mineralizationen_US
dc.subjectmodellingen_US
dc.subjecttriclosanen_US
dc.titleMonitoring Organic Contaminant Concentrations and Carbon Mineralization in Field Soils Receiving Alkaline-Stabilized Biosolidsen_US
dc.date.defence2011-05-25
dc.contributor.departmentNova Scotia Agricultural Collegeen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinerShiv O. Prasheren_US
dc.contributor.graduate-coordinatorHeather Hughesen_US
dc.contributor.thesis-readerGlenn W. Strattonen_US
dc.contributor.thesis-supervisorGordon W. Price, David L. Burtonen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsYesen_US
dc.contributor.copyright-releaseYesen_US
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