Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/1200
DC FieldValueLanguage
dc.contributor.authorHarris, Willie G.-
dc.contributor.authorO'Connor, George A.-
dc.contributor.authorObreza, Thomas A.-
dc.contributor.authorElliott, Herschel A.-
dc.contributor.authorMakris, Konstantinos C.-
dc.date.accessioned2015-03-19T09:24:19Z-
dc.date.accessioned2015-12-02T09:03:06Z-
dc.date.available2015-03-19T09:24:19Z-
dc.date.available2015-12-02T09:03:06Z-
dc.date.issued2005-06-01-
dc.identifier.citationEnvironmental Science & Technology, 2005, Volume 39, Issue 11, Pages 4280-4289en_US
dc.identifier.issn15205851-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/1200-
dc.description.abstractDrinking-water treatment residuals (WTRs) are nonhazardous materials that can be obtained free-of-charge from drinking-water treatment plants to reduce soluble phosphorus (P) concentrations in poorly P sorbing soils. Phosphorus sorption capacities of WTRs can vary 1-2 orders of magnitude, on the basis of short-term equilibration times (up to 7 d), but studies dealing with long-term (weeks to months) P retention by WTRs are lacking. Properties that most affect long-term P sorption capacities are pertinent to the efficacy of WTRs as amendments to stabilize P in soils. This research addressed the long-term (up to 80 d) P sorption/desorption characteristics and kinetics for seven WTRs, including the influence of specific surface area (SSA), porosity, and total C content on the overall magnitude of P sorption by seven WTRs. The data confirm a strong but variable affinity for P by WTRs. Aluminum-based WTRs tended to have higher P sorption capacity than Fe-based WTRs. Phosphorus sorption with time was biphasic in nature for most samples and best fit to a second-order rate model. The P sorption rate dependency was strongly correlated with a hysteretic P desorption, consistent with kinetic limitations on P desorption from micropores. Oxalate-extractable Al + Fe concentrations of the WTRs did not effectively explain long-term (80 d) P sorption capacities of the WTRs. Micropore (CO 2-based) SSAs were greater than BET-N2 SSAs for most WTRs, except those with the lowest (<80 g kg-1) total C content. There was a significant negative linear correlation between the total C content and the CO2/N2 SSA ratio. The data suggest that C in WTRs increases microporosity, but reduces P sorption per unit pore volume or surface area. Hence, variability in C content confounds direct relations among SSA, porosity, and P sorption. Total C, N2-based SSA, and CO 2-based SSAs explained 82% of the variability in the long-term P sorption capacities of the WTRs. Prediction of long-term P sorption capacities for different WTRs may be achieved by taking into account the three proposed variables.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofEnvironmental Science & Technologyen_US
dc.rights© American Chemical Societyen_US
dc.subjectDrinking-water treatment residuals (WTR)en_US
dc.subjectNonhazardous materialsen_US
dc.subjectPhosphorus sorptionen_US
dc.subjectSpecific surface area (SSA)en_US
dc.titlePhysicochemical properties related to long-term phosphorus retention by drinking-water treatment residualsen_US
dc.typeArticleen_US
dc.collaborationUniversity of Texasen_US
dc.collaborationUniversity of Floridaen_US
dc.collaborationPennsylvania State Universityen_US
dc.subject.categoryEarth and Related Environmental Sciencesen_US
dc.journalsSubscriptionen_US
dc.reviewPeer Revieweden
dc.countryUnited Statesen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1021/es0480769en_US
dc.dept.handle123456789/54en
dc.relation.issue11en_US
dc.relation.volume39en_US
cut.common.academicyear2005-2006en_US
dc.identifier.spage4280en_US
dc.identifier.epage4289en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn1520-5851-
crisitem.journal.publisherAmerican Chemical Society-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0001-5251-8619-
crisitem.author.parentorgFaculty of Health Sciences-
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