{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/43659"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/43659","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"Evaluation of different powdered activated carbons in the control of chlorite ion","abstract":"Twelve different powdered activated carbons (PACs) were screened under laboratory conditions to determine their performance in the removal of chlorite ions (ClO₂⁻) and in the production of chloride ions (Cl⁻) and chlorate ions (ClO₃⁻) during that removal. All screenings were conducted in reagent water, at pH 7.0 ± 0.2 pH units, with a standard concentration of 20 mg/liter of powdered activated carbon (PAC) added in each case, and with the process and samples protected from light. One set of screening experiments was conducted with both ClO₂⁻ and chlorine added with the PAC, while the other set contained only ClO₂⁻, and PAC. The chlorine and ClO₂⁻ were added to concentration levels which might be expected in disinfection practice in water treatment plants. Periodic samples were drawn as the mixtures were stirred over a 24 hour period. Each sample was analyzed for Cl⁻, ClO₂⁻, and ClO₃⁻ concentrations utilizing ion chromatography. All PACs were found to reduce ClO₂⁻ to Cl, and ClO₃⁻ was never detected when chlorine was absent. The data provided no consistent significant evidence of ClO₃⁻ formation even when chlorine was present. The rate of ClO₂⁻ removal was most rapid in the first two hours of contact, but slowed to rates below 6 percent per hour after 4 hours of contact. Rates of ClO₂⁻ removal varied with PAC type. The overall rate of ClO₂⁻ removal was also slower, with the total percentage of ClO₂⁻ removal less, when chlorine was present in the mixture.","abstract_html":"Twelve different powdered activated carbons (PACs) were screened under laboratory conditions to determine their performance in the removal of chlorite ions (ClO₂⁻) and in the production of chloride ions (Cl⁻) and chlorate ions (ClO₃⁻) during that removal. All screenings were conducted in reagent water, at pH 7.0 ± 0.2 pH units, with a standard concentration of 20 mg/liter of powdered activated carbon (PAC) added in each case, and with the process and samples protected from light. One set of screening experiments was conducted with both ClO₂⁻ and chlorine added with the PAC, while the other set contained only ClO₂⁻, and PAC. The chlorine and ClO₂⁻ were added to concentration levels which might be expected in disinfection practice in water treatment plants. Periodic samples were drawn as the mixtures were stirred over a 24 hour period. Each sample was analyzed for Cl⁻, ClO₂⁻, and ClO₃⁻ concentrations utilizing ion chromatography. All PACs were found to reduce ClO₂⁻ to Cl, and ClO₃⁻ was never detected when chlorine was absent. The data provided no consistent significant evidence of ClO₃⁻ formation even when chlorine was present. The rate of ClO₂⁻ removal was most rapid in the first two hours of contact, but slowed to rates below 6 percent per hour after 4 hours of contact. Rates of ClO₂⁻ removal varied with PAC type. The overall rate of ClO₂⁻ removal was also slower, with the total percentage of ClO₂⁻ removal less, when chlorine was present in the mixture.","abstract_has_math":false,"creators":["Mitchell, Robert M."],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Environmental Planning","degree_department":"Environmental Engineering","school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1993,"date_issued":"1993","date_published":"1993","updated_at":"2026-07-22T22:20:23Z","subjects":[],"languages":["en"],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-07112009-040246"],"render_values":[{"text":"etd-07112009-040246","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/43659","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.department","label":"Department","values":["Environmental Engineering"]},{"key":"dc:creator","label":"Author","values":["Mitchell, Robert M."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-03-14T21:40:08Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-03-14T21:40:08Z","2009-07-11"]},{"key":"dc:date.issued","label":"Date","values":["1993"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Tech"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.dcmitype","label":"Dc Type Dcmitype","values":["Text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Environmental Planning"]},{"key":"thesis:degree_level","label":"Degree Level","values":["masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Virginia Polytechnic Institute and State University"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["In Copyright"]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://rightsstatements.org/vocab/InC/1.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-07112009-040246"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/43659"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Twelve different powdered activated carbons (PACs) were screened under laboratory conditions to determine their performance in the removal of chlorite ions (ClO₂⁻) and in the production of chloride ions (Cl⁻) and chlorate ions (ClO₃⁻) during that removal. All screenings were conducted in reagent water, at pH 7.0 ± 0.2 pH units, with a standard concentration of 20 mg/liter of powdered activated carbon (PAC) added in each case, and with the process and samples protected from light. One set of screening experiments was conducted with both ClO₂⁻ and chlorine added with the PAC, while the other set contained only ClO₂⁻, and PAC. The chlorine and ClO₂⁻ were added to concentration levels which might be expected in disinfection practice in water treatment plants. Periodic samples were drawn as the mixtures were stirred over a 24 hour period. Each sample was analyzed for Cl⁻, ClO₂⁻, and ClO₃⁻ concentrations utilizing ion chromatography. All PACs were found to reduce ClO₂⁻ to Cl, and ClO₃⁻ was never detected when chlorine was absent. The data provided no consistent significant evidence of ClO₃⁻ formation even when chlorine was present. The rate of ClO₂⁻ removal was most rapid in the first two hours of contact, but slowed to rates below 6 percent per hour after 4 hours of contact. Rates of ClO₂⁻ removal varied with PAC type. The overall rate of ClO₂⁻ removal was also slower, with the total percentage of ClO₂⁻ removal less, when chlorine was present in the mixture."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Master of Science"]},{"key":"dc:format.medium","label":"Dc Format Medium","values":["BTD"]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Evaluation of different powdered activated carbons in the control of chlorite ion"]}]}],"canonical_facts":{"dc:contributor.department":["Environmental Engineering"],"dc:creator":["Mitchell, Robert M."],"dc:date.accessioned":["2014-03-14T21:40:08Z"],"dc:date.available":["2014-03-14T21:40:08Z","2009-07-11"],"dc:date.issued":["1993"],"dc:description.abstract":["Twelve different powdered activated carbons (PACs) were screened under laboratory conditions to determine their performance in the removal of chlorite ions (ClO₂⁻) and in the production of chloride ions (Cl⁻) and chlorate ions (ClO₃⁻) during that removal. All screenings were conducted in reagent water, at pH 7.0 ± 0.2 pH units, with a standard concentration of 20 mg/liter of powdered activated carbon (PAC) added in each case, and with the process and samples protected from light. One set of screening experiments was conducted with both ClO₂⁻ and chlorine added with the PAC, while the other set contained only ClO₂⁻, and PAC. The chlorine and ClO₂⁻ were added to concentration levels which might be expected in disinfection practice in water treatment plants. Periodic samples were drawn as the mixtures were stirred over a 24 hour period. Each sample was analyzed for Cl⁻, ClO₂⁻, and ClO₃⁻ concentrations utilizing ion chromatography. All PACs were found to reduce ClO₂⁻ to Cl, and ClO₃⁻ was never detected when chlorine was absent. The data provided no consistent significant evidence of ClO₃⁻ formation even when chlorine was present. The rate of ClO₂⁻ removal was most rapid in the first two hours of contact, but slowed to rates below 6 percent per hour after 4 hours of contact. Rates of ClO₂⁻ removal varied with PAC type. The overall rate of ClO₂⁻ removal was also slower, with the total percentage of ClO₂⁻ removal less, when chlorine was present in the mixture."],"dc:description.degree":["Master of Science"],"dc:format.medium":["BTD"],"dc:format.mimetype":["application/pdf"],"dc:identifier.other":["etd-07112009-040246"],"dc:identifier.uri":["http://hdl.handle.net/10919/43659"],"dc:language.iso":["en"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["Evaluation of different powdered activated carbons in the control of chlorite ion"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Environmental Planning"],"thesis:degree_level":["masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:20:23Z"}