{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/41675"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/41675","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"Comparison of ion chromatography and flow injection analysis methods for monitoring chlorite and chlorate ions in drinking water","abstract":"Up-coming regulations on chlorine dioxide in drinking water treatment require low level measurement of chlorite ion (CI0₂-) and chlorate ion (CI0₃-). This research investigated analysis of CI0₂- and CI0₃-; in drinking water by flow injection analysis with iodometric detection (FIA) and ion chromatography with conductivity detection (IC). Both the FIA and IC methods were accurate for the determination of CIO₂-; and CIO₃-; in reagent water. The IC method was accurate in drinking water, however, FIA responded to chloramines and other oxidants present in drinking water causing inaccurate analysis of CIO₂-; and CIO₃-; by FIA. The two IC eluants investigated, a carbonate/bicarbonate mixture and a borate/boric acid mixture, performed well. By taking advantage of the slightly different separation abilities of each eluant, the IC method can be modified to maximize resolution of CIO₂-; and CIO₃-; in different drinking water matrices. Chlorite was unstable in chlorinated drinking water but was stable for up to three days when sodium oxalate was added and stable up to eighteen days when ethylene diamine was added as a preservative. Chlorate was stable in drinking water for up to eighteen days with or without a preservative. The propagation of errors method for determining detection limits yielded limits of detection for CIO₂- (mg/L) of 0.05 for FIA, 0.03 for the IC carbonate eluant and 0.01 for the IC borate eluant. For CIO₃- the limits of detection (mg/L) were 0.24 for FIA; 0.11 for the IC carbonate eluant and 0.02 for the borate eluant.","abstract_html":"Up-coming regulations on chlorine dioxide in drinking water treatment require low level measurement of chlorite ion (CI0₂-) and chlorate ion (CI0₃-). This research investigated analysis of CI0₂- and CI0₃-; in drinking water by flow injection analysis with iodometric detection (FIA) and ion chromatography with conductivity detection (IC). Both the FIA and IC methods were accurate for the determination of CIO₂-; and CIO₃-; in reagent water. The IC method was accurate in drinking water, however, FIA responded to chloramines and other oxidants present in drinking water causing inaccurate analysis of CIO₂-; and CIO₃-; by FIA. The two IC eluants investigated, a carbonate/bicarbonate mixture and a borate/boric acid mixture, performed well. By taking advantage of the slightly different separation abilities of each eluant, the IC method can be modified to maximize resolution of CIO₂-; and CIO₃-; in different drinking water matrices. Chlorite was unstable in chlorinated drinking water but was stable for up to three days when sodium oxalate was added and stable up to eighteen days when ethylene diamine was added as a preservative. Chlorate was stable in drinking water for up to eighteen days with or without a preservative. The propagation of errors method for determining detection limits yielded limits of detection for CIO₂- (mg/L) of 0.05 for FIA, 0.03 for the IC carbonate eluant and 0.01 for the IC borate eluant. For CIO₃- the limits of detection (mg/L) were 0.24 for FIA; 0.11 for the IC carbonate eluant and 0.02 for the borate eluant.","abstract_has_math":false,"creators":["Ledder, Tracey"],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Environmental Sciences and Engineering","degree_department":"Environmental Sciences and Engineering","school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1991,"date_issued":"1991-12-05","date_published":"1991-12-05","updated_at":"2026-07-22T22:20:38Z","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-03172010-020312"],"render_values":[{"text":"etd-03172010-020312","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/41675","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.department","label":"Department","values":["Environmental Sciences and Engineering"]},{"key":"dc:creator","label":"Author","values":["Ledder, Tracey"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-03-14T21:31:57Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-03-14T21:31:57Z","2010-03-17"]},{"key":"dc:date.issued","label":"Date","values":["1991-12-05"]},{"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 Sciences and Engineering"]},{"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-03172010-020312"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/41675"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Up-coming regulations on chlorine dioxide in drinking water treatment require low level measurement of chlorite ion (CI0₂-) and chlorate ion (CI0₃-). This research investigated analysis of CI0₂- and CI0₃-; in drinking water by flow injection analysis with iodometric detection (FIA) and ion chromatography with conductivity detection (IC). Both the FIA and IC methods were accurate for the determination of CIO₂-; and CIO₃-; in reagent water. The IC method was accurate in drinking water, however, FIA responded to chloramines and other oxidants present in drinking water causing inaccurate analysis of CIO₂-; and CIO₃-; by FIA. The two IC eluants investigated, a carbonate/bicarbonate mixture and a borate/boric acid mixture, performed well. By taking advantage of the slightly different separation abilities of each eluant, the IC method can be modified to maximize resolution of CIO₂-; and CIO₃-; in different drinking water matrices. Chlorite was unstable in chlorinated drinking water but was stable for up to three days when sodium oxalate was added and stable up to eighteen days when ethylene diamine was added as a preservative. Chlorate was stable in drinking water for up to eighteen days with or without a preservative. The propagation of errors method for determining detection limits yielded limits of detection for CIO₂- (mg/L) of 0.05 for FIA, 0.03 for the IC carbonate eluant and 0.01 for the IC borate eluant. For CIO₃- the limits of detection (mg/L) were 0.24 for FIA; 0.11 for the IC carbonate eluant and 0.02 for the borate eluant."]},{"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":["Comparison of ion chromatography and flow injection analysis methods for monitoring chlorite and chlorate ions in drinking water"]}]}],"canonical_facts":{"dc:contributor.department":["Environmental Sciences and Engineering"],"dc:creator":["Ledder, Tracey"],"dc:date.accessioned":["2014-03-14T21:31:57Z"],"dc:date.available":["2014-03-14T21:31:57Z","2010-03-17"],"dc:date.issued":["1991-12-05"],"dc:description.abstract":["Up-coming regulations on chlorine dioxide in drinking water treatment require low level measurement of chlorite ion (CI0₂-) and chlorate ion (CI0₃-). This research investigated analysis of CI0₂- and CI0₃-; in drinking water by flow injection analysis with iodometric detection (FIA) and ion chromatography with conductivity detection (IC). Both the FIA and IC methods were accurate for the determination of CIO₂-; and CIO₃-; in reagent water. The IC method was accurate in drinking water, however, FIA responded to chloramines and other oxidants present in drinking water causing inaccurate analysis of CIO₂-; and CIO₃-; by FIA. The two IC eluants investigated, a carbonate/bicarbonate mixture and a borate/boric acid mixture, performed well. By taking advantage of the slightly different separation abilities of each eluant, the IC method can be modified to maximize resolution of CIO₂-; and CIO₃-; in different drinking water matrices. Chlorite was unstable in chlorinated drinking water but was stable for up to three days when sodium oxalate was added and stable up to eighteen days when ethylene diamine was added as a preservative. Chlorate was stable in drinking water for up to eighteen days with or without a preservative. The propagation of errors method for determining detection limits yielded limits of detection for CIO₂- (mg/L) of 0.05 for FIA, 0.03 for the IC carbonate eluant and 0.01 for the IC borate eluant. For CIO₃- the limits of detection (mg/L) were 0.24 for FIA; 0.11 for the IC carbonate eluant and 0.02 for the borate eluant."],"dc:description.degree":["Master of Science"],"dc:format.medium":["BTD"],"dc:format.mimetype":["application/pdf"],"dc:identifier.other":["etd-03172010-020312"],"dc:identifier.uri":["http://hdl.handle.net/10919/41675"],"dc:language.iso":["en"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["Comparison of ion chromatography and flow injection analysis methods for monitoring chlorite and chlorate ions in drinking water"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Environmental Sciences and Engineering"],"thesis:degree_level":["masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:20:38Z"}