{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/106143"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/106143","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"Development of a dye sensitized photochemical reduction process for the degradation of polychlorinated biphenyls","abstract":"A method has been developed that can photoreduce polychlorinated biphenyl (PCB) to biphenyl with great speed and efficiency as well as at relatively low cost. This process uses visible light, generated by ordinary incandescent light bulbs, which is absorbed by a common dye sensitizer. The dye molecules, when excited by the absorption of light, can promote a chemical reaction between polychlorinated biphenyls and a hydrocarbon gas such as propane. In this chemical reaction, hydrogen is abstracted from the hydrocarbon gas molecule and is substituted for chlorine on the PCB molecule in a stepwise fashion, which ultimately yields the major reaction product biphenyl. This reaction occurs in a polar aprotic solvent at room temperature and is accelerated by the presence of an alkali metal hydroxide. The final residence of the chlorine appears to be a salt which precipitates from the reaction mixture. This procedure could be applied to the treatment of PCB contaminated transformer oils, soils, and landfill leachates.","abstract_html":"A method has been developed that can photoreduce polychlorinated biphenyl (PCB) to biphenyl with great speed and efficiency as well as at relatively low cost. This process uses visible light, generated by ordinary incandescent light bulbs, which is absorbed by a common dye sensitizer. The dye molecules, when excited by the absorption of light, can promote a chemical reaction between polychlorinated biphenyls and a hydrocarbon gas such as propane. In this chemical reaction, hydrogen is abstracted from the hydrocarbon gas molecule and is substituted for chlorine on the PCB molecule in a stepwise fashion, which ultimately yields the major reaction product biphenyl. This reaction occurs in a polar aprotic solvent at room temperature and is accelerated by the presence of an alkali metal hydroxide. The final residence of the chlorine appears to be a salt which precipitates from the reaction mixture. This procedure could be applied to the treatment of PCB contaminated transformer oils, soils, and landfill leachates.","abstract_has_math":false,"creators":["Stallard, Michael L."],"institution":"Virginia Polytechnic Institute and State University","degree_name":"M.S.","degree_level":"masters","degree_discipline":"Environmental Engineering","degree_department":"Environmental Engineering","school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1986,"date_issued":"1986","date_published":"1986","updated_at":"2026-07-22T22:20:12Z","subjects":[],"languages":["en"],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10919/106143","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":["Stallard, Michael L."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2021-10-26T20:10:18Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2021-10-26T20:10:18Z"]},{"key":"dc:date.issued","label":"Date","values":["1986"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Polytechnic Institute and State University"]},{"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 Engineering"]},{"key":"thesis:degree_level","label":"Degree Level","values":["masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"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.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/106143"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["A method has been developed that can photoreduce polychlorinated biphenyl (PCB) to biphenyl with great speed and efficiency as well as at relatively low cost. This process uses visible light, generated by ordinary incandescent light bulbs, which is absorbed by a common dye sensitizer. The dye molecules, when excited by the absorption of light, can promote a chemical reaction between polychlorinated biphenyls and a hydrocarbon gas such as propane. In this chemical reaction, hydrogen is abstracted from the hydrocarbon gas molecule and is substituted for chlorine on the PCB molecule in a stepwise fashion, which ultimately yields the major reaction product biphenyl. This reaction occurs in a polar aprotic solvent at room temperature and is accelerated by the presence of an alkali metal hydroxide. The final residence of the chlorine appears to be a salt which precipitates from the reaction mixture. This procedure could be applied to the treatment of PCB contaminated transformer oils, soils, and landfill leachates."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["M.S."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Development of a dye sensitized photochemical reduction process for the degradation of polychlorinated biphenyls"]}]}],"canonical_facts":{"dc:contributor.department":["Environmental Engineering"],"dc:creator":["Stallard, Michael L."],"dc:date.accessioned":["2021-10-26T20:10:18Z"],"dc:date.available":["2021-10-26T20:10:18Z"],"dc:date.issued":["1986"],"dc:description.abstract":["A method has been developed that can photoreduce polychlorinated biphenyl (PCB) to biphenyl with great speed and efficiency as well as at relatively low cost. This process uses visible light, generated by ordinary incandescent light bulbs, which is absorbed by a common dye sensitizer. The dye molecules, when excited by the absorption of light, can promote a chemical reaction between polychlorinated biphenyls and a hydrocarbon gas such as propane. In this chemical reaction, hydrogen is abstracted from the hydrocarbon gas molecule and is substituted for chlorine on the PCB molecule in a stepwise fashion, which ultimately yields the major reaction product biphenyl. This reaction occurs in a polar aprotic solvent at room temperature and is accelerated by the presence of an alkali metal hydroxide. The final residence of the chlorine appears to be a salt which precipitates from the reaction mixture. This procedure could be applied to the treatment of PCB contaminated transformer oils, soils, and landfill leachates."],"dc:description.degree":["M.S."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["http://hdl.handle.net/10919/106143"],"dc:language.iso":["en"],"dc:publisher":["Virginia Polytechnic Institute and State University"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:title":["Development of a dye sensitized photochemical reduction process for the degradation of polychlorinated biphenyls"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Environmental Engineering"],"thesis:degree_level":["masters"],"thesis:degree_name":["M.S."],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:20:12Z"}