{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/84104"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/84104","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Environmental Applications of Ultrasound","abstract":"As previously reported, molybdenum carbonyl and tungsten carbonyl were decomposed sonochemically in hexadecane to form porous aggregates of 2--3 nm high surface area Mo2C and W2C particles. The activity of these materials was studied for the catalytic hydrodehalogenation of aliphatic and aromatic halocarbons at low temperatures (T = 200--300°C). Both catalysts were selective, active, and stable for all substrates tested. The HDH of substrates bearing aliphatic C-Cl bonds occurs faster than those with aryl C-Cl bonds. Characterization of post catalytic materials with x-ray diffraction and x-ray photoelectron spectroscopy revealed no change in the bulk structure of the catalyst and chlorination of the surface metal species, respectively.","abstract_html":"As previously reported, molybdenum carbonyl and tungsten carbonyl were decomposed sonochemically in hexadecane to form porous aggregates of 2--3 nm high surface area Mo2C and W2C particles. The activity of these materials was studied for the catalytic hydrodehalogenation of aliphatic and aromatic halocarbons at low temperatures (T = 200--300°C). Both catalysts were selective, active, and stable for all substrates tested. The HDH of substrates bearing aliphatic C-Cl bonds occurs faster than those with aryl C-Cl bonds. Characterization of post catalytic materials with x-ray diffraction and x-ray photoelectron spectroscopy revealed no change in the bulk structure of the catalyst and chlorination of the surface metal species, respectively.","abstract_has_math":false,"creators":["Oxley, James Dean"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Kenneth S. Suslick"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2003,"date_issued":"2003","date_published":"2003","updated_at":"2026-07-22T22:26:22Z","subjects":["Physics, Fluid and Plasma"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(MiAaPQ)AAI3086152"],"render_values":[{"text":"(MiAaPQ)AAI3086152","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/84104","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Kenneth S. 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The activity of these materials was studied for the catalytic hydrodehalogenation of aliphatic and aromatic halocarbons at low temperatures (T = 200--300°C). Both catalysts were selective, active, and stable for all substrates tested. The HDH of substrates bearing aliphatic C-Cl bonds occurs faster than those with aryl C-Cl bonds. Characterization of post catalytic materials with x-ray diffraction and x-ray photoelectron spectroscopy revealed no change in the bulk structure of the catalyst and chlorination of the surface metal species, respectively.","Made available in DSpace on 2015-09-25T22:12:56Z (GMT). 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The activity of these materials was studied for the catalytic hydrodehalogenation of aliphatic and aromatic halocarbons at low temperatures (T = 200--300°C). Both catalysts were selective, active, and stable for all substrates tested. The HDH of substrates bearing aliphatic C-Cl bonds occurs faster than those with aryl C-Cl bonds. Characterization of post catalytic materials with x-ray diffraction and x-ray photoelectron spectroscopy revealed no change in the bulk structure of the catalyst and chlorination of the surface metal species, respectively.","Made available in DSpace on 2015-09-25T22:12:56Z (GMT). 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