File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Abatement of toluene in the plasma-driven catalysis: Mechanism and reaction kinetics

TitleAbatement of toluene in the plasma-driven catalysis: Mechanism and reaction kinetics
Authors
KeywordsMechanism
nonthermal plasma (NTP)
ozone catalytic decomposition
plasma-driven catalysis (PDC)
reaction kinetics
Issue Date2011
PublisherIEEE.
Citation
IEEE Transactions on Plasma Science, 2011, v. 39 n. 3, p. 877-882 How to Cite?
AbstractThe mechanism and reaction kinetics of toluene destruction in a plasma-driven catalysis (PDC) system were studied. The results show that the toluene removal efficiency (TRE) is greatly increased while the level of O 3 by-product is significantly reduced in PDC as compared with that in nonthermal plasma (NTP). The rate constant of toluene destruction in the PDC is more than twice than that in NTP. Among the multiple reactive species responsible for toluene destruction in the PDC, hydroxyl radicals (̇OH) had a small contribution, whereas energetic electrons and atomic oxygen (O) were the most important. The enhanced performance of toluene destruction by PDC was mainly due to greater amounts of O formed during the process. The catalysts improved toluene destruction by catalytic decomposition of O 3 and generation of O. Essentially, better toluene abatement can be achieved by focusing on the increased energy density and improved performance of the catalyst for O 3 decomposition. © 2006 IEEE.
Persistent Identifierhttp://hdl.handle.net/10722/134426
ISSN
2021 Impact Factor: 1.368
2020 SCImago Journal Rankings: 0.460
ISI Accession Number ID
Funding AgencyGrant Number
National Key High Technology Research and Development Program of China2006AA06A310
CRCG of The University of Hong Kong200907176159
Funding Information:

Manuscript received November 12, 2010; revised December 25, 2010; accepted December 25, 2010. Date of publication February 4, 2011; date of current version March 9, 2011. This work was supported in part by the National Key High Technology Research and Development Program of China under Grant 2006AA06A310 and in part by the CRCG of The University of Hong Kong under Grant 200907176159.

References
Grants

 

DC FieldValueLanguage
dc.contributor.authorHuang, Hen_HK
dc.contributor.authorYe, Den_HK
dc.contributor.authorLeung, DYCen_HK
dc.date.accessioned2011-06-17T09:20:15Z-
dc.date.available2011-06-17T09:20:15Z-
dc.date.issued2011en_HK
dc.identifier.citationIEEE Transactions on Plasma Science, 2011, v. 39 n. 3, p. 877-882en_HK
dc.identifier.issn0093-3813en_HK
dc.identifier.urihttp://hdl.handle.net/10722/134426-
dc.description.abstractThe mechanism and reaction kinetics of toluene destruction in a plasma-driven catalysis (PDC) system were studied. The results show that the toluene removal efficiency (TRE) is greatly increased while the level of O 3 by-product is significantly reduced in PDC as compared with that in nonthermal plasma (NTP). The rate constant of toluene destruction in the PDC is more than twice than that in NTP. Among the multiple reactive species responsible for toluene destruction in the PDC, hydroxyl radicals (̇OH) had a small contribution, whereas energetic electrons and atomic oxygen (O) were the most important. The enhanced performance of toluene destruction by PDC was mainly due to greater amounts of O formed during the process. The catalysts improved toluene destruction by catalytic decomposition of O 3 and generation of O. Essentially, better toluene abatement can be achieved by focusing on the increased energy density and improved performance of the catalyst for O 3 decomposition. © 2006 IEEE.en_HK
dc.languageengen_US
dc.publisherIEEE.en_US
dc.relation.ispartofIEEE Transactions on Plasma Scienceen_HK
dc.subjectMechanismen_HK
dc.subjectnonthermal plasma (NTP)en_HK
dc.subjectozone catalytic decompositionen_HK
dc.subjectplasma-driven catalysis (PDC)en_HK
dc.subjectreaction kineticsen_HK
dc.titleAbatement of toluene in the plasma-driven catalysis: Mechanism and reaction kineticsen_HK
dc.typeArticleen_HK
dc.identifier.emailLeung, DYC:ycleung@hku.hken_HK
dc.identifier.authorityLeung, DYC=rp00149en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1109/TPS.2010.2103403en_HK
dc.identifier.scopuseid_2-s2.0-79952622787en_HK
dc.identifier.hkuros185853en_US
dc.identifier.hkuros200075-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-79952622787&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume39en_HK
dc.identifier.issue3en_HK
dc.identifier.spage877en_HK
dc.identifier.epage882en_HK
dc.identifier.isiWOS:000289484600010-
dc.publisher.placeUnited Statesen_HK
dc.relation.projectDestruction of multiple indoor air pollutants using photocatalysis irradiated by ozone-producing UV lamp-
dc.identifier.scopusauthoridHuang, H=24080074500en_HK
dc.identifier.scopusauthoridYe, D=7102368962en_HK
dc.identifier.scopusauthoridLeung, DYC=7203002484en_HK
dc.identifier.issnl0093-3813-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats