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dc.contributor.authorLi, Ziyien_US
dc.contributor.authorLiu, Yingshuen_US
dc.contributor.authorYang, Xiongen_US
dc.contributor.authorXing, Yien_US
dc.contributor.authorTsa, Chuenjinnen_US
dc.contributor.authorWang, Zhanyingen_US
dc.contributor.authorYang, Quanen_US
dc.contributor.authorYang, Ralph T.en_US
dc.date.accessioned2017-04-21T06:55:38Z-
dc.date.available2017-04-21T06:55:38Z-
dc.date.issued2016-02-10en_US
dc.identifier.issn0888-5885en_US
dc.identifier.urihttp://hdl.handle.net/11536/132719-
dc.description.abstractThe desorption performances of naphthalene and pyrene on mesoporous MCM-41, SBA-15, and CMK-3 sorbents are studied on the basis of temperature-programmed desorption experiments over the temperature range of 350-800 K at different heating rates. The kinetic parameters for each sorbate sorbent pair are determined with combined model-fitting methods. The data for naphthalene and pyrene are best fitted with the same kinetic models on MCM-41 (with 1D mesopore channels), in contrast to those on SBA-15 and CMK-3, which have micropore mesopore structures, leading to different desorption mechanisms for these two sorbates. SBA-15 with interconnectivity between adjacent mesopores not only shows high sorption capacities but also offers diffusion advantages in desorption, which contributes to the order of the degree of ease in desorption: SBA-15 > MCM-41 > CMK-3. CMK-3, with higher microporosity and hydrophobicity, shows stronger binding with the adsorbates while still benefiting in pyrene desorption from the consecutive mesoporosity.en_US
dc.language.isoen_USen_US
dc.titleDesorption of Polycyclic Aromatic Hydrocarbons on Mesoporous Sorbents: Thermogravimetric Experiments and Kinetics Studyen_US
dc.identifier.journalINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCHen_US
dc.citation.volume55en_US
dc.citation.issue5en_US
dc.citation.spage1183en_US
dc.citation.epage1191en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000370212000004en_US
Appears in Collections:Articles