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New adsorbents for purification: Selective removal of aromatics

dc.contributor.authorTakahashi, Akiraen_US
dc.contributor.authorYang, Ralph T.en_US
dc.date.accessioned2006-04-19T13:24:47Z
dc.date.available2006-04-19T13:24:47Z
dc.date.issued2002-07en_US
dc.identifier.citationTakahashi, Akira; Yang, Ralph T. (2002)."New adsorbents for purification: Selective removal of aromatics." AIChE Journal 48(7): 1457-1468. <http://hdl.handle.net/2027.42/34245>en_US
dc.identifier.issn0001-1541en_US
dc.identifier.issn1547-5905en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34245
dc.description.abstractAdsorption of benzene and cyclohexane on various Y-zeolites was investigated to develop sorbents for the purification of aliphatics by removal of aromatics. Ag-Y showed superior benzene/cyclohexane selectivities to Na-Y, Pd-Y, and H-USY. Separation factors greater than 10 5 were obtained with Ag-Y at low concentrations of benzene. High selectivities were achieved by the strong interaction between benzene and Ag-Y, while the interaction with cyclohexane was not influenced by the cations. Molecular orbital calculation revealed that benzene formed a classic Π-complexation bond with Ag-Y: donation of electron charges from the p-orbitals of benzene to the vacant s-orbital of the silver (Σ donation) and, simultaneously, back donation of electron charges from d-orbitals of silver to Π*-orbital of benzene (d–Π* back donation). Grand canonical Monte Carlo simulations were also performed for adsorption isotherms. Potential parameters of benzene on Ag-Y, including Π-complexation, were developed first. Simulation and experiments of GCMC agreed excellently for adsorption of benzene on Y-zeolites.en_US
dc.format.extent252428 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherChemical Engineeringen_US
dc.titleNew adsorbents for purification: Selective removal of aromaticsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDept. of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109en_US
dc.contributor.affiliationumDept. of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109 ; Dept. of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34245/1/690480710_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/aic.690480710en_US
dc.identifier.sourceAIChE Journalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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