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dc.contributor.authorChung, Po-Wenen_US
dc.contributor.authorCharmot, Alexandreen_US
dc.contributor.authorClick, Timothyen_US
dc.contributor.authorLin, Yuchunen_US
dc.contributor.authorBae, YounJueen_US
dc.contributor.authorChu, Jhih-Weien_US
dc.contributor.authorKatz, Alexanderen_US
dc.date.accessioned2015-12-02T02:59:19Z-
dc.date.available2015-12-02T02:59:19Z-
dc.date.issued2015-07-07en_US
dc.identifier.issn0743-7463en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.langmuir.5b01115en_US
dc.identifier.urihttp://hdl.handle.net/11536/128044-
dc.description.abstractTo better understand the adsorption of long-chain poly(1 -> 4)beta-D-glucans on carbon surfaces as well as interactions responsible for this adsorption, we use a comparative study involving mesoporous carbon silica composite materials that have been etched to varying degrees and all-atom molecular dynamics simulations. The materials synthesized as part of this etching study consist of an as-synthesized composite material (MCN-MSN), MCN-MSN-0.5 (composite materials consisting of 50% carbon by mass), MCN-MSN-0.3 (composite materials consisting of 70% carbon by mass), and MCN, in which silica etching was conducted using an aqueous ethanolic solution of either NaOH or HF. Data for the adsorption of long-chain glucans to these materials from concentrated aqueous HCl (37 wt %) solution demonstrate a direct relationship between the amount of beta-glu adsorption and the magnitude of exposed carbon mesopore surface area, which systematically increases and is also accompanied by an increase in the mesopore size during silica etching. This demonstrates beta-glu adsorption as occurring on internal carbon mesopores rather than exclusively on the external carbon surface. These experimental data on adsorption were corroborated by molecular dynamics (MD) simulations of beta-glu adsorption to a graphene bilayer separated by a distance of 3.2 nm, chosen to correspond to the carbon mesopore diameter of the experimental system. Simulation results using a variety of beta-glu solvent systems demonstrate the rapid adsorption of a beta-glu strand on the graphitic carbon surface via axial coupling and are consistent with experimentally observed trends in fast adsorption kinetics. Solvent-mediated effects such as small-scale hydrophobicity and preferential interactions with ions are shown to play important roles in modulating glucan adsorption to carbon surfaces, whereas experimental data on hydrophobically modified silica demonstrate that hydrophobicity in and of itself is insufficient to cause beta-glu adsorption from concentrated aqueous HCl solution.en_US
dc.language.isoen_USen_US
dc.titleImportance of Internal Porosity for Glucan Adsorption in Mesoporous Carbon Materialsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.langmuir.5b01115en_US
dc.identifier.journalLANGMUIRen_US
dc.citation.volume31en_US
dc.citation.issue26en_US
dc.citation.spage7288en_US
dc.citation.epage7295en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000357839200015en_US
dc.citation.woscount1en_US
Appears in Collections:Articles