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dc.contributor.author이영무-
dc.date.accessioned2018-03-10T01:53:30Z-
dc.date.available2018-03-10T01:53:30Z-
dc.date.issued2013-10-
dc.identifier.citationMACROMOLECULES, 2013, 46(19), P.7797-7804en_US
dc.identifier.issn0024-9297-
dc.identifier.issn1520-5835-
dc.identifier.urihttp://pubs.acs.org/doi/abs/10.1021/ma400889t-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/44563-
dc.description.abstractOrdered morphologies in disulfonated poly(arylene sulfide sulfone nitrile) (SPSN) copolymers were generated via thermal annealing followed by multiblock copolymer synthesis. While SPSN random copolymers (R-SPSN) showed featureless morphologies, the SPSN multiblock copolymers (B-SPSN) exhibited cocontinuous lamellar morphologies with a center-to-center interdomain size of up to 40 nm. In spite of the well-ordered, interconnected hydrophilic domains, the water self-diffusion coefficient (e.g., D = (0.7-2.0) x 10(-10) m(2) s(-1)) and proton conductivity (e.g., sigma = 0.16-0.20 S cm(-1) in deionized water at 30 degrees C) through B-SPSN were lower than those of the corresponding R-SPSN (e.g., D = (3.5-3.9) x 10(-10) m(2) s(-1) and sigma = 0.21 S cm(-1)) due to the relatively lower water uptake of the B-SPSN after thermal annealing. The reduced water uptake of B-SPSN was beneficial to reduction of peroxide degradation rate. Thermal annealing produced significant gains in morphological ordering and finer control over desired membrane properties for proton conduction applications.en_US
dc.description.sponsorshipThis work was supported by the New & Renewable Energy R&D program (2008-N-FC12-J-01-2-100), Nano-Material Technology Development program (2012M3A7B4049745) of the National Research Foundation, Ministry of Science and Technology of Korea. This material is based upon work supported by the US National Science Foundation under Awards CHE 1057797 and DMR 0844933. We acknowledge the Advanced Photon Source supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract W-31-109-Eng-38, for access to the beamtime SID-D, operated by DND-CAT. The DND-CAT is supported by the E.I. DuPont de Nemours & Co., The Dow Chemical Company, the U.S. National Science Foundation through Grant DMR-9304725, and the State of Illinois through the Department of Commerce and the Board of Higher Education Grant IBHE HECA NWU 96. The diode beam stops were constructed at DuPont by Robert F. Knox and Mark G. Bradigan under J. David Londono's direction.en_US
dc.language.isoenen_US
dc.publisherACS AMERICAN CHEMICAL SOCIETYen_US
dc.subjectPOLYMER ELECTROLYTE MEMBRANESen_US
dc.subjectFUEL-CELL APPLICATIONSen_US
dc.subjectETHER SULFONE)Sen_US
dc.subjectMEDIUM-TEMPERATUREen_US
dc.subjectWATER-RETENTIONen_US
dc.subjectACID GROUPSen_US
dc.subjectCONDUCTIVITYen_US
dc.subjectNAPHTHALENEen_US
dc.subjectTRANSPORTen_US
dc.subjectHUMIDITYen_US
dc.titleSulfonated Poly(arylene sulfide sulfone nitrile) Multiblock Copolymers with Ordered Morphology for Proton Exchange Membranesen_US
dc.typeArticleen_US
dc.relation.no19-
dc.relation.volume46-
dc.identifier.doi10.1021/ma400889t-
dc.relation.page7797-7804-
dc.relation.journalMACROMOLECULES-
dc.contributor.googleauthorShin, Dong Won-
dc.contributor.googleauthorLee, So Young-
dc.contributor.googleauthorLee, Chang Hyun-
dc.contributor.googleauthorLee, Kwan-Soo-
dc.contributor.googleauthorPark, Chi Hoon-
dc.contributor.googleauthorMcGrath, James E.-
dc.contributor.googleauthorZhang, Mingqiang-
dc.contributor.googleauthorMoore, Robert B.-
dc.contributor.googleauthorLingwood, Mark D.-
dc.contributor.googleauthorLee, Young Moo-
dc.relation.code2013011181-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF ENERGY ENGINEERING-
dc.identifier.pidymlee-
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > ENERGY ENGINEERING(에너지공학과) > Articles
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