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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004008naa a2200433 4500
001oai:DiVA.org:umu-223557
003SwePub
008240419s1992 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-2235572 URI
024a https://doi.org/10.1016/0167-2738(92)90288-z2 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Albinsson, I.u Department of Physics, Chalmers University of Technology, Gothenburg, Sweden4 aut
2451 0a Ion association effects and ionic conduction in polyalkalene modified polydimethylsiloxanes
264 1b Elsevier,c 1992
338 a print2 rdacarrier
500 a Conference proceedings published in the journal Solid State Ionics, volumes 53-56 (1992) but also as a monograph (Solid State Ionics -91) by North-Holland, Amsterdam (1992).
520 a Poly (ethylene oxide) and poly (propylene oxide) modified poly (dimethyl siloxane) (PDMS) have been complexed with LiCF3SO3, NaCF3SO3 and KCF3SO3. In order to study ion association in these systems, the nondegenerate symmetric stretch (A1, SO3) Raman modes have been studied as a function of temperature at several different salt concentrations. Ionic conductivity has also been measured. For the poly (ethylene oxide) modified PDMS (PEO-PDMS), ether oxygen to metal ratios ranged from 12500:1 to 9:1. Changing the cation from Li+ to Na+ to K+ increases the conductivity of the complex. Plots of the molar conductivity versus salt concentration show that the characteristic shape and the region of increase in the molar conductivity is influenced most by the fraction of “free” ions which increases with increasing salt concentration. Charged triplets and contact ion-pairs are also present at the higher salt concentrations; the number of triplets increases with concentration and temperature. Non-VTF behaviour is observed. For the poly (propylene oxide) modified PDMS (PPO-PDMS) (with excess PPO), phase separation is observed when these triflate salts are complexed in. These solutions above and below the boundary layer have been studied by Raman spectroscopy revealing that the upper region is siloxane rich. The formation of the boundary layer is attributed to an increasing difference in surface tension between the PPO/salt/PPO-PDMS complexes and the separate PPO, PPO-PDMS components. The boundary layer moves up with increase in salt concentration. There is evidence of “free” ions, contact-ion pairs, triplets and aggregates. Values of conductivity of 2.2×10−6 and 1.6×10−5 S/cm are quoted for 293 K and 8 mol% LiCF3SO3 in respectively PPO-PDMS/PPO and PEO-PDMS/PEO. Both are better conductors than the corresponding 8 mol% PPG4000/LiCF3SO3 complex.
650 7a NATURVETENSKAPx Fysikx Den kondenserade materiens fysik0 (SwePub)103042 hsv//swe
650 7a NATURAL SCIENCESx Physical Sciencesx Condensed Matter Physics0 (SwePub)103042 hsv//eng
653 a Raman scattering
653 a ionic conductivity
653 a poly(dimethyl siloxane)
653 a poly(ethylene oxide)
653 a poly(propylene oxide)
653 a LiCF3SO3
653 a NaCF3SO3
653 a KCF3SO3
653 a alkali triflate salts
700a Jacobsson, Peru Department of Physics, Chalmers University of Technology, Gothenburg, Sweden4 aut
700a Mellander, Bengt-Eriku Department of Physics, Chalmers University of Technology, Gothenburg, Sweden4 aut
700a Stevens, James R.u Department of Physics, Chalmers University of Technology, Gothenburg, Sweden4 aut
710a Department of Physics, Chalmers University of Technology, Gothenburg, Sweden4 org
773t Solid State Ionicsd : Elsevierg 53-56:Part 2, s. 1044-1053q 53-56:Part 2<1044-1053x 0167-2738x 1872-7689
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-223557
8564 8u https://doi.org/10.1016/0167-2738(92)90288-z

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