期刊
ANALYTICAL SCIENCES
卷 24, 期 10, 页码 1315-1320出版社
JAPAN SOC ANALYTICAL CHEMISTRY
DOI: 10.2116/analsci.24.1315
关键词
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资金
- Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [14205120, 15655008, 16750060]
- Grants-in-Aid for Scientific Research [16750060, 15655008, 14205120] Funding Source: KAKEN
The phase-boundary potential at the interface between an aqueous KC] solution (W) and a hydrophobic room-temperature ionic liquid (RTIL), trioctylmethylammonium bis(nonafluorobutylsulfonyl)imide ([TOMA(+)][C4C4N-]), containing dicyclohexano-18-crown-6 (DCH18C6), shows the nernstian response to K+ in W within a polarized potential window of 500mV between [TOMA(+)][C4C4N-] and W, demonstrating that hydrophobic RTILs can be used as a nonvolatile ionic medium for liquid-membrane ion-selective electrodes. The complex formation constant of K+ with DCH18C6 in [TOMA(+)][C4C4N-] is estimated to be on the order of 10(9) from the upper detection limit using a partition equilibrium model in the presence of a neutral ionophore. The response time of the phase-boundary potential is similar to 20 min. Gelled [TOMA(+)][C4C4N-] also shows the nernstian response to K+, although the upper limit is lower probably due to a change in the solvent properties from the non-gelled [TOMA(+)][C4C4N-]. The response time of the gelled [TOMA(+)][C4C4N-] is similar to 5 min, shorter than that of the non-gelled [TOMA(+)][C4C4N-].
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