Thin Layer Coulometry with Ionophore Based Ion-Selective Membranes

被引:71
作者
Grygolowicz-Pawlak, Ewa [1 ]
Bakker, Eric [1 ]
机构
[1] Curtin Univ Technol, Nanochem Res Inst, Dept Chem, Perth, WA 6845, Australia
基金
美国国家卫生研究院; 澳大利亚研究理事会;
关键词
LIQUID-MEMBRANE; BULK OPTODES; SENSORS; ELECTRODES; INTERFACE; POTENTIOMETRY; ELECTROLYSIS; TITRATIONS; VIEW; LEAD;
D O I
10.1021/ac100524z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We are demonstrating here for the first time a thin layer coulometric detection mode for ionophore based liquid ion-selective membranes. Coulometry promises to achieve the design of robust, calibration free sensors that are especially attractive for applications where recalibration in situ is difficult or undesirable. This readout principle is here achieved with porous polypropylene tubing doped with the membrane material and which contains a chlorinated silver wire in the inner compartment, together with the fluidically delivered sample solution. The membrane material consists of the lipophilic plasticizer dodecyl 2-nitrophenyl ether, the lipophilic electrolyte ETH 500, and the calcium ionophore ETH 5234. Importantly and in contrast to earlier work on voltammetric liquid membrane electrodes, the membrane also contains a cation-exchanger salt, KTFPB. This renders the membrane permselective and allows one to observe open circuit potentiometric responses for the device, which is confirmed to follow the expected Nernstian equation. Moreover, as the same cationic species is now potential determining at both interfaces of the membrane, it is possible to use rapidly diffusing and/or thin membrane systems where transport processes at the inner and outer interface of the membrane do not perturb each other or the overall composition of the membrane. The tubing is immersed in an electrolyte solution where the counter and working electrode are placed, and the potentials are applied relative to the measured open circuit potentials. Exhaustive current decays are observed in the range of 10 to 100 mu M calcium chloride. The observed charge, calculated as integrated currents, is linearly dependent on concentration and forms the basis for the coulometric readout of ion-selective membrane electrodes.
引用
收藏
页码:4537 / 4542
页数:6
相关论文
共 33 条
  • [1] NEUTRAL CARRIER BASED ION-SELECTIVE ELECTRODE FOR THE DETERMINATION OF TOTAL CALCIUM IN BLOOD-SERUM
    ANKER, P
    WIELAND, E
    AMMANN, D
    DOHNER, RE
    ASPER, R
    SIMON, W
    [J]. ANALYTICAL CHEMISTRY, 1981, 53 (13) : 1970 - 1974
  • [2] How do pulsed amperometric ion sensors work? A simple PDE model
    Bakker, E
    Meir, AJ
    [J]. SIAM REVIEW, 2003, 45 (02) : 327 - 344
  • [3] Carrier-based ion-selective electrodes and bulk optodes. 1. General characteristics
    Bakker, E
    Buhlmann, P
    Pretsch, E
    [J]. CHEMICAL REVIEWS, 1997, 97 (08) : 3083 - 3132
  • [4] Bakker E., 2007, ANGEW CHEM INT EDIT, V46, P2
  • [5] Beyond potentiometry: Robust electrochemical ion sensor concepts in view of remote chemical sensing
    Bakker, Eric
    Bhakthavatsalam, Vishnupriya
    Gemene, Kebede L.
    [J]. TALANTA, 2008, 75 (03) : 629 - 635
  • [6] BARD AJ, 1966, ANAL CHEM, V38, pR88
  • [7] Selective coulometric release of ions from ion selective polymeric membranes for calibration-free titrations
    Bhakthavatsalam, Vishnupriya
    Shvarev, Alexey
    Bakker, Eric
    [J]. ANALYST, 2006, 131 (08) : 895 - 900
  • [8] Carrier-based ion-selective electrodes and bulk optodes. 2. Ionophores for potentiometric and optical sensors
    Buhlmann, P
    Pretsch, E
    Bakker, E
    [J]. CHEMICAL REVIEWS, 1998, 98 (04) : 1593 - 1687
  • [9] GEHRIG P, 1989, CHIMIA, V43, P377
  • [10] Direct sensing of total acidity by chronopotentiometric flash titrations at polymer membrane ion-selective electrodes
    Gemene, Kebede L.
    Bakker, Eric
    [J]. ANALYTICAL CHEMISTRY, 2008, 80 (10) : 3743 - 3750