Co-ion interference for ion selective electrodes based on charged and neutral ionophores:: A comparison

被引:73
作者
Bühlmann, P [1 ]
Amemiya, S [1 ]
Yajima, S [1 ]
Umezawa, Y [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
关键词
D O I
10.1021/ac9805145
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Interferences from co-ions, i.e., ions with a charge sign opposite to that of the measured ion, limit the upper detection limit of ion-selective electrodes (ISEs) based on electrically neutral or charged ionophores. A theoretical description based on phase boundary equilibria is used here to predict the co-ion interference (Donnan failure) of both types of ISEs quantitatively and to compare the extent of co-ion interference in these two cases. It is shown that, for practically relevant ionophore-site ratios, Donnan failure for ISEs based on electrically charged and neutral ionophore occurs at very similar co-ion concentrations if the charged and the neutral ionophores form complexes of equal stabilities and stoichiometries. With the exception of the selective complexation of the primary ion and charged ionophores, association of two or more ions such as between ionic sites and complexes has only a limited effect on co-ion interference. If relevant at all, ion pairing is predicted to affect upper detection limits more unfavorably in the case of neutral than in the case of charged ionophore-based ISEs. Experimental determination of co-ion interference for ISEs with five different charged and two electrically neutral H+ ionophores shows that co-ion interference increases as the stability of the H+ complexes increases and confirms that co-ion interferences for charged and neutral ionophore-based ISEs indeed occur to an equal extent if their H+ complexes have the same stabilities. These results corroborate the high potentiality of charged ionophore-based ISEs.
引用
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页码:4291 / 4303
页数:13
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共 66 条
[1]   Hydrogen bond based recognition of nucleotides by neutral-carrier ion-selective electrodes [J].
Amemiya, S ;
Buhlmann, P ;
Tohda, K ;
Umezawa, Y .
ANALYTICA CHIMICA ACTA, 1997, 341 (2-3) :129-139
[2]   A phase boundary potential model for apparently "twice-Nernstian" responses of liquid membrane ion-selective electrodes [J].
Amemiya, S ;
Bühlmann, P ;
Umezawa, Y .
ANALYTICAL CHEMISTRY, 1998, 70 (03) :445-454
[3]   Hydrogen bond based recognition of nucleotides by neutral-carrier ion-selective electrodes (vol 341, pg 129, 1997) [J].
Amemiya, S ;
Buhlmann, P ;
Tohda, K ;
Umezawa, Y .
ANALYTICA CHIMICA ACTA, 1997, 351 (1-3) :407-407
[4]   STUDY OF CALCIUM-ION SELECTIVE ELECTRODES CONTAINING SIMON IONOPHORES USING IMPEDANCE METHODS - BULK PROPERTIES [J].
ARMSTRONG, RD ;
TODD, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 257 (1-2) :161-166
[5]   MOBILITY OF NA+ IN PVC MEMBRANES CONTAINING VALINOMYCIN AND DI-BENZO-18-CROWN-6 [J].
ARMSTRONG, RD ;
ASHASSISORKHABI, H .
ELECTROCHIMICA ACTA, 1987, 32 (01) :135-137
[6]   IONIC MOBILITIES IN PVC MEMBRANES [J].
ARMSTRONG, RD ;
TODD, M .
ELECTROCHIMICA ACTA, 1987, 32 (01) :155-157
[7]   SELECTIVITY OF POLYMER MEMBRANE-BASED ION-SELECTIVE ELECTRODES - SELF-CONSISTENT MODEL DESCRIBING THE POTENTIOMETRIC RESPONSE IN MIXED ION SOLUTIONS OF DIFFERENT CHARGE [J].
BAKKER, E ;
MERUVA, RK ;
PRETSCH, E ;
MEYERHOFF, ME .
ANALYTICAL CHEMISTRY, 1994, 66 (19) :3021-3030
[8]   OPTIMUM COMPOSITION OF NEUTRAL CARRIER BASED PH ELECTRODES [J].
BAKKER, E ;
XU, AP ;
PRETSCH, E .
ANALYTICA CHIMICA ACTA, 1994, 295 (03) :253-262
[9]   APPLICABILITY OF THE PHASE-BOUNDARY POTENTIAL MODEL TO THE MECHANISTIC UNDERSTANDING OF SOLVENT POLYMERIC MEMBRANE-BASED ION-SELECTIVE ELECTRODES [J].
BAKKER, E ;
NAGELE, M ;
SCHALLER, U ;
PRETSCH, E .
ELECTROANALYSIS, 1995, 7 (09) :817-822
[10]   SYNTHESIS AND CHARACTERIZATION OF NEUTRAL HYDROGEN ION-SELECTIVE CHROMOIONOPHORES FOR USE IN BULK OPTODES [J].
BAKKER, E ;
LERCHI, M ;
ROSATZIN, T ;
RUSTERHOLZ, B ;
SIMON, W .
ANALYTICA CHIMICA ACTA, 1993, 278 (02) :211-225