期刊
TALANTA
卷 80, 期 5, 页码 1964-1969出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2009.10.055
关键词
pH; Optode; 6,8-Dihydroxypyrene-1,3-disulfonic acid; DHPDS; Photoacidity; Fluorescence ratio
资金
- Swedish Research Council (VR)
- Foundation for Strategic Environmental Research (MISTRA)
- Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS)
This study presents a high-performance ratiometnc pH optode based on the fluorophore 6,8-dihydroxypyrene-1,3-disulfonic acid (DHPDS). The two pH-sensitive terminal hydroxy groups of DHPDS facilitated dual excitation/dual emission (F(1): lambda(1,ex) 420 nm, lambda(1,em) = 462 nm: F(2): lambda(2,ex) = 470 nm, lambda(2,em) = 498 nm) properties for ratiometric (R(F1,F2) = F(1)/F(2)) normalization of sensor signal. The sensor demonstrated an exponentially decreasing ratiometric response with increasing pH, with a linear correlation (R(2) = 0.9936) between (10)log(R(F1,F2)) and pH within the pH interval 6-9. Precision determined as the IUPAC pooled standard deviation for the pH values 6.00, 7.01 and 9.01, was 0.0057 pH units for the fluorosensor and 0.0054 for a commercially available pH electrode used for comparison. Between the end-points of calibration at pH 7.01, the precision of the sensor was 0.0037 pH units Effects from changes in ionic strength (I(tot), 10-700 mM) were more pronounced for the electrode, with a linear (R(2) = 0.9976) increase in response (delta E/delta pH) with increasing I(tot). The DHPDS-based fluorosensor, however, retained sensitivity (delta(10)log(R(F1,F2))/delta pH = 0.8024 +/- 0.0145), though with an overall increase in ratiometnc signal with increasing I(tot). The preserved sensitivity despite changes in ionic strength was possibly a consequence from the dual photo-acidic properties of DHPDS Analytical characteristics of immobilized DHPDS therefore not only facilitated high-performance measurements over a wide pH range, but also opened for straightforward simultaneous measurements of pH and ionic strength (C) 2009 Elsevier B.V. All rights reserved
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