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  • Pitzer model  (3)
  • Solid-phase extraction  (3)
  • 42.75
  • Computational Chemistry and Molecular Modeling
  • Inorganic Chemistry
  • Springer  (6)
  • 1995-1999  (6)
  • 1960-1964
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Keywords
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Pitzer Parameters for the Pertechnetate Ion in the System Na+/K+/Mg2+/Ca2+/Cl−/SO 2 4 −/TcO − 4 /H2O at 25°C (1998)
    Springer
    Journal of solution chemistry 27 (1998), S. 107-120 
    Details
    ISSN: 1572-8927
    Keywords: Sodium pertechnetate ; magnesium pertechnetate ; potassium pertechnetate ; osmotic coefficients ; activity coefficients ; solubility ; seawater system ; Pitzer model ; binary parameters ; mixing parameters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Isopiestic vapor pressure experiments are performed at 25°C with aqueous Mg(TcO4)2 solutions and with ternary mixtures containing various combinations of NaTcO4, Mg(TcO4)2, NaCl, MgCl2, Na2SO4, and MgSO4. The osmotic coefficients of the binary solutions are used to evaluate the binary Pitzer parameters β(0), β(1), and CΦ for Mg(TcO4)2. We previously reported these parameters for NaTcO4. The binary parameters for KTcO4 and Ca(TcO4)2 are evaluated from solubilities of KTcO4 in KCl and CaCl2 solutions, respectively. The mixing parameters Θ TcO 4 − /Cl −, ΨM/TcO 4 − /Cl −, Θ TcO 4 − /SO 4 2− , ΨM/TcO 4 − /SO 4 2− , and ΨNa + /Mg 2+ /TcO4 2− are calculated from either osmotic coefficients or solubilities in the corresponding ternary mixtures. The evaluated set of Pitzer parameters predicts well the activity coefficients and solubilities of KTcO4 in multicomponent systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1022625605743
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  • 2
    Electronic Resource
    Electronic Resource
    Thermodynamics of Cm(III) in Concentrated Salt Solutions: Carbonate Complexation in NaCl Solution at 25°C (1999)
    Springer
    Journal of solution chemistry 28 (1999), S. 447-462 
    Details
    ISSN: 1572-8927
    Keywords: Trivalent actinides ; curium ; americium ; solution thermodynamics ; carbonate complexation ; ionic strength ; Pitzer model ; concentrated solutions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The carbonate complexation reactions of Cm(III) were studied by time-resolved laser fluorescence spectroscopy in 0–6 m NaCl at 25°C. The ionic strength dependence of the stepwise formation constants for the carbonato complexes Cm(CO3) n 3−2n with n = 1, 2, 3, and 4 is described by modeling the activity coefficients of the Cm(III) species with Pitzer's ion-interaction approach. Based on the present results and literature data for Cm(III) and Am (III), the mean carbonate complexation constants at I = 0 are calculated to be: log β 101 o =8.1 ±0.3, log β 102 o =13.0 ± 0.6, log β 103 o =15.2 ± 0.4, and log β 104 o =13.0 ± 0.5. Combining these equilibrium constants at infinite dilution and the evaluated set of Pitzer parameters, a model is obtained, that reliably predicts the thermodynamics of bivalent actinide An(III) carbonate complexation in dilute to concentrated NaCl solution.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1022664013648
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  • 3
    Electronic Resource
    Electronic Resource
    Data correlation in on-line solid-phase extraction-gas chromatography-atomic emission/mass spectrometric detection of unknown microcontaminants (1998)
    Springer
    Chromatographia 48 (1998), S. 273-283 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Atomic emission and MS detection ; Solid-phase extraction ; Aqueous samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A procedure is described for the (non-target) screening of hetero-atom-containing compounds in tap and waste water by correlating data obtained by gas chromatography (GC) using atomic emission (AED) and mass selective (MS) detection. Solid-phase extraction (SPE) was coupled on-line to both GC systems to enable the determination of microcontaminants at the 0.02–1 μg L−1 level in 7–50 mL of aqueous sample. The screening was limited to compounds present in at least one heteroatom-selective GC-AED trace above a predetermined concentration level. These compounds were identified by their partial formulae (AED) and the corresponding mass spectra, which were obtained from the GC-MS chromatogram via the retention index concept. The potential of the approach was demonstrated by the identification of target compounds as well as all unknowns present in tap and waste water above the predetermined threshold of 0.05 μg L−1 (tap water) or 0.5 μg L−1 (waste water).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467683
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  • 4
    Electronic Resource
    Electronic Resource
    On-line coupling of solid-phase extraction and gas chromatography with atomic emission detection for analysis of trace pollutants in aqueous samples (1995)
    Springer
    Chromatographia 40 (1995), S. 119-124 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Atomic emission detection ; Aqueous samples ; Solid-phase extraction ; Organophosphorus pesticides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An on-line, solid-phase extraction gas chromatography atomic-emission detection (SPE-GC-AED) system has been set up using an on-column interface to transfer 100 μl of desorbing solvent to the GC part of the system. Analytical characteristics such as recovery, precision and linearity of calibration plots were comparable with those of the off-line combination of SPE-GC-AED using organophosphorus pesticides as test compounds. The fully on-line set-up causes a marked improvement in detection because of the quantitative transfer of the analytes from the SPE module to the GC: detection limits are as low as 5–20 ng l−1 for the analysis of 10 ml raw and spiked surface water samples using the phosphorus channel. Detection levels can be further enhanced by processing up to 100 ml samples. The integrated analytical system is robust. The potential of the on-line set up has been demonstrated for the analysis of surface water and waste water.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02272157
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  • 5
    Electronic Resource
    Electronic Resource
    The ion product of H2O, dissociation constants of H2CO3 and pitzer parameters in the system Na+/H+/OH−/HCO 3 − /CO 3 2- /ClO 4 − /H2O at 25°C (1996)
    Springer
    Journal of solution chemistry 25 (1996), S. 327-343 
    Details
    ISSN: 1572-8927
    Keywords: Ion product of water ; carbonic acid ; dissociation constants ; NaClO4 solution ; iomic strength ; activity coefficients ; Pitzer model ; mixing parameters ; solution thermodynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The ion product of water and the dissociation constants of carbonic acid have been determined in 0.1, 1.0, 3.0, and 5.0M NaClO4 at 25°C. The ion product of water K w ' has been evaluated by emf measurements with a combined glass electrode in NaClO4 solutions containing 0.001–0.1M HCLO4 or NaOH. The product K H ' K l ' K 2 ' of the Henry constant for CO2 and the dissociation constants for H2CO3 have been determined by titration of carbonate solutions equilibrated with pCO2 =10−3.52 atm, and K 2 ' has been evaluated by potentiometric titration and by measuring the H+ concentration at fixed HCO 3 − and CO 3 2- concentrations. The ion interaction (Pitzer) equations are applied to describe the constants K w ' , K 2 ' and K H ' H 1 ' K 2 ' as a function of the NaClO4 concentration. The experimental data are used to evaluate the mixing parametersΘ i/ClO 4 andΨ i/ClO 4 -/Na+ fori = OH -,HCO 3 - andCO 3 2-
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00972890
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  • 6
    Electronic Resource
    Electronic Resource
    On-line solid-phase extraction-gas chromatography-ion trap tandem mass spectrometric detection for the nanogram per liter analysis of trace pollutants in aqueous samples (1997)
    Springer
    Chromatographia 44 (1997), S. 372-380 
    Details
    ISSN: 1612-1112
    Keywords: Solid-phase extraction ; Gas chromatography ; Ion trap tandem mass spectrometry ; Water samples ; Environmental analysis ; Pesticides ; Bromide ; Nitrite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary On-line solid-phase extraction-gas chromatographyion-trap tandem mass spectrometry (SPE-GC-MS/MS) has been used for the trace-level determination of polar and apolar pesticides. The SPE-GC interface, an Autoloop 2000, was operated at an injection temperature of 90°C which permitted the determination of thermolabile pesticides such as carbofuran and carbaryl. Rectilinear calibration curves were obtained for the analytes tested over a range of 0.1–500 ng L−1, using a sample volume of 10–100 mL for enrichment on an SPE cartridge packed with styrene-divinylbenzene copolymer. The detection limits for the pesticides were in the 0.01–4 ng L−1 range. For a number of pesticides acceptable tandem mass spectra were obtained at levels as low as 0.1 ng L−1 level in real-life water samples. As a demonstration of the applicability of this technique for inorganic anions, bromide and nitrite were converted into 4-bromoacetanilide and 2-phenylphenol, respectively. The reaction products were pooled and subjected to simultaneous analysis by the present method using full-scan mass spectrometric detection. The detection limits were 0.3 and 2 ng L−1, respectively.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02466313
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