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  • Cell & Developmental Biology  (89)
  • thermodynamics  (11)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 26 (1997), S. 63-84 
    ISSN: 1572-8927
    Schlagwort(e): Citric acid ; dissociation constants ; thermodynamics ; potentiometry ; ionic strength
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The three molal dissociation quotients for citric acid were measured potentiometrically with a hydrogen-electrode concentration cell from 5 to 150°C in NaCl solutions at ionic strengths of 0.1, 0.3, 0.6, and 1 molal. The molal dissociation quotients and available literature data at infinite dilution were fitted by empirical equations in the all-anionic form involving an extended Debye-Hückel term and up to five adjustable parameters involving functions of temperature and ionic strength. This treatment yielded the following thermodynamic quantities for the first dissociation equilibrium at $$\begin{gathered} 25^ \circ {\text{C: log }}K_{1{\text{a}}} = - 3.127 \pm 0.002{\text{, }}\Delta H_{{\text{la}}}^{\text{o}} = \hfill \\ 4.1 \pm 0.{\text{2 kJ - mol}}^{{\text{ - 1}}} {\text{, }}\Delta S_{{\text{1a}}}^{\text{o}} = - 46.3 \pm 0.{\text{7 J - K}}^{{\text{ - 1}}} - {\text{mol}}^{{\text{ - 1}}} {\text{, and }}\Delta Cp_{{\text{1a}}}^{\text{o}} = - 162 \pm \hfill \\ {\text{7 J - K}}^{{\text{ - 1}}} - {\text{mol}}^{{\text{ - 1}}} ; \hfill \\ \end{gathered} $$ for the second acid dissociation equilibrium at $$\begin{gathered} 25^ \circ {\text{C: log }}K_{{\text{2a}}} = - 4.759 \pm 0.001{\text{, }}\Delta H_{{\text{2a}}}^{\text{o}} = \hfill \\ 2.2 \pm 0.1,{\text{ }}\Delta S_{{\text{2a}}}^{\text{o}} = - 83.8 \pm 0.4{\text{, and }}\Delta Cp_{{\text{2a}}}^{\text{o}} = - 192 \pm 15 \hfill \\ \end{gathered} $$ , and for the third dissociation equilibrium at $$\begin{gathered} 25^ \circ {\text{C: log }}K_{{\text{3a}}} = - 6.397 \pm 0.002{\text{, }}\Delta H_{{\text{3a}}}^{\text{o}} = \hfill \\ - 3.6 \pm 0.2,{\text{ }}\Delta S_{{\text{3a}}}^{\text{o}} = - 134.5 \pm 0.7{\text{, and }}\Delta Cp_{{\text{3a}}}^{\text{o}} = - 231 \pm 7 \hfill \\ \end{gathered} $$ .
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of statistical physics 7 (1973), S. 337-360 
    ISSN: 1572-9613
    Schlagwort(e): Magnetoelastic system ; phase transition ; renormalization of critical exponents ; Ising model ; statistical mechanics ; soluble models ; thermodynamics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract We examine the soluble magnetoelastic Ising model developed by Baker and Essam and give a detailed discussion of its thermodynamic properties. Particular attention is devoted to the properties of the magnetic phase transition at zero field, which is found to be either first order or second order, depending on whether the experiment is performed at negative or positive pressure.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1573-904X
    Schlagwort(e): enantiomers ; ephedrine ; racemic compound ; binary mixture ; conglomerate ; heat of fusion ; thermodynamics ; solubility ; differential scanning calorimetry ; solid-solid reactions
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Physical mixtures (conglomerates) of the two enantiomers of ephedrine base, each containing 0.5% (w/w) of water, were observed to be converted to the 1:1 racemic compound in the solid, liquid, solution, or vapor state. From a geometrically mixed racemic conglomerate of particle size 250–300 µm (50–60 mesh), the formation of the racemic compound follows second-order kinetics (first order with respect to each enantiomer), with a rate constant of 392 mol−1 hr−1 at 22°C. The reaction appears to proceed via the vapor phase as indicated by the growth of the crystals of the racemic compound between diametrically separated crystals of the two enantiomers in a glass petri dish. The observed kinetics of conversion in the solid state are explained by a homogeneous reaction model via the vapor and/or liquid states. Formation of the racemic compound from the crystals of ephedrine enantiomers in the solution state may explain why Schmidt et al. (Pharm. Res. 5:391–395, 1988) observed a consistently lower aqueous solubility of the mixture than of the pure enantiomers. The solid phase in equilibrium with the solution at the end of the experiment was found to be the racemic compound, whose melting point and heat of fusion are higher than those of the enantiomers. An association reaction, of measurable rate, between the opposite enantiomers in a binary mixture in the solid, liquid, solution, or vapor state to form the racemic compound may be more common than is generally realized.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 22 (1993), S. 125-136 
    ISSN: 1572-8927
    Schlagwort(e): Formic acid ; methanoic acid ; dissociation constant ; thermodynamics ; potentiometry ; ionic strength
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The dissociation quotients of formic acid were measured potentiometrically from 25 to 200°C in NaCl solutions at ionic strengths of 0.1, 0.3 1.0, 3.0, and 5.0 mol-kg−1. The experiments were carried out in a concentration cell with hydrogen electrodes. The resulting molal acid dissociation quotients for formic acid, as well as a set of infinite dilution literature values and a calorimetrically-determined enthalpy of reaction, were fitted by an empirical equation involving an extended Debye Hückel term and seven adjustable parameters involving functions of temperature and ionic strength. This regressional analysis yielded the following thermodynamic quantities for 25°C: logK=−3.755±0.002, ΔHo=−0.09±0.15 kJ-mol−1, ΔSo=−72.2±0.5 J-K−1-mol−1, and ΔC p o =−147±4 J-K−1-mol−1. The isocoulombic form of the equilibrium constant is recommended for extrapolation to higher temperatures.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 19 (1990), S. 159-173 
    ISSN: 1572-8927
    Schlagwort(e): Aluminum ; Bis-tris ; dextrose ; solubility ; Raman ; complex ; thermodynamics ; aqueous
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Gibbsite, Al(OH)3, solubility studies in aqueous NaCl solutions at pH 9 demonstrate that the aluminate anion forms a strong complex with the neutral Bis-tris molecule 2,2-Bis(hydroxymethyl)-2,2′,2″-nitrilotriethanol, at low temperatures. The logarithm of the molal concentration quotient for the reaction $$Al(OH)_4^ - + H_2 [Bis - tris] _ \leftarrow ^ \to Al(OH)_2 [Bis - tris]^ - + 2H_2 O$$ in aqueous NaCl solutions at 0.1 molal ionic strength is 2.63±0.03 at 25°C and 2.6±0.1 at 50°C. Raman spectroscopy of NaOH−NaAl(OH)4 solutions at 25°C quantitatively verifies these results and indicates that a complex with symmetrical vibrational frequencies at 498 and 574 cm−1 is stabilized in the presence of excess Bis-tris in these solutions. Gibbsite solubility and Raman spectroscopy also indicate that a similar complexation reaction between the aluminate anion and dextrose occurs, with a molal equilibrium quotient of 100.65 at 25°C, 0.1 molal ionic strength. These complexation reactions are suggested to be equivalent to the wellknown reactions involving the borate anion and polyhydroxyl sugar-like molecules. Experiments with ethylene glycol, glycerol, mannitol and sucrose indicate no significant complexing of these compounds with the aluminate anion.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 20 (1991), S. 905-927 
    ISSN: 1572-8927
    Schlagwort(e): Oxalic acid ; ethanedioic acid ; dissociation constants ; thermodynamics ; potentiometry ; ionic strength
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The first and second molal dissociation quotients of oxalic acid were measured potentiometrically in a concentration cell fitted with hydrogen electrodes. The emf of oxalic acid-bioxalate solutions was measured relative to an HCl standard solution from 25 to 125°C over 25o intervals at nine ionic strengths ranging from 0.1 to 5.0 molal (NaCl). The molal dissociation quotients and available literature data were treated in the all anionic form by a five-term equation that yielded the following thermodynamic quantities at infinite dilution and 25°C: logK1a=−1.277±0.010, ΔH 1a o =−4.1±1.1 kJ-mol−1, ΔS 1a o =38±4 J-K−1-mol−1, and ΔC p,1a o =−168±41 J-K−1-mol−1. Similar measurements of the bioxalate-oxalate system were made at 25o intervals from 0 to 175°C at seven ionic strengths from 0.1 to 5.0m. A similar regression of the experimentally-derived and published equilibrium quotients using a seven-term equation yielded the following values at infinite dilution and 25°C: logK2a=−4.275±0.006, ΔH 2a o =−6.8±0.5 kJ-mol−1, ΔS 2a o =−105±2 J-K−1-mol−1, and ΔC p,2a o =−261±12 J-K−1-mol−1.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 24 (1995), S. 385-407 
    ISSN: 1572-8927
    Schlagwort(e): Benzoic acid ; dissociation constant ; ionization constant ; potentiometry ; ionic strength ; temperature and pressure dependence ; thermodynamics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The dissociation quotient of benzoic acid was determined potentiometrically in a concentration cell fitted with hydrogen electrodes. The hydrogen ion molality of benzoic acid/benzoate solutions was measured relative to a standard aqueous HCl solution at seven temperatures from 5 to 250°C and at seven ionic strengths ranging from 0.1 to 5.0 molal (NaCl). The molal dissociation quotients and selected literature data were fitted in the isocoulombic (all anionic) form by a six-term equation. This treatment yielded the following thermodynamic quantities for the acid dissociation equilibrium at 25°C and 1 bar: logKa=−4.206±0.006, ΔH a o =0.3±0.3 kJ-mol−1, ΔS a o =−79.6±1.0 J-mol−1-K−1, and ΔC p;a o =−207±5 J-mol−1-K−1. A five-term equation derived to describe the dependence of the dissociation constant on solvent density is accurate to 250°C and 200 MPa.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 26 (1997), S. 63-84 
    ISSN: 1572-8927
    Schlagwort(e): Citric acid ; dissociation constants ; thermodynamics ; potentiometry ; ionic strength
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The three molal dissociation quotients for citric acid were measured potentiometrically with a hydrogen-electrode concentration cell from 5 to 150°C in NaCl solutions at ionic strengths of 0.1, 0.3, 0.6, and 1 molal. The molal dissociation quotients and available literature data at infinite dilution were fitted by empirical equations in the all-anionic form involving an extended Debye-Hückel term and up to five adjustable parameters involving functions of temperature and ionic strength. This treatment yielded the following thermodynamic quantitites for the first dissociation equilibrium at 25°C: logK 1a=−3.127±0.002, ΔH 1a o =4.1±0.2 kJ-mol−1, ΔS 1a o =−46.3±0.7 J-K−1-mol−1, and ΔCp 1a o =−162±7 J-K−1-mol−1; for the second acid dissociation equilibrium at 25°C: logK 2a =−4.759±0.001, ΔH 2a o =2.2±0.1, ΔS 2a o =−83.8±0.4, and ΔCp 2a o =−192±15, and for the third dissociation equilibrium at 25°C: logK 3a=−6.397±0.002, ΔH 3a o =−3.6±0.2, ΔS 3a o =−134.5±0.7, and ΔCp 3a o =−231±7.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 21 (1992), S. 883-900 
    ISSN: 1572-8927
    Schlagwort(e): Malonic acid ; propanedioic acid ; dissociation constants ; thermodynamics ; potentiometry ; ionic strength
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The first and second molal dissociation quotients of malonic acid were measured potentiometrically in a concentration cell fitted with hydrogen electrodes. The hydrogen ion molality of malonic acid/bimalonate solutions was measured relative to a standard aqueous HCl solution from 0 to 100°C over 25° intervals at five ionic strengths ranging from 0.1 to 5.0 molal (NaCl). The molal dissociation quotients and available literature data were treated in the all anionic form by a seven-term equation. This treatment yielded the following thermodynamic quantities for the first acid dissociation equilibrium at 25°C: logK 1a =-2.852±0.003, ΔH 1a /o =0.1±0.3 kJ-mol−1, ΔS 1a o =−54.4±1.0 J-mol−1-K−1, and ΔC p,1a o =−185±20 J-mol−1-K−1. Measurements of the bimalonate/malonate system were made over the same intervals of temperature and ionic strength. A similar regression of the present and previously published equilibrium quotients using a seven-term equation yielded the following values for the second acid dissociation equilibrium at 25°C: logK2a=−5.697±0.001, ΔH 2a o =−5.13±0.11 kJ-mol−1, ΔS 2a o =−126.3±0.4 J-mol−1-K−1, and ΔC p,2a o =−250+10 J-mol−1-K−1.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 18 (1989), S. 545-559 
    ISSN: 1572-8927
    Schlagwort(e): 2,2-Bis(hydroxymethyl)-2,2′,2″-nitrilotriethanol ; equilibrium constant ; thermodynamics ; buffer ; association ; salt effect ; temperature dependence
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The ionic strength and temperature dependencies of the molal acid association quotients of 2,2-Bis(hydroxymethyl)-2,2′,2″-nitrilotriethanol (also abbreviated as bis-tris) were determined potentiometrically in a concentration cell fitted with hydrogen electrodes. The emf was recorded for equimolal bis-tris/bis- trisHCl buffer solutions from 5 to 125°C at approximately 25°C intervals, and at nine ionic strengths from 0.05 to 5.0m (NaCl). The molal association quotients, combined with infinite dilution values from the literature, are described precisely by a seven parameter equation which yielded the following thermodynamic quantities at infinite dilution and 25°C: logK=6.481±0.003, ΔH o =−28.5±0.2 kJ-mol −1 , ΔS o =28.5±0.8 J-K −1 -mol −1 , and ΔC P o =−22±5 J-K −1 -mol −1 . The equation incorporates a simple three term expression for logK, but requires four terms to describe the rather complex ionic strength dependence despite the reaction being isocoulombic. The molal association quotients from this study and the literature were also subjected to the Pitzer ion interaction treatment.
    Materialart: Digitale Medien
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