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  • Chemistry  (24)
  • hydrothermal solutions  (6)
  • Analytical Chemistry and Spectroscopy  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 18 (1989), S. 1133-1152 
    ISSN: 1572-8927
    Keywords: Nickel oxide ; aqueous solutions ; metal ion hydrolysis ; phosphato-complexing ; equilibrium constant ; thermodynamics ; dehydration ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined, flowing autoclave facility was used to investigate the solubility/phase behavior of nickel oxide (NiO) in aqueous sodium phosphate solutions between 290 and 560 K. A layer of hydrous nickel oxide was concluded to exist on the nickel oxide surface below 468 K; only at higher temperatures did the anhydrous nickel oxide phase control the nickel ion solubility behavior. The measured solubility behavior was examined via a nickel(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reaction equilibria were obtained from a least-squares analysis of the data. The existence of two new nickel ion complexes are reported for the first time: Ni(OH)2(HPO4)= and Ni(OH)3(H2PO4)=. The positive entropy change associated with the formation of Ni(OH)3(H2PO4)= leads to its dominance in alkaline phosphate solutions at elevated temperatures.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 21 (1992), S. 1153-1176 
    ISSN: 1572-8927
    Keywords: Zinc oxide ; aqueous solutions ; metal ion hydrolysis ; phosphato-complexing ; equilibrium constant ; thermodynamics ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined, flowing autoclave facility is used to investigate the solubility/phase behavior of zinc(II) oxide in aqueous sodium phosphate solutions at temperatures between 17 and 287°C. ZnO solubilities are observed to increase continuously with temperature and phosphate concentration. At higher phosphate concentrations, a solid phase transformation to NaZnPO4 is observed. NaZnPO4 solubilities are retrograde with temperature. The measured solubility behavior is examined via a Zn(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reaction equilibria are obtained from a least-squares analysis of the data. The existence of two new zinc(II) ion complexes, Zn(OH)2(HPO4)2− and Zn(OH)3(H2PO4)2−, is reported for the first time. A summary of thermochemical properties for species in the systems ZnO−H2O and ZnO−Na2O−P2O5−H2O is also provided.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 21 (1992), S. 179-200 
    ISSN: 1572-8927
    Keywords: Copper oxide ; aqueous solutions ; metal ion hydrolysis ; phosphato complexing ; equilibrium constant ; thermodynamics ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined, flowing autoclave facility is used to investigate the solubility behavior of copper(II) oxide (CuO) in aqueous sodium phosphate solutions at temperatures between 19 and 262°C. Copper solubilities are observed to increase continuously with temperature and phosphate concentration. The measured solubility behavior is examined via a Cu(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reactions are obtained from a leastsquares analysis of the data. Altogether, thermochemical properties are established for five anionic complexes: Cu(OH) 3 − , Cu(OH) 4 2− , Cu(OH) 2 (HPO 4 ) 2− , Cu(OH) 3 (H 2 PO 4 ) 2− , and Cu(OH) 2 (PO 4 ) 3− . Precise thermochemical parameters are also derived for the Cu(OH)+ hydroxocomplex based on CuO solubility behavior previously observed (Ref. 3) for pure water at elevated temperatures. The relative ease of Cu(II) ion hydrolysis is such that Cu(OH) 3 − species become the preferred hydroxocomplex for pH≥9.4.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 24 (1995), S. 837-877 
    ISSN: 1572-8927
    Keywords: Magnetite ; iron oxide ; ferrous and ferric ion hydrolysis ; phosphatocomplexing ; equilibrium constant ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined flowing autocláve facility was used to investigate the solubility behavior of magnetite (Fe3O4) in alkaline sodium phosphate and ammonium hydroxide solutions between 21 and 288°C. Measured iron solubilities were interpreted via a Fe(II)/Fe(III) ion hydroxo-, phosphato-, and ammino-complexing model and thermodynamic functions for these equilibria were obtained from a least-squares analysis of the data. A total of 14 iron ion species were fitted. Complexing equilibria are reported for 8 new species: Fe(OH)(HPO4)−, Fe(OH)2(HPO4)2−, Fe(OH)3(HPO4)2−, Fe(OH)(NH3)+, Fe(OH)2(PO4)3−, Fe(OH)4(HPO4)3−, Fe(OH)2(H2PO4)−, and Fe(OH)3(H2PO4)3−. At elevated temperatures, hydrolysis and phosphato complexing tended to stabilize Fe(III) relative to Fe(II), as evidenced by free energy changes fitted to the oxidation reactions. $$\begin{gathered} Fe(OH)_3^ - + H_2 O_ \leftarrow ^ \to Fe(OH)_4^ - + (1/2)H_2 (g) \hfill \\ Fe(OH)_2^{} (HPO_4 )^{2 - } + H_2 O_ \leftarrow ^ \to Fe(OH)_3 (HPO_4 )^{2 - } + (1/2)H_2 (g) \hfill \\ \end{gathered}$$ For temperatures below 83°C and for a dissolved hydrogen concentration of 234 μmol-kg−1, the activity of ferrous iron in aqueous solution is controlled by a hydrous Fe(II) oxide solid phase rather than magnetite.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 27 (1998), S. 33-66 
    ISSN: 1572-8927
    Keywords: Chromium(III) oxide ; eskolaite ; chromium(III) oxide hydroxide ; chromium(III) hydroxide dehydration ; ferrous chromite ; aqueous solutions ; chromium(III) ion hydrolysis ; phosphatocomplexing ; equilibrium constant ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined, flowing autoclave facility is used to investigate the solubility behavior of Cr2O3 and FeCr2O4 in alkaline sodium phosphate, sodium hydroxide, and ammonium hydroxide solutions between 21 and 288°C. Baseline Cr(III) ion solubilities were found to be on the order of 0.1 nmolal, which were enhanced by the formation of anionic hydroxo and phosphato complexes. At temperatures below 51°C, the activity of Cr(III) ions in aqueous solution is controlled by a Cr(OH)3·3H2O solid phase rather than Cr2O3; above 51°C the saturating solid phase is γ-CrOOH. Measured chromium solubilities were interpreted via a Cr(III) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reaction equilibria were obtained from least-squares analyses of the data. The existence of four new Cr(III) ion complexes is reported: Cr(OH)3(H2PO4)−, Cr(OH)3(HPO4)2−, Cr(OH)3(PO4)3−, and Cr(OH)4(HPO4)-(H2PO4)4−. The last species is the dominant Cr(III) ion complex in concentrated, alkaline phosphate solutions at elevated temperatures.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 22 (1993), S. 601-623 
    ISSN: 1572-8927
    Keywords: Titatium(IV) oxide ; rutile ; aqueous solutions ; metal ion hydrolysis ; phosphatocomplexing ; equilibrium constant ; thermodynamics ; pressurized water ; hydrothermal solutions ; corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A platinum-lined, flowing autoclave facility was used to investigate the solubility behavior of titanium dioxide (TiO2) in aqueous sodium phosphate, sodium hydroxide and ammonium hydroxide solutions between 17 and 288°. Baseline Ti(IV) solubilities were found to be on the order of one nanomolal, which were enhanced by the formation of anionic hydroxo- and phosphato-complexes. The measured solubility behavior was examined via a titanium(IV) ion hydrolysis/complexing reaction equilibria were obtained from a least squares analysis of the data. The existence of three new Ti(IV) ion complexes is reported for the first time: Ti(OH)4(HPO4)2−, Ti(OH)5(H2PO4)2− and Ti(OH)5(HPO4)3−. The triply-charged anionic complex was the dominant Ti(IV) species in concentrated, alkaline phosphate solutions at elevated temperatures. This complex is expected to exhibit C.N.=4 (i.e., Ti(OH)2OPO 4 3− ). A summary of thermochemical properties for species in the systems TiO2-H2O and TiO2-P2O5-H2O is also provided.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 1435-1450 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissociation of beef liver and bacterial (Micrococcus lysodeikticus) catalases by the action of sodium n-dodecyl sulfate (SDS) has been investigated as a function of SDS concetration and time by ultracentrifugation. The rate of dissociation of beef liver catalase is found to be much faster than that for bacterial catalase in 25 mM SDS at pH 7.0. Beef liver catalase is dissociated into its four subunits after 24 h, whereas bacterial catalase is not completely dissociated after 36 days of incubation. The binding of SDS to beef liver catalase obeys a Hill equation with a cooperativity exponent of 2.0 and a binding constant of 440. The initial interaction of SDS with beef liver catalase can be detected by microcalorimetry, whereas the mixing of SDS with bacterial catalase is athermal. Bacterial catalase retains enzymic activity in the presence of SDS, whereas beef liver catalase is completely deactivated at SDS concentrations above 5 mM. Beef liver catalase is more sensitive to acid denaturation than bacterial catalase, and the rate of dissociation for both catalases is sixth-order in proton concentration. Comparison of the amino acid analysis of the two catalases shows that bacterial catalase has a smaller number of lysyl residues and a larger number of glutamyl residues than beef liver catalase. Taken together these structural differences could lead to a reduced affinity of bacterial catalase for the binding of SDS as observed.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 3-16 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: We investigated the effect of concentration on the Brownian diffusion of uncharged rigid spheres. Monosize silica spheres were prepared according to the method of Stöber (1968). The particles were sterically stabilized by chemisorption of stearic alcohol at their surface by the method developed by van Helden (1981).Particle radius was 14.5 nm from electron micrographs of the coated particles. Osmotic pressure measurements of the sterically stabilized particles dispersed in cyclohexane showed that the particles behaved as hard spheres. The measurements agreed well with predictions from the Carnahan-Starling equation over the concentration range 0.0458 〈 φ 〈 0.37 where φ is the volume fraction of the particles in the suspension. Viscosity measurements of silica dispersions were made over the concentration range 0 〈 φ 〈 0.25. The relative viscosity over the range 0 〈 φ 〈 0.2 was fitted by ηr = 1 + 2.4φ + 7.1φ2. The coefficients 2.4 and 7.1 in this equation are in good agreement with the theoretical values of 2.5 and 6.2 obtained by Einstein(1906) and Batchelor(1977), respectively. The Brownian diffusion coefficient of the particles dispersed in cyclohexane was measured over the concentration range 0.0055 〈 φ 〈 0.248 using Taylor's hydrodynamic stability method. A laser fiber-optic system was used to measure the transient concentration profile along the capillary as indicated by a fluorescent dye. This technique offers the advantage of being direct and nonintrusive. The experimental diffusivity data were found to be well described by the generalized Stokes-Einstein equation(Batchelor, 1976) over the entire concentration range studied.
    Additional Material: 12 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 34 (1988), S. 2059-2062 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 1555-1557 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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