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  • Polymer and Materials Science  (17)
  • Biochemistry and Biotechnology  (5)
  • Engineering General  (4)
  • Pitzer model  (3)
  • thermal diffusivity  (3)
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  • 1
    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
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  • 2
    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
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  • 3
    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
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 17 (1996), S. 695-703 
    ISSN: 1572-9567
    Keywords: AC calorimetry ; CVD diamond film ; Debye phonon model ; grain boundary ; thermal conductivity ; thermal diffusivity ; U-process
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Diamond films 60 and 170 µm in thickness were grown by PACVD (plasma-assisted chemical vapor deposition) under similar conditions. The thermal diffusivity of these freestanding films was measured between 100 and 300 K using AC calorimetry. Radiation heat loss from the surface was estimated by analyzing both the amplitude and the phase shift of a lock-in amplifier signal. Thermal conductivity was calculated using the specific heat data of natural diamond. At room temperature, the thermal conductivity of the 60 and 170 υm films is 9 and 16 W-cm−1. K−1 respectively, which is 40–70% that of natural diamond, The temperature dependence of thermal conductivity of the CVD diamond films is similar to that of natural diamond, Phonon scattering processes are considered using the Debye model, The microsize of the grain boundary has a significant effect on the mean free path of phonons at low temperatures. The grain in CVD diamond film is grown as a columnar structure, Thus, the thicker film has the larger mean grain size and the higher thermal conductivity. Scanning electron microscopy (SEM) and Raman spectroscopy were used to study the microstructure of the CVD diamond films. In this experiment, we evaluated the quality of CVD diamond film of the whole sample by measuring the thermal conductivity.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 19 (1998), S. 281-290 
    ISSN: 1572-9567
    Keywords: GaAs ; impurities ; phonons ; photothermal displacement technique ; semiconductors ; Si ; thermal conductivity ; thermal diffusivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Thermal conductivity and thermal diffusivity of Si and GaAs wafers were measured using the photothermal displacement technique, and the temperature dependence of these two quantities was investigated. Thermal diffusivity was obtained from the phase difference between the heating source and the signal, and thermal conductivity was determined from the maximum value of the signal amplitude in the temperature range 80 to 300 K. It was verified that an increase in doping concentration gives rise to a decrease in thermal conductivity at low temperatures. The experimental results obtained on samples with different types and doping concentrations are consistent with those expected from theoretical considerations.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-9567
    Keywords: antireflection coating ; parameter estimation ; photoacoustic effect ; thermal diffusivity ; through-plane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract In this study, we designed and developed two-layer antireflection (AR) optical coating samples on glass substrates, using different evaporation conditions of coating rates and substrate temperatures for two dielectric materials, MgF2 and ZnS, with different refractive indices. The through-plane thermal diffusivity of these systems was measured using the photoacoustic effect. The optical thicknesses of MgF2 and ZnS layers were fixed at 5λ/4 (λ=514.5 nm) and λ, respectively, and the thermal diffusivities of the samples were obtained from the measured amplitude of the photoacoustic signals by changing the chopping frequency of the Ar+ laser beam. The results demonstrated that the thermal diffusivity of the sample fabricated under the conditions of 10μÅ·s−1 and 150°C had the maximum value and that the results were directly related to the microstructure of the film system.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Composite reverse osmosis membranes of ionically crosslinked poly(acrylic acid) (PAA) have been prepared. The process consists of coating a porous polysulfone membrane with a thin layer of dilute solution of PAA, drying the thin liquid layer, and ionically crosslinking the PAA in solutions of different salts. The influence of some important preparation parameters on the properties of these membranes was investigated. It was found that all these membranes possessed ion exchange properties and could be ion exchanged; some of them have been found to be suitable for the desalination of low concentration salt solutions. By comparison to cellulose acetate (CA) membranes, higher rejection of phenols may be an interesting property of these membranes.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 4017-4027 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The synthesis of sulfonated poly(phenylene oxide) polymer was investigated. The poly(phenylene oxide) was synthesized through oxidative coupling from 2,6-dimethyl-phenol with copper (I) chloride-pyridine catalyst and sulfonated using chlorosulfonic acid. The effects of catalyst concentration, solvent, and other experimental variables on the kinetics of the polymerization of poly(phenylene oxide) and its subsequent sulfonation are reported in detail.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 2117-2131 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Sulfonated polystyrene latex particles were used as acid catalysts in the continuous inversion of sucrose at 50-70°C. The particles (surface charge 168 μeq/g) were confined in a stirred reactor with a semipermeable membrane; sucrose solution was pumped in, and product solution was pumped out. The catalytic activity of the particles was unchanged after 20 days continuous use. Variation of particle size (0.13 and 0.42 μm) and stirring rate showed that internal and external mass transfer was not a controlling factor. The kinetics were pseudo-first-order; the rate constant at 70°C was 2.30/N min as compared with 0.07/N min for macroporous sulfonated ion-exchange resin; the apparent activation energy was 111 kJ/mol as compared with 121 kJ/mol for the homogeneous acid-catalyzed reaction. The faster rate was attributed to the very great surface area, high charge density, and lack of internal diffusional resistance of the latex particles. The proposed mechanism comprised adsorption of sucrose on the particle surface, followed by inversion and desorption of product.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3187-3199 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previous attempts to prepare monodisperse styrene/sodium styrene sulfonate copolymer latexes by batch, seeded, and semicontinuous emulsion polymerization were unsuccessful at high concentrations of the functional comonomer. Broad, and sometimes bimodal, size distributions, and large amounts of water soluble homopolymer were obtained. After removal of free monomer, solute and adsorbed homopolymer and copolymer, the overall incorporation of the functional comonomer was found to be low. To overcome these problems, a two stage “shot-growth” or in situ seeding technique was developed. A first stage copolymerization was carried out with a low concentration of sodium styrene sulfonate: the purpose of the functional comonomer was to enhance the stability and regulate the size of the seed particles. When this reaction had reached high conversion (〉 90%), a second stage monomer mixture was added. The ratio of styrene to sodium styrene sulfonate in this mixture determined the final surface charge density. The mechanism by which the NaSS is incorporated in the polymer particles is considered to be by solution copolymerization with solute styrene monomer to form surface active oligoradicals. These radicals adsorb on the particle surface, initiate polymerization and become inextricably bound, preventing their transfer back to the aqueous phase. By this means, it was possible to vary independently the particle size and surface charge density. High concentrations of functional comonomer could be polymerized without undue wastage (incorporations were only slightly less than 100%) or loss of monodispersity. In extreme cases, the area per functional group fell below the theoretical minimum, indicating considerable hydration of the surface layers.
    Additional Material: 6 Ill.
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