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  • 1
    ISSN: 1572-8927
    Schlagwort(e): Electrochemical thermodynamics ; standard emfs ; standard potentials ; activity coefficients ; nonaqueous solvents ; mixed solvents ; aqueous-organic solvent mixtures ; hydration numbers ; amalgam electrode
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The electromotive force of the amalgam cell {NaxHg1-x‖NaCl(m)‖AgCl‖Ag} has been measured at 25°C as a function of the mole fraction x of Na in amalgams and of the molality m of NaCl in (ethylene glycol + water), (acetonitrile + water), and (1,4-dioxane + water) mixed solvents, containing up to 0.8 mass fraction of the organic component, with relative permittivities ε ≥ 27. The relevant standard molal electromotive forces $$E_{\text{m}}^ \circ $$ have been determined, together with the mean molal activity coefficient γ± of NaCl as a function of its molality. In the case of (ethylene glycol + water) mixtures, a linear dependence of $$E_{\text{m}}^ \circ $$ on the mass fraction of ethylene glycol is observed, which is quite unusual, The Debye-Hückel equation is applicable successfully over the whole range of molalities explored, which extends to the vicinity of the solubility limit of NaCl in each solvent. The dependence of the standard emf on the logarithm of the volume fraction of water in the aqueous-organic solvent mixtures have been analyzed in terms of Feakins and French's theory, leading to a primary hydration number 7.2 for NaCl, in good agreement with previous results employing different methods.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 27 (1998), S. 1-16 
    ISSN: 1572-8927
    Schlagwort(e): Transference cells ; transference numbers ; salt bridges ; mixed solvents
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Electromotive forces (emf) were measured in the transference cells: Ag∣AgCl∣- Nacl (m2) in Z∥ NaCl (m1) in Z∣AgCl∣Ag and NaxHg1-x∣NaCl (m1) in Z∥ NaCl (m2) in Z∣NaxHg1-x (where NaxHg1-x denotes a flowing Na–amalgam electrode and Z an aqueous-organic solvent mixture) at various molalities m 2 〉 m1 of NaCl in Z = (ethylene glycol + water), (acetonitrile + water) and (1,4-dioxane + water), with mass fractions of the organic components ≤0.8. The transference number of Na+ in (ethylene glycol + water) and (1,4-dioxane + water) varies little with respect to that in pure water medium, whereas in (acetonitrile + water) it increases remarkably with increasing proportion of acetonitrile so as to approach equitransference, behavior similar to that previously found in (methanol + water) and in (ethanol + water). At acetonitrile mass fraction 0.6 NaCl is sufficiently close to equitransference to emerge as a useful salt bridge, nearly at the same level as the popular aqueous KCl.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 28 (1999), S. 1329-1340 
    ISSN: 1572-8927
    Schlagwort(e): Transference cells ; transference numbers ; salt bridges ; mixed solvents
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The electromotive forces (emf) E A and E C of the following concentration cells with transference: $${\text{Ag}}\left| {{\text{AgCl}}} \right|{\text{KCl (}}m_2 {\text{)}}\left\| {{\text{KCl(}}m_1 {\text{)}}\left| {{\text{AgCl}}} \right|{\text{Ag and K}}_{\text{x}} {\text{Hg}}_{{\text{1}} - {\text{x}}} |{\text{KCl(}}m_1 {\text{)}}} \right\|{\text{KCl(}}m_2 {\text{)|K}}_{\text{x}} {\text{Hg}}_{{\text{1}} - {\text{x}}} ,$$ respectively, together with the emfs E MAX of the corresponding double cell without transference: $${\text{K}}_{\text{x}} {\text{Hg}}_{{\text{1}} - {\text{x}}} \left| {{\text{KCl(}}m_1 {\text{)}}} \right|{\text{AgCl}}\left| {{\text{Ag}} - {\text{Ag}}} \right|{\text{AgCl}}\left| {{\text{KCl(}}m_2 {\text{)}}} \right|{\text{K}}_{\text{x}} {\text{Hg}}_{{\text{1}} - {\text{x}}} $$ have been measured at KCl molalities m (m 1 fixed and m 2 varied, with m 2〉m 1) approximately up to the KCl solubility limit in 12 solvent mixtures for the three aqueous–organic solvent systems (ethylene glycol+water), (acetonitrile + water), and (1,4-dioxane + water) up to 0.8 mass fraction of organic component. For all the cases explored, the E A vs. E MAX relation is linear over the whole KCl molality range. The ionic transference numbers t of KCl determined therefrom show a curvilinear dependence on the mass fraction of the organic component of the relevant solvent mixture and are found to fall in the range 0.52–0.48, viz., within ±4% of exact equitransference (t + = t − = 0.5). In particular, KCl becomes exactly equitransferent (i.e., an ideal salt bridge) in aqueous mixtures with the following mass fractions of organic component: 0.4 ethylene glycol and 0.09 acetonitrile, as well as 0.12 methanol, and 0.08 and 0.34 ethanol from our recent work. Even if use of KCl as a salt bridge would be somewhat restricted by its limited solubility in high mass fractions of dioxane and acetonitrile and pending extension of investigation to other mixed-solvent systems, the above figures characterize KCl as a fairly good “intersolvental” salt bridge in electrochemistry, electroanalysis, and corrosion science.
    Materialart: Digitale Medien
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