Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1572-8927
    Keywords: Transference cells ; transference numbers ; salt bridges ; mixed solvents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 28 (1999), S. 1329-1340 
    ISSN: 1572-8927
    Keywords: Transference cells ; transference numbers ; salt bridges ; mixed solvents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1572-8927
    Keywords: pH standards ; aqueous—organic solvents ; medium effects ; ionization constants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Determination of primary standards for pH measurements in glycerol + water solventmixtures has been carried out based on reversible emf measurements of the cellPt|H2|KHPh (m PS) + KCl (m Cl)|AgCl|Ag|Ptwhere KHPh denotes the potassium hydrogen phthalate buffer solution of molalitym PS = 0.05 mol-kg−1, at glycerol mass fractions w G = 0.2 and 0.4, within thetemperature range −10 to 40°C. A multilinear regression procedure as a functionof electrolyte molality, glycerol mass fraction w G, and temperature T has beenapplied for the data processing leading to the values of primary standards pHPS.These can be represented by the following regression equationpHPS = (4.007037±0.001113) + (3.55844±0.01776)x G+(0.39622±0.01410)z + (4.3084±0.3377)z 2− (50.66±10.53)x G z 2 + (457.10±78.48)x G 2 z 2where z = (T − 298.15)/298.15. Parallel values of the first ionization constantof o-phthalic acid (H2Ph; benzene-1,2-dicarboxylic acid, the parent acid of KHPh),which are essential for the above calculations, have been determined fromreversible emf measurements of the cellPt|H2|H2Ph (m 1) + KHPh (m 2) + KCl (m 3)|AgCl|Ag|Ptover the range of solvent composition and temperatures mentioned above.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...