2018
DOI: 10.21577/0100-4042.20170216
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Measuring the Conductivity of Very Dilute Electrolyte Solutions, Drop by Drop

Abstract: Undergraduate experiments on ionic conductivity are common practice in general chemistry and advanced physical chemistry laboratories. Often, the conductivities are measured for solutions prepared for various salts, in a range of concentrations, and the relationship between solution conductivity and concentration is interpreted in terms of the Kohlrausch law. Contaminations can dominate the conductivity of the solutions such that students might obtain unsatisfactory results for analysis. Here, the experience o… Show more

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Cited by 4 publications
(4 citation statements)
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“…As shown in Figure 6, the conductivities were 0.00 mS/cm for methanol only (0.0M TBD), rising to 3.74 mS/cm for 0.1M TBD in methanol. The change in the methanol conductivity with TBD concentration follows a general trend in conductivity for formations of ions from weak acids and bases due to equilibrium limitations (Martínez, 2018).…”
Section: Resultsmentioning
confidence: 95%
“…As shown in Figure 6, the conductivities were 0.00 mS/cm for methanol only (0.0M TBD), rising to 3.74 mS/cm for 0.1M TBD in methanol. The change in the methanol conductivity with TBD concentration follows a general trend in conductivity for formations of ions from weak acids and bases due to equilibrium limitations (Martínez, 2018).…”
Section: Resultsmentioning
confidence: 95%
“…At innite dilution, the conductivity is simply directly proportional to the ion concentration in solution c. 13,14 However, this model fails at the dilute domain (0 < c < 10 À3 mol L À1 ) since the conductivity depends additionally on a squared root term of the conducting salt concentration. 15 Kohlrausch formulated these ndings into an empirical law with an adjustable parameter, 15,16 later addressed by Onsager by considering that ions are dragged not only by hydrodynamic effects, but also by electrophoretic and relaxation phenomena as in the Debye-Hückel theory. The Debye-Hückel-Onsager (DHO) theory effectively upgrades Kohlrausch's law into a fully theoretical law, without adjustable parameters:…”
Section: Introductionmentioning
confidence: 99%
“…13,14 However, this model fails at the dilute domain (0 < c < 10 −3 mol L −1 ) since the conductivity depends additionally on a squared root term of the conducting salt concentration. 15 Kohlrausch formulated these findings into an empirical law with an adjustable parameter, 15,16 later addressed by Onsager by considering that ions are dragged not only by hydrodynamic effects, but also by electrophoretic and relaxation phenomena as in the Debye–Hückel theory. The Debye–Hückel–Onsager (DHO) theory effectively upgrades Kohlrausch's law into a fully theoretical law, without adjustable parameters: 17 where κ 0 is the limiting conductivity, A 1–3 enclose multiple constants, and T , ε and η represent the solution's temperature, permittivity and viscosity, respectively.…”
Section: Introductionmentioning
confidence: 99%
“…At infinite dilution, the conductivity is simply directly proportional to the ion concentration in solution c. 13,14 However, this model fails at the dilute domain (0 < c < 10 -3 mol/L) since the conductivity depends additionally on a squared root term of the conducting salt concentration. 15 Kohlrausch formulated these findings into an empirical law with an adjustable parameter, 15,16 later addressed by Onsager by considering that ions are dragged not only by hydrodynamic effects, but also by electrophoretic and relaxation phenomena as in the Debye-Hückel theory. The Debye-Hückel-Onsager (DHO) theory effectively upgrades Kohlrausch's law into a fully theoretical law, without adjustable parameters: 17…”
Section: Introductionmentioning
confidence: 99%