TY - JOUR
T1 - An investigation of Harned's rule for predicting the activity coefficients of strong aqueous electrolyte solution mixtures at 25 ºC
AU - Rowland, Darren
AU - May, Peter M.
PY - 2017/1/12
Y1 - 2017/1/12
N2 - From a critical evaluation of the relevant literature Harned coefficients at 25 degrees C and their corresponding trace activity coefficients are reported for 72 mixtures of strong aqueous electrolytes with a common ion. The work confirms the generality of Harned's rule in its simplest form, that is, with only one (linear) term. Uncertainties in predicted mean activity coefficients are typically less than 0.01, comparable with the experimental reproducibility. Unless there are good grounds to suggest that significant changes in chemical speciation are occurring, experimental measurements that do not conform to the rule should be regarded with suspicion. We find that the estimates of errors made by authors of single potentiometric investigations are often as much as an order of magnitude too optimistic. Even the work of Harped and colleagues, which was typically of high quality, is sometimes much worse than is claimed or implied in the literature. The unfortunately common practice of introducing a quadratic term (as a second adjustable parameter) to extend Harned's rule is unjustified, within the true current limits of experimental error. Harned's rule with just one coefficient provides a description of aqueous strong electrolyte mixing thermodynamics which is widely applicable, satisfactorily accurate, and without sign of any systematic problem. © 2016 American Chemical Society
AB - From a critical evaluation of the relevant literature Harned coefficients at 25 degrees C and their corresponding trace activity coefficients are reported for 72 mixtures of strong aqueous electrolytes with a common ion. The work confirms the generality of Harned's rule in its simplest form, that is, with only one (linear) term. Uncertainties in predicted mean activity coefficients are typically less than 0.01, comparable with the experimental reproducibility. Unless there are good grounds to suggest that significant changes in chemical speciation are occurring, experimental measurements that do not conform to the rule should be regarded with suspicion. We find that the estimates of errors made by authors of single potentiometric investigations are often as much as an order of magnitude too optimistic. Even the work of Harped and colleagues, which was typically of high quality, is sometimes much worse than is claimed or implied in the literature. The unfortunately common practice of introducing a quadratic term (as a second adjustable parameter) to extend Harned's rule is unjustified, within the true current limits of experimental error. Harned's rule with just one coefficient provides a description of aqueous strong electrolyte mixing thermodynamics which is widely applicable, satisfactorily accurate, and without sign of any systematic problem. © 2016 American Chemical Society
KW - MEAN ACTIVITY-COEFFICIENTS
KW - CONSTANT TOTAL MOLALITY
KW - ORDER ELECTROSTATIC TERMS
KW - VALENCE TYPE CHLORIDE
KW - THERMODYNAMIC PROPERTIES DETERMINATION
KW - SODIUM AMALGAM ELECTRODES
KW - EXPERT SPECIATION SYSTEM
KW - BRINE-SALT EQUILIBRIA
KW - BROMIDE PLUS WATER
KW - HYDROCHLORIC-ACID
U2 - 10.1021/acs.jced.6b00651
DO - 10.1021/acs.jced.6b00651
M3 - Article
SN - 0021-9568
VL - 62
SP - 310
EP - 327
JO - Journal of Chemical & Engineering Data
JF - Journal of Chemical & Engineering Data
IS - 1
ER -