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Conversely, when pH = pK a, the concentration of HA is equal to the concentration of A −. The buffer region extends over the approximate range pK a ± 2. Buffering is weak outside the range pK a ± 1. At pH ≤ pK a − 2 the substance is said to be fully protonated and at pH ≥ pK a + 2 it is fully dissociated (deprotonated).
Lawrence Joseph Henderson was a biological chemist and Karl Albert Hasselbalch was a physiologist who studied pH. [2] [3] In 1908, Lawrence Joseph Henderson [4] derived an equation to calculate the hydrogen ion concentration of a bicarbonate buffer solution, which rearranged looks like this:
Speciation of ions refers to the changing concentration of varying forms of an ion as the pH of the solution changes. [1]The ratio of acid, AH and conjugate base, A −, concentrations varies as the difference between the pH and the pK a varies, in accordance with the Henderson-Hasselbalch equation.
The pH of a simple solution of an acid in water is determined by both and the acid concentration. For weak acid solutions, it depends on the degree of dissociation, which may be determined by an equilibrium calculation. For concentrated solutions of acids, especially strong acids for which pH < 0, the value is a better measure of acidity than ...
At 298 K, 1 pH unit is approximately equal to 59 mV. [2] When the electrode is calibrated with solutions of known concentration, by means of a strong acid–strong base titration, for example, a modified Nernst equation is assumed. = + [] where s is an empirical slope factor.
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Phase behavior Triple point: 150 K (−123 °C), 0.00043 Pa Critical point: 514 K (241 °C), 63 bar Std enthalpy change of fusion, Δ fus H o +4.9 kJ/mol
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