n.
An equation expressing the pH of a buffer solution as a function of the concentration of the weak acid or base and the salt components of the buffer.
| Medical Dictionary: Hen·der·son-Has·sel·balch equation |
An equation expressing the pH of a buffer solution as a function of the concentration of the weak acid or base and the salt components of the buffer.
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| Veterinary Dictionary: Henderson–Hasselbalch equation |
An equation by which the pH of a buffer solution, blood plasma being such a one, can be determined:$$\hbox{pH=pK\'^\prime}+\log{[\hbox{BA}]\over[\hbox{HA}]}$$
where pK′ is the negative log of the dissociation constant of a weak acid in a buffer solution, [HA] is the concentration in the buffer solution of the weak acid and [BA] is the concentration of a salt of that acid.
| Wikipedia: Henderson–Hasselbalch equation |
In chemistry, the Henderson–Hasselbalch (often misspelled as Henderson–Hasselbach) equation describes the derivation of pH as a measure of acidity (using pKa, the acid dissociation constant) in biological and chemical systems. The equation is also useful for estimating the pH of a buffer solution and finding the equilibrium pH in acid-base reactions (it is widely used to calculate isoelectric point of the proteins).
Two equivalent forms of the equation are
![\textrm{pH} = \textrm{pK}_{a}+ \log \frac{[\textrm{A}^-]}{[\textrm{HA}]}](http://wpcontent.answers.com/math/a/a/0/aa0d5016a357f0b5679b5924e3bdde67.png)
and
![\textrm{pH} = \textrm{pK}_{a}+\log \left ( \frac{[\textrm{conjugate base}]}{[\textrm{acid}]} \right ).](http://wpcontent.answers.com/math/9/d/0/9d0ec0924282dcb12abdc1f0d379ecac.png)
Here, pKa is − log(Ka) where Ka is the acid dissociation constant, that is:
for the non-specific Brønsted acid-base reaction: 
In these equations, A − denotes the ionic form of the relevant acid. Bracketed quantities such as [base] and [acid] denote the molar concentration of the quantity enclosed.
In analogy to the above equations, the following equation is valid:
![\textrm{pOH} = \textrm{pK}_{b}+ \log \left ( \frac{[\textrm{BH}^+]}{[\textrm{B}]} \right )](http://wpcontent.answers.com/math/7/3/6/736f4f31c1b23b09276c93b4c01910c7.png)
Where BH+ denotes the conjugate acid of the corresponding base B.
Contents |
Lawrence Joseph Henderson wrote an equation, in 1908, describing the use of carbonic acid as a buffer solution. Karl Albert Hasselbalch later re-expressed that formula in logarithmic terms, resulting in the Henderson–Hasselbalch equation [1]. Hasselbalch was using the formula to study metabolic acidosis.
There are some significant approximations implicit in the Henderson–Hasselbalch equation. The most significant is the assumption that the concentration of the acid and its conjugate base at equilibrium will remain the same as the former concentration. This neglects the dissociation of the acid and the hydrolysis of the base. The dissociation of water itself is neglected as well. These approximations will fail when dealing with relatively strong acids or bases (pKa more than a couple units away from 7), dilute or very concentrated solutions (less than 1 mM or greater than 1M), or heavily skewed acid/base ratios (more than 100 to 1).
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| buffer1 | |
| Karl Albert Hasselbalch | |
| Charlot equation |
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