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- The title of this article should be pH. The initial letter is capitalized due to technical restrictions.
|Acids and bases:|
pH is a measure of the acidity of a solution, in terms of activity of hydrogen ions (H+), standing for potential of Hydrogen. For dilute solutions, however, it is convenient to substitute the activity of the hydrogen ions with the molarity (mol/L) of the hydrogen ions (however, this is not necessarily accurate at higher concentrations  ).
In aqueous systems, the hydrogen ion activity is dictated by the dissociation constant of water (Kw = 1.011 × 10−14 M2 at 25 °C) and interactions with other ions in solution. Due to this dissociation constant, a neutral solution (hydrogen ion activity equals hydroxide ion activity) has a pH of approximately 7. Aqueous solutions with pH values lower than 7 are considered acidic, while pH values higher than 7 are considered basic.
The concept was introduced by S.P.L. Sørensen in 1909, and is purported to mean "pondus hydrogenii" in Latin. However, most other sources attribute the name to the French term pouvoir hydrogène.    In English, pH can stand for "hydrogen power,"   "power of hydrogen,"   or "potential of hydrogen."   All of these terms are technically correct.
Though pH is generally expressed without units, it is not an arbitrary scale; the number arises from a definition based on the activity of hydrogen ions in the solution. The pH scale is a reverse logarithmic representation of relative hydrogen proton (H+) concentration. Most scales are linear in nature and progress in a smooth incremental manner. On the pH scale, a shift up in value by one number represents a ten-fold decrease in value. For example, a shift in pH from 2 to 3 represents a decrease in total concentration of ten times less H+ concentration, and a shift from 2 to 4 represents a one-hundred fold decrease (10 X 10) in H+ concentration.
The precise formula for calculating pH is:
aH+ denotes the activity of H+ ions, and is unitless.
In dilute solutions (such as tap water), the activity is approximately equal to the numeric value of the concentration of the H+ ion, denoted as [H+] (or more accurately written, [H3O+]), measured in moles per litre (also known as molarity). Therefore, it is often convenient to define pH as:
For both definitions, log10 denotes the base-10 logarithm, therefore pH defines a logarithmic scale of acidity. The straight bars, indicating absolute value, make pH a unit-less quantity. For example, if one makes a lemonade with a H+ concentration of 0.0050 moles per litre, its pH would be:
A solution of pH = 8.2 will have an [H+] concentration of 10−8.2 mol/L, or about 6.31 × 10−9 mol/L. Thus, its hydrogen activity aH+ is around 6.31 × 10-9. A solution with an [H+] concentration of 4.5 × 10−4 mol/L will have a pH value of 3.35.
In solution at 25 °C, a pH of 7 indicates neutrality (i.e. the pH of pure water) because water naturally dissociates into H+ and OH− ions with equal concentrations of 1×10−7 mol/L. A lower pH value (for example pH 3) indicates increasing strength of acidity, and a higher pH value (for example pH 11) indicates increasing strength of basicity. Note, however, that pure water, when exposed to the atmosphere, will take in carbon dioxide, some of which reacts with water to form carbonic acid and H+, thereby lowering the pH to about 5.7.
Neutral pH at 25 °C is not exactly 7. pH is an experimental value, so it has an associated error. Since the dissociation constant of water is (1.011 ± 0.005) × 10-14, pH of water at 25 °C would be 6.998 ± 0.001. The value is consistent, however, with neutral pH being 7.00 to two significant figures, which is near enough for most people to assume that it is exactly 7. The pH of water gets smaller with higher temperatures. For example, at 50 °C, pH of water is 6.55 ± 0.01. This means that a diluted solution is neutral at 50 °C when its pH is around 6.55 and that a pH of 7.00 is basic.
Most substances have a pH in the range 0 to 14, although extremely acidic or extremely basic substances may have pH less than 0 or greater than 14. An example is acid mine runoff, with a pH = -3.6. Note that this does not translate to a molar concentration of 3981 M.
However, in a concentration cell both εo are equal so the equation becomes
By using the standard hydrogen electrode, with H2 gas at 1 atm and an unknown molarity of H+ ions, and in which 2 moles of electrons are transferred for every mole of reaction, the equation may be set up as follows:
Arbitrarily, the potential of hydrogen, or pH, is defined as . Therefore,
or, by substitution,
The "pH" of any other substance may also be found (e.g. the potential of silver ions, or pAg+) by deriving a similar equation using the same process. These other equations for potentials will not be the same, however, as the number of moles of electrons transferred (n) will differ for the different reactions.
Calculation of pH for weak and strong acids
Values of pH for weak and strong acids can be approximated using certain assumptions.
Under the Brønsted-Lowry theory, stronger or weaker acids are a relative concept. But here we define a strong acid as a species which is a much stronger acid than the hydronium (H3O+) ion. In that case the dissociation reaction (strictly HX+H2O↔H3O++X− but simplified as HX↔H++X−) goes to completion, i.e. no unreacted acid remains in solution. Dissolving the strong acid HCl in water can therefore be expressed:
- HCl(aq) → H+ + Cl−
This means that in a 0.01 mol/L solution of HCl it is approximated that there is a concentration of 0.01 mol/L dissolved hydrogen ions. From above, the pH is: pH = −log10 [H+]:
- pH = −log (0.01)
which equals 2.
For weak acids, the dissociation reaction does not go to completion. An equilibrium is reached between the hydrogen ions and the conjugate base. The following shows the equilibrium reaction between methanoic acid and its ions:
- HCOOH(aq) ↔ H+ + HCOO−
It is necessary to know the value of the equilibrium constant of the reaction for each acid in order to calculate its pH. In the context of pH, this is termed the acidity constant of the acid but is worked out in the same way (see chemical equilibrium):
- Ka = [hydrogen ions][acid ions] / [acid]
For HCOOH, Ka = 1.6 × 10−4
When calculating the pH of a weak acid, it is usually assumed that the water does not provide any hydrogen ions. This simplifies the calculation, and the concentration provided by water, 1×10−7 mol, is usually insignificant.
With a 0.1 mol/L solution of methanoic acid (HCOOH), the acidity constant is equal to:
- Ka = [H+][HCOO−] / [HCOOH]
Given that an unknown amount of the acid has dissociated, [HCOOH] will be reduced by this amount, while [H+] and [HCOO−] will each be increased by this amount. Therefore, [HCOOH] may be replaced by 0.1 − x, and [H+] and [HCOO−] may each be replaced by x, giving us the following equation:
Solving this for x yields 3.9×10−3, which is the concentration of hydrogen ions after dissociation. Therefore the pH is −log(3.9×10−3), or about 2.4
|Gastric acid||<center>1.5 – 2.0|
|Orange or apple juice||<center>3.5|
|Tea or healthy skin||<center>5.5|
|Healthy human saliva||<center>6.5 – 7.4|
|Blood||<center>7.34 – 7.45|
|Hand soap||<center>9.0 – 10.0|
pH can be measured:
- by addition of a pH indicator into the studying solution. The indicator color varies depending on the pH of the solution. Using indicators, qualitative determinations can be made with universal indicators that have broad color variability over a wide pH range and quantitative determinations can be made using indicators that have strong color variability over a small pH range. Extremely precise measurements can be made over a wide pH range using indicators that have multiple equilibriums (ie H2I) in conjunction with spectrophotometric methods to determine the relative abundance of each pH dependent component that make up the color of solution, or
- by using a pH meter together with pH-selective electrodes (pH glass electrode, hydrogen electrode, quinhydrone electrode, ion sensitive field effect transistor and other).
There is also pOH, in a sense the opposite of pH, which measures the concentration of OH− ions, or the basicity. Since water self ionizes, and notating [OH−] as the concentration of hydroxide ions, we have
where Kw is the ionization constant of water.
by logarithmic identities, we then have the relationship:
This formula is valid exactly for temperature = 298.15 K (25 °C) only, but is acceptable for most lab calculations.
- ↑ http://www.jp.horiba.com/story_e/ph/ph01_03.htm
- ↑ http://chem.lapeer.org/Chem2Docs/pHFacts.html
- ↑ 3.0 3.1 http://www.madsci.org/posts/archives/sep2001/1000136604.Sh.r.html
- ↑ 4.0 4.1 Davis, R.E.; Metcalfe, H.C.; Williams, J.E.; Castka, J.F. et al. (2002) Aqueous Solutions and the Concept of pH. In Modern Chemistry, pp. 485. Austin: Holt, Rinehart and Winston
- ↑ 5.0 5.1 http://encarta.msn.com/encyclopedia_761552883/pH.html
- ↑ 6.0 6.1 http://bcn.boulder.co.us/basin/data/COBWQ/info/pH.html
- ↑ http://www.coastwidelabs.com/Technical%20Articles/ph__the_power_of_hydrogen.htm
- ↑ 8.0 8.1 http://hyperphysics.phy-astr.gsu.edu/HBASE/Chemical/ph.html
- ↑ http://wordnet.princeton.edu/perl/webwn?s=ph
- ↑ http://www.morrisonlabs.com/ph_study_guide.htm
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