Site pages
Current course
Participants
General
18 February - 24 February
25 February - 3 March
4 March - 10 March
11 March - 17 March
18 March - 24 March
25 March - 31 March
1 April - 7 April
8 April - 14 April
15 April - 21 April
22 April - 28 April
Alkalinity
Alkalinity or AT is a measure of the ability of a solution to neutralize acids to the equivalence point of carbonate or bicarbonate. Alkalinity is closely related to the acid neutralizing capacity (ANC) of a solution and ANC is often incorrectly used to refer to alkalinity. The alkalinity is equal to the stoichiometric sum of the bases in solution. In the natural environment carbonate alkalinity tends to make up most of the total alkalinity due to the common occurrence and dissolution of carbonate rocks and presence of carbon dioxide in the atmosphere. Other common natural components that can contribute to alkalinity include borate, hydroxide, phosphate, silicate, nitrate, dissolved ammonia, the conjugate bases of some organic acids and sulfide.
Theoretical treatment of alkalinity In typical groundwater or seawater the measured alkalinity is set to be equal to: AT = [HCO3−]T + 2[CO3−2]T + [B(OH)4−]T + [OH−]T + 2[PO4−3]T + [HPO4−2]T + [SiO(OH)3−]T − [H+]sws − [HSO4−] (Subscript T indicates the total concentration of the species in the solution as measured. This is opposite to the free concentration, which takes into account the significant amount of ion pair interactions that occur in seawater.) Alkalinity can be measured by titrating a sample with a strong acid until all the buffering capacity of the aforementioned ions above the pH of bicarbonate or carbonate is consumed. This point is functionally set to pH 4.5. At this point, all the bases of interest have been protonated to the zero level species, hence they no longer cause alkalinity. For example, the following reactions take place during the addition of acid to a typical seawater solution: HCO3− + H+ → CO2 + H2O CO3−2 + 2H+ → CO2 + H2O B(OH)4− + H+ → B(OH)3 + H2O OH− + H+ → H2O PO4−3 + 2H+ → H2PO4− HPO4−2 + H+ → H2PO4− [SiO(OH)3−] + H+ → [Si(OH)40] It can be seen from the above protonation reactions that most bases consume one proton (H+) to become a neutral species, thus increasing alkalinity by one per equivalent. CO3−2 however, will consume two protons before becoming a zero level species (CO2), thus it increases alkalinity by two per mole of CO3−2. [H+] and [HSO4−] decrease alkalintiy, as they act as sources of protons. They are often represented collectively as [H+]T. Alkalinity is typically reported as mg/l as CaCO3. This can be converted into milliEquivalents per liter (mEq/l) by dividing by 50 (the approximate MW of CaCO3/2). |