Alkalinity

Not to be confused with alkali or base (chemistry).

Sea surface alkalinity (from the GLODAP climatology).

Alkalinity (from Arabic: القلوية, romanized: al-qaly, lit. 'ashes of the saltwort')[1] is the capacity of water to resist acidification.[2] It should not be confused with basicity, which is an absolute measurement on the pH scale. Alkalinity is the strength of a buffer solution composed of weak acids and their conjugate bases. It is measured by titrating the solution with an acid such as HCl until its pH changes abruptly, or it reaches a known endpoint where that happens. Alkalinity is expressed in units of concentration, such as meq/L (milliequivalents per liter), μeq/kg (microequivalents per kilogram), or mg/L CaCO₃ (milligrams per liter of calcium carbonate).[3] Each of these measurements corresponds to an amount of acid added as a titrant.

In freshwater, particularly those on non-limestone terrains, alkalinities are low and involve a lot of ions. In the ocean, on the other hand, alkalinity is completely dominated by carbonate and bicarbonate plus a small contribution from borate.[4]

Although alkalinity is primarily a term used by limnologists[5] and oceanographers,[3] it is also used by hydrologists to describe temporary hardness. Moreover, measuring alkalinity is important in determining a stream's ability to neutralize acidic pollution from rainfall or wastewater. It is one of the best measures of the sensitivity of the stream to acid inputs.[6] There can be long-term changes in the alkalinity of streams and rivers in response to human disturbances such as acid rain generated by SO_x and NO_x emissions.[7]

History

In 1884, Professor Wilhelm (William) Dittmar of Anderson College, now the University of Strathclyde, analysed 77 pristine seawater samples from around the world brought back by the Challenger expedition. He found that in seawater the major ions were in a fixed ratio, confirming the hypothesis of Johan Georg Forchhammer, that is now known as the Principle of Constant Proportions. However, there was one exception. Dittmar found that the concentration of calcium was slightly greater in the deep ocean, and named this increase alkalinity.^[citation needed]

Also in 1884, Svante Arrhenius submitted his PhD theses in which he advocated the existence of ions in solution, and defined acids as hydronium ion donors and bases as hydroxide ion donors. For that work, he received the Nobel Prize in Chemistry in 1903.^[citation needed] See also Svante Arrhenius#Ionic disassociation.

Simplified summary

Alkalinity roughly refers to the molar amount of bases in a solution that can be converted to uncharged species by a strong acid. For example, 1 mole of HCO^−
₃ in solution represents 1 molar equivalent, while 1 mole of CO^2−
₃ is 2 molar equivalents because twice as many H^+ ions would be necessary to balance the charge. The total charge of a solution always equals zero.[8] This leads to a parallel definition of alkalinity that is based upon the charge balance of ions in a solution.

${\displaystyle \sum ({\text{cations}})=\sum ({\text{anions}})}$

Certain ions, including Na^+, K^+, Ca^2+, Mg^2+, Cl^−, SO^2−
₄, and NO^−
₃ are "conservative" such that they are unaffected by changes in temperature, pressure or pH.[8] Others such as HCO^−
₃ are affected by changes in pH, temperature, and pressure. By isolating the conservative ions on one side of this charge balance equation, the nonconservative ions which accept or donate protons and thus define alkalinity are clustered on the other side of the equation.

${\displaystyle {\begin{aligned}&\sum ({\text{conservative cations}})-\sum ({\text{conservative anions}})=\\&\quad [\mathrm {HCO_{3}^{-}} ]+2[\mathrm {CO_{3}^{2-}} ]+[\mathrm {B(OH)_{4}^{-}} ]+[\mathrm {OH^{-}} ]+[\mathrm {HPO_{4}^{2-}} ]+2[\mathrm {PO_{4}^{3-}} ]+[\mathrm {H_{3}SiO_{4}^{-}} ]+[\mathrm {NH_{3}} ]+[\mathrm {HS^{-}} ]-[\mathrm {H^{+}} ]-[\mathrm {HSO_{4}^{-}} ]-[\mathrm {HF} ]-[\mathrm {H_{3}PO_{4}} ]-[\mathrm {HNO_{2}} ]\end{aligned}}}$

This combined charge balance and proton balance is called total alkalinity.[9] Total alkalinity is not (much) affected by temperature, pressure, or pH, and is thus itself a conservative measurement, which increases its usefulness in aquatic systems. All anions except HCO^−
₃ and CO^2−
₃ have low concentrations in Earth's surface water (streams, rivers, and lakes). Thus carbonate alkalinity, which is equal to [HCO^−
₃] + 2[CO^2−
₃] is also approximately equal to the total alkalinity in surface water.[8]

Detailed description

Alkalinity measures the ability of a solution to neutralize acids to the equivalence point of carbonate or bicarbonate, defined as pH 4.5 for many oceanographic/limnological studies.[10] The alkalinity is equal to the stoichiometric sum of the bases in solution. In most Earth surface waters carbonate alkalinity tends to make up most of the total alkalinity due to the common occurrence and dissolution of carbonate rocks and other geological weathering processes that produce carbonate anions. Other common natural components that can contribute to alkalinity include borate, hydroxide, phosphate, silicate, dissolved ammonia, and the conjugate bases of organic acids (e.g., acetate). Solutions produced in a laboratory may contain a virtually limitless number of species that contribute to alkalinity. Alkalinity is frequently given as molar equivalents per liter of solution or per kilogram of solvent. In commercial (e.g. the swimming pool industry) and regulatory contexts, alkalinity might also be given in parts per million of equivalent calcium carbonate (ppm CaCO₃)^[citation needed]. Alkalinity is sometimes incorrectly used interchangeably with basicity. For example, the addition of CO₂ lowers the pH of a solution, thus reducing basicity while alkalinity remains unchanged (see example below).

A variety of titrants, endpoints, and indicators are specified for various alkalinity measurement methods. Hydrochloric and sulfuric acids are common acid titrants, while phenolpthalein, methyl red, and bromocresol green are common indicators.[11]

Theoretical treatment

In typical groundwater or seawater, the measured total alkalinity is set equal to:

A_T = [HCO^−
₃]_T + 2[CO^2−
₃]_T + [B(OH)^−
₄]_T + [OH^−]_T + 2[PO^3−
₄]_T + [HPO^2−
₄]_T + [SiO(OH)^−
₃]_T − [H^+]_sws − [HSO^−
₄]

(Subscript T indicates the total concentration of the species in the solution as measured. This is opposed 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. In the carbonate system the bicarbonate ions [HCO^−
₃] and the carbonate ions [CO^2−
₃] have become converted to carbonic acid [H₂CO₃] at this pH. This pH is also called the CO₂ equivalence point where the major component in water is dissolved CO₂ which is converted to H₂CO₃ in an aqueous solution. There are no strong acids or bases at this point. Therefore, the alkalinity is modeled and quantified with respect to the CO₂ equivalence point. Because the alkalinity is measured with respect to the CO₂ equivalence point, the dissolution of CO₂, although it adds acid and dissolved inorganic carbon, does not change the alkalinity. In natural conditions, the dissolution of basic rocks and addition of ammonia [NH₃] or organic amines leads to the addition of base to natural waters at the CO₂ equivalence point. The dissolved base in water increases the pH and titrates an equivalent amount of CO₂ to bicarbonate ion and carbonate ion. At equilibrium, the water contains a certain amount of alkalinity contributed by the concentration of weak acid anions. Conversely, the addition of acid converts weak acid anions to CO₂ and continuous addition of strong acids can cause the alkalinity to become less than zero.[12] For example, the following reactions take place during the addition of acid to a typical seawater solution:

B(OH)^−
₄ + H^+ → B(OH)₃ + H₂O

OH^− + H^+ → H₂O

PO^3−
₄ + 2 H^+ → H
₂PO^−
₄

HPO^2−
₄ + H^+ → H
₂PO^−
₄

[SiO(OH)^−
₃] + H^+ → [Si(OH)₄]

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. CO^2−
₃ however, will consume two protons before becoming a zero-level species (CO₂), thus it increases alkalinity by two per mole of CO^2−
₃. [H^+] and [HSO^−
₄] decrease alkalinity, as they act as sources of protons. They are often represented collectively as [H^+]_T.

Alkalinity is typically reported as mg/L as CaCO₃. (The conjunction "as" is appropriate in this case because the alkalinity results from a mixture of ions but is reported "as if" all of this is due to CaCO₃.) This can be converted into milliequivalents per Liter (meq/L) by dividing by 50 (the approximate MW of CaCO₃ divided by 2).

Carbon dioxide interactions

Addition of CO₂

Addition (or removal) of CO₂ to a solution does not change its alkalinity, since the net reaction produces the same number of equivalents of positively contributing species (H^+) as negative contributing species (HCO^−
₃ and/or CO^2−
₃). Adding CO₂ to the solution lowers its pH, but does not affect alkalinity.

At all pH values:

CO₂ + H₂O ⇌ HCO^−
₃ + H^+

Only at high (basic) pH values:

HCO^−
₃ + H^+ ⇌ CO^2−
₃ + 2 H^+

Dissolution of carbonate rock

Addition of CO₂ to a solution in contact with a solid can (over time) affect the alkalinity, especially for carbonate minerals in contact with groundwater or seawater. The dissolution (or precipitation) of carbonate rock has a strong influence on the alkalinity. This is because carbonate rock is composed of CaCO₃ and its dissociation will add Ca^2+ and CO^2−
₃ into solution. Ca^2+ will not influence alkalinity, but CO^2−
₃ will increase alkalinity by 2 units. Increased dissolution of carbonate rock by acidification from acid rain and mining has contributed to increased alkalinity concentrations in some major rivers throughout the eastern U.S.[7] The following reaction shows how acid rain, containing sulfuric acid, can have the effect of increasing river alkalinity by increasing the amount of bicarbonate ion:

2 CaCO₃ + H₂SO₄ → 2 Ca^2+ + 2 HCO^−
₃ + SO^2−
₄

Another way of writing this is:

CaCO₃ + H^+ ⇌ Ca^2+ + HCO^−
₃

The lower the pH, the higher the concentration of bicarbonate will be. This shows how a lower pH can lead to higher alkalinity if the amount of bicarbonate produced is greater than the amount of H^+ remaining after the reaction. This is the case since the amount of acid in the rainwater is low. If this alkaline groundwater later comes into contact with the atmosphere, it can lose CO₂, precipitate carbonate, and thereby become less alkaline again. When carbonate minerals, water, and the atmosphere are all in equilibrium, the reversible reaction

CaCO₃ + 2 H^+ ⇌ Ca^2+ + CO₂ + H₂O

shows that pH will be related to calcium ion concentration, with lower pH going with higher calcium ion concentration. In this case, the higher the pH, the more bicarbonate and carbonate ion there will be, in contrast to the paradoxical situation described above, where one does not have equilibrium with the atmosphere.

Changes to oceanic alkalinity

See also: Ocean § Alkalinity, pH § pH in the ocean, Ocean acidification, and Effects of climate change on oceans

In the ocean, alkalinity is completely dominated by carbonate and bicarbonate plus a small contribution from borate.[4]

Thus the chemical equation for alkalinity in seawater is:

A_T = [HCO₃^−] + 2[CO₃^2-] + [B(OH)₄^−]

There are many methods of alkalinity generation in the ocean. Perhaps the most well known is the dissolution of calcium carbonate to form Ca^2+ and CO^2−
₃ (carbonate). The carbonate ion has the potential to absorb two hydrogen ions. Therefore, it causes a net increase in ocean alkalinity. Calcium carbonate dissolution occurs in regions of the ocean which are undersaturated with respect to calcium carbonate.

The increasing carbon dioxide level in the atmosphere, due to carbon dioxide emissions, results in increasing absorption of CO₂ from the atmosphere into the oceans.[13] This does not affect the ocean's alkalinity[14]: 2252  but it does result in a reduction in pH value (called ocean acidification).[15] Ocean alkalinity enhancement has been proposed as one option to add alkalinity to the ocean and therefore buffer against pH changes.[16]: 181 

Biological processes have a much greater impact on oceanic alkalinity on short (minutes to centuries) timescales.[17] Denitrification and sulfate reduction occur in oxygen-limited environments. Both of these processes consume hydrogen ions (thus increasing alkalinity) and release gases (N₂ or H₂S), which eventually escape into the atmosphere. Nitrification and sulfide oxidation both decrease alkalinity by releasing protons as a byproduct of oxidation reactions.[18]

Global temporal and spatial variability

The ocean's alkalinity varies over time, most significantly over geologic timescales (millennia). Changes in the balance between terrestrial weathering and sedimentation of carbonate minerals (for example, as a function of ocean acidification) are the primary long-term drivers of alkalinity in the ocean.[19] Over human timescales, mean ocean alkalinity is relatively stable.[20] Seasonal and annual variability of mean ocean alkalinity is very low.[21]

Alkalinity varies by location depending on evaporation/precipitation, advection of water, biological processes, and geochemical processes.[4]

River dominated mixing also occurs close to the shore; it is strongest close to the mouth of a large river. Here, the rivers can act as either a source or a sink of alkalinity. A_T follows the outflow of the river and has a linear relationship with salinity.[21]

Oceanic alkalinity also follows general trends based on latitude and depth. It has been shown that A_T is often inversely proportional to sea surface temperature (SST). Therefore, it generally increases with high latitudes and depths. As a result, upwelling areas (where water from the deep ocean is pushed to the surface) also have higher alkalinity values.[22]

There are many programs to measure, record, and study oceanic alkalinity, together with many of the other characteristics of seawater, like temperature and salinity. These include: GEOSECS (Geochemical Ocean Sections Study),[23] TTO/NAS (Transient Tracers in the Ocean/North Atlantic Study), JGOFS (Joint Global Ocean Flux Study),[24] WOCE (World Ocean Circulation Experiment),[25] CARINA (Carbon dioxide in the Atlantic Ocean).[26]

Interventions to add alkalinity

This section is an excerpt from Ocean acidification § Carbon removal technologies which add alkalinity.[edit]

Some carbon removal techniques add alkalinity to the ocean and therefore immediately buffer pH changes which might help the organisms in the region that the extra alkalinity is added to. The two technologies that fall into this category are ocean alkalinity enhancement and electrochemical methods.[27] Eventually, due to diffusion, that alkalinity addition will be quite small to distant waters. This is why the term local ocean acidification mitigation is used. Both of these technologies have the potential to operate on a large scale and to be efficient at removing carbon dioxide.[27]: Table 9.1  However, they are expensive, have many risks and side effects and currently have a low technology readiness level.[28]: 12–36 

See also

• Alkali soils
• Base (chemistry)
• Biological pump
• Dealkalization of water
• Global Ocean Data Analysis Project

References

1. "alkali". Dictionary.com Unabridged (Online). n.d. Retrieved 2018-09-30.
2. "What is alkalinity?". Water Research Center. 2014. Retrieved 5 February 2018.
3. Dickson, Andrew G. (1992). "The development of the alkalinity concept in marine chemistry". Marine Chemistry. 40 (1–2): 49–63. Bibcode:1992MarCh..40...49D. doi:10.1016/0304-4203(92)90047-E.
4. Chester, R.; Jickells, Tim (2012). "Chapter 9: Nutrients oxygen organic carbon and the carbon cycle in seawater". Marine geochemistry (3rd ed.). Chichester, West Sussex, UK: Wiley/Blackwell. ISBN 978-1-118-34909-0. OCLC 781078031.
5. Mattson, M. D. (2014-01-01), "Alkalinity of Freshwater☆", Reference Module in Earth Systems and Environmental Sciences, Elsevier, doi:10.1016/b978-0-12-409548-9.09397-0, ISBN 978-0-12-409548-9, retrieved 2023-01-09
6. "Total Alkalinity". United States Environment Protection Agency. Retrieved 6 March 2013.
7. Kaushal, S. S.; Likens, G. E.; Utz, R. M.; Pace, M. L.; Grese, M.; Yepsen, M. (2013). "Increased river alkalinization in the Eastern U.S.". Environmental Science & Technology. 47 (18): 10302–10311. doi:10.1021/es401046s. PMID 23883395.
8. Drever, James I. (1988). The Geochemistry of Natural Waters, Second Edition. Englewood Cliffs, NJ: Prentice Hall. ISBN 0-13-351396-3.
9. Wolf-Gladrow, Dieter A.; Zeebe, Richard E.; Klaas, Christine; Körtzinger, Arne; Dickson, Andrew G. (July 2007). "Total alkalinity: The explicit conservative expression and its application to biogeochemical processes". Marine Chemistry. 106 (1–2): 287–300. Bibcode:2007MarCh.106..287W. doi:10.1016/j.marchem.2007.01.006.
10. Dickson, A.G. (June 1981). "An exact definition of total alkalinity and a procedure for the estimation of alkalinity and total inorganic carbon from titration data". Deep Sea Research Part A. Oceanographic Research Papers. 28 (6): 609–623. Bibcode:1981DSRA...28..609D. doi:10.1016/0198-0149(81)90121-7.
11. 2320 alkalinity, Standard Methods for the Examination of Water and Wastewater, American Public Health Association, 2017-08-27, doi:10.2105/smww.2882.023 (inactive 1 November 2024), ISBN 9780875532998, retrieved 2022-12-01
12. Benjamin. Mark M. 2015. Water Chemistry. 2nd Ed. Long Grove, Illinois: Waveland Press, Inc.
13. Doney, Scott C.; Busch, D. Shallin; Cooley, Sarah R.; Kroeker, Kristy J. (2020-10-17). "The Impacts of Ocean Acidification on Marine Ecosystems and Reliant Human Communities". Annual Review of Environment and Resources. 45 (1): 83–112. doi:10.1146/annurev-environ-012320-083019. S2CID 225741986. Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
14. IPCC, 2021: Annex VII: Glossary Archived 5 June 2022 at the Wayback Machine [Matthews, J.B.R., V. Möller, R. van Diemen, J.S. Fuglestvedt, V. Masson-Delmotte, C.  Méndez, S. Semenov, A. Reisinger (eds.)]. In Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change Archived 9 August 2021 at the Wayback Machine [Masson-Delmotte, V., P. Zhai, A. Pirani, S.L. Connors, C. Péan, S. Berger, N. Caud, Y. Chen, L. Goldfarb, M.I. Gomis, M. Huang, K. Leitzell, E. Lonnoy, J.B.R. Matthews, T.K. Maycock, T. Waterfield, O. Yelekçi, R. Yu, and B. Zhou (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA
15. Doney, Scott C.; Busch, D. Shallin; Cooley, Sarah R.; Kroeker, Kristy J. (2020-10-17). "The Impacts of Ocean Acidification on Marine Ecosystems and Reliant Human Communities". Annual Review of Environment and Resources. 45 (1): 83–112. doi:10.1146/annurev-environ-012320-083019. S2CID 225741986. Text was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
16. A Research Strategy for Ocean-based Carbon Dioxide Removal and Sequestration. 2022. doi:10.17226/26278. ISBN 978-0-309-08761-2. PMID 35533244. S2CID 245089649.
17. Emerson, Steven; Hedges, John (2008). Chemical oceanography and the marine carbon cycle. Cambridge: Cambridge University Press. ISBN 978-0-511-64987-5. OCLC 558876135.
18. Stumm, Werner; Morgan, James J. (1996). Aquatic chemistry : chemical equilibria and rates in natural waters (3rd ed.). New York: Wiley. ISBN 0-471-51184-6. OCLC 31754493.
19. Zeebe, Richard E.; Wolf-Gladrow, Dieter A. (2001). CO2 in seawater : equilibrium, kinetics, isotopes. Amsterdam: Elsevier. ISBN 978-0-08-052922-6. OCLC 246683387.
20. Doney, Scott C.; Fabry, Victoria J.; Feely, Richard A.; Kleypas, Joan A. (2009-01-01). "Ocean Acidification: The Other CO 2 Problem". Annual Review of Marine Science. 1 (1): 169–192. Bibcode:2009ARMS....1..169D. doi:10.1146/annurev.marine.010908.163834. ISSN 1941-1405. PMID 21141034.
21. Thomas, H.; Schiettecatte, L.-S.; et al. Enhanced Ocean Carbon Storage from Anaerobic Alkalinity Generation in Coastal Sediments. Biogeosciences Discussions. 2008, 5, 3575–3591
22. Millero, F. J.; Lee, K.; Roche, M. Distribution of alkalinity in the surface waters of the major oceans. Marine Chemistry. 1998, 60, 111-130.
23. "dataset: GEOSECS". iridl.ldeo.columbia.edu. Retrieved 2023-03-28.
24. "Home : Woods Hole Oceanographic Institution". 2012-03-14. Archived from the original on 2012-03-14. Retrieved 2023-03-28.
25. "WOCE Global Data Resource". 2011-10-16. Archived from the original on 2011-10-16. Retrieved 2023-03-28.
26. "CARINA". www.pmel.noaa.gov. Retrieved 2023-03-28.
27. A Research Strategy for Ocean-based Carbon Dioxide Removal and Sequestration. 2022. doi:10.17226/26278. ISBN 978-0-309-08761-2. PMID 35533244. S2CID 245089649.
28. IPCC (2022) Chapter 12: Cross sectoral perspectives Archived 13 October 2022 at the Wayback Machine in Climate Change 2022: Mitigation of Climate Change. Contribution of Working Group III to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change Archived 2 August 2022 at the Wayback Machine, Cambridge University Press, Cambridge, United Kingdom and New York, NY, US

External links

• DOE (1994) "[1],"Handbook of methods for the analysis of the various parameters of the carbon dioxide system in sea water. Version 2, A. G. Dickson & C. Goyet, eds. ORNL/CDIAC-74.

Carbonate system calculators

The following packages calculate the state of the carbonate system in seawater (including pH):

• CO2SYS Archived 2011-10-14 at the Wayback Machine, available as a stand-alone executable, Excel spreadsheet, or MATLAB script.
• seacarb, a R package for Windows, Mac OS X and Linux (also available here)
• CSYS, a Matlab script