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Oxygen solubility

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Oxygen solubility


The oxygen solubility, SO2 [碌M/kPa] = [(碌mol路L-1)/kPa], expresses the oxygen concentration in solution in equilibrium with the oxygen pressure in a gas phase, as a function of temperature and composition of the solution. The inverse of oxygen solubility is related to the activity of dissolved oxygen. The oxygen solubility in solution, SO2(aq), depends on temperature and the concentrations of solutes in solution, whereas the dissolved oxygen concentration at equilibrium with air, cO2*(aq), depends on SO2(aq), barometric pressure and temperature. SO2(aq) in pure water is 10.56 碌M/kPa at 37 掳C and 12.56 碌M/kPa at 25 掳C. At standard barometric pressure (100 kPa), cO2*(aq) is 207.3 碌M at 37 掳C (19.6 kPa partial oxygen pressure) or 254.7 碌M at 25 掳C (20.3 kPa partial oxygen pressure). In MiR05 and serum, the corresponding saturation concentrations are lower due to the oxygen solubility factor: 191 and 184 碌M at 37 掳C or 234 and 227 碌M at 25 掳C.

Abbreviation: SO2 [碌M/kPa]

Reference: MiPNet06.03 POS-calibration-SOP

Communicated by Gnaiger E 2010-10-21 (last update 2021-12-19)

Oxygen solubility in gas (g) versus aqueous solution (aq)

At room temperature or 37 掳C, the concentration of oxygen is 30- to 40-fold higher in the gas phase compared to the aqueous phase in equilibrium with the gas phase. This explains why even a small gas bubble in an aqueous volume of a respirometer causes enormous errors in the measurement of respiration. And it is the reason why we need red blood cells with hemoglobin, to boost the total oxygen concentration carried in the blood. The ideal gas law plays a central role in elucidating the behavior of gases dissolved in aqueous solution, where the gas interacts with a very different environment compared to the gas phase. Following the track of a few equations derived in this overview provides a deep understanding of the rationale implemented in the oxygen calibration algorithms in HRR (MiPNet06.03 POS-calibration-SOP).
The key quantities in the gas law are:
  1. Gas pressure, p [Pa]: 1 atm = 101.325 kPa; standard pressure is 100 kPa.
  2. Temperature, T [K]: Temperature in 掳C is converted to absolute temperature as T[K] = TC[掳 C] + 273.15.
  3. Amount of substance, n [mol].
  4. Volume, V [m3]: Concentration, c = nV-1.
  5. Gas constant, R = 8.314462618 J路mol-1路K-1.
Four forms of the gas law are used in the derivations below:
Eq. a:  pV = nRT ; the fundamental format: pressure-volume work [Pa路m3]=[J] 
Eq. b:  p = cRT ; pressure [Pa] and concentration: c=nV-1  
--------------------- Compare chemical potential:  = 掳 + ln(c/c掳)路RT; 掳=0 and =1 in the gas phase
Eq. c:  Vn-1 = RTp-1 ; the molar volume, Vm [m3路mol-1]=[J路mol-1路Pa-1] 
Eq. d:  cp-1 = RT-1 ; the solubility, S [mol路m-3路Pa-1]=[mol路J-1] 
Solubility is defined as concentration per pressure,
Eq. 1:  SG(g) = cG/p
The solubility of an ideal gas in the gas phase, SG(g), can be calculated simply from the ideal gas law, since the activity coefficient of an ideal gas in the gas phase equals one, =1. Arranging the ideal gas law (Eq. a) to obtain solubility (Eq. d),
Eq. 2:  SG(g) = cG/p = RT-1
cG=nGV-1 is the inverse of the molar volume, Vm,G (Eq. c; Cohen 2008 IUPAC Green Book),
Eq. 3:  Vm,G(g) = VnG-1 = RTp-1
where the last expression is another form of the ideal gas law (Eq. c). Prior to 1982 the standard pressure has been defined as 101.325 kPa (STPD). Inserting this standard pressure, standard temperature of 273.15 K, and the corresponding value of RT=2271 J/mol into Eq. 3, yields the familiar value for the molar volume of an ideal gas of 22.414 L鈭檓ol-1. But Vm,G(g) = 22.711 L鈭檓ol-1 at 100 kPa, compared to Vm,O2(g) = 22.689 L鈭檓ol-1 under these standard conditions. The ratio of these molar volumes is 0.999, such that we can practically treat oxygen in the gas phase as an ideal gas.
A distinction has to be made between solubility of an ideal gas in the gas phase, SG(g), with an activity coefficient equal to one, and oxygen solubility of a real gas in the aqueous phase, such as SO2(aq), with an activity coefficient, O2, obtained from the experimentally determined solubility of dissolved oxygen.
The definition of (relative) activity of oxygen is (concentration basis; Cohen 2008 IUPAC Green Book),
Eq. 4:  aO2 = O2cO2c-1 ; c掳=1 mol路L-1 
At equilibrium between the gas phase and aqueous phase at a constant pressure, p, the activity of oxygen is equal in the two phases,
Eq. 5:  aO2*(aq) = aO2*(g) 
c掳 cancels when inserting Eq. 4 into Eq. 5, and solving for the aqueous activity coefficient,
Eq. 6:  O2(aq) = O2(g)路cO2*(g)路cO2*(aq)-1 
The equilibrium concentrations, c*, in Eq. 6 are obtained from the solubilities (Eq. 1), and the gas pressure cancels in the ratio, since p is equal in both phases,
Eq. 7:  O2(aq) = O2(g)路SO2(g)路SO2(aq)-1 
Table 1
Oxygen solubilities (Forstner and Gnaiger 1983; MiPNet06.03 POS-calibration-SOP) and the constants defined above are used in these equations to obtain the activity coefficient of dissolved oxygen (Eq. 7) as a function of temperature, summarized in Tab. 1.
The solubility of an ideal gas in the gas phase, SG(g) [碌M路kPa-1] (Eq. 2), is compared in Tab. 1 to the oxygen solubility in pure water, SO2(aq) (for which frequently the abbreviated symbol SO2 is sufficient), and in MiR05. The activity coefficient of dissolved oxygen, O2(aq), is the ratio of the oxygen solubility in gas to aqueous solution (Eq. 7), which is a concentration ratio at equilibrium, cO2*(g)/cO2*(aq) (Eq. 6; O2(g)=1). O2(aq) increases from 20 at 0 掳C to 38 at 40 掳C (Tab. 1). Importantly, the activities and chemical potentials of oxygen in the gas and aqueous phase are equal at equilibrium, when concentrations in the aquesous phase vary 20- to 40-fold, taking into account that the aqueous phase under experimental conditions with mitochondria or cells is a physiological salt solution (MiR05; Tab. 1), in which the oxygen solubility is further reduced (see Oxygen solubility factor).
The definition of activity in the gas and aqueous phase depends on the definition of the standard state. In this context, it is 'advantageous to choose the standard state of unit activity as that in which the partial pressure of the gas is unity at a given temperature' (Hitchman and Gnaiger 1983).

Numerical examples for oxygen solubility and the activity of dissolved oxygen

Further application of the concept of oxygen solubility introduced above requires the following constants:
  • (a) The volume fraction of oxygen in dry air is constant at 0.20946.
  • (b) The saturation water vapour pressure at 25 掳C is 3.17 kPa. The partial pressure of oxygen in water vapour saturated air at 25 掳C and barometric pressure of 100 kPa equals (100-3.17)路0.20946 = 20.28 kPa. The oxygen solubility in pure water at 25 掳C is 12.56 碌M/kPa (Tab. 1).
  • (c) The saturation water vapour pressure at 37 掳C is 6.27 kPa. The partial pressure of oxygen in water vapour saturated air at 37 掳C and barometric pressure of 100 kPa equals (100-6.27)路0.20946 = 19.63 kPa. The oxygen solubility in pure water at 37 掳C is 10.56 碌M/kPa (Tab. 1).
  • (d) The oxygen solubility factor of the medium MiR05 relative to pure water is 0.92 at 25 掳C and 37 掳C (Tab. 1).

  1. An aqueous solution of pure water in equilibrium with air at standard barometric pressure (100 kPa) is heated from 25 掳C to 37 掳C, maintaining equilibrium between the aqueous and gaseous phase, achieved by continuous stirring of the aqueous phase in the 'open chamber'. The concentration of dissolved oxygen changes from 254.7 碌M at 25 掳C to 207.3 碌M at 37 掳C. The partial pressure of oxygen changes from 20.3 to 19.6 kPa.
  2. An aqueous solution of pure water in equilibrium with air at standard barometric pressure (100 kPa) changed from pure water to a physiological salt solution (MiR05) at 37 掳C. The concentration of dissolved oxygen changes from 207.3 碌M in pure water to 190.7 碌M in MiR05. The partial pressure of oxygen remains constant at 19.6 kPa.
  3. An aqueous solution (MiR05) in equilibrium with air at standard barometric pressure (100 kPa) and 25 掳C is heated in a closed system from the initial temperature of 25 掳C to 37 掳C. If we ignore in a first approximation the thermal volume expansion of water [K-1], the concentration remains constant at 234.4 碌M, since oxygen cannot be exchanged across the boundaries of the closed system. The actual concentration at 37 掳C (233.6 碌M) declines relative to = 0 K-1 by <0.4 % ( = 0.000207路K-1 at 20 掳C and 0.000385路K-1 at 40 掳C (The Physics Hypertextbook, retrieved 2021-12-19). The partial pressure of oxygen pO2 is initially 20.3 kPa at 25 掳C (234.4/11.56). pO2 increases upon heating by 12 掳C to 37 掳C in the closed system to pO2 = 24.0 kPa (233.6/9.72). The total partial pressure of the gases in solution increases to >100 kPa, which leads to gas bubble formation, if the closed system is maintained at constant barometric pressure, as is the case in a respirometer with a chamber that is closed by a stopper with a titration capillary, through which the excess aqueous volume of thermal expansion escapes and the barometric pressure is kept constant.


Bioblast linkReferenceYear
Cohen ER, Cvitas T, Frey JG, Holmstr枚m B, Kuchitsu K, Marquardt R, Mills I, Pavese F, Quack M, Stohner J, Strauss HL, Takami M, Thor HL (2008) Quantities, Units and Symbols in Physical Chemistry. IUPAC Green Book 3rd Edition, 2nd Printing, IUPAC & RSC Publishing, Cambridge.2008
Forstner H, Gnaiger E (1983) Calculation of equilibrium oxygen concentration. In: Gnaiger E, Forstner H (eds) Polarographic oxygen sensors. Aquatic and physiological applications. Springer, Berlin, Heidelberg, New York:321-33.1983
Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. 2020.2
Gnaiger E et al 鈥 MitoEAGLE Task Group (2020) Mitochondrial physiology. 2020.1
Hitchman ML, Gnaiger E (1983) A thermodynamic consideration of permeability coefficients of membranes. In: Polarographic Oxygen Sensors. Aquatic and Physiological Applications. Gnaiger E, Forstner H (eds), Springer, Berlin, Heidelberg, New York:31-6.1983
O2k Quality Control 1: Polarographic oxygen sensors and accuracy of calibration.


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Molar mass
Barometric pressure
Chemiosmotic pressure
Gas pressure
Osmotic pressure
Oxygen pressure
Solubility = concentration/pressure
Solubility factor
Oxygen solubility
Boltzmann constant
Gas constant
Related keyword lists
Keywords: Oxygen signal
Keywords: Normalization


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