Information about Henry's Law
In chemistry, Henry's law is one of the gas laws, formulated by William Henry. It states that:
where:
Taking the natural logarithm of the formula, gives us the more commonly used formula:[1]
Some values for k include:
when these gases are dissolved in water at 298 kelvin.
Note that in the above, the unit of concentration was chosen to be molarity. Hence the dimensional units: L is liters of solution, atm is the partial pressure of the gaseous solute above the solution (in atmospheres of absolute pressure), and mol is the moles of the gaseous solute in the solution. Also note that the Henry's Law constant, k, varies with the solvent and the temperature.
As discussed in the next section, there are other forms of Henry's Law each of which defines the constant k differently and requires different dimensional units.[2] The form of the equation presented above is consistent with the given example numerical values for oxygen, carbon dioxide and hydrogen and with their corresponding dimensional units.
where:
As can be seen by comparing the equations in the above table, the Henry's Law constant
is simply the inverse of the constant
. Since all
may be referred to as the Henry's Law constant, readers of the technical literature must be quite careful to note which version of the Henry's Law equation is being used.[2]
It should also be noted the Henry's Law is a limiting law that only applies for dilute enough solutions. The range of concentrations in which it applies becomes narrower the more the system diverges from non-ideal behavior. Roughly speaking, that is the more chemically different the solute is from the solvent.
It also only applies for solutions where the solvent does not react chemically with the gas being dissolved. A common example of a gas that does react with the solvent is carbon dioxide, which rapidly forms hydrated carbon dioxide and then carbonic acid (H2CO3) with water.
where
The above equation is an approximation only and should be used only when no better experimentally derived formula for a given gas exists.
The following table lists some values for constant C (dimension of kelvins) in the equation above:
Because solubility of gases is decreasing with increasing temperature, the partial pressure a given gas concentration has in liquid must increase. While heating water (saturated with nitrogen) from 25°C to 95°C the solubility will decrease to about 43% of its initial value. This can be verified when heating water in a pot. Small bubbles evolve and rise, long before the water reaches boiling temperature. Similarly, carbon dioxide from a carbonated drink escapes much faster when the drink is not cooled because of the increased partial pressure of CO2 in higher temperatures. Partial pressure of CO2 in seawater doubles with every 16 K increase in temperature.[5]
The constant C may be regarded as:
where
where:
where:
If the solution is ideal, both components follow Raoult's law over the entire composition range, but Henry noticed that at low concentrations of non-ideal solutions, the constant of proportionality is not p*. Therefore Henry's law uses an empirically-derived constant, k, based on an infinitely-dilute solution, i.e. x = 0, that is specific to the components in the mixture and the temperature.
In most systems, the laws can only be applied over very limited concentrations at the extreme ends of the mole-fraction range. Raoult's law, which uses the vapor pressure of the pure component, is best used for the major component (solvent) and in mixtures of similar components. Henry's law applies to the minor component (solute) in dilute solutions.
In ideal-dilute solutions, the minor component follows Henry's law, while the solvent obeys Raoult's law. This is proved by the Gibbs-Duhem equation.
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- At a constant temperature, the amount of a given gas dissolved in a given type and volume of liquid is directly proportional to the partial pressure of that gas in equilibrium with that liquid.
Formula and Henry constant
A formula for Henry's Law is:where:
is approximately 2.7182818, the base of the natural logarithm (also called Euler's number)
is the partial pressure of the solute above the solution
is the concentration of the solute in the solution (in one of its many units)
is the Henry's Law constant, which has units such as L·atm/mol, atm/(mol fraction) or Pa·m3/mol.
Taking the natural logarithm of the formula, gives us the more commonly used formula:[1]
Some values for k include:
- oxygen (O2) : 769.2 L·atm/mol
- carbon dioxide (CO2) : 29.4 L·atm/mol
- hydrogen (H2) : 1282.1 L·atm/mol
when these gases are dissolved in water at 298 kelvin.
Note that in the above, the unit of concentration was chosen to be molarity. Hence the dimensional units: L is liters of solution, atm is the partial pressure of the gaseous solute above the solution (in atmospheres of absolute pressure), and mol is the moles of the gaseous solute in the solution. Also note that the Henry's Law constant, k, varies with the solvent and the temperature.
As discussed in the next section, there are other forms of Henry's Law each of which defines the constant k differently and requires different dimensional units.[2] The form of the equation presented above is consistent with the given example numerical values for oxygen, carbon dioxide and hydrogen and with their corresponding dimensional units.
Other Forms of Henry's Law
There are various other forms Henry's Law which are discussed in the technical literature.[3][4][2]| equation: | ![]() | ![]() | ![]() | ![]() |
|---|---|---|---|---|
| dimension: | ![]() | ![]() | ![]() | ![]() |
| O2 | 769.23 | 1.3 E-3 | 4.259 E4 | 3.180 E-2 |
| H2 | 1282.05 | 7.8 E-4 | 7.099 E4 | 1.907 E-2 |
| CO2 | 29.41 | 3.4 E-2 | 0.163 E4 | 0.8317 |
| N2 | 1639.34 | 6.1 E-4 | 9.077 E4 | 1.492 E-2 |
| He | 2702.7 | 3.7 E-4 | 14.97 E4 | 9.051 E-3 |
| Ne | 2222.22 | 4.5 E-4 | 12.30 E4 | 1.101 E-2 |
| Ar | 714.28 | 1.4 E-3 | 3.955 E4 | 3.425 E-2 |
| CO | 1052.63 | 9.5 E-4 | 5.828 E4 | 2.324 E-2 |
where:
= liters of solution
= partial pressure of gas above the solution, in atmospheres of absolute pressure
= mole fraction of gas in solution = moles of gas per total moles ≈ moles of gas per mole of water
= atmospheres of absolute pressure
As can be seen by comparing the equations in the above table, the Henry's Law constant
is simply the inverse of the constant
. Since all
may be referred to as the Henry's Law constant, readers of the technical literature must be quite careful to note which version of the Henry's Law equation is being used.[2]
It should also be noted the Henry's Law is a limiting law that only applies for dilute enough solutions. The range of concentrations in which it applies becomes narrower the more the system diverges from non-ideal behavior. Roughly speaking, that is the more chemically different the solute is from the solvent.
It also only applies for solutions where the solvent does not react chemically with the gas being dissolved. A common example of a gas that does react with the solvent is carbon dioxide, which rapidly forms hydrated carbon dioxide and then carbonic acid (H2CO3) with water.
Temperature dependence of the Henry constant
When the temperature of a system changes, the Henry constant will also change.[2] This is why some people prefer to name it Henry coefficient. There are multiple equations assessing the effect of temperature on the constant. A simple example is [4], which is a form of the van 't Hoff equation:where
- k for a given temperature is the Henry's Law constant (as defined in the first section of this article), identical with kH,pc defined in Table 1,
- T is in kelvins,
- the index
(Theta) refers to the standard temperature (298K).
The above equation is an approximation only and should be used only when no better experimentally derived formula for a given gas exists.
The following table lists some values for constant C (dimension of kelvins) in the equation above:
| Gas | O2 | H2 | CO2 | N2 | He | Ne | Ar | CO |
| C | 1700 | 500 | 2400 | 1300 | 230 | 490 | 1300 | 1300 |
The constant C may be regarded as:
where
is the enthalpy of solution
is the gas constant.
Henry's law in geophysics
In geophysics a version of Henry's law applies to the solubility of a noble gas in contact with silicate melt. One equation used iswhere:
- subscript m = melt
- subscript g = gas phase
= the number densities of the solute gas in the melt and gas phase
an inverse temperature scale
= the Boltzmann constant
and
= the excess chemical potential of the solute in the two phases.
Henry's law versus Raoult's law
Both Henry's law and Raoult's law state that the vapor pressure of a component, p, is proportional to its concentration.- Henry's law:

- Raoult's law:

where:
is the mole fraction of the component;
is the Henry constant; (Note that the numerical value and dimensions of this constant change when mole fractions are used rather than molarity, as seen in Table 1.)
is the equilibrium vapor pressure of the pure component.
If the solution is ideal, both components follow Raoult's law over the entire composition range, but Henry noticed that at low concentrations of non-ideal solutions, the constant of proportionality is not p*. Therefore Henry's law uses an empirically-derived constant, k, based on an infinitely-dilute solution, i.e. x = 0, that is specific to the components in the mixture and the temperature.
In most systems, the laws can only be applied over very limited concentrations at the extreme ends of the mole-fraction range. Raoult's law, which uses the vapor pressure of the pure component, is best used for the major component (solvent) and in mixtures of similar components. Henry's law applies to the minor component (solute) in dilute solutions.
In ideal-dilute solutions, the minor component follows Henry's law, while the solvent obeys Raoult's law. This is proved by the Gibbs-Duhem equation.
See also
References
1. ^ University of Delware physical chemistry lecture
2. ^ Francis L. Smith and Allan H. Harvey (September 2007). "Avoid Common Pitfalls When Using Henry's Law". CEP (Chemical Engineering Progress). ISSN 0360-7275.
3. ^ University of Arizona chemistry class notes
4. ^ An extensive list of Henry's Law constants, and a conversion tool
5. ^ Takahashi, T; Sutherland, SC; Sweeney, C; Poisson, A; Metzl, N; Tilbrook, B; Bates, N; Wanninkhof, R; Feely, RA; Sabine, C; Olafsson, J; Nojiri, Y "Global sea-air CO2 flux based on climatological surface ocean pCO2 and seasonal biological and temperature effects" Deep-Sea Research (Part II, Topical Studies in Oceanography) [Deep-Sea Research (II Top. Stud. Oceanogr.)] 49, 9-10, pp. 1601-1622, 2002
2. ^ Francis L. Smith and Allan H. Harvey (September 2007). "Avoid Common Pitfalls When Using Henry's Law". CEP (Chemical Engineering Progress). ISSN 0360-7275.
3. ^ University of Arizona chemistry class notes
4. ^ An extensive list of Henry's Law constants, and a conversion tool
5. ^ Takahashi, T; Sutherland, SC; Sweeney, C; Poisson, A; Metzl, N; Tilbrook, B; Bates, N; Wanninkhof, R; Feely, RA; Sabine, C; Olafsson, J; Nojiri, Y "Global sea-air CO2 flux based on climatological surface ocean pCO2 and seasonal biological and temperature effects" Deep-Sea Research (Part II, Topical Studies in Oceanography) [Deep-Sea Research (II Top. Stud. Oceanogr.)] 49, 9-10, pp. 1601-1622, 2002
External links
- www.henrys-law.org - Large compilation of Henry's law constants
- New 'no air tanks' diving system, based on Henry's law - An article with flash presentation
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The gas laws are a set of laws that describe the relationship between thermodynamic temperature (T), pressure (P) and volume (V) of gases. They are a loose collection of rules developed between the late Renaissance and early 19th century.
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William Henry (December 12, 1775—September 2, 1836) was an English chemist.
William Henry, the son of Thomas Henry (1734-1816), an apothecary and writer on chemistry, was born in Manchester.
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William Henry, the son of Thomas Henry (1734-1816), an apothecary and writer on chemistry, was born in Manchester.
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In a mixture of ideal gases, each gas has a partial pressure which is the pressure which the gas would have if it alone occupied the volume. The total pressure of a gas mixture is the sum of the partial pressures of each individual gas in the mixture.
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The natural logarithm, formerly known as the hyperbolic logarithm, is the logarithm to the base e, where e is an irrational constant approximately equal to 2.718281828459.
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e is the unique real number such that the value of the derivative (slope of the tangent line) of f(x) = ex at the point x = 0 is exactly 1.
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In a mixture of ideal gases, each gas has a partial pressure which is the pressure which the gas would have if it alone occupied the volume. The total pressure of a gas mixture is the sum of the partial pressures of each individual gas in the mixture.
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This article is about chemical solutions. For other uses, see Solution (disambiguation).
In chemistry, a solution is a homogeneous mixture composed of two or more substances...... Click the link for more information.
This article is about chemical solutions. For other uses, see Solution (disambiguation).
In chemistry, a solution is a homogeneous mixture composed of two or more substances...... Click the link for more information.
In chemistry, concentration is the measure of how much of a given substance there is mixed with another substance. This can apply to any sort of chemical mixture, but most frequently the concept is limited to homogeneous solutions, where it refers to the amount of
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The natural logarithm, formerly known as the hyperbolic logarithm, is the logarithm to the base e, where e is an irrational constant approximately equal to 2.718281828459.
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2, −1
(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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Carbon dioxide is a chemical compound composed of two oxygen atoms covalently bonded to a single carbon atom. It is a gas at standard temperature and pressure and exists in Earth's atmosphere in this state.
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1, −1
(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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Water is a common chemical substance that is essential to all known forms of life.[1] In typical usage, water refers only to its liquid form or state, but the substance also has a solid state, ice, and a gaseous state, water vapor.
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The kelvin (symbol: K) is a unit increment of temperature and is one of the seven SI base units. The Kelvin scale is a thermodynamic (absolute) temperature scale where absolute zero — the coldest possible temperature — is zero kelvins
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2, −1
(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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(neutral oxide)
Electronegativity 3.44 (Pauling scale)
Ionization energies
(more) 1st: 1313.9 kJmol−1
2nd: 3388.3 kJmol−1
3rd: 5300.5 kJmol−1
Atomic radius 60 pm
Atomic radius (calc.
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1, −1
(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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(amphoteric oxide)
Electronegativity 2.20 (Pauling scale) More
Atomic radius 25 pm
Atomic radius (calc.) 53 pm
Covalent radius 37 pm
Van der Waals radius 120 pm
Miscellaneous
Thermal conductivity (300 K) 180.
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Carbon dioxide is a chemical compound composed of two oxygen atoms covalently bonded to a single carbon atom. It is a gas at standard temperature and pressure and exists in Earth's atmosphere in this state.
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3, 5, 4, 2
(strongly acidic oxide)
Electronegativity 3.04 (Pauling scale)
Ionization energies
(more) 1st: 1402.3 kJmol−1
2nd: 2856 kJmol−1
3rd: 4578.1 kJmol−1
Atomic radius 65 pm
Atomic radius (calc.
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(strongly acidic oxide)
Electronegativity 3.04 (Pauling scale)
Ionization energies
(more) 1st: 1402.3 kJmol−1
2nd: 2856 kJmol−1
3rd: 4578.1 kJmol−1
Atomic radius 65 pm
Atomic radius (calc.
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Helium (He) is a colorless, odorless, tasteless, non-toxic, inert monatomic chemical element that heads the noble gas series in the periodic table and whose atomic number is 2.
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90.48% Ne is stable with 10 neutrons
21Ne 0.27% Ne is stable with 11 neutrons
22Ne 9.25% Ne is stable with 12 neutrons
References
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21Ne 0.27% Ne is stable with 11 neutrons
22Ne 9.25% Ne is stable with 12 neutrons
References
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Argon (IPA:/ˈɑːgɒn/) is a chemical element designated by the symbol Ar. Argon has atomic number 18 and is the third element in group 18 of the periodic table (noble gases).
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Carbon monoxide, with the chemical formula CO, is a colorless, odorless, and tasteless gas. It is the product of the incomplete combustion of carbon-containing compounds, notably in internal-combustion engines.
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The mole (symbol: mol) is the SI base unit that measures an amount of substance. One mole contains Avogadro's number (approximately 6.0221023) entities.
A mole is much like "a dozen" in that both are absolute numbers (having no units) and can describe any type of
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A mole is much like "a dozen" in that both are absolute numbers (having no units) and can describe any type of
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The litre or liter (see spelling differences) is a unit of volume. There are two official symbols, namely the Latin letter L both in lower and upper case: l and L.
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In a mixture of ideal gases, each gas has a partial pressure which is the pressure which the gas would have if it alone occupied the volume. The total pressure of a gas mixture is the sum of the partial pressures of each individual gas in the mixture.
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Standard atmosphere is a pressure defined as 101 325 Pa and used as unit of pressure (symbol: atm). Standard atmosphere is a non-SI unit that is internationally recognized.
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Pressure (symbol: p) is the force per unit area applied on a surface in a direction perpendicular to that surface.
Gauge pressure is the pressure relative to the local atmospheric or ambient pressure.
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Gauge pressure is the pressure relative to the local atmospheric or ambient pressure.
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In chemistry, the mole fraction of a component in a mixture is the relative proportion of molecules belonging to the component to those in the mixture, by number of molecules. It is one way of measuring concentration.
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