Backgroundstates that "supposed that the separation of gas particles one from another in the phase bears the ratio of a small whole number to their interatomic distance in solution. Henry's law follows as a consequence if this ratio is a constant for each gas at a given temperature."
Applications of Henry's law; In production of carbonated beverages: Under high pressure, solubility of increases. On opening the bottle to atmospheric pressure, solubility decreases and the gas bubbles are released from the liquid. ; For climbers or people living at high altitude: Concentration of in the blood and tissues is so low that they feel weak and are unable to think properly, a condition called hypoxia. ; In underwater diving: Gas is breathed at the ambient pressure which increases with depth due to the . Solubility of gases increase at depth in accordance with Henry's law, so the body tissues take on more gas over time until saturated for the depth. When ascending the diver is decompressed and the solubility of the gases dissolved in the tissues decreases accordingly. If the supersaturation is too great, bubbles may form and grow, and the presence of these bubbles can cause blockages in capillaries, or distortion in the more solid tissues which can cause damage known as . To avoid this injury the diver must ascend slow enough that the excess dissolved gas is carried away by the blood and released into the lung gas.
Fundamental types and variants of Henry's law constantsThere are many ways to define the proportionality constant of Henry's law, which can be subdivided into two fundamental types: One possibility is to put the aqueous phase into the numerator and the gaseous phase into the denominator ("aq/gas"). This results in the Henry's law solubility constant . Its value increases with increased solubility. Alternatively, numerator and denominator can be switched ("gas/aq"), which results in the Henry's law volatility constant . The value of decreases with increased solubility. There are several variants of both fundamental types. This results from the multiplicity of quantities that can be chosen to describe the composition of the two phases. Typical choices for the aqueous phase are (), (), and molar mixing ratio (). For the gas phase, molar concentration () and () are often used. It is not possible to use the gas-phase mixing ratio () because at a given gas-phase mixing ratio, the aqueous-phase concentration depends on the total pressure and thus the ratio is not a constant. To specify the exact variant of the Henry's law constant, two superscripts are used. They refer to the numerator and the denominator of the definition. For example, refers to the Henry solubility defined as .
Henry's law solubility constants
Henry solubility defined via concentration ()Atmospheric chemists often define the Henry solubility as :. Here is the concentration of a species in the aqueous phase, and is the partial pressure of that species in the gas phase under equilibrium conditions. The SI unit for is mol/(m3·Pa); however, often the unit M/atm is used, since is usually expressed in M (1M = 1 mol/dm3) and in atm (1atm = 101325Pa).
The dimensionless Henry solubilityThe Henry solubility can also be expressed as the dimensionless ratio between the aqueous-phase concentration of a species and its gas-phase concentration : :. For an ideal gas, the conversion is : where is the gas constant, and is the temperature. Sometimes, this dimensionless constant is called the ''water–air partitioning coefficient'' . It is closely related to the various, slightly different definitions of the ''Ostwald coefficient'' , as discussed by Battino (1984).
Henry solubility defined via aqueous-phase mixing ratio ()Another Henry's law solubility constant is : . Here is the molar mixing ratio in the aqueous phase. For a dilute aqueous solution the conversion between and is: :, where is the density of water and is the molar mass of water. Thus :. The SI unit for is Pa−1, although atm−1 is still frequently used.
Henry solubility defined via molality ()It can be advantageous to describe the aqueous phase in terms of molality instead of concentration. The molality of a solution does not change with , since it refers to the ''mass'' of the solvent. In contrast, the concentration does change with , since the density of a solution and thus its volume are temperature-dependent. Defining the aqueous-phase composition via molality has the advantage that any temperature dependence of the Henry's law constant is a true solubility phenomenon and not introduced indirectly via a density change of the solution. Using molality, the Henry solubility can be defined as : Here is used as the symbol for molality (instead of ) to avoid confusion with the symbol for mass. The SI unit for is mol/(kg·Pa). There is no simple way to calculate from , since the conversion between concentration and molality involves ''all'' solutes of a solution. For a solution with a total of solutes with indices , the conversion is: : where is the density of the solution, and are the molar masses. Here is identical to one of the in the denominator. If there is only one solute, the equation simplifies to : Henry's law is only valid for dilute solutions where and . In this case the conversion reduces further to : and thus :
The Bunsen coefficientAccording to Sazonov and Shaw, the dimensionless Bunsen coefficient is defined as "the volume of saturating gas, V1, reduced to T° = 273.15 K, p° = 1 bar, which is absorbed by unit volume V2* of pure solvent at the temperature of measurement and partial pressure of 1 bar." If the gas is ideal, the pressure cancels out, and the conversion to is simply :, with = 273.15K. Note, that according to this definition, the conversion factor is ''not'' temperature-dependent. Independent of the temperature that the Bunsen coefficient refers to, 273.15K is always used for the conversion. The Bunsen coefficient, which is named after Robert Bunsen, has been used mainly in the older literature.
The Kuenen coefficientAccording to Sazonov and Shaw, the Kuenen coefficient is defined as "the volume of saturating gas V(g), reduced to T° = 273.15 K, p° = bar, which is dissolved by unit mass of pure solvent at the temperature of measurement and partial pressure 1 bar." If the gas is ideal, the relation to is :, where is the density of the solvent, and = 273.15 K. The SI unit for is m3/kg. The Kuenen coefficient, which is named after Johannes Kuenen, has been used mainly in the older literature, and IUPAC considers it to be obsolete.
Henry's law volatility constants
The Henry volatility defined via concentration ()A common way to define a Henry volatility is dividing the partial pressure by the aqueous-phase concentration: : The SI unit for is Pa·m3/mol.
The Henry volatility defined via aqueous-phase mixing ratio ()Another Henry volatility is : The SI unit for is Pa. However, atm is still frequently used.
The dimensionless Henry volatilityThe Henry volatility can also be expressed as the dimensionless ratio between the gas-phase concentration of a species and its aqueous-phase concentration : : In chemical engineering and environmental chemistry, this dimensionless constant is often called the ''air–water partitioning coefficient'' .
Values of Henry's law constantsA large compilation of Henry's law constants has been published by Sander (2015). A few selected values are shown in the table below:
Temperature dependenceWhen the temperature of a system changes, the Henry constant also changes. The temperature dependence of equilibrium constants can generally be described with the van 't Hoff equation, which also applies to Henry's law constants: : where is the enthalpy of dissolution. Note that the letter in the symbol refers to enthalpy and is not related to the letter for Henry's law constants. Integrating the above equation and creating an expression based on at the reference temperature = 298.15 K yields: : The van 't Hoff equation in this form is only valid for a limited temperature range in which does not change much with temperature. The following table lists some temperature dependencies: Solubility of permanent gases usually decreases with increasing temperature at around room temperature. However, for aqueous solutions, the Henry's law solubility constant for many species goes through a minimum. For most permanent gases, the minimum is below 120 °C. Often, the smaller the gas molecule (and the lower the gas solubility in water), the lower the temperature of the maximum of the Henry's law constant. Thus, the maximum is at about 30 °C for helium, 92 to 93 °C for argon, nitrogen and oxygen, and 114 °C for xenon.
Effective Henry's law constantsThe Henry's law constants mentioned so far do not consider any chemical equilibria in the aqueous phase. This type is called the ''intrinsic'', or ''physical'', Henry's law constant. For example, the intrinsic Henry's law solubility constant of formaldehyde can be defined as : In aqueous solution, formaldehyde is almost completely hydrated: :
Dependence on ionic strength (Sechenov equation)Values of Henry's law constants for aqueous solutions depend on the composition of the solution, i.e., on its ionic strength and on dissolved organics. In general, the solubility of a gas decreases with increasing salinity ("salting out"). However, a "salting in" effect has also been observed, for example for the effective Henry's law constant of glyoxal. The effect can be described with the Sechenov equation, named after the Russian physiologist Ivan Sechenov (sometimes the German transliteration "Setschenow" of the Cyrillic name Се́ченов is used). There are many alternative ways to define the Sechenov equation, depending on how the aqueous-phase composition is described (based on concentration, molality, or molar fraction) and which variant of the Henry's law constant is used. Describing the solution in terms of molality is preferred because molality is invariant to temperature and to the addition of dry salt to the solution. Thus, the Sechenov equation can be written as : where is the Henry's law constant in pure water, is the Henry's law constant in the salt solution, is the molality-based Sechenov constant, and is the molality of the salt.
Non-ideal solutionsHenry's law has been shown to apply to a wide range of solutes in the limit of ''infinite dilution'' (''x'' → 0), including non-volatile substances such as sucrose. In these cases, it is necessary to state the law in terms of chemical potentials. For a solute in an ideal dilute solution, the chemical potential depends only on the concentration. For non-ideal solutions, the activity coefficients of the components must be taken into account: :, where for a volatile solute; ''c''° = 1 mol/L. For non-ideal solutions, the activity coefficient ''γc'' depends on the concentration and must be determined at the concentration of interest. The activity coefficient can also be obtained for non-volatile solutes, where the vapor pressure of the pure substance is negligible, by using the Gibbs-Duhem relation: : By measuring the change in vapor pressure (and hence chemical potential) of the solvent, the chemical potential of the solute can be deduced. The standard state for a dilute solution is also defined in terms of infinite-dilution behavior. Although the standard concentration ''c''° is taken to be 1 mol/l by convention, the standard state is a hypothetical solution of 1 mol/l in which the solute has its limiting infinite-dilution properties. This has the effect that all non-ideal behavior is described by the activity coefficient: the activity coefficient at 1 mol/l is not necessarily unity (and is frequently quite different from unity). All the relations above can also be expressed in terms of molality, molalities ''b'' rather than concentrations, e.g.: : where for a volatile solute; ''b''° = 1 mol/kg. The standard chemical potential ''μm''°, the activity coefficient ''γm'' and the Henry's law constant ''K''H,''b'' all have different numerical values when molalities are used in place of concentrations.
Solvent mixturesHenry law constant H2, M for a gas 2 in a mixture of solvents 1 and 3 is related to the constants for individual solvents H21 and H23: : where a13 is the interaction parameter of the solvents from Wohl expansion of the excess chemical potential of the ternary mixtures.
In geochemistryIn geochemistry, a version of Henry's law applies to the solubility of a noble gas in contact with silicate melt. One equation used is : where :''C'' is the number concentrations of the solute gas in the melt and gas phases, :''β'' = 1/''k''B''T'', an inverse temperature parameter (''k''B is the Boltzmann constant), :''µ''E is the excess chemical potentials of the solute gas in the two phases.
Comparison to Raoult's lawHenry's law is a limiting law that only applies for "sufficiently dilute" solutions, while Raoult's law is generally valid when the liquid phase is almost pure or for mixtures of similar substances. The range of concentrations in which Henry's law applies becomes narrower the more the system diverges from ideal behavior. Roughly speaking, that is the more chemically "different" the solute is from the solvent. For a dilute solution, the concentration of the solute is approximately proportional to its mole fraction ''x'', and Henry's law can be written as : This can be compared with Raoult's law: : where ''p''* is the vapor pressure of the pure component. At first sight, Raoult's law appears to be a special case of Henry's law, where ''K''H = ''p''*. This is true for pairs of closely related substances, such as benzene and toluene, which obey Raoult's law over the entire composition range: such mixtures are called ''ideal mixtures''. The general case is that both laws are Limit of a function, limit laws, and they apply at opposite ends of the composition range. The vapor pressure of the component in large excess, such as the solvent for a dilute solution, is proportional to its mole fraction, and the constant of proportionality is the vapor pressure of the pure substance (Raoult's law). The vapor pressure of the solute is also proportional to the solute's mole fraction, but the constant of proportionality is different and must be determined experimentally (Henry's law). In mathematical terms: :Raoult's law: :Henry's law: Raoult's law can also be related to non-gas solutes.
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