## Introduction

#### Web Version 1.0

A database containing solubilities originally published in the IUPAC (International Union for Pure and Applied Chemistry) - NIST Solubility Data Series is now available online.

Mutual solubilities and liquid-liquid equilibria of binary, ternary and quaternary systems are presented. Typical solvents and solutes include water, sea water, heavy water, inorganic compounds, and a variety of organic compounds such as hydrocarbons, halogenated hydrocarbons, alcohols, acids, esters and nitrogen compounds. For many systems, sufficient data were available to allow critical evaluation. Data are expressed as mass and mole fractions as well as the originally reported units.

Scope: There are over 67,500 solubility measurements, compiled from 18 volumes of the IUPAC Solubility Data Series. There are about 1800 chemical substances in the database and 5200 systems, of which 473 have been critically evaluated. The database has over 1800 references.

*Updated: March, 2006*

IUPAC-NIST Solubility Data Series

V.P. Sazonov and D.G. Shaw

### 1. Introduction to the Solubility Data Series

1.1 The Nature of the Project

The Solubility Data Project (SDP) has as its aim a comprehensive review of published data for solubilities of gases, liquids and solids in liquids or solids. Data of suitable precision are compiled for each publication on data sheets in a uniform format. The data for each system are evaluated and, where data from different sources agree sufficiently, recommended values are proposed. The evaluation sheets, recommended values, and compiled data sheets are published on consecutive pages.

This series is concerned primarily with liquid-liquid systems, but a limited number or related solid-liquid, fluid-fluid and multi-component (organic-water-salt) systems are included where it is considered logical and appropriate. Solubilities at elevated and low temperatures and at elevated pressures have also been included, as it is considered inappropriate to establish artificial limits on the data presented if they are considered relevant or useful.

For some systems, the two components may be miscible in all proportions at certain temperatures and pressures. Data on reported miscibility gaps and upper and lower critical solution temperatures are included where appropriate and when available.

1.2. Compilations and Evaluations

The formats for the compilations and critical evaluations have been standardized for all volumes. A description of these formats follows.

1.3. Compilations

The format used for the compilations is, for the most part, self-explanatory. A compilation sheet is divided into boxes, with detailed contents described below.

*Components*: Each component is listed according to IUPAC name, formula, and
Chemical Abstracts (CA) Registry Number. The Chemical Abstracts name is also included if this differs from
the IUPAC name, as are trivial names if appropriate. IUPAC and common names are cross-referenced to
Chemical Abstracts names in the System Index. The formula is given either in terms of the IUPAC or Hill
^{1} system and the choice of formula is governed by what is usual
for most current users: i.e., IUPAC for inorganic compounds, and Hill system for organic compounds.
Components are ordered on a given compilation sheet according to:

- saturating components;
- non-saturating components in alphanumerical order;
- solvents in alphanumerical order.

The saturating components are arranged in order according to the IUPAC 18-column periodic table with two additional rows: Columns 1 and 2: H, alkali elements, ammonium, alkaline earth elements;

- Columns 3 to 12: transition elements;
- Columns 13 to 17: boron, carbon, nitrogen groups; chalcogenides, halogens;
- Column 18: noble gases;
- Row 1: Ce to Lu;
- Row 2: Th to the end of the known elements, in order of atomic number.

Organic compounds within each Hill formula are ordered in the following succession:

- by degree of unsaturation;
- by order of increasing chain length in the parent hydrocarbon;
- by order of increasing chain length of hydrocarbon branches;
- numerically by position of unsaturation;
- numerically by position by substitution;
- alphabetically by IUPAC name.

Example:

C_{5}H_{8} |
cyclopentane |

2-methyl-1,3-butadiene | |

1,4-pentadiene | |

1-pentyne | |

C_{5}H_{10} |
cyclopentane |

3-methyl-1-butene | |

2-methyl-2-butene | |

1-pentene | |

2-pentene | |

C_{5}H_{12} |
2,2-dimethylpropane |

2-methylbutane | |

pentane | |

C_{5}H_{12}O |
2,2-dimethyl-1-propanol |

2-methyl-1-butanol | |

2-methyl-2-butanol | |

3-methyl-1-butanol | |

3-methyl-2-butanol | |

1-pentanol | |

2-pentanol | |

3-pentanol | |

C_{6}H_{12}O |
cyclohexanol |

4-methyl-1-penten-3-ol | |

1-hexen-3-ol | |

4-hexen-3-ol |

Deuterated (2H) compounds follow immediately the corresponding H compounds.

*Original Measurements*: References are abbreviated in the forms given by
Chemical Abstracts Service Source Index (CASSI). Names originally in other than Roman alphabets are given
as transliterated by Chemical Abstracts. In the case of multiple entries (for example, translations) an
asterisk indicates the publication used for compilation of the data.

*Variables*: Ranges of temperature, pressure, etc. are indicated here.

*Prepared by*: The names of all compilers are given here.

*Experimental Values*: Components are described as (1), (2), etc., as defined
in the "Components" box. Data are reported in the units used in the original publication, with the
exception that modern names for units and quantities are used; e.g., mass per cent for weight per cent; mol
dm^{–3} for molar; etc. In most cases, both mass and molar values are given. Usually, only one
type of value (e.g., mass per cent) is found in the original paper, and the compiler has added the other
type of value (e.g., mole per cent) from computer calculations based on 1989 atomic weights
^{2}. Temperatures are expressed as *t*/°C, *t*/°F or
*T*/K as in the original; if necessary, conversions to *T*/K are made, sometimes in the
compilations, and always in the critical evaluation. However, the author's units are expressed according to
IUPAC recommendations^{3} as far as possible.

Errors in calculations, fitting equations, etc. are noted, and where possible corrected. Material inserted by the compiler is identified by the word "compiler" or by the compiler's name in parentheses or in a footnote. In addition, compiler-calculated values of mole or mass fractions are included if the original data do not use these units. If densities are reported in the original paper, conversions from this is done in the evaluation, with the values and sources of the densities concentrations to mole fractions are included, but otherwise being quoted and referenced.

Details of smoothing equations (with limits) are included if they are present in the original publication and if the temperature or pressure ranges are wide enough to justify this procedure and if the compiler finds that the equations are consistent with the data.

The precision of the original data is preserved when derived quantities are calculated, if necessary by the inclusion of one additional significant figure. In some cases graphs have been included, either to illustrate presented data more clearly, or if this is the only information in the original. Full grids are not usually inserted as it is not intended that users should read data from the graphs.

*Method*: The apparatus and procedure are mentioned briefly. Abbreviations used
in Chemical Abstracts are often used here to save space, reference being made to sources of further detail
if these are cited in the original paper.

*Source and Purity of Materials*: For each component, referred to as (1), (2),
etc., the following information (in this order and in abbreviated form) is provided if available in the
original paper: source and specified method of preparation; properties; degree of purity.

*Estimated Errors*: If estimated errors were omitted by the original authors,
and if relevant information is available, the compilers have attempted to estimate errors (identified by
"compiler" or the compiler's name in parentheses or in a footnote) from the internal consistency of data
and type of apparatus used. Methods used by the compilers for estimating and reporting errors are based
on Ku and Eisenhart^{4}.

*Comments and/or Additional Data*: Many compilations include this section which
provides short comments relevant to the general nature of the work or additional experimental and
thermodynamic data which are judged by the compiler to be of value to the reader.

*References*: The format for these follows the format for the Original
Measurements box, except that final page numbers are omitted. References (usually cited in the original
paper) are given where relevant to interpretation of the compiled data, or where cross-reference can be
made to other compilations.

1.4. Evaluations

The evaluator's task is to assess the reliability and quality of the data, to estimate errors where necessary, and to recommend "best" values. The evaluation takes the form of a summary in which all the data supplied by the compiler have been critically reviewed. There are only three boxes on a typical evaluation sheet, and these are described below.

*Components*: The format is the same as on the Compilation sheets.

*Evaluator*: The name and affiliation of the evaluator(s) and date up to
which the literature was checked.

*Critical Evaluation*:

(a) Critical text. The evaluator checks that the compiled data are correct, assesses their reliability and quality, estimates errors where necessary, and recommends numerical values based on all the published data (including theses, reports and patents) for each given system. Thus, the evaluator reviews the merits or shortcomings of the various data. Only published data are considered. Documented rejection of some published data may occur at this stage, and the corresponding compilations may be removed.

The solubility of comparatively few systems is known with sufficient accuracy to enable a set of recommended values to be presented. Although many systems have been studied by at least two workers, the range of temperatures is often sufficiently different to make meaningful comparison impossible.

Occasionally, it is not clear why two groups of workers obtained very different but internally consistent sets of results at the same temperature, although both sets of results were obtained by reliable methods. In such cases, a definitive assessment may not be possible. In some cases, two or more sets of data have been classified as tentative even though the sets are mutually inconsistent.

(b) Fitting equations. If the use of a smoothing equation is justifiable the evaluator may provide an equation representing the solubility as a function of the variables reported on all the compilation sheets, stating the limits within which it should be used.

(c) Graphical summary. In addition to (b) above, graphical summaries are often given.

(d) Recommended values. Data are recommended if the results of at least two independent groups are available and they are in good agreement, and if the evaluator has no doubt as to the adequacy and reliability of the applied experimental and computational procedures. Data are reported as tentative if only one set of measurements is available, or if the evaluator considers some aspect of the computational or experimental method as mildly undesirable but estimates that it should cause only minor errors. Data are considered as doubtful if the evaluator considers some aspect of the computational or experimental method as undesirable but still considers the data to have some value where the order of magnitude of the solubility is needed. Data determined by an inadequate method or under ill-defined conditions are rejected. However, references to these data are included in the evaluation together with a comment by the evaluator as to the reason for their rejection.

(e) References. All pertinent references are given here, including all those publications appearing in the accompanying compilation sheets and those which, by virtue of their poor precision, have been rejected and not compiled.

(f) Units. While the original data may be reported in the units used by the
investigators, the final recommended values are reported in SI units^{3
} when the data can be converted accurately.

1.5. Quantities and Units Used in Compilation and Evaluation of Solubility Data

1.5.1. Mixtures, Solutions and Solubilities

A *mixture*^{5,6
} describes a gaseous, liquid or solid phase containing more than one substance, where the substances
are all treated in the same way.

A *solution*^{5,6
} describes a liquid or solid phase containing more than one substance, when for convenience one of
the substances, which is called the *solvent*, and may itself be a mixture, is treated differently
than the other substances, which are called *solutes*. If the sum of the mole fractions of the solutes
is small compared to unity, the solution is called a *dilute solution*.

The *solubility* of a solute 1 (solid, liquid or gas) is the analytical
composition of a saturated solution, expressed in terms of the proportion of the designated solute in a
designated solvent^{7}.

"Saturated" implies equilibrium with respect to the processes of dissolution and demixing; the equilibrium may be stable or metastable. The solubility of a substance in metastable equilibrium is usually greater than that of the same substance in stable equilibrium.(Strictly speaking, it is the activity of the substance in metastable equilibrium that is greater.) Care must be taken to distinguish true metastability from supersaturation, where equilibrium does not exist.

Either point of view, mixture or solution, may be taken in describing solubility. The two points of view find their expression in the reference states used for definition of activities, activity coefficients and osmotic coefficients. Note that the composition of a saturated mixture (or solution) can be described in terms of any suitable set of thermodynamic components.

1.5.2. Physicochemical Quantities and Units

Solubilities of solids have been the subject of research for a long time, and have been
expressed in a great many ways, as described below. In each case, specification of the temperature and
either partial or total pressure of the saturating gaseous component is necessary. The nomenclature and
units follow, where possible.^{3} A few quantities follow
the ISO standards^{8} or the German
standard^{9};
see a review by Cvitaš^{10} for details.

A note on nomenclature

The nomenclature of the IUPAC Green Book^{3}
calls the solute component B and the solvent component A. In compilations and evaluations, the first-named
component (component 1) is the solute, and the second (component 2 for a two-component system) is the
solvent. The reader should bear these distinctions in nomenclature in mind when comparing equations
given here with those in the Green Book.

1. *Mole fraction* of substance 1, *x*_{1} or *x*(1)
(condensed phases),*y*_{1} (gases):

where *n _{s}* is the amount of substance of

*s*, and

*c*is the number of distinct substances present (often the number of thermodynamic components in the system).

*Mole percent*of substance 1 is 100

*x*

_{1}.

2. *Ionic mole fractions* of salt *i*,* x _{i}*

_{+},

*x*

_{i}_{–}: For a mixture of s binary salts

*i*, each of which ionizes completely into n

_{s+}cations and nu

_{s–}anions, with nu

_{s}= nu

_{s+}+ nu

_{s–}and a mixture of

*p*non-electrolytes

*j*, of which some may be solvent components, a generalization of the definition in

^{11}gives:

The sum of these mole fractions is unity, so that, with *c* = *s* + *p*,

General conversions to other units in multicomponent systems are complicated. For a three-component system containing non-electrolyte 1, electrolyte 2 and solvent 3.

These relations are used in solubility equations for salts, and for tabulation of salt effects on solubilities of gases (see below).

3. *Mass fraction* of substance 1, *w*_{1} or *w*(1):

where *gs* is the mass of substance *s*. *Mass percent* of substance
1 is 100*w*_{1}. The equivalent terms *weight fraction*, *weight percent* and
*g* (1)/100*g* *solution* are no longer used.

4. Molality of solute 1 in a solvent 2, *m*_{1}:

SI base units: mol kg^{–1}. Here, *M*_{2} is the molar mass of the solvent.

5. *Aquamolality*, *Solvomolality* of substance 1 in a mixed solvent with
components 2, 3^{12},*m*_{1}^{(3)}:

SI base units: mol kg^{–1}. Here, the average molar mass of the solvent is

and x_{2}' is the solvent mole fraction of component 2. This term is used most
frequently in discussing comparative solubilities in water (component 2) and heavy water (component 3)
and in their mixtures.

6. *Amount concentration* of solute 1 in a solution of volume *V*,*c*_{1}:

SI base units: mol m^{–3}. The symbol c_{1} is preferred to [formula
of solute], but both are used. The old terms molarity, molar and moles per unit volume are no longer used.

7. *Mole ratio*,*r*_{A,B} (dimensionless)
^{10}

*r*_{A,B} = *n*_{1}/*n*_{2}. (11)

Mass ratio, Z_{A,B}, may be defined analogously^{10}.

Mole and mass fractions are appropriate to either the mixture or the solution point of view. The other quantities are appropriate to the solution point of view only. Conversions between pairs of these quantities can be carried out using the equations given in Table 1 at the end of this Introduction. Other useful quantities will be defined in the prefaces to individual volumes or on specific data sheets.

8. *Mass concentration* of solute 1 in a solution of volume *V*,
*p*1: SI base units: kg m^{–3}.

*ρ*_{1} = *g*_{1}/*V* (12)

9.* Ionic strength*, I_{m} (molality basis), or I_{c} (concentration basis):

*I _{m}* = ½ Σ

_{i}m_{i}z_{i}^{2}

*I*= ½ Σ

_{c}

_{i}c_{i}z_{i}^{2}(13)

where *z _{i}* is the charge number of ion i. While these quantities are
not used generally to express solubilities, they are use to express the compositions of non-saturating
components. For a single salt I with ions of charges

*z*,

_{+}*z*,

_{-}
*I _{m}*

_{ }=

*|z*

_{+}z_{-}|vm_{i}*I*

_{c}_{ }=

*|z*(14)

_{+}z_{-}|vc_{i}Mole and mass fractions are appropriate to either the mixture or the solution point of view. the other quantities are appropriate to the solution point of view only. Conversions between some pairs of these quantities can be carried out using the equations given in Table 1 at the end of this Introduction. Other useful quantities will be defined in the prefaces to individual volumes or on specific data sheets.

In addition to these well defined SI-based units, other units have been used to express the solubilities of gases. Units and nomenclature follow, as modified by IUPAC recommendations. The equations describing Bunsen, Kuenen, Ostwald and absorption coefficients, as well as Henry's law constants, hold for ideal gases and perfect solutions only. Corrections of non-ideality should be made where possible. The corrections are less than 1 % for most gases near atmospheric pressure.

In much published data, the reference pressure is 1 atm = 0.101325 MPa rather than 1 bar = 0.1 MPa.

10. *Bunsen coefficient*, α (dimensionless):

The volume of saturating
gas, *V*_{1}, reduced to *T °* = 273.15 K, *p*° = 1 bar, which is absorbed by unit
volume *V*_{2}* of pure solvent at the temperature of measurement and partial pressure
*p*° = 1 bar. If the gas is ideal, Henry's law (see below) holds, and the liquid is incompressible, then

*α = ( V °*

_{1}/

*V**

*) = (*

_{2}*V*

_{1}/

*V**

*) (*

_{2}*T°/T*) (15)

11. *Kuenen coefficient, S*: The volume of saturating gas, *V*(g), reduced
to *T°* = 273.15 K, *p*° = 1 bar, which is dissolved by unit mass of pure solvent at the
temperature of measurement and partial pressure 1 bar. Thus,

*S = V*

_{1}

*T°*/

*g*

_{2}

*T*=

*αV*

_{m,2}/

*M*

*(16)*

_{2}SI base units: m^{3} kg^{-1}. Here, *M*_{2} is the molar
mass of the solvent. The Kuenen coefficient is proportional to the molality of the dissolved gas.

12.* Ostwald coefficient, L* (dimensionless) :

The volume of saturating gas,
*V*_{1}, absorbed by a volume *V*_{2}* of pure solvent at the temperature and
pressure of the measurement. Thus,

*L* = (*V*_{1}/*V*** _{2}*) = (

*αT*/

*T°*) (

*p°/p*) (17)

The Ostwald coefficient is equal to the ratio of the amount concentrations in the gas and in the liquid.

13.* Absorption coefficient, β* (dimensionless):>The most common of several
definitions of absorption coefficient is the volume of gas, reduced to *T °* = 273.15, p° = 1 bar
absorbed per unit volume of pure solvent at a total pressure of 1 bar. The absorption and Bunsen
coefficients are therefore very similar, and are connected by

β = α (1 - *p*_{2}/*p°*) (18)

14.* Henry's Law constant, K _{H}*:

*K _{H}* = lim

_{x→0 }(

*p*

_{1}/

*x*

_{1}) (19)

SI base units: Pa. Unfortunately, the definition is used often at finite mole fraction, even though this is a limiting law. The following have also been defined at Henry's Law constants:

*K*_{2} = *p*_{1}/*c*_{1}
*K _{c}* =

*c*

_{1}

^{g}/

*c*

_{1}(20)

where superscript g refers to the gas phase. *K*_{2} has SI base units
Pa m^{3} mol^{-1}, and *K*_{c} is dimensionless. The Henry's Law constant
has also been called the Henry coefficient. Henry's Law can be used, with great caution, to convert
data from the experimental pressure to 1 bar if the mole fraction of the gas in the liquid is small, and
the difference in pressures is small.

The relations between the mole fraction solubility and the various quantities given above are as follows. Note again that these relations hold for ideal gaseous and perfect solution phases only.

*x*_{1} = 1/[1 + (*RT°*/*p°*_{1}*V**_{m,2} α)] = 1/[1 + (*RT °*/ *p°*_{1}*M*_{2}*S*)]

= 1/[1 + (*RT*/*p*_{1}*V**_{m,2} *L*)] = 1/[1 + (*RT °*/ *p°**V**_{m,2}*β)]* (21)

15. *Salt effects on the Solubility of Gases*

These are often reported as Sechenov (Setchenow, Setschenow) salt effect parameters
*y* which are defined in various ways. The general semi-empirical Sechenov equation is

log(*z*_{1}°/*z*_{1}) = *k _{syz} y* (22)

where solubility is expressed in quantities *z*, with superscript o designating
pure solvent, and salt composition is expressed in quantities y. The quantities *c*_{2},
*m*_{2}, *x'*_{2}, *I*_{m}, and *I*_{c} are used for
*y*, and quantities *c*_{1}, *m*_{1}, *x*_{1+}, α, *S*
and *L* for *z*, giving 30 definitions of *k _{syz}*. Here, components 1 and 2 are
the gaseous solute and electrolyte, respectively. The ratios of

*z*-values are the same for

*z*=

*c*

_{1}, α, and

*L*and for

*m*

_{1}and

*S*, leaving 15 distinct definitions. If

*z*is the same, the definitions of

*k*are related simply through 10 equations between pairs of

_{syz}*c*

_{2},

*m*

_{2},

*x'*

_{2},

*I*

_{m}, and

*I*

_{c}. Some relations among the definitions, in terms of

*k*,

_{scc}*k*,

_{smm}*k*, are:

_{sxx}
*k _{scc}* =

*k*=

_{scα}*k*= (

_{scL}*m*

_{2}/

*c*

_{2})

*k*= (

_{smc}*x'*

_{2}/

*c*

_{2})

*k*= (

_{sxc}*I*/

_{c}*c*

_{2})

*k*

_{sIcc}
*k _{smm}* = (

*x'*

_{2}/

*m*

_{2})

*k*=

_{sxm}*k*= (

_{smS}*c*

_{2}/

*m*

_{2})

*k*= (

_{scm}*I*/

_{m}*m*

_{2})

*k*(23)

_{sImm}
*k _{sxx}* = (

*c*

_{2}/

*x'*

_{2})

*k*= (

_{scx}*m*

_{2}/

*x'*

_{2})

*k*= (

_{smx}*I*/

_{m}*x'*

_{2})

*k*= (

_{sImx}*I*/

_{c}*x'*

_{2})

*k*

_{sIcx}These relations hold when a single salt is present; note that the relations between
ionic strength and either molality or concentration are simple. If more than one salt is present, the
ionic strength is the only practical quantity to be used for *y*.

Conversions between pairs of *k _{scc}*,

*k*,

_{smm}*k*are more complicated, and can be found using Eqn [5] and Table 1 at the end of the Introduction. For example,

_{sxx}
*k _{sxx}* = ƒ

*(m)*[(

*k*/ν

_{smm}_{2+}) + (1/

*m*

_{2}) log(ƒ(

*m*)/ƒ(

*m*°))] (24)

where

ƒ(*m*) = 1 + (*m*_{1} + ν_{2}*m*_{2})*M*_{3}
ƒ(*m*)*°* = 1 + (*m °*_{1}*m°*_{2})*M*_{3} (25)

Errors in the salt effect parameters, as defined above, can be large. If the relative
standard deviation in measurement of solubility is *s*(*c*_{1})/*c*_{1}, the
relative standard deviation in *k _{scc}* is

*s*(*k _{scc}*)/

*k*= (√2/

_{scc}*c*

_{2}

*k*ln 10)(

_{scc}*s*(

*c*

_{1})/

*c*

_{1}) (26)

For example, for *k _{scc}* = 0.1 and

*c*

_{2}= 0.01 mol dm

^{-3},

*s*(

*k*) /

_{scc}*k*is 30 % when

_{scc}*s*(

*c*

_{1}) /

*c*

_{1}= 0.05 % and 1200 % when

*s*(

*c*

_{1}) /

*c*

_{1}= 2 %. At

*c*

_{2}= 1 mol dm

^{-3}, the corresponding errors are 0.3 % and 12 %, respectively.

If the solubility of a gas is greater than about *x* = 0.01 at partial pressure 1
bar, then several other factors must be taken into account, such as the density of the solution or the
partial molar volume of the dissolved gas. In addition, corrections should be made for non-ideality of the gas.

In addition, the following definitions concerning density are useful in conversions between concentrations and other quantities.

16.* Density (gas)*, *ρ*, or γ:

ρ = *g*/*V* (27)

SI base units: kg m^{–3}. Here *g* is the total mass of the system.

17. *Relative density*, *d* = ρ/ρ°: the ratio of the density of a
mixture at temperature *t*, pressure *p* to the density of a reference substance at temperature
*t'*, pressure *p*'. For liquid solutions, the reference substance is often water at 4 °C, 1 bar.
(In some cases 1 atm is used instead of 1 bar.) The term *specific* gravity is no longer used.

*Thermodynamics of Solubility* Thermodynamic analysis of solubility phenomena
provides a rational basis for the construction of functions to represent solubility data, and thus aids
in evaluation, and sometimes enables thermodynamic quantities to be extracted. Both these are often
difficult to achieve because of a lack of experimental or theoretical activity coefficients. Where
thermodynamic quantities can be found, they are not evaluated critically, since this task would involve
examination of a large body of data that is not directly relevant to solubility. Where possible, procedures
for evaluation are based on established thermodynamic methods. Specific procedures used in a particular
volume will be described in the Preface to that volume.

Only one thermodynamic result is mentioned here: the temperature dependence of solubility. Sometimes it is possible to fit the mole fraction solubility at various temperatures using the equation

ln *x*_{1} = *A* + *B*(*T*/K) + *C*ln(*T*/K) + *D ^{2}*(

*T*/K) (28)

where *A, B*, C and *D* are constants to be determined from least-squares
fitting of the data. Sometimes, to avoid singular matrices of the least-squares normal equations, *T*
is scaled; e.g., *T* is replaced by *T*/100.

If the gas and the solution of the dissolved gas are ideal, the coefficients can be used to find standard thermodynamic functions for transfer of the gas from the vapor to the liquid phase at the standard pressure (1 bar) and infinitely-dilute dissolved gas, as follows.

Δ*G°*_{m,1}/*R* = - *A* - *B* - *C*(*T*/K)ln(*T*/K) - *D*(*T*/K)^{2} (29)

Δ*S°*_{m,1}/*R* = *A* + *C*ln(*T*/K) + *C* + 2*D*(*T*/K) (30)

Δ*H°*_{m,1}/*R* = - *B* + *C*(*T*/K) + *D*(*T*/K)^{2} (31)

Δ*C° _{mp}*/

*R*=

*C*+ 2

*D*(

*T*/K) (32)

Alternatively (but equivalently), the standard state of infinitely-dilute dissolved gas
can be described as a hypothetical ideal gas at mole fraction *x*_{1} = 1, *p* = 1 bar.

TABLE 1. Interconversions between quantities used as measures of solubilities
*c*-component systems containing *c*-1 solutes i and single solvent *c* (ρ—density
of solution; *M _{i}*—molar masses of

*i*. For relations for two-component systems, set summations to 0.)

1.6. References for the Introduction

^{1}E. A. Hill, J. Am. Chem. Soc.**22**, 478 (1990).^{2}IUPAC Commission on Atomic Weights and Isotopic Abundances. Pure Appl. Chem.**63**, 975 (1989).*^{3}I. Mills et al., eds.*Quantities, Units and Symbols in Physical Chemistry*(The Green Book) (Blackwell Scientific Publications. Oxford, UK, 1993).^{4}H. H. Ku, , p. 73; C. Eisenhart, p. 69; in H. H. Ku, ed.,*Precision Measurement and Calibration*. NBS Special Publication 300, Vol. 1. (Washington, 1969).^{5}J. Regaudy, S. P. Klesney,*Nomenclature of Organic Chemistry*(IUPAC), (The Blue Book) (Pergamon, Oxford, 1979).^{6}V. Gold*et al*., eds.*Compendium of Chemical Technology*(The Gold Book) (Blackwell Scientific Publications. Oxford, UK, 1987).^{7}H. Freiser, G. H. Nancollas, eds.*Compendium of Analytical Nomenclature*(The Orange Book) (Blackwell Scientific Publications, Oxford, UK, 1987). Sect. 9.1.8.^{8}ISO Standards Handbook,*Quantities and Units*(International Standards Organization, Geneva, 1993).^{9}German Standard, DIN 1310,*Zusammungsetzung von Mischphasen*(Beuth Verlag, Berlin, 1984).^{10}T. Cvitaš, Chem. International**17**, No. 4, 123 (1995).^{11}R. A. Robinson, R. H. Stokes,*Electrolyte Solutions*, 2nd ed. (Butterworths, London, 1959).^{12}J. W. Lorimer, in R. Cohen-Adad, J. W. Lorimer,*Alkali Metal and Ammonium Chlorides in Water and Heavy Water (Binary Systems)*, IUPAC Solubility Data Series, Vol. 47. (Pergamon Press, Oxford, UK, 1991). p. 495.

This section was written by:

A. F. M. Barton, Perth, WA, Australia; F. W. Getzen,
Raleigh, NC, USA; G. T. Hefter, Perth, WA, Australia; D. G. Shaw, Fairbanks, AK, USA - December, 1995

*There is now a 2001 update, IUPAC Commission on Atomic Weights and Isotopic Abundances. Pure Appl. Chem.
**75**, 1107 (2003).