1. Introduction
Thermodynamics has established in chemistry principally as a science determining possibility and direction of chemical transformations and giving conditions for their final, equilibrium state. Thermodynamics is usually thought to tell nothing about rates of these processes, their velocity of approaching equilibrium. Rates of chemical reactions belong to the domain of chemical kinetics. However, as thermodynamics gives some restriction on the course of chemical reactions, similar restrictions on their rates are continuously looked for. Similarly, because thermodynamic potentials are often formulated as driving forces for various processes, a thermodynamic driving force for reactions rates is searched for.
Two such approaches will be discussed in this article. The first one are restrictions put by thermodynamics on values of rate constants in mass action rate equations. The second one is the use of the chemical potential as a general driving force for chemical reactions and also “directly” in rate equations. These two problems are in fact connected and are related to expressing reaction rate as a function of pertinent independent variables.
Relationships between chemical thermodynamics and kinetics traditionally emerge from the ways that both disciplines use to describe equilibrium state of chemical reactions (chemically reacting systems or mixtures in general). Equilibrium is the main domain of classical, equilibrium, thermodynamics that has elaborated elegant criteria (or, perhaps, definitions) of equilibria and has shown how they naturally lead to the well known equilibrium constant. On the other hand, kinetics describes the way to equilibrium, i.e. the nonequilibrium state of chemical reactions, but also gives a clear idea on reaction equilibrium. Combining these two views various results on compatibility between thermodynamics and kinetics, on thermodynamic restrictions to kinetics etc. were published. The main idea can be illustrated on the trivial example of decomposition reaction
Chemical potential (
(note that the equivalence of thermodynamic and kinetic equilibrium constants is supposed again;
2. Restrictions put by thermodynamics on values of rate constants
2.1. Basic thermodynamic restrictions on rate constants coming from equilibrium
Perhaps the only one work which clearly distinguishes kinetic and thermodynamic equilibrium constant is the kinetic textbook by Eckert and coworkers (Eckert et al., 1986); the former is in it called the empirical equilibrium constant. This book stresses different approaches of thermodynamics and kinetics to equilibrium. In thermodynamics, equilibrium is defined as a state of minimum free energy (Gibbs energy) and its description is based on stoichiometric equation and thermodynamic equilibrium constant containing activities. Different stoichiometric equations of the same chemical equation can give different values of thermodynamic equilibrium constant, however, equilibrium composition is independent on selected stoichiometric equation. Kinetic description of equilibrium is based on zero overall reaction rate, on supposed reaction mechanism or network (reaction scheme) and corresponding kinetic (rate) equation. Kinetic equilibrium constant usually contains concentrations. According to that book, thermodynamic equilibrium data should be introduced into kinetic equations indirectly as shown in the Scheme 1.
Simple example reveals basic problems. Decomposition of carbon monoxide occurs (at the pressure
Standard state of gaseous components is selected as the ideal gas at 101 kPa and for solid component as the pure component at the actual pressure (due to negligible effects of pressure on behavior of solid components, the dependence of the standard state on pressure can be neglected here). Ideal behavior is supposed. Then
On contrary, the ratio of rate constants is given by
It is clear that thermodynamic and kinetic equilibrium constants need not be equivalent even in ideal systems. For example, the former does not contain concentration of carbon and though this could be remedied by stating that carbon amount does not affect reaction rate and its concentration is included in the reverse rate constant, even then the kinetic equilibrium constant could depend on carbon amount in contrast to the thermodynamic equilibrium constant. Some discrepancies could not be remedied by restricting on elementary reactions only – in this example the presence of
Let us use the same example to illustrate the procedure suggested by Eckert et al. (1986). At 1300 K and 202 kPa the molar standard Gibbs energies are (Novák et al., 1999):
and this is real and true result of thermodynamic restriction on values of rate constants valid at given temperature. More precisely, this is a restriction put on the ratio of rate constants, values of which are supposed to be independent on equilibrium, in other words, dependent on temperature (and perhaps on pressure) only and therefore this restriction is valid also out of equilibrium at given temperature. The numerical value of this restriction is dependent on temperature and should be recalculated at every temperature using the value of equilibrium constant at that temperature.
Thus, simple and safe way how to relate thermodynamics and kinetics, thermodynamic and kinetic equilibrium constants, and rate constants is that shown in Scheme 1. However, it gives no general equations and should be applied specifically for each specific reaction (reacting system) and reaction conditions (temperature, at least). There are also works that try to resolve relationship between the two types of equilibrium constant more generally and, in the same time, correctly and consistently. They were reviewed previously and only main results are presented here, in the next section. But before doing so, let us note that kinetic equilibrium constant can be used as a useful indicator of the distance of actual state of reacting mixture from equilibrium and to follow its approach to equilibrium. In the previous example, actual value of the fraction
2.2. General thermodynamic restrictions on rate constants
As noted in the preceding section there are several works that do not rely on simple identification of thermodynamic and kinetic equilibrium constants. Hollingsworth (1952a, 1952b) generalized restriction on the ratio of forward and reverse reaction rates (f) defined by
Hollingsworth showed that sufficient condition for consistent kinetic and thermodynamic description of equilibrium is
where
where
in the neighbourhood of
Blum (Blum & Luus, 1964) considered a general mass action rate law formulated as follows:
where
where
General law (10) is rarely used in chemical kinetics, in reactions of ions it probably does not work (Laidler, 1965; Boudart, 1968). It can be transformed, particularly simply in ideal systems, to concentrations. Samohýl (personal communication) pointed out that criteria (12) may be problematic, especially for practically irreversible reactions. For example, reaction orders for reaction
2.3. Independence of reactions, Wegscheider conditions
Wegscheider conditions belong also among “thermodynamic restrictions” on rate constants and have been introduced more than one hundred years ago (Wegscheider, 1902). In fact, they are also based on equivalence between thermodynamic and kinetic equilibrium constants disputed in previous sections. Recently, matrix algebra approaches to find these conditions were described (Vlad & Ross, 2009). Essential part of them is to find (in)dependent chemical reactions. Problem of independent and dependent reactions is an interesting issue sometimes found also in studies on kinetics and thermodynamics of reacting mixtures. As a rule, a reaction scheme, i.e. a set of stoichiometric equations (whether elementary or nonelementary), is proposed, stoichiometric coefficients are arranged into stoichiometric matrix and linear (matrix) algebra is applied to find its rank which determines the number of linearly (stoichiometrically) independent reactions; all other reactions can be obtained as linear combinations of independent ones. This procedure can be viewed as an a posteriori analysis of the proposed reaction mechanism or network. Bowen has shown (Bowen, 1968) that using not only matrix but also vector algebra interesting results can be obtained on the basis of knowing only components of reacting mixture, i.e. with no reaction scheme. This is a priori type of analysis and is used in continuum nonequilibrium (rational) thermodynamics. Because Bowen’s results are important for this article they are briefly reviewed now for reader’s convenience.
Let a reacting mixture be composed from n components (compounds) which are formed by
Although compounds are destroyed or created in chemical reactions the atoms are preserved. If
This result expresses, in other words, the mass conservation.
Atomic numbers can be arranged in matrix
In this way only linearly independent relations from (14) are retained and from the chemical point of view it means that instead of (some) atoms with masses
Example. Mixture of
Multiplying each of the
To proceed further we use relations (15) and (16) because in contrast to relations (13) and (14) the matrix
where the latter equality follows using (15). Because the matrix
that appear in (18) are linearly independent and thus form a basis of a h-dimensional subspace W of the space U (remember that
which shows that M can be expressed in the basis of the subspace W or
which means that J is perpendicular to all basis vectors of the subspace W, consequently, J lies in the complementary orthogonal subspace V,
Let us now select basis vectors in the subspace V and denote them
Because of orthogonality of subspaces V and W, their bases conform to equation
which can be alternatively written in matrix form as
Meaning of the matrix
Second, because the vector of molar masses M is in the subspace W, it is perpendicular to all vectors
as follows after substitution from (20), (22), (220. Eq. (26) shows that matrix
Vector algebra thus shows that chemical transformations fulfilling persistence of atoms (mass conservation) can be equivalently described either by component reaction rates or by rates of independent reactions. The number of the former is equal to the number of components (n) whereas the number of the latter is lower (n–h) which could decrease the dimensionality of the problem of description of reaction rates. In kinetic practice, however, changes in component concentrations (amounts) are measured, i.e. data on component rates and not on rates of individual reactions are collected. Reactions, in the form of reaction schemes, are suggested a posteriori on the basis of detected components, their concentrations changing in time and chemical insight. Then dependencies between reactions can be searched. Vector analysis offers rather different procedure outlined in Scheme 2. Dependencies are revealed at the beginning and then only independent reactions are included in the (kinetic) analysis. Vector analysis also shows how to transform (measured) component rates into (suggested, selected) rates of independent reactions. This transformation is made by standard procedure for interchange between vector bases or between vector coordinates in different bases. First, the contravariant metric tensor with components
Of course, so far we have seen only relationships between reaction rates and no explicit equations for them like, e.g., the kinetic mass action law. Analysis based only on permanence of atoms cannot give such equations – they belong to the domain of chemical kinetics although they can also be devised by thermodynamics, see Section 4.
Simple example on Wegscheider conditions was presented by Vlad and Ross (Vlad & Ross, 2009) – isomerization taking place in two ways:
Vlad and Ross note that if the (thermodynamic) equilibrium constant is
It can be easily checked that in this mixture of one kind of atom and two components the rank of the matrix
Then the only one independent reaction rate is in the form
should be valid for any concentrations. Sufficient conditions for this are
i.e. “kinetic part” of Wegscheider condition (29). Substituting derived expressions for
There is a thermodynamic method giving kinetic description in terms of independent reactions as noted in Scheme 2, see Section 4.
More complex reaction mixture and scheme was discussed by Ederer and Gilles (Ederer & Gilles, 2007). Their mixture was composed from six formal components (A, B, C, AB, BC, ABC) formed by three atoms (A, B, C). Three independent reactions are possible in this mixture while four reactions were considered by Ederer and Gilles (Ederer & Gilles, 2007)
Let us suppose that the fourth reaction rate can be expressed through the other three rates:
i.e., Wegscheider condition derived in (Ederer & Gilles, 2007) from equilibrium considerations. Thus also here Wegscheider condition seems to be a result of mutual dependence of reaction rates and not a necessary consistency condition between thermodynamics and kinetics.
If reactions
Remember that, e.g.,
Eq. (27) gives more complex expressions for independent rates, e.g.
Message from the analysis of independence of reactions in this example is that it is sufficient to measure three component rates only (
Algebraically more rigorous is this analysis in the case of first order reactions as was illustrated on a mixture of three isomers and their triangular reaction scheme which is traditional example used to discuss consistency between thermodynamics and kinetics. Here, Wegscheider relations are consequences of linear dependence of traditional mass action reaction rates (Pekař, 2007).
2.4. Note on standard states
Preceding sections demonstrated that one of the main problems to be solved when relating thermodynamics and kinetics is the transformation between activities and concentration variables. This is closely related to the selection of standard state (important and often overlooked aspect of relating thermodynamic and kinetic equilibrium constants) and to chemical potential. Standard states are therefore briefly reviewed in this section and chemical potential is subject of the following section.
Rates of chemical reactions are mostly expressed in terms of concentrations. Among standard states introduced and commonly used in thermodynamics there is only one based on concentration – the standard state of nonelectrolyte solute on concentration basis. Only this standard state can be directly used in kinetic equations. Standard state in gaseous phase or mixture is defined through (partial) pressure or fugacity. As shown above even in mixture of ideal gases it is impossible to simply use this standard state in concentration based kinetic equations. Although kinetic equations could be reformulated into partial pressures there still remains problem with the fact that standard pressure is fixed (at 1 atm or, nowadays, at 105 Pa) and its recalculation to actual pressure in reacting mixture may cause incompatibility of thermodynamic and kinetic equilibrium constants (see the factor prel in the example above in Section 2.1). This opens another problem – the very selection of standard state, particularly in relation to activity discussed in subsequent section. In principle, it can be selected arbitrarily, as dependent only on temperature or on temperature and pressure. Standard states strictly based on the (fixed) standard pressure are of the former type and only such will be considered in this article. All other states, including states dependent also on pressure, will be called the reference state; the same approach is used, e.g. by de Voe (de Voe, 2001).
The value of thermodynamic equilibrium constant and its dependence or independence on pressure is thus dependent on the selected standard (or reference) state. This is quite uncommon in chemical kinetics where the dependence of rate constants is not a matter of selection of standard states but result of experimental evidence or some theory of reaction rates. As a rule, rate constant is always function of temperature. Sometimes also the dependence on pressure is considered but this is usually the case of nonelementary reactions. Consequently, attempts to relate thermodynamic and kinetic equilibrium constants should select standard state consistently with functional dependence of rate constants. On the other hand, the method of Scheme 1 is self-consistent in this aspect because equilibrium composition is independent of the selection of standard state.
3. Chemical potential and activity revise
Chemical potential is used in discussions on thermodynamic implications on reaction rates, particularly in the form of (stoichiometric) difference between chemical potentials of reaction products and reactants and through its explicit relationship to concentrations (activities, in general). Before going into this type of analysis basic information is recapitulated.
Chemical potential is in classical, equilibrium thermodynamics defined as a partial derivative of Gibbs energy (G):
Although another definitions through another thermodynamic quantities are possible (and equivalent with this one), the definition using the Gibbs energy is the most useful for chemical thermodynamics. Chemical potential expresses the effect of composition and this effect is also essential in chemical kinetics. To make the mathematical definition of the chemical potential applicable in practice its relationship to composition (concentration) should be stated explicitly. Practical chemical thermodynamics suggests that this is an easy task but we must be very careful and bear all (tacit) presumptions in mind to arrive at proper conclusions. Generally the explicit relationship between chemical composition and chemical potential is stated defining the activity of a component
which can be transformed to
but this still lacks direct interconnection/linkage to measurable concentrations. Just this is the main problem of applying chemical potential (and activities) in rate equations which systematically use molar concentrations. Even when reaction rates would be expressed using activities in place of concentrations the activities should be properly calculated from the measured concentrations, in other words, the concentrations should be correctly transformed to the activities. Activity is very easily related to measurable composition variable in the case of mixture of ideal gases. Providing that Gibbs energy is a function of temperature, pressure and molar amounts, following relation is well known from thermodynamics for the partial molar volume:
Integration from the standard state to some actual state then yields
Comparing with the definition of activity it follows
Application of this relationship was illustrated in the example given above. Note that (44) was not derived from the definition of activity but comparing the properties of chemical potential in the ideal gas mixture (43) with the definition of activity. Note also that the partial derivative in the original definition of chemical potential is in general a function of molar amounts (contents) of all components but eq. (44) states that the chemical potential of a component
In a real gas mixture, non-idealities should be taken into account, usually by substituting fugacity (
The fugacity can be eliminated in favor of directly measurable quantities using the fugacity coefficient
and its relationship to the partial molar volume and the total pressure (de Voe, 2001):
It should be stressed that in derivation of the expression for the fugacity coefficient it was assumed that the Gibbs energy is a function of (only) temperature, pressure, and molar amounts of all components. Comparing with the definition of activity we have
If kinetic equations for mixture of real gases are written in partial pressures then thermodynamic and kinetic equilibrium constants are incompatible due to the presence of fugacity coefficient or the integral in eq. (47). Kinetic equations for mixture of real gases could be formulated in terms of fugacities instead of concentrations (or partial pressures) to achieve compatibility between thermodynamic and kinetic equilibrium constants but even than the same problem remains with the presence of the standard pressure in thermodynamic relations. Kinetic equations formulated in fugacities are really rare – some success in this way was demonstrated by Eckert and Boudart (Eckert & Boudart, 1963) while Mason (Mason, 1965) showed, using the same data, that fugacities need not remedy the whole situation.
Similar derivation for liquid state (solutions) has different basis. It stems from the equilibrium between liquid and gaseous phase in which the following identity holds:
which has, in fact, inspired the definition of an ideal (liquid, solid, or gas) mixture as a mixture with the chemical potential defined, at a given T and p, as
Then the activity of a (non-electrolyte) component in real solution is written as
The main problems with using activities defined for liquid systems can be summarized as follows. Activity is based on molar fractions whereas kinetic uses concentrations. Although there are formulas for the conversion of these variables they do not allow direct substitution, they introduce other variables (e.g., solution density) and lead to rather complex expression of thermodynamic equilibrium constant in concentrations. Whereas concentrations of all species are independent (variables) this is not true for molar fractions – value of one from them is unambiguously determined by values of remaining ones. Chemical potential in liquid and activity based on it are introduced on the basis of (liquid-gas) equilibrium while kinetics essentially works with reactions out of equilibrium. Applicability of equilibrium-based formulated in fugacities are really rare in nonequilibrium states deserves further study. The problem with molar fractions can be resolved by the use of molar concentration based Henry’s law giving for ideal-dilute solution
It is clear from this basic overview that chemical potential, activity and their interrelation are in principle equilibrium quantities which, in kinetic applications, are to be used for non-equilibrium situations. Let us now trace one relatively simple non-equilibrium approach to description of chemically reacting systems and its results regarding the chemical potential. Samohýl has developed rational thermodynamic approach for chemically reacting fluids with linear transport properties (henceforth called briefly linear fluids) and these fluids seem to include many (non-electrolyte) systems encountered in chemistry (Samohýl & Malijevský, 1976; Samohýl, 1982, 1987). This is a continuum mechanics based approach working with densities of quantities and specific quantities (considered locally, in other words, as fields but this is not crucial for the present text) therefore it primarily uses densities of components (more precisely, the density of component mass) instead of their molar concentrations or fractions that are common in chemistry. This density, in fact, is known in chemistry as a mass concentration with dimension of mass per (unit) volume and can be thus easily recalculated to concentration quantities more common in chemistry. Chemical potential of a reacting component α is defined in this theory as follows:
Here
The specific free energy
In the case of linear fluids it can be proved that free energy is function of densities and temperature only,
where the last transformation was made using the following transformation of (specific) chemical potential into the traditional chemical potential (which will be called the molar chemical potential henceforth):
It should be stressed that chemical potential of component α as defined by (51) is a function of densities of all components, i.e. of
Although the functions (dependencies) given above were derived for specific case of linear fluids they are still too general. Yet simpler fluid model is the simple mixture of fluids which is defined as mixture of linear fluids constitutive (state) equations of which are independent on density gradients. Then it can be shown (Samohýl, 1982, 1987) that
and, consequently, also that
that is slightly more general than the common model of ideal gas for which
where
which looks like a function of ρα and T only, i.e. the simple mixture function
4. Solution offered by rational thermodynamics
Rational thermodynamics offers certain solution to problems presented so far. It should be stressed that this is by no means totally general theory resolving all possible cases. But it clearly states assumptions and models, i. e. scope of its potential application.
The first assumption, besides standard balances and entropic inequality (see, e.g., Samohýl, 1982, 1987), or model is the mixture of linear fluids in which the functional form of reaction rates was proved:
Activity (39) is supposed to be equal to molar concentrations (divided by unit standard concentration), which is possible for ideal gases, at least (Samohýl, 1982, 1987). Combining this definition of activity with the proved fact that in equilibrium
Some equilibrium concentrations can be thus expressed using the others and (59) and substituted in the approximating polynomial that equals zero in equilibrium. Equilibrium polynomial should vanish for any concentrations what leads to vanishing of some of its coefficients. Because the coefficients are independent of equilibrium these results are valid also out of it and the final simplified approximating polynomial, called thermodynamic polynomial, follows and represents rate equation of mass action type. More details on this method can be found elsewhere (Samohýl & Malijevský, 1976; Pekař, 2009, 2010). Here it is illustrated on two examples relevant for this article.
First example is the mixture of two isomers discussed in Section 2. 3. Rate of the only one independent reaction, selected as A = B, is approximated by a polynomial of the second degree:
The concentration of B is expressed from the equilibrium constant,
Eq. (61) should be valid for any values of equilibrium concentrations, consequently
Substituting (62) into (60) the final thermodynamic polynomial (of the second degree) results:
Note, that coefficients
This example illustrated how thermodynamics can be consistently connected to kinetics considering only independent reactions and results of nonequilibrium thermodynamics with no need of additional consistency conditions.
Example of simple combination reaction
that represents the function
This is thermodynamically correct expression (for the supposed thermodynamic model) of the function
Rational thermodynamics thus provides efficient connection to reaction kinetics. However, even this is not totally universal theory; on the other hand, presumptions are clearly stated. First, the procedure applies to linear fluids only. Second, as presented here it is restricted to mixtures of ideal gases. This restriction can be easily removed, if activities are used instead of concentrations, i.e. if functions
5. Conclusion
Two approaches relating thermodynamics and chemical kinetics were discussed in this article. The first one were restrictions put by thermodynamics on the values of rate constants in mass action rate equations. This can be also formulated as a problem of relation, or even equivalence, between the true thermodynamic equilibrium constant and the ratio of forward and reversed rate constants. The second discussed approach was the use of chemical potential as a general driving force for chemical reaction and “directly” in rate equations. Both approaches are closely connected through the question of using activities, that are common in thermodynamics, in place of concentrations in kinetic equations and the problem of expressing activities as function of concentrations.
Thermodynamic equilibrium constant and the ratio of forward and reversed rate constants are conceptually different and cannot be identified. Restrictions following from the former on values of rate constants should be found indirectly as shown in Scheme 1.
Direct introduction of chemical potential into traditional mass action rate equations is incorrect due to incompatibility of concentrations and activities and is problematic even in ideal systems.
Rational thermodynamic treatment of chemically reacting mixtures of fluids with linear transport properties offers some solution to these problems whenever its clearly stated assumptions are met in real reacting systems of interest. No compatibility conditions, no Wegscheider relations (that have been shown to be results of dependence among reactions) are then necessary, thermodynamic equilibrium constants appear in rate equations, thermodynamics and kinetics are connected quite naturally. The role of (“thermodynamically”) independent reactions in formulating rate equations and in kinetics in general is clarified.
Future research should focus attention on the applicability of dependences of chemical potential on concentrations known from equilibrium thermodynamics in nonequilibrium states, or on the related problem of consistent use of activities and corresponding standard states in rate equations.
Though practical chemical kinetics has been successfully surviving without special incorporation of thermodynamic requirements, except perhaps equilibrium results, tighter connection of kinetics with thermodynamics is desirable not only from the theoretical point of view but may be of practical importance considering increasing interest in analyzing of complex biochemical network or increasing computational capabilities for correct modeling of complex reaction systems. The latter when combined with proper thermodynamic requirements might contribute to more effective practical, industrial exploitation of chemical processes.
Acknowledgments
The author is with the Centre of Materials Research at the Faculty of Chemistry, Brno University of Technology; the Centre is supported by project No. CZ.1.05/2.1.00/01.0012 from ERDF. The author is indebted to Ivan Samohýl for many valuable discussions on rational thermodynamics.
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