Advanced solution inThermodynamics

 

Thermodynamic Datenbase und Process Design

Thermodynamic calculation and Process modelling

Content
1. Calculation of an equilibrium state in AsTher
2. Answer to the questions whether and how a process can be modelled or represented using thermodynamic calculations.

Examples and explanations
An example shows how a process concept is created and a process analysis is carried out using thermodynamic calculations.
Determination of substantial composition based on elementary analysis of a material

1. Calculation of an equilibrium state in AsTher
The initial state for calculating an equilibrium state is a hypothetical mixture consisting of the selected substances in all states of matter: gas, liquid, solid, and plasma.
The Lagrange coefficients of the elements in the equilibrium state are determined iteratively according to the phases, ensuring an elemental balance between the input composition and the calculated composition.

When the 'Calculation Option' 'Maximum Entropy' is selected
the calculation is terminated when,
the given pressure is reached in the gas phase,
or
when the sum of the activities of the substances in a phase corresponds to the system pressure.
The sum of the chemical activity of substances: is not in each phase Σ a i ≈ 1 

When the 'Calculation Option' 'Maximum Entropy' is not selected
Calculation is terminated when the sum of the frugalities and activities of the substances in a phase corresponds to the system pressure.
In several case, the sum of the activity or fugacity in a phase can not correspond to the system pressure,
In this case, the application may display a message, or the reason can be seen from the calculation results.
The sum of the chemical activity of substances for each phase: Σ ai ≈ 1

In both case of the calculation options, the following applies to each reaction:  a A + b B = c C + d D

K=( [A]a . [B]b)/( [C]c . [D]d) = exp(-ΔG°/R T)
[A], [B], [C], [D]: Activity or fugacity of the substances in the equilibrium state

ΔG° = c G°C + d G°D -  a G°A - b G°B
G°i:[J/mol]:  The molar free energy of substance i at the temperature T and pressure P in the equilibrium state.

 

In the thermodynamic modelling of high-temperature reactors with multiple liquid phases, we achieve a nearly exact representation of the processes by selecting the algorithm 'Maximum entropy'.
As a result of high turbulence, liquid, solid particles and gas bubble exist in other phases for a short time (e.g.  liquid metals dispersed in slag, or aerosol, metals dispersed in slag or aerosol) .

It is probably not in every phase Σ a i ≈ 1 in a short time

 

2. Answer to the questions whether and how a process can be modelled or represented using thermodynamic calculations.

Using an example, it is shown how a process concept is created and a process analysis is carried out using thermodynamic calculations.

When we intend to create a thermodynamic model of a process, some of the circumstances to be considered are:

2.1. Reactions are possible
Example, when an O2 molecule meets a CH4 molecule at 800 C, it reacts immediately, because the ignition temperature of CH4 is exceeded.
The extent of the reaction between O2 and CH4 is determined by natural laws and thermodynamics.
O2 also reacts immediately with C, CO, CH3OH, CH4 and several other substances at 800 C.

The cooling process of exhaust gases below 500 °C is difficult to calculate, even with an optimized reactor, since the ignition temperature of several substances, including CH4 and CO, is exceeded.
If a reaction cannot occur, thermodynamic calculations are only of limited use.

2.2. Flows, turbulence and geometry, sufficient mixing is ensured
It depends on how fast an O2  molecule hits z.B. a CH4  molecule.
An important factor is the turbulence (Re number) and the geometry of the reactor

2.3. The assumed temperature is approximately everywhere in the reactor.
In a reactor with an optimized flow and an approximately uniform local temperature, the product composition can be calculated thermodynamically with sufficient accuracy.

2.4. Liquid metal oxides are often unaffected by CO(g), CH4 (g), or H2 (g).
The reason why liquid metal oxides do not react with substances in the gaseous or solid state is often due, among other things, to the surface tension or the activity coefficient of MeOx(l) at the surface.
Based on measurements, the activity coefficients of MeOx(l) can be determined using thermodynamic calculations.

2.5 Carbon in the pure solid phase does not react directly with liquid metal oxides (FeO in a blast furnace).
Carbon only reacts with FeO(l) when carbon is dissolved in the liquid phase with the addition of CaO and SiO2 .

2.6. Thermodynamic calculations are helpful in determining which product composition can be formed
when, for example, a given amount of O2 reacts with the input material.
By comparing the calculated and measured composition of the products, we determine which O2 fraction reacts in the reactor and what the proportion of leak air is.

2.7. Reliable heat and mass balance using thermodynamic calculations
The heat and mass balance of a process requires substantial composition of the input materials and products.
Often we only have the elementary composition of the input materials, residues from other processes and/or natural ores.
Thermodynamic calculations make it possible to determine the substantial composition of a material.
How such calculations are carried out reliably is explained in DeterminationOfSubstantialComposition.pdf.

2.8. Process analysis, and incident prevention
Thermodynamic calculations enable reliable process analysis.
We obtain information about the behaviour of environmentally relevant substances and elements (e.g. As, Cd, Cl, Hg, Sb, Tl )depending on the process conditions
and the accompanying substances (e.g. BaO, MgO, SiO, FeO) in the input material.

We can avoid multiple incidents caused by unwanted substances in a phase, e.g: Substances containing the elements Cl, Cd, Hg, S, Tl in the exhaust gas or Substances containing the elements Tl, S in a metal phase