Girolami method
The Girolami method,^{[1]} named after Gregory Girolami, is a predictive method for estimating densities of pure liquid components at room temperature. The objective of this method is the simple prediction of the density and not high precision.
Contents
ProcedureEdit
The method uses purely additive volume contributions for single atoms and additional correction factors for components with special functional groups which cause a volume contraction and therefore a higher density. The Girolami method can be described as a mixture of an atom and group contribution method.
Atom contributionsEdit
The method uses the following contributions for the different atoms:
Element | Relative volume V_{i} |
---|---|
Hydrogen | 1 |
Lithium to Fluorine | 2 |
Sodium to Chlorine | 4 |
Potassium to Bromine | 5 |
Rubidium to Iodine | 7.5 |
Cesium to Bismuth | 9 |
A scaled molecular volume is calculated by
and the density is derived by
with the molecular weight M. The scaling factor 5 is used to obtain the density in g·cm^{−3}.
Group contributionEdit
For some components Girolami found smaller volumes and higher densities than calculated solely by the atom contributions. For components with
- a hydroxylic function (Alcohols)
- a carboxylic function (Carboxylic acids)
- a primary or secondary amine function
- an amide group (incl. amides substituted at the nitrogen)
- a sulfoxide group
- a sulfone group
- a ring (non-condensed),
it is sufficient to add 10% to the density obtained by the main equation. For sulfone groups it is necessary to use this factor twice (20%).
Another specific case are condensed ring systems like Naphthalene. The density has to increased by 7.5% for every ring; for Naphthalene the resulting factor would be 15%.
If multiple corrections are needed their factors have to be added but not over 130% in total.
Example calculationEdit
Component | M [^{g}/_{mol}] |
Volume V_{S} | Corrections | Calculated density [g·cm^{−3}] |
Exp. density [g·cm^{−3}] |
---|---|---|---|---|---|
Cyclohexanol | 100 | (6×2)+(13×1)+(1×2)=26 | One ring and a hydroxylic group = 120% | d=^{1.2*100}/_{5×26}=0.92 | 0.962 |
Dimethylethylphosphine | 90 | (4×2)+(11×1)+(1×4)=23 | No corrections | d=^{90}/_{5×23}=0.78 | 0.76 |
Ethylenediamine | 60 | (2×2)+(8×1)+(2×2)=16 | Two primary amine groups = 120% | d=^{1.2×60}/_{5×16}=0.90 | 0.899 |
Sulfolane | 120 | (4×2)+(8×1)+(2×2)+(1×4)=24 | One ring and two S=O bonds = 130% | d=^{1.3×120}/_{5×24}=1.30 | 1.262 |
1-Bromonaphthalene | 207 | (10×2)+(7×1)+(1×5)=32 | Two condensed rings = 115% | d=^{1,15×207}/_{5×32}=1.49 | 1.483 |
QualityEdit
The author has given a mean quadratic error (RMS) of 0.049 g·cm^{−3} for 166 checked components. Only for two components (acetonitrile and dibromochloromethane) has an error greater than 0.1 g·cm ^{−3} been found.
ReferencesEdit
- ^ Gregory S. Girolami, A Simple "Back of the Envelope" Method for Estimating the Densities and Molecular Volumes of Liquids and Solids, Journal of Chemical Education, 71(11), 962-964 (1994)