Acentric factor (ω) – typical magnitude and definition insight The acentric factor ω is defined by ω = −log10(Pr_sat) at Tr = 0.7. What is the usual magnitude range of ω for real substances?

Difficulty: Easy

Correct Answer: < 1

Explanation:


Introduction / Context:
The acentric factor (ω) is a shape- and polarity-related parameter introduced by Pitzer to improve corresponding-states correlations for vapor pressures and compressibility. It is widely used with cubic equations of state (e.g., Soave–Redlich–Kwong, Peng–Robinson).


Given Data / Assumptions:

  • Definition: ω = −log10(Pr_sat) at Tr = 0.7.
  • Pr_sat = Psat / Pc and Tr = T / Tc.
  • Simple spherical molecules (e.g., argon, methane) have small ω; complex/polar molecules have larger ω.


Concept / Approach:
By construction, ω measures the deviation of a substance from the simple spherical model. For many common fluids, ω falls between roughly 0 and 1. Light gases like methane have ω near 0.01, while heavier or more polar substances like water are around 0.34, and aromatics may approach ~0.6–0.9. Values greater than 1 are unusual and reserved for highly non-ideal species under specific definitions; thus the safe, general statement is ω < 1 for typical substances.


Step-by-Step Solution:

Recall definition point Tr = 0.7 used to evaluate Pr_sat.Recognize typical ω values from data tables (0 ≲ ω ≲ 1).Conclude the best universal choice among options is “< 1”.


Verification / Alternative check:
Databanks list ω(CH4) ≈ 0.011, ω(N2) ≈ 0.037, ω(H2O) ≈ 0.344, ω(benzene) ≈ 0.212, all less than 1.


Why Other Options Are Wrong:

  • > 2 or > 1: Not representative of typical fluids.
  • < 3: Trivially true but uninformative; the conventional characterization is ω well below 1.


Common Pitfalls:
Assuming ω relates directly to critical compressibility factor; although correlated, ω specifically parameterizes vapor-pressure behavior at a reduced temperature.


Final Answer:
< 1

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