This
paper improves upon a standard method of determining the Flory–Huggins
χ parameter, whereby experimental order–disorder transitions
(ODTs) of symmetric diblock polymer melts are fit to the mean-field
prediction, (χN)ODT = 10.495. The
improvement is achieved by switching to an accurate prediction of
(χN)ODT from Glaser et al. (Phys. Rev. Lett. 2014, 113, 068302), supplemented
with corrections for the small degrees of polydispersity and compositional
asymmetry that inevitably exist in real diblock polymers. The first
correction is evaluated by simulating polydisperse diblocks over a
wide range of invariant polymerization indices, and the second correction
is extracted from analogous simulations for compositionally asymmetric
diblocks by Ghasimakbari and Morse (Macromolecules 2020, 53, 7399). The resulting calibration method
is then demonstrated on 19 different chemical pairs, using previously
published experimental data. It provides a considerable increase in
accuracy, but yet is nearly as simple to apply as the original version.