Rheological properties of rotator and crystalline phases of alkanes

TL;DR

This study develops a method to measure and compare the shear rheological properties of rotator and crystalline phases in alkanes, revealing significant differences and dependencies on molecular length and temperature.

Contribution

A novel methodology for rheological measurement of alkane phases and comprehensive characterization of their properties across different chain lengths and compositions.

Findings

Rotator phases have storage and loss moduli about 10 times lower than crystalline phases.

Rheological properties of crystal phases depend mainly on subcooling temperature.

Rotator phases become softer as alkane chain length increases.

Abstract

Linear long-chain organic molecules are known to form lamellar intermediate phases (called also rotator phases) between their fully ordered crystalline phases and their isotropic liquid phases. The properties of intermediate rotator phases are crucially important for various industrial and living nature processes, but the data for their rheological properties are almost missing, due to the specific difficulties in the respective experiments. In the current study we describe a methodology for measuring and comparing the shear rheological properties of rotator (R) and crystalline (C) phases formed in bulk hydrocarbons at temperatures below the melting temperature. We apply this approach to characterize the rheological properties of R and C phases formed upon cooling of alkanes with chain length varied between 17 and 30 carbon atoms. For comparison, we study also several alkane mixtures and one alkene with double bond at the end of its chain. The obtained results show that the storage and loss moduli of the rotator phases are ca. 10-times lower than those of the respective crystalline phases. We found also that the rheological properties of the crystal phases depend mainly on the subcooling temperature below the crystallization temperature, while the R phases become softer with the increase of the molecular length. We explain these results by assuming that the rheological properties of the crystal phases are determined mainly by the sliding of the ordered crystal domains with respect to each other, while in the rotator phases we have multiple defects in the molecular packing which increase with the alkane length. The proposed methodology and the obtained results serve as a solid basis for further rheological studies of this important class of technological systems.