Abstract

Kinetic theory and acoustic measurements have proven that the bulk viscosity associated with the expansion or compression effect cannot be ignored in compressible fluids except for monatomic gases. A new theoretical formula for the bulk viscosity coefficient (BVC) $\unicode[STIX]{x1D701}$ is derived by the continuum medium methodology, which provides a further understanding of the bulk viscosity, i.e. $\unicode[STIX]{x1D701}$ is equal to the product of the bulk modulus $K$ and the relaxation time $\unicode[STIX]{x1D70F}$ ($\unicode[STIX]{x1D701}=K\unicode[STIX]{x1D70F}$). The continuum and kinetic theories present consistent results from macro- and microperspectives respectively, only differing in terms of a coefficient. The theoretical predictions of the BVC in diatomic molecules, such as $\text{N}_{2}$, $\text{O}_{2}$ and CO, show good agreement with the experimental data over a wide range of temperature. In addition, the vibrational contributions to $\unicode[STIX]{x1D701}$ are controlled by a rapid exponential decrease at high temperatures, while at low temperatures a slow linear increase proceeds for the rotational cases. The relaxation time $\unicode[STIX]{x1D70F}$, collision number $Z$, BVC $\unicode[STIX]{x1D701}$ and ratio of bulk-to-shear viscosities $\unicode[STIX]{x1D701}/\unicode[STIX]{x1D707}$ in the vibrational mode are found to be several orders of magnitude larger than those in the rotational mode.

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