arXiv subjects

Øivind Wilhelmsen

Publications and source records attributed to Øivind Wilhelmsen.

6 recordsLinked to original sources

arXiv2022

Steady-state two-phase flow of compressible and incompressible fluids in a capillary tube of varying radius

We study immiscible two-phase flow of a compressible and an incompressible fluid inside a capillary tube of varying radius under steady-state conditions. The incompressible fluid is Newtonian and the compressible fluid is an inviscid ideal gas. The surface tension associated with the interfaces between the two fluids introduces capillary forces that vary along the tube due to the variation in the tube radius. The interplay between effects due to the capillary forces and the compressibility results in a set of properties that are different from incompressible two-phase flow. As the fluids move towards the outlet, the bubbles of the compressible fluid grow in volume due to the decrease in pressure. The volumetric growth of the compressible bubbles makes the volumetric flow rate at the outlet higher than at the inlet. The growth is not only a function of the pressure drop across the tube, but also of the ambient pressure. Furthermore, the capillary forces create an effective threshold below which there is no flow. Above the threshold, the system shows a weak non-linearity between the flow rates and the effective pressure drop, where the non-linearity also depends on the absolute pressures across the tube.

physics.flu-dyn↗

arXiv2021

Theory and simulation of shock waves: Entropyproduction and energy conversion

We have considered a shock wave as a surface of discontinuity and computed the entropy production using non-equilibrium thermodynamics for surfaces. The results from this method, which we call the "Gibbs excess method" (GEM), were compared with results from three alternative methods, all based on the entropy balance in the shock front region, but with different assumptions about local equilibrium. Non-equilibrium molecular dynamics (NEMD) simulations were used to simulate a thermal blast in a one-component gas consisting of particles interacting with the Lennard-Jones/spline potential. This provided data for the theoretical analysis. Two cases were studied, a weak shock with Mach number $M \approx 2$ and a strong shock with $M \approx 6$ and with a Prandtl number of the gas $Pr \approx 1.4$ in both cases. The four theoretical methods gave consistent results for the time-dependent surface excess entropy production for both Mach numbers. The internal energy was found to deviate only slightly from equilibrium values in the shock front. The pressure profile was found to be consistent with the Navier-Stokes equations. The entropy production in the weak and strong shocks were approximately proportional to the square of the Mach number and decayed with time at approximately the same relative rate. In both cases, some 97 \% of the total entropy production in the gas occurred in the shock wave. The GEM showed that most of the shock's kinetic energy was converted reversibly into enthalpy and entropy, and a small amount was dissipated as produced entropy. The shock waves traveled at almost constant speed and we found that the overpressure determined from NEMD simulations agreed well with the Rankine-Hugoniot conditions for steady-state shocks.

physics.flu-dyn↗

arXiv2020

A combined fluid-dynamic and thermodynamic model to predict the onset of rapid phase transitions in LNG spills

Transport of liquefied natural gas (LNG) by ship occurs globally on a massive scale. The large temperature difference between LNG and water means LNG will boil violently if spilled onto water. This may cause a physical explosion known as rapid phase transition (RPT). Since RPT results from a complex interplay between physical phenomena on several scales, the risk of its occurrence is difficult to estimate. In this work, we present a combined fluid-dynamic and thermodynamic model to predict the onset of delayed RPT. On the basis of the full coupled model, we derive analytical solutions for the location and time of delayed RPT in an axisymmetric steady-state spill of LNG onto water. These equations are shown to be accurate when compared to simulation results for a range of relevant parameters. The relative discrepancy between the analytic solutions and predictions from the full coupled model is within 2% for the RPT position and within 8% for the time of RPT. This provides a simple procedure to quantify the risk of occurrence for delayed RPT for LNG on water. Due to its modular formulation, the full coupled model can straightforwardly be extended to study RPT in other systems.

physics.flu-dyn↗

arXiv2019

Tolman lengths and rigidity constants from free-energy functionals -- General expressions and comparison of theories

The leading order terms in a curvature expansion of the surface tension, the Tolman length (first order), and rigidities (second order) have been shown to play an important role in the description of nucleation processes. This work presents general and rigorous expressions to compute these quantities for any non-local density functional theory (DFT). The expressions hold for pure fluids and mixtures, and reduce to the known expressions from density gradient theory (DGT). The framework is applied to a Helmholtz energy functional based on the perturbed chain polar statistical associating fluid theory (PCP-SAFT) and is used for an extensive investigation of curvature corrections for pure fluids and mixtures. Predictions from the full DFT are compared to two simpler theories: predictive density gradient theory (pDGT), that has a density and temperature dependent influence matrix derived from DFT, and DGT, where the influence parameter reproduces the surface tension as predicted from DFT. All models are based on the same equation of state and predict similar Tolman lengths and spherical rigidities for small molecules, but the deviations between DFT and DGT increase with chain length for the alkanes. For all components except water, we find that DGT underpredicts the value of the Tolman length, but overpredicts the value of the spherical rigidity. An important basis for the calculation is an accurate prediction of the planar surface tension. Therefore, further work is required to accurately extract Tolman lengths and rigidities of alkanols, because DFT with PCP-SAFT does not accurately predict surface tensions of these fluids.

cond-mat.soft↗

arXiv2019

A consistent reduction of the two-layer shallow-water equations to an accurate one-layer spreading model

The gravity-driven spreading of one fluid in contact with another fluid is of key importance to a range of topics. To describe these phenomena, the two-layer shallow-water equations is commonly employed. When one layer is significantly deeper than the other, it is common to approximate the system with the much simpler one-layer shallow water equations. So far, it has been assumed that this approximation is invalid near shocks, and one has applied additional front conditions for the shock speed. In this paper, we prove mathematically that an effective one-layer model can be derived from the two-layer equations that correctly captures the behaviour of shocks and contact discontinuities without any additional closure relations. The proof yields a novel formulation of an effective one-layer shallow water model. The result shows that simplification to an effective one-layer model is well justified mathematically and can be made without additional knowledge of the shock behaviour. The shock speed in the proposed model is consistent with empirical models and identical to the front conditions that have been found theoretically by e.g. von Kármán and by Benjamin. This suggests that the breakdown of the shallow-water equations in the vicinity of shocks is less severe than previously thought. We further investigate the applicability of the shallow water framework to shocks by studying shocks in one-dimensional lock-exchange/lock-release. We derive expressions for the Froude number that are in good agreement with the widely employed expression by Benjamin. We then solve the equations numerically to illustrate how quickly the proposed model converges to solutions of the full two-layer shallow-water equations. We also compare numerical results using our model with results from dam break experiments. Predictions from the one-layer model are found to be in good agreement with experiments.

physics.flu-dyn↗

arXiv2019

Thermodynamic stability of droplets, bubbles and thick films in open and closed pores

A fluid in a pore can form diverse heterogeneous structures. We combine a capillary description with the cubic-plus-association equation of state to study the thermodynamic stability of droplets, bubbles and films of water at 358 K in a cylindrically symmetric pore. The equilibrium structure depends strongly on the size of the pore and whether the pore is closed or connected to a particle reservoir. A new methodology is presented to analyze the thermodynamic stability of films, where the integral that describes the total energy of the system is approximated by a quadrature rule. We show that, for large pores, the thermodynamic stability limit of adsorbed droplets and bubbles in both open and closed pores is governed by their mechanical stability, which is closely linked to the pore shape. This is also the case for a film in a closed pore. In open pores, the film is chemically unstable except for very low film-phase contact angles and for a limited range in external pressure. This result emphasizes the need to invoke a complete thermodynamic stability analysis, and not restrict the discussion to mechanical stability. A common feature for most of the heterogeneous structures examined is the appearance of regions where the structure is metastable with respect to a pore filled with a homogeneous fluid. In the closed pores, these regions grow considerably in size when the pores become smaller. [...] Complete phase diagrams are presented that compare all the investigated structures. In open pores at equilibrium, the most stable structure is either the homogeneous phase or adsorbed droplets and bubbles, depending on the type of phase in the external reservoir. Smaller pores allow for droplets and bubbles to adsorb for a larger span in pressure. In closed pores, most of the investigated configurations can occur depending on the total density, the contact angle and the pore shape. [...]

physics.comp-ph↗