### Refine

#### Department, Institute

#### Document Type

- Article (10)
- Part of a Book (2)
- Conference Object (1)
- Doctoral Thesis (1)

#### Keywords

- High-performance computing (2)
- Molecular modeling (2)
- Numerical optimization (2)
- Adams-Moulton (1)
- Automation (1)
- BDF (1)
- Computational fluid dynamics (1)
- Force field (1)
- Force field parameters (1)
- Irreguläre Gitter (1)

The paper describes methods for calculating chemical equilibria based on a constrained Gibbs free energy minimization. The methods allow the treatment of multicomponent systems with multiple phases, including gaseous phases, condensed phases, and stoichiometric phases. A special aspect is the detection and treatment of miscibility gaps. The underlying mathematical problem is described in detail together with the algorithmic approach for its solution. Results are presented for some test cases, including the computation of phase diagrams for ternary systems.

A central goal of molecular simulations is to predict physical or chemical properties such that costly and elaborate experiments can be minimized. The reliable generation of molecular models is a critical issue to do so. Hence, striving for semiautomated and fully automated parameterization of entire force fields for molecular simulations, the authors developed several modular program packages in recent years. The programs run with limited user interactions and can be executed in parallel on modern computer clusters. Various interlinked resolutions of molecular modeling are addressed: For intramolecular interactions, a force-field optimization package named Wolf2Pack has been developed that transfers knowledge gained from quantum mechanics to Newtonian-based molecular models. For intermolecular interactions, especially Lennard–Jones parameters, a modular optimization toolkit of programs and scripts has been created combining global and local optimization algorithms. Global optimization is performed by a tool named CoSMoS, while local optimization is done by the gradient-based optimization workflow named GROW or by a derivative-free method called SpaGrOW. The overall goal of all program packages is to realize an easy, efficient, and user-friendly development of reliable force-field parameters in a reasonable time. The various tools are needed and interlinked since different stages of the optimization process demand different courses of action. In this paper, the conception of all programs involved is presented and how they communicate with each other.

Transition point prediction in a multicomponent lattice Boltzmann model: Forcing scheme dependencies
(2018)

Pseudopotential-based lattice Boltzmann models are widely used for numerical simulations of multiphase flows. In the special case of multicomponent systems, the overall dynamics are characterized by the conservation equations for mass and momentum as well as an additional advection diffusion equation for each component. In the present study, we investigate how the latter is affected by the forcing scheme, i.e., by the way the underlying interparticle forces are incorporated into the lattice Boltzmann equation. By comparing two model formulations for pure multicomponent systems, namely the standard model [X. Shan and G. D. Doolen, J. Stat. Phys. 81, 379 (1995)] and the explicit forcing model [M. L. Porter et al., Phys. Rev. E 86, 036701 (2012)], we reveal that the diffusion characteristics drastically change. We derive a generalized, potential function-dependent expression for the transition point from the miscible to the immiscible regime and demonstrate that it is shifted between the models. The theoretical predictions for both the transition point and the mutual diffusion coefficient are validated in simulations of static droplets and decaying sinusoidal concentration waves, respectively. To show the universality of our analysis, two common and one new potential function are investigated. As the shift in the diffusion characteristics directly affects the interfacial properties, we additionally show that phenomena related to the interfacial tension such as the modeling of contact angles are influenced as well.

Pseudopotential-based Lattice Boltzmann models provide an efficient means to simulate multiphase flows. Although thoroughly analysed and extended, they still suffer from various numerical deficiencies, such as stability issues at large density and viscosity ratios as well as spurious velocities in interfacial regions. In this work, we show how to optimize the model numerically with regard to the latter. This optimized scheme is analysed in static as well as oscillating droplet simulations and is compared to different higher-order isotropic schemes. We found that the optimized scheme substantially lowers spurious velocities and competes well with comparable schemes in both test cases.

In dieser Arbeit werden neuartige methodische Erweiterungen der Lattice-Boltzmann-Methode (LBM) entwickelt, die effizientere Simulationen inkompressibler Wirbelströmungen ermöglichen. Diese Erweiterungen beheben zwei Hauptprobleme der Standard-LBM: ihre Instabilität in unteraufgelösten turbulenten Simulationen und ihre Beschränkung auf reguläre Rechengitter. Dazu wird zunächst eine Pseudo-Entropische Stabilisierung (PES) entwickelt. Diese kombiniert Ansätze der Multiple-Relaxation-Time (MRT)-Modelle und der Entropischen LBM zu einem expliziten, lokalen und flexiblen Stabilisierungsoperator. Diese Modifikation des Kollisionsschritts erlaubt selbst auf stark unteraufgelösten Gittern stabile und qualitativ korrekte Simulationen. Zur Erweiterung der LBM auf irreguläre Rechengitter wird zunächst eine moderne Discontinuous-Galerkin-LBM untersucht und um stabilere Zeitintegratoren ergänzt. Diese Studie demonstriert die drastischen Schwächen existierender LBMAnsätze auf irregulären Gittern. Basierend auf den gewonnenen Erkenntnissen gelingt die Formulierung einer neuartigen Semi-Lagrangeschen LBM (SLLBM). Diese ermöglicht in einzigartigerWeise sowohl die Verwendung irregulärer Gitter und großer Zeitschritte als auch eine hohe räumliche Konvergenzordnung. Anhand von Beispielsimulationen wird demonstriert, wieso dieser Ansatz anderen aktuellen Off-Lattice-Boltzmann-Methoden (OLBMs) in Effizienz und Genauigkeit überlegen ist. Weitere neuartige Aspekte dieser Arbeit sind die Entwicklung eines modularen Off-Lattice-Boltzmann-Codes und die Erweiterung der LBM um implizite Mehrschrittverfahren, mit denen eine Erhöhung der zeitlichen Konvergenzordnung gelingt.

The lattice Boltzmann method is a simulation technique in computational fluid dynamics. In its standard formulation, it is restricted to regular computation grids, second-order spatial accuracy, and a unity Courant-Friedrichs-Lewy (CFL) number. This paper advances the standard lattice Boltzmann method by introducing a semi-Lagrangian streaming step. The proposed method allows significantly larger time steps, unstructured grids, and higher-order accurate representations of the solution to be used. The appealing properties of the approach are demonstrated in simulations of a two-dimensional Taylor-Green vortex, doubly periodic shear layers, and a three-dimensional Taylor-Green vortex.

Atomistic biomolecular simulations predominantly utilize additive force fields (FF), where the electrostatic potential is modeled by fixed point charges. Among other consequences, the lack of polarizability in these models undermines the balance of hydrophilic/hydrophobic non-bonded interactions. Simulations of water/alkane systems using the TIP3P water model and CHARMM36 parameters reveal a 1 kcal/mol over-estimate of the experimental transfer free energy of water to hexadecane; more recent optimized water models (SPC/E, TIP4P/2005, TIP4P-Ew, TIP3P-FB, TIP4P-FB, OPC, TIP4P-D) overestimate this transfer free energy by approximately 2 kcal/mol. In contrast, the polarizable SWM4-NDP and SWM6 water models reproduce experimental values to within statistical error. As an alternative to explicitly modeling polarizability, this paper develops an efficient automated workflow to optimize pair-specific Lennard-Jones parameters within an additive FF. Water/hexadecane is used as a prototype and the free energy of water transfer to hexadecane as a target. The optimized model yields quantitative agreement with the experimental transfer free energy and improves the water/hexadecane interfacial tension by 6%. Simulations of five different lipid bilayers show a strong increase of water permeabilities compared to the unmodified CHARMM36 lipid FF which consistently improves match with experiment: the order-of-magnitude underestimate for monounsaturated bilayers is rectified and the factor of 2.8 - 4 underestimate for saturated bilayers is turned into a factor of 1.5 - 3 overestimate. While agreement with experiment is decreased for the diffusion constant of water in hexadecane, alkane transfer free energies, and the bilayers' area per lipid, the method provides a permeant-specific route to achieve a wide range of heterogeneous observables via rapidly optimized pairwise parameters.

This Review illustrates the evaluation of permeability of lipid membranes from molecular dynamics (MD) simulation primarily using water and oxygen as examples. Membrane entrance, translocation, and exit of these simple permeants (one hydrophilic and one hydrophobic) can be simulated by conventional MD, and permeabilities can be evaluated directly by Fick's First Law, transition rates, and a global Bayesian analysis of the inhomogeneous solubility-diffusion model. The assorted results, many of which are applicable to simulations of nonbiological membranes, highlight the limitations of the homogeneous solubility diffusion model; support the utility of inhomogeneous solubility diffusion and compartmental models; underscore the need for comparison with experiment for both simple solvent systems (such as water/hexadecane) and well-characterized membranes; and demonstrate the need for microsecond simulations for even simple permeants like water and oxygen. Undulations, subdiffusion, fractional viscosity dependence, periodic boundary conditions, and recent developments in the field are also discussed. Last, while enhanced sampling methods and increasingly sophisticated treatments of diffusion add substantially to the repertoire of simulation-based approaches, they do not address directly the critical need for force fields with polarizability and multipoles, and constant pH methods.

Automated parameterization of intermolecular pair potentials using global optimization techniques
(2014)

In this work, different global optimization techniques are assessed for the automated development of molecular force fields, as used in molecular dynamics and Monte Carlo simulations. The quest of finding suitable force field parameters is treated as a mathematical minimization problem. Intricate problem characteristics such as extremely costly and even abortive simulations, noisy simulation results, and especially multiple local minima naturally lead to the use of sophisticated global optimization algorithms. Five diverse algorithms (pure random search, recursive random search, CMA-ES, differential evolution, and taboo search) are compared to our own tailor-made solution named CoSMoS. CoSMoS is an automated workflow. It models the parameters’ influence on the simulation observables to detect a globally optimal set of parameters. It is shown how and why this approach is superior to other algorithms. Applied to suitable test functions and simulations for phosgene, CoSMoS effectively reduces the number of required simulations and real time for the optimization task.

Ionic liquids are highly relevant for industrial applications as they stand out due to their special chemical and physical features, e.g. low vapor pressure, low melting point or extraordinary solution properties. The goal of this work is to study the capability of the three ionic liquids [C2MIM][NTf2], [C12MIM][NTf2] and [C2MIM][EtSO4] to diffuse through a POPC membrane (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine). To achieve this, we used molecular simulation techniques, which on the one hand give insight into specific domains of the membrane and on the other hand compute partition coefficients and free energy profiles of solutes in lipid membranes, which cannot be measured by labor experiments. To be as accurate as possible we parameterized a new united atom force field for the ionic liquid of type 1-alkyl-3-methylimidazoliumethylsulfate [CnMIM][EtSO4] with n = 1,2,4,6,8. Like the other IL force field for [CnMIM][NTf2] (see Köddermann et al., ChemPhysChem 14, 3368–3374, 2013) used in this work, the new one was derived to reproduce experimental densities and self-diffusion coefficients. The new force field reproduces the experimental data extremely well. Using this force field, the influences of cation and anion exchanges as well as the variation of the chain length on the free energy could be analyzed. We performed umbrella-sampling to characterize the free energy profile of one ion pair, accompanied by a second one, in solution, at the membrane interface, and inside the membrane. In the outlook we present our intention to parameterize force fields in a systematic and user-friendly way. We will use the combination of two optimization toolkits, developed at SCAI: The global optimization toolkit CoSMoS and the local optimization techniques implemented in the software package GROW.

Molecular simulations are an important tool in the study of aqueous salt solutions. To predict the physical properties accurately and reliably, the molecular models must be tailored to reproduce experimental data. In this work, a combination of recent global and local optimization tools is used to derive force fields for MgCl2 (aq) and CaCl2 (aq). The molecular models for the ions are based on a Lennard-Jones (LJ) potential with a superimposed point charge. The LJ parameters are adjusted to reproduce the bulk density and shear viscosity of the different solutions at 1 bar and temperatures of 293.15, 303.15, and 318.15 K. It is shown that the σ-value of chloride consistently has the strongest influence on the system properties. The optimized force field for MgCl2 (aq) provides both properties in good agreement with the experimental data over a wide range of salt concentrations. For CaCl2 (aq), a compromise was made between the bulk density and shear viscosity, since reproducing the two properties requires two different choices of the LJ parameters. This is demonstrated by studying metamodels of the simulated data, which are generated to visualize the correlation between the parameters and observables by using projection plots. Consequently, in order to derive a transferable force field, an error of ∼3% on the bulk density has to be tolerated to yield the shear viscosity in satisfactory agreement with experimental data.