Liquid Formation Research Articles

Dynamic analysis of adsorbate behavior in nanopores: Liquid bridge formation, cavitation, and contact angle evaluation via molecular dynamics simulations

To explore the internal transport mechanisms and evolutionary processes within nanopore, molecular dynamic simulations were employed to explore the formation of liquid bridges and the evolution of menisci. The adsorption–desorption isotherms were obtained, and the dynamic behavior of the adsorbate was analyzed. Results revealed two distinct processes governing the behavior of the adsorbate within nanopore. At low pressure ratios, a molecular adsorption layer initially grows continuously on the pore surface. As the pressure ratio increases, an additional mechanism emerges, characterized by the formation of a liquid bridge near the nanopore mouth. This leads to pore filling as the liquid bridge expands and retreats towards the pore’s closed end. During desorption, cavitation occurs, which can be characterized as an activation process. Once initiated, cavitation intensifies, progressively increasing the number of cavities. The convergence of these cavities undermines the stability of the liquid bridge, ultimately resulting in its collapse and the rapid evaporation of the adsorbate molecules. Additionally, we further calculated the contact angle at the vapor–liquid interface using the Kelvin equation. The results indicated a deviation of less than 5 % compared to our simulations, suggesting that the Kelvin equation is applicable for materials with pore sizes of at least 3.6 nm.

Clr4SUV39H1 ubiquitination and non-coding RNA mediate transcriptional silencing of heterochromatin via Swi6 phase separation

Transcriptional silencing by RNAi paradoxically relies on transcription, but how the transition from transcription to silencing is achieved has remained unclear. The Cryptic Loci Regulator complex (CLRC) in Schizosaccharomyces pombe is a cullin-ring E3 ligase required for silencing that is recruited by RNAi. We found that the E2 ubiquitin conjugating enzyme Ubc4 interacts with CLRC and mono-ubiquitinates the histone H3K9 methyltransferase Clr4SUV39H1, promoting the transition from co-transcriptional gene silencing (H3K9me2) to transcriptional gene silencing (H3K9me3). Ubiquitination of Clr4 occurs in an intrinsically disordered region (Clr4IDR), which undergoes liquid droplet formation in vitro, along with Swi6HP1 the effector of transcriptional gene silencing. Our data suggests that phase separation is exquisitely sensitive to non-coding RNA (ncRNA) which promotes self-association of Clr4, chromatin association, and di-, but not tri- methylation instead. Ubc4-CLRC also targets the transcriptional co-activator Bdf2BRD4, down-regulating centromeric transcription and small RNA (sRNA) production. The deubiquitinase Ubp3 counteracts both activities.

Numerical Study on Droplet Splashing Behavior of Slag‐Splashing for Converter Protection Using Volume of Fluid‐Discrete Phase Model Two‐Way Conversion Model

Limited quantitative research exists on the complex phenomenon of slag splashing in converters. A comprehensive modeling framework is developed to fill this gap, integrating a 3D two‐phase flow model with a volume of fluid‐discrete phase model two‐way conversion model. This framework explores droplet behavior during splashing for converter protection, encompassing the mutual conversion between slag and discrete droplets induced by top‐blowing oxygen. It also tracks the trajectories of all droplets, enabling a detailed quantitative analysis of the splashing process. The Eulerian wall film model is used to simulate liquid film formation on the converter wall. Model predictions are validated against 1:10 scale experimental data from a 50 t converter. This assessment covers splashing rates, droplet locations, and size distribution under various operating conditions. Parametric studies identified an optimal top‐blowing flow rate of 8.80 Nm3 h−1 and an oxygen lance height of 233.2 mm, balancing splashing effectiveness with production cost and safety.

Enhancing strength and ductility of CuCrZr high-conductivity alloy via lamellar heterostructures on grain boundaries

Heterogeneous lamellar structure materials have attracted extensive attention due to their exceptional strength and ductility. In this study, Y element was introduced into CuCrZr alloys to adjust the liquid phase formation temperature of the CuZrY phase during the solution annealing process. By employing cold rolling deformation prior to annealing to elongate the grains, the liquid phase was promoted to wet the elongated grain boundaries during the annealing process, ultimately forming lamellar CuZrY heterostructures distributed along the grain boundaries. The heterogeneous lamellar structure, the grain boundary distribution characteristics, and the effect of Y on stacking fault energy enhanced the hetero-deformation induced working hardening, thereby improving both the strength and ductility of the CuCrZrY alloy. Besides, the investigated CuCrZrY alloy achieved an excellent combination of tensile strength, uniform elongation, electrical conductivity and thermal conductivity, with values of 527 MPa, 10.66%, 83% IACS and 335.5 W/(m·K), respectively. Therefore, the method of controlling liquid phase temperature through composition adjustment and liquid phase infiltration path through grain deformation offers new possibilities for the design of heterogeneous lamellar structure materials.

Modelling nematic liquid crystal in fractal dimensions

In this paper we present a fractal Berreman's model which account for azimuthal surface anchoring of nematic liquid crystals which play a leading role nowadays in biomedical field and pharmaceutical controlled release dosage forms. The model is based on the concept of "product-like fractal measure" in anisotropic media which permits to describe liquid crystals formation in terms of fractal dimensions. It was observed that fractal dimensions affect both the polar azimuthal angle and the Franck excess elastic energy density of the distortion. For fractal dimensions close to unity, our analysis reveals the emergence of fluctuations and large deformations in the dynamical variables of the theory which suggest the presence of non-linear elastic instabilities or emergence of defect structures in liquid crystals. These fluctuations fade away for fractal dimensions much less than unity. We have evaluated the elastic energy per unit of area which is found to depend on the square of the fractal dimension. This leads to a decrease of the saturation voltage which is necessary to reduce the elastic energy of liquid crystals films in order to minimize the elastic energy. This reduction may describe nematic liquid crystals free from deformations, singularities or weak anchoring surfaces.

Noble metal-free tandem catalysis enables efficient upcycling plastic waste into liquid fuel components

The lack of effective approaches for upcycling waste plastic has led to severe environmental pollution and squandering of carbon resources. While hydrocracking macromolecular polyolefins over typical metal-zeolite catalyst produces high quality liquid fuel components, the limited activity of base metal and restricted accessibility of acid sites within microporous zeolite renders this process still not in practical scale. A tandem catalyst comprising Ni-WO3/Al2O3 and Beta zeolite was developed for consecutive hydrocracking polyolefins, achieving a yield of 86.2 % of primarily gasoline-jet ranged hydrocarbons (mainly C5-C16 and minor C16+) at 280 °C. The incorporation of tungsten species onto Ni/Al2O3 largely enhances the surface acidity and accelerates the primary cracking process that converts polyethylene (PE) into medium-sized intermediates, which would readily diffuse into the pore networks of Beta and undergo further cracking to yield desired liquid hydrocarbons. In addition, this tandem catalyst also promotes facile hydrocracking of consumer-grade plastic waste and maintains excellent stability over 5 recycling tests. The noble-metal-free catalyst achieves an impressive liquid formation rate of 5.74 g·gcat.−1·h−1, rivaling the noble metal-based catalyst and demonstrating high application prospects.

Thermodynamic and computational approaches to the stability and structural transformation of Xe + large-molecule guest substance (LMGS) hydrates

In this study, the influence of different types of large-molecule liquid substances (LMGSs) and formation conditions on the stability and structural transformation of Xe + LMGS hydrates was investigated using phase equilibria, powder X-ray diffraction (PXRD), 129Xe NMR spectroscopy, and molecular dynamics (MD) simulations. The phase equilibria of Xe hydrates in the presence of three different LMGS types (neohexane [NH], methylcyclopentane [MCP], and methylcyclohexane [MCH]) were measured in the pressure range of 0.1–1.0 MPa. The equilibrium curves of Xe + MCH and Xe + NH hydrates shifted away from that of pure Xe hydrate under low pressure, whereas they coincided with that of pure Xe hydrate under high pressure. Interestingly, the equilibrium curve of Xe + MCP hydrate aligned with that of pure Xe hydrate throughout the pressure range. PXRD and 129Xe NMR analyses demonstrated that the equilibrium curve shift under low pressure was caused by the formation of sH (Xe + LMGS) hydrates, which was attributed to the inclusion of NH or MCH. However, MCP did not participate in sH hydrate formation with Xe. MD simulations revealed that MCP in the large cages did not contribute to the thermodynamic or dynamic stability of sH hydrates. The findings of this study provide valuable insights into the development of hydrate-based noble gas capture and storage.

Design and batch fabrication of anisotropic microparticles toward small-scale robots using microfluidics: recent advances.

Small-scale robots with shape anisotropy have garnered significant scientific interest due to their enhanced mobility and precise control in recent years. Traditionally, these miniature robots are manufactured using established techniques such as molding, 3D printing, and microfabrication. However, the advent of microfluidics in recent years has emerged as a promising manufacturing technology, capitalizing on the precise and dynamic manipulation of fluids at the microscale to fabricate various complex-shaped anisotropic particles. This offers a versatile and controlled platform, enabling the efficient fabrication of small-scale robots with tailored morphologies and advanced functionalities from the microfluidic-derived anisotropic microparticles at high throughput. This review highlights the recent advances in the microfluidic fabrication of anisotropic microparticles and their potential applications in small-scale robots. In this review, the term 'small-scale robots' broadly encompasses micromotors endowed with capabilities for locomotion and manipulation. Firstly, the fundamental strategies for liquid template formation and the methodologies for generating anisotropic microparticles within the microfluidic system are briefly introduced. Subsequently, the functionality of shape-anisotropic particles in forming components for small-scale robots and actuation mechanisms are emphasized. Attention is then directed towards the diverse applications of these microparticle-derived microrobots in a variety of fields, including pollution remediation, cell microcarriers, drug delivery, and biofilm eradication. Finally, we discuss future directions for the fabrication and development of miniature robots from microfluidics, shedding light on the evolving landscape of this field.

Dissolution Behaviors of Recycled Cement Paste and Lime in EAF Slag Under Static Conditions

AbstractRecycled cement paste (RCP) is a CaO-rich resource that is recycled from waste concrete and waste cement. For reducing environmental impact and promoting comprehensive resource utilization, RCP could partially replace lime as flux in electric arc furnace (EAF) steelmaking process. In this study, the dissolution behaviors of RCP and lime in EAF slag at 1400 °C and 1500 °C were investigated using static dissolution experiments. The measured dissolution rate constant of lime at 1400 °C and 1500 °C is 3.12×10−5 and 8.42×10−5 m/s, respectively, while that for RCP is 1.37×10−4 and 2.91×10−4 m/s, respectively. For the lime dissolution, a dense dicalcium silicate (C2S) product layer was generated at the dissolution interface, with the diffusion of Ca2+ in the C2S layer being the limiting step for the lime dissolution. However, for the RCP dissolution, no product layer was observed at the dissolution interface. Instead, a dissolution intermediate layer forms due to slag penetration. During the dissolution of RCP, Ca2+ and SiO44− diffuse from RCP layer to slag, while Fe2+ and AlO45− diffuse from slag to RCP layer accumulating in the dissolution intermediate layer. Furthermore, a dissolution model was developed based on current experimental results, which helps to predict dynamic dissolution process of lime and RCP in EAF slag. In general, the dissolution rate of RCP in EAF slag was much higher than that of lime, partially adding RCP as flux in EAF could accelerate the liquid slag formation in EAF steelmaking process.

Coupled Discrete Phase and Eulerian Wall Film Models for Drug Deposition Efficacy Analysis in Human Respiratory Airways.

The current study explores the effectiveness of drug particle deposition into human respiratory airways to cure various pulmonary-bound ailments. It has been assumed that drug solutions are inhaled in the form of tiny droplets or mist, which after striking create a thin layer along the inner surface of airways where the virus initially resides to infect the human body. A coupled Eulerian wall film (EWF) and discrete phase model (DPM) based simulation approach is used to capture these dynamics. Here, the Lagrangian DPM technique tracks the dynamics of tiny droplets, while the liquid layer formation after striking is captured using the Eulerian thin film approximations or the EWF model. Previous studies in this field primarily employed only the DPM method, which is inadequate to predict the poststriking dynamics of drug layer deposition and their spread to neutralize the respiratory virus. The drug delivery effectiveness is characterized by three different particle sizes, 1, 5, and 10 μm at the inhalation rates of 15, 30, and 60 L per minute (LPM). It has been found that the size of the drug particles significantly influences drug delivery effectiveness. The film thickness increases monotonically with particle sizes and inhalation rates. However, this increase in averaged film thickness is prominent in the range 5 to 10 μm (≈60%) compared to 1 to 5 μm (≈10%) droplet sizes at generation level 4 (G4). The other deposition parameters, e.g., deposition fraction, deposition density, and area coverage) roughly show similar behavior with the increase in droplet sizes. Therefore, it is recommended to vary the droplet sizes between 5 and 10 μm for better deposition effectiveness. The sizes of more than 10 μm mostly stuck into the oral cavity and cannot reach the targeted generations. In contrast, less than 5 μm may reach much deeper generations than the targeted one.

Nanoheterogeneity in Protic and Aprotic Alkylimidazolium Bistriflimide Ionic Liquids

Many ionic liquids, including alkylimidazolium salts, form a nanoheterogeneous structure with polar and apolar domains in their liquid phase. Using molecular dynamics simulations, the influence of the structure of the cations of a series of aprotic ([CnC1Im][TFSI], [CnCnIm][TFSI]) and protic ([HCnIm][TFSI]) alkylimidazolium bistrilimides on the domain structure of their liquid phase was studied. The characteristic sizes of domains and the extent of domain segregation in different liquids have been compared. It has been shown that the latter, but not the former, is a key factor determining the magnitude of the Gibbs free energy of cavity formation in nanostructured ionic liquids, which in turn governs their solvation properties.

Liquid crystal droplets formation and stabilization during phase transition process

Abstract The study of phase transition processes in liquid crystals (LCs) remains challenging. Most thermotropic LCs exhibit a narrow temperature range and a rapid phase transition from the isotropic (ISO) to the nematic (N) phase, which make it difficult to capture and manipulate the phase transition process. In this study, we observed the evolution of small droplets during the ISO-N phase transition in ferroelectric nematic (NF) LC RM734. After doping with metal nanoparticles (NPs), the temperature range of the phase transition broadened, and the droplets formed during the phase transition remained stable, with their diameter increasing linearly with temperature. In addition, droplets doped with NPs can be well controlled by an external electric field. This discovery not only aids in understanding the fundamental mechanisms of LC phase transitions but also provides a simple alternative method for preparing droplets, which is potentially valuable for applications in optoelectronic devices and sensors.

Calcined colemanite as an additive for iron ore sintering process

During sintering process, iron ores, fluxes and coke are agglomerated into a desirable blast furnace feed. The degrading iron ore quality and environmental norms has forced sinter producers to look for additives which can improve the sintering process efficiency. For the current work, use of calcined colemanite as an additive was studied by adding it from 0% to 4% within the sinter raw blend through lab-scale pot trials. During the sintering process, calcined colemanite forms a Calcium Borosilicate (Ca11B2Si4O22) phase at temperature above 400 °C which latter gets dissociated within the liquid melt thus increasing the liquid slag formation. Increasing calcined colemanite up to 2% increases tumbler index from 56.27% to 61.67%, decreasing thereafter to 55.33% at 4% of calcined colemanite. The sinter yield (+5 mm) is also found to be maximum of 89.39% at 2% of calcined colemanite. An increase in calcined colemanite from 0% to 4% increases sintering time from 20 to 26 min, decreasing the overall sinter productivity from 2.35 to 1.99 t/m2/h. Before integrating calcined colemanite within the sintering process at plant scale, its cost and efficacy must be considered. An alternate approach can be combining it with an organic binder where the two can complement each other in providing the required sinter properties.

Free Energy Evaluation of Cavity Formation in Metastable Liquid Based on Stochastic Thermodynamics.

Nucleation is a fundamental and general process at the initial stage of first-order phase transition. Although various models based on the classical nucleation theory (CNT) have been proposed to explain the energetics and kinetics of nucleation, detailed understanding at nanoscale is still required. Here, in view of the homogeneous bubble nucleation, we focus on cavity formation, in which evaluation of the size dependence of free energy change is the key issue. We propose the application of a formula in stochastic thermodynamics, the Jarzynski equality, for data analysis of molecular dynamics (MD) simulation to evaluate the free energy of cavity formation. As a test case, we performed a series of MD simulations with a Lennard-Jones (LJ) fluid system. By applying an external spherical force field to equilibrated LJ liquid, we evaluated the free energy change during cavity growth as the Jarzynski's ensemble average of required works. A fairly smooth free energy curve was obtained as a function of bubble radius in metastable liquid of mildly negative pressure conditions.

Numerical Study of Liquid Water Formation and Transport in Porous Media

Fundamental understanding of liquid water formation and transport in fuel cells is of great importance for achieving high durability, reliability, and maximizing cell performance. For low temperature fuel cells, water may exist as vapor or liquid phase and is involved in various electrochemical reactions and transport mechanisms. The condensation process occurs when local water vapor pressure exceeds the saturation pressure. In this work, we first investigate the permeation of liquid water in the gas diffusion layer (GDL). To this aim, a two-dimensional isothermal model considering reconstructed GDL microstructure in conjunction with VOF model is implemented. The effects of mixed wettability of materials, operating temperature, and Polytetrafluoroethylene (PTFE) loadings on liquid water transport in the porous media are investigated numerically. The liquid water breakthrough and the capillary fingering regime are captured and compared. The results show that liquid water saturation in the GDL increases with decreasing PTFE loadings. Moreover, the results demonstrated that the local microstructure in the GDL has a strong effect and can dominate the overall water distribution. To further study water condensation, the isothermal model is expanded to non-isothermal for including physics of phase change heat transfer and species transport. In addition, anisotropic thermal conductivity is incorporated to study its effect on temperature distribution and liquid water distribution. The results show that initially the liquid water is formed as micro droplets and then these micro droplets are combined to form large droplets. Moreover, the impacts of water generation rate, temperature gradient, operating pressure, and contact angle on condensation have been investigated. The findings of this work are expected to provide insights into designing more reliable GDL in fuel cells. Figure 1

Structure, Microheterogeneity, and Transport Properties of Ethaline Decoded by X-ray/Neutron Scattering and MD Simulation.

Ethaline, a deep eutectic solvent (DES) composed of choline chloride (ChCl)-ethylene glycol (EG) in a 1:2 molar ratio, is garnering significant interest for its wide potential applications. The nature of liquid formation and the structure of H-bonds within ethaline were investigated by X-ray scattering (XRS), neutron scattering (NS), and MD simulations. The sum of the dissociation energy barriers of Ch-EG (3.31 kJ·mol-1) and EG-Cl (4.28 kJ·mol-1) exceeds that of Ch-Cl (5.97 kJ·mol-1). This results in a more pronounced solvation of ChCl by EG compared to ChCl association, facilitating the solubilization of ChCl crystals by EG to form a DES. A partial radial distribution function (PDF) reveals that Cl- solvation is dominated by the hydroxyl group of EG, while the methylene group dominates Ch+ solvation. The spatial distribution function (SDF) shows that the distribution of EG and Cl- around Ch+ partially overlaps with that of the quaternary ammonium group. However, the center of mass distance of Ch-Cl (4.95 Å) is significantly lower than that of Ch-EG (5.65 Å), suggesting a favorable advantage for Cl- in this competition. Chain and ring structure distributions provide direct evidence of the microheterogeneity of ethaline. Hydroxyl groups on the EG promote the formation of a chain structure in ethaline, while methylene groups favor a ring structure. H-bond, carbon H-bond, and Cl- bridge bond restrict Cl- diffusion. This new understanding is crucial for a deeper comprehension of the microstructure of ethaline and for elucidating its mechanisms in applications.

Experimental investigation and thermodynamic modelling of WC-Fe-Ni-Co-Cr cemented carbides

This work investigates the effect of Cr addition into the FeCoNi binder phase of the cemented carbides (WC-FeCoNi) using experimental and computational techniques. Liquid phase formation temperatures and C contents of WC-Fe-Ni-Co-Cr alloys were used as experimental results. Based on this, a thermodynamic modelling was conducted on the W-C-Fe-Ni-Co-Cr system using the CALPHAD (CALculation of PHAse Diagrams) approach. Taking into account the experimental and theoretical results, it was shown that the error in the solidus and liquidus temperatures were lower in the database generated in this work in comparison to the commercial thermodynamic databases for steels and cemented carbides. Using the database developed in the present work, the experimental data can be well reproduced.In addition, the maximum solubility of Cr to avoid the formation of Cr-rich carbides was also deduced from this study.

Thermodynamics analysis and experimental investigation of EAF slag based ceramics materials for circular economy

The disposal of electric arc furnace (EAF) slag is often problematic, with most of it ending up being landfilled rather than recycled. Incorporating EAF slag into the typical clay-feldspar-quartz system to produce useful ceramics offers a potential and environmentally safer option. Thermodynamics package FactSage 8.2 was employed to predict the equilibrium-products of sintering process of EAF slag mixtures at different temperatures ranging from 600 to 1600 °C. Subsequent ceramic products were fabricated at a temperature of 1150 °C following the thermodynamic analysis by considering the fraction of liquid formation and the viscosity of the system. These products were further subjected to X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses and compared to the thermodynamic predictions. The physical performance of the products was also examined by evaluating the shrinkage, water absorption, apparent porosity, bulk density and modulus of rupture (MOR). When EAF slag was added to the base mixture, there was a positive trend of improvement in the physical properties and specifically, MOR peak value of 37.56 MPa was obtained when 40 % EAF slag was added. However, the MOR value as well as other physical properties started to decline when the base mixture had more than 40 % EAF slag. Conclusively, incorporating 40 % EAF slag improved the final product and correlated with the thermodynamic studies, process parameters, and experimental assessments of the ceramic tiles.

Thermomechanical and thermodynamic analysis of the sintering process of Mn-based oxygen carrier in chemical looping gasification of biomass

The Mn-based oxygen carrier (OC) owns a great oxygen carrying capacity and a high reactivity in the chemical looping gasification of biomass. However, the sintering of the Mn-based OC can cause serious defluidization or even the shut-down of the biomass chemical looping gasifier. In this study, the sintering kinetics and mechanism of Mn-based OC in the gasification of two typical biomass ash were revealed by thermomechanical and thermodynamic analysis. It revealed that the manganese silicate was converted to iwakiite (MnFe2O4) and liquid at high temperatures in the high-Mn OC (OC2), leading to the liquid sintering mechanism and high apparent activation energy of sintering (Es), with a maximum shrinkage rate of 6.14 %/oC. Conversely, the solid sintering mechanism of the low-Mn OC (OC1) was attributed to the FeMn2O4 crystallization, leading to a low shrinkage rate (The maximum shrinkage rate was 0.30 %/oC). The sintering rate of Mn-based OC was closely related to the liquid content, and the biomass ash addition advantaged the liquid formation. Therefore, the Es of OC1 was increased from 44 kJ/mol to 151 kJ/mol at the 15 wt% addition of corn straw ash, and Es of OC2 was increased from 72 kJ/mol to 93–107 kJ/mol at 20 wt% addition of biomass ash. Element distribution analysis supported that Ca in sawdust ash improved the bonding between Mn and Si, improving the Mn-based minerals crystallization and OC expansion. However, the K in corn straw ash facilitated the melting of rhodonite(MnSiO3), and the expansion of Mn-based OC was inhibited. This study provides valuable insights into the sintering mechanism of the Mn-based oxygen carrier and its relationship with liquid evolution behavior in the chemical looping gasification of biomass.

Determination Of Two-Phase Flow Regimes Of A Condensing Water-Air Mixture In An Array Of Micro Channels

Proton exchange membrane (PEM) full cells (FCs) are a promising alternative to combustion engines for mobile applications. Their signature low operating temperature leads to the possible existence of product water in its liquid form. Liquid water formation and transport are important phenomena to understand and model in order to facilitate the development of new, more efficient PEMFCs. This contribution investigates the two-phase flow phenomena separately by introducing a gaseous air-vapor mixture into an optically accessible fuel cell flow plate with 14 parallel micro channels (confinement number Co = 7.3) and a carbon paper inlay representing the FC's gas diffusion layer and bringing it to the point of onset of condensation. Special care is taken to provide a controlled and reproducible air-vapor mixture with low pressure pulsation. One key feature of the experiment is that the flow plate used is designed to be as similar to a regular research fuel cell flow plate as possible, retaining its channel surface properties and electrical parameters. It can also be heated to a given temperature to mimic the fuel cell operating conditions. Therefore, the same plate can also be used in in-situ experiments in an operated fuel cell. An air mass flow rate of 500 - 1000 mLn / min with relative humidities of 75% - 95% at 65°C and 75°C was investigated. The emerging flow patterns were captured using a high-speed camera at 250 Hz and categorized using canonical two-phase flow regime nomenclature. It is shown that the present setup can produce the relevant two-phase flow patterns that can be found in operated fuel cells as reported by previous studies and is furthermore equipped to investigate flow states not easily reached with an operated fuel cell (e.g. flooded channels).