2,344 research outputs found

    Evidence of slippage breakdown for a superhydrophobic microchannel

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    © 2014 AIP Publishing LLC.A full characterization of the water flow past a silicon superhydrophobic surface with longitudinal micro-grooves enclosed in a microfluidic device is presented. Fluorescence microscopy images of the flow seeded with fluorescent passive tracers were digitally processed to measure both the velocity field and the position and shape of the liquid-air interfaces at the superhydrophobic surface. The simultaneous access to the meniscus and velocity profiles allows us to put under a strict test the no-shear boundary condition at the liquid-air interface. Surprisingly, our measurements show that air pockets in the surface cavities can sustain non-zero interfacial shear stresses, thereby hampering the friction reduction capabilities of the surface. The effects of the meniscus position and shape as well as of the liquid-air interfacial friction on the surface performances are separately assessed and quantified

    Slip behavior in liquid films on surfaces of patterned wettability: Comparison between continuum and molecular dynamics simulations

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    We investigate the behavior of the slip length in Newtonian liquids subject to planar shear bounded by substrates with mixed boundary conditions. The upper wall, consisting of a homogenous surface of finite or vanishing slip, moves at a constant speed parallel to a lower stationary wall, whose surface is patterned with an array of stripes representing alternating regions of no-shear and finite or no-slip. Velocity fields and effective slip lengths are computed both from molecular dynamics (MD) simulations and solution of the Stokes equation for flow configurations either parallel or perpendicular to the stripes. Excellent agreement between the hydrodynamic and MD results is obtained when the normalized width of the slip regions, a/σO(10)a/\sigma \gtrsim {\cal O}(10), where σ\sigma is the (fluid) molecular diameter characterizing the Lennard-Jones interaction. In this regime, the effective slip length increases monotonically with a/σa/\sigma to a saturation value. For a/σO(10)a/\sigma \lesssim {\cal O}(10) and transverse flow configurations, the non-uniform interaction potential at the lower wall constitutes a rough surface whose molecular scale corrugations strongly reduce the effective slip length below the hydrodynamic results. The translational symmetry for longitudinal flow eliminates the influence of molecular scale roughness; however, the reduced molecular ordering above the wetting regions of finite slip for small values of a/σa/\sigma increases the value of the effective slip length far above the hydrodynamic predictions. The strong inverse correlation between the effective slip length and the liquid structure factor representative of the first fluid layer near the patterned wall illustrates the influence of molecular ordering effects on slip in non-inertial flows.Comment: 12 pages, 10 figures Web reference added for animations: http://www.egr.msu.edu/~priezjev/bubble/bubble.htm

    Two-dimensional conical dispersion in ZrTe5 evidenced by optical spectroscopy

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    Zirconium pentatelluride was recently reported to be a 3D Dirac semimetal, with a single conical band, located at the center of the Brillouin zone. The cone's lack of protection by the lattice symmetry immediately sparked vast discussions about the size and topological/trivial nature of a possible gap opening. Here we report on a combined optical and transport study of ZrTe5, which reveals an alternative view of electronic bands in this material. We conclude that the dispersion is approximately linear only in the a-c plane, while remaining relatively flat and parabolic in the third direction (along the b axis). Therefore, the electronic states in ZrTe5 cannot be described using the model of 3D Dirac massless electrons, even when staying at energies well above the band gap 6 meV found in our experiments at low temperatures.Comment: Physical Review Letters 122, 217402 (2019). Corrected acknowledgment

    Nanoscale fluid flows in the vicinity of patterned surfaces

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    Molecular dynamics simulations of dense and rarefied fluids comprising small chain molecules in chemically patterned nano-channels predict a novel switching from Poiseuille to plug flow along the channel. We also demonstrate behavior akin to the lotus effect for a nanodrop on a chemically patterned substrate. Our results show that one can control and exploit the behavior of fluids at the nanoscale using chemical patterning.Comment: Phys. Rev. Lett. in pres

    Dynamic surface decoupling in a sheared polymer melt

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    We propose that several mechanisms contribute to friction in a polymer melt adsorbed at a structured surface. The first one is the well known disentanglement of bulk polymer chains from the surface layer. However, if the surface is ideal at the atomic scale, the adsorbed parts of polymer chains can move along the equipotential lines of the surface potential. This gives rise to a strong slippage of the melt. For high shear rates chains partially desorb. However, the friction force on adsorbed chains increases, resulting in quasi-stick boundary conditions. We propose that the adsorbed layers can be efficiently used to adjust the friction force between the polymer melt and the surface

    Exploring the volatile composition of comets C/2012 F6 (Lemmon) and C/2012 S1 (ISON) with ALMA

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    Comets formed in the outer and cold parts of the disk which eventually evolved into our Solar System. Assuming that the comets have undergone no major processing, studying their composition provides insight in the pristine composition of the Solar Nebula. We derive production rates for a number of volatile coma species and explore how molecular line ratios can help constrain the uncertainties of these rates. We analyse observations obtained with the Atacama Large Millimetre/Submillimetre Array of the volatile composition of the comae of comets C/2012 F6 (Lemmon) and C/2012 S1 (ISON) at heliocentric distances of ~1.45 AU and ~0.56 AU, respectively. Assuming a Haser profile with constant outflow velocity, we model the line intensity of each transition using a 3D radiative transfer code and derive molecular production rates and parent scale lengths. We report the first detection of CS in comet ISON obtained with the ALMA array and derive a parent scale length for CS of ~200 km. Due to the high spatial resolution of ALMA, resulting in a synthesised beam with a size slightly smaller than the derived parent scale length, we are able to tentatively identify CS as a daughter species, i.e., a species produced in the coma and/or sublimated from icy grains, rather than a parent species. In addition we report the detection of several CH3OH transitions and confirm the previously reported detections of HCN, HNC and H2CO as well as dust in the coma of each comet, and report 3sigma upper limits for HCO+. We derive molecular production rates relative to water of 0.2% for CS, 0.06-0.1% for HCN, 0.003-0.05% for HNC, 0.1-0.2% for H2CO and 0.5-1.0% for CH3OH, and show that the modelling uncertainties due to unknown collision rates and kinematic temperatures are modest and can be mitigated by available observations of different transitions of HCN.Comment: 10 pages, 4 figures, 2 tables. Accepted for publication in A&

    Diffusion in pores and its dependence on boundary conditions

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    We study the influence of the boundary conditions at the solid liquid interface on diffusion in a confined fluid. Using an hydrodynamic approach, we compute numerical estimates for the diffusion of a particle confined between two planes. Partial slip is shown to significantly influence the diffusion coefficient near a wall. Analytical expressions are derived in the low and high confinement limits, and are in good agreement with numerical results. These calculations indicate that diffusion of tagged particles could be used as a sensitive probe of the solid-liquid boundary conditions.Comment: soumis \`a J.Phys. Cond. Matt. special issue on "Diffusion in Liquids, Polymers, Biophysics and Chemical Dynamics

    Drainage of a nanoconfined simple fluid: rate effects on squeeze-out dynamics

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    We investigate the effect of loading rate on drainage in molecularly thin films of a simple fluid made of quasi-spherical molecules (octamethylcyclotetrasiloxane, OMCTS). We find that (i) rapidly confined OMCTS retains its tendency to organize into layers parallel to the confining surfaces, and (ii) flow resistance in such layered films can be described by bulklike viscous forces if one accounts for the existence of one monolayer immobilized on each surfaces. The latter result is fully consistent with the recent work of Becker and Mugele, who reached a similar conclusion by analyzing the dynamics of squeeze-out fronts in OMCTS [T. Becker and F. Mugele, Phys. Rev. Lett. {\bf 91} 166104(2003)]. Furthermore, we show that the confinement rate controls the nature of the thinning transitions: layer-by-layer expulsion of molecules in metastable, slowly confined films proceeds by a nucleation/growth mechanism, whereas deeply and rapidly quenched films are unstable and undergo thinning transitions akin to spinodal decomposition

    Organics in comet 67P – a first comparative analysis of mass spectra from ROSINA–DFMS, COSAC and Ptolemy

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    The ESA Rosetta spacecraft followed comet 67P at a close distance for more than 2 yr. In addition, it deployed the lander Philae on to the surface of the comet. The (surface) composition of the comet is of great interest to understand the origin and evolution of comets. By combining measurements made on the comet itself and in the coma, we probe the nature of this surface material and compare it to remote sensing observations. We compare data from the double focusing mass spectrometer (DFMS) of the ROSINA experiment on ESA's Rosetta mission and previously published data from the two mass spectrometers COSAC (COmetary Sampling And Composition) and Ptolemy on the lander. The mass spectra of all three instruments show very similar patterns of mainly CHO-bearing molecules that sublimate at temperatures of 275 K. The DFMS data also show a great variety of CH-, CHN-, CHS-, CHO2- and CHNO-bearing saturated and unsaturated species. Methyl isocyanate, propanal and glycol aldehyde suggested by the earlier analysis of the measured COSAC spectrum could not be confirmed. The presence of polyoxymethylene in the Ptolemy spectrum was found to be unlikely. However, the signature of the aromatic compound toluene was identified in DFMS and Ptolemy data. Comparison with remote sensing instruments confirms the complex nature of the organics on the surface of 67P, which is much more diverse than anticipated
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