Drop mobility on chemically heterogeneous and lubricant-impregnated surfaces

Controlling the motion of liquid drops in contact with a solid surface has broad technological implications in many different areas ranging from textiles to microfluidics and heat exchangers. The wettability of a surface is determined by specifying the apparent contact angle and contact angle hysteresis (CAH) that depend on the surface chemistry and morphology. The presence of chemical inhomogeneity and morphological disorder usually increases CAH. A liquid substrate, whose surface is atomically flat and homogenous, is then expected to exhibit a very low CAH. Low CAH determines high drop mobility, while high CAH favours drop pinning. Very slippery surfaces with exceptional omniphobicity are obtained by impregnating a textured solid with a lubricant. To guide and control the motion of drops, the solid surface can be decorated with suitable chemical patterns. In this review, we briefly outline the main results obtained in the past few years to passively control drop motion and produce robust omniphobic surfaces, highlighting some of the most promising applications of these novel functional surfaces

Droplet breakup driven by shear thinning solutions in a microfluidic T-Junction

Droplet-based microfluidics turned out to be an efficient and adjustable platform for digital analysis, encapsulation of cells, drug formulation, and polymerase chain reaction. Typically, for most biomedical applications, the handling of complex, non-Newtonian fluids is involved, e.g. synovial and salivary fluids, collagen, and gel scaffolds. In this study we investigate the problem of droplet formation occurring in a microfluidic T-shaped junction, when the continuous phase is made of shear thinning liquids. At first, we review in detail the breakup process providing extensive, side-by-side comparisons between Newtonian and non-Newtonian liquids over unexplored ranges of flow conditions and viscous responses. The non-Newtonian liquid carrying the droplets is made of Xanthan solutions, a stiff rod-like polysaccharide displaying a marked shear thinning rheology. By defining an effective Capillary number, a simple yet effective methodology is used to account for the shear-dependent viscous response occurring at the breakup. The droplet size can be predicted over a wide range of flow conditions simply by knowing the rheology of the bulk continuous phase. Experimental results are complemented with numerical simulations of purely shear thinning fluids using Lattice Boltzmann models. The good agreement between the experimental and numerical data confirm the validity of the proposed rescaling with the effective Capillary number.Comment: Manuscript: 11 pages 5 figures, 65 References. Textual Supplemental Material: 6 pages 3 figure. Video Supplemental Materials: 2 movie

Single File Flow of Biomimetic Beads for Continuous SERS Recording in a Microfluidic Device

A major challenge in cancer treatment is the quantification of biomarkers associated with a specific cancer type. Important biomarkers are the circulating tumor cells (CTCs) detached from the main cancer and circulating in the blood. CTCs are very rare and their identification is still an issue. Although CTCs quantification can be estimated by using fluorescent markers, all the fluorescence techniques are strongly limited by the number of emissions (therefore markers) that can be discriminated with one exciting line, by their bleaching characteristics, and by the intrinsic autofluorescence of biological samples. An emerging technique that can overcome these limitations is Surface Enhanced Raman Scattering (SERS). Signals of vibrational origin with intensity similar to those of fluorescence, but narrower bandwidths, can be easily discriminated even by exciting with a single laser line. We recently showed the benefit of this method with cells fixed on a surface. However, this approach is too demanding to be applied in clinical routine. To effectively increase the throughput of the SERS analysis, microfluidics represents a promising tool. We report two different hydrodynamic strategies, based on device geometry and liquids viscosity, to successfully combine a microfluidic design with SERS

Lithium niobate micromachining for the fabrication of microfluidic droplet generators

In this paper, we present the first microfluidic junctions for droplet generation directly engraved on lithium niobate crystals by micromachining techniques, preparatory to a fully integrated opto-microfluidics lab-on-chip system. In particular, laser ablation technique and the mechanical micromachining technique are exploited to realise microfluidic channels in T-and cross junction configurations. The quality of both lateral and bottom surfaces of the channels are therefore compared together with a detailed study of their roughness measured by means of atomic force microscopy in order to evaluate the final performance achievable in an optofluidic device. Finally, the microfluidics performances of these water-in-oil droplets generators are investigated depending on these micromachining techniques, with particular focus on a wide range of droplet generation rates

Thermolubricity of gas monolayers on graphene

Nanofriction of Xe, Kr and N2 monolayers deposited on graphene was explored with a quartz crystal microbalance (QCM) at temperatures between 25 and 50 K. Graphene was grown by chemical vapour deposition and transferred to the QCM electrodes with a polymer stamp. Graphene was found to strongly adhere to the gold electrodes at temperatures as low as 5 K and at frequencies up to 5 MHz. At low temperatures, the Xe monolayers are fully pinned to the graphene surface. Above 30 K, the Xe film slides and the depinning onset coverage beyond which the film starts sliding decreases with temperature. Similar measurements repeated on bare gold show an enhanced slippage of the Xe films and a decrease of the depinning temperature below 25 K. Nanofriction measurements of Kr and N2 confirm this scenario. This thermolubric behaviour is explained in terms of a recent theory of the size dependence of static friction between adsorbed islands and crystalline substrates

Drop motion induced by vertical vibrations

We have studied the motion of liquid drops on an inclined plate subject to vertical vibrations. The liquids comprised distilled water and different aqueous solutions of glycerol, ethanol and isopropanol spanning the range 1–39 mm2 s−1 in kinematic viscosities and 40–72 mN m−1 in surface tension. At sufficiently low oscillating amplitudes, the drops are always pinned to the surface. Vibrating the plate above a certain amplitude yields sliding of the drop. Further increasing the oscillating amplitude drives the drop upward against gravity. In the case of the most hydrophilic aqueous solutions, this motion is not observed and the drop only slides downward. Images taken with a fast camera show that the drop profile evolves in a different way during sliding and climbing. In particular, the climbing drop experiences a much bigger variation in its profile during an oscillating period. Complementary numerical simulations of 2D drops based on a diffuse interface approach confirm the experimental findings. The overall qualitative behavior is reproduced suggesting that the contact line pinning due to contact angle hysteresis is not necessary to explain the drop climbing