Collective Effects in Ionic Liquid [emim][Tf2N] and Ionic Paramagnetic Nitrate Solutions without Long-Range Structuring.

Mesoscopic shear elasticity has been revealed in ordinary liquids both experimentally by reinforcing the liquid/surface interfacial energy and theoretically by nonextensive models. The elastic effects are here examined in the frame of small molecules with strong electrostatic interactions such as room temperature ionic liquids [emim][Tf2N] and nitrate solutions exhibiting paramagnetic properties. We first show that these charged fluids also exhibit a nonzero low-frequency shear elasticity at the submillimeter scale, highlighting their resistance to shear stress. A neutron scattering study completes the dynamic mechanical analysis of the paramagnetic nitrate solution, evidencing that the magnetic properties do not induce the formation of a structure in the solution. We conclude that the elastic correlations contained in liquids usually considered as viscous away from any phase transition contribute in an effective way to collective effects under external stress whether mechanical or magnetic fields.

Capillary-size flow of human blood plasma: Revealing hidden elasticity and scale dependence.

The dynamical mechanical analysis of blood generally uses models inspired by conventional flows, assuming scale-independent homogeneous flows and without considering fluid-surface boundary interactions. The present experimental study highlights the relevance of using an approach in line with physiological reality providing a strong interaction between the fluid and the boundary interface. New dynamic properties of human blood plasma are found: a finite shear elastic response (solid-like property) is identified in nearly static conditions, which also depends on the scale (being reinforced at small scales). The elastic behavior is confirmed by the induction, without heat transfer, of local hot and cold thermodynamic states evidencing a thermo-mechanical coupling in blood plasma so far known only in elastic materials. This finding opens new routes for medical diagnosis and device fabrication.

Highlighting Thermo-Elastic Effects in Confined Fluids.

The recent identification of a finite shear elasticity in mesoscopic fluids has motivated the search of other solid-like properties of liquids. We present an innovative thermal approach of liquids. We identify a dynamic thermo-elastic mesoscopic behavior by building the thermal image produced by different liquids upon applying a low frequency mechanical shear field. We selected three fluids: a low molecular weight polybutylacrylate (PBuA), polypropyleneglycol (PPG), and glycerol. We demonstrate that a part of the energy of the shear strain is converted in cold and hot shear bands varying synchronously with the applied shear field. This thermodynamic change suggests a coupling to shear elastic modes in agreement with the low frequency shear elasticity theoretically foreseen and experimentally demonstrated.

Strain-induced violation of temperature uniformity in mesoscale liquids.

Thermo-elasticity couples the deformation of an elastic (solid) body to its temperature and vice-versa. It is a solid-like property. Highlighting such property in liquids is a paradigm shift: it requires long-range collective interactions that are not considered in current liquid descriptions. The present microthermal studies provide evidence for such solid-like correlations. It is shown that ordinary liquids emit a modulated thermal signal when applying a low frequency (Hz) mechanical shear stress. The liquid splits in several tenths microns wide hot and cold thermal bands, all varying synchronously and separately with the applied stress wave reaching a sizable amplitude of ± 0.2 °C. Thermomechanical coupling challenges fluid dynamics: it reveals that the liquid does not dissipate the energy of shear waves at low frequency, but converts it in non-uniform thermodynamic states. The dynamic thermal changes work in an adiabatic way supporting the hypothesis of the excitation of macroscopic elastic correlations whose range is limited to several tens of microns, in accordance with recent non-extensive theoretical models. The proof of thermomechanical coupling opens the way to a new generation of energy-efficient temperature converters.

Bringing to Light Hidden Elasticity in the Liquid State Using In-Situ Pretransitional Liquid Crystal Swarms.

The present work reveals that at the sub-millimeter length-scale, molecules in the liquid state are not dynamically free but elastically correlated. It is possible to "visualize" these hidden elastic correlations by using the birefringent properties of pretransitional swarms persistent in liquids presenting a weak first order transition. The strategy consists in observing the optical response of the isotropic phase of mesogenic fluids to a weak (low energy) mechanical excitation. We show that a synchronized optical response is observable at frequencies as low as 0.01Hz and at temperatures far away from any phase transition (up to at least 15°C above the transition). The observation of a synchronized optical signal at very low frequencies points out a collective response and supports the existence of long-range elastic (solid-like) correlations existing at the sub-millimeter length-scale in agreement to weak solid-like responses already identified in various liquids including liquid water. This concept of elastically linked molecules differs deeply with the academic view of molecules moving freely in the liquid state and has profound consequences on the mechanisms governing collective effects as glass formation, gelation and transport, or synchronized processes in physiological media.

Highlighting a Cooling Regime in Liquids under Submillimeter Flows.

The shear flow of ordinary liquids is for the first time observed at the submillimeter scale by thermal imaging. We report on microinfrared experiments, showing that liquids as important as water flowing on wetting surfaces produce cooling, while the academic view would foresee heating production. This apparent counterintuitive cooling effect shows that the increase of the internal energy due to the flow can result in different shapes, including a cooling process, before reaching the conventional heating regime at higher shear rates. This unknown property might be interpreted as a transient stretching state of the liquid. Shearing liquids might be a promising alternative compared to conventional endothermic processes (gas expansion or vaporization of a liquid, the Peltier effect, and so forth).

Identification of a low-frequency elastic behaviour in liquid water.

This article deals with the identification of solid-like properties measured at room temperature at a sub-millimetre length scale in liquid water. At a macroscopic scale, normal liquids (i.e. above melting temperature), and in particular water, are typically and empirically defined by the absence of shear elasticity, in contrast to solids or plastic fluids that require a stress threshold for flowing. A novel method optimizing the transmission of the shear stress to the sample enables a more complete probe of the mechanical response of liquids. It reveals that glass formers and viscous alkanes actually exhibit finite macroscopic shear elasticity away from any phase transition. This protocol is here applied for the first time to liquid water at room temperature, revealing, at the sub-millimetre scale, a low-frequency solid-like property.

Shear-induced isotropic to nematic transition of liquid-crystal polymers: identification of gap thickness and slipping effects.

The shear-induced isotropic-nematic transition is a generic property of liquid-crystalline polymer melts which is identified by the emergence in the isotropic phase of a strong birefringence above a critical shear rate. Although spectacular, this transition cannot be explained on the basis of a conventional approach (coupling with pretransitional fluctuations or with viscoelastic relaxation times). We investigate the asymptotic rheo-optical behavior of the shear-induced phase. The sample is an unentangled cyanobiphenyl side-chain polyacrylate. We show that the birefringence increases almost linearly and then saturates above a given shear rate depending on the gap thickness. Similarly, the shear stress versus shear rate curve exhibits for the same thickness and using the same substrate (quartz), an overshoot occurring at about the same shear rates followed by the stress plateau (indicating a stress-optical equivalence). In contrast, when the substrate is different, the stress-optical equivalence is no more valid. We interpret the overshoot and the plateau observed in birefringence and in shear stress curves as the entrance in a so far unidentified macroscopic sliding regime. The slipping mechanism is corroborated by the recent identification of macroscopic long-range correlations in unentangled polymer melt and contrasts with a description in terms of a nucleation-growth process as in wormlike micellar solutions.

New light on old wisdoms on molten polymers: conformation, slippage and shear banding in sheared entangled and unentangled melts.

The flow of viscoelastic materials is usually interpreted as resulting from intramolecular properties. Typically, the non-linear flow behaviour and sluggish relaxation dynamics in entangled polymers are interpreted by a disentanglement process. This molecular interpretation has never been validated by direct observation. We report here on in situ observations of polymer melts under steady-state shear flow using neutron scattering and particle tracking velocimetry. It is shown that the chains remain largely undeformed under steady-state shear flow whereas wall slippage and shear-banding are identified in both entangled and unentangled polymer melts. These observations are of prime importance; they reveal that the flow mechanism and its viscoelastic signature reflect a collective effect and not properties of individual chains.