Ref HAL: hal-02374362_v1
Ref Arxiv: 1812.06484
DOI: 10.1039/c9sm01172b
WoS: WOS:000493519700010
Ref. & Cit.: NASA ADS
Exporter : BibTex | endNote
1 Citation
Résumé:

Cells and tissues have the remarkable ability to actively generate the forces required to change theirshape. This active mechanical behavior is largely mediated by the actin cytoskeleton, a crosslinkednetwork of actin filaments that is contracted by myosin motors. Experiments and active gel theorieshave established that the length scale over which gel contraction occurs is governed by a balancebetween molecular motor activity and crosslink density. By contrast, the dynamics that govern thecontractile activity of the cytoskeleton remain poorly understood. Here we investigate the microscopicdynamics of reconstituted actin–myosin networks using simultaneous real-space video microscopy andFourier-space dynamic light scattering. Light scattering reveals different regimes of microscopicdynamics as a function of sample age. We uncover two dynamical precursors that precede macroscopicgel contraction. One is characterized by a progressive acceleration of stress-induced rearrangements,while the other consists of sudden, heterogeneous rearrangements. Intriguingly, our findings suggest aqualitative analogy between self-driven rupture and collapse of active gels and the delayed rupture ofpassive gels observed in earlier studies of colloidal gels under external loads.

Ref HAL: hal-02344464_v1
Ref Arxiv: 2011.07825
DOI: 10.1038/s41598-019-50164-6
WoS: WOS:000487586600003
Ref. & Cit.: NASA ADS
Exporter : BibTex | endNote
7 Citations
Résumé:

The peculiar linear temperature-dependent swelling of core-shell microgels has been conjectured to be linked to the core-shell architecture combining materials of different transition temperatures. Here the structure of pNIPMAM-core and pNNPAM-shell microgels in water is studied as a function of temperature using small-angle neutron scattering with selective deuteration. Photon correlation spectroscopy is used to scrutinize the swelling behaviour of the colloidal particles and reveals linear swelling. Moreover, these experiments are also employed to check the influence of deuteration on swelling. Using a form free multi-shell reverse Monte Carlo approach, the small-angle scattering data are converted into radial monomer density profiles. The comparison of ‘core-only’ particles consisting of identical cores to fully hydrogenated core-shell microgels, and finally to H core/D shell architectures unambiguously shows that core and shell monomers display gradient profiles with strong interpenetration, leading to cores embedded in shells which are bigger than their isolated ‘core only’ precursor particles. This surprising result is further generalized to different core cross linker contents, for temperature ranges encompassing both transitions. Our analysis demonstrates that the internal structure of pNIPMAM-core and pNNPAM-shell microgels is heterogeneous and strongly interpenetrated, presumably allowing only progressive core swelling at temperatures intermediate to both transition temperatures, thus promoting linear swelling behaviour.

Ref HAL: hal-02341812_v1
DOI: 10.1021/acs.jpcc.9b05798
WoS: 000493865700022
Exporter : BibTex | endNote
2 Citations
Résumé:

We have investigated the wetting and surface diffusion of mesoporous colloidal silica particles at the water surface and the adsorption of cationic cetyltrimethylammonium (CTA+) surfactant on these particles. Porous silica colloids diffuse at the surface of water and in the volume, interacting with cationic surfactants that can adsorb inside the pores of the particles. We observed that surfactant adsorption on mesoporous silica depends dramatically not only on the particle pore size but also on specific counterion effects. We measured striking differences both on a macroscopic property of the interface, i.e., surface tension, and also at a single particle level by evaluating the translational diffusion of partially wetted particles at the fluid interface. We varied the pore size from 2 to 7 nm and explored the effects of ions possessing different hydration number and kosmotropic/chaotropic character. At concentrations lower than the critical micellar concentration, we evidence that cationic surfactants adsorb on silica as surface micelles and surfactant adsorption inside the pores occurs only if the pore diameter is larger than the size of surface micelles. With a view to understand the surprising different adsorption behavior of CTA+OH– and CTA+Br– on porous silica particles, we investigated the effect of counterions on the surfactant adsorption on porous silica colloids by tuning the pH and the counterion properties.

Ref HAL: hal-02339367_v1
Exporter : BibTex | endNote
Résumé:

Les techniques de microrhéologie basées sur le suivi optique de particules microniques sont très intéressantes lorsqu’il s’agit de mesurer les propriétés viscoélastiques de fluides complexes de petit volume. Elles peuvent également paraître très intéressantes pour sonder localement des milieux hétérogènes. Dans le cas de milieux anisotropes comme les cristaux liquides nématiques, ces techniques doivent cependant être utilisées avec précaution. Nous l’illustrerons à travers le cas d’un cristal liquide lyotrope, le cromoglycate de sodium (DSCG) pour lequel nous avons examiné la pertinence des données rhéologiques extraites à partir de la dynamique de microparticules.Le mouvement Brownien, inhabituel, de microsphères dans la phase nématique de ce système avait en effet attiré récemment l’attention [1,2] suggérant un couplage complexe entre les fluctuations du directeur et les fluctuations de positions des billes. Bien qu’il ait été récemment proposé que des mesures par suivi de particules puissent être utilisées pour obtenir les différentes viscosités de la phase nématique [3], ce phénomène peut en effet conduire à des mesures rhéologiques incohérentes. Afin d’explorer ces différents problèmes, nous avons étudié le mouvement Brownien de particules dans des échantillons alignés en cellules minces (épaisseur 50µm) tout en variant à la fois la concentration de DSCG et la taille des particules (0.5, 1, 3, and 6µm de diamètre).Des propriétés viscoélastiques effectives ont été extraites de nos mesures de microrhéologie passive ainsi que de mesures actives basées sur l’utilisation de pinces optiques et le mouvement forcé des particules[4]. Nos résultats expliquent pourquoi différents comportements viscoélastiques ont été obtenus précédemment sur ce même système et l’origine des modules élastiques mesurés.

Ref HAL: hal-02301216_v1
Exporter : BibTex | endNote
Résumé:

Heliconal nematic twist bend (NTB) phases are usually not well oriented in planar commercial cells, even in thin (~1 µm) ones where a micron-sized periodic texture is usually observed [1,2,3] (see Fig.1-a). The origin of the stripe patterns is attributed to the rapid shrinking of the pseudo-layers below the N-NTB phase transition temperature, which yields an undulation instability. The observed periodicity is found to be twice the cell gap [1].We have explored the effect of the strength of the anchorings of the substrates on the resulting patterns. We used polymer aligning layers of tunable azimuthal and zenithal strengths to design liquid crystal cells with surface anchorings ranging from ultraweak to strong. We then have studied the patterns formed by the NTB phase of 1,7-bis-4-(4-cyanobiphenyl) heptane (CB7CB). We will show how the period of the stripes can be varied in a large range in cells of the same thickness but with different anchoring preparations. With adequate anchoring conditions (see Fig.1-b-c), an excellent and spontaneous planar alignment of the NTB phase of CB7CB can be obtained much below the phase transition temperature.
References:
[1] Panov V.P. et al, Phys. Rev. Lett., 2010, 105; 167801.
[2] Challa P. K. et al, Phys. Rev. E: Stat., Nonlinear, Soft Matter Phys., 2014, 89, 060501.
[3] Vaupotič N. et al., Chem. Phys. Chem., 2018, 19,2566.

Ref HAL: hal-02301192_v1
Exporter : BibTex | endNote
Résumé:

Confinement of colloidal particles in thin liquid films is typically accompanied with interfacial deformations which give rise to long-range capillary forces, attractive in most of the cases [1]. In simple fluids, these long-range capillary forces compete mostly with the isotropic electrostatic interactions. In nematic[2] or smectic[3] liquid crystal free films, other long-range anisotropic interactions related to bulk distortions of the surrounding fluid appear and new equilibrium positions or the possibility of forming new types of 2D colloidal assemblies appear via original elasto-capillarity couplings.
In a previous work [4], using spatially resolved retardation and easy-axis maps, we have analysed quantitatively the 2D interfaces deformation and the nematic textures observed around isolated particles (see Fig.1) embedded in thin nematic films with hybrid anchoring conditions. Using numerical methods, we have explained quantitatively the different textures and the formation of topological defects. Contrary to what is classically observed in aligned nematic cells, the equilibrium patterns (such as the elastic dipole) due to a microsphere can be much larger than the particle size (as shown in Fig.1).
Here we have focused on the overall colloidal interactions and the equilibrium positions between spherical or anisotropic particles. We have experimentally characterized the equilibrium configuration of isolated colloidal pairs. Using a 2D model of the nematic elasticity and finite element approaches, we have also numerically characterized the pair interaction and explained the textures observed. These new spontaneous organizations in thin nematic films offer new ways to self-assemble complex colloidal systems in 2D.
References:
[1] P.A. Kralchevsky, K. Nagayama, Adv Colloid Interface Sci ,2000, 85, 145.
[2] H.Jeridi, M.A.Gharbi, T.Othman, Ch.Blanc, Proc Natl Acad Sci USA, 2015, 112, 14771.
[3] M.A.Gharbi et al., Langmuir, 2018, 34, 2006.
[4] H. Jeridi, M. Tasinkevych, T. Othman, and Ch. Blanc, Langmuir, 2016, 32, 9097.

Ref HAL: hal-02301167_v1
Exporter : BibTex | endNote
Résumé:

L’existence d’une phase « Nematique twist Bend » (NTB) a été prédite par I.Dozov dès 2001 [1] mais n’a été observée expérimentalement qu’en 2010 [2]. Cette phase est assez originale car elle présente optiquement des défauts de type coniques focales sans réel ordre translationnel observable en diffusion des rayons X. Généralement cette phase est présente à des températures élevées (au-dessus de 100°C) dans les corps purs. L’ajout d’un nématogène [comme le 4-Cyano-4'-pentylbiphenyl (5CB)] à un composé NTB [tels que le 1,7-bis (4-cyanobiphényl-4-yl) heptane (CB7CB)] permet de diminuer fortement la plage d’existence de la phase NTB [3] tout en modifiant continûment les propriétés thermiques et diélectriques. Dans ce travail, nous avons exploré les modifications dues à l’ajout au CB7CB de smectogènes, et en particulier du 4′-octyl-4-biphénylcarbonitrile (8CB). Le diagramme de phase de ce dernier mélange binaire présente des caractéristiques surprenantes. Malgré leur ressemblance macroscopique, les phases SmA et NTB semblent ainsi incompatibles et restent séparées par une phase nématique s’étendant à très basse température (-20 ° C) pour une fraction CB7CB de ϕ_c≈20%. Nous avons par ailleurs caractérisé les propriétés optiques, thermiques, diélectriques et d’ancrage des phases N et NTB des mélanges. Les propriétés optiques sont très différentes de celles du CB7CB sur une large gamme de composition et de forts effets pré-transitionnels sont observables à l'approche de ϕ_c≈20%. Les propriétés d’ancrage (fig1) sont également significativement modifiées par l'ajout de 8CB au CB7CB ce qui facilite l'alignement homéotrope, très difficilement obtenu pour le CB7CB.