Structuration and deformation of colloidal hydrogels.

The aim of the present paper is to determine the optimum conditions for the formation of homogeneous colloidal silica hydrogels by aggregation and drying processes, avoiding mechanical instabilities at the surface. Aggregation is controlled by adding monovalent salt to the silica nano-particle suspension while the drying of the sol is also modulated by changing the evaporation rate. A phase diagram reveals two regions in the parameter plane, ionic strength versus evaporation rate: a region where the drop undergoes an isotropic shrinkage and forms the required homogeneous gel and a region where mechanical instabilities appear due to the formation of a solid skin at the gel surface. The frontier between these two regions can be determined by equating the following two characteristic times: the gelation time and the time for skin formation. Permeability measurements of the final gel provide an estimate of the drying stress which is compared to the yield stress of the material. In accordance with the determined phase diagram, our study shows that instabilities appear when the drying stress is larger than the yield stress.

Revealing crystalline domains in a mollusc shell single-crystalline prism.

Biomineralization integrates complex processes leading to an extraordinary diversity of calcareous biomineral crystalline architectures, in intriguing contrast with the consistent presence of a sub-micrometric granular structure. Hence, gaining access to the crystalline architecture at the mesoscale, that is, over a few granules, is key to building realistic biomineralization scenarios. Here we provide the nanoscale spatial arrangement of the crystalline structure within the 'single-crystalline' prisms of the prismatic layer of a Pinctada margaritifera shell, exploiting three-dimensional X-ray Bragg ptychography microscopy. We reveal the details of the mesocrystalline organization, evidencing a crystalline coherence extending over a few granules. We additionally prove the existence of larger iso-oriented crystalline domains, slightly misoriented with respect to each other, around one unique rotation axis, and whose shapes are correlated with iso-strain domains. The highlighted mesocrystalline properties support recent biomineralization models involving partial fusion of oriented nanoparticle assembly and/or liquid droplet precursors.

Neutron reflectivity measurements at the oil/water interface for the study of stimuli-responsive emulsions⋆.

Stable stimuli-responsive emulsions between oil and water are formed with an amphiphilic block copolymer bearing polystyrene (PS) and poly(dimethylaminoethyl methacrylate) (PDMAEMA) moieties. Different kinds of emulsions like direct, multiple or inverse ones are reproducibly formed as a function of chemical parameters such as p H and salt concentration. To test the correlation between the different nature of the emulsion and the conformation of the polymer chain at the interface, neutron reflectometry at the oil/water interface was carried out. An original sample cell was built and the procedure to get reliable results with it on the FIGARO reflectometer at the Institut Laue-Langevin is described. Results show that for direct emulsions, the copolymer is much more extended on the water side than on the oil side. In the case where multiple emulsions are stabilized, the conformation is strongly modified and is compatible with a more equilibrated extension of the chain on both sides. The inverse case shows that the extension in oil is stronger than in water. These results are discussed in term of polymer brushes (charged or neutral) extension with respect to salt addition and hydrophobic interactions.

Correction: Breaking of the Bancroft rule for multiple emulsions stabilized by a single stimulable polymer.

Correction for 'Breaking of the Bancroft rule for multiple emulsions stabilized by a single stimulable polymer' by L. Besnard et al., Soft Matter, 2014, 10, 7073-7087.

Breaking of the Bancroft rule for multiple emulsions stabilized by a single stimulable polymer.

We investigated emulsions of water and toluene stabilized by (co)polymers consisting of styrene (S) and 2-(dimethylamino)ethyl methacrylate (DMAEMA) monomer units with different compositions and structures such as a PDMAEMA homopolymer, a P(S-co-DMAEMA) random copolymer and various PS-b-PDMAEMA and PS-b-(S-co-DMAEMA) block copolymers. The model system is used to study the fundamental conditions under which the different kinds of polymer-stabilized emulsions (direct oil in water, inverse water in oil and multiple emulsions) are stabilized or destabilized by pH change (at constant temperature). Polymer properties like chain conformation at the toluene-water interface as probed by SANS and neutron reflectivity at the liquid-liquid interface, the oil-water partitioning of the polymer chains (Bancroft's rule of thumb) as determined by UV spectroscopy and interfacial tensions measured by the rising and spinning drop techniques are determined. Overall, results evidence that the curvature sign, as defined by positive and negative values as the chain segments occupy preferentially the water and toluene sides of the interface respectively, reliably predicts the emulsion kind. In contrast, the Bancroft rule failed at foreseeing the emulsion type. In the region of near zero curvature the crossover from direct to inverse emulsions occurs through the formation of either unstable coexisting direct and inverse emulsions (i) or multiple emulsions (ii). The high compact adsorption of the chains at the interface as shown by low interfacial tension values does not allow to discriminate between both cases. However, the toluene-water partitioning of the polymeric emulsifier is still a key factor driving the formation of (i) or (ii) emulsions. Interestingly, the stabilization of the multiple emulsions can be tuned to a large extent as the toluene-water polymer partitioning can be adjusted using quite a large number of physico-chemical parameters linked to polymer architecture like diblock length ratio or polymer total molar mass, for example. Moreover, we show that monitoring the oil-water partitioning aspect of the emulsion system can also be used to lower the interfacial tension at low pH to values slightly higher than 0.01 mN m(-1), irrespective of the curvature sign.

A silicone-based slippery polymer coating with humidity-dependent nanoscale topography.

HYPOTHESIS: Slippery Omniphobic Covalently Attached Liquids (SOCAL) have been proposed for making omnirepellent thin films of self-assembled dimethylsiloxane polymer brushes grafted from silica surfaces. Smooth and flat at very small scale, these fluid surfaces could exhibit a more complex multiscale structure though showing very weak contact angle hysteresis (less than 5°). EXPERIMENT: In this work, coatings were deposited on glass surfaces from an acidic dimethoxydimethylsilane solution under carefully controlled relative humidity. Ellipsometry mapping was used to analyze the surface structuration with nanometric thickness sensitivity. The sliding properties were determined using a drop shape analyzer with a tilting device, and chemical analyses of the coatings were performed using on-surface techniques (XPS, ATR-FTIR spectroscopy). FINDINGS: Coated materials possessed an unexpected surface structure with multiscale semispherical-like features, which surprisingly, did not increase the contact angle hysteresis. A careful study of some parameters of the coating process and the related evolution of the surface properties allowed us to propose a new model of the chemical organization of the polymer to support this remarkable liquid-like behavior. These structures are made of end-grafted strongly adsorbed Guiselin brushes with humidity-dependent thickness: the higher the humidity, the thinner and the more slippery the coating.

Huge Seebeck coefficients in nonaqueous electrolytes.

The Seebeck coefficients of the nonaqueous electrolytes tetrabutylammonium nitrate, tetraoctylphosphonium bromide, and tetradodecylammonium nitrate in 1-octanol, 1-dodecanol, and ethylene-glycol are measured in a temperature range from T = 30 °C to T = 45 °C. The Seebeck coefficient is generally of the order of a few hundreds of microvolts per Kelvin for aqueous solution of inorganic ions. Here we report huge values of 7 mV/K at 0.1 M concentration for tetrabutylammonium nitrate in 1-dodecanol. These striking results open the question of unexpectedly large kosmotrope or "structure making" effects of tetraalkylammonium ions on the structure of alcohols.

[Quantification of carotid stenosis by doppler ultrasonography: update]. / Quantification des sténoses carotidiennes par échographie doppler: mise au point.

In presence of an internal carotid artery stenosis, the evaluation of the degree of narrowing is a major issue for the achievement of most appropriate therapeutic strategy. Angiography has been for a long time considered as the gold standard, nevertheless non-invasive imaging methods are becoming of major importance. Among these techniques, duplex ultrasound is the most widely considered at the first stage. This is the single technique to provide in single stage anatomical and functional information. Criteria for carotid artery stenosis are well established. Despite this amount of data, one must notice a wide heterogeneity among different non-invasive vascular lab. Among the limits of ultrasound, discrepancy in the methodology of carotid artery stenosis evaluation is of major concern. Harmonization of reporting carotid stenosis grading should be a major issue for the optimization of the technique.

Capillary electrophoresis of associative diblock copolymers.

Water soluble diblock copolymers composed of a long poly(styrene sulfonate) chain (between 200 and 400 monomers) and a short poly(ethylene propylene) or poly(tert.-butylstyrene) hydrophobic end (20-50 monomers) are highly associative and form micelles in aqueous solution. The micelles are composed of a small hydrophobic core and a polyelectrolyte corona, the dimensions of which can be estimated by neutron and light scattering. These physical techniques are, however, not amenable to discriminate easily between the free copolymer and the copolymer micelle. Capillary electrophoresis was implemented in this work as a new and effective tool to investigate the behaviour of such associative copolymer systems. Since the rate of exchange between the micellised and free states is very slow in comparison with the time scale of the electrophoretic process, the electropherograms of the diblock copolymers obtained in plain aqueous borate buffers exhibit two peaks assigned to the two states mentioned above. The identification of the two peaks was first made on the basis of the retention orders of the two peaks equally obtained in similar conditions by size-exclusion chromatography. The copolymer micelles appeared to have a smaller electrophoretic mobility than the free copolymers. This peak assignment is also consistent with the observed ratio of the time-corrected peak areas and peak dispersions. The effects of the copolymer concentration, electric field, temperature and hydroorganic composition of the medium was also studied. Such systems do not exhibit a defined concentration threshold equivalent to a classical critical micelle concentration. Adding methanol to the electrolyte resulted in the progressive loss of baseline return between the two peaks, which might be attributed to a slight increase in the rate of exchange between the two states. Finally, adding a neutral surfactant to the electrolyte at a concentration in excess of its critical micelle concentration resulted in a decrease in the electrophoretic mobility of the peak attributed to the free copoplymer, while the electrophoretic mobility of the copolymer micelle remained unperturbed.

[Relations of the duration of pre-existing angina pectoris, collateral circulation and left ventricular function after isolated coronary occlusion with or without myocardial infarction]. / Interrelations entre durée d'angine de poitrine préexistante, circulation de suppléance et fonction ventriculaire gauche après occlusion coronaire isolée avec ou sans infarctus myocardique.

The aim of this retrospective study was to determine the relationship between the duration of preceding angina pectoris, collateral circulation and left ventricular function after isolated coronary occlusion with or without myocardial infarction. Coronary angiography of 138 consecutive patients showed isolated and complete occlusions of the left anterior descending (58 patients) or right coronary artery (80 patients). One hundred and four patients had myocardial infarction with (Group A, n = 21) or without (Group B, n = 83) preceding angina pectoris and 34 had angina without myocardial infarction (Group C). The left ventricular ejection fraction was measured by ventriculography in the 30 degrees right anterior oblique projection. The collateral circulation was assessed by coronary angiography and evaluated as follows: no flow or flow limited to collateral branches (subgroup 1) and partial or complete filling of the epicardial arterial segment (subgroup 2). In the global population the left ventricular ejection fraction was higher and the duration of preceding angina pectoris was longer in the subgroups with a well developed collateral circulation. There was no difference in ejection fraction between Groups A and B (presence of myocardial infarction), on the other hand, within each of the groups, a good collateral circulation (subgroup 2) was associated with a significantly higher ejection fraction. Group C (without infarction) patients had better ejection fractions than Groups A or B, especially when the collateral circulation was poorly developed. Within Group C, the quality of the collateral circulation did not seem to affect the ejection fraction. The left ventricular ejection fraction is lower in patients with isolated coronary occlusion and myocardial infarction.(ABSTRACT TRUNCATED AT 250 WORDS)

Oil-in-water microemulsions stabilized by charged diblock copolymers.

We present here oil-in-water microemulsions stabilized by charged diblock copolymers alone, along with their structural characterization by small-angle neutron scattering measurements. They consist of swollen spherical micelles containing small amounts of oil in their core, which is surrounded by a corona of stretched polyelectrolyte chains. Structural changes, including core size variations, are evidenced when using a cosurfactant, or upon addition of salt, through a contraction of the charged corona. Attempts to relate the micellar structure to the individual copolymer characteristics are also presented, and show that the size of the hydrophobic block mainly determines that of the micelles.