Mesurer nécessite d'évaluer les incertitudes de mesure. Une mesure scientifique n'a de sens qu'accompagnée de son incertitude, ce qui permet de fixer le nombre de chiffres significatifs de sa valeur numérique. Ceci permet par exemple de vérifier la conformité d'une série de pièces usinées à un cahier des charges qualité.Les méthodes de calcul des incertitudes-types conformes aux recommandations internationales sont présentées progressivement, après avoir distingué les erreurs des incertitudes.Des vidéos d'expérience, accompagnées de cours et de nombreux exercices, devraient vous permettre d'exprimer correctement vos résultats de mesure, quelle que soit la grandeur mesurée et les appareils utilisés.https://socles3.unisciel.fr/course/view.php?id=555

Silica aerogels have many potential applications, including as host matrices for chemical species or nuclear waste storage. For these applications, the permeability is a key parameter and data show that the silica aerogels have poor permeability (~10-60 nm 2). In this chapter we review the method to measure the liquid and gas permeability in gels, aerogels and composite aerogels. Ideally, permeability does not depend on the type of pore fluid, therefore permeability measured using gas should be the same as that measured using water. We measured gas and water permeability in sets of nano composite silica aerogels. Experimental results show that gas permeability in aerogels was larger than water permeability by almost two orders of magnitude. The observed difference in gas and water permeability was analyzed from the point of view of the slip regime (Klinkenberg correction), and transition regime (Knudsen correction), the slip flow of gas at pore walls enhance the gas flow when pore sizes are small. This work addresses the problem of estimating permeability with high porosity materials such as aerogels. The effects of structural parameters of porous media (pore volume, tortuosity, fractal features) on the Klinkenberg and Knudsen corrections are discussed and the different models proposed in the literature are tested.

ObjectiveDentin, enamel and the transition zone, called the dentin-enamel junction (DEJ), have an organization and properties that play a critical role in tooth resilience and in stopping the propagation of cracks. Understanding their chemical and micro-biomechanical properties is then of foremost importance. The aim of this study is to apply Brillouin microscopy on a complex biological structure, that is, the DEJ, and to compare these results with those obtained with Raman microscopy.DesignBoth techniques allow noncontact measurements at the microscopic scale. Brillouin microscopy is based on the interaction between acoustic phonons and laser photons and gives a relation between the frequency shift of the scattered light and the stiffness of the sample. Raman spectra contain peaks related to specific chemical bonds.ResultsComparison of the Brillouin and Raman cartographies reveals correlations between mechanical and chemical properties. Indeed, the shapes of the phosphate content and stiffness curves are similar. The two spectroscopies give compatible values for the mean distance between two tubules, i.e., 4–6 µm. Moreover, for the first time, the daily cross striations of enamel could be studied, indicating a relationship between the variation in the phosphate concentration and the variation in the rigidity within the enamel prisms.ConclusionsWe demonstrate here the possibility of using Brillouin scattering microscopy to both study complex biological materials such as the enamel-dentin junction and visualize secondary structures. Correlations between the chemical composition and mechanical properties could help in better understanding the tissue histology.

An experimental program is oriented to the mechanical behaviour of the Interfacial Transition Zone (ITZ) exposed to leaching, for a single mix. Leaching kinetics of the degraded depth, measured through grey level on cross sections, reveals a maximum gap of 10 % between ITZ and bulk cement paste. ITZ, with a main thickness of 15 µm suffers a significant decalcification, which is reflected on the mechanical properties of the bond. Grey level, Calcium/Silicon (Ca/Si) molar ratio and Young’s modulus in the degraded zone present similar evolution. Effect of ITZ causing cracking and then debonding is noticed, through chemical analysis, image observation and mechanical tests.

The development of artificial receptors able to selectively recognize a target protein is of particular interest in separation, diagnostics, and therapeutics fields. Herein, we disclose a method to prepare biomimetic and functionalized protein imprints in biocompatible conditions avoiding any protein denaturation. For that purpose, a set of different hybrid silylated amino acid derivatives were synthesized and used without tetraethyl orthosilicate to prepare our molecularly imprinted polymers, allowing to reduce to a minimum of the silicon amount, in order to obtain imprints made almost entirely of amino acids to mimic paratope surfaces of antibodies. Such functional building blocks were polymerized on the surface of magnetic silica nanoparticles at pH 8.5 in ultrapure water in the presence of two globular proteins: cytochrome C or lysozyme. The resulting imprinted hybrid materials were evaluated for their adsorption capacity, specificity, and selectivity by quartz-crystal microbalance with dissipation and magnetic enzyme-linked immunosorbent assay (ELISA) assays. High imprinting factors of 8.7 were measured for these biomimetic hybrid materials (corresponding to approximately 4000 and 450 ng of protein per cm2 immobilized on molecularly imprinted polymers and non-imprinted polymer nanoparticles, respectively), representing a significant breakthrough in sol-gel-based molecular imprinting materials. Moreover, competition experiments performed by magnetic ELISA (mELISA) show very good specificity of our imprints at the usual concentrations of ELISA measurements.