Mixed Lubrication with C18 Fatty Acids: Effect of Unsaturation

In this paper, the lubrication mechanism of fatty acids is revisited with a new approach combining experimental and computational chemistry studies. The lubricating properties of single and mixtures of stearic, oleic and linoleic acids in a synthetic Poly-Alpha-Olefin base oil (PAO4) on iron oxide surface are investigated under mixed boundary regime with temperatures from 50 °C up to 150 °C. Low friction coefficient (about 0.055) with no visible wear is reported in the presence of single stearic acid at high temperature. This lubricating behavior is inhibited in the presence of unsaturated fatty acids highlighting an anti-synergic effect of a saturated/unsaturated mixture, especially at 150 °C. To understand the anti-synergic effect and the adsorption mechanism of these molecules, molecular dynamic (MD) and quantum chemistry simulations are performed to evaluate their diffusion coefficient in PAO4 and their adsorption mechanism on iron oxide at different temperatures. MD simulation results show a faster diffusion toward the surface for unsaturated fatty acids than for saturated fatty acid at all the studied temperatures. This means that unsaturated molecules arrive and mainly adsorb before stearic acid on the surface leading to a tribological behavior of the mixture characteristic of the unsaturated molecule. Computational chemistry suggests that all fatty acids (saturated and unsaturated) adsorption mechanism is due to the chemisorption of the carboxylic group on iron oxide surface with no desorption up to 150 °C.     

The evolution of the exhaust diesel soot adsorptive properties after NO2 exposure and according to their SOF content

Several samples of exhaust diesel soot are investigated by inverse gas chromatography and linear solvation energy relationship (LSER) modelling according to their soluble organic fraction content and their time of exposure in oxidative conditions. The results demonstrate the evolution of the adsorptive properties of the studied materials towards volatile compounds during the oxidation under NO₂.     

Crystallization Mechanisms and Rates of Cyclopentane Hydrates Formation in Brine

Clathrate hydrates most often grow at the interface between liquid water and another fluid phase (hydrocarbon) acting as a provider for the hydrate guest molecules, and some transfer through this shell is required for the hydrate growth to proceed, thus self‐limiting the reaction rate. An optical microscope and a horizontal reaction cell are utilized to capture the shell growth phenomenology and to estimate the hydrate layer growth rates from sequential pictures. Cyclopentane (CP) is chosen as the hydrate‐forming molecule to obtain hydrates at low pressure. Experimental hydrate layer growth rates are provided for the CP+brine system, using various combinations of salts and degrees of subcooling.     

Improving the transfer of near infrared prediction models by orthogonal methods

Eight calibration transfer methods based on the removal of orthogonal signal were compared for the standardization of whole soybean protein and oil models. Dynamic orthogonal projection (DOP), transfer by orthogonal projection (TOP), error removal by orthogonal subtraction (EROS), orthogonal signal correction (OSC), and orthogonal projections to latent structures (O-PLS) as well as the modification and extension of some of these methods were compared in the transfer of models in intra and inter-brand situations using two Foss Infratecs and two Bruins OmegAnalyzerGs. For each brand, a master was designated and its models transferred onto the second unit of its network and the two units of the second brand. Calibration models were transferable from brand to brand with similar or better precision than when each instrument was calibrated on its own calibration set (for Infratec 1229, the relative predictive determinant (RPD) increased in intra and inter-brand calibration transfer situations from 10.42 to 11.45 and 10.57, with DOP and EROS respectively). Performance of each method was different across parameters, instruments, and validation sets. DOP modifications on the determination of the difference matrix showed promising results while TOP and EROS extensions to include variability specifically present in certain crop years did not bring any beneficial effects.     

Preparation of Phospholipid Multilayer Patterns of Controlled Size and Thickness by Capillary Assembly on a Microstructured Substrate

By dragging a phospholipid solution on microstructured silicon surfaces, phospholipid molecules are selectively deposited inside the microstructures to get regular phospholipid multilayer patterns of controlled thickness over a large scale (～cm²). By varying the dragging speed, the thickness of the patterns varies between 28 and 100 nm on average (7 to 25 bilayers). Electroswelling of phospholipid multilayer patterns leads to the formation of giant liposomes of controlled size and narrow size distributions.     

Influence of the suspension flocculated state on the microstructure of alumina spheres elaborated by colloidal granulation

A process of granulation by a colloidal method based on ceramic powder agglomeration makes it possible to produce millimetric spheres with a very homogeneous distribution in terms of shape and size. The starting suspension consists of a mixture of alumina submicrometer particles and silica nanoparticles such as mSiO₂/mAl₂O₃ = 1.1%. Heterocoagulation between the two oxides occurs forming a flocculated network the structure of which can be modified by a shear application. The outer appearance of the spheres is nearly perfect whereas the inner structure exhibits some defects (cracks and porosity). It has been shown that the green spheres are more porous as well as the grains of the starting suspension are less flocculated. During the drying step, the high mobility of these agglomerates increases the overall density on the surface and leads to the formation of a spherical empty cavity in the sphere centre.     

Compaction index of cement paste of normal consistency

Knowing the virtual packing densities of all the components in a mixture is necessary to calculate its granular packing density with the compressible packing model. The calculation of these virtual packing densities is based on real packing density measurements carried out according to specific operating modes, each one with a different compaction index K. For powders, the current method consists in adding water to powder in a mixer until obtaining a smooth paste (K = 6.7). But this method remains subjective since the degree of smoothness achieved is estimated by the operator. The objective of this work is to put forward a more rational alternative method based on tests of normal consistency used in cement plants. This paper presents experiments on binary mixtures (cement–mineral admixtures), with or without superplasticizer, which have resulted in a compaction index K = 4.8. Using these results, the amount of water (given in the technical data sheet) needed to obtain a normal consistency allows the calculation of virtual packing densities of standardized cements. However, if a superplasticizer is used it is necessary to carry out this test. Its saturation proportion can also be estimated with the test of normal consistency.     

A performance study of plane wave finite element methods with a Padé-type artificial boundary condition in acoustic scattering

This paper proposes an original numerical method and studies its performance for solving high-frequency scattering problems involving elongated scatterers. The approach is based on coupling a high-order Padé-type non-reflecting boundary condition with plane wave finite element formulations. It is shown that for some numerical examples the approximate solution of suitable accuracy can be obtained using a small number of degrees of freedom.     

Fifth International Deer Biology Congress

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Fifth International Deer Biology Congress