Experimental investigation into squeal under reciprocating sliding

Experiments on squeal under reciprocating sliding were performed by means of a ball against a block. Vibration accelerations, sound pressure level of squeal and tangential force were measured simultaneously. Under certain test conditions, the reciprocating sliding can create a whole process from squeal generation to disappearance. Based on power spectral density (PSD) and short-time Fourier transform (STFT) analyses on the vibration accelerations in that process, it was found that the dominant frequencies of the friction-induced vibrations associated with squeal is not varied. Examination of the friction–velocity slope shows that there is no invariable correlation between the negative friction–velocity slope and occurrence of squeal. Squeal can occur in regions with both negative and positive friction–velocity slopes.     

Nanoparticle detachment: a possible link between macro- and nanotribology?

Although particle detachment is a common phenomenon associated with most tribological processes, it seldom occurs that each piece of elemental debris can be considered as the result of a single event. Such an association has been revealed by the systematic study of a specific system, where a pin of graphite is made to rub against thoroughly polished steel. While the discontinuous nature of the transfer film allows a quantitative assessment of the volume of transfer h _e to be made by 3D optical-profilometry, the linear dependence of the rate of particle detachment dh _e/dn (n=number of rubbing cycles) with the logarithm of sliding speed v strongly suggests the existence of a particular type of stick–slip, where each stick may lead to the detachment of a debris particle. The variations in size of these debris with environment as revealed by AFM, further suggest that the global rate of particle detachment is of the form: dh _e/dn=Nx _i , where N is the number of stick–slip events per rubbing cycle, x the proportion of stick events leading to a cohesive rupture, and _i the mean volume of an elemental particle. While this relation is apparently supported by most experimental results, its actual validation can only be made by experiments at the level of single (nanoscale) asperities, carried out under well-controlled experimental conditions.     

Interactions of diuron with dissolved organic matter from organic amendments

Diuron is frequently detected in some drinking water reservoirs under the Burgundy vineyards, where organic amendments are applied. The environmental effect of these amendments on pesticide transport is ambiguous: on the one hand it could enhance their retention by increasing soil organic carbon content; on the other hand, dissolved organic matter (DOM) could facilitate their transport. Elutions were performed using columns packed with glass beads in order to investigate DOM-diuron interactions, and the possible co-transport of diuron and DOM. Four organic amendments (A, B, C and D) were tested; C and D were sampled at fresh (F) and mature (M) stages. An increase in diuron leaching was observed only for A and D_F amendments (up to 16% compared to the DOM-free blank samples), suggesting a DOM effect on diuron transport. These results could be explained by the higher DOM leaching for A and D_F compared to B, C_F, C_M and D_M increasing diuron-DOM interactions. These interactions seem to be related to the aromatic and aliphatic content of the DOM, determining formation of hydrogen and non-covalent bonds. The degree of organic matter maturity does not seem to have any effect with amendment C, while a reduction in diuron leaching is observed between D_F and D_M. After equilibrium dialysis measurement of diuron-DOM complexes, it appeared that less than 3% of the diuron applied corresponded to complexes with a molecular weight > 1000 Da. Complexes < 1000 Da could also take part in this facilitated transport.     

Low temperature adsorption of ethylene and butadiene on platinum and palladium surfaces: A theoretical study of the diσ/π competition

The different low temperature coordination modes of ethylene and butadiene on a platinum (111) face, (110) face and on a palladium (111) face are compared on the basis of extended Hückel calculations. The nature of the chemical interaction between the olefin and the surface is detailed and the electronic factors that govern the coordination mode of the hydrocarbon are underlined. The different surfaces are modelled by a 49 or a 44 atoms cluster. A correction is applied in the calculation in order to minimize the artefact introduced by this cluster representation of an extended surface. For the adsorption, the respective importance of two electrons interactions and four electrons repulsions is the key point for the determination of the preferred mode. The di- coordination is more stable on platinum (111) but on the platinum (110) face the coordination yields the same adsorption energy than the di- one. This is roughly the same result for the palladium (111) face. The mode is there favored by a decrease of the four electrons repulsions caused either by a smaller number of metal neighbours for the surface atom (Pt(110)) or by a reduced radial expansion of the metal orbitals (Pd(111)). This coordination is associated with a smaller hybridization of the ethylene molecule. The results are extended to the adsorption of butadiene and this allows a qualitative explanation of the better selectivity for butadiene partial hydrogenation on palladium compared with platinum.     

Bunsen section thermodynamic model for hydrogen production by the sulfur–iodine cycle

A model for the Bunsen section of the Sulfur–Iodine thermo-chemical cycle is proposed, where sulfur dioxide reacts with excess water and iodine to produce two demixing liquid aqueous phases (H₂SO₄ rich and HI rich) in equilibrium. Considering the mild temperature and pressure conditions, the UNIQUAC activity coefficient model combined with Engels' solvation model is used. The complete model is discussed, with HI solvation by water and by iodine as well as H₂SO₄ solvation by water, leading to a very high complexity with almost hundred parameters to be estimated from experimental data. Taking into account the water excess, a successful reduced model with only 15 parameters is proposed after defining new apparent species. Acids total dissociation and total H⁺ solvation by water are the main assumptions. Results show a good agreement with published experimental data between 25 °C and 120 °C.     

Countercurrent reactor design and flowsheet for iodine-sulfur thermochemical water splitting process

A conceptual design is presented for the I/S process for the production of hydrogen using a high-temperature nuclear heat source to split water. The process includes a countercurrent reactor being developed by CEA within the framework of an international collaboration (I-NERI project) with DOE at General Atomics (San Diego, CA). A ProsimPlus? model of the flowsheet indicates 600 kJ high-temperature heat and 69 kJ electric power are consumed per mole of H₂ product (with an assumed pressure of 120 bars). The net thermal efficiency would be 38% (HHV basis) if electric power is available at a conversion efficiency of 45%.     

Size Effect on Properties of Varistors Made From Zinc Oxide Nanoparticles Through Low Temperature Spark Plasma Sintering

Conditions for the elaboration of nanostructured varistors by spark plasma sintering (SPS) are investigated, using 8‐nm zinc oxide nanoparticles synthesized following an organometallic approach. A binary system constituted of zinc oxide and bismuth oxide nanoparticles is used for this purpose. It is synthesized at room temperature in an organic solution through the hydrolysis of dicyclohexylzinc and bismuth acetate precursors. Sintering of this material is performed by SPS at various temperatures and dwell times. The determination of the microstructure and the chemical composition of the as‐prepared ceramics are based on scanning electron microscopy and X‐ray diffraction analysis. The nonlinear electrical characteristics are evidenced by current–voltage measurements. The breakdown voltage of these nanostructured varistors strongly depends on grain sizes. The results show that nanostructured varistors are obtained by SPS at sintering temperatures ranging from 550 to 600 °C.     

Temperature Modulation Measurements of the Thermal Properties of Nanosystems at Low Temperatures

We report on the dynamic measurements of thermal properties of nanosystems at very low temperatures. These techniques are based on the modulation of the temperature and hence leads to highly sensitive measurements. We will discuss the intrinsic limitations of these methods when the thermal properties of nano-objects are studied at very low temperatures, much below 1 K. Firstly, we will present thermal conductance measurements using the 3ω method. This technique is limited at low temperatures due to the significant increase of the mean free path. Secondly, heat capacity measurements using ac calorimetry are outlined, and again restrictions occur due to the continuous temperature gradient inherent to that technique. Propositions are made in order to overcome these limitations.