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Carbon nanotubes and silica nanoparticles are allowed to self-assemble into a nanocomposite by first forming an aqueous suspension, then depositing one drop after the other and finally letting them evaporate. Two types of composites are prepared. One by forming alternate layers and the other by forming several layers of a pre-mixed suspension. The thickness, thermal and electrical conductivity of the composites are measured versus the number of depositions. The pre-mixed composites showed an increase in the values in both the parallel and perpendicular directions of both the electrical and thermal conductivities, making them suitable for electrodes or battery-like applications. The values of the electrical and thermal conductivities in the perpendicular direction for the first composite decrease and increase, respectively, while for the parallel direction the values are significantly constant. As such, they would be useful as electrical insulators for optimal cooling. Thickness measurements showed that the pre-mixed composite is the denser one, due to a better alignment of the carbon nanotubes.

Evaporation can cause instability due to cooling effects on the density and surface tension. This causes, respectively, Rayleigh and Marangoni instabilities. When these instabilities grow sufficiently, self-sustained convection occurs. This convection causes changes into the evaporation rate and heat transfer rate. This also could change the heat transfer via the evaporation rate and can be important for industrial applications. It is the purpose of this paper to investigate the relation that exists between the overall evaporation rate and a set of parameters: temperature, gas flow and liquid thickness. Three-dimensional numerical simulations have been performed for this purpose and the results have been validated by means of an experimental setup, on which the numerical geometry has been based, characterized by a liquid evaporating through an opening in a cover sheet under a shear gas flow. It is shown that the temperature and the gas flow increase the evaporation rate. More interestingly, a maximum is observable for the evaporation rate as function of the liquid thickness. The explanation for these phenomena are drawn from the 3D numerical simulations. It appears that the maximum evaporation rate as a function of the liquid thickness depends on the confinement of the convection cells by the cover sheet, being assisted by the gas flow.

Early detection of ice formation on surfaces is a crucial requirement in many applications such as wind turbines, aeroplane’s wings, and radar domes. This paper presents the concept of a heat-pulse ice detection system. Its principle consists of recording the temperature evolution and assessing the relaxation time after the surfaces are subject to a heat excitation generated by an electrical pulse. The sensor comprises thin graphene films embedded in pre-preg layers of aeronautical grade as well as thermocouples to record the temperatures profiles at given locations. The criterion of ice detection exploits the high thermal capacity of ice compared to the air to capture the formation of icy spots. Numerical simulations and comparison with experimental investigations have been carried out to validate the principle and criteria of the ice detection system.

Carbon nanotubes are allowed to self-assemble by depositing a droplet of a water dispersion thereof and letting it evaporate on a polycarbonate substrate. The effect of the number of droplets, evaporated on the same deposition spot, on the self-assembly density is assessed to be more than proportional for the first five depositions. The obtained nanoporous nanostructures are further tested for their electrical resistance and wettability. Two concentrations are used. It is found that a higher concentration and more importantly a higher number of droplet depositions causes the electrical resistance to decrease up to four orders of magnitude and the static contact angle to decrease more than three times. The contact angle hysteresis also increases due to an increasing advancing contact angle and a decreasing receding one. This is explained by the degree of coverage of the substrate by the carbon nanotubes as is also shown by scanning electron microscope images. A better coverage is suggested to cause more pinning for an advancing droplet and a higher capillary force for a receding droplet.

A thermodynamic model for transient heat conduction in ceramic-polymer nanocomposites is proposed. The model takes into account particle’s size, particle’s volume fraction, and interface characteristics with emphasis on the effect of agglomeration of particles on the effective thermal conductivity of the nanocomposite. The originality of the present work is its basement on extended irreversible thermodynamics, combining nano- and continuum-scales without invoking molecular dynamics. The model is compared to experimental data using the examples of SiO 2 , AlN and MgO nanoparticles embedded in epoxy resin. The analysis is limited to spherical nanoparticles. The dependence of the degree of agglomeration with respect of the volume fraction of particles is also discussed and a power-law relation is established through a kinetic mechanism and experiments performed in our laboratory. This relation is used in our theoretical model, resulting into a good agreement with experiments. It is shown that the effective thermal conductivity may either increase or decrease with the degree of agglomeration.

The aim of this work is to understand the changes in the observed phenomena during particle-laden drop impact. The impact of millimeter-size drops was investigated onto hydrophilic (glass) and hydrophobic (polycarbonate) substrates. The drops were dispersions of water and spherical and nearly iso-dense hydrophobic particles with diameters of 200 and 500 μm. The impact was studied by side and bottom view images in the range 150 ≤ We ≤ 750 and 7100 ≤ Re ≤ 16400. The particles suppressed the appearance of singular jetting and drop partial rebound but promoted splashing, receding breakup, and rupture. The drops with 200 μm particles spread in two phases: fast and slow, caused by inertial and capillary forces, respectively. Also, the increase in volume fraction of 200 μm particle led to a linear decrease in the maximum spreading factor caused by the inertia force on both hydrophilic and hydrophobic substrates. The explanation of this reduction was argued to be the result of energy dissipation through frictional losses between particles and the substrate.

The splat morphology after the impact of suspension drops on hydrophilic (glass) and hydrophobic (polycarbonate) substrates was investigated. The suspensions were mixtures of water and spherical hydrophobic particles with diameter of 200μm or 500μm. The impact was studied by side, bottom and angled view images. At Reynolds and Weber numbers in the range 150⩽We⩽750 and 7100⩽Re⩽16,400, the particles distributed in a monolayer on the hydrophilic substrates. It was found that the 200μm particles self-arranged as rings or disks on the hydrophilic substrates. On hydrophobic substrates, many particles were at the air-water interface and 200μm formed a crown-like structure. The current study for impact of particle-laden drops shows that the morphology of splats depends on the substrate wettability, the particle size and impact velocity. We developed correlations for the inner and outer diameter of the particle distribution on the hydrophilic substrates, and for the crown height on hydrophobic substrates. The proposed correlations capture the character of the particle distributions after drop impact that depends on particle volume fraction, the wettability of both particles and the substrate, and the dimensionless numbers such as Reynolds and Weber.