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We study the surfactant-induced fracture of carbon nanotube layers at the air-water interface. The interfacial cracks exhibit branched morphologies. The propagation velocity V of the cracks follows a power law as [Formula: see text] , which is independent of the surface coverage of the layers as well as the surfactant concentration. However, the crack morphology changes from lightning-like to flower-like with the increasing of SDS concentration. A higher surfactant concentration does not accelerate the crack propagation velocity, whereas it significantly enhances the crack areas due to the stronger interfacial compression effect. Our results may shed light on the understanding of branching dynamics of interfacial cracks for 2-dimensional viscoelastic systems.

This paper presents an exploration of the phase separation behavior and pattern formation in a binary fluid with temperature-dependent viscosity via a coupled lattice Boltzmann method (LBM). By introducing a viscosity-temperature relation into the LBM, the coupling effects of the viscosity-temperature coefficient [Formula: see text] , initial viscosity [Formula: see text] and thermal diffusion coefficient [Formula: see text] , on the phase separation were successfully described. The calculated results indicated that an increase in initial viscosity and viscosity-temperature coefficient, or a decrease in the thermal diffusion coefficient, can lead to the orientation of isotropic growth fronts over a wide range of viscosity. The results showed that droplet-type phase structures and lamellar phase structures with domain orientation parallel or perpendicular to the walls can be obtained in equilibrium by controlling the initial viscosity, thermal diffusivity, and the viscosity-temperature coefficient. Furthermore, the dataset was rearranged for growth kinetics of domain growth and thermal diffusion fronts in a plot by the spherically averaged structure factor and the ratio of separated and continuous phases. The analysis revealed two different temporal regimes: spinodal decomposition and domain growth stages, which further quantified the coupled effects of temperature and viscosity on the evolution of temperature-dependent phase separation. These numerical results provide guidance for setting optimum temperature ranges to obtain expected phase separation structures for systems with temperature-dependent viscosity.

We have studied the wetting behaviors of surfaces with a single micro-scale structure and a double micro/nano hierarchical structure, respectively. We have found the delayed wetting phenomenon on the single micro scale surface, which indicates that the wetting state transits from the initial Cassie state to the Cassie impregnating one. Furthermore, the droplet rebound becomes incomplete on the single micro scale surface when the impact velocity exceeds a critical value. On the contrary, complete rebound can still be observed when impacting on the micro/nano hierarchical structure. We proposed that, under static deposition the wetting transition occurs though the contact line depinning mechanism, whereas it occurs via sagging mechanism under a dynamic impact. Our results may be helpful for the understanding of superhydrophobicity and the wetting transition on complex structures.

The cracking behavior accompanied with the drying of colloidal droplets containing polytetrafluoroethylene (PTFE) nanoparticles was studied. During evaporation, due to the stretching effect of the liquid zone, the receding wet front leads to the formation of radialized surface wrinkling in the gel zone. This indicates the building of a macroscopic stress field with a similar distribution. As a result, the cracks in the deposited films are in a radial arrangement. The propagation velocity of the cracks depends on the thickness of the film, ∼ H (3/5). In addition, sodium dodecylsulfate (SDS) additives can be used to tune crack behavior by causing a reduction of the capillary force between particles. The results highlight the significance of the receding wet front in building the drying deposition stress field and may be helpful in other fields related to drying and cracking processes.

We have developed a straightforward method to tune the wettability of an aluminum substrate within a contact angle (CA) range from 2(°) to 170(°) by chemical deposition in CuCl2 solution and fluoroalkylsilane (FAS) modification. The CA of the as-deposited surface decreases with deposition time due to the growth of fractal copper dendrites, which enhance the surface roughness significantly. After subsequent modification with FAS, a superhydrophobic surface with CA 170(°) and sliding angle less than 5(°) has been obtained. With the increase of CA, the maximum spreading of water droplets is reduced. A bouncing behavior is observed for droplets impinging on the superhydrophobic substrate, suggesting its potential application as a self-cleaning surface.

We have investigated the rheological behaviour of silica nanoparticle layers at the air-water interface. Both compressed and deposited layers have been studied in Langmuir troughs and with a bicone rheometer. The compressed layers are more homogeneous and rigid, and the elastic response to continuous, step and oscillatory compression are similar, provided the compression is fast enough and relaxation is prevented. The deposited layers are less rigid and more viscoelastic. Their shear moduli deduced from the oscillatory uniaxial compression are much smaller than those deduced from pure shear deformation suggesting that the effective shear rate is smaller than expected in the compression measurements.