•Bubble-particle attachment is fundamental for understanding flotation process.•Advances in macroscopic experimental approaches to flotation are reviewed.•Nanoscale techniques to probe surface forces and liquid film drainage are reviewed.•Synchronous detection of forces and film drainage profile is a promising trend.Bubble-particle interaction is of great theoretical and practical importance in flotation. Significant progress has been achieved over the past years and the process of bubble-particle collision is reasonably well understood. This, however, is not the case for bubble-particle attachment leading to three-phase contact line formation due to the difficulty in both theoretical analysis and experimental verification. For attachment, surface forces play a major role. They control the thinning and rupture of the liquid film between the bubble and the particle. The coupling between force, bubble deformation and film drainage is critical to understand the underlying mechanism responsible for bubble-particle attachment. In this review we first discuss the advances in macroscopic experimental methods for characterizing bubble-particle attachment such as induction timer and high speed visualization. Then we focus on advances in measuring the force and drainage of thin liquid films between an air bubble and a solid surface at a nanometer scale. Advances, limits, challenges, and future research opportunities are discussed. By combining atomic force microscopy and reflection interference contrast microscopy, the force, bubble deformation, and liquid film drainage can be measured simultaneously. The simultaneous measurement of the interaction force and the spatiotemporal evolution of the confined liquid film hold great promise to shed new light on flotation.Download high-res image (187KB)Download full-size image

Nanofibers composed of silica nanoparticles, used as structural building blocks, and polystyrene nanoparticles introduced as sacrificial material are fabricated by bicolloidal electrospinning. During fiber calcination, sacrificial particles are combusted leaving voids with controlled average sizes. The mechanical properties of the sintered silica fibers with voids are investigated by suspending the nanofiber over a gap and performing three-point bending experiments with atomic force microscopy. We investigate three different cases: fibers without voids and with 60 or 260 nm voids. For each case, we study how the introduction of the voids can be used to control the mechanical stiffness and fracture properties of the fibers. Fibers with no voids break in their majority at a single fracture point (70% of cases), segmenting the fiber into two pieces, while the remaining cases (30%) fracture at multiple points, leaving a gap in the suspended fiber. On the other hand, fibers with 60 nm voids fracture in only 25% of the cases at a single point, breaking predominantly at multiple points (75%). Finally, fibers with 260 nm voids fracture roughly in equal proportions leaving two and multiple pieces (46% vs 54%, respectively). The present study is a prerequisite for processes involving the controlled sectioning of nanofibers to yield anisometric particles.

The hydrodynamic drainage force between a spherical silica particle and a soft, elastic polydimethylsiloxane surface was measured using the colloidal probe technique. The experimental force curves were compared to finite element simulations and an analytical model. The hydrodynamic repulsion decreased when the particle approached the soft surface as compared to a hard substrate. In contrast, when the particle was pulled away from the surface again, the attractive hydrodynamic force was increased. The hydrodynamic attraction increased because the effective area of the narrow gap between sphere and the plane on soft surfaces is larger than on rigid ones.

Local dielectric spectroscopy (LDS) was employed to analyze the miscible blend composed of poly(vinyl acetate) (PVAc) and poly(ethylene oxide) (PEO). The two homopolymers have very different relaxation times and glass transition temperatures. The aim was to study the dynamic heterogeneity in films as a function of the film thickness. Measurements of the local blend composition at the nanoscale have shown that LDS is sensitive to the dynamic heterogeneity. In thinner films, phase segregation occurs, and the kinetics of phase demixing was studied using as a probe the change in local composition. These results open new possibilities for studying interdiffusion and adhesion at polymer–polymer interfaces as a function of annealing temperature with LDS.

One way of measuring adhesion forces in fine powders is to place the particles on a surface, retract the surface with a high acceleration, and observe their detachment due to their inertia. To induce detachment of micrometer-sized particles, an acceleration in the order of 500 000g is required. We developed a device in which such high acceleration is provided by a Hopkinson bar and measured via laser vibrometry. Using a Hopkinson bar, the fundamental limit of mechanically possible accelerations is reached, since higher values cause material failure. Particle detachment is detected by optical video microscopy. With subsequent automated data evaluation a statistical distribution of adhesion forces is obtained. To validate the method, adhesion forces for ensembles of single polystyrene and silica particles on a polystyrene coated steel surface were measured under ambient conditions. We were able to investigate more than 150 individual particles in one experiment and obtained adhesion values of particles in a diameter range of 3–13 μm. Measured adhesion forces of small particles agreed with values from colloidal probe measurements and theoretical predictions. However, we observe a stronger increase of adhesion for particles with a diameter larger than roughly 7–10 μm. We suggest that this discrepancy is caused by surface roughness and heterogeneity. Large particles adjust and find a stable position on the surface due to their inertia while small particles tend to remain at the position of first contact. The new device will be applicable to study a broad variety of different particle–surface combinations on a routine basis, including strongly cohesive powders like pharmaceutical drugs for treatment of lung diseases.