The mutual interaction between small oscillating cavitation bubbles (R 0 Ͻ10 m) in a strong acoustic field ͑P a Ͼ1 bar, f ϭ20 kHz͒ is investigated numerically. We assume spherical symmetry and a coupling of the bubble oscillations. Our results show that the strength and even the directions of the resulting secondary Bjerknes forces differ considerably from predictions of the well-known linear theory. This is of immediate consequence for understanding and modeling structure formation processes in acoustic cavitation and multibubble sonoluminescence. ͓S1063-651X͑97͒01909-0͔

The fluid dynamic interaction of cavitation bubbles with adherent cells on a substrate is experimentally investigated. We find that the nonspherical collapse of bubbles near to the boundary is responsible for cell detachment. High-speed photography reveals that a wall bounded flow leads to the detachment of cells. Cells at the edge of the circular area of detachment are found to be permanently porated, whereas cells at some distance from the detachment area undergo viable cell membrane poration (sonoporation). The wall flow field leading to cell detachment is modeled with a self-similar solution for a wall jet, together with a kinetic ansatz of adhesive bond rupture. The self-similar solution for the delta-type wall jet compares very well with the full solution of the Navier-Stokes equation for a jet of finite thickness. Apart from annular sites of sonoporation we also find more homogenous patterns of molecule delivery with no cell detachment.

Heterogeneous bubble nucleation at surfaces has been notorious because of its irreproducibility. Here controlled multibubble surface cavitation is achieved by using a hydrophobic surface patterned with microcavities. The expansion of the nuclei in the microcavities is triggered by a fast lowering of the liquid pressure. The procedure allows us to control and fix the bubble distance within the bubble cluster. We observe a perfect quantitative reproducibility of the cavitation events where the inner bubbles in the two-dimensional cluster are shielded by the outer ones, reflected by their later expansion and their delayed collapse. Apart from the final bubble collapse phase (when jetting flows directed towards the cluster's center develop), the bubble dynamics can be quantitatively described by an extended Rayleigh-Plesset equation, taking pressure modification through the surrounding bubbles into account.

Nanobubbles can be observed with optical microscopy using the total-internal-reflection-fluorescence excitation. We report on total-internal-reflection-fluorescence visualization using rhodamine 6G at 5 μM concentration which results in strongly contrasting pictures. The preferential absorption and the high spatial resolution allow us to detect nanobubbles with diameters of 230 nm and above. We resolve the nucleation dynamics during the water-ethanol-water exchange: within 4 min after exchange the bubbles nucleate and form a stable population. Additionally, we demonstrate that tracer particles near to the nanobubbles are following Brownian motion: the remaining drift flow is weaker than a few micrometers per second at a distance of 400 nm from the nanobubble's center.

The dynamics of cavitation bubbles on water is investigated for bubbles produced optically and acoustically. Single bubble dynamics is studied with laser produced bubbles and high speed photography with framing rates up to 20.8 million frames per second. Examples for jet formation and shock wave emission are given. Acoustic cavitation is produced in water in the interior of piezoelectric cylinders of different sizes (up to 12 cm inner diameter). The filementary structure composed of bubbles is investigated and their light emission (sonoluminescence) studied for various driving strengths.