Cavitation Nucleation

Cavitation nucleation is the initiation of vapor bubbles within a liquid when local conditions allow a stable or transient cavity to form, making it a key process in fluid engineering. Nuclei arise from dissolved gas, microscopic surface imperfections, or suspended particles, and can expand when pressure falls below the liquid’s vapor pressure; subsequent pressure recovery may cause rapid bubble collapse and intense local forces. Understanding nucleation helps engineers predict cavitation in pumps, turbines, propellers, valves, and hydraulic systems, where it can reduce performance, generate noise and vibration, and damage surfaces. Controlling pressure, dissolved gas, and surface conditions supports safer, more efficient designs.

Cavitation Nucleation - Related Videos

Research

JoVE Journal - Engineering
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Controllable Nucleation of Cavitation from Plasmonic Gold Nanoparticles for Enhancing High Intensity Focused Ultrasound Applications

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Cited by 4 •

2018

This protocol demonstrates the controllable nucleation of cavitation in gel phantoms, through simultaneous exposure to both near-infrared pulsed laser light and high intensity focused ultrasound (HIFU). The cavitation activity can then be used for enhancing imaging and/or therapeutic uses of HIFU.

Research

JoVE Journal - Chemistry

Activating Molecules, Ions, and Solid Particles with Acoustic Cavitation

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Cited by 6 •

2014

Acoustic cavitation in liquids submitted to power ultrasound creates transient extreme conditions inside the collapsing bubbles, which are the origin of unusual chemical reactivity and light emission, known as sonoluminescence. In the presence of noble gases, nonequilibrium plasma is formed. The "hot" particles and the photons generated by collapsing bubbles are able to excite species in solution.

Visualization of Cell Cycle Variations and Determination of Nucleation in Postnatal Cardiomyocytes

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Cited by 5 •

2017

To distinguish cell division from cell cycle variations in cardiomyocytes, we present protocols using two transgenic mouse lines: Myh6-H2B-mCh transgenic mice, for the unequivocal identification of cardiomyocyte nuclei, and CAG-eGFP-anillin mice, for distinguishing cell division from cell cycle variations.

Nitrogen Cavitation and Differential Centrifugation Allows for Monitoring the Distribution of Peripheral Membrane Proteins in Cultured Cells

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Cited by 15 •

2017

Here we present protocols for detergent-free homogenization of cultured mammalian cells based on nitrogen cavitation and subsequent separation of cytosolic and membrane-bound proteins by ultracentrifugation. This method is ideal for monitoring the partitioning of peripheral membrane proteins between soluble and membrane fractions.

Automated Microfluidic Blood Lysis Protocol for Enrichment of Circulating Nucleated Cells

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Cited by 4 •

2009

An automated microfluidic device was developed for circulating nucleated cell enrichment from peripheral blood via erythrocyte lysis that ensures isolation of high quality sample without cell loss.

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