Despite the prevalence of surface bubbles in many natural phenomena and engineering applications, the effect of surfactants on their surface residence time is not clear. Numerous experimental studies and theoretical models exist but a clear understanding of the film drainage phenomena is still lacking. In particular, theoretical work predicting the drainage rate of the thin film between a bubble and the free surface in the presence and absence of surfactants usually makes use of the lubrication theory. On the other hand, in numerous natural situations and experimental works, the bubble approaches the free surface from a certain distance and forms a thin film at a later stage. This article attempts to bridge these two approaches. In particular, in this article, we review these works and compare them to our direct numerical simulations where we study the coupled influence of bubble deformation and surfactants on the rising and drainage process of a bubble beneath a free surface. In the present study, the level-set method is used to capture the air-liquid interfaces, and the transport equation of surfactants is solved in an Eulerian framework. The axisymmetric simulations capture the bubble acceleration, deformation, and rest (or drainage) phases from nondeformable to deformable bubbles, as measured by the Bond number (), and from surfactant-free to surfactant-coated bubbles, as measured by the Langmuir number (). The results show that the distance between the bubble and the free surface decays exponentially for surfactant-free interfaces ( = 0), and this decay is faster for nondeformable bubbles ( ≪ 1) than for deformable ones ( ≫ 1). The presence of surfactants ( > 0) slows the decay of , exponentially for large bubbles ( ≫ 1) and algebraically for small ones ( ≪ 1). For ≈ 1, the lifetime is the longest and is associated with the (Marangoni) elasticity of the interfaces.
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http://dx.doi.org/10.1021/acs.langmuir.9b03597 | DOI Listing |
Science
January 2025
Department of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Phase diagrams and crystallography are standard tools for studying structural phase transitions, whereas acquiring kinetic information at the atomistic level has been considered essential but challenging. The η-to-θ phase transition of alumina is unidirectional in bulk and retains the crystal lattice orientation. We report a rare example of a statistical kinetics study showing that for nanoparticles on a bulk Al(OH) surface, this phase transition occurs nondeterministically through an ergodic equilibrium through the molten state, and the memory of the lattice orientation is lost in this process.
View Article and Find Full Text PDFAnal Chem
January 2025
Key Laboratory of Optic-Electric Sensing and Analytical Chemistry for Life Science, MOE; College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China.
J Phys Chem Lett
January 2025
Graduate School of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashiosaka, Osaka 577-8502, Japan.
Selective modification of chemically active sites on supports, such as steps, edges, and corners, with metal nanoparticles (NPs) is a challenging topic in the fields of catalysis and photocatalysis. However, the formation of site-selective, high-density metal NPs on a support has not yet been achieved. Radial ZnO mesocrystals composed of hexagonal nanowires (NWs) with {101̅0} sidewalls were synthesized by a simple solution-phase method.
View Article and Find Full Text PDFFront Oncol
January 2025
Department of Gynecologic Oncology, Chongqing Health Center for Women and Children, Chongqing, China.
Background: Emerging surgical methods are utilized to treat endometrial cancer. The study aimed to assess the efficacy and safety of four common surgical methods of hysterectomy.
Methods: We systematically searched the PubMed, Cochrane Library databases, Medline, EMBASE and Web of Science from their inception until April 30, 2024.
ACS Appl Nano Mater
January 2025
Atomic Manipulation and Spectroscopy Group (AMS), Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Bellaterra, 08193 Barcelona, Spain.
Despite the outstanding progress in photonic sensor devices, a major limitation for its application as label-free biosensors for biomedical analysis lies in the surface biofunctionalization step, that is, the reliable immobilization of the biorecognition element onto the sensor surface. Here, we report the integration of bottom-up synthesized nanoporous graphene onto bimodal waveguide interferometric biosensors as an atomically precise biofunctionalization scaffold. This combination leverages the high sensitivity of bimodal waveguide interferometers and the large functional surface area of nanoporous graphene to create highly sensitive, selective, and robust biosensors for the direct immunoassay detection of C-reactive protein (CRP), an inflammatory biomarker widely used in the clinical diagnosis of infections and sepsis.
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