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Relevant bibliographies by topics / Solid-liquid interface

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Academic literature on the topic 'Solid-liquid interface'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 June 2025

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Journal articles on the topic "Solid-liquid interface"

1

Storaska, Garrett A., and James M. Howe. "In-Situ TEM Investigation of the Solid/Liquid Interface in Al-Si Alloys." Microscopy and Microanalysis 6, S2 (2000): 1068–69. http://dx.doi.org/10.1017/s1431927600037831.

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The solid/liquid interface is a junction between two condensed phases with completely different atomic arrangements. At the interface between the periodically ordered solid and the amorphous liquid, the atoms adopt a structure that minimizes the excess energy due to the abrupt change between the surrounding phases. Faceted and diffuse interfaces describe two extremes in morphology of a solid/liquid interface. In a faceted interface, the change from solid to liquid occurs over one atomic layer, however periodic order extends into the first few liquid layers adjacent to the crystalline solid, as predicted by numerous models.1 The faceted interface advances by nucleation and growth of ledges on the interface. A diffuse interface has a structure in which the change from solid to liquid occurs over several atomic layers. This interface contains many ledges to which liquid atoms may attach continuously as the interface advances.

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Ariga, Katsuhiko. "Liquid–Liquid and Liquid–Solid Interfacial Nanoarchitectonics." Molecules 29, no. 13 (2024): 3168. http://dx.doi.org/10.3390/molecules29133168.

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Nanoscale science is becoming increasingly important and prominent, and further development will necessitate integration with other material chemistries. In other words, it involves the construction of a methodology to build up materials based on nanoscale knowledge. This is also the beginning of the concept of post-nanotechnology. This role belongs to nanoarchitectonics, which has been rapidly developing in recent years. However, the scope of application of nanoarchitectonics is wide, and it is somewhat difficult to compile everything. Therefore, this review article will introduce the concepts of liquid and interface, which are the keywords for the organization of functional material systems in biological systems. The target interfaces are liquid–liquid interface, liquid–solid interface, and so on. Recent examples are summarized under the categories of molecular assembly, metal-organic framework and covalent organic framework, and living cell. In addition, the latest research on the liquid interfacial nanoarchitectonics of organic semiconductor film is also discussed. The final conclusive section summarizes these features and discusses the necessary components for the development of liquid interfacial nanoarchitectonics.

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Howe, J. M. "Quantification of order in the liquid at a solid-liquid interface by high-resolution transmission electron microscopy (HRTEM)." Proceedings, annual meeting, Electron Microscopy Society of America 54 (August 11, 1996): 114–15. http://dx.doi.org/10.1017/s0424820100163034.

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A number of different theoretical approaches have been used to model the atomic structure and properties of solid-liquid interfaces. Most calculations indicate that ordering occurs in the first several layers of the liquid, adjacent to the crystal surface. In contrast to the numerous theoretical investigations, there have been no direct experimental observations of the atomic structure of a solid-liquid interface for comparison. Saka et al. examined solid-liquid interfaces in In and In-Sb at lattice-fringe resolution in the TEM, but their data do not reveal information about the atomic structure of the liquid phase. The purpose of this study is to determine the atomic structure of a solid-liquid interface using a highly viscous supercooled liquid, i.e., a crystal-amorphous interface.

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Lozovskii, V. N., A. N. Ovcharenko, and V. P. Popov. "Liquid-solid interface stability." Progress in Crystal Growth and Characterization 13, no. 3 (1986): 145–62. http://dx.doi.org/10.1016/0146-3535(86)90018-3.

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Fan, Feng Ru. "(Invited) novel Charged Interfaces for Catalysis and Energy Conversion." ECS Meeting Abstracts MA2023-01, no. 34 (2023): 1885. http://dx.doi.org/10.1149/ma2023-01341885mtgabs.

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Charged interfaces are ubiquitous in many research fields such as electrochemistry, catalysis, and energy chemistry, and are key places where physical and chemical processes occur. The charged interface structure can also be affected by external fields such as light, electricity, and force, and becomes the key to regulating chemical reactions. It is of great significance for the development of surface and interface science, electrochemistry, catalysis and energy science to deeply understand the physical and chemical reaction process and mechanism of various charged interface systems, and to clarify the interaction between interface structure and reacting species. It is extremely challenging to rationally design, construct, and characterize various novel charged interfaces, and then comprehensively and deeply study their physical and chemical processes and mechanisms. By constructing new charged interface structures such as solid/solid triboelectric interface, micro-droplet charged liquid/gas interface, and metal/two-dimensional material charged interface, we study the reaction process and mechanism of the charged interface and develop new energy conversion pathways. A series of innovative research results: Discovered a new mechanism of triboelectric power generation, expanding the new direction of charged interface structure in energy conversion; established and developed epitaxial growth modes of various interface structures; accurately characterized the electron transport of charged interface structure and surface charge distribution and other physical and chemical properties. We have developed new systems such as solid/dielectric/liquid charged interfaces based on electrodes/dielectric layers/electrolytes and liquid/gas charged interfaces based on microdroplets, and explored new applications in energy conversion and electrocatalysis. Applying a voltage to the electrode/dielectric layer/electrolyte interface can polarize the dielectric layer and adsorb ions in the electrolyte, forming a special "sandwich" electric double layer. Different from the solid/solid charged interface formed by triboelectrification or light excitation, this is a new solid/dielectric/liquid charged interface system based on electrostatic adsorption. Based on this interface system, a new nanoscale power generation device is designed, which can effectively convert mechanical energy into electrical energy, and has high output performance. A new liquid/gas charged interface based on micro-droplets was constructed by means of electrospray, a new strategy for confining the liquid/gas charged interface was proposed, and a high-performance electrolytic water catalyst was prepared. The physical and chemical mechanism of accelerated chemical reactions at the liquid/gas charged interface is revealed, and the desolvation effect and interface confinement effect are proved to be effective ways to construct defect-rich electrocatalysts.

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Veen, J. F. van der, and H. Reichert. "Structural Ordering at the Solid–Liquid Interface." MRS Bulletin 29, no. 12 (2004): 958–62. http://dx.doi.org/10.1557/mrs2004.267.

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AbstractMany processes in nature and technology are based on the static and dynamic properties of solid–liquid interfaces. Prominent examples are crystal growth, melting, and recrystallization. These processes are strongly affected by the local structure at the solid–liquid interface. Therefore, it is mandatory to understand the change in the structure across the interface. The break of the translational symmetry at the interface induces ordering phenomena, and interactions between the liquid's molecules and the atomically corrugated solid surface may induce additional ordering effects. In the past decade, new techniques have been developed to investigate the structural properties of such (deeply) buried interfaces in their natural environment. These methods are based on deeply penetrating probes such as brilliant x-ray beams, providing full access to the structure parallel and perpendicular to the interface. Here, we review the results of a number of case studies including liquid metals in contact with Group IV elements (diamond and silicon), where charge transfer effects at the interface may come into play. Another particularly important liquid in our environment is water. The structural properties of water vary widely as it is brought in contact with other materials. We will then proceed from these seemingly simple cases to complex fluids such as colloids.

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D'Antona, Nicholas R., Nadia F. Barnard, Paul A. Kempler, and Shannon W. Boettcher. "Proton Transfer Kinetics at a Defect-Free Liquid-Liquid Interface." ECS Meeting Abstracts MA2024-01, no. 44 (2024): 2444. http://dx.doi.org/10.1149/ma2024-01442444mtgabs.

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Proton transfer at electrochemical interfaces is fundamentally important for many areas of science and technology, yet kinetic measurements of this elementary step are often convoluted by inhomogeneous electrode surface structures. We show that facilitated proton transfer at the interface between two immiscible electrolyte solutions (ITIES) can serve as a model system to study proton transfer kinetics in the absence of defects found at solid|electrolyte interfaces. Diffusion-controlled micropipette voltammetry revealed that 2,6-diphenylpyridine (DPP) facilitated direct proton transfer across the liquid|liquid interface and voltammetry at nanopipette-supported interfaces yielded activation-controlled ion transfer currents. The exchange current density for proton transfer at the ITIES is comparable to exchange current densities recently reported for H-UPD on Pt (111) and provides the first direct means of comparing ion transfer kinetics between solid|liquid and liquid|liquid interfaces, supporting the development of a general theory of ion transfer kinetics.

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Spencer, B. J., S. H. Davis, G. B. McFadden, and P. W. Voorhees. "Effects of Elastic Stress on the Stability of a Solid-Liquid Interface." Applied Mechanics Reviews 43, no. 5S (1990): S54—S55. http://dx.doi.org/10.1115/1.3120850.

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The effects of elastic stress on the stability of solid-liquid interfaces under a variety of conditions are discussed. In the cases discussed, the nonuniform composition field in the solid, which accompanies either the melting process or the development of a perturbation on the solid-liquid interface during solidification, generates nonhydrostatic stresses in the solid. Such compositionally generated elastic stresses have been shown experimentally to induce a solidifying solid-liquid interface to become unstable. We are in the process of analyzing the effects of these stresses on the conditions for morphological stability of a directionally solidified binary alloy.

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Saka, H., K. Sasaki, S. Tsukimoto, and S. Arai. "In situ Observation of Solid–liquid Interfaces by Transmission Electron Microscopy." Journal of Materials Research 20, no. 7 (2005): 1629–40. http://dx.doi.org/10.1557/jmr.2005.0212.

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Recent progress in in situ observation of solid–liquid interfaces by means of transmission electron microscopy, carried out by the Nagoya group, was reviewed. The results obtained on pure materials are discussed based on Jackson's theory. The structure of the solid–liquid interfaces of eutectic alloys was also observed. The in situ observation technique of solid–liquid interface is applied to industrially important reactions which include liquid phases.

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Saleman, Abdul Rafeq, Mohamad Shukri Zakaria, Ridhwan Jumaidin, Nur Hazwani Mokhtar, and Nor Aslily Sarkam. "Molecular Dynamics Study: Correlation of Heat Conduction Across S-L Interfaces Between Constant Heat Flux and Shear Applied to Liquid Systems." Journal of Mechanical Engineering 19, no. 3 (2022): 33–53. http://dx.doi.org/10.24191/jmeche.v19i3.19795.

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Heat conduction (HC) at solid-liquid (S-L) interfaces play a significant role in the performance of engineering systems. Thus, this study investigates HC at S-L interfaces and its correlation between constant heat flux (CHF) and shear applied to liquid (SAL) systems using non-equilibrium molecular dynamics simulation. The S-L interface consists of solids with the face-centred cubic (FCC) lattice of (110), (111) and (100) planes facing the liquid. The solid is modelled by Morse potential whereas the liquid is modelled by Lennard Jones potential. The interaction between solid-liquid was modelled by Lorentz-Bertholet combining rules. The temperature and heat flux of the system is evaluated to correlate the HC at the S-L interface which reflect by the interfacial thermal resistance (ITR). The results suggest that the surfaces of FCC influence ITR at the S-L interface. The (110) surface for both cases of CHF and SAL has the lowest ITR as compared to other surfaces. In general, ITR for the case of SAL is higher than the CHF. SAL disturbs the adsorption behaviour of liquid at the S-L interfaces, thus reducing the HC. In conclusion, the surface of FCC and liquid experiencing shear do influence the characteristics of HC at the S-L interface.

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Dissertations / Theses on the topic "Solid-liquid interface"

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Denk, Matthias. "Structural investigation of solid liquid interfaces metal semiconductor interface /." [S.l. : s.n.], 2006. http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-29148.

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McDermott, D. C. "Adsorption at the solid/liquid interface." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317917.

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Marsh, Richard James. "Protein adsorption at the solid/liquid interface." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624796.

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Sun, Chen-guang. "Non-covalent bonding at the solid-liquid interface." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610589.

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Curwen, Thomas Daniel. "Kinetics of surfactant adsorption at the solid-liquid interface." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442388.

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Xu, Dan. "The adsorption of nanoparticles at the solid-liquid interface." Thesis, University of Leeds, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.577526.

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This study aims to investigate the adsorption of nanoparticles at the solid-water interface. Surface treatments with nanoparticles have been increasingly explored for a broad range of potential applications. However, the adsorption behaviour of inorganic nanoparticles has not been well studied to-date. Nanoparticle adsorption can be affected by several factors, such as the type of solid substrate, nanoparticle shape, nanoparticle concentration and salt concentration in the nanoparticle suspension, Two types of nanoparticles are used in this thesis: spherical Ludox silica (20 nm) and disk-like laponite clay (25 nm across, 1 nm thick). The adsorption of Laponite nanoparticles at the solid-water interface on various substrates and over a range of Laponite concentrations has been investigated using a quartz crystal microbalance (QCM) and an optical reflectometer (OR). Adsorption of laponite was only observed on a positively charged poly(diallyldimethylammonium chloride) (PDADMAC) surface, whereas no adsorption was seen on hydrophilic/hydrophobic, negative or neutrally charged surfaces. This shows that when fully wetted, Laponite adsorption depends primarily on the surface charge. The adsorption of both Laponite and Ludox silica onto PDADMAC coated surfaces over the first few seconds were studied by OR. The initial adsorption rate of Laponite was faster than Ludox, possibly due to reorientation of the laponite nanoparticles as they approach the substrate. Over longer times, the QCM data for Ludox III nanopartic1es demonstrated more complex adsorption behaviour than Laponite, demonstrating intermixing processes taking place within the PDADMAC-Ludox layer. The effect of a monovalent salt (NaCI) on the adsorption behaviour of both PDADMAC and Ludox nanopartic1es was also investigated using QCM. These data suggest that the adsorbed amount of Ludox increase with NaCI concentration. This can be explained by the roughening of the PDADMAC surface at high salt concentrations leading to more Ludox nanopartic1es adsorbing per unit area. Preliminary evidence for less intermixing between the PDADMAC and the Ludox when the PDADMAC layer was adsorbed and then pre-dried was also found.

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Patel, Asha. "Adsorption studies of polysiloxanes at the solid/liquid interface." Thesis, University of York, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304063.

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Hjalmarsson, Nicklas. "Ionic liquids : The solid-liquid interface and surface forces." Doctoral thesis, KTH, Yt- och korrosionsvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-186267.

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Ionic liquids (ILs) present new approaches for controlling interactions at the solid-liquid interface. ILs are defined as liquids consisting of bulky and asymmetric ions, with a melting point below 373 K. Owing to their amphiphilic character they are powerful solvents but also possess other interesting properties. For example, ILs can self-assemble and are attracted to surfaces due to their charged nature. As a result, they are capable of forming nanostructures both in bulk and at interfaces. This thesis describes how the solid-IL interface responds to external influences such as elevated temperatures, the addition of salt and polarisation. An improved understanding of how these factors govern the surface composition can provide tools for tuning systems to specific applications such as friction. Normal and friction forces are measured for ethylammonium nitrate (EAN) immersed between a mica surface and a silica probe, at different temperatures or salt concentrations. The results demonstrate that an increase in temperature or low concentrations of added salt only induce small changes in the interfacial structure and that the boundary layer properties remain intact. In contrast, at sufficiently large salt concentrations the smaller lithium ion prevails and the surface composition changes. The interfacial layer of a similar IL is also investigated upon the addition of salt and the results reveal that lithium ions affect the surface composition differently depending on the ion structure of the IL. This demonstrates that the surface selectivity strongly depends on the ion chemistry. Remarkably, a repulsive double layer force manifests itself for EAN at 393 K, which is not observed for lower temperatures. This indicates a temperature dependent change in EAN’s microscopic association behaviour and has general implications for how ILs are perceived. A new method is developed based on a quartz crystal microbalance to investigate how the surface compositions of ILs respond to polarisation. The approach demonstrates that interfacial layers of both a neat IL and an IL dissolved in oil can be controlled using potentials of different magnitudes and signs. Furthermore, the method enables two independent approaches for monitoring the charges during polarisation which can be used to quantify the surface composition. The technique also provides information on ion kinetics and surface selectivity. This work contributes to the fundamental understanding of the solid-IL interface and demonstrates that the surface composition of ILs can be controlled and monitored using different approaches.<br>Jonvätskor möjliggör nya tillvägagångssätt för att kontrollera interaktioner vid gränsskiktet mellan fasta ytor och vätskor. Jonvätskor definieras som vätskor som består av stora och asymmetriska joner med en smältpunkt under 373 K. På grund av sin amfifila karaktär är de starka lösningsmedel men har också andra intressanta egenskaper. Jonvätskor kan till exempel självorganisera sig och attraheras till ytor på grund av sin laddning. En följd av detta är att de bildar nanostrukturer både i bulk och på ytor. Denna avhandling beskriver hur gränsskiktet mellan fasta ytor och jonvätskor svarar på yttre påverkan såsom en ökning i temperatur, tillsättning av ett salt samt polarisering. En ökad förståelse för hur dessa faktorer styr ytkompositionen av jonvätskor kan bidra med verktyg för att kontrollera system till specifika applikationer såsom friktion. Normala- och friktionskrafter mäts för etylammonium nitrat (EAN) mellan en glimmeryta och en kolloidprob vid olika temperaturer eller saltkoncentrationer. Resultaten visar att en ökning av temperatur eller låga koncentrationer av tillsatt salt bara marginellt framkallar ändringar i strukturen på gränsytan och att det adsorberade lagret förblir intakt. När saltkoncentrationen emellertid var tillräckligt hög får den mindre litiumjonen överhanden och ytsammansättningen ändras. Ytlagret av en liknande jonvätska undersöks också vid tillsättning av salt och resultaten avslöjar att litiumjoner påverkar ytsammansättningen annorlunda beroende på jonstrukturen av jonvätskan. Detta visar att ytselektiviteten starkt beror på jonkemin. En repulsiv dubbellagerkraft yttrar sig anmärkningsvärt för EAN vid 393 K vilket inte observeras vid lägre temperaturer. Detta indikerar en ändring i EANs mikroskopiska sammansättningsbeteende och har generella återverkningar för hur jonvätskor uppfattas. En ny metod har utvecklats baserad på en kvartskristall mikrovåg för att undersöka hur ytsammansättningen av jonvätskor reagerar på polarisering. Denna metod visar att det adsorberade lagret av både en ren jonvätska och en jonvätska löst i olja kan kontrolleras genom att applicera spänningar med olika tecken och storlekar. Dessutom möjliggör metoden två oberoende tillvägagångssätt för att övervaka laddningarna under polarisering vilket kan användas för att kvantifiera ytsammansättningen. Tekniken ger också information om jonkinetik och ytselektivitet. Detta arbete bidrar till den grundläggande förståelsen av gränsskiktet mellan fasta ytor och jonvätskor och visar att ytsammansättningen av jonvätskor kan kontrolleras och övervakas med olika tillvägagångssätt.<br><p>QC 20160518</p>

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Stocker, Isabella Natalie. "Adsorption at the calcite-liquid interface." Thesis, University of Cambridge, 2013. https://www.repository.cam.ac.uk/handle/1810/252293.

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Brügger, Georges. "Evanescent wave techniques for nanoparticle deposition at liquid-solid interface /." [S.l.] : [s.n.], 2009. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000288123.

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Books on the topic "Solid-liquid interface"

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Halley, J. Woods, ed. Solid-Liquid Interface Theory. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0789.

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1938-, Halley J. Woods, American Chemical Society. Division of Colloid and Surface Chemistry., and American Chemical Society Meeting, eds. Solid-liquid interface theory. American Chemical Society, 2001.

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Gewirth, Andrew A., and Hans Siegenthaler, eds. Nanoscale Probes of the Solid/Liquid Interface. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8435-7.

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Royal Society of Chemistry (Great Britain). Faraday Division., ed. The Liquid/solid interface at high resolution. Faraday Division, Royal Society of Chemistry, 1993.

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Royal Society of Chemistry. Faraday Division. and General discussion on the liquid/solid interface at high resolution (1992 : University of Newcastle-upon-Tyne), eds. The liquid/solid interface at high resolution. Royal Society of Chemistry, Faraday Division, 1992.

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Gewirth, Andrew A. Nanoscale Probes of the Solid/Liquid Interface. Springer Netherlands, 1995.

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A, Gewirth Andrew, Siegenthaler Hans, North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Study Institute on Nanoscale Probes of the Solid/Liquid Interface (1993 : Sophia-Antipolis, France), eds. Nanoscale probes of the solid/liquid interface. Kluwer Academic Publishers, 1995.

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Mauri, Roberto. Multiphase microfluidics: The diffuse interface model. Springer Verlag, 2012.

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J, Brown. Acoustic fields of a laser generated ultrasound source at a liquid/solid interface. UMIST, 1994.

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A, Wheeler A., and National Institute of Standards and Technology (U.S.), eds. On the Gibbs adsorption equation and diffuse interface models. U.S. Dept. of Commerce, Technology Administration, National Institute of Standards and Technology, 2001.

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Book chapters on the topic "Solid-liquid interface"

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Tadros, Tharwat. "Interface, Solid-liquid." In Encyclopedia of Colloid and Interface Science. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-20665-8_110.

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Memming, Rüdiger. "Solid-Liquid Interface." In Semiconductor Electrochemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527688685.ch5.

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Morrison, S. Roy. "The Solid/Liquid Interface." In The Chemical Physics of Surfaces. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2498-8_8.

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Blinov, Lev M. "Liquid Crystal – Solid Interface." In Structure and Properties of Liquid Crystals. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-8829-1_10.

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Zajac, Jerzy Jozef. "Calorimetry at the Solid–Liquid Interface." In Calorimetry and Thermal Methods in Catalysis. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-11954-5_6.

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Perronet, Karen, and Fabrice Charra. "STM-Induced Photoemission at Solid-Liquid Interface." In Organic Nanophotonics. Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0103-8_11.

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Gramsbergen, E. F., and G. H. Wegdam. "Brillouin Scattering near a Solid-Liquid Interface." In Static and Dynamic Properties of Liquids. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74907-0_12.

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Rohrer, H. "Solid-Liquid: The Interface of the Future." In Nanoscale Probes of the Solid/Liquid Interface. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8435-7_1.

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Berkowitz, Brian, Ishai Dror, and Bruno Yaron. "Abiotic Transformation at the Solid–Liquid Interface." In Contaminant Geochemistry. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-54777-5_14.

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Siegenthaler, H., E. Ammann, P. F. Indermühle, and G. Repphun. "Nanoscale Probes of the Solid — Liquid Interface." In Nanoscale Science and Technology. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5024-8_20.

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Conference papers on the topic "Solid-liquid interface"

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Wang, Wei, Shuai Wang, Zicheng Sa, et al. "Size Effect of IMC Growth in Liquid-Solid Reflow Reaction at SAC305/Cu Interface." In 2024 25th International Conference on Electronic Packaging Technology (ICEPT). IEEE, 2024. http://dx.doi.org/10.1109/icept63120.2024.10668650.

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Lewis, T. J. "The solid-liquid interface." In IEE Colloquium on An Engineering Review of Liquid Insulation. IEE, 1997. http://dx.doi.org/10.1049/ic:19970014.

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Daher, Ali, Amine Ammar, and Abbas Hijazi. "Dynamics of solid nanoparticles near a liquid-liquid interface." In PROCEEDINGS OF THE 21ST INTERNATIONAL ESAFORM CONFERENCE ON MATERIAL FORMING: ESAFORM 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5034924.

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Daley, P. F. "Conversion coefficients at a liquid/solid interface." In SEG Technical Program Expanded Abstracts 2001. Society of Exploration Geophysicists, 2001. http://dx.doi.org/10.1190/1.1816553.

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Argirakis, I. "The liquid-solid interface: the effect of negative liquid discharge." In Seventh International Conference on Dielectric Materials, Measurements and Applications. IEE, 1996. http://dx.doi.org/10.1049/cp:19961010.

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Martini, A., S. Lichter, R. Q. Snurr, and Q. Wang. "Solid-Liquid Interface Slip as a Rate Process." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44022.

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Thin film lubrication may be significantly affected by slip at the solid-liquid interface. Slip occurs when there is a jump in the mean speed between the walls and the first layer of liquid molecules. Using molecular simulation, we show that the amount of slip is greatly affected by solvation pressure and that this dependence can be accounted for by treating slip as a rate process. This treatment enables formulation of a quantitative relationship between solvation pressure and interface slip.

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Kamanina, Natalia V., and Vladimir I. Berendyaev. "Influence of solid/liquid crystal interface on characteristics of liquid crystal cells." In Optoelectronics and High-Power Lasers & Applications, edited by Richard L. Sutherland. SPIE, 1998. http://dx.doi.org/10.1117/12.305502.

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Liu, Haibo, Sreedevi Krishnan, and H. S. Udaykumar. "A Fast Sharp Interface Method for Solid, Liquid and Gas Interface Calculations." In 16th AIAA Computational Fluid Dynamics Conference. American Institute of Aeronautics and Astronautics, 2003. http://dx.doi.org/10.2514/6.2003-4108.

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Ueki, Yoshitaka, Tomoya Oyabu, and Masahiko Shibahara. "THERMAL RESISTANCE OF NANOPARTICLE LAYER DEPOSITED SOLID-LIQUID INTERFACE." In International Heat Transfer Conference 16. Begellhouse, 2018. http://dx.doi.org/10.1615/ihtc16.tpm.022135.

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Duffy, David C., Paul B. Davies, Colin D. Bain, Robert N. Ward, and Andrew M. Creeth. "Sum frequency vibrational spectroscopy of the solid-liquid interface." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Janice M. Hicks, Wilson Ho, and Hai-Lung Dai. SPIE, 1995. http://dx.doi.org/10.1117/12.221487.

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Reports on the topic "Solid-liquid interface"

1

Blum, L., and D. A. Huckaby. Exact Results for the Structured Liquid-Solid Interface. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada232992.

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Blum, L., and D. A. Huckaby. Exact Results for the Structured Liquid-Solid Interface. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada222762.

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3

Carlson, A. B. Liquid effluent services and solid waste disposal interface control document. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10102583.

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Prof. P. Somasundaran. BEHAVIOR OF SURFACTANT MIXTURE AT SOLID/LIQUID AND OIL/LIQUID INTERFACE IN CHEMICAL FLOODING SYSTEMS. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/811903.

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Butler, P. D., W. A. Hamilton, J. B. Hayter, L. J. Magid, and T. M. Slawecki. Effect of a solid/liquid interface on bulk solution structures under flow. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/532532.

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Greager, T. M. ,. Westinghouse Hanford. Interface control document between liquid effluent services and solid waste disposal division. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/658890.

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Yang, Yuan. Scalable Enrichment of 48Ca at the Solid/liquid Interface by Chemical and Electrochemical Methods. Office of Scientific and Technical Information (OSTI), 2024. http://dx.doi.org/10.2172/2475193.

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Vera, Jose, and Ken Evans. PR186-203600-Z01 Impact of Drag Reducing Agents on Corrosion Management. Pipeline Research Council International, Inc. (PRCI), 2021. http://dx.doi.org/10.55274/r0012177.

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The purpose of this research was to understand the potential impact of drag reducing agents (DRA) on internal corrosion of liquid hydrocarbon pipelines. The first task of this project included a comprehensive review of literature and knowledge, both in public domain and from industry experience, on the effect of DRA on water and solid transport in liquid hydrocarbons, and possible interactions with other performance chemicals typically used in the oil and gas industry. This was the basis for defining the final bench test methodology and test matrix to be performed in the second task. A novel bench-top apparatus was designed based on a vertical Couette cell approach, and a test methodology was successfully implemented to evaluate the potential effect(s) of DRA on water accumulation and localized corrosion at the oil/water interface. A test matrix was conducted with two DRAs (a water based and an oil based) and two corrosion inhibitors (a water soluble and an oil soluble) at a given test condition (3.5% NaCl saturated with 97%CO2/3%O2, pH ~6 at 80 oF). There is a related webinar.

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Allen, Jeffrey, and Guillermo Riveros. Mesoscale multiphysics simulations of the fused deposition additive manufacturing process. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/48595.

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As part of an ongoing effort to better understand the multiscale effects of fused deposition additive manufacturing, this work centers on a multiphysics, mesoscale approach for the simulation of the extrusion and solidification processes associated with fused deposition modeling. Restricting the work to a single line scan, we focus on the application of polylactic acid. In addition to heat, momentum, and mass transfer, the solid-liquid–vapor interface is simulated using a front-tracking, level-set method. The results focus on the evolving temperature, viscosity, and volume fraction and are cast within a set of parametric studies to include the nozzle and extrusion velocities as well as the extrusion temperature. Among other findings, it was observed that fused deposition modeling can be effectively modeled using a front-tracking method (i.e., the level-set method) in concert with a moving mesh and temperature-dependent porosity function.

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DR. PAUL WYNBLATT. ENERGETICS OF SOLID/SOLID AND LIQUID/SOLID INTERFACES. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/833421.

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