Relevant bibliographies by topics / Porous Liquid

Academic literature on the topic 'Porous Liquid'

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Published: 10 December 2022
Last updated: 20 February 2023

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Journal articles on the topic "Porous Liquid"

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Liu, Yutong, Yang Bai, and Tao Tian. "Preparation of Porous Liquid Based on Silicalite-1." Materials 12, no. 23 (December 1, 2019): 3984. http://dx.doi.org/10.3390/ma12233984.

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Solid porous materials, like zeolites, have been widely used in a variety of fields such as size-and-shape-selective absorption/separation and catalysis because of their porosity. However, there are few liquid materials that exhibit permanent porosity. Porous liquids are a novel material that combine the properties of fluidity and permanent porosity. They have potential applications in many fields such as gas separation, storage and transport. Herein, we report a novel Type 1 porous liquid prepared based on silicalite-1. The pore size of this porous liquid was determined by positron annihilation lifetime spectroscopy (PALS), and the CO2 capacities were determined by the intelligent gravimetric analyzer (IGA). The unique properties of this porous liquid can promote its application in many fields such as gas storage and transport.
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Wang, Zenghui, Pingping Zhao, Jimin Wu, Jun Gao, Lianzheng Zhang, and Dongmei Xu. "ZIF-8-porous ionic liquids for the extraction of 2,2,3,3-tetrafluoro-1-propanol and water mixture." New Journal of Chemistry 45, no. 19 (2021): 8557–62. http://dx.doi.org/10.1039/d1nj01053k.

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Frisken, B. J., Andrea J. Liu, and David S. Cannell. "Critical Fluids in Porous Media." MRS Bulletin 19, no. 5 (May 1994): 19–24. http://dx.doi.org/10.1557/s0883769400036526.

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The behavior of fluids confined in porous materials has been of interest to engineers and scientists for many decades. Among the applications driving this research are the use of porous membranes to achieve liquid-liquid separations and to deionize water, the use of porous materials as beds for catalysis, and the need to extract liquids (especially oil and water) from such media. Many of these applications depend on transport, which is governed by flow or diffusion in the imbibed fluids. Both the flow and diffusion of multiphase fluids in porous media, however, strongly depend on the morphology of phase-separated domains, and on the kinetics of domain growth. Thus, it is worthwhile to study the behavior of multiphase fluids in porous media in the absence of flow. Recently, much attention has focused on even simpler systems that still capture these essential features, namely, near-critical binary liquid mixtures and vapor-liquid systems in model porous media, such as Vycor and dilute silica gels. Although near-critical fluids may seem rather artificial as models for multiphase liquids, there are several advantages associated with them. In general, domain morphology and growth kinetics are governed primarily by competition between interfacial tension and the preferential attraction of one phase to the surface of the medium. In near-critical fluids, the relative strength of these two energy scales is sensitive to temperature, and can therefore be altered in a controlled fashion. In addition, the kinetics of domain growth are sensitive to the temperature quench depth, and can be controlled.
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de Boer, Reint. "Thermodynamics of Phase Transitions in Porous Media." Applied Mechanics Reviews 48, no. 10 (October 1, 1995): 613–22. http://dx.doi.org/10.1115/1.3005042.

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Under certain circumstances, phase transitions can occur in porous media consisting of a porous solid saturated with liquids and gases, for example, due to a freezing process, the liquid or parts of the liquid can turn into ice, which is then connected with the porous solid, or due to a drying process, the liquid or parts of the liquid are converted to vapor, which is then a component of the gas phase. Although some special proboems of phase transitions in porous media have already been treated, a general theory on the basis of thermodynamics is still to be explored. The present paper is concerned with the development of thermodynamic restrictions for the constitutive relations of an elastic, compressible porous solid, filled with two compressible fluids, whereby it is assumed that the three phases have different temperatures. The investigations reveal that the mass changes are essentially, among others, connected to the differences of the chemical potentials and the energy transitions to the differences of the reciprocal of the temperatures, which is well-known in classical thermodynamics of gases.
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Hemming, Ellen B., Anthony F. Masters, and Thomas Maschmeyer. "Immobilisation of Homogeneous Pd Catalysts within a Type I Porous Liquid." Australian Journal of Chemistry 73, no. 12 (2020): 1296. http://dx.doi.org/10.1071/ch20256.

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An N-heterocyclic carbene-based palladium complex was successfully immobilised on the inner surfaces of hollow silica nanospheres. The external surfaces of these spheres were functionalised with a corona-canopy to produce a Type I porous liquid. To confirm the successful immobilisation of the catalytic precursor, the porous liquid system was explored using the Heck reaction as a model reaction. This work demonstrated that homogeneous catalysts can be successfully immobilised within porous liquids in principle and that the approach used could be readily adapted for the immobilisation of other systems.
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Sheng, Zhizhi, Jian Zhang, Jing Liu, Yunmao Zhang, Xinyu Chen, and Xu Hou. "Liquid-based porous membranes." Chemical Society Reviews 49, no. 22 (2020): 7907–28. http://dx.doi.org/10.1039/d0cs00347f.

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Costa Gomes, Margarida, Laure Pison, Ctirad Červinka, and Agilio Padua. "Porous Ionic Liquids or Liquid Metal-Organic Frameworks?" Angewandte Chemie 130, no. 37 (August 10, 2018): 12085–88. http://dx.doi.org/10.1002/ange.201805495.

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Costa Gomes, Margarida, Laure Pison, Ctirad Červinka, and Agilio Padua. "Porous Ionic Liquids or Liquid Metal-Organic Frameworks?" Angewandte Chemie International Edition 57, no. 37 (August 10, 2018): 11909–12. http://dx.doi.org/10.1002/anie.201805495.

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Sun, Zhenning, Zhengyu Cao, Yan Li, Qiuya Zhang, Xiaofang Zhang, Jiangang Qian, Lei Jiang, and Dongliang Tian. "Switchable smart porous surface for controllable liquid transportation." Materials Horizons 9, no. 2 (2022): 780–90. http://dx.doi.org/10.1039/d1mh01820e.

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Magnetic field induced switchable morphology of composite porous surfaces has been demonstrated for controllable liquid transportation, which can be used as a valve to dynamically control the moving and permeation behavior of non-miscible liquids.
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Sliwinska-Bartkowiak, M., S. L. Sowers, and K. E. Gubbins. "Liquid−Liquid Phase Equilibria in Porous Materials†." Langmuir 13, no. 5 (March 1997): 1182–88. http://dx.doi.org/10.1021/la960004a.

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Dissertations / Theses on the topic "Porous Liquid"

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Stevar, M. S. P. "Dissolution dynamics of liquid/liquid binary mixtures in porous media." Thesis, University of Southampton, 2013. https://eprints.soton.ac.uk/349974/.

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In this project has been undertaken an experimental study aimed at understanding the dissolution dynamics of binary mixtures within porous media. The porous medium can be roughly represented as a network of capillary tubes. This allowed for the initial research to be focused on understanding the dissolution dynamics of binary mixtures (i.e. glycerol/water, soybean oil/hexane, and isobutyric acid/water) within single capillary tubes. Further, the dissolution process was investigated within a 2D micromodel built as a network of capillary tubes. In the experiments with the capillary tubes, the dissolution (i.e. the interfacial mass transfer) could be isolated from the hydrodynamic motion while using glycerol/water and soybean oil/hexane binary mixtures. Despite the fact that these are fully miscible liquids, the interface could be observed for rather long time periods. In particular, two phase boundaries were observed moving from the ends into the middle section of the capillary tube with the speeds v∼D^1/3t^-2/3d^2(D, t and d are the coefficient of diffusion, time and diameter of the capillary tube, respectively). The boundaries slowly smeared but their smearing occurred very slow in comparison to their motion. The motion of the phase boundaries cannot be explained by the dependency of the diffusion coefficient on concentration, and could possibly be explained by the effect of barodiffusion. In addition, these solute/solvent boundaries were endowed with non-zero interfacial tension. This experimental study also revealed that the solvent penetration into the micromodel is diffusion-dominated for completely miscible binary mixtures. This is however non-Fickian diffusion with the dissolution rate dV/dt∼D^1/3t^-0.4 for almost the entire duration of the experiment (V is the volume occupied by the solvent, D is the diffusion coefficient and t is time). For the IBA/water mixture the experiments performed at undercritical temperatures revealed that the diffusive mass transport was negligible despite the mixture being out of its thermodynamic equilibrium. Despite a seeming simplicity of the experiments, to the author’s best knowledge, there is no theory that could correctly describe the observed diffusional penetration of a solvent into a solute-filled capillary tube and hence, into a more complex porous volume.
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Shin, Youn-Ok. "Vapor and liquid equilibria in porous media." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0022/MQ50659.pdf.

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Shin, Youn-Ok 1971. "Vapor and liquid equilibria in porous media." Thesis, McGill University, 1999. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=21323.

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The alteration of the vapor and liquid equilibrium (VLE) of volatile organic mixtures by using porous media at the liquid-vapor interface was studied. Kelvin, assuming ideal behavior of fluids, first introduced the vapor pressure of liquid over a meniscus as a function of its surface tension and the radius of the curvature. A thermodynamic model (SSmod model) predicting the VLE of non-ideal organic mixtures in porous media was developed as a function of pore sizes based on the pressure equations available in literature. The model was used to predict the VLE of two aqueous alcohol solutions, ethanol-water and propanol-water, and two binary alcohol solutions, methanol-isopropanol and ethanol-octane. Experiments were conducted using sintered metal and fritted glass plates as porous media and compared with the model predictions. The model predictions for the actual pore diameters tested showed good agreement with the experimental results.
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Monser, Lotfi Ibrahim. "Modified porous graphitic carbon for liquid chromatography." Thesis, University of Hull, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318379.

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Russo, Ann. "Immiscible Liquid Dissolution in Heterogeneous Porous Media." Diss., The University of Arizona, 2008. http://hdl.handle.net/10150/194522.

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Immiscible liquids, including chlorinated solvents, have proven to be a lasting source of subsurface contamination at many hazardous waste sites. Continued improvement of site characterization and determination of applicable remediation technologies can be achieved by further understanding of the transport and fate of these contaminants. The transport and fate of trichloroethene (TCE) was investigated through miscible displacement and dissolution experiments. Miscible displacement experiments were conducted using homogeneously packed columns with several porous media encompassing a range of particle size distributions. Immiscible liquid dissolution was investigated using homogeneously packed columns containing a residual saturation of trichloroethene. The same porous media were used for immiscible liquid dissolution experiments. Mathematical modeling of miscible displacement and dissolution experiments was conducted using a one-dimensional single region or multi-region model. Imaging of immiscible liquid dissolution was also conducted, using Synchrotron X-ray Microtomography imaging at Argonne National Laboratory, Argonne, IL. Dissolution experiments exhibited nonideal dissolution behavior that was apparent in observed effluent data and in collected imaging data. Nonideal behavior was manifested as secondary regions of relatively constant aqueous concentrations occurring for a number of pore volumes. This behavior was observed to increase in magnitude as particle size distribution of the porous media increased. During imaging, immiscible liquid blobs were observed to dissolve throughout the column during dissolution. This behavior is also indicative of nonideal dissolution, as it would be expected that dissolution would first occur for the blobs nearest the inlet and then proceed upward through the column as dissolution progressed. In many cases, a multi-region modeling approach was necessary to successfully represent the nonideal behavior observed. Comparisons were made between the natural porous media used for this research and a well-sorted sand. Nonideal dissolution was not observed in the well-sorted sand.
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Guo, Tianle. "Effects of buoyancy forces on miscible liquid-liquid displacements in porous media." Thesis, University of Ottawa (Canada), 1994. http://hdl.handle.net/10393/6825.

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The effects of gravity forces on the miscible displacement of one fluid (aqueous glycerol solution) by another fluid (pure water) in a vertical consolidated porous medium have been investigated. A set of horizontal displacement experiments was performed for comparison with two sets of vertical-upward and vertical-downward displacements. It was found that gravitational forces (i.e. buoyancy forces) can be an important factor in determining the displacement pattern where fluids having different densities and different flowrates are involved. In a given porous medium system, the principal variables which affect the displacement efficiency of oil (or any other miscible liquid) by water are the viscosity ratio, density difference, and displacement flowrate. Increasing the viscosity ratio will decrease the oil recovery; however, when the viscosity ratio is close to unity, good oil recovery will be obtained. The injection flowrate is also critical. At low injection flowrates, the effects of gravity become relatively more important. At high flowrates, gravity forces have less effect on the displacement efficiency. In vertical-upward displacements, buoyancy forces play a negative role since they tend to promote viscous fingering and consequently lower the oil recovery (when $\rm \rho\sb{oil}>\rho\sb{water}$). On the other hand, in vertical-downward displacements, buoyancy forces tend to stabilize the displacement process, and high oil recoveries can be obtained. Comparing the horizontal displacement patterns with those of the two vertical displacements, it was found that buoyancy forces can exert very significant effects on fingering phenomena.
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Zhdanov, Sergey. "Kinetics of spreading over porous substrate." Thesis, Loughborough University, 2002. https://dspace.lboro.ac.uk/2134/33884.

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The spreading of small liquid drops over thin and thick porous layers (dry or saturated with the same liquid) has been investigated in the case of both complete wetting (silicone oils of different viscosities) and partial wetting (aqueous SDS solutions of different concentrations). Consideration has been carried out from both experimental and theoretical points of view. Nitrocellulose membranes of different porosity and averaged pore size were used as a model of thin porous layers, glass and metal filters were used as a model of thick porous substrates. It has been shown, that the spreading process follows the power law in time in the case of spreading of silicon oil drops over porous substrate saturated with the same oil. The liquid flow in the spreading drop has been matched with the flow in the porous substrate. Both the exponent and the pre-exponential factor of the power law have been predicted and compared with our experimental data, which shows the good agreement. An effective lubrication coefficient has been introduced, which accounts for an effective slippage of liquids over porous substrates. This coefficient has been both theoretically predicted and experimentally verified.
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Pourmand, Payam. "NMR detection of liquid dynamics in porous matrices." Thesis, KTH, Skolan för kemivetenskap (CHE), 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-145864.

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Porous materials or a porous media can be encountered in our everyday life, both in industrial and household systems and in the nature. Generally speaking all solid and semisolid materials are porous to some degree e.g. different dense rock types, plastics etc. Porous materials are constantly finding more and more applications, both in industry and research. Many commercially important process in the industry utilize porous media e.g. flow of fluids through porous media for separation process and porous catalyst supports. This has strongly contributed to the development of porous media with controlled properties, which can be utilized for understanding the behavior of liquids confined in the material, and the morphology of these synthetic materials. This thesis work brings some insight and understanding of porous materials i.e. Controlled Pore Glass (CPG). Report also contains a brief explanation of Nuclear Magnetic Resonance (NMR) spectroscopy, diffusion NMR and other techniques such as Mercury porosimetry. The first part of the thesis is focused on determining the required amount of liquid i.e. octanol needed to achieve full pore saturation for different CPGs with varying pore sizes. This was achieved by taking into account that the transverse relaxation time T2 is sensitive in the ms-ns of motional correlation times, and that there are physical factors in porous material which affect the T2. Second part, diffusion NMR is used to study self-diffusion of octanol confined in CPG, thus bringing some insight on mass transfer limitations within porous systems. The report present results obtained from experiments with NMR and Diffusion NMR, discusses the issues that can arise when investigating porous materials and suggest solutions
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Dias, H. "Gas and liquid chromatography on porous graphitic carbon." Thesis, University of Edinburgh, 1990. http://hdl.handle.net/1842/13643.

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A new hydrophobic support material, Porous Graphitic (or Graphitised) Carbon (PGC) has been studied using both Liquid (LC) and Gas Chromatography (GC). The heat of adsorbtion (AH) of typical LC solvents determined on PGC, using GC, showed that AH increased with the molecular area (Ax) of solvents for well graphitised carbons, but that AH/Ax values were similar for all solvents studied. By definition, AH/Ax is a measure of eluotropic strength. The results reveal that a strong eluotropic series does not exist on carbon. A strong eluotropic series does exist on silica. In this case, AH/Ax values of solvents were dependent upon their eluotropic strengths (Eo), determined by LC. GC work was carried out using alcohols, ketones and aliphatic hydrocarbons on PGC, modified with different amounts of Carbowax 1500. Symmetrical peaks were obtained with coated materials. The column efficiency (N), first increased and then dropped with increasing Carbowax content on the PGC surface. The retention of ketones and hydrocarbons decreased with increasing amount of Carbowax on PGC. In the case of alcohols, the retention decreased with the initial introduction of Carbowax on to PGC. Some alcohols displayed enhanced retention at 0.10% of Carbowax. All alcohols showed increased retention at the monolayer coverage of Carbowax. In the quest for a perfect material for adsorption GC, PGC samples were hydrogen treated at elevated temperatures (230-1030°C). All hydrogen treated samples failed to display signficantly improved chromatographic properties. PGC was then treated with toluene in a stream of either hydrogen (at 630°C) or nitrogen (at 630°C or 300°C) to eliminate any active sites present on the surface. Hexane was used us an alternative to toluene at 630°C in a stream of hydrogen. Such surface treatments yielded improved materials for adsorption GC. On heating the columns (beyond 230"C), containing these materials, with carrier gas running through the columns, the Chromatography deteriorated in the cases of toluene-treated PGC whilst the Chromatography of the hexane-treatcd PGC remained unaffected. LC work on some aromatic compounds using PGC, coated with surfactants such as Tween 80 or Span 80 showed that, analyte retention decreased with increasing surfactant concentration (up to 0.03% of Tween and 0.02% of Span) in the eluent. N dropped with the introduction of Tween to the PGC. Increasing the ratio of water to mcthanol in the eluent, at a constant eluent concentration of surfactant, resulted in diminishing N, increasing eluent polarity and analyte retention values. Ion pairing was carried out on PGC using cetyltrimethylammonium-bromide (CTAB) as the ion pairing agent, at an eluent pH of 12.5. The retention of solutes, that ionise under these conditions, increased whereas the retention of analytes, that do not ionise, decreased with increasing eluent concentration of CTAB. The coated or chemically modified PGC surfaces are useful in GC whilst the dynamically coated PGC surfaces are important in LC. Such surface treatments can alter the following properties of PGC; (a) Retention characteristics, (b) the selectivity and (c) chromatographic efficiency.
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Wan, Quian-Hong. "Surface modification of porous graphite for liquid chromatography." Thesis, University of Edinburgh, 1992. http://hdl.handle.net/1842/13187.

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Surface modification of porous graphite has been studied in detail by liquid chromatography. The non-polar nature of the graphite provides the basis for adsorptive modification by which the graphite surface is either deactivated or functionized. While the elimination of geometric heterogeneity is achieved by adsorption of trace polyaromatic compounds, the specialist in selectivity is conferred to the graphite by a monolayer coating of modifiers. A number of strategies are used for different purposes. These include dynamic coating, insoluble coating and cross-linked coating. The chromatographic properties of the modified materials are evaluated in terms of efficiency, selectivity and stability. With the exception for cross-linked coating, the modified materials show performances better than those of the original graphite. Applications to adsorption, ion exchange, chiral and exclusion chromatography are demonstrated. These new packings are found particularly useful in the separation of inorganic anions, amino acid and hydroxy acid enantiomers. They give excellent peak symmetry and long term stability. The mechanisms of retention on the graphite based materials are characterised and discussed.
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Books on the topic "Porous Liquid"

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A, Galwey, ed. Liquid and vapor flows in porous bodies: Surface phenomena. Amsterdam: Gordon & Breach, 1999.

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Churaev, N. V. Liquid and vapor flows in porous bodies: Surface phenomena. Amsterdam, The Netherlands: Gordon & Breach Science Publishers, 2000.

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Philip, Crawford Gregory, and Žumer Slobodan, eds. Liquid crystals in complex geometries: Formed by polymer and porous networks. London: Taylor & Francis, 1996.

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Yoon, B. G. A study of the liquid absorption properties of porous construction materials. Manchester: UMIST, 1993.

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Buchlin, J.-M. OPERA II: A test facility to study the thermohydraulics of liquid saturated self heated porous media. Rhode Saint Genese, Belgium: von Karman Institute for Fluid Dynamics, 1986.

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Borman, V. D. Dynamics of infiltration of a nanoporous media with a nonwetting liquid. Hauppauge, N.Y: Nova Science Publishers, 2010.

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Olagunju, M. O. A study of efficient recovery of liquid from fine air-liquid mists of the form generated in gas turbine bearing chambers using a rotating porous disc. London: University of East London, 1998.

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New materials permeable to water vapor. Berlin: Springer, 1999.

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1931-, Lowell S., and Lowell S. 1931-, eds. Characterization of porous solids and powders: Surface area, pore size, and density. 4th ed. Boston: Kluwer Academic Publishers, 2004.

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Dukhin, Andrei S., and Philip J. Goetz. Characterization of liquids, nano- and microparticulates, and porous bodies using ultrasound. 2nd ed. Amsterdam: Elsevier, 2010.

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Book chapters on the topic "Porous Liquid"

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Rurali, Riccardo. "Gas and Liquid Doping Gas and liquid doping of Porous Silicon." In Handbook of Porous Silicon, 639–45. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-05744-6_66.

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Aybers, M. N. "Liquid Seeping Into Porous Ground." In Convective Heat and Mass Transfer in Porous Media, 1061–69. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3220-6_38.

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Rurali, Riccardo. "Gas and Liquid Doping of Porous Silicon." In Handbook of Porous Silicon, 1–7. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04508-5_66-1.

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Rurali, Riccardo. "Gas and Liquid Doping of Porous Silicon." In Handbook of Porous Silicon, 973–79. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-71381-6_66.

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Zhang, Haifei. "Porous Materials by Templating of Small Liquid Drops." In Hierarchically Structured Porous Materials, 209–39. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639588.ch7.

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Dani, Alessandro, Valentina Crocellà, Giulio Latini, and Silvia Bordiga. "CHAPTER 2. Porous Ionic Liquid Materials." In Polymerized Ionic Liquids, 23–82. Cambridge: Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/9781788010535-00023.

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Barrulas, Raquel V., Marcileia Zanatta, and Marta C. Corvo. "Porous Ionic Liquid Derived Materials for CO2 Emissions Mitigation." In Advanced Functional Porous Materials, 613–59. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-85397-6_20.

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Concha A., Fernando. "Flow Through Rigid Porous Media." In Solid-Liquid Separation in the Mining Industry, 119–42. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-02484-4_6.

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Ehlers, W., and W. Volk. "Localization Phenomena in Liquid-Saturated and Empty Porous Solids." In Porous Media: Theory and Experiments, 159–77. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4579-4_10.

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De Boer, Reint, and Joachim Bluhm. "Phase Transitions in Gas- and Liquid-Saturated Porous Solids." In Porous Media: Theory and Experiments, 249–67. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4579-4_16.

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Conference papers on the topic "Porous Liquid"

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Zijl, Wouter. "LIQUID-LIQUID MOTION IN POROUS AND FRACTURED MEDIA." In International Symposium on Liquid-Liquid Two Phase Flow and Transport Phenomena. Connecticut: Begellhouse, 1997. http://dx.doi.org/10.1615/ichmt.1997.intsymliqtwophaseflowtranspphen.430.

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Zidansek, A., S. Kralj, G. Lahajnar, Slobodan Zumer, and Robert Blinc. "Deuteron NMR study of an 8CB liquid crystal confined to porous glass." In Liquid Crystals, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, Jerzy Zielinski, and Jozef Zmija. SPIE, 1998. http://dx.doi.org/10.1117/12.299982.

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Rozanski, Stanislaw A., and Friedrich Kremer. "Dielectric properties of nematic liquid crystals in porous membranes." In Liquid Crystals: Materials Science and Applications, edited by Jozef Zmija. SPIE, 1995. http://dx.doi.org/10.1117/12.215567.

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Nilsson Pingel, Torben. "Liquid transport in porous paperboard coatings." In European Microscopy Congress 2020. Royal Microscopical Society, 2021. http://dx.doi.org/10.22443/rms.emc2020.1117.

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Mao, Aihua, Mingle Wang, Yong-jin Liu, Huamin Wang, and Guiqing Li. "Liquid wetting across porous anisotropic textiles." In SA '17: SIGGRAPH Asia 2017. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3145690.3145713.

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Razavi, Reza, and Stephen A. Sarles. "Modeling and Experiments on Liquid-Infused, Mechanically Activated Porous Materials." In ASME 2016 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/smasis2016-9046.

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The goal of our research is to develop new understanding regarding the design and fabrication of mechanically activated liquid-infused porous films. Our unique approach is to consider a thin, elastic material that features well-defined pores, which are plugged with an infusing liquid that preferentially wets to the walls of the pores. By tuning the geometry of the pores, liquid-filled pores can be rearranged into a configuration that creates an open pore by applying stretch to the solid material, and they close (i.e. heal) again when the stretch is removed. Impregnating the pores with liquid seeks to avoid limitations that prevent complete pore closure and allows for tailoring of the pore geometry to drive liquid redistribution in the pore. The specific objective of this research is to study the effects of pore geometry and liquid wetting for creating fully reversible, stretch-activated pores. Our approach is both computational and experimental: Surface Evolver software is utilized to predict minimal energy wetting states of liquid in various pore shapes, and experiments on porous elastomers infused with either water or mineral oil allow measurements of stretch-induced changes in wetting properties and porosity. Both modeling and experiments demonstrate that a tear-shaped pore, which consists of a circular pore that features a taper extending in a radial direction, can enable reversible opening and closing of the pore via liquid redistribution. Our results indicate that infusing liquids with lower surface tensions and lower contact angles on walls of the pore exhibit better reversibility during the application of stretch.
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Gustavesen, R. L., and S. A. Sheffield. "Unreacted Hugoniots for porous and liquid explosives." In High-pressure science and technology—1993. AIP, 1994. http://dx.doi.org/10.1063/1.46239.

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Kon, Akira, Ryouta Ito, Michinori Honma, Toshiaki Nose, and Yoshiaki Watanabe. "Quasi-optic millimeter-wave device application of liquid crystal material by using porous PMMA matrix." In Emerging Liquid Crystal Technologies XIII, edited by Igor Muševič, Liang-Chy Chien, Dirk J. Broer, and Vladimir G. Chigrinov. SPIE, 2018. http://dx.doi.org/10.1117/12.2295062.

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Loboiko, Alexander I., Vladimir V. Likhanskii, and Oleg V. Khoruzhii. "INVESTIGATION OF EFFECT OF A SPATIAL INHOMOGENEITY ON THE VAPOUR-LIQUID FLOW DYNAMICS IN HEAT-GENERATION POROUS MEDIUM." In International Symposium on Liquid-Liquid Two Phase Flow and Transport Phenomena. Connecticut: Begellhouse, 1997. http://dx.doi.org/10.1615/ichmt.1997.intsymliqtwophaseflowtranspphen.410.

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Binh-Khiem, Nguyen, Kiyoshi Matsumoto, and Isao Shimoyama. "Porous Parylene and effects of liquid on Parylene films deposited on liquid." In 2011 IEEE 24th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2011. http://dx.doi.org/10.1109/memsys.2011.5734374.

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Reports on the topic "Porous Liquid"

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Stubos, A. K., C. Satik, and Y. C. Yortsos. Effects of capillary heterogeneity on vapor-liquid counterflow in porous media. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/10159907.

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Stubos, A. K., C. Satik, and Y. C. Yortsos. Effects of capillary heterogeneity on vapor-liquid counterflow in porous media. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/5121949.

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Cooper, Gene R. Moments on a Coning Projectile by a Spinning Liquid in Porous Media. Fort Belvoir, VA: Defense Technical Information Center, September 2005. http://dx.doi.org/10.21236/ada444065.

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FLACH, GREGORY. Porous Medium Analysis or Interstitial Liquid Removal from Tank 41 and Tank 3. Office of Scientific and Technical Information (OSTI), March 2004. http://dx.doi.org/10.2172/822653.

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Nitao, J. J., and T. A. Buscheck. On the movement of a liquid front in an unsaturated, fractured porous medium, Part 1. Office of Scientific and Technical Information (OSTI), June 1989. http://dx.doi.org/10.2172/137640.

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Cooper, Gene R. Moments on a Coning M864 by a Liquid Payload: The Candlestick Problem and Porous Media. Fort Belvoir, VA: Defense Technical Information Center, July 2006. http://dx.doi.org/10.21236/ada453380.

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Kaplan, Daniel, Kenneth Gibbs, Abdullah Mamun, and Brian Powell. Non-Destructive Imaging of a Liquid Moving Through Porous Media Using a Computer Tomography Scanner. Office of Scientific and Technical Information (OSTI), August 2020. http://dx.doi.org/10.2172/1647017.

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Takigawa, D. Y. The effect of porous support composition and operating parameters on the performance of supported liquid membranes. Office of Scientific and Technical Information (OSTI), February 1991. http://dx.doi.org/10.2172/6235612.

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Tsimpanogiannis, Ioannis N., and Yanis C. Yortsos. An Effective Continuum Model for the Liquid-to-Gas Phase Change in a Porous Medium Driven by Solute Diffusion: II. Constant Liquid Withdrawal Rates. Office of Scientific and Technical Information (OSTI), August 2001. http://dx.doi.org/10.2172/784396.

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Nitao, J. J. On the movement of a liquid front in an unsaturated, fractured porous medium, Part 2, Mathematical theory. Office of Scientific and Technical Information (OSTI), June 1989. http://dx.doi.org/10.2172/137641.

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