Wetting and Spreading of Nanofluids on Solid Surfaces Driven by the Structural Disjoining Pressure: Statics Analysis and Experiments
The wetting and spreading of nanofluids composed of liquid suspensions of nanoparticles have significant technological applications. Recent studies have revealed that, compared to the spreading of base liquids without nanoparticles, the spreading of wetting nanofluids on solid surfaces is enhanced b...
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Veröffentlicht in: | Langmuir 2011-04, Vol.27 (7), p.3324-3335 |
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description | The wetting and spreading of nanofluids composed of liquid suspensions of nanoparticles have significant technological applications. Recent studies have revealed that, compared to the spreading of base liquids without nanoparticles, the spreading of wetting nanofluids on solid surfaces is enhanced by the structural disjoining pressure. Here, we present our experimental observations and the results of the statics analysis based on the augmented Laplace equation (which takes into account the contribution of the structural disjoining pressure) on the effects of the nanoparticle concentration, nanoparticle size, contact angle, and drop size (i.e., the capillary and hydrostatic pressure); we examined the effects on the displacement of the drop-meniscus profile and spontaneous spreading of a nanofluid as a film on a solid surface. Our analyses indicate that a suitable combination of the nanoparticle concentration, nanoparticle size, contact angle, and capillary pressure can result not only in the displacement of the three-phase contact line but also in the spontaneous spreading of the nanofluid as a film on a solid surface. We show here, for the first time, that the complete wetting and spontaneous spreading of the nanofluid as a film driven by the structural disjoining pressure gradient (arising due to the nanoparticle ordering in the confined wedge film) is possible by decreasing the nanoparticle size and the interfacial tension, even at a nonzero equilibrium contact angle. Experiments were conducted on the spreading of a nanofluid composed of 5, 10, 12.5, and 20 vol % silica suspensions of 20 nm (geometric diameter) particles. A drop of canola oil was placed underneath the glass surface surrounded by the nanofluid, and the spreading of the nanofluid was monitored using an advanced optical technique. The effect of an electrolyte, such as sodium chloride, on the nanofluid spreading phenomena was also explored. On the basis of the experimental results, we can conclude that a nanofluid with an effective particle size (including the electrical double layer) of about 40 nm, a low equilibrium contact angle (30 vol %) is desirable for the dynamic spreading of a nanofluid system with an interfacial tension of 0.5 mN/m. Our experimental observations also validate the major predications of our theoretical analysis. |
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Recent studies have revealed that, compared to the spreading of base liquids without nanoparticles, the spreading of wetting nanofluids on solid surfaces is enhanced by the structural disjoining pressure. Here, we present our experimental observations and the results of the statics analysis based on the augmented Laplace equation (which takes into account the contribution of the structural disjoining pressure) on the effects of the nanoparticle concentration, nanoparticle size, contact angle, and drop size (i.e., the capillary and hydrostatic pressure); we examined the effects on the displacement of the drop-meniscus profile and spontaneous spreading of a nanofluid as a film on a solid surface. Our analyses indicate that a suitable combination of the nanoparticle concentration, nanoparticle size, contact angle, and capillary pressure can result not only in the displacement of the three-phase contact line but also in the spontaneous spreading of the nanofluid as a film on a solid surface. We show here, for the first time, that the complete wetting and spontaneous spreading of the nanofluid as a film driven by the structural disjoining pressure gradient (arising due to the nanoparticle ordering in the confined wedge film) is possible by decreasing the nanoparticle size and the interfacial tension, even at a nonzero equilibrium contact angle. Experiments were conducted on the spreading of a nanofluid composed of 5, 10, 12.5, and 20 vol % silica suspensions of 20 nm (geometric diameter) particles. A drop of canola oil was placed underneath the glass surface surrounded by the nanofluid, and the spreading of the nanofluid was monitored using an advanced optical technique. The effect of an electrolyte, such as sodium chloride, on the nanofluid spreading phenomena was also explored. On the basis of the experimental results, we can conclude that a nanofluid with an effective particle size (including the electrical double layer) of about 40 nm, a low equilibrium contact angle (<3°), and a high effective volume concentration (>30 vol %) is desirable for the dynamic spreading of a nanofluid system with an interfacial tension of 0.5 mN/m. 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Recent studies have revealed that, compared to the spreading of base liquids without nanoparticles, the spreading of wetting nanofluids on solid surfaces is enhanced by the structural disjoining pressure. Here, we present our experimental observations and the results of the statics analysis based on the augmented Laplace equation (which takes into account the contribution of the structural disjoining pressure) on the effects of the nanoparticle concentration, nanoparticle size, contact angle, and drop size (i.e., the capillary and hydrostatic pressure); we examined the effects on the displacement of the drop-meniscus profile and spontaneous spreading of a nanofluid as a film on a solid surface. Our analyses indicate that a suitable combination of the nanoparticle concentration, nanoparticle size, contact angle, and capillary pressure can result not only in the displacement of the three-phase contact line but also in the spontaneous spreading of the nanofluid as a film on a solid surface. We show here, for the first time, that the complete wetting and spontaneous spreading of the nanofluid as a film driven by the structural disjoining pressure gradient (arising due to the nanoparticle ordering in the confined wedge film) is possible by decreasing the nanoparticle size and the interfacial tension, even at a nonzero equilibrium contact angle. Experiments were conducted on the spreading of a nanofluid composed of 5, 10, 12.5, and 20 vol % silica suspensions of 20 nm (geometric diameter) particles. A drop of canola oil was placed underneath the glass surface surrounded by the nanofluid, and the spreading of the nanofluid was monitored using an advanced optical technique. The effect of an electrolyte, such as sodium chloride, on the nanofluid spreading phenomena was also explored. On the basis of the experimental results, we can conclude that a nanofluid with an effective particle size (including the electrical double layer) of about 40 nm, a low equilibrium contact angle (<3°), and a high effective volume concentration (>30 vol %) is desirable for the dynamic spreading of a nanofluid system with an interfacial tension of 0.5 mN/m. Our experimental observations also validate the major predications of our theoretical analysis.</description><subject>Canola Oil</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Colloids: Surfactants and Self-Assembly, Dispersions, Emulsions, Foams</subject><subject>Electrolytes</subject><subject>Exact sciences and technology</subject><subject>Fatty Acids, Monounsaturated - chemistry</subject><subject>General and physical chemistry</subject><subject>Nanoparticles - chemistry</subject><subject>Nanotechnology - methods</subject><subject>Physical and chemical studies. Granulometry. Electrokinetic phenomena</subject><subject>Pressure</subject><subject>Solid-liquid interface</subject><subject>Surface physical chemistry</subject><subject>Wettability</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E1vEzEQBmALgWgoHPgDyBeEOCz4a7NZblVbPqQKkALiuJr1zoIjxw4eG5E7PxyHhnDhZFnz6B37ZeyxFC-kUPKlBymMEma8wxayVaJpV6q7yxaiM7rpzFKfsQdEGyFEr01_n50pqftWGbFgv75gzi585RAmvt4lhOlwizN_DyHOvriJeAx8Hb2roKQZLBK_Su4HBj7uef6GfJ1Tsbkk8PzK0Sa6cMj4mJCoJHxV55CdJX4RwO_J0Z9l1z93mNwWQ6aH7N4MnvDR8Txnn19ff7p829x8ePPu8uKmASNFbsw4Aup-tp22ndRWWD0pJbFf2RGsXcFSG6GndpJWA8q2syDscgZs2zpF1Ofs2W3uLsXvBSkPW0cWvYeAsdCwanvT606pKp_fSpsiUcJ52NW3QtoPUgyHzodT59U-OaaWcYvTSf4tuYKnRwBkwc8JgnX0z5maJ-uHTg4sDZtYUq2L_rPwN2rXl8M</recordid><startdate>20110405</startdate><enddate>20110405</enddate><creator>Kondiparty, Kirti</creator><creator>Nikolov, Alex</creator><creator>Wu, Stanley</creator><creator>Wasan, Darsh</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110405</creationdate><title>Wetting and Spreading of Nanofluids on Solid Surfaces Driven by the Structural Disjoining Pressure: Statics Analysis and Experiments</title><author>Kondiparty, Kirti ; Nikolov, Alex ; Wu, Stanley ; Wasan, Darsh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a410t-4bbae39fc73c713c0c3d221e98cbacc8a63403d5d1c3ae157ca0c6fae55cc8ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Canola Oil</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Colloids: Surfactants and Self-Assembly, Dispersions, Emulsions, Foams</topic><topic>Electrolytes</topic><topic>Exact sciences and technology</topic><topic>Fatty Acids, Monounsaturated - chemistry</topic><topic>General and physical chemistry</topic><topic>Nanoparticles - chemistry</topic><topic>Nanotechnology - methods</topic><topic>Physical and chemical studies. Granulometry. Electrokinetic phenomena</topic><topic>Pressure</topic><topic>Solid-liquid interface</topic><topic>Surface physical chemistry</topic><topic>Wettability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kondiparty, Kirti</creatorcontrib><creatorcontrib>Nikolov, Alex</creatorcontrib><creatorcontrib>Wu, Stanley</creatorcontrib><creatorcontrib>Wasan, Darsh</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kondiparty, Kirti</au><au>Nikolov, Alex</au><au>Wu, Stanley</au><au>Wasan, Darsh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Wetting and Spreading of Nanofluids on Solid Surfaces Driven by the Structural Disjoining Pressure: Statics Analysis and Experiments</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2011-04-05</date><risdate>2011</risdate><volume>27</volume><issue>7</issue><spage>3324</spage><epage>3335</epage><pages>3324-3335</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>The wetting and spreading of nanofluids composed of liquid suspensions of nanoparticles have significant technological applications. Recent studies have revealed that, compared to the spreading of base liquids without nanoparticles, the spreading of wetting nanofluids on solid surfaces is enhanced by the structural disjoining pressure. Here, we present our experimental observations and the results of the statics analysis based on the augmented Laplace equation (which takes into account the contribution of the structural disjoining pressure) on the effects of the nanoparticle concentration, nanoparticle size, contact angle, and drop size (i.e., the capillary and hydrostatic pressure); we examined the effects on the displacement of the drop-meniscus profile and spontaneous spreading of a nanofluid as a film on a solid surface. Our analyses indicate that a suitable combination of the nanoparticle concentration, nanoparticle size, contact angle, and capillary pressure can result not only in the displacement of the three-phase contact line but also in the spontaneous spreading of the nanofluid as a film on a solid surface. We show here, for the first time, that the complete wetting and spontaneous spreading of the nanofluid as a film driven by the structural disjoining pressure gradient (arising due to the nanoparticle ordering in the confined wedge film) is possible by decreasing the nanoparticle size and the interfacial tension, even at a nonzero equilibrium contact angle. Experiments were conducted on the spreading of a nanofluid composed of 5, 10, 12.5, and 20 vol % silica suspensions of 20 nm (geometric diameter) particles. A drop of canola oil was placed underneath the glass surface surrounded by the nanofluid, and the spreading of the nanofluid was monitored using an advanced optical technique. The effect of an electrolyte, such as sodium chloride, on the nanofluid spreading phenomena was also explored. On the basis of the experimental results, we can conclude that a nanofluid with an effective particle size (including the electrical double layer) of about 40 nm, a low equilibrium contact angle (<3°), and a high effective volume concentration (>30 vol %) is desirable for the dynamic spreading of a nanofluid system with an interfacial tension of 0.5 mN/m. Our experimental observations also validate the major predications of our theoretical analysis.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21395240</pmid><doi>10.1021/la104204b</doi><tpages>12</tpages></addata></record> |
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subjects | Canola Oil Chemistry Colloidal state and disperse state Colloids: Surfactants and Self-Assembly, Dispersions, Emulsions, Foams Electrolytes Exact sciences and technology Fatty Acids, Monounsaturated - chemistry General and physical chemistry Nanoparticles - chemistry Nanotechnology - methods Physical and chemical studies. Granulometry. Electrokinetic phenomena Pressure Solid-liquid interface Surface physical chemistry Wettability |
title | Wetting and Spreading of Nanofluids on Solid Surfaces Driven by the Structural Disjoining Pressure: Statics Analysis and Experiments |
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