Dissertationen zum Thema „Wetting behavior“
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Monast, Patrick. „Wetting behavior of ternary mixtures containing surfactants“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ64410.pdf.
Der volle Inhalt der QuelleStables, Christa Lauren. „Wetting and Penetration Behavior of Resin/Wood Interfaces“. Thesis, Virginia Tech, 2017. http://hdl.handle.net/10919/79700.
Der volle Inhalt der QuelleMaster of Science
Lodge, Richard. „Wetting behavior and surface potential characteristics of human hair“. The Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=osu1165335748.
Der volle Inhalt der QuelleTsao, Joanna W. „Influence of nanoscale roughness on wetting behavior in liquid/liquid systems“. Thesis, Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/53045.
Der volle Inhalt der QuelleAziz, Hossain. „COMPUTATIONAL AND EXPERIMENTAL INVESTIGATION ON THE WETTING BEHAVIOR OF DROPLET-FIBER SYSTEMS“. VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/5910.
Der volle Inhalt der QuelleRosemond, St Julien Palmer III. „Characterization of the wetting behavior of place exchanged mixed-monolayer-protected gold nanoparticles“. Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/58273.
Der volle Inhalt der QuelleCataloged from PDF version of thesis.
Includes bibliographical references (p. 22-24).
Mixed-monolayer-protected gold nanoparticles have been shown to have self assembling ligand shells. Given certain ligand concentrations, the NP shell can spontaneously form complex ordered domains with domain spacing as small as five angstroms. It has been proven that the solubility of NPs synthesized using a one step method is almost solely dependent on the corresponding ligand shell morphology. We have attempted to get a better understanding of the morphological differences between NPs synthesized in one step and those synthesized through place exchange by comparing their solubility characteristics. Both types NPs were functionalized using different concentrations two immiscible ligands. The place exchanged NPs almost certainly form a type of ripple shell morphology due to the presence of nonmonotonic solubility peaks in polar solvents at low hydrophilic ligand concentrations. Based on the solubility results, we conclude that the ligand shell morphology must be different for place exchanged and one step nanoparticles. The differences are most likely due to the mechanism by which place exchange populates the nanoparticles.
by St. Julien Palmer Rosemond III.
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Patel, Nirajkumar. „Micro scale flow behavior, fiber wetting and void formation in liquid composite molding“. The Ohio State University, 1994. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299253097.
Der volle Inhalt der QuelleNalagatla, Dinesh Reddy. „INFLUENCE OF SURFACE ROUGHNESS OF COPPER SUBSTRATE ON WETTING BEHAVIOR OF MOLTEN SOLDER ALLOYS“. UKnowledge, 2007. http://uknowledge.uky.edu/gradschool_theses/488.
Der volle Inhalt der QuelleSmyth, Katherine Marie. „Wetting hysteresis and droplet roll off behavior on superhydrophobic surfaces by Katherine Marie Smyth“. Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/59918.
Der volle Inhalt der QuelleCataloged from PDF version of thesis.
Includes bibliographical references (p. 55-56).
Various states of hydrophobic wetting and hysteresis are observed when water droplets are deposited on micro-post surfaces of different post densities. Hysteresis is commonly defined as the difference between the advancing and receding contact angle and after many decades of research, the mechanisms governing hysteresis are still not fully understood. Particularly, stick-slip behavior of the three-phase contact line has been observed and qualitatively attributed to surface or chemical heterogeneities, but the behavior has yet to be quantified. In this thesis, contact line motion particularly focused on stick-slip behavior and its influence on drop width and contact angle was examined as a new approach to understanding hysteresis as pertaining to micro-textured surfaces. This work focuses on developing a fundamental understanding and physical model of the stick-slip behavior of the contact line and preliminarily explores the influence of contact line velocity on this stick-slip behavior and contact angle. By characterizing stick-slip behavior and hysteresis on micro-post surfaces, models can be developed that in the future can aid in surface design for optimal wetting behavior in industrial and power plant applications. Additionally, the pinning parameter has been used to predict roll off angle on micro-post surfaces for a variety of post densities and these predictions have been experimentally verified. With further definition of the pinning parameter to include surface roughness and impact phenomena, the pinning parameter can be used in surface design for droplet shedding in industrial applications.
S.B.
Denham, Martha H. „The Use of Laboratory Testing to Understand the Behavior of Collapsible Soil Upon Wetting“. PDXScholar, 1992. https://pdxscholar.library.pdx.edu/open_access_etds/4664.
Der volle Inhalt der QuelleAttinger, Daniel. „An investigation of microdroplet surface deposition : transient behavior, wetting angle dynamics and substrate melting phenomenon /“. Zürich : [s.n.], 2001. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=14004.
Der volle Inhalt der QuelleWorbs, Peter. „Wetting behavior of titanium carbide films for carbon-copper braze joints in high heat flux components“. kostenfrei, 2009. http://mediatum2.ub.tum.de/node?id=823480.
Der volle Inhalt der QuelleSadeghpour, Nima. „The Influence of Surface Roughness and Its Geometry on Dynamic Behavior of Water Droplets“. Thesis, University of North Texas, 2014. https://digital.library.unt.edu/ark:/67531/metadc700094/.
Der volle Inhalt der QuelleAnnavarapu, Rama Kishore. „Elastocapillary Behavior and Wettability Control in Nanoporous Microstructures“. University of Toledo / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1544705326035201.
Der volle Inhalt der QuelleGrimmer, Philipp E. S. [Verfasser], und Thomas [Akademischer Betreuer] Hirth. „Wetting, de-icing and anti-icing behavior of microstructured and plasma-coated polyurethane films / Philipp E. S. Grimmer ; Betreuer: Thomas Hirth“. Stuttgart : Universitätsbibliothek der Universität Stuttgart, 2019. http://d-nb.info/1181099285/34.
Der volle Inhalt der QuelleLarson, Hans Christian. „Replacement Rates of Initially Hydrocarbon-Filled Microscopic Cavities with Water“. BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/7496.
Der volle Inhalt der QuelleRose, Lesley Anne. „Wetting behavior of Fe-Ni-Co-Cu-O-S melts against olivine and chromite as a function of melt composition, oxygen fugacity, and pressure“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape4/PQDD_0018/MQ53464.pdf.
Der volle Inhalt der QuelleBrunson, Kennard Marcellus. „Synthesis and Characterization of methylene bis (p-cyclohexyl isocyanate)-poly (tetramethyl oxide) based Polyurethane Elastomers“. VCU Scholars Compass, 2005. http://scholarscompass.vcu.edu/etd/1211.
Der volle Inhalt der QuelleSetu, Siti Aminah. „Interfacial instabilities and wetting behaviour in confinement“. Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:7848f713-437b-4be8-b5f8-8232fcd59667.
Der volle Inhalt der QuelleRazak, Huzaifah Haritsah Abdul. „Wetting behaviour of colloid-polymer mixtures in confinement“. Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:e75a8463-fe02-46f3-ba95-7d7b40c955cb.
Der volle Inhalt der QuelleDavid, Samuel. „Investigation of the Wetting Behaviour of Evaporating Drops“. Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/12174.
Der volle Inhalt der QuelleKnauf, Jan [Verfasser], Alexander [Akademischer Betreuer] Böker, Karsten [Akademischer Betreuer] Reihs, Alexander [Gutachter] Böker, Karsten [Gutachter] Reihs und Hans-Jürgen [Gutachter] Butt. „Synthesis of highly fluorinated precursors and their deposition conditions for self-assembled monolayers with defined small-scale surface structures as templates for the manipulation of wetting behavior / Jan Knauf ; Gutachter: Alexander Böker, Karsten Reihs, Hans-Jürgen Butt ; Alexander Böker, Karsten Reihs“. Potsdam : Universität Potsdam, 2020. http://d-nb.info/1219662925/34.
Der volle Inhalt der QuelleWijeratne, Susil. „Liquid drop flow behaviour in unsaturated non-wetting packed beds /“. [St. Lucia, Qld.], 2002. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16336.pdf.
Der volle Inhalt der QuelleFrenzel, Ralf, Christa Blank, Karina Grundke, Veneta Hein, Bernd Schmidt, Frank Simon, Michael Thieme und Hartmut Worch. „Wettability of Methacrylate Copolymer Films Deposited on Anodically Oxidized and Roughened Aluminium Surfaces“. Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-107056.
Der volle Inhalt der QuelleCrichton, Donna. „The interaction of oils with surfactant monolayers at the air-water surface“. Thesis, University of Hull, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310247.
Der volle Inhalt der QuelleStark, Alyssa Yeager. „The Effect of Water on the Gecko Adhesive System“. University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1405334677.
Der volle Inhalt der QuelleFrenzel, Ralf, Christa Blank, Karina Grundke, Veneta Hein, Bernd Schmidt, Frank Simon, Michael Thieme und Hartmut Worch. „Wettability of Methacrylate Copolymer Films Deposited on Anodically Oxidized and Roughened Aluminium Surfaces“. Technische Universität Dresden, 2009. https://tud.qucosa.de/id/qucosa%3A26713.
Der volle Inhalt der QuelleLeboeuf, Sébastien. „Dynamic wetting and heat transfer behaviour of aluminium droplets impinging and solidifying on copper substrates“. Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=81548.
Der volle Inhalt der QuelleGermanà, Sarah. „HLAS reactive binder in detergent granulation : relationship between phase behaviour and wetting and adhesive properties“. Thesis, University College London (University of London), 2009. http://discovery.ucl.ac.uk/19792/.
Der volle Inhalt der QuelleKlinter, Andreas. „Wetting behaviour of aluminum alloys on ceramic substrates and its effect on the stability of aluminum foams“. Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:8881/R/?func=dbin-jump-full&object_id=92344.
Der volle Inhalt der QuelleVilla, Stefano. „Behaviour of a Colloid close to an Air-Water Interface : Interactions and Dynamics“. Thesis, Montpellier, 2018. http://www.theses.fr/2018MONTS074/document.
Der volle Inhalt der QuelleDespite the relevance to environmental, biological and industrial processes, the motion of a colloidal particle close to a fluid interface and the way it interacts with the water surface are still largely elusive and intriguing physical phenomena.In this thesis, we explore the motion dynamics and the interaction of individual colloidal particles close to an air-water interface in thermal equilibrium.In order to investigate them without perturbing or altering the experimental system, we designed and built a dual-wave reflection interference microscope working with an air-water interface geometry. Contrary to other established experimental techniques, our set-up allows accurate measurements of the absolute particle-interface distance and thus does not require any calibration or assumption to know the location of the interface. Highly resolved 3D particle trajectories close to the interface were obtained, from which information on particle diffusion close to the interface and particle-interface interactions are obtained.The system shows two different potential energy landscapes resulting in two different equilibrium particle-interface distances. The larger one can be fairly explained by Van der Waals and electrostatic interactions combined with gravity. The shorter one highlights the existence of an unexpected additional attractive interaction. The possible origins of such an interaction are discussed.Using a method of analysis of the particle mean square displacements in a generic potential we developed, we were able to access to particle drag coefficients as a function of the distance from the interface. Peculiarly, the air-water interface acts as a slip boundary for the particle motion parallel to the interface and as a no-slip boundary for the particle motion perpendicular to the interface. This experimental result can be partially rationalized considering recent models based on surface incompressibility. However, some discrepancies between experiments and theories remain. Experimental drag coefficients are larger than the hydrodynamic predictions and depend on the particle electrical charge, pointing therefore to a possible role of electrokinetic phenomena.Finally, the particle trapping at the air-water interface and its contact angle were observed while tuning the ionic strength of the aqueous solution and varying the surface state of the colloids
Postill, Harry E. „Weather-driven clay cut slope behaviour in a changing climate“. Thesis, Loughborough University, 2018. https://dspace.lboro.ac.uk/2134/35832.
Der volle Inhalt der QuelleKemppainen, K. (Kalle). „Towards simplified deinking systems:a study of the effects of ageing, pre-wetting and alternative pulping strategy on ink behaviour in pulping“. Doctoral thesis, Oulun yliopisto, 2014. http://urn.fi/urn:isbn:9789526203805.
Der volle Inhalt der QuelleTiivistelmä Siistausprosessin tavoitteena on tuottaa keräyspapereista valmistettua vaaleaa ja puhdasta massaa, jota voidaan käyttää uusien paperituotteiden valmistamiseen. Siistausprosesseja pyritään yksinkertaistamaan nykyisten monimutkaisten prosessien korkeiden tuotantokustannusten ja materiaalitappioiden vuoksi. Eräs edellytys siistausprosessien yksinkertaistamiselle on, että kuiduissa kiinni olevan musteen pitoisuus, massan likapitoisuus ja musteen liiallinen pilkkoutuminen minimoidaan siistausprosessin ensimmäisessä vaiheessa, pulpperoinnissa. Täten on tärkeää tunnistaa musteen käyttäytymiseen pulpperoinnissa vaikuttavat tekijät, etsiä uusia mahdollisuuksia parantaa musteen irrotusta keräyspapereista sekä kehittää pulpperointimenetelmiä, joilla voitaisiin prosessoida tehokkaasti eri painomenetelmillä painettuja papereita. Tämän työn tavoitteena oli saada uutta tietoa siitä miten ympäristöolosuhteet, joille keräyspaperit voivat altistua varastoinnin ja kuljetuksen aikana, vaikuttavat musteen käyttäytymiseen pulpperoinnissa. Lisäksi tavoitteena oli selvittää voitaisiinko kuituihin kiinni jääneen musteen pitoisuutta vähentää esiliottamalla keräyspapereita sopivissa kemiallisissa olosuhteissa ennen pulpperointia ja poistamalla irronneet mustepartikkelit massan seasta pulpperoinnin aikana. Tulokset osoittavat, että jos tietyt keräyspaperit ovat erittäin kosteita ja altistuvat korkealle lämpötilalle riittävän pitkän ajan ennen pulpperointia, tulee musteen irrottaminen kuiduista pulpperoinnissa vaikeammaksi ja tuotettu massa likaisemmaksi, kuin sellaisista keräyspapereista, jotka ovat altistuneet kuivina korkealle lämpötilalle. Kuituihin kiinnittyneen musteen pitoisuutta voidaan vähentää esiliottamalla tiettyjä keräyspapereita alkalisilla siistauskemikaaleilla sopivissa olosuhteissa ennen pulpperointia. Esiliotuksen kyky parantaa musteen irrotusta kuiduista pulpperoinnissa riippuu voimakkaasti esiliotusvaiheen alkalisuudesta, lämpötilasta ja kestosta. Kun irronneet mikroskooppiset mustepartikkelit poistetaan massasta useassa vaiheessa pulpperoinnin aikana, voidaan paperin kuidutusta, musteen irrottamista kuiduista ja likapilkkujen hajottamista jatkaa ilman että haitallista musteen takaisin kiinnittymistä kuituihin tapahtuu. Tämä mahdollistaa esimerkiksi vesipohjaisten musteiden ja lasertulosteiden samanaikaisen prosessoinnin
Pena, Alvarez Ana Azucena. „Micro/nano patterning of silicon and NiP/Al disks by nanosecond and femtosecond laser sources“. Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/micronano-patterning-of-silicon-and-nipal-disks-by-nanosecond-and-femtosecond-laser-sources(fcd519c6-bf51-4b73-b3ff-e3cbdd1bcffc).html.
Der volle Inhalt der QuelleSeghini, Maria Carolina. „Mechanical Analysis and Fibre/Matrix Interface Optimization for Next Generation of Basalt-Plant Fibre Hybrid Composites“. Electronic Thesis or Diss., Chasseneuil-du-Poitou, Ecole nationale supérieure de mécanique et d'aérotechnique, 2020. http://www.theses.fr/2020ESMA0003.
Der volle Inhalt der QuelleGlobal awareness of environmental issues has resulted in the emergence of “green” composites, in which natural fibres are used to replace synthetic ones. However, in semi-or structural applications, it can be inconvenient to use composites based on natural fibres. A possible solution to this problem is the development of hybrid composite materials, combining together plies of natural and synthetic fibres. In this framework, the aim of this research project was to develop basalt-flax fibre hybrid composites with a view to obtaining more environmentally friendly composites for semi-structural applications. Hybrid composites were produced through vacuum infusion molding with epoxy matrix.For comparison purposes, 100% flax fibre composites and 100% basalt fibre composites were also manufactured. A quasi-static and dynamic mechanical characterization showed that the hybridization allows the production of a composite with intermediate mechanical performances compared to those possessed by flax and basalt composites. However, the damage analysis has revealed the need to optimize the fibre/matrix interface adhesion quality, in order to increase the mechanical properties of the resulting hybrid composites. For this reason, different surface modification treatments have been specifically designed and investigated for flax and basalt fibres. Flax and basalt fibres were treated by the physical process of Plasma Enhanced Chemical Vapor Deposition. Flax fibres were also subjected to two chemical treatments using enzymatic species and supercritical CO2. The effects of the surface modification treatments on the thermal stability, morphology and mechanical properties of flax and basalt fibres have been investigated. The degree and extent of fibre/matrix adhesion were analyzed by micromechanical fragmentation tests on monofilament composites. The adhesion quality between fibres and both epoxy and vinylester matrices has been assessed in terms of critical fragment length, debonding length and interfacial shear strength. High-resolution μ-CT has been used to support the analysis of the damage mechanisms during fragmentation tests. For both flax and basalt fibres, the best results were obtained after the plasma polymer deposition process. This process was able to produce a homogeneous tetravinylsilane coating on the surface of basalt and flax fibres, which resulted in a significant increase in the fibre/matrix adhesion, thus paving the way for the next generation of more environmentally friendly hybrid composites for semi-structural applications
Lo, Yu-yun, und 羅御云. „Wetting Behavior on Zwitterionic Sulfobetaine Surfaces“. Thesis, 2015. http://ndltd.ncl.edu.tw/handle/69793398457647124586.
Der volle Inhalt der Quelle國立中央大學
化學工程與材料工程學系
103
In this study, (N,N-Dimethylaminopropyl)trimethoxysilane and 1,3-Propane sultone reacted to form Sulfobetaine silane(SBSi). SBSi is modified on glasses in the process of hydrolysis and condensation. By area and contact line variety to realize wetting behavior on SBSi substrates. Solution is divided into two sections, pure solution (water and hexadecane) and solution adding nonvolatile solute(cellobiose, poly(vinyl alcohol), poly(ethylene glycol), graphite oxide nanoparticle). Water spreads on SBSi substrates, area of water increasing. Then due to evaporation, area of water decreases. Hexadecane is nonvolatile solution. Hexadecane keeps spreading even passing an hour, area of hexadecane increasing. It indicates that SBSi substrates are superhydrophilic surfaces. Dipping solution on it, solution shows spontaneous spreading. Water and hexadecane are total wetting on SBSi substrates. When a SBSi substrate is placed in solution that with nonvolatile solute, bubble moves on substrates. As a result, it’s still total wetting. Nonvolatile solute deposition induces pinning behavior. In cellobiose, poly(vinyl alcohol) and graphite oxide nanoparticle solution experiments all indicate above results. Notably, poly(ethylene glycol)(PEG) solution is a special case. PEG solution doesn’t occur pinning behavior. Therefore, due to unequal evaporation rate, it can move non-directionally on level SBSi substrates. If let PEG solution deform, it can return to hemispherical shape no depending on another force. It shows that PEG solution is no hysteresis on SBSi substrates.
Pratten, Don H. „Wettability and wetting behavior of elastomeric impression materials“. 1987. http://books.google.com/books?id=S6w9AAAAMAAJ.
Der volle Inhalt der QuelleWang, Tzu-Yu, und 王姿妤. „Exotic wetting behavior of surfactant drops on SBSi“. Thesis, 2017. http://ndltd.ncl.edu.tw/handle/82143038671779098633.
Der volle Inhalt der Quelle國立中央大學
化學工程與材料工程學系
105
The total wetting surface which is a kind of zwitterionic surface is fabricated by grafting the sulfobetain silane (SBSi) on glass slices. It is considered that there is a water film on the surface because of highly hydrate chemical groups. It can be observed different contact angle with dropping diiodomethane on SBSi which is in different relative humidity (RH). With increasing the relative humidity, the contact angle is larger in the reason that diiodomethane is insoluble in water. The other indirect evident is that the maximum wetting area of water drops on SBSi surface grows because more equilibrium water molecules bring benefits to the spreading of liquid. In the same ambient, it is observed the enormously different behavior between wet and dry surface no matter which electric charge surfactant droplets drop on the SBSi surface. When the liquid droplets drop on the SBSi surface containing a water film in the atmosphere, the droplets show the different behaviors depending on the electric charge of surfactant. Experiments show that droplets of cationic surfactant on SBSi surface present the phenomena of dewetting, because surfactant ions would be adsorbed on the SBSi surface. However, the droplets tend to stick on the dry surface and the contact angle of drops is about 40. For the case of anionic and nonionic surfactant, it shows the fingering pattern on the wet SBSi surface and the wetting behavior on the dry one.
Tu, Sheng-Hung, und 涂勝宏. „Wetting behavior on copper wafers after etch cleaning processes“. Thesis, 2014. http://ndltd.ncl.edu.tw/handle/99724006810611796942.
Der volle Inhalt der Quelle國立中央大學
化學工程與材料工程學系
102
The thin CuO flm is acquired by a quick dip of copper in H2O2 solutions at room temperature. The CuO filmq appears smooth and exhibits superhydrophilic nature. The composition change cannot be verifed by X-ray photoelectron spectroscopy but can be manifested by the water contact angle. In the ambient condition, the thickness of the oxidized layer and the surface hydrophobicity grow gradually, while the chemical composition of the overall oxidized film remains essentially unchanged. That is, in the vacuum, the growth rate of the hydrophobicity is significantly elevated, revealing deoxidation on the upmost surface. Our results indicate that growing hydrophobicity on the CuO film is spontaneous and the reversible wettability transition can be observed by H2O2 oxidation and vacuum deoxidation. The wet cleaning process in semiconductor fabrication often involves the immersion of the copper wafer into etching solutions and thereby its surface properties are significantly altered. The wetting behavior of a copper film deposited on silicon wafer is investigated after a short dip in various etching solutions. The etchants include glacial acetic acid and dilute solutions of nitric acid, hydrofluoric acid, and tetramethylammonium hydroxide. A thin oxide layer always remains on the surface of as-received Cu wafers when they are subject to etching treatments. A pure Cu wafer can be obtained by the glacial acetic acid treatment and its water contact angle (CA) is about 45. As the pure Cu wafer is placed in the ambient condition, the oxide thickness grows rapidly to the range of 10 to 20 Å within 3 hours and the CA on the hydrophilic surface also rises. In the vacuum, it is surprising to find that the CA and surface roughness of the pure Cu wafer can grows significantly. These interesting results may be attributed to the rearrangement of surface Cu atoms to reduce the surface free energy.
Liu, Shue-Ching, und 劉淑卿. „Wetting behavior of Na2O-Al2O3-P2O5 glasses at high temperature“. Thesis, 2003. http://ndltd.ncl.edu.tw/handle/78050544214403923416.
Der volle Inhalt der Quelle大同大學
材料工程研究所
91
Abstract Sessile drop method is used to discuss the derive difference in wetting angle、density and surface tension by using contact angle measurement instruments. The melting Na2O-Al2O3-P2O5 glass is placed on a platinum substrate, whose composition is changed(increase Al2O3 ratio and relatively decrease Na2O、P2O5 ratio). In this experiment, drying mixing method is used to mix oxide(NaH2PO4•H2O and α- Al2O3). The Na-Al-P glass is prepared by melting the mix oxide in the high temperature, and it is identifyed by XRD identification、ICP analysis、DTA analysis、TMA analysis、contact angle ( θ ) and surface tension (σ) measurement. From the XRD identification, the productions of Na-Al-P glass show amorphous phase. Due to the result of ICP, there is only slight deviation in the compo-sition of the glasses. The DTA result can be observed the crystalline temperature (TP ) of Na-Al-P glass. The outcome of the softening point temp- erature (Tds )、glass transition temperature (Tg ) and coefficient of thermal expansion (α) of Na-Al-P glass can be measured in TMA. The thermal expansion coefficient reduced and Tg、Tds increased of Na-Al-P glass as the increased ratio of Al2O3 ( which confirm to the literature ). From the result of DTA , the TP of the NP46.3A7.5 composition is 572.79℃, which is the most high temperature among the five compositions. The difference between TP and Tds of NP46.3A7.5 is the maximum value for five compositions. The NP46.3A7.5 is the more stable composition for all samples from the result of the wetting test.
Wang, Yu-Qian, und 王育謙. „Wetting Behavior Between Electroless Nickel and Sn-Zn-Al Solder“. Thesis, 1997. http://ndltd.ncl.edu.tw/handle/02008454074858220984.
Der volle Inhalt der QuelleHuang, Rui-Hong, und 黃瑞鴻. „Orientational Wetting Behavior of Liquid Crystal Mixtures on the Glass“. Thesis, 1998. http://ndltd.ncl.edu.tw/handle/26266778366246306680.
Der volle Inhalt der QuelleWang, Yu-Chien, und 王育謙. „Wetting Behavior Between Electroless Nickel and Sn-Zn-Al Solder“. Thesis, 1997. http://ndltd.ncl.edu.tw/handle/38467090652350630105.
Der volle Inhalt der Quelle國立成功大學
材料科學(工程)學系
85
This study is to investigate the wetting behavior between the copper substrate which was deposited with electroless nickel as a diffusion barrier for the ternary eutectic Sn-Zn-Al solder. The copper plating was deposited on the electroless nickel to improve the wetting behavior. The wetting experiment was conducted with the wetting balance for the two systems of Cu/Ni- P and Cu/Ni-P/Cu Plating at various temperature and fluxes. The interfacial reactions between the solder and these two systems after heat treatment were examined with Scanning Electron Microscope and with X-ray diffraction. The contact angle investigation was applied for estimating the temperature needed for the occurrence of solder wetting without flux. The experimental results for the Ni-P/solder system showed that good wetting was achieved only at high temperature (above 350℃) and with high concentration of active fluxes (above 5g/l DMAHCl). The solder layer contains pores. The crystallization of electroless nickel layer and less active fluxes could not improve wetting. The experiment results of the Ni-P/Cu system showed that the surface coverage of solder on Ni-P/Cu was more than that on Ni-P at low concentration of fluxes (above 2.5g/l DMAHCl), although it also showed partial wetting. The results of the interfacial elemental line - scanning showed that the Zn atom diffused to the interface between the solder and copper. The X-ray showed that the interaction between solder and Ni-P/Cu resulted in the formation of g-Cu5Zn8 compound which further avoids the tin diffusing into the layer of copper plating.
Hsu, Chia-Hao, und 許家豪. „The wetting behavior of polymeric drop on polymer brush surfaces“. Thesis, 2017. http://ndltd.ncl.edu.tw/handle/b9zy3w.
Der volle Inhalt der Quelle國立臺灣大學
化學工程學研究所
105
The study of the stability of polymeric thin films on solid substrates is of significant importance in many practical applications such as the manufactures of organic solar cells and organic light-emitting diode. However, films on nonwettable substrates tend to exhibit unstable behavior. To resolve this issue, the modification of a nonwettable surface can be accomplished by coating the surface with an appropriate monolayer. Polymer brush is a typical example of applicable candidates. However, an autophobic behavior is observed due to entropic repulsion even if the brushed layer is composed of identical molecules as those forming the films. In this work, dissipative particle dynamics is performed to study the wetting phenomena of polymeric thin films on top of solid substrates or surfaces coated polymer brush. We start by investigating the effects of polymer length and solid-liquid affinity on the shape and contact angle of a polymeric droplet. The interfacial tensions of solid-liquid, solid-gas and liquid-gas are measured and the Young’s equation is employed to estimate the contact angle. The resulting contact angles are consistent with those obtained directly from simulations verifying that validity of our simulation work. The influences of the molecular lengths of the polymeric films and polymeric brushes on the wetting behaviors of the coated films are examined. It is found that the wettability can be improved by decreasing the molecular lengths of the polymeric films while increasing the lengths of polymer brushes. The stability of a thin film depends on the penetration length of the polymers into the brush layers. Moreover, there exists a critical value of grafting density beyond which the autophobic behavior becomes significant as grafting density increases. The rupture process of a polymer thin film has also been studied. The dewetting velocity increases with increasing grafting density. Our simulation results are consistent with the experimental observation and can be applied to improve adhesion of polymeric thin films on a solid substrate.
Xu, Wei-Shiang, und 徐惟祥. „Spreading Behavior of Drops on a Total Wetting Surface:MDPD Simulation“. Thesis, 2017. http://ndltd.ncl.edu.tw/handle/56491894009021587103.
Der volle Inhalt der Quelle國立中央大學
化學工程與材料工程學系
105
Liquid drops spontaneously spreading on a solid surface is referred to as the total wetting phenomenon. A typical example is the continuous expansion of a silicon drop on various surfaces. The time evolution of the drop radius can be described by the power law r(t) ∼ tn with the exponent 1/10, known as Tanners law. In this work, the spreading dynamics of a nanodrop on a total wetting surface under saturated humidity and no-slip condition has been explored by many-body dissipative particle dynamics simulation. The influences of surface roughness and wettability in terms of spreading coefficient on the spontaneous spreading behavior are studied. It is found that the exponent n is 0.2 on smooth surface, and the exponent grows with increasing the spreading coefficient. The reason for the difference with Tanner’s law is that the formation of precursor film with the drop spreading process. As we remove the effect of the precursor film, the drop radius and contact angle behavior agree with Tanner’s law and the spreading law is independent of the spreading coefficient. In addition, The drop spreading velocity on rough surface is lower than that on smooth surface and the spreading process also follow Tanner’s law. It shows the surface roughness will prevent the growing of the precursor film and the resistance rises with increasing the cavity size. Furthermore, the drop spreading velocity is significantly lower and the drop becomes very thin for a long time because the most of the liquid beads stuck in the cavity. The forced spreading that is similar to the thin film flow on the surface under external force are investigated as well. As a result, the drop spreading motion which is vertical to external force also consistent with Tanner’s law and the precursor film is produced in the spreading process with this direction. On the forced direction, the rear part of the liquid drop will slide on smooth surface due to without surface roughness that can make pinning force to impede the movement of the contact line. In contrast, the rear part of the liquid drop will pinning on rough surface. Moreover, the precursor film can’t be observed on forced direction, since the forced flow velocity is faster than the velocity of expansion with precursor. In addition, the flow velocity with the forced direction will be affected by the precursor and the surface roughness will make the flow velocity significant slower.
Yeh, Ming-Chih, und 葉銘智. „A Study of Effect of Molecular Structure on Wetting Behavior“. Thesis, 2003. http://ndltd.ncl.edu.tw/handle/54233306699418977739.
Der volle Inhalt der Quelle國立臺灣大學
化學工程學研究所
91
For three phases, alpha, beta,and gamma in equilibrium, the wetting behavior of the middle beta phase can be easily realized by the contact angle spanned by the alpha and the gamma interfaces, such as nonwetting, partial wetting, and complete wetting. The transition from a partial wetting regime to a complete wetting (or nonwetting) regime, or vice versa, is called a wetting transition. A wetting transition was found to be induced by altering thermodynamic variables, such as temperature, pressure, and salinity, etc, to bring the system close to its criticality. It was also pointed out that a wetting transition might be more relevant to the preferential adsorption behavior at interface or the short-range intermolecular forces rather than the critical phenomena. In this work, the effect of molecular structure on wetting behavior was both experimentally and theoretically investigated. In the experimental section, alcohols which including linear-chain alcohol, branched-chain alcohol, and linear-chain alcohol with additional oxyethylene groups, were chosen to examine the effect of structure upon wetting transitions. By employing surface and interfacial tension measurement, the wetting behavior and the location of a wetting transition could be deduced. It was found that for the water + linear alcohol homologs systems, the alcohol-rich phase tends to completely wets the air-aqueous interface as chain length decreases. For water + polyoxyethylene alcohol systems, a wetting transition from partial wetting nonwetting may occur with decreasing temperature and increasing number of oxyethylene groups. For water + isomeric alcohol systems, a wetting transition from partial wetting to complete wetting takes place while the molecular structure changes from a primary linear alcohol to a tertiary branched alcohol. Otherwise, in the theoretical approach, the influences of intermolecular force, molecule size, and molecule anisotropy on wetting phenomena were scrutinized by two density functional theories (DFT). The effect of tuning intermolecular forces was analyzed by a density functional theory combined with statistical associating fluid theory (SAFT-DFT), and good agreements with experimental results for water + polyoxyethylene alcohol systems were achieved. In addition, the order of a wetting transition was also found to be fine tuned by the range of attraction force and the association strength. Two wetting transitions with different orders in one system are revealed in this calculation. Besides, the sequential transitions from nonwetting partial wetting complete wetting for water + oil + alcohol mixtures was observed to be associated with the amphiphilicity of the alcohol. Finally, the molecular anisotropy was considered using an interaction site model coupled with a density functional theory (ISM-DFT). This method was applied to examine the influence of hydrocarbon-chain structure, flexibility, and the hydrophilicity of the polar head. The wetting transition induced by molecular structure change was successfully predicted. Furthermore, satisfactory predictions for the effect of chain length and hydrophilicity upon wetting behavior are also illustrated.
Su, Cheng-Hao, und 蘇晟豪. „A Study on Phase Behavior and Wetting Behavior of the Ternary Water + Oil + CiPj System“. Thesis, 2011. http://ndltd.ncl.edu.tw/handle/27558504128881170960.
Der volle Inhalt der Quelle國立臺灣大學
化學工程學研究所
99
In this study, we investigate the phase behavior and the wetting behavior of the ternary water + oil + nonionic surfactant system. The oils are n-alkanes and the nonionic surfactants are CiPj. The symbol CiPj is the abbreviation of a propylene glycol ether CH3(CH2)i-1(OCH2CH(CH3))jOH. There are three-liquid-phase- coexisting regions in water + decane + C3P1, water + dodecane + C3P1, water + tetradecane + C3P1, water + hexadecane + C3P1, water + dodecane + C3P2, water + tetradecane + C3P2, and water + hexadecane + C3P2 systems. Experiments of fish-shaped phase diagrams for these seven systems under atmospheric pressure were performed at constant water/n-alkane weight ratio (1/1) to locate the critical end points. The ternary system of the alkane with the longer carbon chain length has the higher upper and lower critical solution temperatures and the larger three-liquid-coexisting temperature window in the fish-shaped phase diagram. The upper and lower critical solution temperatures are lower in these systems with larger j number of C3Pj. Precise liquid-liquid equilibrium data of mixtures for six ternary systems water + alkane (dodecane, tetradencane, and hexadecane) + C3Pj (j=1 or 2) under atmospheric pressure were determined by using gas chromatography. The evolution of phase behavior of the ternary water + n-alkane + C3Pj system as a function of temperature is qualitatively consistent with that of the water + oil + CiEj system. The experimental liquid-liquid equilibrium data were successfully correlated with the NRTL model. We use pedant drop method to measure the interfacial tensions and investigate the wetting behavior of four ternary systems, water + dodecane + C3P1, water + tetradecane + C3P1, water + hexadecane + C3P1, and water + hexadecane + C3P2 system. In these ternary systems, the middle surfactant-rich phase exhibits complete wetting in the temperature window of the three-liquid-phase-coexisting region.
Woracek, Robin. „Wetting Behavior of Polymer Melts with Refractory Coatings at High Temperature“. 2009. http://trace.tennessee.edu/utk_gradthes/574.
Der volle Inhalt der QuelleHong, Ting-Syu, und 洪庭旭. „Wetting Behavior of Surfactant Solutions on Hydrophobic Surfaces: Copper and Teflon“. Thesis, 2007. http://ndltd.ncl.edu.tw/handle/14722073420473158256.
Der volle Inhalt der Quelle國立中央大學
化學工程與材料工程研究所
95
Drop wetting on material surface that is decided by Young’s equation. Gas-solid tension, solid-liquid tension and liquid-gas tension are balance on wetting substrate. Between liquid and solid is display a angle that the angle is call: “Contact Angle”. In the research, steady of wetting behavior of surfactant solutions on the hydrophobic surfaces: Copper and Teflon. We know that have low γsg (Cu=21.2mN/m,Teflon=6.78mN/m) and high contact angle (Cu~100°,Teflon~130°) on Cu and Teflon surfaces. Because of hydrophobic property surfaces, therefore use surfactant solutions to decrease γgl,γsl and contact angle for achieve wetting effectiveness. We find out contact angle of nonionic surfactants are not change when reach CMC, but contact angle of anionic surfactants are continue decrease when reach high CMC on Cu and Teflon surfaces. Contact angle of cationic surfactants are not change on Cu surface, but that continue decrease when reach concentration on Teflon surface. However, contact angle of two tail ionic surfactants are always continue decrease with concentration increase on Cu and Teflon surfaces.
Yang, Yung-Jih, und 楊詠茹. „Modeling the Wetting Behavior of Heterogeneous Patterned Surface by Numerical Method“. Thesis, 2011. http://ndltd.ncl.edu.tw/handle/03792616605172661827.
Der volle Inhalt der Quelle國立臺灣大學
化學工程學研究所
99
There are two sections in our studies. First part is a simple and cheap method for fabrication of superhydrophobic surface and the wetting behaviors on structured hydrophilic or hydrophobic surfaces are also studied. The other part is the study of wetting behavior on 2 μm striped heterogeneous surface. Wetting behavior plays an important role in various industries, and has been studied for a long while. Lower the surface energy and enhance the surface roughness are the method to prepare superhydrophobic surface. We are able to combine and modify a soft-embossing technique and surface modification of a self-assembled monolayer to establish a standard operation procedure for manufacturing superhydrophobic surfaces. Two issues are addressed in this part of study. First, the water contact angles of surfaces without modification are discrepant with the Wenzel and Cassie models. Second, the different polymer surfaces with modification can change their characteristics from hydrophilicity to hydrophobicity. Further, different polymer surfaces have the same contact angle only if they have the same structure before modification. And the results are quite consistent with Wenzel and Cassie models. Besides, we examine contact angle of liquid droplet on 2 μm striped surface by the Matlab modeling and also determine equilibrium contact angle (ECA), advancing contact angle (ACA) and receding contact angle (RCA) from free energy curve obtained by the Surface Evolver. The ECA (78°) from the Matlab modeling is totally consistent with the Cassie model, but is quite different from the results (83°~85°) shown in the Surface Evolver. However, the tendencies of ECAs from both methods are the same – oscillation with small liquid and approaching a constant with larger liquid. In our system, ACA is always a constant (110°) but RCA is volume-dependent. RCA oscillates at first, and finally falls into a certain narrow region (70°~80°). Our result also indicates that the contact line of liquid drop inclines to be a slightly ellipse-like shape, not a perfect circle-like shape. Further, we make a discussion about the thickness of contact angle transition region. The dimensionless thickness from hydrophobic to hydrophilic surface is almost 0.22, and the dimensionless thickness from hydrophilic to hydrophobic surface decreases from 0.02 to 0.0027 as increasing liquid volume.