Дисертації з теми "Polymer solutions Elastic properties"
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Farmer, David John. "Elastic measurements in ultra-thin polymer structures." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/33073/.
Повний текст джерелаWhang, Kyu-ho. "Static and Flow Properties of Dilute Polymer Solutions." Thesis, University of North Texas, 1991. https://digital.library.unt.edu/ark:/67531/metadc501073/.
Повний текст джерелаGutsul, O. V. "The rheological and electrical properties of polymer-colloid solutions." Thesis, БДМУ, 2020. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/18320.
Повний текст джерелаEastman, John. "The shear and extensional flow properties of polymer/surfactant solutions." Thesis, University of Bristol, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319075.
Повний текст джерелаDe, Joannis Jason. "Equilibrium properties of polymer solutions at surfaces Monte Carlo simulations /." [Florida] : State University System of Florida, 2000. http://etd.fcla.edu/etd/uf/2000/ane5947/dissertation%5Fdone.pdf.
Повний текст джерелаTitle from first page of PDF file. Document formatted into pages; contains ix, 242 p.; also contains graphics. Vita. Includes bibliographical references (p. 232-241).
Sukhadia, Tejas. "Prediction of phase equilibria in solutions : an associative reformulation of thermodynamic theories of solutions." Diss., Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/11886.
Повний текст джерелаBaranowski, Roman. "The properties of polymer/solvent systems at surfaces and interfaces." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq25767.pdf.
Повний текст джерелаMueller, A. J. "Extensional flow of macromolecules in solution." Thesis, University of Bristol, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234875.
Повний текст джерелаOmowunmi, Sunday Chima. "Modelling the nonlinear dynamics of polymer solutions in complex flows." Thesis, University of Manchester, 2011. https://www.research.manchester.ac.uk/portal/en/theses/modelling-the-nonlinear-dynamics-of-polymer-solutions-in-complex-flows(3230a688-0ea4-4620-bda1-396346feb645).html.
Повний текст джерелаLaRiviere, Daniel John Christopher. "Viscometric properties of dilute lubricating oil-polymer solutions over a wide temperature range." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ30961.pdf.
Повний текст джерелаFuruya, Tsutomu. "Structure Formation and Physical Properties of Aqueous Polymer Solutions and Hydrogels with Additives." Kyoto University, 2019. http://hdl.handle.net/2433/236625.
Повний текст джерелаAshrafi, Behnam. "Theoretical and experimental investigations of the elastic properties of carbon nanotube-reinforced polymer thin films." Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=21910.
Повний текст джерелаLes nano-composites sont une nouvelle classe de matériaux prometteurs pour les composants mécaniques de microstructures telles que les micro-actuateurs et micro-résonateurs. Ce travail présente une combinaison d'études théoriques et expérimentales sur l'utilité de composites renforcés par des nanotubes de carbone pour la conception de microstructures. Dans la partie théorique de cette recherche, les effets du rapport de forme, de la dispersion, de l'alignement et de la fraction volumique des nanotubes sur le module élastique et la vitesse d'onde longitudinale ont été analysés en utilisant la théorie de Mori-Tanaka. Les limites calculées du module d'Young et de la vitesse d'onde capturent la tendance des résultats expérimentaux rapportés dans la littérature. Les nano-composites à matrice polymère renforcée avec des SWNT alignés et dispersés ont été identifiés comme d'excellents candidats pour de petites structures dont les propriétés rivalisent avec les structures métalliques ou céramiques utilisées dans la présente génération de systèmes micro-électro-mécaniques (MEMS). La partie expérimentale de cette recherche focalise sur la fabrication et la caractérisation de films polymères minces renforcés avec des nanotubes de carbone. Du aux difficultés rencontrées avec les techniques traditionnelles pour la caractérisation du module élastique de films polymère minces, une nouvelle technique, un test en flexion par nano-indentation, a été développée avec succès. La technique a été d'abord vérifiée numériquement par la 00 méthode d'éléments finis. Puis des films polymère minces avec des propriétés connues ont été utilisés pour vérifier cette technique expérimentalement. Par la suite, des films minces (épaisseur variant de 50 à 70 μm) de nano-composite à matrice époxy et vinyle-ester renforcées avec de faibles concentrations de SWNT (1% par masse) ont été fabriqués et caractérisés avec succès
Desruisseaux, Claude. "The electrophoretic properties of end-labeled DNA molecules in gels, polymer solutions and free-solutions, a theoretical and experimental study." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0017/NQ48096.pdf.
Повний текст джерелаLadin, Dmitry. "Study of the rheological properties of polymer/gas solutions based on a foam extrusion system." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape4/PQDD_0017/MQ49787.pdf.
Повний текст джерелаRaviprasad, Muniyamuthu. "Influence of Molecular Interactions on Elastic Properties and Oxygen Diffusion in PolyButylene Terephthalate Polymer: A Molecular Dynamics Study." Thesis, North Dakota State University, 2012. https://hdl.handle.net/10365/26732.
Повний текст джерелаNSF-EPSCoR FlexEM Grant
Park, Simon S. "On-line measurement of the PVT properties of polymer/CO¦2 solutions using a gear pump." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0003/MQ46081.pdf.
Повний текст джерелаSmith, Steven Richard. "Equilibrium and dynamic properties of side-chain liquid-crystalline polymers in dilute nematic solutions." Case Western Reserve University School of Graduate Studies / OhioLINK, 1995. http://rave.ohiolink.edu/etdc/view?acc_num=case1058202738.
Повний текст джерелаNanavati, Hemant. "Molecular modeling of the elastic and photoelastic properties of crosslinked polymer networks: a statistical segment approach / by Hemant Nanavati." Diss., Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/8227.
Повний текст джерелаLi, Yumeng. "Multiscale Modeling of the Effects of Nanoscale Load Transfer on the Effective Elastic Properties of Carbon Nanotube-Polymer Nanocomposites." Diss., Virginia Tech, 2015. http://hdl.handle.net/10919/51197.
Повний текст джерелаPh. D.
Vlattas, Cosmas. "A study of the mechanical properties of liquid crystal polymer fibres and their adhesion to epoxy resin using Laser Raman Spectroscopy." Thesis, Queen Mary, University of London, 1995. http://qmro.qmul.ac.uk/xmlui/handle/123456789/25566.
Повний текст джерелаWoelfle, Caroline. "Study of Nanoparticle/Polymer Composites: I) Microstructures and Nonlinear Optical Solutions Based on Single-Walled Carbon Nanotubes and Polymers and II) Optical Properties of Quantum Dot/Polymer Composites." Diss., Virginia Tech, 2006. http://hdl.handle.net/10919/26657.
Повний текст джерелаPh. D.
Rodrigues, Ferreira Elizabete. "Finite-amplitude waves in deformed elastic materials." Doctoral thesis, Universite Libre de Bruxelles, 2008. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210464.
Повний текст джерелаAprès un rappel des équations de base de l'élasticité non linéaire (Chapitre 1), on considère tout d'abord la classe générale des matériaux incompressibles. Pour ces matériaux, on montre que la propagation d'ondes transversales polarisées linéairement est possible pour des choix appropriés des directions de polarisation et de propagation. De plus, on propose des généralisations des modèles classiques de "Mooney-Rivlin" et "néo-Hookéen" qui conduisent à de nouvelles solutions. Bien que le contexte soit tri-dimensionnel, il s'avère que toutes ces ondes sont régies par des équations d'ondes scalaires non linéaires uni-dimensionelles. Dans le cas de solutions du type ondes simples, on met en évidence une propriété remarquable du flux et de la densité d'énergie.
Dans les Chapitres 3 et 4, on se limite à un modèle particulier de matériaux compressibles appelé "modèle restreint de Blatz-Ko", qui est une version compressible du modèle néo-Hookéen.
En milieu infini (Chapitre 3), on montre que des ondes transversales polarisées linéairement, faisant intervenir deux variables spatiales, peuvent se propager. Bien que la théorie soit non linéaire, le champ de déplacement de ces ondes est régi par une version anisotrope de l'équation d'onde bi-dimensionnelle classique. En particulier, on présente des solutions à symétrie "cylindrique elliptique" analogues aux ondes cylindriques. Comme cas particulier, on obtient aussi des ondes planes inhomogènes atténuées à la fois dans l'espace et dans le temps. De plus, on montre que diverses superpositions appropriées de solutions sont possibles. Dans chaque cas, on étudie les propriétés du flux et de la densité d'énergie. En particulier, dans le cas de superpositions il s'avère que des termes d'interactions interviennent dans les expressions de la densité et du flux d'énergie.
Finalement (Chapitre 4), on présente une solution exacte qui constitue une généralisation non linéaire de l'onde de Love classique. On considère ici un espace semi-infini, appelé "substrat" recouvert par une couche. Le substrat et la couche sont constitués de deux matériaux restreints de Blatz-Ko pré-déformés. L'onde non linéaire de Love est constituée d'un mouvement non atténué dans la couche et d'une onde plane inhomogène dans le substrat, choisies de manière à satisfaire aux conditions aux limites. La relation de dispersion qui en résulte est analysée en détail. On présente de plus des propriétés générales du flux et de la densité d'énergie dans le substrat et dans la couche.
The context of this thesis is the non linear elasticity theory, also called "finite elasticity".
Results are obtained for finite-amplitude waves in non linear elastic materials which are first subjected to a large homogeneous static deformation. Although the materials are assumed to be isotropic, anisotropic behaviour for wave propagation is induced by the static deformation.
After recalling the basic equations of the non linear elasticity theory (Chapter 1), we first consider general incompressible materials. For such materials, linearly polarized transverse plane waves solutions are obtained for adequate choices of the polarization and propagation directions (Chapter 2). Also, extensions of the classical Mooney-Rivlin and neo-Hookean models are introduced, for which more solutions are obtained. Although we use the full three dimensional elasticity theory, it turns out that all these waves are governed by scalar one-dimensional non linear wave equations. In the case of simple wave solutions of these equations, a remarkable property of the energy flux and energy density is exhibited.
In Chapter 3 and 4, a special model of compressible material is considered: the special Blatz-Ko model, which is a compressible counterpart of the incompressible neo-Hookean model.
In unbounded media (Chapter 3), linearly polarized two-dimensional transverse waves are obtained. Although the theory is non linear, the displacement field of these waves is governed by a linear equation which may be seen as an anisotropic version of the classical two-dimensional wave equation. In particular, solutions analogous to cylindrical waves, but with an "elliptic cylindrical symmetry" are presented. Special solutions representing "damped inhomogeneous plane waves" are also derived: such waves are attenuated both in space and time. Moreover, various appropriate superpositions of solutions are shown to be possible. In each case, the properties of the energy density and the energy flux are investigated. In particular, in the case of superpositions, it is seen that interaction terms enter the expressions for the energy density and the energy flux.
Finally (Chapter 4), an exact finite-amplitude Love wave solution is presented. Here, an half-space, called "substrate", is assumed to be covered by a layer, both made of different prestrained special Blatz-Ko materials. The Love surface wave solution consists of an unattenuated wave motion in the layer and an inhomogeneous plane wave in the substrate, which are combined to satisfy the exact boundary conditions. A dispersion relation is obtained and analysed. General properties of the energy flux and the energy density in the substrate and the layer are exhibited.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Seidel, Gary Don. "Micromechanics modeling of the multifunctional nature of carbon nanotube-polymer nanocomposites." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1881.
Повний текст джерелаIngremeau, François. "Solutions de polymères sous écoulement : liens entre propriétés microscopiques et manifestations macroscopiques." Phd thesis, Université Sciences et Technologies - Bordeaux I, 2013. http://tel.archives-ouvertes.fr/tel-00912345.
Повний текст джерелаWhite, Christopher Cleaveland. "High frequency viscoelastic properties of polymer solutions." 1994. http://catalog.hathitrust.org/api/volumes/oclc/32426410.html.
Повний текст джерелаRadtke, Douglas Robert. "High frequency viscoelastic properties of polymer solutions." 1986. http://catalog.hathitrust.org/api/volumes/oclc/13959796.html.
Повний текст джерелаTypescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 298-305).
BEARDEN, DANIEL WESLEY. "A QUASI-ELASTIC NEUTRON SCATTERING STUDY OF HYDROGEN DYNAMICS IN AQUEOUS POLYMER SOLUTIONS." Thesis, 1986. http://hdl.handle.net/1911/16036.
Повний текст джерелаRahman, Shamsur. "Shear & Extensional Effects in Internal Flows of Dilute Polymer Solutions." Thesis, 2011. http://hdl.handle.net/1807/31400.
Повний текст джерела"Interaction of polymer chains in solution." 2003. http://library.cuhk.edu.hk/record=b6073531.
Повний текст джерела"May 2003."
Thesis (Ph.D.)--Chinese University of Hong Kong, 2003.
Includes bibliographical references.
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Mode of access: World Wide Web.
Abstracts in English and Chinese.
Tuan, Yu-Chun, and 段友竣. "P-V-T Properties of Polymer Blend Solutions at Elevated Pressures." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/14845623823414079024.
Повний текст джерела國立臺灣科技大學
化學工程系
89
P-V-T data have been measured for binary and ternary mixtures composed of anisole, PEG-200, PPG-425, and PEGME-350 with a high-pressure densimeter in a temperature range of 298.15 K to 348.15 K and the pressures up to 50 MPa. The variations of densities and excess volumes with composition, temperature, and pressure were investigated. The excess volumes were found to change from positive to negative with increasing the mole fraction of PPG-425 in the PPG-425 + anisole and PPG-425 + PEGME-350. The Redlich-Kister model correlated well the excess volumes at fixed temperature and pressure. The Tait equation correlated accurately the density data over the entire pressure range. The isothermal compressibilities were calculated with the aid of the Tait equation. The magnitudes of the isothermal compressibility follow the order of anisole > PPG-425 > PEGME -350 >PEG-200. Both the FOV( Flory-Orwoll-Vrij ) and the Schotte equations of state were also employed to correlate the P-V-T data. The values of the binary interaction parameters were determined from the specific volumes of binary mixtures. The equations of state with those determined binary interaction parameters predicted the P-V-T properties to within acceptable accuracy for the three ternary mixtures composed of anisole with polymer blends of PEG-200, PPG-425 or PEGME-350.
"Thermally induced association/dissociation of polymers in dilute solutions." Thesis, 2008. http://library.cuhk.edu.hk/record=b6074635.
Повний текст джерелаChapter 2 details the theories of static and dynamic laser light scattering (LLS) as well as the instrumental set-up. In addition, the invention and set-up of differential refractometer are briefly discussed.
Chapter 3 summarizes laser light-scattering (LLS) and stopped-flow studies of association of cyclic- and linear-poly( N-isopropylacrylamide) (c-PNIPAM and l-PNIPAM) chains in dilute aqueous solutions. Dynamic and static LLS results reveal that the heating leads to a microphase transition. Resultant structures of interchain aggregates depend on the heating rate and the chain structure. In comparison with l-PNIPAM chains, a slow heating of c-PNIPAM chains in the solution results in stable mesoglobules with a lower average aggregation number, a looser structure and a smaller average size (∼290 nm). The temperature-jump induced association of c -PNIPAM chains in the stopped-flow measurement reveals two kinetic stages; namely, the loose packing of contracted c-PNIPAM chains and further contraction-induced fragmentation of initially packed c-PNIPAM chains due to the lack of interchain entanglements. On the other hand, for l-PNIPAM chains, the intrachain contraction and interchain penetration/entanglement simultaneously occur as the temperatures increases, leading to larger and more compact aggregates whose size increases with the solution temperature.
Chapter 4 discusses the association of water-soluble PNIPAM-monolayer-protected gold particles in dilute dispersions induced by heating the dispersions to different final temperatures higher than the lower critical solution temperature (LCST) of PNIPAM chains via the slow and fast processes. LLS was used to trace and characterize the association process, supplemented by transmission electron microscopy (TEM) measurements. The slow heating-and-cooling cycle reveals that the association and dissociation of PNIPAM-protected gold nanoparticles can be easily induced by altering the solution temperatures and the association and dissociation are fully reversible. Fast heating the dispersion to three different temperatures reveals that both the aggregation rate and average aggregation number increase with the dispersion temperature. Furthermore, the fast heating leads to the formation of fractal aggregates. The fractal dimensions of such formed aggregates continuously increases as the time evolves, which can be ascribed to the simultaneous dissociation that leads to the restructuring and rearrangement of the aggregates, resulting in denser structures. It is interesting to note that the structure of aggregate always remains fractal during the whole process.
Chapter 5 shows how water-dispersible nanosized semiconductor CdS particles (quantum dots, QDs) can be synthesized with a protective layer of covalently grafting linear thermally sensitive PNIPAM chains as well as how these CdS particles can be induced into reversible association and dissociation via an alteration of the dispersion temperature. The formation and fragmentation of these QDs aggregates were systematically investigated by laser light scattering (LLS) and confirmed by transmission electron microscopy (TEM). There exists a hysteresis in one heating-and-cooling cycle. The CdS particles stabilized with shorter PNIPAM chains (Mn = 15,000 g/mol) can associate to form larger and denser spherical aggregates with a much higher aggregation number than those grafted with longer PNIPAM chains ( Mn = 31,000 g/mol) in the heating process. The dissociation (fragmentation) in the cooling process has two stages: initially, the aggregates dissociate as the temperature decreases, and then, the fragmentation stops over a wider temperature range before its final complete dissociation at a lower temperature. We attribute such a two-stage fragmentation to a balanced effect of inter- and intra-chain hydrogen bonding as well as to the hydrophobic interaction between PNIPAM chains and CdS particles.
In this Ph.D. thesis, temperature-induced association and dissociation of various polymeric systems were systematically investigated by a combination of static and dynamic laser light scattering (LLS), supplemented by other methods, such as stopped-flow temperature jump, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR).
Ye, Jing.
Adviser: Wu Chi.
Source: Dissertation Abstracts International, Volume: 70-06, Section: B, page: 3533.
Thesis (Ph.D.)--Chinese University of Hong Kong, 2008.
Includes bibliographical references.
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstracts in English and Chinese.
School code: 1307.
CHIEN, WANG MENG, and 王孟堅. "PVT Properties of Polymer Solutions of Oligomeric Propylene Glycols at Elevated Pressures." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/03147839633058066084.
Повний текст джерела國立臺灣科技大學
化學工程系
91
Abstract In this study, the densities of polymer solutions were measured with a high-pressure vibrating tube densimeter at temperatures from 298.15 K to 348.15 K and pressures up to 50 MPa. The investigated mixtures include two binary and three ternary systems, containing 1-octanol, acetophenone, anisole, PEGME-350, and PPG-425. The Tait model and a semi-empirical model can correlate accurately the experimental density data over the entire pressure range. The experimental density data were used to calculate the excess volumes, which showed that the excess volumes change from positive to negative as the mole fraction of PPG-425 increasing from zero to unity for 1-octanol + PPG-425 and acetophenone + PPG-425 systems. The excess volumes can be correlated with the Redlich-Kister model. The experimental binary PVT data were also correlated with the FOV, the Schotte, and the Polymer CPHC equations of state, respectively, to determine the binary interaction parameters. By using the parameters determined from experimental data of pure components and binary mixtures, the equations of state predicted the specific volumes of the ternary polymer solutions to within reasonable accuracy.
Ho, Kuan-Li, and 何寬澧. "PVT Properties for Polymer Solutions of PEG and PEGME at Elevated Pressures." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/74320316410957594360.
Повний текст джерела國立臺灣科技大學
化學工程系
90
In this study, we measured the densities for mixed solvents and polymer solutions by a high-pressure densimeter. The mixtures include two binary and three ternary systems, containing anisole, acetophenone, PEG-200, and PEGME-350. Operating temperatures were in a range of 298.15 K to 348.15 K and the pressures were up to 50 MPa. Tait model and a choosed semi-empirical model can correlate accurately the density data. The isothermal compressibilities were calculated with the aid of Tait constants. The magnitudes of the isothermal compressibility follow the order of anisole>acetophenone>PEGME-350>PEG-200. The R-K model was applied to correlate the excess volumes of each binary system. The FOV and the Schotte equations of state were also applied to correlate the PVT data. Both models correlated well the specific volumes of each binary system. With the parameters determined from pure materials and binary systems, the equations of state were used to predict the specific volumes for multi-component polymer solutions. However, the predicted results appear to be larger than the experimental values.
Kuang, Lee Cheng, and 李正光. "Coarse-Grained Molecular Dynamics Simulation of the Aggregation Properties in Conjugated Polymer Solutions." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/09502101302967051096.
Повний текст джерела國立中正大學
化學工程研究所
93
Coarse-grained molecular dynamics simulation, which has been developed consistently from atomistic molecular dynamics simulation and retains the information of chemical structure, is utilized to investigate the aggregation properties of conjugated polymer solutions. Essential single-chain structural parameters including self-diffusivity, radius of gyration, and persistent length are reported. Representative aggregation realizations in two distinct solvent are contrasted and discussed in view of related experimental findings.
Koh, Andrew Yew Chiang. "Preparation, characterisation and properties of thermally-responsive copolymers and emulsions : a thesis submitted towards the degree of Doctor of Philosophy / by Andrew Yew Chiang Koh." 2003. http://hdl.handle.net/2440/21984.
Повний текст джерелаIncludes bibliographical references (leaves 261-270)
xvi, 271, [16] leaves : ill. ; 30 cm.
Title page, contents and abstract only. The complete thesis in print form is available from the University Library.
Thesis (Ph.D.)--University of Adelaide, School of Chemistry and Physics, 2003
Koh, Andrew Yew Chiang. "Preparation, characterisation and properties of thermally-responsive copolymers and emulsions : a thesis submitted towards the degree of Doctor of Philosophy / by Andrew Yew Chiang Koh." Thesis, 2003. http://hdl.handle.net/2440/21984.
Повний текст джерелаCrain, Patrick Michael. "Polymer/solvent interactions as revealed by dynamic viscoelastic and oscillatory flow birefringence properties for polystyrene solutions." 1991. http://catalog.hathitrust.org/api/volumes/oclc/25662306.html.
Повний текст джерелаTypescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 295-300).
"Laser light scattering studies of some special polymers in solution." 1997. http://library.cuhk.edu.hk/record=b5889179.
Повний текст джерелаAbstract also in Chinese.
Thesis (M.Phil.)--Chinese University of Hong Kong, 1997.
Includes bibliographical references.
Abstract --- p.i
Abstract (Chinese) --- p.iii
Acknowledgment --- p.iv
Contents --- p.v
Abbreviations --- p.viii
List of Figures --- p.xiv
List of Tables --- p.xvii
Chapter 1. --- Introduction --- p.1
Chapter 2. --- Theoretical background --- p.4
Chapter 2.1 --- Static laser light scattering --- p.5
Chapter 2.2 --- Dynamic laser light scattering --- p.5
Chapter 2.3 --- Gel Permeation Chromatography --- p.6
Chapter 2.4 --- Chain Flexibility --- p.9
Chapter 2.4.1 --- Flexible chains --- p.9
Chapter 2.4.2 --- Stiff chains --- p.12
Chapter 2.5 --- Calibration between translational diffusion coefficient D and molar mass M --- p.14
Chapter 2.5.1 --- Conversion between line-Width and molar Mass distributions --- p.14
Chapter 2.5.2 --- Using a set of Narrowly Distributed Standards --- p.15
Chapter 2.5.3 --- Using Two or More Broadly Distributed Samples --- p.16
Chapter 2.6 --- "Calibration by off-line GPC, Static and Dynamic LLS" --- p.16
Chapter 2.7 --- References --- p.19
Chapter 3. --- Experimental --- p.21
Chapter 3.1 --- Laser Light Scattering Instrumentation --- p.21
Chapter 3.2 --- Refractive index increment measurement --- p.23
Chapter 3.3 --- Gel permeation chromatography --- p.24
Chapter 3.4 --- References --- p.25
Chapter 4. --- Laser Light Scattering Studies of Soluble High Performance Fluorine- containing Polyimides --- p.26
Chapter 4.1 --- Introduction --- p.26
Chapter 4.2 --- Sample Preparation --- p.28
Chapter 4.3 --- Results and Discussion --- p.28
Chapter 4.4 --- Conclusion --- p.40
Chapter 4.5 --- References --- p.42
Chapter 5. --- Characterization of novel optically active conjugated polyarylenes and poly(aryleneethynylene)s by a combination of Laser Light Scattering and Gel Permeation Chromatography --- p.45
Chapter 5.1 --- Introduction --- p.45
Chapter 5.2 --- Sample Preparation --- p.48
Chapter 5.3 --- Results and Discussion --- p.48
Chapter 5.4 --- Conclusion --- p.56
Chapter 5.5 --- References --- p.61
Appendix --- p.62
Chapter A.1 --- Static laser light scattering --- p.62
Chapter A.1.1 --- Scattering from a small particle --- p.62
Chapter A. 1.2 --- Scattering from a large particle --- p.62
Chapter A. 1.3 --- Scattering by macroscopic systems and Theory of Fluctuations --- p.65
Chapter A.1.3.1 --- Scattering by gases and liquids --- p.67
Chapter A. 1.4 --- Scattering by solutions of small molecules --- p.68
Chapter A. 1.4.1 --- Scattering from polymer solution --- p.70
Chapter A.2 --- Dynamic laser light scattering --- p.71
Chapter A.2.1 --- Line-width measurement --- p.75
Chapter A.2.2 --- Data analysis --- p.77
Ayranci, Cagri. "Predicting the Elastic Properties of Two Dimensionally Braided Tubular Composite Structures Towards the Design of Braid-Reinforced Polymer Medical Catheters." Phd thesis, 2010. http://hdl.handle.net/10048/1169.
Повний текст джерелаChang, Chih-Shun, and 張智舜. "The Aggregation and Gelation Behavior and Its Effect on the Photophysical Properties of Polyfluorenes Conjugated Polymer in Solutions." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/05975675913493408263.
Повний текст джерела國立臺灣科技大學
高分子系
98
In this work, we provided insights into effect of the concentration, aging time, temperature, and blended conjugated polymers on the aggregation, gelation mechanism and its effect on the photophysical properties of polyfluorenes conjugate polymer in solutions with Static light scattering (SLS), Dynamic light scattering (DLS), Polarized optical microscopy(POM), Wide-angle X-ray diffraction (WAXD) UV-visble absorption(UV-vis), and Photoluminescence (PL) spectra. Firstly, Poly(9,9-dioctylfluorene-2,7-diyl) (PF8), in a good solvent toluene. The conformational structure characterized by the radius of gyration (Rg) and the persistence length (lp) of PF8 in the dilute toluene solution depended strongly on temperature, where the conjugated chains exhibited a more extended conformation as the temperature was raised. The inter-chain interaction above the overlap concentration induced aggregation of PF8 to form network clusters in the solution. Gelation took place when the semidilute PF8 solutions were cooled and subsequently aged at -20 oC. The gel composed of the dynamically arrested PF8-enriched phase and the isotropic phase due to the occurrence of a phase-separation at the subambient temperature. The PF8-enriched phase was mesomorphic, consisting of sheetlike aggregates or membranes. A fraction of the PF8 chains or segments within these sheetlike aggregates formed the beta-phase which dominated the photoluminescence of the gel. The gel structure could be disrupted by heating to ca. 45 oC, above which the corresponding PL spectra displayed a blue shift because of reduced amount of the beta-phase. Then, we provided insights into effect of the concentration, temperature, and aging time on the aggregation, and gelation mechanism and its effect on the photophysical properties of poly(9,9-dioctylfluorene) (PF8), with a poor solvent, methylcyclohexane (MCH), induced by aging and spinning rate at room temperature. Light scattering and optical microscopy revealed that the gelation was driven by a phase-separation occurred through a spinodal decomposition mechanism. Although the spinodal decomposition could proceed to the late stage, the interconnected morphology was arrested to give rise to the gel property of the system. The liquid crystalline phase was further found to consist of sheetlike aggregates as revealed by polarized optical microscopy(POM), in which a fraction of the PF8 chains formed the beta-phase that dominated the photoluminescence (PL) spectrum of the gel. The PF8/MCH gel could be disintegrated by moderate heating to ca. 70 oC. This gel-to-sol transition was accompanied with the disruptions of the sheetlike aggregates and the ??phase that led to homogenization of the solution. In the solid state, the photophysical spectra and crystallinity of thin films changed with increasing spinning rate at spin-coat film attested that the beta-phase in PF8/MCH thin film was deformed accompanied by shear force. Finally, we provided a constant weight content (1.0wt%) but various ratios of PF2/6 in PF8/PF2/6 blended conjugated polymer, aging time, and temperature on the gelation mechanism of Poly(9,9-dioctylfluorene)/Poly[9,9-di-(2-ethylhexyl)-fluorenyl] (PF8/PF2/6) in MCH solution. At PF8/PF2/6/MCH solutions and gels, dynamic light scattering revealed that the sheetlike aggregates (beta-phase) of PF8 conjugate polymer restricted by PF2/6. However, the gelation mechanism of PF8/PF2/6/MCH solutions was driven by the phase-separation occurred through a spinodal decomposition. Herein, the spinodal decomposition temperature, Tsp, gel-to-sol transition temperature, Tg-s, and gelation temperature, Tgel of PF8/PF2/6/MCH solutions decreased as PF2/6 was increased. The fraction of the PF8 chains formed the beta-phase that dominated the photoluminescence (PL) spectrum of the gel was revealed by Avrami equation to prove that the scale of beta-phase from 2-D to 1-D as PF2/6 was increased. The beta-phase of PF8/PF2/6/MCH gel could be disintegrated by moderate heating and increase PF2/6. These results proved that disrupted the sheetlike aggregates and the beta-phase by PF2/6 that led to reduce the intensities at 470 and 490 nm of the PL spectrum.
Chuang, Ching-Heng, and 莊靖恆. "Morphology and Electronic Properties of Semiconducting Polymer and Branched Polyethylene Blends and the synthesis of Self-Healing and elastic random copolymer." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/8wkqrq.
Повний текст джерелаStokich, Theodore M. "The influence of polymer/solvent interactions on the viscoelastic and oscillatory flow birefringence properties of polystyrene and polyisoprene solutions." 1988. http://catalog.hathitrust.org/api/volumes/oclc/19759530.html.
Повний текст джерелаSharma, Rati. "Theoretical Approaches to the Study of Fluctuation Phenomena in Various Polymeric Systems." Thesis, 2013. http://etd.iisc.ernet.in/2005/3338.
Повний текст джерела