Thèses sur le sujet « Liquid crystalline elastomer »
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Hessberger, Tristan [Verfasser]. « Microfluidic preparation of liquid crystalline elastomer actuators / Tristan Hessberger ». Mainz : Universitätsbibliothek Mainz, 2018. http://d-nb.info/1162864419/34.
Texte intégralMcKenzie, Blayne M. « Metallo-Responsive Liquid Crystalline Monomers, Polymers and Networks ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1295565872.
Texte intégralBurke, Kelly Anne. « Structure-Property Relationships in Main-Chain Liquid Crystalline Networks ». Cleveland, Ohio : Case Western Reserve University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1270660447.
Texte intégralDepartment of Macromolecular Science and Engineering Title from PDF (viewed on 2010-05-25) Includes abstract Includes bibliographical references and appendices Available online via the OhioLINK ETD Center
Matkar, Rushikesh Ashok. « Phase Diagrams and Kinetics of Solid-Liquid Phase Transitions in Crystalline Polymer Blends ». University of Akron / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=akron1189533285.
Texte intégralPatel, Sangdil Ishwarlal. « Memory effects in liquid crystalline elastomers ». Thesis, University of Reading, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394061.
Texte intégralBrannum, Michelle T. « Functional Performance of Liquid Crystalline Elastomers ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1549025445138734.
Texte intégralGibson, John. « Reconfigurable Antennas Using Liquid Crystalline Elastomers ». FIU Digital Commons, 2018. https://digitalcommons.fiu.edu/etd/3706.
Texte intégralAragrag, Najib. « Synthesis and characterisation of thermotropic liquid crystalline elastomers ». Thesis, University of Reading, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541980.
Texte intégralBeattie, Helen Naomi. « The synthesis and evaluation of poly- and mono-domain elastomers based on polysiloxanes ». Thesis, University of Hull, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.262446.
Texte intégralHasson, Craig. « Preparation and properties of liquid crystalline elastomers with chiral nematic structure ». Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326186.
Texte intégralFleischmann, Eva-Kristina [Verfasser]. « Liquid crystalline elastomers as stimuli-responsive microactuators / Eva-Kristina Fleischmann ». Mainz : Universitätsbibliothek Mainz, 2013. http://d-nb.info/1034339249/34.
Texte intégralRen, Wanting. « Structure-property Relations of Siloxane-based Main Chain Liquid Crystalline Elastomers and Related Linear Polymers ». Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/16248.
Texte intégralBrenn, William Alexander. « Stimuli-responsive Materials From Thiol-based Networks ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case149192088155293.
Texte intégralOdarchenko, Yaroslav. « Tailoring the mesoscopic structure and orientation of semicrystalline and liquid-crystalline polymers : from 1D- to 2D-confinement ». Phd thesis, Université de Haute Alsace - Mulhouse, 2012. http://tel.archives-ouvertes.fr/tel-01062091.
Texte intégralMelchert, Christian. « Entwicklung multi-stimuli sensitiver Materialien auf der Basis von flüssigkristallinen Elastomeren ». Phd thesis, Universität Potsdam, 2012. http://opus.kobv.de/ubp/volltexte/2012/6286/.
Texte intégralActively moving polymers are high scientific significance due to their ability to move actively in response to an external stimulus. Most notably shape-change and shape-memory polymers are in the focus of current research. Shape-changing polymers exhibit a non-contact deformation from a permanent into a temporary shape, which is just stable as long the material is exposed to an external stimulus. In contrast shape-memory polymers are capable of a fixed temporary shape due to the formation of additional temporary netpoints, while the deformation is proceed by applying mechanical stress. A polymeric material, which combines both functions would result into a material that possesses the advantages of the shape-change, as well as the shape-memory effect. In this work, the coupling of two known functions is investigated which results into a new switchable function. Therefore, two different concepts were developed requiring different material structures. For the first concept monodomain, smectic liquid-crystalline elastomers (LCE) containing azobenzene moieties were prepared and the coupling of the light-induced shape-change with the thermally-induced shape-memory effect was investigated. These oriented LCE's exhibit a non-contact deformation into a temporary shape, above the glass transition temperature (Tg), due to the irradiation with UV-light. The temporary shape could be fixed by cooling the material below Tg, while the irradiation with light was kept constant. The permanent shape could be recovered by additional heating above Tg. This process could be repeated several times. Therefore, a new switchable function was developed, which based on the coupling of the light-induced shape-change with the thermally induced shape-memory effect. The second concept required a multi-component system and the coupling of the thermally-induced shape-memory withe the light-induced shape-change effect was investigated. The multi component system consists of a LCE-core and a photosensitive layer. Nematic, main-chain elastomers were prepared, which possess of low transition temperatures and high actuation performances. The photosensitive layer consists of cinnamylidene acetic moieties, that were attached to a siloxane backbone, while the photoreversibility of the light-induced [2+2]-cycloaddition was shown. Furthermore, the photosensitive layer was covalently attached to the surface of the LCE-core. While both components showed their functionality, the coupling of the thermally-induced shape-change with the light-induced shape-memory effect was not successful up to now. The Adjustment of both components on each other has to be improved. Mainly the variation of the layer thickness of both structural components should be in the focus of future work.
MARTELLA, DANIELE. « Towards microrobotics : new liquid crystalline elastomer based photoactive microstructures ». Doctoral thesis, 2015. http://hdl.handle.net/2158/1079711.
Texte intégralPontes, Rita Valério. « Cellulose nanorods in liquid crystalline elastomers for improved actuators ». Master's thesis, 2014. http://hdl.handle.net/10362/14172.
Texte intégralLin, Wen-Jahn, et 林文章. « Studies on the properties and characterization of Side Chain Liquid Crystalline Polyurethane Elastomers ». Thesis, 1996. http://ndltd.ncl.edu.tw/handle/04885018454367710976.
Texte intégral孫時傑. « Studies on the synthesis and properties of thermotropic liquid crystalline polycarbonates and elastomers ». Thesis, 1996. http://ndltd.ncl.edu.tw/handle/59100843817581817405.
Texte intégralMenzel, Andreas [Verfasser]. « Nonlinear macroscopic description of liquid crystalline elastomers in external fields / vorgelegt von Andreas Menzel ». 2009. http://d-nb.info/993161375/34.
Texte intégralRamón, Giménez Laura [Verfasser]. « Smectic a side-chain liquid crystalline elastomers containing lithium salts / vorgelegt von Laura Ramón Giménez ». 2009. http://d-nb.info/995853452/34.
Texte intégral許再發. « The investigations on the synthesis and properties of novel thermotropic liquid crystalline polymers and elastomers ». Thesis, 1998. http://ndltd.ncl.edu.tw/handle/57943362564647994048.
Texte intégralGrandinetti, Bruno. « Development of light-responsive materials for biomedical applications - A perspective on the use of Liquid Crystalline Elastomers as artificial muscles and cell culture substrates ». Doctoral thesis, 2022. http://hdl.handle.net/2158/1265117.
Texte intégralLi-Ling, Chung, et 鍾麗玲. « Studies on the Synthesis and Properties of Semi-Aromatic Thermotropic Liquid Crystalline Poly(amide-ester) and Polyester Elastomers ». Thesis, 1998. http://ndltd.ncl.edu.tw/handle/55487298959277022208.
Texte intégral中原大學
化學工程研究所
86
A series of semi-aromatic thermotropic liquid crystalline poly(amide-ester) and polyester elastomers were prepared by direct polycondensation from various aromatic diacid (e.g. TPA, DBAC or PEG4) with various aromatic diamine (e.g. ODA, BDAM or NDAM), various diols (e.g. PhHQ, BPO, MHQ, BP, PEG-200, PEG-600, PEG-1000 or isosorbide), respectively, in the presence of diphenyl chlorophosphate(DPCP), LiCl and pyridine. In order to investigate the relationship between the structures and the LC properties of the synthesized poly(amide-ester) and polyester elastomers, all of the synthesized polymers were examined by DSC, polarized microscope with a heating stage, WAXD, TGA and DMA. For preparing LC poly(amide-ester)s and polyester elastomers with long soft segments, it was found that aspect ratio of the hard segments should be extented. However, on the other hand, the transition temperatures of the hard segment were suppose to be reduced to show LC properties, because the thermostabilities of the soft segments were relatively poor. Synthesizing alternating LC elastomers could lower the transation temperation temperature effectively. In this study, we also attempted to prepare novel cholesteric LC elastomers by introducing the amount of isosorbide, as a chiral diol monomer, which is lower than 25 mole ﹪. In addition, the synthesized poly(amide-ester) and polyester elastomers possessed excellent thermostabilties (the 5 wt ﹪ loss temperature is higher than 400 ℃).
Long, Chung Shing, et 鍾新龍. « Studies on the Synthesis and Properties of Side Chain Crosslinkable Thermotropic Liquid Crystalline Polymer and its Elastomers(Ⅱ) ». Thesis, 1999. http://ndltd.ncl.edu.tw/handle/92519366537418135025.
Texte intégral中原大學
化學工程學系
87
In the first part of this study, a diamine monomer, (2,2’-diacryloyl-4,4’-diaminobiphenyl), containing crosslinkable and mesogen functional group was synthesized using 2-2’-diacryloyl-4,4’-dinitrobiphenyl as the starting material by various kind of reduction methods. In order to investigate the influence of the reduction methods on the yield and structure of diamine monomer, the reduction products were analyzed and identified by FTIR, NMR and elemetal analysis. The nitro functional group reduced into amine group by using calcium chloride mixing with iron powder and hydrochloric acid containing iron powder as the reduction agents would not reduce carbon-carbon double bond simultaneously. However, by using others reduction agents, the carbon-carbon double would be reduced with nitro group at the same time. In the second part, the diamine monomer synthesized by using hydrochloric acid and iron powder as the reduction agent reacted with various diacids, diols, and aromatic acids, which contain hydroxy group in one end and carboxyl group in the other end, were polymerized by using direct polycodensation to obtain a series of side chain crosslinkable aromatic poly(amide-ester)s. In order to investigate the effect of the kind of monomer and its structure on the thermal properties of obtained polymer, the obtained polymers were measured by DSC, TGA, and polarized microscope with a heating stage. The polymer synthesized by introducing of PEG4 diacid monomer which containing flexible spacer possessed lower melting point and higher inherent viscosity than those of polymers synthesized from TPA, IPA, and NAAC diacid monomers. Furthermore, except polymer 3a, all of the polymers did not exhibt thermotropic liquid crystalline properties.
Lupi, Flavia. « Photopolymerization approaches towards smart responsive surfaces and materials ». Doctoral thesis, 2020. http://hdl.handle.net/2158/1191501.
Texte intégralBellis, Isabella De. « Photonic crystals based on smart polymers. A new route for tunable devices ». Doctoral thesis, 2021. http://hdl.handle.net/2158/1236030.
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