Thèses sur le sujet « Free radical photo polymerisation »
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Dobie, Christopher George. « A Study of Bulk Free-Radical Photo Copolymerisation and Surfactant Free Emulsion Polymerisation Using Intensified Processing Methods ». Thesis, University of Newcastle Upon Tyne, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512198.
Texte intégralShooter, Andrew James. « Living free radical polymerisation ». Thesis, University of Warwick, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263817.
Texte intégralParkes, Caroline Margaret. « 'Living'/Controlled free-radical polymerisation ». Thesis, University of Manchester, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.488186.
Texte intégralEason, Michael Douglas. « Water-soluble polymers from controlled free-radical polymerisation ». Thesis, University of Warwick, 2000. http://wrap.warwick.ac.uk/36687/.
Texte intégralLudlow, Andrew John. « Free radical polymerisation studies of 4-substituted styrenes ». Thesis, London South Bank University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336419.
Texte intégralHart-Smith, Gene On Chemistry Faculty of Science UNSW. « Mass spectrometric investigations into free radical polymerisation reaction mechanisms ». Awarded by:University of New South Wales. Chemistry, 2009. http://handle.unsw.edu.au/1959.4/44621.
Texte intégralLi, Jianing. « Free radical polymerisation in supercritical carbon dioxide expanded phase ». Thesis, University of Nottingham, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576539.
Texte intégralArsu, Nergis. « Some aspects of free radical polymerisation in UV-curing ». Thesis, City University London, 1993. http://openaccess.city.ac.uk/8266/.
Texte intégralPullen, Graeme K. « 2-substituted anthraquinones as photoinitiators of free radical polymerisation ». Thesis, Manchester Metropolitan University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320492.
Texte intégralFraser, Kathryn. « An investigation of nitroxide-mediated polymerisation ». Thesis, University of York, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288036.
Texte intégralKurinczuk, Andrew H. « The kinetics of free radical bulk polymerisation at high conversion ». Thesis, Loughborough University, 1991. https://dspace.lboro.ac.uk/2134/7117.
Texte intégralDieudonne, Lucile. « Synthesis, characterisation and cytotoxicity evaluation of novel polymeric carriers for polymer therapeutics : from free radical polymerisation to atom transfer radical polymerisation ». Thesis, Cardiff University, 2008. http://orca.cf.ac.uk/55722/.
Texte intégralTat, Nguyen Cam. « A novel free radical polymerisation approach to hyperbranched poly(methyl methacrylate) ». Thesis, Imperial College London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417994.
Texte intégralMortamet, Anne-Cecile. « Redox free radical polymerisation of 4-methylstyrene : thermal and spectroscopic characterisations ». Thesis, University of Strathclyde, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.502357.
Texte intégralTai, Hongyun. « Free radical heterogeneous polymerisation of vinylidene fluoride in supercritical carbon dioxide ». Thesis, University of Nottingham, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428931.
Texte intégralMouillat, Claire G. J. « Application of UV curing to the preparation of composite materials ». Thesis, University of Kent, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360968.
Texte intégralMcAllister, Thomas D. « Expanding the scope of free-radical dispersion polymerisation in supercritical carbon dioxide ». Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/46744/.
Texte intégralAdash, Uma. « Synthetic and kinetic investigations into living free-radical polymerisation used in the preparation of polymer therapeutics ». Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1282.
Texte intégralBirchall, Andrew Carl. « The synthesis of novel homochiral polymers from amino acids ». Thesis, Bangor University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310924.
Texte intégralBradley, Grant. « Hexaarylbisimidazoles as initiators of acrylate polymerisation : some new synthesis and application ». Thesis, University of Kent, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360967.
Texte intégralChaffey-Millar, Hugh William Chemical Sciences & Engineering Faculty of Engineering UNSW. « An experimental and computational study of two state of the art living free radical polymerisation techniques ». Awarded by:University of New South Wales. Chemical Sciences & ; Engineering, 2008. http://handle.unsw.edu.au/1959.4/41421.
Texte intégralLussini, Vanessa C. « The synthesis and evaluation of polyaromatic profluorescent nitroxide probes for the detection of photo-oxidative polymer degradation ». Thesis, Queensland University of Technology, 2019. https://eprints.qut.edu.au/127299/1/Vanessa_Lussini_Thesis.pdf.
Texte intégralEngland, Richard Mark. « Free Radical Polymerisation of Linear and Highly Branched Polymers Using Reversible Addition Fragmentation chain-Transfer and an Alkylation Reaction with a Silyl Enol Ether ». Thesis, University of Sheffield, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522023.
Texte intégralVidyasagar, Ajay Kumar. « Volume Phase Transitions in Surface-Tethered, Photo-Cross-Linked Poly(N-isopropylacrylamide) Networks ». Scholar Commons, 2010. https://scholarcommons.usf.edu/etd/1798.
Texte intégralBlinco, James Peter. « The synthesis and application of novel profluorescent nitroxides as probes for polymer degradation ». Queensland University of Technology, 2008. http://eprints.qut.edu.au/26376/.
Texte intégralBlinco, James P. « The synthesis and application of novel profluorescent nitroxides as probes for polymer degradation ». Thesis, Queensland University of Technology, 2008. https://eprints.qut.edu.au/26376/1/James_Blinco_Thesis.pdf.
Texte intégralTAUFER, MICHEL. « Polymerisation et caracterisations de materiaux de coeur pour fibres optiques transparentes et scintillantes ». Toulouse 3, 1989. http://www.theses.fr/1989TOU30031.
Texte intégralRoth, Jan. « Funktionalisierung von Silikonoberflächen ». Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1234268177738-70409.
Texte intégralRoth, Jan. « Funktionalisierung von Silikonoberflächen ». Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A23701.
Texte intégralPrandato, Emeline. « Relations structure-propriétés et résistance à l’endommagement de vernis acrylate photo-polymérisables pour substrats thermoplastiques : évaluation de monomères bio-sourcés et de nano-charges ». Thesis, Lyon, INSA, 2013. http://www.theses.fr/2013ISAL0103/document.
Texte intégralThe aim of this work was to develop 100% solids photo-polymerizable acrylate coatings, intended to protect thermoplastic pieces made of polycarbonate against mechanical damage, in particular scratches. The relationships between the composition, the structure and the properties of these coatings were examined. For this purpose the morphology, the thermomechanical properties and the scratch resistance of the materials, assessed by micro-scratch tests, were studied. The kinetics of the polymer network formation was also studied by photo-DSC experiments. All the materials feature a high elastic modulus and a broad mechanical relaxation in dynamic thermomechanical analysis. A 100% solids petro-based coating (standard) constituted the starting point of this work. First it was compared to a commercial photo-polymerizable coating containing solvents, specially designed to protect thermoplastic pieces. This commercial coating turned out to be more efficient against scratches. In a second time was studied the influence of the percentage of a multicyclic monomer, taking part in the composition of the standard petro-based coating, on the properties of the latter. The modification of its proportion does not bring any advantage concerning the scratch resistance. Silica, alumina and zirconia nanoparticles, dispersed in an acrylate monomer, were then incorporated in the standard petro-based coating. A particular organization of the silica or alumina nanoparticles in the materials could be observed by transmission electron microscopy. A high filler content is required to observe an increase in the elastic modulus and an enhancement of the scratch resistance of the coating (≥15% by weight for the nano-silica). Moreover, no change of the photo-polymerization kinetics was noticed through the addition of 5% by weight of nano-silica in the coating. Finally, some of the petro-based acrylate compounds of the standard coating were substituted by commercially available bio-based acrylate monomers. Both types of coatings feature similar polymerization kinetics. The conclusions concerning the comparison of the scratch resistance of the bio-based and standard petro-based coatings depend on their thickness. The incorporation of a bio-based monoacrylate compound in low thickness coatings tends to improve the elastic recovery. Isobornyl acrylate is particularly interesting since it also tends to delay the apparition of cracks along the scratch
Mansri, Ali. « Synthese et etude de polymeres styreniques porteurs de chaines laterales polycetoniques ». Le Mans, 1987. http://www.theses.fr/1987LEMA1025.
Texte intégralSun, L., Anaïs Pitto-Barry, A. W. Thomas, M. Inam, K. E. B. Doncom, A. P. Dove et R. K. O'Reilly. « Core functionalization of semi-crystalline polymeric cylindrical nanoparticles using photo-initiated thiol–ene radical reactions ». 2016. http://hdl.handle.net/10454/15390.
Texte intégralSequential ring-opening and reversible addition–fragmentation chain transfer (RAFT) polymerization was used to form a triblock copolymer of tetrahydropyran acrylate (THPA), 5-methyl-5-allyloxycarbonyl-1,3-dioxan-2-one (MAC) and L-lactide. Concurrent deprotection of the THPA block and crystallization-driven self-assembly (CDSA) was undertaken and allowed for the formation of cylindrical micelles bearing allyl handles in a short outer core segment. These handles were further functionalized by different thiols using photo-initiated thiol–ene radical reactions to demonstrate that the incorporation of an amorphous PMAC block within the core does not disrupt CDSA and can be used to load the cylindrical nanoparticles with cargo.
Royal Society (Great Britain), Engineering and Physical Sciences Research Council (EPSRC), European Research Council (ERC)
Szablan, Zachary Peter Chemical Sciences & Engineering Faculty of Engineering UNSW. « Living free radical and photo initiation studies of acrylate, methacrylate and itaconate polymerization systems ». 2008. http://handle.unsw.edu.au/1959.4/41255.
Texte intégralEl, Rezzi Véronique. « Chain-transfer kinetics for free-radical homo- and coplymerizations of styrene and methyl methacrylate in supercritical carbon dioxide ». Doctoral thesis, 2001. http://hdl.handle.net/11858/00-1735-0000-0006-B0E3-8.
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