Дисертації з теми "Self-assembly systems"
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Fox, Michael Jacob. "Stochastic self-assembly." Thesis, Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/34741.
Повний текст джерелаRazali, Azaima. "Self assembly in gel systems." Thesis, University of Bristol, 2018. http://hdl.handle.net/1983/77bc44c6-4aed-4548-90f6-4c2f6975e522.
Повний текст джерелаFejer, Szilard. "Self-assembly in complex systems." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611771.
Повний текст джерелаKwiecinski, James Andrew. "Self-assembly in mechanical systems." Thesis, University of Oxford, 2018. http://ora.ox.ac.uk/objects/uuid:a3b521ad-be4a-4152-aaa6-f9a002060c48.
Повний текст джерелаAntzoulatos, Nikolas. "Towards self-adaptable intelligent assembly systems." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/39583/.
Повний текст джерелаTerrazas, Angulo German. "Automated evolutionary design of self-assembly and self-organising systems." Thesis, University of Nottingham, 2009. http://eprints.nottingham.ac.uk/10648/.
Повний текст джерелаXiong, Xiaorong. "Controlled multi-batch self-assembly of micro devices /." Thesis, Connect to this title online; UW restricted, 2004. http://hdl.handle.net/1773/5917.
Повний текст джерелаPuntambekar, Smita. "Molecular self assembly in fluorocarbon surfactant/water systems." Thesis, University of Central Lancashire, 2000. http://clok.uclan.ac.uk/20906/.
Повний текст джерелаBrust, Mathias. "The self-assembly of nanostructured gold-dithiol systems." Thesis, University of Liverpool, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260334.
Повний текст джерелаBranda, Neil R. (Neil Robin). "Synthetic recognition systems : self-assembly and metal chelation." Thesis, Massachusetts Institute of Technology, 1994. http://hdl.handle.net/1721.1/17367.
Повний текст джерелаSpiteri, Ludovic. "Self-assembly of dipolar particles." Thesis, Université de Lorraine, 2018. http://www.theses.fr/2018LORR0261/document.
Повний текст джерелаThis thesis covers the self-assembly of dipolar (magnetic/dielectric) particles. These systems are abundant in condensed matter physics (magnetic molecules and nanoparticles, magnetic colloidal particles, magnetotactic bacteria, etc). They also represent a fundamental challenge owing to the both long range and anisotropic nature of the pair interaction. The main objective of this research work is to predict the microstructures of these systems by properly handling the intricate dipole-dipole interaction combined with steric and possibly confinement effects. Understanding and revisiting the interaction of dipolar filaments such as needles or chains made up of dipolar beads is a first important achievement in this thesis. Indeed, the chains are the fundamental building blocks of many dipolar systems especially under applied external magnetic field. Then, the columnar aggregation of dipolar chains is investigated which naturally leads to the study of the bulk dipolar crystals. A new phase is discovered there. The more generic case of helical chains is discussed by considering limiting situations such as straight linear chains and zigzag chains. The association of dipolar chains in two-dimensions forms ribbons then a monolayer with triangular lattice symmetry. The interesting response of such a layer to an imposed perpendicular magnetic is addressed as well. It is demonstrated that rhombicity can be induced that way. Finally, sedimenting paramagnetic particles in a tilted monolayer in presence of a magnetic field are investigated by experiments, theory and simulations. The gravity-mediated ordering is found to be a promising route to elaborate tailored two-dimensional patterns
Campbell, V. E. "Subcomponent self-assembly : from topological complexity to dynamic systems." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597267.
Повний текст джерелаKarpenko, Daria. "Active Tile Self-assembly and Simulations of Computational Systems." Scholar Commons, 2015. https://scholarcommons.usf.edu/etd/5519.
Повний текст джерелаCooper, Christopher G. F. "Self-assembled systems for molecular device applications." Link to electronic thesis, 2004. http://www.wpi.edu/Pubs/ETD/Available/etd-0430104-152257/.
Повний текст джерелаFerreira, Pedro. "An agent-based self-configuration methodology for modular assembly systems." Thesis, University of Nottingham, 2011. http://eprints.nottingham.ac.uk/12325/.
Повний текст джерелаGazzaz, Hanna Asaad. "Kinetics of metal ion complex formation in self-assembly systems." Thesis, University of East Anglia, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365019.
Повний текст джерелаGreco, E. "Synthesis of self-assembly systems with multiple hydrogen bonding interactions." Thesis, University College London (University of London), 2009. http://discovery.ucl.ac.uk/17980/.
Повний текст джерелаRosa, Rogério Paulo Guerreiro. "Assessing self-organization and emergence in Evolvable Assembly Systems (EAS)." Master's thesis, Faculdade de Ciências e Tecnologia, 2013. http://hdl.handle.net/10362/10990.
Повний текст джерелаThere is a growing interest from industry in the applications of distributed IT. Currently, most modern plants use distributed controllers either to control production processes, monitor them or both. Despite the efforts on the last years to improve the implementation of the new manufacturing paradigms, the industry is still mainly using traditional controllers. Now, more than ever, with an economic crisis the costumers are searching for cheap and customized products, which represents a great opportunity for the new paradigms to claim their space in the market. Most of the research on distributed manufacturing is regarding the control and communication infrastructure. They are key aspects for self-organization and there is a lack of study on the metrics that regulate the self-organization and autonomous response of modern production paradigms. This thesis presents a probabilistic framework that promotes self-organization on a multiagent system based on a new manufacturing concept, the Evolvable Assembly Systems/Evolvable Production Systems. A methodology is proposed to assess the impact of self-organization on the system behavior, by the application of the probabilistic framework that has the dual purpose of controlling and explaining the system dynamics. The probabilistic framework shows the likelihood of some resources being allocated to the production process. This information is constantly updated and exchanged by the agents that compose the system. The emergent effect of this self-organization dynamic is an even load balancing across the system without any centralized controller. The target systems of this work are therefore small systems with small production batches but with a high variability of production conditions and products. The agents that compose the system originated in the agent based architecture of the FP7-IDEAS proejct. This work has extended these agents and the outcome has been tested in the IDEAS demonstrators, as the changes have been incorporated in the latest version of the architecture, and in a simulation and more controlled environment were the proposed metric and its influence were assessed.
Phoomboplab, Tirawat. "Self-resilient production systems : framework for design synthesis of multi-station assembly systems." Thesis, University of Warwick, 2012. http://wrap.warwick.ac.uk/59325/.
Повний текст джерелаWood, Kris Cameron. "Nanostructured gene and drug delivery systems based on molecular self-assembly." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39350.
Повний текст джерелаIncludes bibliographical references.
Molecular self-assembly describes the assembly of molecular components into complex, supramolecular structures governed by weak, non-covalent interactions. In recent years, molecular self-assembly has been used extensively as a means of creating materials and devices with well-controlled, nanometer-scale architectural features. In this thesis, molecular self-assembly is used as a tool for the fabrication of both gene and drug delivery systems which, by virtue of their well-controlled architectural features, possess advantageous properties relative to traditional materials used in these applications. The first part of this thesis describes the solution-phase self-assembly of a new family of linear-dendritic "hybrid" polymers with plasmid DNA for applications in gene therapy. It begins with an overview of the design of next-generation, non-viral gene delivery systems and continues through the synthesis and validation of hybrid polymer systems, which possess modular functionalities for DNA binding, endosomal escape, steric stabilization, and tissue targeting. This part of the thesis concludes with applications of these systems to two areas of clinical interest: DNA vaccination and tumor targeted gene therapy.
(cont.) The second part of this thesis describes the directed self-assembly of polymeric thin films which are capable of degrading in response to either passive or active stimuli to release their contents. It begins with a description of passive release thin films which degrade by basic hydrolysis to release precise quantities of model drug compounds. These systems can be engineered to release their contents on time scales ranging from hours to weeks and can also be designed to release multiple drugs either in series or in parallel. Later, field-activated thin films which release their contents in response to an external, electrical stimulus are described and characterized in detail. Together, these approaches combine rapid and inexpensive processing, the ability to conformally coat any surface regardless of composition, size, or shape, and the ability to release multi-drug or multi-dose schedules, and as such they may find applications in a range of areas.
by Kris Cameron Wood.
Ph.D.
Steinbach, Gabi, Dennis Nissen, Manfred Albrecht, Ekaterina V. Novak, Pedro A. Sánchez, Sofia S. Kantorovich, Sibylle Gemming, and Artur Erbe. "Bistable self-assembly in homogeneous colloidal systems for flexible modular architectures." Universitätsbibliothek Chemnitz, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-202517.
Повний текст джерелаDieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
Wu, Yuchao. "Cucurbit[n]uril-based colloidal self-assembly in hybrid polymeric systems." Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/270021.
Повний текст джерелаGe, Chen. "Nanopatterning on metallic and ceramic systems via self-assembly and polymer system via replica molding." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461180232.
Повний текст джерелаBhise, Anil Dnyanoba. "A biomimetic approach for synthesizing artificial light-harvesting systems using self-assembly." Karlsruhe : FZKA, 2004. http://bibliothek.fzk.de/zb/berichte/FZKA7174.pdf.
Повний текст джерелаBhise, Anil Dnyanoba. "A biomimetic approach for synthesizing artificial light-harvesting systems using self-assembly /." Karlsruhe : Forschungszentrum, 2005. http://www.gbv.de/dms/bs/toc/503994367.pdf.
Повний текст джерелаAuch als elektronische Ressource vorh. Literaturverz. S. 126 - 133. Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden. Zsfassung in dt. Sprache.
Hong, Young Ki. "Surface tension self-assembly for three dimensional micro-opto-electro-mechanical systems." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429321.
Повний текст джерелаChen, Chao. "Self-assembly studies of hybrid nanoparticle-protein cage systems and icosahedral viruses." [Bloomington, Ind.] : Indiana University, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3331353.
Повний текст джерелаTitle from PDF t.p. (viewed on Jul 27, 2009). Source: Dissertation Abstracts International, Volume: 69-11, Section: B, page: 6818. Adviser: Bogdan Dragnea.
Serpe, Michael Joseph. "Self-Assembly of Poly(N-isopropylacrylamide) Microgel Thin Films." Diss., Georgia Institute of Technology, 2004. http://hdl.handle.net/1853/4806.
Повний текст джерелаMcKnight, Patrick T. "Finite Element Analysis of Thermoelectric Systems with Applications in Self Assembly and Haptics." Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/3630.
Повний текст джерелаWhite, Claire Michelle. "Ruthenium polypyridyl complexes designed for the non-covalent self-assembly of supramolecular systems." Thesis, University of Bristol, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265497.
Повний текст джерелаGray, Sarah Jane. "Dissipative particle dynamics simulations of surfactant systems : phase diagrams, phases and self-assembly." Thesis, Durham University, 2018. http://etheses.dur.ac.uk/12641/.
Повний текст джерелаHristova, Yana Roumenova. "Subcomponent self-assembly of diverse metallo-supramolecular systems from 3,3'-bipyridine-6,6'-dicarboxaldehyde." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610122.
Повний текст джерелаValkov, Eugene. "Design and analysis of self-assembling protein systems." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670100.
Повний текст джерелаAl-Milaji, Karam Nashwan. "Material Interactions and Self-Assembly in Inkjet Printing." VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/6053.
Повний текст джерелаLim, Yun Fong. "Some Generalizations of Bucket Brigade Assembly Lines." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/6910.
Повний текст джерелаZaucha, Michael Thomas. "Biomechanics and biaxial mechanical stimulation of self-assembly tissue engineered blood vessels." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/39532.
Повний текст джерелаMathews, Nithin. "Beyond self-assembly: Mergeable nervous systems, spatially targeted communication, and supervised morphogenesis for autonomous robots." Doctoral thesis, Universite Libre de Bruxelles, 2018. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/267717.
Повний текст джерелаDoctorat en Sciences de l'ingénieur et technologie
info:eu-repo/semantics/nonPublished
Hannon, Adam Floyd. "Modeling and theoretical design methods for directed self-assembly of thin film block copolymer systems." Thesis, Massachusetts Institute of Technology, 2014. http://hdl.handle.net/1721.1/89842.
Повний текст джерелаThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 321-324).
Block copolymers (BCPs) have become a highly studied material for lithographic applications due to their ability to self-assemble into complex periodic patterns with feature resolutions ranging from a few to 100s nm. BCPs form a wide variety of patterns due the combination of their enthalpic interactions promoting immiscibility between the blocks and the bonding constraint through their chain topology. The morphologies formed can be tailored through a directed self-assembly (DSA) process using chemical or topographical templates to achieve a desired thin film pattern. This method combines the traditional top-down lithographic methods with the bottom-up self-assembly process to obtain greater control over long range order, the local morphology, and overall throughput of the patterns produced. This work looks at key modeling challenges in optimizing BCP DSA to achieve precision morphology control, reproducibility, and defect control. Modeling techniques based on field theoretic simulations are used to both characterize and predict the morphological behavior of a variety of BCPs under a variety of processing conditions including solvent annealing and DSA under topographical boundary conditions. These methods aid experimental studies by saving time in performing experiments over wide parameter spaces as well as elucidating information that may not be available by current experimental techniques. Both forward simulation approaches are studied where parameters are varied over a wide range with phase diagrams of potential morphologies characterized and inverse design approaches where given target patterns are taken as simulation input and required conditions to produce those patterns are outputted from the simulation for experimental testing. The studies ultimately help identify the key control parameters in BCP DSA and enable a vast array of possible utility in the field.
by Adam Floyd Hannon.
Sc. D.
Ma, Shucong. "Subcomponent self-assembly of metal-organic supramolecular systems utilising synthesised organic ligands and metal templates." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608203.
Повний текст джерелаKhan, Siddique J. "Brownian dynamics study of the self-assembly of ligated gold nanoparticles and other colloidal systems." Diss., Kansas State University, 2012. http://hdl.handle.net/2097/13508.
Повний текст джерелаDepartment of Physics
Amit Chakrabarti
We carry out Brownian Dynamics Simulations to study the self-assembly of ligated gold nanoparticles for various ligand chain lengths. First, we develop a phenomenological model for an effective nanoparticle-nanoparticle pair potential by treating the ligands as flexible polymer chains. Besides van der Waals interactions, we incorporate both the free energy of mixing and elastic contributions from compression of the ligands in our effective pair potentials. The separation of the nanoparticles at the potential minimum compares well with experimental results of gold nanoparticle superlattice constants for various ligand lengths. Next, we use the calculated pair potentials as input to Brownian dynamics simulations for studying the formation of nanoparticle assembly in three dimensions. For dodecanethiol ligated nanoparticles in toluene, our model gives a relatively shallower well depth and the clusters formed after a temperature quench are compact in morphology. Simulation results for the kinetics of cluster growth in this case are compared with phase separations in binary mixtures. For decanethiol ligated nanoparticles, the model well depth is found to be deeper, and simulations show hybrid, fractal-like morphology for the clusters. Cluster morphology in this case shows a compact structure at short length scales and a fractal structure at large length scales. Growth kinetics for this deeper potential depth is compared with the diffusion-limited cluster-cluster aggregation (DLCA) model. We also did simulation studies of nanoparticle supercluster (NPSC) nucleation from a temperature quenched system. Induction periods are observed with times that yield a reasonable supercluster interfacial tension via classical nucleation theory (CNT). However, only the largest pre-nucleating clusters are dense and the cluster size can occasionally range greater than the critical size in the pre-nucleation regime until a cluster with low enough energy occurs, then nucleation ensues. Late in the nucleation process the clusters display a crystalline structure that is a random mix of fcc and hcp lattices and indistinguishable from a randomized icosahedra structure. Next, we present results from detailed three-dimensional Brownian dynamics simulations of the self-assembly process in quenched short-range attractive colloids. Clusters obtained in the simulations range from dense faceted crystals to fractal aggregates which show ramified morphology on large length scales but close-packed crystalline morphology on short length scales. For low volume fractions of the colloids, the morphology and crystal structure of a nucleating cluster are studied at various times after the quench. As the volume fraction of the colloids is increased, growth of clusters is controlled by cluster diffusion and cluster-cluster interactions. For shallower quenches and low volume fractions, clusters are compact and the growth-law exponent agrees well with Binder–Stauffer predictions and with recent experimental results. As the volume fraction is increased, clusters do not completely coalesce when they meet each other and the kinetics crosses over to diffusion-limited cluster-cluster aggregation (DLCA) limit. For deeper quenches, clusters are fractals even at low volume fractions and the growth kinetics asymptotically reaches the irreversible DLCA case.
Wang, Han. "Developing Novel Drug Delivery Systems For Platinum-based Anticancer Drugs Using Coordination-driven Self-assembly." Kent State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1595260147978142.
Повний текст джерелаShokri, Roozbeh [Verfasser], and Günter [Akademischer Betreuer] Reiter. "Self-Assembly of supra-molecular systems on graphene or graphite = Selbstorganisation von Supramolekularen Systemen auf Graphen oder Graphit." Freiburg : Universität, 2013. http://d-nb.info/1123475415/34.
Повний текст джерелаHaedler, Andreas T. [Verfasser], and Hans-Werner [Akademischer Betreuer] Schmidt. "Synthesis, Self-Assembly and Photophysical Properties of Multichromophoric Systems / Andreas T. Haedler. Betreuer: Hans-Werner Schmidt." Bayreuth : Universität Bayreuth, 2015. http://d-nb.info/1074461843/34.
Повний текст джерелаNicoll, Sarah Louise. "Covalently-linked self-assembling peptide-amphiphile hydrogels for cell scaffolding applications." Thesis, University of Aberdeen, 2012. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=186975.
Повний текст джерелаPerera, Uduwanage Gayani E. "STM Investigation of Charge-Transfer and Spintronic Molecular Systems." Ohio University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1300141817.
Повний текст джерелаPranger, Lawrence A. "Reactive molding and self-assembly techniques for controlling the interface and dispersion of the particulate phase in nanocomposites." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26551.
Повний текст джерелаCommittee Chair: Tannenbaum, Rina; Committee Member: Garmestani, Hamid; Committee Member: Jacob, Karl; Committee Member: Patterson, Tim; Committee Member: Singh, Preet. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Tison, Christopher Kirby. "Programmable, isothermal disassembly of DNA-linked colloidal particles." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/28189.
Повний текст джерелаCommittee Chair: Milam, Valeria; Committee Member: Boyan, Barbara; Committee Member: Li, Mo; Committee Member: McDevitt, Todd; Committee Member: Sandhage, Ken.
Nguyen, Duong Thuy. "Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc822738/.
Повний текст джерелаHurley, Margaret M. "Analysis of the dipolar lattice gas as a model for self-assembly in 1 and 2-dimensional systems /." The Ohio State University, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487780393265179.
Повний текст джерелаSommer, Samantha. "Hybrid Metal-Ligand Hydrogen-Bonded (MLHB) Architectures Based on the Quinolone Subunit: Understanding and Expanding the Accessible Space of Supramolecular Systems." Thesis, University of Oregon, 2015. http://hdl.handle.net/1794/19298.
Повний текст джерела10000-01-01