Дисертації з теми "Polymers brushes"
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Gunkel, Gesine. "Antibiofouling polymer brushes." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608096.
Повний текст джерелаUğur, Gökce. "Interface Structure of Diblock Copolymer Brushes and Surface Dynamics of Homopolymer Brushes and Bilayers of Untethered Chains on Brushes." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1311005794.
Повний текст джерелаFleet, Reda Ali. "Synthesis and characterization of glycopolymer brushes." Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/5132.
Повний текст джерелаWei, Yuan. "Probing Local Structure and Dynamics of Polymer Brushes with Neutron Scattering." Case Western Reserve University School of Graduate Studies / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1624963009022896.
Повний текст джерелаSun, Liang. "Structure and Dynamics of Swollen Polymer Brushes." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1499675793233755.
Повний текст джерелаKelby, Timothy Simon. "Smart brushes on flexible substrates : probing the chemomechanical properties of stimulus-responsive polymer brushes." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610331.
Повний текст джерелаConlin, Emma L. "Design and synthesis of liquid crystalline polymer brushes and hydrogen bonded polymers /." Available to subscribers only, 2005. http://proquest.umi.com/pqdweb?did=1079664771&sid=2&Fmt=2&clientId=1509&RQT=309&VName=PQD.
Повний текст джерелаPiaoran, Ye. "Synthesis of Polymers and Polymer Brushes through RAFT Polymerization via Flow Chemistry." Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1491229581133419.
Повний текст джерелаTan, Khooi Yeei. "Smart surfaces using responsive polymer brushes." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607743.
Повний текст джерелаYang, Fengyu. "Development of Polyacrylamide-Based Biomaterials in Hydrogels and Brushes." University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1555603442979042.
Повний текст джерелаConstable, Andrew N. "Functionalization of Silica Micro-capillaries and Silica Nanoparticles via Polymer Brushes." University of Akron / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=akron1221746490.
Повний текст джерелаChen, Xiaoping. "Synthesis and characterization of polymers incorporating N-alkyl urea-peptoid sequences." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1382951885.
Повний текст джерелаConstable, Andrew N. "Functionalization of silica micro-capillaries and silica nanoparticles via polymber brushes." Akron, OH : University of Akron, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=akron1221746490.
Повний текст джерела"December, 2008." Title from electronic dissertation title page (viewed 12/28/2008) Advisor, Roderic P. Quirk; Committee members, Scott Collins, Ali Dhinojwala, Li Jia, Mark D. Soucek; Department Chair, Ali Dhinojwala; Dean of the College, Stephen Z. D. Cheng; Dean of the Graduate School, George R. Newkome. Includes bibliographical references.
Beck, Catherine Keel. "Characterization of Spin Coated Polymers in Nano-environments as a Function of Film Thickness." Thesis, Virginia Tech, 2001. http://hdl.handle.net/10919/34548.
Повний текст джерелаMaster of Science
Bialas, Sabrina. "Lambda-orthogonal photoresists." Thesis, Queensland University of Technology, 2021. https://eprints.qut.edu.au/212724/1/Sabrina%20Bialas%20Thesis.pdf.
Повний текст джерелаSchollier, Audrey. "Probing protein adsorption modes onto poly(ethylene glycol) brushes by neutron reflection." Doctoral thesis, Universite Libre de Bruxelles, 2011. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209952.
Повний текст джерелаA clear understanding of the mechanism of protein adsorption onto polymer brushes is still missing. The first models describing the interactions of a polymer brush with adsorbing particles predicted two adsorption modes: primary adsorption at the grafting surface, and secondary adsorption at the outer edge of the brush (occurring for large cylindrical proteins). Primary adsorption can be repressed by increasing the grafting density of the brush, and secondary adsorption by increasing its thickness, in agreement with the experiments reported in the literature. But experimental evidences (a maximum in the adsorbed amount observed for long brushes) suggested then the existence of a third mode: ternary adsorption within the brush itself, due to attractive interactions between the protein and the brush. Standard techniques can in general only probe the total adsorbed amount. The aim of this work was to separate primary and ternary adsorption isotherms, by using neutron reflectivity and deuterated proteins. As neutrons interact differently with hydrogen and deuterium atoms, the contrast between the hydrogenated brush and the deuterated protein is high enough to separate the two contributions.
We studied the adsorption of deuterated myoglobin on PEG brushes with different degrees of polymerisation (N = 56, 146 and 770), and as a function of the area per grafted chain. The contribution of primary and ternary adsorption was separated for the different systems, and the adsorbed amount was extracted and the adsorption isotherms compared to the theoretical predictions. The ability to distinguish between the different adsorption modes, and the quantification of their relative contribution to the overall amount of adsorbed proteins, represents a major advance in optimising surface properties. In particular, the occurrence of ternary adsorption onto PEG brushes affects their status as tool for repressing protein adsorption.
L’adsorption de protéines aux interfaces a un rôle important pour certaines applications pharmaceutiques ou biotechnologiques. En effet, plusieurs processus indésirables sont liés à l’adsorption de protéines, par exemple l’encrassement de lentilles de contact, la coagulation dans des appareils contenant du sang, l’inflammation d’organes artificiels ou encore la diminution du temps de circulation dans le corps de protéines ou liposomes thérapeutiques. Certains polymères, tels que le polyéthylène glycol (PEG), sont utilisés pour réprimer l’adsorption de protéines :en greffant une brosse de PEG sur la surface, une couche est créée entre la protéine et celle-ci qui diminue, voire même réprime complètement l’adsorption. Comprendre le mécanisme qui entrave l’adsorption aux interfaces est un sujet de recherche actif, qui pourrait mener à des améliorations significatives dans la conception de biomatériaux.
À ce jour, la compréhension du mécanisme d’adsorption de protéines sur des brosses de polymère n’est pas claire. Les premiers modèles décrivant les interactions entre brosses de polymères et particules adsorbantes prédisaient deux modes d’adsorption :l’adsorption primaire sur la surface de greffage, et l’adsorption secondaire à l’extérieur de la brosse (pour les grandes protéines cylindriques uniquement). L’adsorption primaire peut-être réprimée en augmentant la densité de greffage de la brosse, et l’adsorption secondaire en augmentant son épaisseur, en accord avec les expériences reportées dans la littérature. Mais d’autres évidences expérimentales (un maximum dans la quantité adsorbée observé pour les brosses longues) ont ensuite suggéré l’existence d’un troisième mode :l’adsorption ternaire à l’intérieur même de la brosse, due aux interactions attractives entre la protéine et la brosse.
Les techniques standards peuvent en général mesurer la quantité adsorbée totale. Le but de ce travail était de séparer les isothermes d’adsorption primaire et ternaire, en utilisant la réflectivité de neutrons et des protéines deutérées. Comme les neutrons interagissent différemment avec les atomes d’hydrogène ou de deutérium, le contraste entre la brosse hydrogénée et la protéine deutérée est ainsi suffisant pour séparer les deux contributions.
Nous avons étudié l’adsorption de myoglobine deutérée sur des brosses de PEG avec différents degrés de polymérisation (N = 56, 146 and 770), en fonction de l’aire par chaîne Σ. La contribution des adsorptions primaire et ternaire put être séparée pour les différents systèmes, et les quantités adsorbées extraites pour finalement comparer les isothermes d’adsorption aux prédictions théoriques. La possibilité de distinguer les différents modes d’adsorption, et la quantification de leur contribution relative à la quantité totale de protéines adsorbées représente une avancée majeure dans l’optimisation des propriétés des surfaces. L’adsorption ternaire dans les brosses de PEG en particulier remet en question leur utilisation pour réprimer l’adsorption de protéines.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Lankshear, Ethan Robert. "Covalently anchored polymerisation initiator monolayers for polymer brush growth." Thesis, University of Canterbury. Chemistry, 2015. http://hdl.handle.net/10092/10415.
Повний текст джерелаRaynor, Jenny E. "Surface modification of titanium substrates with polymer brushes to control cell adhesion for bioapplications." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26653.
Повний текст джерелаCommittee Chair: Collard, David M.; Committee Co-Chair: Garcia, Andres J.; Committee Member: France, Stefan; Committee Member: Ragauskas, Arthur; Committee Member: Temenoff, Johnna. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Schellkopf, Leonard. "Investigation of Polymer Systems in Solutions with Electron Microscopy and Scattering Methods." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-167948.
Повний текст джерелаHamelinck, Paul Johan. "Functional surface-initiated polymers : device applications and polymerization techniques." Thesis, University of Cambridge, 2008. https://www.repository.cam.ac.uk/handle/1810/270327.
Повний текст джерелаChen, Hong. "Development of multi-functional polymeric biomaterials." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1490706379312092.
Повний текст джерелаRodriguez, Loureiro Ignacio [Verfasser], Emanuel [Akademischer Betreuer] Schneck, Svetlana [Gutachter] Santer, and Olivier [Gutachter] Diat. "Structural characterization of single and interacting soft interfaces displaying brushes of synthetic or biomolecular polymers / Ignacio Rodriguez Loureiro ; Gutachter: Svetlana Santer, Olivier Diat ; Betreuer: Emanuel Schneck." Potsdam : Universität Potsdam, 2018. http://d-nb.info/121840440X/34.
Повний текст джерелаEdmondson, S. "Functional polymer brushes." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.598765.
Повний текст джерелаChen, Tao, Ihsan Amin, and Rainer Jordan. "Patterned polymer brushes." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-138928.
Повний текст джерелаDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
Chen, Tao, Ihsan Amin, and Rainer Jordan. "Patterned polymer brushes." Royal Society of Chemistry, 2012. https://tud.qucosa.de/id/qucosa%3A27793.
Повний текст джерелаDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
Mirous, Brian K. "SYNTHESIS AND PRESUMPTIVE CROSSLINKING OF STIMULI-RESPONSIVE DIBLOCK POLYMER BRUSHES." University of Akron / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=akron1144783034.
Повний текст джерелаScheibelein, Christoph [Verfasser]. "Mechanical Activation of Polymer Brushes and the Evolution of Stable Brush Architectures / Christoph Scheibelein." München : Verlag Dr. Hut, 2018. http://d-nb.info/1168535026/34.
Повний текст джерелаKönig, Meike. "Functional Coatings with Polymer Brushes." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-126365.
Повний текст джерелаRoderick, Christopher. "Stability analysis of polymer brushes." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85644.
Повний текст джерелаRomeis, Dirk. "Conformational Transitions in Polymer Brushes." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-139354.
Повний текст джерелаNkoua, Ngavouka Maryse Dadina. "Conformational properties of variable density DNA nanobrushes." Doctoral thesis, Università degli studi di Trieste, 2015. http://hdl.handle.net/10077/11129.
Повний текст джерелаAdvanced nanotechnologies allow the manipulation of molecules with nanoscale precision, and can be used for the production of sensitive devices for protein or nucleic acids detection for clinical use. DNA nano-assemblies are an excellent route for ultrasensitive DNA/RNA detection and for DNA-protein conjugated immobilization, for bio interaction studies, through the careful detection of single strand DNA (ssDNA) hybridization with complementary target sequences. For DNA nanoscale devices, the control of DNA surface density and conformation is crucial in order to achieve the highest reproducibility and to optimize the sensitivity. An improved understanding of the chemical and physical properties of the nanoscale DNA assemblies and of the recognition process is necessary for device performance optimization. In this framework, we first focused on the understanding of the mechanisms that optimize and limit hybridization efficiency in variable density DNA monolayers. We performed Atomic Force Microscopy (AFM) assisted-Nanografting and AFM measurements to realize reference patches into a DNA self-assembled monolayer, and to carefully monitoring DNA hybridization. We then performed molecular dynamics (MD) simulations, in collaboration with a theoretical group, to capture the energetic hybridization limit in high dense DNA monolayers. We found that no more than 44% of the substrate ssDNA can be successfully hybridized, limited by molecular and electrostatic crowding effect connected to the highly charged nature of DNA. To further capture the conformational properties of DNA monolayers, and their relation to biorecognition, we characterized the ionic strength effect on ssDNA nano-assembled of different density by careful AFM topography measurements in liquid environment. We confined ssDNA brushes with controlled surface densities within a bio-repellent self-assembled monolayer. We then monitored the topographic brush height variation upon changing salt type (NaCl, KCl, CaCl2 and MgCl2 ) and concentration inside the liquid cell. We showed that the measured height is related to scaling law of salt concentration, in agreement with the theory of polyelectrolyte brush. Using this scaling model to fit our experimental data, we quantified structural parameters such as the average internucleotide distance (d) for ssDNA brushes of different, estimated surface density σ, featuring a strong dependence of d on different salts species. This result is crucial for the structural designing of synthetic nucleic acids and, more generally, nucleic acid-based devices with controlled physical behaviors. In the last part of the work, we apply all knowledge learned on hybridization mechanism to a clinical problem. We studied the hybridization mechanism to distinguish single base mismatch and to detect at high sensitivity, without any labeling and amplification, microRNAs (miRNAs) connected to hearth failure disease. Our results demonstrate that the AFM nanolithography can serve as a sensitive and selective readout system to discriminate single nucleotide polymorphism. Also, our device allows for the detection of more than one sequence of miRNAs on a same assay with target in picomolar (100pM) range concentration.
I recenti sviluppi delle nanotecnologie permettono di manipolare singole molecole con precisione nanometrica, e possono essere utilizzati per la produzione di dispositivi innovativi ad alta sensitivita` per la rivelazione di proteine e acidi nucleici, per usi clinici. Nanostrutture di DNA a singolo filamento rappresentano una eccellente soluzione per la rivelazione ultrasensibile di frammenti di DNA/RNA e per l’immobilizzazione di coniugati DNA-proteina per studi di bioriconoscimento, attaverso lo studio dell’ibridazione del DNA con le sequenze target complementari. Nello sviluppo di dipositivi alle nanoscale basati sul DNA, il controllo di parametri quali la densita` di superficie e la conformazione del DNA, risulta cruciale per raggiungere gli alti livelli di riproducibilita` richiesti e per ottimizzare la sensitivita`. Studiare e capire in dettaglio le proprieta` chimico -fisiche di strutture alle nanoscale di DNA a singolo filamento, e del relativo processo di bioriconoscimento risulta quindi fondamentale per ottimizzare le prestazioni del dispositivo associato. In questo contesto, ci siamo dapprima focalizzati sullo studio dei meccanismi che ottimizzano e limitano l’efficienza di ibridazione in monolayer di DNA. Usando il microscopio a forza atomica (AFM) e una tecnica di nanolitografia basata sull’AFM, il nanografting, abbiamo costruito delle nanostrutture di riferimento in film di DNA autoassemblati, ad alta densita`, ed abbiamo accuratamente monitorato con l’AFM e con simulazioni di dinamica molecolare, il limite di ibridazione in tali film. In collaborazione con un gruppo di fisici teorici, abbiamo trovato un limite di ibridazione pari a circa il 44% delle sequenze probe, collegandolo a effetti di repulsione elettrostatica dovuta all’ alta densita` a di carica nei monolayer di DNA, un polielettrolita altamente carico in soluzione. In un secondo tempo, per cogliere le proprieta` conformazionali dei monolayer di DNA, e la loro relazione con la capacita` di bioriconoscimento, abbiamo creato delle nanostrutture di DNA a singolo filamento, a densit variabile, in un monostrato autoassemblato di molecole bio-repellenti, e caratterizzato l’effetto della forza ionica della soluzione a mezzo di misure topografiche fatte con l’ AFM, in liquido. Da misure di variazione dell’ altezza topografica delle nanostrutture di DNA in funzione dei diversi sali usati in soluzione (NaCl, KCl, CaCl2 and MgCl2 ) e della loro concentrazione, abbiamo dimostrato che, per ogni sale, l’ altezza` legata alla concentrazione da una legge di scala, in accordo con la teoria dei polyelectrolyte brush. Utilizzando questa legge di scala, abbiamo fatto un fit dei dati sperimentali, quantificando un importante parametro strutturale, la distanza media tra nucleotidi nel filamento (d), per nanostrutture di DNA con divesra densita`, anch’essa stimata dal nostro fit. Questo risultato e` fondamentale per il disegno di acidi nucleici sintetici e piu` in generale per la progettazione di dispositivi miniaturizzati per la rivelazione di acidi nucleici. Nella parte finale di questo lavoro di tesi, abbiamo applicato le conoscenze acquisite sui meccanismi di ibridazione del DNA su scale nanometriche, per realizzare dispositivi utili a scopi clinici. Abbiamo studiato il meccanismo di ibridazione per distinguere un mismatch tra due filamenti complementari di DNA relativo a una singola base e alla rivelazione di micro-RNA, biomarcatori rilevanti per monitorare specifiche malattie quali, nel presente caso, malattie cardiovascolari. Abbiamo dimostrato che i nostri nanodispositivi dimostrano un’ottima risoluzione (100 pM o meglio) e che possono essere utilizzati senza bisogno di amplificazione del materiale genetico originale, o di altre modificazioni, in estratti provenienti da plasmi umani. Queste piattaforme possono essere ulteriormente sviluppate per il monitoraggio di polimorfismi di singolo nucleotide, estremamente rilevanti dal punto di vista clinico
XXVII Ciclo
1986
Soga, K. Geoffrey (Kenneth Geoffrey). "Equilibrium phase separation in polymer brushes." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=40445.
Повний текст джерелаNawroth, Jonas F., Claudia Neisser, Artur Erbe, and Rainer Jordan. "Nanopatterned polymer brushes by reactive writing." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-214281.
Повний текст джерелаNawroth, Jonas F., Claudia Neisser, Artur Erbe, and Rainer Jordan. "Nanopatterned polymer brushes by reactive writing." Royal Society of Chemistry, 2016. https://tud.qucosa.de/id/qucosa%3A29980.
Повний текст джерелаLee, Thomas. "Tunable nanopatterns formed by polymer brushes." Thesis, The University of Sydney, 2013. http://hdl.handle.net/2123/10519.
Повний текст джерелаKalan, Steven V. "Surface Modification of Silicon Through Thermal Annealing and Rinsing of Solvent Cast Polystyrene Films." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1316651768.
Повний текст джерелаJia, Haidong. "Polymer brushes at nanoparticle and planar interfaces." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526480.
Повний текст джерелаOren, Ron. "Probing the internal structure of polymer brushes." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611682.
Повний текст джерелаGaluschko, André. "Molecular dynamics simulations of sheared polymer brushes." Strasbourg, 2010. https://publication-theses.unistra.fr/public/theses_doctorat/2010/GALUSCHKO_Andre_2010.pdf.
Повний текст джерелаBisen, Milind Dhaniram. "Synthesis and Characterization of Siloles, Silole-Containing Polymers and Photoswitchable Polymer Brush." OpenSIUC, 2015. https://opensiuc.lib.siu.edu/dissertations/990.
Повний текст джерелаKhanduyeva, Natalya. "Conjugated Polymer Brushes (Poly(3-hexylthiophene) brushes): new electro- and photo-active molecular architectures." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1232556562686-70575.
Повний текст джерелаKhanduyeva, Natalya. "Conjugated Polymer Brushes (Poly(3-hexylthiophene) brushes): new electro- and photo-active molecular architectures." Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A23635.
Повний текст джерелаWilshaw, Claire Tamsin. "Directed phase separation of polymer blends on binary-patterned polymer brushes." Thesis, University of Sheffield, 2009. http://etheses.whiterose.ac.uk/573/.
Повний текст джерелаVan, Velzen Vera. "Enhancing the functionality of hydrogels using molecular polymer brushes." Thesis, Queensland University of Technology, 2021. https://eprints.qut.edu.au/226153/1/Vera_Van%20Velzen_Thesis.pdf.
Повний текст джерелаGupta, Smrati. "Immobilization of Inorganic Nanoparticles on Responsive Polymer Brushes." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2008. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1222086844714-55891.
Повний текст джерелаChen, Meng. "Synthesis and properties of surface-grown polymer brushes." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443606.
Повний текст джерелаRigby, Matthew. "A friction study of densely grafted polymer brushes." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123065.
Повний текст джерелаLa présente thèse aborde le développement d'une nouvelle méthode pour les mesures de friction à l'aide d'un microscope à force atomique. Elle est comparée à la méthode standard pour vérification. Cette nouvelle méthode est utilisée afin d'investiguer les propriétés dans le régime de la limite de lubrification d'un nouvel échantillon de brosse de polymères à très haute densité. Aucune corrélation n'a été trouvé entre le coefficient de friction et le pH ou la concentration de sel du fluide environnant. Le coefficient de friction mesuré est de l'ordre de 0.1.
Pelras, Theophile Werner Louis. "Nanostructured Soft Matter from Compartmentalised Molecular Polymer Brushes." Thesis, The University of Sydney, 2019. http://hdl.handle.net/2123/21150.
Повний текст джерелаWu, Zhenghao. "Investigating the Effects of Grafting and Chain Stiffness on Nanoconfined Polymers from Molecular Dynamics Simulation." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1525861929889197.
Повний текст джерелаPardo-Figuerez, Maria M. "Designing neuronal networks with chemically modified substrates : an improved approach to conventional in vitro neural systems." Thesis, Loughborough University, 2018. https://dspace.lboro.ac.uk/2134/27941.
Повний текст джерела