Dissertations / Theses: 'Polymer Metal Composite'

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Mokhtari, Morgane. "FeCr composites : from metal/metal to metal/polymer via micro/nano metallic foam, exploitation of liquid metal dealloying process." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSEI088/document.

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Les métaux micro ou nanoporeux sont très attrayants notamment pour leur grande surface spécifique. Le désalliage dans un bain de métal liquide permet une dissolution sélective d'une espèce chimique (l'élément soluble) à partir d'un alliage d'origine (le précurseur) composé de l'élément soluble et d'un élément cible (qui deviendra nano/micro poreux) non soluble dans le bain de métal liquide. Quand le précurseur est plongé dans le bain de métal liquide, à son contact, l'élément soluble va se dissoudre dans le bain tandis que l'élément cible va en parallèle se réorganiser spontanément afin de former une structure poreuse. Quand l'échantillon est retiré du bain, il est sous la forme d'une structure bi-continue composée de deux phases : l'une étant la structure poreuse composée de l'élément cible et l'autre est une phase dans laquelle est présente l'élément du bain avec l'élément sacrificiel en solution solide. Cette phase peut être dissoute par une attaque chimique afin d’obtenir le métal nano/micro poreux. Les objectifs principaux de cette thèse sont l'élaboration et la caractérisation microstructurale et mécanique de 3 différents types de matériaux par désalliage dans un bain de métal liquide : des composites métal-métal (FeCr-Mg), des métaux poreux (FeCr) et des composites métal-polymère (FeCr-matrice époxy). Le dernier objectif est l'évaluation des possibilités d'utiliser la technique de désalliage dans un bain de métal liquide dans un contexte industriel. L'étude de la microstructure est basée sur des observations 3D faites par tomographie aux rayons X et des analyses 2D réalisées en microscopie électronique (SEM, EDX, EBSD). Pour mieux comprendre le désalliage, le procédé a été suivi in situ en tomographie aux rayons X et diffraction. Enfin, les propriétés mécaniques ont été évaluées par nanoindentation et compression
Nanoporous metals have attracted considerable attention for their excellent functional properties. The first developed technique used to prepare such nanoporous noble metals is dealloying in aqueous solution. Porous structures with less noble metals such as Ti or Fe are highly desired for various applications including energy-harvesting devices. The less noble metals, unstable in aqueous solution, are oxidized immediately when they contact water at a given potential so aqueous dealloying is only possible for noble metals. To overcome this limitation, a new dealloying method using a metallic melt instead of aqueous solution was developed. Liquid metal dealloying is a selective dissolution phenomenon of a mono-phase alloy solid precursor: one component (referred as soluble component) being soluble in the metallic melt while the other (referred as targeted component) is not. When the solid precursor contacts the metallic melt, only atoms of the soluble component dissolve into the melt inducing a spontaneously organized bi-continuous structure (targeted+sacrificial phases), at a microstructure level. This sacrificial phase can finally be removed by chemical etching to obtain the final nanoporous materials. Because this is a water-free process, it has enabled the preparation of nanoporous structures in less noble metals such as Ti, Si, Fe, Nb, Co and Cr. The objectives of this study are the fabrication and the microstructure and mechanical characterization of 3 different types of materials by dealloying process : (i) metal/metal composites (FeCr-Mg), (ii) porous metal (FeCr) (iii) metal/polymer composites (FeCr-epoxy resin). The last objective is the evaluation of the possibilities to apply liquid metal dealloying in an industrial context. The microstructure study was based on 3D observation by X-ray tomography and 2D analysis with electron microscopy (SEM, SEM-EDX, SEM-EBSD). To have a better understanding of the dealloying, the process was followed in situ by X-ray tomography and X-ray diffraction. Finally the mechanical properties were evaluated by nanoindentation and compression

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Bhat, Nikhil Dilip. "Modeling and precision control of ionic polymer metal composite." Thesis, Texas A&M University, 2003. http://hdl.handle.net/1969.1/1152.

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This thesis describes the open-loop behavior of an ionic polymer metal composite (IPMC) strip as a novel actuator, the empirical force and position models, the control system and the improved dynamic characteristics with the feedback control implemented. Ionic polymer metal composite is a novel polymer in the class of electroactive polymers. IPMC consists of a base polymer coated with electrodes made up of highly conducting pure metals such as gold. The actuation behavior of IPMC can be attributed to the bending of an IPMC strip upon application of voltage across its thickness. The main reasons for the bending are ion migration on the application of voltage and swelling and contraction caused by water content. An experimental setup to study the open-loop force and tip displacement of an IPMC strip in a cantilever configuration was developed, and real time controllers were implemented. In open loop, the force response of the IPMC strip of dimensions 25 mm x 3.9 mm x 0.16 mm to a 1.2-V step input is studied. The open-loop rise time was 0.08 s and the percent overshoot was 131.62 %, while the settling time was about 10 s. Based on this open-loop step response using a least-square curve-fitting methodology, a fourth-order empirical transfer function from the voltage input to the force output was derived. The tip displacement response of an IPMC strip of dimensions 23 mm x 3.96 mm x 0.16 mm to a 1.2-V step input was also studied. The step response exhibited a 205.34 % overshoot with a rise time of 0.08 s, and the settling time was 27 s. A fourth-order empirical transfer function from the step input to the tip displacement as output was also derived. Based on the derived transfer functions lead-lag feedback controllers were designed for precision control of both force and displacement. The control objectives were to decrease the settling time and the percent overshoot, and achieve reference input tracking. After implementing the controllers, the percent overshoot decreased to 30% while the settling time was reduced to 1.5 s in case of force control. With position control, the settling time was reduced to 1 s while the percent overshoot decreased to 20%. Precision micro-scale force and position-control capabilities of the IPMC were also demonstrated. A 4 ?N force resolution was achieved, with a force noise of 0.904-?N rms. The position resolution was 20 ?m with a position noise of 7.6-?m rms.

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Yusuf, Suhaila Mohamad. "Development of an ionic polymer metal composite (IPMC) microgripper." Thesis, University of Leeds, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550855.

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Ionic Polymer Metal Composite (IPMC) is a class of electroactive polymer , that is receiving great attention due to its advantages of large bending deflection, low power consumption and driving voltage. Although there is still no commercial application of IPMC, it has been actively investigated by researchers for the past decade. The IPMC has been identified as a potential material to be used in the specific application of sensor and/or actuation, such as microgripper and micropump. This research deals with the characterisation of small scale IPMC with the ultimate objective to develop a simple microgripper to demonstrate the ability of the IPMC to grasp a micro object. A vision system has been developed to perform image processing to measure the displacement of IPMC. New algorithms of edge detection and displacement measurement have been introduced to characterise the IPMC. Comparison between laser sensor measurements and vision systems measurement has been carried out and the results showed that the vision system is a reliable measurement. Characterisation of small scale IPMC is carried out to prove the claim that miniaturization of IPMC is possible without degrading its performance. The characterisation of the IPMC actuator is divided into two major works - the displacement and blocked force measurements. The results showed that small scale characteristics are in line with the results that have been published by other researchers for larger scale of IPMC, hence supported the claim. The dynamic sensory behaviour of the IPMC has also been characterised. The results showed that the sensor functions are better in terms of producing consistent output signals when it is dehydrated. With such finding, the possibility of using the IPMC as the actuator and sensor at the same time for micro gripper application is not promising because the actuator needs to be fully hydrated in order to work better while the sensor is working better in a dehydrated condition. The final part in this research work is to develop a simple micro gripper. A two-finger microgripper with size of lOmm x 2rnrn x O.2mm is controlled by a vision feedback system to grasp small objects. For a demonstration purposes, an object with diameter of lmm was successfully grasped in 4.6 seconds.

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Anyaogu, Kelechi C. "Stabilized metal nanoparticle-polymer composites preparation, characterization and potential applications /." Bowling Green, Ohio : Bowling Green State University, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=bgsu1222126708.

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Graham, Adam. "Electrical properties and vapour sensing characteristics of a novel metal-polymer composite." Thesis, Durham University, 2008. http://etheses.dur.ac.uk/2376/.

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Quantum Tunnelling Composite (QTC) is a metal polymer composite, commercialised and produced using a patented manufacture process. This process ensures that the metal particles within an elastomerie polymer matrix maintain a highly fractal surface morphology where nano-scale point features are retained on the particles and are coated in polymer. This structure provides unique electronic behaviour including very high resistivity, of order 10 ΜΩ, above the expected percolation threshold and an exponential increase in conductivity under all types of mechanical deformation. Increase in sample compression leads to a lower electrical resistance through the material. Current-voltage characteristics show a hysteresis effect due to current storage in the QTC material as a current is passed. The hysteresis is shown to be reduced as the applied compression on the material is increased until an Ohmic regime is reached at very high compressions, above 70% linear compression. At these high compressions Joule heating is also proven to occur as a result of the power dissipated in the sample by I-V cycling. The Joule heating is sufficient to influence the physical characteristics of the sample and expand it, creating a current limiting device. QTC samples loaded with acicular electro-conductive particles in small fractions, less than 10% by weight, showed less sensitivity to applied compression in terms of electrical response. These samples appear to exhibit less white noise characteristics and indicate a combination of field assisted quantum tunnelling and percolation mechanism, Intrinsically conductive QTC samples were developed. These were made using QTC granules mixed into a polymer solvent solution. Upon depositing onto electrodes the solvent was allowed to evaporate leaving the constituent polymer binding the QTC granules together, compressing them into a conductive state. Samples were exposed to volatile organic compound (VOC) vapours in the concentration range 10 ppm to 100,000 ppm, causing swelling and void filling in the binding polymer. Combinations of these processes caused an increase in sample resistance, from ~50 Ω to excess of 10 ΜΩ. Sample composition and physical parameters have significant effect upon the response characteristics of the sensors. A system of experiments was undertaken and optimum sample composition was determined. Response to environmental changes were investigated^ namely temperature response and response to varying concentration of exposed solvent. It was found that samples produced using Polyphenylene Oxide ( PPO) and Polyvinyl Chloride (PVC) based binding polymer were more resistant to temperature change from 30 С to 80 С due to their molecular structures. Sensor response to different vapour concentrations was found to exhibit two distinct response regimes. High concentration exposures were found to exhibit a swelling mechanism with a CASE-II diffusion model fitting the data well. Whereas at low concentrations a void-filling based change in sample dielectric constant was attributed to the electronic response to vapour exposure. These predictions were also confirmed using a Quartz Crystal Microbalance (QCM) to measure mass uptake of vapour molecules and polymer density under similar test conditions.

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Skinner, Anna Penn. "Ion Conducting Polyelectrolytes in Conductive Network Composites and Humidity Sensing Applications for Ionic Polymer-Metal Composite Actuators." Thesis, Virginia Tech, 2016. http://hdl.handle.net/10919/71683.

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Ionic polymer-metal composites (IPMCs) are widely studied for their potential as electromechanical sensors and actuators. Bending of the IMPC depends on internal ion motion under an electric potential, and the addition of an ionic liquid and ionic self-assembled multilayer (ISAM) conductive network composite (CNC) strongly enhances bending and improves lifetime. Ion conducting polyelectrolytes poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPS) and Nafion® were incorporated into an ISAM CNC film with poly(allylamine hydrochloride) (PAH) and anionic gold nanoparticles actuators to further improve bending. CNC films were optimized for bending through pH adjustments in PAH and adding NaCl to the PAMPS and Nafion® solutions. PAMPS-containing actuators showed larger and faster bending than those containing Nafion® in the CNC. The IPMC actuator was also evaluated for its potential as a humidity sensor based on its relative humidity (RH) dependent steady-state current. The detection range is at least 10-80%RH, with 5%RH increment differentiation and likely better resolution. Effects of CNC presence and thickness were studied, in conjunction with ionic liquid at a range of RH values. A thin CNC (pH 4 PAH) produced the greatest current differentiation between RH values. The current's response speed to a large RH decrease was approximately 4 times faster than that of a fast commercial digital hygrometer. Additionally, the presence of a CNC and ionic liquid improved the current response time. These results indicate that an IPMC based humidity sensor using a CNC and ionic liquid is very promising and merits further study.
Master of Science

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Sun, Weizhen. "Microstructure-based FE Modeling and Measurements of Magnetic Properties of Polymer Matrix-Metal Composites." Thesis, Virginia Tech, 2017. http://hdl.handle.net/10919/74946.

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An increasing need for smaller, higher-power-density devices is driving the development of more advanced topologies for use in power architectures. The challenge, however, is to reduce the size of the passive components in circuit boards (e.g., the inductors), which are typically the most bulky. There are two ways to approach this problem. The first is to redesign the flux in the inductor in order to minimize its size; the second is to optimize the magnetic properties of the constituent magnetic materials, which include permeability, density, resistivity, core loss density, saturation magnetization value, fluidity, sintering temperature, and others. Compared to altering the nature of solid magnetic materials to reduce space constraints, modifying the magnetic composite is preferred. The most popular candidates for use in magnetic composites are magnetic powders and polymer composites. In particular, when metal alloys are chosen as magnetic powders they have high initial permeability, high saturation magnetization values, but low electrical resistivity. Since polymers can serve as insulation materials, mixing metal alloys with polymers will increase electrical resistivity. The most common metal alloy used is nickel-iron (permalloy) and Metglas. Since existing modeling methods are limited in (a) that multiphasic composites cannot be utilized and (b) the volume fraction of magnetic particles must be low, this investigation was designed to utilize FE (finite element) simulation to analyze how magnetic properties change with the distribution of permalloy powder or Metglas flakes in composites. The primary magnetic properties of interest in this study are permeability and core loss density. Furthermore two kinds of magnetic composites were utilized in this investigation: a benzocyclobutene (BCB) matrix-permalloy and a benzocyclobutene (BCB) matrix-permalloy-based amorphous alloy (Metglas 2705M) material. In our FE simulations, a BCB matrix-permalloy composite was utilized in a body-centered cubic model with half-diameter smaller particles serving as padding. The composite was placed in a uniform magnetic field surrounded by a material whose relative permeability was equal to zero in simulation. In comparison to experimental results, our model was able to predict permeability of composites with volume fraction higher than 52%. It must be noted, however, that although our model was able to predict permeability with only 10% off, it was less effective with respect to core loss density findings. The FE model also showed that permeability will increase with an increasing volume fraction of magnetic particles in the composite. To modify the properties of the composite material, the model of the BCB matrix-permalloy-Metglas composite followed model simulations up to the point at which flakes were inserted in BCB matrix-permalloy composite. The thickness of flakes was found to be an important factor in influencing resulting magnetic properties. Specifically, when the thickness of flakes decreased to quarter size at the same volume fraction, the permeability increased by 15%, while core loss density decreased to a quarter of the original value. The analysis described herein of the important relationship between magnetic properties and the composites is expected to aid in the development and design of new magnetic composite materials.
Master of Science

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Hands, Philip James Walton. "Vapour sensing applications and electrical conduction mechanisms of a novel metal-polymer composite." Thesis, Durham University, 2003. http://etheses.dur.ac.uk/4084/.

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A novel metal-polymer composite is presented, comprised of a micron-sized nickel powder dispersed within a silicone polymer matrix. The composite is intrinsically electrically insulating, but displays a dramatic increase in conductivity under compression, tension and torsion. The electrical response to applied compression is characterised. Combined with electron microscopy, the large sensitivity to compression is shown to be due to the uniquely spiky morphology of the filler particles. Low mechanical energy mixing techniques are essential for retaining these sharp tips. In addition, wetting of the nickel particles by the silicone polymer is highly effective, resulting in negligible inter-particle contact between metallic grains even at very high loadings and compressions. Current-voltage characteristics are highly non-linear, displaying peaks, hysteresis, negative differential resistance, trap-filling and radio frequency emission. Evidence points towards an inter-particle conduction mechanism dominated by field emission and Fowler-Nordheim tunnelling, made possible by localised field enhancements at the sharp tips. A novel mechanism of grain charging and the 'pinching-off of conduction pathways is also suggested. Granular forms of the composite display dramatic increases in resistance when exposed to organic solvent vapours, transduced by a polymer swelling mechanism. Responses are dependent upon vapour concentration, and differential responses are obtained with other polymers, indicating excellent potential for applications in artificial olfactory devices (electronic noses). Polymer-solvent interactions follow both Fickian and anomalous diffusion characteristics, and follow basic trends predicted by solubility parameters.

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Jadhav, Niteen. "Novel Conducting Polymer Containing Composite Coatings for the Corrosion Protection of Metal Alloys." Diss., North Dakota State University, 2013. https://hdl.handle.net/10365/27037.

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Corrosion is a persistent problem faced by manmade structures made up of metal alloys. Aluminum 2024-T3 is high strength, light weight alloy used in aerospace applications. It suffers from the problem of corrosion due to its composition. Cold rolled steel is employed in structural applications but undergoes severe corrosion when exposed to corrosive conditions. Coatings are one of the best avenues to protect metal alloys from the corrosion. Traditional coating systems such as barrier type coatings, metal rich coatings, and inhibitor containing coatings have their own drawbacks. Conducting polymers (CPs), such as polypyrrole (PPy) can be used for the corrosion protection of the metals. Redox activity in conjunction with corrosion inhibiting ion release ability make CPs as a promising candidate for the replacement for hexavalent chromates. However CPs porous nature, inherent insolubility, stiff chains, and poor mechanical properties pose significant hindrance towards their implementation in coatings. In order to overcome the problems associated with the CPs and to extract maximum functionality out of them, conducting polymer containing composites (CPCC) were developed. CPCC combines CPs with inorganic pigments in unique ways and pave for excellent properties. In this work, series of composites of PPy/Inorganic pigments (aluminum flakes, iron oxide, micaceous iron oxide, and titanium dioxide) were synthesized by ecofriendly, facile chemical oxidative polymerization. Core and shell morphologies of PPy with titanium dioxide and iron oxide were synthesized and employed for the corrosion protection of cold rolled steel substrate. Various dopants such as phosphate, nitrate, molybdate, vanadate, and tungstate were incorporated in the backbone of PPy. These composites were characterized for morphology, elemental composition, and conductivity by various techniques. Furthermore coatings based on these composite pigments were formulated on Aluminum 2024-T3 and cold rolled steel substrates. These coatings were exposed to salt spray and prohesion test conditions and electrochemically evaluated against corrosion by Electrochemical Impedance Spectroscopy (EIS), DC Polarization, galvanic coupling and Scanning Vibrating Electrode Technique (SVET). Effect of solvent in the composite synthesis and PPy morphology in the final composite on the protective properties of coating was investigated. Effect of corrosion inhibiting anions on the final performance properties was also evaluated.
U.S. Army Research Laboratory (Grant No. W911NF-09-2-0014, W911NF-10-2-0082, and W911NF-11-2-0027)

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Seo, Geon S. "Time evolution of current and displacement of ion-exchange polymer/metal composite actuators." Diss., The University of Arizona, 2004. http://hdl.handle.net/10150/280748.

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This dissertation describes the development of a coupled model for the analysis of a novel polymer/metal composite (IPMC) actuator under large external voltage. A general continuum model describing the transport and deformation processes of solid polymer electrolyte is proposed. The formulation is based on global integral postulates for the mass conservation, charge conservation, momentum equilibrium, the first law of thermodynamics, and the second law of thermodynamics. The global equations are localized in the volume and on the material surfaces bounding the polymer. The model is simplified to a three-component system comprised of a fixed negatively charged polymeric matrix, protons, and free water molecules within the polymer matrix. Among these species, water molecules are considered as the dominant specie responsible for the deformation of the IPMC actuators. In this work, the electrochemical process occurring at both electrodes is analyzed as boundary conditions during the deformation of actuator in the regime of large voltage (over 1.2 V). These are used in the framework of overpotential theory to develop boundary conditions for the water transport in the bulk of polymer. The proposed coupled model successfully captures the stress relaxation phenomenon due to water redistribution governed by diffusion. The fabrication process are described, and experiments including the role of initial water content on the electro-mechanical response of the actuator are also discussed. Comparison of simulations and experimental data showed good agreement.

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Ji, Yijie. "Metal Organic Frameworks Derived Nickel Sulfide/Graphene Composite for Lithium-Sulfur Batteries." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron152233332526446.

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Bhaskar, A. "Design and synthesis of metal organic framework (MOF) - polymer composite membranes for gas separation." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2015. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2063.

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Tiwari, Rashi. "Modeling and characterization of the mechanoelectric response of ionic polymer metal composite (IPMC) energy harvesters." abstract and full text PDF (UNR users only), 2009. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3387826.

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Kaleli, Kadir. "Nano Structural Metal Composites: Synthesis, Structural And Thermal Characterization." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/12609674/index.pdf.

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In this work , metal functional polymers, namely Cr-PS-b-P2VP, Co-PS-b-P2VP, Au-PS-b-P2VP, Fe-PS-b-P2VP and Mo-PS-b-P2VP were prepared by thermal reaction of hexacarbonylchromium, Cr(CO)6, octacarbonyldicobalt,Co2(CO)8, hydrogentetrachloroaurate(III), H(AuCl4).4H2O, trichloroiron(III), FeCl3.6H2O, molybdenum(VI)oxide, MoO3 and PS-b-P2VP. TEM images indicated formation of AuIII, Cr and Co nanoparticles. On the other hand, crystalline structures were detected for Fe-PS-b-P2VP and Mo-PS-b-P2VP. Samples involving nanoparticles were further characterized by FTIR, UV-Vis and direct pyrolysis mass spectroscopy techniques. FTIR analysis indicated dissapearance of characteristic carbonyl peaks of Cr(CO)6 and Co2(CO)8 for Cr-PS-b-P2VP and Co-PS-b-P2VP samples. The appearance of a peak at about 467 cm-1 supported the formation of metal-nitrogen bond. Pyrolysis mass spectrometry analysis showed an increase in the thermal stability of P2VP chains involving coordinated pyridine units. The thermal stability of these chains increased in the order Co<
Cr <
Au3+ indicating stronger coordination in the same order.

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Francart, Charles. "Experimental and numerical study of the mechanical behavior of metal/polymer multilayer composite for ballistic protection." Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAD033/document.

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L’étude présentée porte sur le développement d’un modèle numérique destiné à évaluer les performances balistiques d’une structure multicouche polymère/métal frittée par procédé SPS. Les matériaux sont un alliage d’aluminium 7020 et un polyimide thermoplastique amorphe qui sont ensuite assemblés avec une résine epoxy. Le comportement mécanique de ces trois matériaux a été étudié sur de larges gammes de vitesses de déformations (de 0.0001 /s à 50.000 /s) et de températures (de -70°C à 500°C) correspondant aux conditions extrêmes rencontrées lors d’impacts à hautes vitesses. Afin d’améliorer la précision des résultats, des approches analytiques ont été développées autant pour la modélisation du métal que pour celle les polymères. Après la calibration des modèles, ces derniers ont été implémenté dans ABAQUS®/Explicit (éléments finis) via des subroutines VUMAT en code FORTRAN. Des essais d’impacts de billes à hautes vitesses ont été réalisés sur des cibles monocouches pour valider les modèles numériques. De nombreuses configurations de composites multicouches ont ensuite été étudiées numériquement et leurs performances balistiques ont été comparées
The present study deals with the development of a numerical model to evaluate the ballistic performance of a polymer/metal multilayer structure sintered by SPS. The materials are an aluminum alloy 7020 and an amorphous thermoplastic polyimide which are then assembled using an epoxy resin. The mechanical behavior of these three materials has been studied over wide ranges of strain rates (from 0.0001 / s to 50,000 / s) and temperatures (from -70 °C to 500 °C) corresponding to the extreme conditions encountered during impacts at high velocities. In order to improve the accuracy of the results, analytical approaches have been developed both for the modeling of the metal and for the polymers. After the calibration of the models, these models were implemented in ABAQUS® / Explicit (finite elements) via VUMAT subroutines in FORTRAN code. Ball impact tests at high velocities were performed on monolayer targets to validate numerical models. Numerous configurations of multilayer composites were then studied numerically and their ballistic performances have been compared

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Davidson, Jacob Daniel. "Actuation and Charge Transport Modeling of Ionic Liquid-Ionic Polymer Transducers." Thesis, Virginia Tech, 2010. http://hdl.handle.net/10919/31204.

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Ionic polymer transducers (IPTs) are soft sensors and actuators which operate through a coupling of micro-scale chemical, electrical, and mechanical mechanisms. The use of ionic liquid as solvent for an IPT has been shown to dramatically increase transducer lifetime in free-air use, while also allowing for higher applied voltages without electrolysis. This work aims to further the understanding of the dominant mechanisms of IPT actuation and how these are affected when an ionic liquid is used as solvent. A micromechanical model of IPT actuation is developed following a previous approach given by Nemat-Nasser, and the dominant relationships in actuation are demonstrated through an analysis of electrostatic cluster interactions. The elastic modulus of Nafion as a function of ionic liquid uptake is measured using uniaxial tension tests and modeled in a micromechanical framework, showing an excellent fit to the data. Charge transport is modeled by considering both the cation and anion of the ionic liquid as mobile charge carriers, a phenomenon which is unique to ionic liquid IPTs as compared to their water-based counterparts. Numerical simulations are performed using the finite element method, and a modified theory of ion transport is discussed which can be extended to accurately describe electrochemical migration of ionic liquid ions at higher applied voltages. The results presented here demonstrate the dominant mechanisms of IPT actuation and identify those unique to ionic liquid IPTs, giving directions for future research and transducer development.
Master of Science

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Osiecki, Tomasz, Colin Gerstenberger, Holger Seidlitz, Alexander Hackert, and Lothar Kroll. "Behavior of Cathodic dip Paint Coated Fiber Reinforced Polymer/Metal Hybrids." Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-175536.

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Increasing mechanical, economic and environmental requirements lead to multi material designs, wherein different classes of materials and manufacturing processes are merged to realize lightweight components with a high level of functional integration. Particularly in automotive industry the use of corresponding technologies will rise in the near future, as they can provide a significant contribution to weight reduction, energy conservation and therefore to the protection of natural resources. Especially the use of continuous fiber reinforced polymers (FRP) with thermoplastic matrices offers advantages for automotive components, due to its good specific characteristics and its suitability for mass production. In conjunction with isotropic materials, such as steel or aluminum, optimized lightweight structures can be produced, whose properties can be easily adapted to the given component requirements. The present paper deals with the development of innovative hybrid laminates with low residual stresses, made of thin-walled steel sheets and glass fiber reinforced thermoplastic (GFRP) prepregs layers. Thereby the interlaminar shear strength (ILSS) was increased by an optimization of the FRP/metal-interfaces, carried out by examining the influence of several pre-operations like sanding, cleaning with organic solvents and applying primer systems. Based on these findings optimized compound samples were prepared and tested under realistic Cathodic dip paint conditions to determine the influence on the ILSS.

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Gasparin, Alexandre Luis. "Adesão metal-polímero: dispositivos de medição e correlações físico-químicas." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2011. http://hdl.handle.net/10183/37831.

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Uma maneira de quantificar a resistência da interface de materiais compósitos é medindo a tensão necessária para separar o filme do substrato. Esta tensão é frequentemente usada como um parâmetro de projeto para desenvolver estes materiais. Entretanto, muitos métodos de medição da adesão não são capazes de eliminar as falhas de coesão das falhas de adesão filme/substrato. Neste trabalho um novo método de medição de adesão é proposto com o objetivo de eliminar a interferência da falha de coesão por cisalhamento, inerente ao filme delaminado, da medida da tensão normal de adesão feita por método padrão. O novo método provou ser eficiente e seus resultados mostraram serem mais precisos que os do método normalizado. Foram testados os seguintes compostos obtidos por evaporação de cobre usando canhão de elétrons através do processo de deposição física de vapor (PVD), formando um filme metálico sobre quatro substratos poliméricos: polipropileno (PP), poliamida 6 (PA 6), poliestireno de alto impacto (HIPS) e poli(tereftalato) de etileno (PET). A análise de espectroscopia de retroespalhamento Rutherford foi utilizada para caracterizar os filmes e o ângulo de contato para caracterizar a interface. As superfícies dos polímeros foram modificadas através de flambagem e lixamento para validar os resultados do novo método. Finalmente os polímeros delaminados através dos métodos padrão e proposto foram observados por microscopia óptica e eletrônica de varredura (MEV), comprovando assim, que somente no método novo ocorre a separação da interface metal-polímero livre da influência da falha coesiva do filme de cobre.
One of the methods to quantify the interface strength of composites is to measure the tensile stress necessary to separate a film from the substrate surface. Such value is often used as a project parameter to develop the composite. However, most of methods cannot avoid the interference of the cohesion bulk failures from the film/substrate adhesion measures. In this work a new method is proposed in order to eliminate the influence of the cohesion shear failure inherent to the delaminated film of the normal adhesion stress measured by the standard method. The new method has proved to work and their results have become more accurate than the standard pull-off method. The experiment consisted in delaminate a copper film deposited by physical vapor evaporation (PVD) through electron gun on four polymers: polypropylene (PP), polyamide 6 (PA 6), high impact polystyrene (HIPS) and polyethylene terephthalate (PET). The Rutherford backscattering spectrometry was used to characterize the films and the contact angle analysis to characterize the interfaces. The polymer surfaces have also been modified to verify the adhesion strengths of the copper film through sanding and flaming processes to validate the new method. Finally the substrates delaminated were analyzed for both methods, standard and proposed, through optical and scanning electron microscopies, proving that only the new method is effective in pulling-off the metal/polymer interface without the cohesive failure influence of the copper film.

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Dogruer, Deniz. "The development of a hydrodynamic model for the segmented ionic polymer metal composite (IPMC) for underwater applications and the potential use of IPMCs for energy harvesting." abstract and full text PDF (free order & download UNR users only), 2006. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1438915.

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Shen, Yubin. "The chemical and mechanical behaviors of polymer / reactive metal systems under high strain rates." Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/45804.

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As one category of energetic materials, impact-initiated reactive materials are able to release a high amount of stored chemical energy under high strain rate impact loading, and are used extensively in civil and military applications. In general, polymers are introduced as binder materials to trap the reactive metal powders inside, and also act as an oxidizing agent for the metal ingredient. Since critical attention has been paid on the metal / metal reaction, only a few types of polymer / reactive metal interactions have been studied in the literature. With the higher requirement of materials resistant to different thermal and mechanical environments, the understanding and characterization of polymer / reactive metal interactions are in great demand. In this study, PTFE (Polytetrafluoroethylene) 7A / Ti (Titanium) composites were studied under high strain rates by utilizing the Taylor impact and SHPB tests. Taylor impact tests with different impact velocities, sample dimensions and sample configurations were conducted on the composite, equipped with a high-speed camera for tracking transient images during the sudden process. SHPB and Instron tests were carried out to obtain the stress vs. strain curves of the composite under a wide range of strain rates, the result of which were also utilized for fitting the constitutive relations of the composite based on the modified Johnson-Cook strength model. Thermal analyses by DTA tests under different flow rates accompanied with XRD identification were conducted to study the reaction mechanism between PTFE 7A and Ti when only heat was provided. Numerical simulations on Taylor impact tests and microstructural deformations were also performed to validate the constitutive model built for the composite system, and to investigate the possible reaction mechanism between two components. The results obtained from the high strain rate tests, thermal analyses and numerical simulations were combined to provide a systematic study on the reaction mechanism between PTFE and Ti in the composite systems, which will be instructive for future energetic studies on other polymer / reactive metal systems.

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Yang, Xiaojiao. "Synthesis and Characterization of Hybrid Metal-Metallic Oxide Composite Nanofibers by Electrospinning and Their Applications." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSE1022/document.

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Nous présentons dans ce manuscrit l'élaboration par électrofilage (ES) de nanofibres hybrides métal/oxyde métallique (HMMOC) et leurs caractérisations physico-chimiques. Leurs utilisations dans le cadre d’applications de type « énergie » et « environnement » ont été évaluées. En particulier, la photocatalyse de nanofibres TiO2-Au pour la dégradation en solution aqueuse du bleu de méthylène et l’utilisation de nanofibres WO3-Au comme capteurs de gaz (VOCs) ont été examinées. En lien étroit avec les résultats obtenus sur l'évaluation des performances comme photocatalyseurs ou capteurs à gaz de ces nouvelles structures HMMOC, l'influence de nombreux paramètres a été étudiée : la concentration en ions aurique, la méthode utilisée pour introduire ces derniers à l’intérieur ou les déposer à la surface des nanofibres d’oxydes et finalement le traitement thermique. En effet, on peut soit mélanger directement, avant la procédure d’électrofilage, la solution contenant les ions aurique à la solution polymérique (composée de PVP, PAN, ou PVA contenant le précurseur d'oxyde métallique), soit déposer sous forme de goutte cette solution d’ions Au à la surface des nanofibres d’oxyde métallique une fois la procédure d’électrofilage effectuée. Quant au traitement thermique, il joue un rôle multiple puisqu’il permet à la fois, d’éliminer les composés organiques des solutions polymériques, participant ainsi à la structuration de la partie oxyde du HMMOC, mais aussi de réduire les ions Au sous forme de nanoparticules.Des résultats prometteurs en photocatalyse ont été obtenus sur des fibres optimisées de TiO2 contenant des nanoparticules d’Au de 10 nm (concentration en Au : 4 wt%). En effet, pour cet échantillon, on montre une dégradation 3 fois plus rapide du bleu de méthylène en solution aqueuse que celle obtenue sur les nanofibres de TiO2 de références et sur le catalyseur commercial P25. De la même manière, des nanofibres de WO3 décorées de nanoparticules d’Au de 10 nm, utilisées comme capteurs de gaz, permettent d’obtenir une réponse 60 fois plus importante que dans le cas de nanofibres de WO3 pure et en améliorant grandement la sélectivité par rapport au n-butanol
We present in this manuscript the elaboration by Electrospinning (ES) process of hybrid metal-metallic oxide composite (HMMOC) nanofibers (NFs), and their physical-chemical characterizations. Their applications, especially the photocatalysis of TiO2-Au composite NFs for photocatalytic degradation for methylene blue (MB) in an aqueous solution and WO3-Au composite NFs for gas sensing of the volatile organic compounds (VOCs) have been investigated. According to the performance evaluation results as photocatalyst or gas sensors, the influence of many parameters have been studied: gold ions concentration, the way to introduce them into or at the NFs surface, typically by mixing them into the polymeric solution (composed of PVP, PAN, or PVA with the metallic oxide precursor) before the ES process or by simple droplet deposition onto the NFs after ES process, and finally the annealing treatment. This latter plays an important role since it both removes the organic components of the polymeric solution, thus forming the metal oxide and in-situ participates to the Au reduction.Concerning the photocatalytic properties, an optimized HMMOC material based on TiO2 NFs including 10 nm Au nanoparticles (NPs) has been obtained and shows 3 times significantly improvement of MB degradation compared to pure TiO2 NFs and the commercial catalyst P25. For gas sensing elaboration, we have shown that a HMMOC material based on WO3 NFs decorated at their surface with 10 nm Au NPs can exhibit 60 times higher response and significantly improved selectivity toward n-butanol compared with pure WO3 NFs

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Vickers, Jason Aaron. "The development and implementation of an ionic-polymer-metal-composite propelled vessel guided by a goal-seeking algorithm." Thesis, Texas A&M University, 2003. http://hdl.handle.net/1969.1/5936.

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This thesis describes the use of an ultrasonic goal-seeking algorithm while using ionic polymer metal composite (IPMC), an electroactive polymer, as the actuator to drive a vessel towards a goal. The signal transmitting and receiving circuits as well as the goal seeking algorithm are described in detail. Two test vessels were created; one was a larger vessel that contained all necessary components for autonomy. The second was a smaller vessel that contained only the sensors and IPMC strips, and all power and signals were transmitted via an umbilical cord. To increase the propulsive efforts of the second, smaller vessel, fins were added to the IPMC strips, increasing the surface area over 700%, determined to yield a 22-fold force increase. After extensive testing, it was found that the three IPMC strips, used as oscillating fins, could not generate enough propulsion to move either vessel, with or without fins. With the addition of fins, the oscillating frequency was reduced from 0.86-Hz to 0.25-Hz. However, the goal-seeking algorithm was successful in guiding the vessel towards the target, an ultrasonic transmitter. When moved manually according to the instructions given by the algorithm, the vessel successfully reached the goal. Using assumptions based on prior experiments regarding the speed of an IPMC propelled vessel, the trial in which the goal was to the left of the axis required 18.2% more time to arrive at the goal than the trial in which the goal was to the right. This significant difference is due to the goal-seeking algorithmÃ¢ÂÂs means to acquire the strongest signal. After the research had concluded and the propulsors failed to yield desired results, many factors were considered to rationalize the observations. The operating frequency was reduced, and it was found that, by the impulse-momentum theorem, that the propulsive force was reduced proportionally. The literature surveyed addressed undulatory motion, which produces constant propulsive force, not oscillatory, which yields intermittent propulsive force. These reasons among others were produced to rationalize the results and prove the cause of negative results was inherent to the actuators themselves. All rational options have been considered to yield positive results.

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Mallavarapu, Kiran. "Feedback Control of Ionic Polymer Actuators." Thesis, Virginia Tech, 2001. http://hdl.handle.net/10919/34154.

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An ionic polymer actuator consists of a thin Nafion-117 sheet plated with gold or platinum on both sides. An ionic polymer actuator undergoes large deformation in the presence of low applied voltage across its thickness and exhibits low impedance. They can also be used as large displacement sensors by bending them to induce stresses and generate a voltage response. They operate best in a humid environment. Ionic polymer actuators have been used for various practical applications such as bio-mimetic robotic propulsion, flexible low mass robotic arms, propellors for swimming robotic structures, linear and platform type robotic actuators and active catheter systems. One of the disadvantages of ionic polymer actuators is that their settling time to a unit step voltage is on the order of 5-20 seconds in a cantilever configuration. The slow time constant of an ionic polymer limits the actuation bandwidth. The characteristics of ionic polymer actuators, low force and large displacement (as compared to other actuator technologies such as PZT or PVDF), cannot be used in applications requiring a faster response time for a given actuation signal. Due to this limitation, many applications will not be able to make use of the large displacement effectively because of the limited bandwidth of the actuator. Another disadvantage of using an ionic polymer actuator is that the stiffness of the actuator is a function of the hydration of the polymer. Difficulties in controlling the hydration, which changes with respect to time, results in inconsistencies in the mechanical response exhibited by the polymers during continual usage. Several physical models of ionic polymer actuators have been proposed. The physical phenomenon responsible for the bending is not completely understood and no clear set of principles have been able to explain the motion of the polymers completely. Physical phenomena like ionic motion, back diffusion of water and electrostatic force have been used to explain these models. This research demonstrates the use of feedback control to overcome the limitation of slow settling time. First, an empirical model of the ionic polymers developed by Kanno was modified by studying the step response of these actuators. The empirical model is used to design a feedback compensator by state space modeling techniques. Since the ionic polymer actuator has a slow settling time in the open-loop, the design objectives are to minimize the settling time and constrain the control voltage to be less than a prescribed value. The controller is designed using Linear Quadratic Regulator (LQR) techniques which reduced the number of design parameters to one variable. Simulations are performed which show settling times of 0.03 seconds for closed-loop feedback control are possible as compared to the open-loop settling time of 16-18 seconds. The maximum control voltage varied from 1.2 Volts to 3.5 Volts depending on the LQR design parameter. The controller is implemented and results obtained are consistent with the simulations. Closed-loop settling time is observed to be 4-8 seconds and the ratio of the peak response to the steady-state response is reduced by an order of magnitude. Discrepancies between the experiment and the simulations are attributed to the inconsistencies in the resonant frequency of the actuator. Experiments demonstrate that changes in the surface hydration of the polymer result in 20\% variations in the actuator resonance. Variations in the actuator resonance require a more conservative compensator design, thus limiting the performance of the feedback control system.
Master of Science

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Zedde, Nicola. "Dynamic mechanical-thermal, microstructural and mechanical analysis of ultra-light polymer-metal composites: influence of forming." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2016.

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A really particular and innovative metal-polymer sandwich material is Hybrix. Hybrix is a product developed and manufactured by Lamera AB, Gothenburg, Sweden. This innovative hybrid material is composed by two relatively thin metal layers if compared to the core thickness. The most used metals are aluminum and stainless steel and are separated by a core of nylon fibres oriented perpendicularly to the metal plates. The core is then completed by adhesive layers applied at the PA66-metal interface that once cured maintain the nylon fibres in position. This special material is very light and formable. Moreover Hybrix, depending on the specific metal which is used, can achieve a good corrosion resistance and it can be cut and punched easily. Hybrix architecture itself provides extremely good bending stiffness, damping properties, insulation capability, etc., which again, of course, change in magnitude depending in the metal alloy which is used, its thickness and core thickness. For these reasons nowadays it shows potential for all the applications which have the above mentioned characteristic as a requirement. Finally Hybrix can be processed with tools used in regular metal sheet industry and can be handled as solid metal sheets. In this master thesis project, pre-formed parts of Hybrix were studied and characterized. Previous work on Hybrix was focused on analyze its market potential and different adhesive to be used in the core. All the tests were carried out on flat unformed specimens. However, in order to have a complete description of this material also the effect of the forming process must be taken into account. Thus the main activities of the present master thesis are the following: Dynamic Mechanical-Thermal Analysis (DMTA) on unformed Hybrix samples of different thickness and on pre-strained Hybrix samples, pure epoxy adhesive samples analysis and finally moisture effects evaluation on Hybrix composite structure.

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MARCHISIO, SILVIA. "Composite Materials reinforced by Carbon Nanotubes." Doctoral thesis, Politecnico di Torino, 2013. http://hdl.handle.net/11583/2506164.

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The work of this Ph.D. thesis has been realised in the field of a promising and largely studied technological material: the carbon nanotubes (CNTs). Since 1991 a large number of attempts have been conducted, trying to exploit the outstanding potential of this carbonaceous material, in order to improve the properties of several matrices. The most important application is the production of polymer matrices composites (PMCs), but in last decades an increasing number of metal matrix ones (MMCs) have been presented and recently also ceramic matrix (CMCs) applications have been attempted. Despite massive efforts focused on CNTs-composites, the potential of employing this reinforcement materials has not yet been fully exploited. This lack is substantially due to the difficulties associated with the dispersion of entangled carbon nanotubes during processing and poor interfacial interaction between CNTs and matrix materials. Because of these reasons the very first aspect of this work has been the study of the dispersion state of nanotubes. The aim of the experiments was not only to obtain a good dispersion and distribution of the CNTs, but also to evaluate their dispersion grade. Indeed, due to their nanosize and to their carbonaceous nature, few simple experimental techniques result suitable for this purpose. The second part of the work consisted in the application of the carbon nanotubes to the production of new materials for technological applications, with improved mechanical properties. Three composite materials with different matrices have been designed, developed and produced: a polymer matrix composite, a ceramic matrix and a metal matrix one. For PMCs a polyvinyl butyral matrix has been used and the composites were obtained by a deeply studied technique: the tape casting technology. The same approach was also used in the case of CMCs: tape casted silicon carbide matrix composites reinforced by carbon nanotubes have been produced. Finally a third matrix has been experimented: MMCs were investigated starting from pure aluminium powders. For Al matrix composites a particular technique was used: the sintering was obtained starting from a powder metallurgy approach and exploiting electric current and pressure (Electric Current Assisted Sintering approach). For all the three different composite materials, after the development of the production route and the preparation of several specimens, a characterization step followed. The materials were characterized in terms of physical properties, morphology and microstructure, and mechanical behaviour.

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Khdhayyer, Muhanned. "Mixed matrix membranes comprising metal organic frameworks and high free volume polymers for gas separations." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/mixed-matrix-membranes-comprising-metal-organic-frameworks-and-high-free-volume-polymers-for-gas-separations(172f6a4f-a531-44ae-979c-bbbd170f33db).html.

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This research aimed to develop new composite membranes using a polymer of intrinsic microporosity (PIM-1) and metal organic frameworks (MOFs) for use in gas separations. PIM-1 was successfully synthesised using the high temperature method (40 min, 160 oC) and the resulting polymer was cast into membranes. PIM-1 membranes were chemically modified by reacting hexamethylenediamine (HMDA) with the nitrile group of PIM-1 to form HMDA-modified PIM-1 membranes. Surfaces of PIM-1 membranes were also modified by basic hydrolysis to form amide-modified PIM-1 membranes. These polymer materials were characterized by different techniques (GPC, NMR, ATR-IR, TGA, Elemental analysis and nitrogen sorption analysis). In addition, eight MOF materials [MIL-101(Cr), ED-g-MIL-101(Cr), TEPA-g-MIL-101(Cr), MIL-101(Cr)-NH2, MIL-101(Al)-NH2, UiO-66(Zr), UiO-66-NH2 and UiO-66(COOH)2] were successfully synthesized. They were chosen due to having high surface areas and large porosity. These MOF compounds were characterized using PXRD, SEM, TGA, and low pressure N2.Successful PIM-1/MOF MMMs were fabricated utilising PIM-1 and the MOFs outlined above with various loadings. The highest MOF loading achieved was 28.6 wt. %, apart from MIL-101(Cr)-NH2, for which it was 23.1 wt. %, and MIL-101(Al)-NH2, for which it was 19.8 wt. %. The morphology of MMMs was characterized by scanning electron microscopy (SEM), proving the dispersion of MOF fillers. Novel PIM-1 supported MOF membranes were successfully prepared by depositing ZIF-8 and HKUST-1 layers on the surfaces of unmodified and modified PIM-1 membranes. These materials were characterized using PXRD, SEM, ATR-IR and SEM-EDX. Gas permeation properties of the MOF/PIM-1 MMMs and PIM-1 supported MOF membranes were determined using a time lag method. Most MMMs tested showed an increase in the permeability and stable selectivity as the MOF amount was increased. However, this was not true for MIL-101(Al)-NH2, where the permeability and selectivity decreased. In contrast, PIM-1 supported ZIF-8 and HKUST-1 membranes caused a sharp decrease in the permeability and increase in the selectivity.

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Hu, Qingchun. "Fabrication and characterization of poly(amide-imides)/TiO₂ nanocomposite gas separation membranes." Diss., This resource online, 1996. http://scholar.lib.vt.edu/theses/available/etd-10022008-063009/.

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Diaz, Mendoza Alvaro. "Conception of a fibrous composite material for the retention of heavy metals." Thesis, Lyon, 2020. http://www.theses.fr/2020LYSEI125.

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La contamination par les métaux lourds est un problème actuel qui affecte les écosystèmes et leurs organismes constitutifs. Ce problème a été reconnu dans le monde entier comme l'un des plus grands défis de notre époque. Depuis le milieu du siècle dernier, les innovations dans le domaine de la science des matériaux ont permis de mettre au point de nouvelles méthodes pour faire face à ce risque, avec des techniques telles que la précipitation chimique ou la flottation. Toutefois, il reste encore beaucoup à faire dans ce domaine. En outre, des recherches récentes ont exploré comment combiner des biomolécules telles que les protéines avec des matériaux tels que les polymères pour créer des solutions plus actives. Ce travail de thèse vise à créer un prototype de matériau adsorbant hybride capable de capturer spécifiquement les ions métalliques divalents Ni(II), Cd(II) et Pb(II) grâce à la présence d'une métalloprotéine synthétique dans sa structure. Pour atteindre cet objectif, le travail de thèse se concentre sur le développement d'une métalloprotéine synthétique capable de capturer spécifiquement les trois ions métalliques cibles, de la conception in silico à sa synthèse in vivo. D'autre part, le support de matériau est traité avec la technique d'électrofilage qui consiste en un matériau membranaire fibreux, étant optimisé pour accueillir la métalloprotéine synthétique dans sa structure. En outre, une méthode permettant d'intégrer la métalloprotéine dans le support polymère est recherchée. Ceci est réalisé au moyen d'une voie de greffage à travers des nanoparticules de silice modifiées en surface. À la fin, l'intégration des deux composants crée le prototype attendu de matériau biosorbant synthétique. Ce matériau a été caractérisé afin d'évaluer sa capacité à adsorber les trois ions métalliques d'intérêt, ce qui permet de dégager certaines tendances des perspectives futures de développement pour créer des matériaux plus efficaces pour l'industrie
Heavy metal contamination is a current problem which affects the ecosystems and their constituent organisms. This problem has been worldwide recognized as one of the biggest challenges of our time. Since the middle of the last century, innovations in the material science field have developed new methods to confront this risk, with techniques such as chemical precipitation or flotation. However, there is still significant room for improvement in this line. Furthermore, recent research has explored how to combine biomolecules such as proteins with materials like polymers to create more active solutions. This thesis work seeks to create a prototype hybrid biosorbent material capable to capture specifically the divalent metal ions Ni(II), Cd(II) and Pb(II) thanks to the presence of a synthetic metalloprotein in its structure. To address this objective, the thesis work focuses on the development of a synthetic metalloprotein capable to specifically capture the three target metal ions, from the in silico conception to its in vivo synthesis. On the other hand, the biosorbent material support is processed with the electrospinning technique that consists of a fibrous membrane material, being optimized to host the synthetic metalloprotein in its structure. Additionally, a method to integrate the metalloprotein into the polymeric support is researched. This is achieved by means of a grafting route through surface modified silica nanoparticles. At the end, the integration of both components creates the expected prototype synthetic biosorbent material. This material has been characterized to evaluate its capacity to adsorb the three metal ions of interest, providing some trends of the future perspectives for further development to create more efficient materials for the industry

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Park, Jong Keun. "Anisotropic Morphologies and Properties in Perfluorosulfonate Ionomer-Based Materials." Diss., Virginia Tech, 2009. http://hdl.handle.net/10919/40486.

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The overall goal of this investigation was to elucidate specific structure-property relationships in perfluorosulfonate ionomers (PFSIs)-related materials. The project can be broken into two primary foci. First, we explored the current state of understanding related to morphology-property relationships in PFSIs with specific attention to the nano-scale organization of the ionic and crystalline domains. Specifically, the effect of uniaxial orientation on the structure and transport properties of NafionÂ® membranes was examined. Small angle X-ray scattering (SAXS) experiments on dry membranes that were uniaxially elongated showed a strong anisotropic morphology which was shown to persist over the swelling process without a significant relaxation. Hermanâ s order parameters for the ionomer peak were strongly influenced by uniaxial deformation, which supports the presence of cylindrical rather than spherical morphology for ionic domains. Comparison of the water diffusion coefficients between unoriented and oriented samples revealed that uniaxial deformation of NafionÂ® membranes essentially enhances transport ability in one direction (i.e., the parallel to draw direction) and suppresses in the other two directions (i.e., two orthogonal directions relative to the stretching direction). Based on 1-dimensional analyses of oriented SAXS patterns at the azimuthal angle 90o, three recent models (lamellar model, semicrystalline rod-like model and fringed-micelle model) for the morphology of PFSIs were critically evaluated. The loss of meridional scattering, different orientation behavior of the crystalline and ionic domains, and inherent chain stiffness precludes the possibility of a chain-folded lamellar morphology. While the inter-aggregate dimensions remain constant at high draw ratios, the inter-crystalline spacings decrease significantly. Coupled with the distinctly different orientation behavior, these observations preclude the existence of crystallites solely within rod-like aggregates. While the worm-like ionic channel model was able to explain the behavior of SAXS and wide angle X-ray scattering (WAXS) relatively well, this model also had limitations such as (1) crystalline domains directly linked to the ionic domain (and thus a lack of amorphous domains) and (2) a presence of only a single ionic channel between two neighboring crystallites. Second, electroactive materials, specifically ionic polymer-metal composites (IPMCs) that undergo bending motions with the stimulus of a relatively weak electric field were fabricated. To understand the role of the nanoscale morphology of the membrane matrix in affecting the actuation behavior of IPMC systems, we evaluated actuation performance of IPMCs subjected to uniaxial orientation. The PFSI nanostructure altered by uniaxial orientation mimicked the fibrillar structure of biological muscle tissue and yielded a new anisotropic actuation response. It was evident that IPMCs cut from films oriented perpendicular to the draw direction yielded displacement values that were significantly greater than that of unoriented IPMCs. In contrast, IPMCs cut from films oriented parallel to the draw direction appeared to resist bending and yield displacement values that were much less than that of the unoriented IPMC. This anisotropic actuation behavior was attributed to the contribution of the nanoscale morphology to the bulk bending modulus. Overall, this study clearly demonstrated, for the first time, the importance of the nanoscale morphology in affecting/controlling the actuation behavior in IPMC systems.
Ph. D.

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Nishikitani, Yoshinori. "Polymères et oligomères conducteurs : matériaux pour l'électronique." Paris 13, 1989. http://www.theses.fr/1989PA132005.

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Etude de films composites formés de polymères conducteurs et de polymères classiques. Etude des propriètés semiconductrices de polymères conjugués dédopés avec inclusion controlée de métaux (cette inclusion augmente l'efficacité des transferts de charge interchaines dans le polymère)

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Jain, Vaibhav. "Applications of Layer-by-Layer Films in Electrochromic Devices and Bending Actuators." Diss., Virginia Tech, 2009. http://hdl.handle.net/10919/28907.

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This thesis presents work done to improve the switching speed and contrast performance of electrochromic devices. Layer-by-Layer (LbL) assembly was used to deposit thin electrochromic films of materials ranging from organic, inorganic, conducting polymers, etc. The focus was on developing new materials with high contrast and long lifecycles. A detailed switching-speed study of solid-state EC devices of already-developed (PEDOT (Poly(3,4-ethylenedioxythiophene)), polyviologen, inorganic) materials and some new materials (Prodot-Sultone) was performed. Work was done to achieve the optimum thickness and number of bilayers in LbL films resulting in high-contrast and fast switching. Device sizes were varied for comparison of the performance of the lab-made prototype device with the commercially available â small pixelâ size displays. Symmetrical EC devices were fabricated and tested whenever conducting polymers are used as an EC material. This symmetrical configuration utilizes conducting polymers as an electroactive layer on each of two ITO-coated substrates; potential is applied to the two layers of similar conducting polymers and the device changes color from one redox state to another. This method, along with LbL film assembly, are the main factors in the improvement of switching speed results over already-published work in the literature. PEDOT results show that EC devices fabricated by LbL assembly with a switching speed of less than 30 ms make EC flat-panel displays possible by adjusting film thickness, device size, and type of material. The high contrast value (84%) for RuP suggests that its LbL films can be used for low-power consumption displays where contrast, not fastest switching, is the prime importance. In addition to the electrochromic work, this thesis also includes a section on the application of LbL assembly in fabricating electromechanical bending actuators. For bending actuators based on ionic polymer metal composites (IPMCs), a new class of conductive composite network (CNC) electrode was investigated, based on LbL self-assembled multilayers of conductive gold (Au) nanoparticles. The CNC of an electromechanical actuator fabricated with 100 bilayers of polyallylamine hydrochloride (PAH)/Au NPs exhibits high strain value of 6.8% with an actuation speed of 0.18 seconds for a 26 Âµm thick IPMC with 0.4 Âµm thick LbL CNCs under 4 volts.
Ph. D.

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MIGLIORINI, LORENZO. "DEVELOPMENT OF FUNCTIONAL NANOCOMPOSITE MATERIALS TOWARDS BIODEGRADABLE SOFT ROBOTICS AND FLEXIBLE ELECTRONICS." Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/704286.

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World population is continuously growing, as well as the influence we have on the ecosystem’s natural equilibrium. Moreover, such growth is not homogeneous and it results in an overall increase of older people. Humanity’s activity, growth and aging leads to many challenging issues to address: among them, there are the spread of suddenly and/or chronic diseases, malnutrition, resource pressure and environmental pollution. Research in the novel field of biodegradable soft robotics and electronics can help dealing with these issues. In fact, to face the aging of the population, it is necessary an improvement in rehabilitation technologies, physiological and continuous monitoring, as well as personalized care and therapy. Also in the agricultural sector, an accurate and efficient direct measure of the plants health conditions would be of help especially in the less-developed countries. But since living beings, such as humans and plants, are constituted by soft tissues that continuously change their size and shapes, today’s traditional technologies, based on rigid materials, may not be able to provide an efficient interaction necessary to satisfy these needs: the mechanical mismatch is too prohibitive. Instead, soft robotic systems and devices can be designed to combine active functionalities with soft mechanical properties that can allow them to efficiently and safely interact with soft living tissues. Soft implantable biomedical devices, smart rehabilitation devices and compliant sensors for plants are all applications that can be achieved with soft technologies. The development of sophisticated autonomous soft systems needs the integration on a unique soft body or platform of many functionalities (such as mechanical actuation, energy harvesting, storage and delivery, sensing capabilities). A great research interest is recently arising on this topic, but yet not so many groups are focusing their efforts in the use of natural-derived and biodegradable raw materials. In fact, resource pressure and environmental pollution are becoming more and more critical problems. It should be completely avoided the use of in exhaustion, pollutant, toxic and non-degradable resources, such as lithium, petroleum derivatives, halogenated compounds and organic solvents. So-obtained biodegradable soft systems and devices could then be manufactured in high number and deployed in the environment to fulfil their duties without the need to recover them, since they can safely degrade in the environment. The aim of the current Ph.D. project is the use of natural-derived and biodegradable polymers and substances as building blocks for the development of smart composite materials that could operate as functional elements in a soft robotic system or device. Soft mechanical properties and electronic/ionic conductive properties are here combined together within smart nanocomposite materials. The use of supersonic cluster beam deposition (SCBD) technique enabled the fabrication of cluster-assembled Au electrodes that can partially penetrate into the surface of soft materials, providing an efficient solution to the challenge of coupling conductive metallic layers and soft deformable polymeric substrates. In this work, cellulose derivatives and poly(3-hydroxybutyrate) bioplastic are used as building blocks for the development of both underwater and in-air soft electromechanical actuators that are characterized and tested. A cellulosic matrix is blended with natural-derived ionic liquids to design and manufacture completely biodegradable supercapacitors, extremely interesting energy storage devices. Lastly, ultrathin Au electrodes are here deposited on biodegradable cellulose acetate sheets, in order to develop transparent flexible electronics as well as bidirectional resistive-type strain sensors. The results obtained in this work can be regarded as a preliminary study towards the realization of full natural-derived and biodegradable soft robotic and electronic systems and devices.

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33

Ferreira, Henrique Perez. "Modificação de poli(fluoreto de vinilideno) induzida por radiação gama para aplicação como compósito ionomérico de metal-polímero." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/85/85134/tde-07112012-073635/.

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Foi estudada a enxertia de estireno induzida por radiação gama em filmes de poli(fluoreto de vinilideno) (PVDF) com espessura de 0,125 mm com doses entre 1 e 100 kGy em presença de soluções de estireno/N,Ndimetilformamida (DMF) (1:1, v/v) e estireno/tolueno (1:1, v/v) com taxa de dose de 5 kGy.h-1 por meio do método simultâneo de irradiação sob atmosfera de nitrogênio e em temperatura ambiente, usando raios gama de uma fonte de Co- 60. Depois de enxertados, os polímeros foram sulfonados em soluções de ácido clorossulfônico/1,2-dicloroetano (2 e 10 %). Os filmes foram caracterizados antes e depois de cada modificação com o cálculo do Grau de enxertia, (DOG), espectrometria no infravermelho (FT-IR), microscopia eletrônica de varredura (MEV), calorimetria exploratória diferencial (DSC) e termogravimetria (TG/DTG). Os resultados do grau de enxertia mostraram que a enxertia aumenta com o aumento da dose e varia enormemente de acordo com o solvente utilizado, com enxertias cerca de 20 vezes maiores quando do uso da DMF em relação ao do tolueno. Foi possível confirmar a enxertia do estireno por FT-IR graças ao aparecimento de novos picos característicos e por TG/DTG e DSC por meio das alterações do comportamento térmico dos materiais enxertados/sulfonados. Os materiais sulfonados ainda foram caracterizados por suas capacidades de troca iônica (IEC), que mostraram que tanto os aumentos do grau de enxertia quanto os da concentração do ácido clorossulfônico aumentam o IEC. Os resultados mostraram que é possível obter materiais com capacidades de troca iônica com possibilidade de aplicação como compósitos ionoméricos de metal-polímero.
Gamma-radiation-induced grafting of styrene into poly(vinylidene fluoride) (PVDF) films with 0.125 mm thickness at doses from 1 to 100 kGy in the presence of a styrene/N,N- dimethylformamide (DMF) solution (1:1, v/v) and styrene/toluene (1:1, v/v) at dose rate of 5 kGy h-1 was carried out by simultaneous method under nitrogen atmosphere at room temperature, using gamma rays from a Co-60. After grafting reactions, the polymer was then sulfonated in chlorosulfonic acid/1,2-dichloroethane (2 and 10%) for 3 hours. The films were characterized before and after modification by calculating the degree of grafting (DOG), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and thermogravimetry (TG/DTG). DOG results show that grafting increases with dose, and varies enormously depending on the solvent used, with DOGs about 20 times greater in DMF than in toluene. It was possible to confirm the grafting of styrene by FT-IR due to the appearance of the new characteristic peaks and by the TG and DSC which exhibited changes in the thermal behavior of the grafted/sulfonated material. Sulfonated material was also characterized by ion exchange capacity (IEC) showed that both DOG and sulfonic acid concentration increase IEC values. Results showed that it is possible to obtain materials with ion exchange capacity of possible application as ionic polymer-metal composites.

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34

Nestler, Daisy Julia. "Beitrag zum Thema VERBUNDWERKSTOFFE - WERKSTOFFVERBUNDE." Doctoral thesis, Universitätsbibliothek Chemnitz, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-134459.

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Vielschichtige Eigenschaftsprofile benötigen zunehmend moderne Verbundwerkstoffe und Werkstoffverbunde einschließlich der raschen Entfaltung neuer Fertigungstechnologien, da der monolithische Werkstoff bzw. ein einziger Werkstoff den heutigen komplexen Anforderungen nicht mehr genügen kann. Zukünftige Werkstoffsysteme haben wirtschaftlich eine Schlüsselposition und sind auf den Wachstumsmärkten von grundlegender Bedeutung. Gefragt sind maßgeschneiderte Leichtbauwerkstoffe (tailor-made composites) mit einem adaptierten Design. Dazu müssen Konzepte entwickelt werden, um die Kombination der Komponenten optimal zu gestalten. Das erfordert werkstoffspezifisches Wissen und Korrelationsvermögen sowie die Gestaltung komplexer Technologien, auch unter dem Aspekt der kontinuierlichen Massen- und Großserienfertigung (in-line, in-situ) und damit der Kostenreduzierung bislang teurer Verbundwerkstoffe und Werkstoffverbunde. In der vorliegenden Arbeit wird in vergleichbarer und vergleichender Art und Weise sowie abstrahierter Form ein Bogen über das Gesamtgebiet der Verbundwerkstoffe und Werkstoffverbunde gespannt. Eine zusammenfassende Publikation über dieses noch sehr junge, aber bereits breit aufgestellte Wissenschaftsgebiet fehlt bislang. Das ist der Separierung der einzelnen, fest aufgeteilten Gruppierungen der Verbundwerkstoffe geschuldet. Querverbindungen werden selten hergestellt. Dieses Defizit in einem gewissen Maße auszugleichen, ist Ziel der Arbeit. Besondere Berücksichtigung finden Begriffsbestimmungen und Klassifikationen, Herstellungsverfahren und Eigenschaften der Werkstoffe. Es werden klare Strukturierungen und Übersichten herausgearbeitet. Zuordnungen von etablierten und neuen Technologien sollen zur Begriffsstabilität der Terminologien „Mischbauweise“ und „Hybrider Verbund“ beitragen. Zudem wird die Problematik „Recycling und Recyclingtechnologien“ diskutiert. Zusammenfassend werden Handlungsfelder zukünftiger Forschungs- und Entwicklungsprojekte spezifiziert. Aus dem Blickwinkel der verschiedenen Herstellungsrouten insbesondere für Halbzeuge und Bauteile und der dabei gewonnenen Erkenntnisse werden verallgemeinerte Konzepte für tailor-made Verbundwerkstoffe und Werkstoffverbunde vorgeschlagen („Stellschraubenschema“). Diese allgemeinen Werkstoffkonzepte werden auf eigene aktuelle Forschungsprojekte der Schwerpunktthemen Metallmatrix- und Polymermatrix-Verbundwerkstoffe sowie der hybriden Werkstoffverbunde appliziert. Forschungsfelder für zukünftige Projekte werden abgeleitet. Besonderes Augenmerk gilt den hybriden Verbunden als tragende Säule zukünftiger Entwicklungen im Leichtbau. Hier spielen in-line- und in-situ-Prozesse eine entscheidende Rolle für eine großseriennahe, kosteneffiziente und ressourcenschonende Produktion
Complex property profiles require increasingly advanced composite materials and material compounds, including the rapid deployment of new production technologies, because the monolithic material or a single material can no longer satisfy today's complex requirements. Future material systems are fundamentally important to growth markets, in which they have an economically key position. Tailor-made lightweight materials (tailor-made composites) with an adapted design are needed. These concepts have to be developed to design the optimum combination of components. This requires material-specific knowledge and the ability to make correlations, as well as the design of complex technologies. Continuous large-scale and mass production (in-line, in-situ), thus reducing the costs of previously expensive composite materials and material compounds, is also necessary. The present work spans the entire field of composite materials and material compounds in a comparable and comparative manner and abstract form. A summarizing publication on this still very new, but already broad-based scientific field is not yet available. The separation of the individual, firmly divided groups of the composite materials is the reason for this. Cross-connections are rarely made. The objective of this work is to compensate to some extent for this deficiency. Special consideration is given to definitions and classifications, manufacturing processes and the properties of the materials. Clear structures and overviews are presented. Mapping established and new technologies will contribute to the stability of the terms "mixed material compounds" and "hybrid material compounds". In addition, the problem of recycling and recycling technologies is discussed. In summary, areas for future research and development projects will be specified. Generalized concepts for tailor-made composite materials and material compounds are proposed ("adjusting screw scheme") with an eye toward various production routes, especially for semi-finished products and components, and the associated findings. These general material concepts are applied to own current research projects pertaining to metal-matrix and polymer-matrix composites and hybrid material compounds. Research fields for future projects are extrapolated. Particular attention is paid to hybrid material compounds as the mainstay of future developments in lightweight construction. In-line and in-situ processes play a key role for large-scale, cost- and resource-efficient production

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35

Liang, Wenfeng. "Metal Organic Composites Derived Tin Dioxide/C Nanoparticles For Sodium-Ion Battery." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1460304081.

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36

Nestler, Daisy Julia. "Beitrag zum Thema VERBUNDWERKSTOFFE - WERKSTOFFVERBUNDE: Status quo und Forschungsansätze." Doctoral thesis, Universitätsverlag Chemnitz, 2012. https://monarch.qucosa.de/id/qucosa%3A20009.

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Vielschichtige Eigenschaftsprofile benötigen zunehmend moderne Verbundwerkstoffe und Werkstoffverbunde einschließlich der raschen Entfaltung neuer Fertigungstechnologien, da der monolithische Werkstoff bzw. ein einziger Werkstoff den heutigen komplexen Anforderungen nicht mehr genügen kann. Zukünftige Werkstoffsysteme haben wirtschaftlich eine Schlüsselposition und sind auf den Wachstumsmärkten von grundlegender Bedeutung. Gefragt sind maßgeschneiderte Leichtbauwerkstoffe (tailor-made composites) mit einem adaptierten Design. Dazu müssen Konzepte entwickelt werden, um die Kombination der Komponenten optimal zu gestalten. Das erfordert werkstoffspezifisches Wissen und Korrelationsvermögen sowie die Gestaltung komplexer Technologien, auch unter dem Aspekt der kontinuierlichen Massen- und Großserienfertigung (in-line, in-situ) und damit der Kostenreduzierung bislang teurer Verbundwerkstoffe und Werkstoffverbunde. In der vorliegenden Arbeit wird in vergleichbarer und vergleichender Art und Weise sowie abstrahierter Form ein Bogen über das Gesamtgebiet der Verbundwerkstoffe und Werkstoffverbunde gespannt. Eine zusammenfassende Publikation über dieses noch sehr junge, aber bereits breit aufgestellte Wissenschaftsgebiet fehlt bislang. Das ist der Separierung der einzelnen, fest aufgeteilten Gruppierungen der Verbundwerkstoffe geschuldet. Querverbindungen werden selten hergestellt. Dieses Defizit in einem gewissen Maße auszugleichen, ist Ziel der Arbeit. Besondere Berücksichtigung finden Begriffsbestimmungen und Klassifikationen, Herstellungsverfahren und Eigenschaften der Werkstoffe. Es werden klare Strukturierungen und Übersichten herausgearbeitet. Zuordnungen von etablierten und neuen Technologien sollen zur Begriffsstabilität der Terminologien „Mischbauweise“ und „Hybrider Verbund“ beitragen. Zudem wird die Problematik „Recycling und Recyclingtechnologien“ diskutiert. Zusammenfassend werden Handlungsfelder zukünftiger Forschungs- und Entwicklungsprojekte spezifiziert. Aus dem Blickwinkel der verschiedenen Herstellungsrouten insbesondere für Halbzeuge und Bauteile und der dabei gewonnenen Erkenntnisse werden verallgemeinerte Konzepte für tailor-made Verbundwerkstoffe und Werkstoffverbunde vorgeschlagen („Stellschraubenschema“). Diese allgemeinen Werkstoffkonzepte werden auf eigene aktuelle Forschungsprojekte der Schwerpunktthemen Metallmatrix- und Polymermatrix-Verbundwerkstoffe sowie der hybriden Werkstoffverbunde appliziert. Forschungsfelder für zukünftige Projekte werden abgeleitet. Besonderes Augenmerk gilt den hybriden Verbunden als tragende Säule zukünftiger Entwicklungen im Leichtbau. Hier spielen in-line- und in-situ-Prozesse eine entscheidende Rolle für eine großseriennahe, kosteneffiziente und ressourcenschonende Produktion.
Complex property profiles require increasingly advanced composite materials and material compounds, including the rapid deployment of new production technologies, because the monolithic material or a single material can no longer satisfy today's complex requirements. Future material systems are fundamentally important to growth markets, in which they have an economically key position. Tailor-made lightweight materials (tailor-made composites) with an adapted design are needed. These concepts have to be developed to design the optimum combination of components. This requires material-specific knowledge and the ability to make correlations, as well as the design of complex technologies. Continuous large-scale and mass production (in-line, in-situ), thus reducing the costs of previously expensive composite materials and material compounds, is also necessary. The present work spans the entire field of composite materials and material compounds in a comparable and comparative manner and abstract form. A summarizing publication on this still very new, but already broad-based scientific field is not yet available. The separation of the individual, firmly divided groups of the composite materials is the reason for this. Cross-connections are rarely made. The objective of this work is to compensate to some extent for this deficiency. Special consideration is given to definitions and classifications, manufacturing processes and the properties of the materials. Clear structures and overviews are presented. Mapping established and new technologies will contribute to the stability of the terms "mixed material compounds" and "hybrid material compounds". In addition, the problem of recycling and recycling technologies is discussed. In summary, areas for future research and development projects will be specified. Generalized concepts for tailor-made composite materials and material compounds are proposed ("adjusting screw scheme") with an eye toward various production routes, especially for semi-finished products and components, and the associated findings. These general material concepts are applied to own current research projects pertaining to metal-matrix and polymer-matrix composites and hybrid material compounds. Research fields for future projects are extrapolated. Particular attention is paid to hybrid material compounds as the mainstay of future developments in lightweight construction. In-line and in-situ processes play a key role for large-scale, cost- and resource-efficient production.

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37

Olea, Mejia Oscar Fernando. "Micro and nano composites composed of a polymer matrix and a metal disperse phase." Thesis, University of North Texas, 2007. https://digital.library.unt.edu/ark:/67531/metadc5135/.

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Low density polyethylene (LDPE) and Hytrel (a thermoplastic elastomer) were used as polymeric matrices in polymer + metal composites. The concentration of micrometric (Al, Ag and Ni) as well as nanometric particles (Al and Ag) was varied from 0 to 10 %. Composites were prepared by blending followed by injection molding. The resulting samples were analyzed by scanning electron microscopy (SEM) and focused ion beam (FIB) in order to determine their microstructure. Certain mechanical properties of the composites were also determined. Static and dynamic friction was measured. The scratch resistance of the specimens was determined. A study of the wear mechanisms in the samples was performed. The Al micro- and nanoparticles as well as Ni microparticles are well dispersed throughout the material while Ag micro and nanoparticles tend to form agglomerates. Generally the presence of microcomposites affects negatively the mechanical properties. For the nanoparticles, composites with a higher elastic modulus than that of the neat materials are achievable. For both micro- and nanocomposites it is feasible to lower the friction values with respective to the neat polymers. The addition of metal particles to polymers also improves the scratch resistance of the composites, particularly so for microcomposites. The inclusion of Ag and Ni particles causes an increase in the wear loss volume while Al can reduce the wear for both polymeric matrices.

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38

Bae, Tae-Hyun. "Engineering nanoporous materials for application in gas separation membranes." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/42712.

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The main theme of this dissertation is to engineer nanoporous materials and nanostructured surfaces for applications in gas separation membranes. Tunable methods have been developed to create inorganic hydroxide nanostructures on zeolite surfaces, and used to control the inorganic/polymer interfacial morphology in zeolite/polymer composite membranes. The study of the structure-property relationships in this material system showed that appropriate tuning of the surface modification methods leads to quite promising structural and permeation properties of the membranes made with the modified zeolites. First, a facile solvothermal deposition process was developed to prepare roughened inorganic nanostructures on zeolite pure silica MFI crystal surfaces. The functionalized zeolite crystals resulted in high-quality ̒mixed matrix̕ membranes, wherein the zeolite crystals were well-adhered to the polymeric matrix. Substantially enhanced gas separation characteristics were observed in mixed matrix membranes containing solvothermally modified MFI crystals. Gas permeation measurements on membranes containing nonporous uncalcined MFI revealed that the performance enhancements were due to significantly enhanced MFI-polymer adhesion and distribution of the MFI crystals. Solvothermal deposition of inorganic nanostructures was successfully applied to aluminosilicate LTA surfaces. Solvothermal treatment of LTA was tuned to deposit smaller/finer Mg(OH)₂ nanostructures, resulting in a more highly roughened zeolite surface. Characterization of particles and mixed matrix membranes revealed that the solvothermally surface-treated LTA particles were promising for application in mixed matrix membranes. Zeolite LTA materials with highly roughened surfaces were also successfully prepared by a new method: the ion-exchange-induced growth of Mg(OH)₂ nanostructures using the zeolite as the source of the Mg²⁺ ions. The size/shape of the inorganic nanostructures was tuned by adjusting several parameters such as the pH of the reagent solution and the amount of magnesium in the substrates and systematic modification of reaction conditions allowed generation of a good candidate for application in mixed matrix membranes. Zeolite/polymer adhesion properties in mixed matrix membranes were improved after the surface treatment compared to the untreated bare LTA. Surface modified zeolite 5A/6FDA-DAM mixed matrix membranes showed significant enhancement in CO₂ permeability with slight increases in CO₂/CH₄ selectivity as compared to the pure polymer membrane. The CO₂/CH₄ selectivity of the membrane containing surface treated zeolite 5A was much higher than that of membrane with untreated zeolite 5A. In addition, the use of metal organic framework (MOF) materials has been explored in mixed matrix membrane applications. ZIF-90 crystals with submicron and 2-μm sizes were successfully synthesized by a nonsolvent induced crystallization technique. Structural investigation revealed that the ZIF-90 particles synthesized by this method had high crystallinity, microporosity and thermal stability. The ZIF-90 particles showed good adhesion with polymers in mixed matrix membranes without any compatibilization. A significant increase in CO₂ permeability was observed without sacrificing CO₂/CH₄ selectivity when Ultem® and Matrimd® were used as the polymer matrix. In contrast, mixed matrix membranes with the highly permeable polymer 6FDA-DAM showed substantial enhancement in both permeability and selectivity, as the transport properties of the two phases were more closely matched.

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39

Anyaogu, Kelechi Chigboo. "Stabilized Metal Nanoparticle-Polymer Composites: Preparation, Characterization and Potential Applications." Bowling Green State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1222126708.

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40

Safa, Meer N. "Poly (Ionic Liquid) Based Electrolyte for Lithium Battery Application." FIU Digital Commons, 2018. https://digitalcommons.fiu.edu/etd/3746.

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The demand for electric vehicles is increasing rapidly as the world is preparing for a fossil fuel-free future in the automotive field. Lithium battery technologies are the most effective options to replace fossil fuels due to their higher energy densities. However, safety remains a major concern in using lithium as the anode, and the development of non-volatile, non-flammable, high conductivity electrolytes is of great importance. In this dissertation, a gel polymer electrolyte (GPE) consisting of ionic liquid, lithium salt, and a polymer has been developed for their application in lithium batteries. A comparative study between GPE and ionic liquid electrolyte (ILE) containing batteries shows a superior cyclic performance up to 5C rate and a better rate capability for 40 cycles for cells with GPE at room temperature. The improvement is attributed to GPE’s improved stability voltage window against lithium as well as higher lithium transference number. The performance of the GPE in lithium-sulfur battery system using sulfur-CNT cathodes shows superior rate capability for the GPE versus ILE for up to 1C rates. Also, GPE containing batteries had higher capacity retention versus ILE when cycled for 500 cycles vii at C/2 rate. Electrochemical impedance spectroscopy (EIS) studies reveal interfacial impedances for ILE containing batteries grew faster than in GPE batteries. The accumulation of insoluble Li2S2/Li2S on the electrodes decreases the active material thus contributes to capacity fading. SEM imaging of cycled cathodes reveals cracks on the surface of cathode recovered from ILE batteries. On the other hand, the improved electrochemical performance of GPE batteries indicates better and more stable passivation layer formation on the surface of the electrodes. Composite GPE (cGPE) containing micro glass fillers were studied to determine their electrochemical performance in Li batteries. GPE with 1 wt% micro fillers show superior rate capability for up to 7C and also cyclic stability for 300 cycles at C/2 rate. In situ, EIS also reveals a rapid increase in charge transfer resistance in GPE batteries, responsible for lowering the capacity during cycling. Improved ion transport properties due to ion-complex formations in the presence of the micro fillers, is evidenced by improved lithium transference number, ionic conduction, and ion-pair dissociation detected using Raman spectroscopy.

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41

Koo, Yiu, and 顧耀. "Synthesis of metal-containing thiophene-based conjugated polymers for photovoltaic applications." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B41897262.

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42

Koo, Yiu. "Synthesis of metal-containing thiophene-based conjugated polymers for photovoltaic applications." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B41897262.

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43

Claude, Elisabeth. "Synthèse et optimisation des propriétés magnétiques et morphologiques de poudres d'alliages terres rares-métaux de transition par le procédé de réduction-diffusion (ORD), destinées à l'élaboration d'aimants permanents composites à matrice polymère." Grenoble INPG, 1994. http://www.theses.fr/1994INPG0126.

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L'industrie de l'aimant permanent est en pleine expansion et notamment celle des aimants lies a matrice polymere. Ces derniers presentent certains avantages par rapport aux aimants frittes (formes plus complexes, meilleure resistance aux chocs, prix plus faibles) qui les destinent a des applications de grandes distributions comme l'automobile, l'electromenager ne comportant pas d'etape de frittage au cours de son procede d'elaboration, le plastoaimant a ses proprietes magnetiques fixees par celles de la poudre qui le constitue. C'est pourquoi, la poudre utilisee doit avoir une forte coercivite, une aimantation a saturation elevee et une granulometrie monodomaine tres homogene. Le procede de reduction diffusion (ord) permet la synthese d'alliages terres rares metaux de transition 3d sous forme de poudre micronique. Ils presentent les caracteristiques requises pour leurs emplois dans l'industrie des plastoaimants, soit directement comme les alliages smco#5, prco#5, pr#2co#1#4b, soit indirectement comme la phase sm#2fe#1#7. En effet, cette derniere devient interessante apres nitruration car son nitrure a une anisotropie magnetocristalline uniaxiale elevee. Une nouvelle technique tout a fait originale de nitruration chimique de la phase sm#2fe#1#7 par de l'azoture de sodium a ete developpee pour elaborer sm#2fe#1#7n#3. Une etude parallelement menee permet d'expliquer que les phenomenes de degradation de la coercivite sous l'effet de la corrosion en milieu humide de ces alliages sont en partie dus a une hydruration partielle du cur des grains de la poudre resultant de l'hydrolyse de leur surface

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44

Xue, Siqi. "Organic-modifier-free pathways for the preparation of polymer-metal oxide nanocomposites." Diss., Connect to online resource - MSU authorized users, 2007.

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45

Corradi, Roberto. "Conducting polymer-silica colloidal composites." Thesis, University of Sussex, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263866.

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46

Joshi, Sharmad Vinod. "Characterization of 3D printed metal oxide composite polymers." Miami University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=miami1595511295182678.

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47

Baccouche, Yousra. "Caractérisation non linéaire de l'endommagement des matériaux composites par ondes guidées." Phd thesis, Université du Maine, 2013. http://tel.archives-ouvertes.fr/tel-00840424.

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La sensibilité des méthodes acoustiques non-linéaires à la présence ainsi qu'à l'évolution des microendommagements a été prouvée dans différents travaux sur une large gamme de matériaux. Parmi les méthodes appliquées figure la résonance non-linéaire dont la sensibilité à l'endommagement est prouvée pour un seul mode de vibration à travers la décroissance de la fréquence de résonance ƒ et celle facteur de qualité Q en fonction de la déformation dynamique. Ainsi, les paramètres non-linéaires hystérétiques (NLH) ƒ et Q ne sont connus que dans une gamme fréquentielle réduite. Le présent travail de thèse propose l'utilisation d'une approche originale permettant de suivre la dispersion des paramètres ƒ et Q à travers la génération d'ondes guidées dans des plaques en composites à matrices polymère et métallique. De plus, l'approche en ondes guidées a également permis de définir un nouveau paramètre NLH V liée au mode de Lamb A0. L'un des résultats originaux de ce travail est que le rapport V/ƒ s'avère constant (~ 2) quelle que soit la fréquence considérée et ce pour les deux types de composites. Ce résultat prometteur montre pour la première fois qu'il est possible de généraliser le comportement NLH dans les structures en plaques moyennant le formalisme de Lamb. Finalement, le travail de thèse s'est également intéressé à la définition d'un nouveau paramètre NLH large bande, noté ∆S, afin de suivre la sensibilité du spectre de vibration à l'endommagement. Les mesures ont montré que ∆S pouvait se distinguer de par une réponse pouvant être nonlinéaire dès les premiers niveaux d'excitation ou à partir d'un niveau seuil. Ce résultat très prometteur montre à quel point il est important d'élargir le domaine fréquentiel pour une détection précoce de l'endommagement et ce même à des niveaux d'excitation où l'on croyait le matériau se comporter de façon linéaire.

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48

Ng, Po-king. "Molecular and polymeric metal complexes for electroluminescence applications." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20979435.

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49

Pallon, Love. "Polyethylene/metal oxide nanocomposites for electrical insulation in future HVDC-cables : probing properties from nano to macro." Doctoral thesis, KTH, Polymera material, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-193591.

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Nanocomposites of polyethylene and metal oxide nanoparticles have shown to be a feasible approachto the next generation of insulation in high voltage direct current cables. In order to reach an operationvoltage of 1 MV new insulation materials with reduced conductivity and increased breakdown strengthas compared to modern low-density polyethylene (LDPE) is needed.In this work polyethylene MgO nanocomposites for electrical insulation has been produced andcharacterized both from an electrical and material perspective. The MgO nanoparticles weresynthesized into polycrystalline nanoparticles with a large specific surface area (167 m2 g–1). Meltprocessing by extrusion resulted in evenly dispersed MgO nanoparticles in LDPE for the silane surfacemodified MgO as compared to the unmodified MgO. All systems showed a reduction in conductivityby up to two orders of magnitude at low loading levels (1–3 wt.%), but where the surface modifiedsystems were able to retain reduced conductivity even at loading levels of 9 wt.%. A maximuminteraction radius to influence the conductivity of the MgO nanoparticles was theoretically determinedto ca. 800 nm. The interaction radius was in turn experimentally observed around Al2O3 nanoparticlesembedded in LDPE using Intermodulation electrostatic force microscopy. By applying a voltage on theAFM-tip charge injection and extraction around the Al2O3 nanoparticles was observed, visualizing theexistence of additional localized energy states on, and around, the nanoparticles. Ptychography wasused to reveal nanometre features in 3D of electrical trees formed under DC-conditions. Thevisualization showed that the electrical tree grows by pre-step voids in front of the propagatingchannels, facilitating further growth, much in analogy to mechanical crack propagation (Griffithconcept). An electromechanical effect was attributed as possible mechanism for the formation of the voids.
Nanokompositer av polyeten och metalloxidpartiklar anses vara möjliga material att använda i morgondagens isolationshölje till högspänningskablar för likström. För att nå en transmissionsspänning på 1 MV behövs isolationsmaterial som i jämförelse med dagens polyeten har lägre elektrisk ledningsförmåga, högre styrka mot elektriskt genomslag och som kan kontrollera ansamling av rymdladdningar. De senaste årens forskning har visat att kompositer av polyeten med nanopartiklar av metalloxider har potential att nå dessa egenskaper. I det här arbetet har kompositer av polyeten och nanopartiklar av MgO för elektrisk isolation producerats och karaktäriserats. Nanopartiklar av MgO har framställts från en vattenbaserad utfällning med efterföljande calcinering, vilket resulterade i polykristallina partiklar med en mycket stor specifik ytarea (167m2 g-1). MgO-nanopartiklarna ytmodifierades i n-heptan genom att kovalent binda oktyl(trietoxi)silan och oktadekyl(trimetoxi)silan till partiklarna för att skapa en hydrofob och skyddande yta. Extrudering av de ytmodifierade MgO nanopartiklarna tillsammans med polyeten resulterade i en utmärkt dispergering med jämnt fördelad partiklar i hela kompositen, vilket ska jämföras med de omodifierade partiklarna som till stor utsträckning bildade agglomerat i polymeren. Alla kompositer med låg fyllnadsgrad (1–3 vikt% MgO) visade upp till 100 gånger lägre elektrisk konduktivitet jämfört med värdet för ofylld polyeten. Vid högre koncentrationer av omodifierade MgO förbättrades inte de isolerande egenskaperna på grund av för stor andel agglomerat, medan kompositerna med de ytmodifierade fyllmedlen som var väl dispergerade behöll en kraftig reducerad elektrisk konduktivitet upp till 9 vikt% fyllnadshalt. Den minsta interaktionsradien för MgO-nanopartiklarna för att minska den elektriska konduktiviten i kompositerna fastställdes med bildanalys och simuleringar till ca 800 nm. Den teoretiskt beräknade interaktionsradien kompletterades med observation av en experimentell interaktionsradie genom att mäta laddningsfördelningen över en Al2O3-nanopartikle i en polyetenfilm med intermodulation (frekvens-mixning) elektrostatisk kraftmikroskop (ImEFM), vilket är en ny AFM-metod för att mäta ytpotentialer. Genom att lägga på en spänning på AFM-kantilevern kunde det visualiseras hur laddningar, både injicerades och extraherades, från nanopartiklarna men inte från polyeten. Det tolkades som att extra energinivåer skapades på och runt nanopartiklarna som fungerar för att fånga in laddningar, ekvivalent med den gängse tolkningen att nanopartiklar introducera extra elektronfällor i den polymera matrisen i nanokompositer. Nanotomografi användes för att avbilda elektriska träd i tre dimensioner. Avbildningen av det elektriska trädet visade att tillväxten av trädet hade skett genom bildning av håligheter framför den framväxande trädstrukturen. Håligheterna leder till försvagning av materialet framför det propagerande trädet och förenklar på det sättet fortsatt tillväxt. Bildningen av håligheter framför trädstrukturen uppvisar en analogi till propagering av sprickor vid mekanisk belastning, i enlighet med Griffiths koncept.

QC 20161006

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Sahu, Laxmi Kumari D'Souza Nandika Anne. "Bulk and interfacial effects on density in polymer nanocomposites." [Denton, Tex.] : University of North Texas, 2007. http://digital.library.unt.edu/permalink/meta-dc-3619.

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Dissertations / Theses on the topic 'Polymer Metal Composite'

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