Yes / This paper investigates the coupled effect of functionalized multiwall carbon nanotubes (MWCNTs-COOH), nanomontmorillonite (NM), and sodium dodecyl benzene sulfonate (SDBS) anionic surfactant on compressive and flexural strengths of cement paste. The response surface methodology (RSM) was used to optimize the content of the two nanomaterials and surfactant, and to analyze the effect of their interactions on mechanical properties and microstructural characteristics of the paste. Test results indicate that the simultaneous use of NM and MWCNT can lead to 30% gain in compressive strength and 40% increase in flexural strength. Using analysis of variance, it was possible to predict the optimal weight percentage of nanomaterials. Atomic Force Microscope observations showed that the use of NM and MWCNT can reduce the surface roughness of cement paste and refine porosity, thus reducing the risk of cracking at the cement matrix and improving the homogeneity of the microstructure.

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The advancement of each component of aerospace vehicles is necessary as the continual demand for more aggressive missions are created. Improvements in propulsion and guidance system electronics are invaluable; however without material development to protect the vehicle from its environment those advances will not have a practical application. Thermal protection systems (TPS) are required in both external applications; for example on reentry vehicles, as well as in internal applications; to protect the casing of rockets and missiles. This dissertation focuses on a specific type of internal solid rocket motor TPS, ablatives. Ablatives have been used for decades on aerospace vehicles. To protect the motor from the hostile environment, these materials pyrolyze and char. Both of these mechanisms produce a boundary between the combustion gases and the motor as well as release the heat that the decomposed material has absorbed. These sacrificial materials are intended to protect the casing that it is attached to. With the development of polymer nanocomposites (PNCs) in the last couple of decades, it is of interest to see how these two fields can merge. Three different nanomaterials (carbon nanofibers, multiwall carbon nanotubes, and nanoclays) are examined to observe how each behaves in environments that simulate the motor firing conditions. These nanomaterials are individually added to a thermoplastic polyurethane elastomer (TPU) at different loadings, creating three distinct families of polymer nanocomposites. To describe a materials ablative performance, a number of material properties must be individually studied; such as thermal, density, porosity, char strength, and rheology. Different experiments are conducted to isolate specific ablative processes in order to identify how each nanomaterial affects the ablative performance. This dissertation first describes each material and the ablative processes which are characterized by each experiment. Then basic material properties of each family of materials are described. Degradation and flammability experiments then describe the degassing processes. Studies of the material char are then performed after full blown rocket experiments are done. These tests have shown that of the three nanomaterials, nanoclay enhances the TPU ablative performance the most while the CNF provides the least enhancement. / text

Vertically aligned Multiwalled Carbon Nanotubes (MWCNTs) were grown in the pores of Anodized Aluminum Oxide (AAO) templates and investigated for resistive sensor applications. High Sensitivity of 23% to low concentration (100 ppm) of ammonia was observed. An equivalent circuit model was developed to understand the current flow path in the resistive sensor. This helped us in achieving high sensitivities through amorphous carbon (a-C) layer thickness tailoring by employing post-growth processing techniques like plasma etching. A simulation model in MATLAB was developed to calculate the device resistance and the change in the sensitivity as a function of device parameters. The steady state response and transient response of the model to the number of ammonia molecules and its adsorption rate were studied. Effects of oxygen plasma, argon plasma and water plasma etch on thinning of the a-C layer were studied. In order to enhance the sensitivity, the top and bottom a-C layers were replaced by a more conductive metal layer. This also helped in understanding the current flow in the device and in the estimation of the resistivity of the a-C layer.

Multiwall carbon nanotubes (MWNTs) have extraordinary mechanical and thermal transport properties. They significantly improve the static and dynamic mechanical properties of acrylic orthopaedic bone cement when added to the dry cement polymer powder. Understanding the role MWNTs play on bone cement polymerization temperatures will lead to improved mechanical integrity of the cement-bone interface in joint arthroplasties. It was determined through thermal testing that MWNTs increased the polymerization time of the methylmethacrylate by 45-460% and decreased the peak exothermic temperature of bone cement with and without antibiotics. The flow of heat produced during polymerizing cement was reduced 25-85% with the addition of MWNTs to the cement powder. This decreases the probability of thermal necrosis and “hot” spots caused by high exothermic polymerization temperatures that can destroy the bone adjacent to the cement. These high temperatures also affect the potency and range of antibiotics used in arthroplasty. Isothermal and elution studies determined that MWNTs altered the heat flow and amount of antibiotic release from bone cement during polymerization. Antibiotic elution from bone cement containing MWNTs could match the elution seen in pure cement. The alteration of the flow of heat from bone cement leads to new options for heat-labile antibiotics in total joint arthroplasty.

The interactions which occur between both polar and non-polar fluid phases and surfaces of various carbon materials: Activated Carbon (AC), non-porous Carbon Black (CB) and Multiwall Carbon Nanotubes (MWCNTs)with different surface chemistry have been studied. These are currently of great interest as they govern the interfacial behaviour of carbons in a wide range of applications; separation adn composite technologies being two prime examples. Consequently, techniques for chemical modification of carbon surfaces ar also of interest. Surface oxygen functional groups have been introduced, or modified, using the following oxidation techniques: liquid-phase oxidation (both AC and CB), Fenton and Birch reduction treatment (MWCNTs) and in a more controlled manner using gas-phase ozone treatment (CB). The chemistry of all the resulting carbon surfaces were characterised using X-ray Photoelectron Spectroscopy (XPS), which gives a quick and direct quantitative measure of the external surface composition. This technique, which has not yet been extensively employed in detailed adsorption studies, is a promising alternative to Temperature Programmed Desorption (TPD) and Boehm titration method in the determination of oxygen and other surface groups. Physical effects of the various surface modifications have been studied using a variety of techniques appropriate for the material in question. Scanning Electron Microscopy (SEM) images show some deteriorating effects of the liquid-phase oxidations on the structure of both activated carbon and carbon black materials. Conversely, surface areas from nitrogen adsorption at 77oK, coupled witj immersion calorimetry data for toluene, show thet the physical structure of the carbon blacks is not modified by ozone treatment. This has allowed a detailed study of the effects of surface oxygen level (i.e. polarity) on vapour adsorption. Regarding the MWCNT materials, detailed High-Resolution Electron Microscopy (HRTEM) photographs show that the multi-wall structure of the nanotubes in not significantly disrupted during the introduction of active functional groups by the Fenton or Birch treatment and therefore keeping intact their mechanical properties which augurs well for their use as reinforcement in composite structures whilst also improving their dispersion properties in polar fluids. A systematic shift to higher adsorption values, due to the increasing specific interactions between the alcohol -OH groups and the surface oxygen groups, is observed in all the isotherms of alcohols from the CB series as the total surface oxygen concentration ([O]T) increases. Moreover, this effect was observed to be most significant for methanol confirming that the mechanism of adsorption is dominated by hydrogen bonding and therefore dependant on the surface concentration of oxygen sites; whereas it becomes less marked in the case of ethanol and isopropanol respectively due to the increasing non-specific, dispersion, interactions of the alkyl chain with the non-polar carbon surface. Overall correlations were observed between the surface oxygen concentration [O]T, the resulting enthalpy of immersion -^Hi values and the characteristic energy E of the Dubinin-Radushkevich-Kaganer (DRK) equation obtained for toluene and these alcohols and the influence of the carbon surface chemistry on the character of the adsorption isotherms is also discussed. This behaviour is also observed and much more pronounced in the case of water adsorption on other oxidised carbon materials (AC, CB and MWCNT) due to the higher polarity of water molecules. The water adsorption data were analysed using in particular the Dubinin-Serpinsky (DS) equation and also some of its recent variations such as Barton and D'Arcy & Watt equations. The DS2 and various Barton equations were found to fit best the AC and CB materials modified by liquid-phase oxidations and also for the CB 03 series with increasing level of oxidation while both D'Arcy & Watt equations gave the best fittings for the MWCNTs materials. It was also shown that the resulting parameters ao (for the DS equation) describing the surface concentration of primary polar adsorption sites and as the limiting water adsorption value were both linked to the surface oxygen level [O]T. Regarding interfacial bonding, the oxidised CB and MWCNT materials are expected to show an improved physicochemical wetting of their surfaces by various resin compunds

Electron Beam Induced Deposition (EBID) is an emerging additive nanomanufacturing tool which enables growth of complex 3-D parts from a variety of materials with nanoscale resolution. Fundamentals of EBID and its application to making a robust, low-contact-resistance electromechanical junction between a Multiwall Carbon Nanotube (MWNT) and a metal electrode are investigated in this thesis research. MWNTs are promising candidates for next generation electrical and electronic devices, and one of the main challenges in MWNT utilization is a high intrinsic contact resistance of the MWNT-metal electrode junction interface. EBID of an amorphous carbon interface has previously been demonstrated to simultaneously lower the electrical contact resistance and to improve mechanical characteristics of the MWNT-electrode junction. In this work, factors contributing to the EBID formation of the carbon joint between a MWNT and an electrode are systematically explored via complimentary experimental and theoretical investigations. A comprehensive dynamic model of EBID using residual hydrocarbons as a precursor molecule is developed by coupling the precursor mass transport, electron transport and scattering, and surface deposition reaction. The model is validated by comparison with experiments and is used to identify different EBID growth regimes and the growth rates and shapes of EBID deposits for each regime. In addition, the impact of MWNT properties, the electron beam impingement location and energy on the EBID-made carbon joint between the MWNT and the metal electrode is critically evaluated. Lastly, the dominant factors contributing to the overall electrical resistance of the MWNT-based electrical interconnect and relative importance of the mechanical contact area of the EBID-made carbon joint to MWNT vs. that to the metal electrode are determined using carefully designed experiments.

In this thesis, bulk and local scale spectroscopic and microscopic tools have been applied to investigate the purified raw material of SWCNT and synthesized MWBNNT, BN-nanocapsules, B-doped SWCNT and SiC nanostructures. Using bulk scale sensitive techniques, including optical absorption spectroscopy, Raman spectroscopy, high-resolution electron energy-loss spectroscopy, the average response of the whole sample is obtained. On the other hand, on a local scale transmission and scanning electron microscopy as well as TEM-electron energy-loss spectroscopy provide information on single tubes or other nanostructures. First, diverse chemical and oxidation methods for the purification of as-produced SWCNT were presented. Purified samples were investigated using TEM and OAS. The analysis of the optical absorption spectra in the UV-Vis energy range revealed that some of the chemical treatments are harmful to nanotubes. In contrast to the chemical treatments an oxygen burning procedure was used on the raw material in high vacuum and a temperature range 450?650oC. The purification processes of SWCNT by HNO3 and oxygen burning procedures resulted in SWCNT comprised of selected diameters and a reduced diameter distribution. Both HNO3 and oxygen burning treatments can be used to selectively remove SWCNT with smaller diameters from the samples. In addition, an adapted substitution reaction was used for the synthesis of multiwall boron nitride nanotubes. It was shown that the IR-response of MWBNNT can be used as a fingerprint to analyse MWBNNT. As in h-BN for the analysis one has to be aware of the sample texture and the LO-TO splitting of the IR-active modes. TEM images and B1s and N 1s excitation edges of the grown material reveal the presence of multiwall BN nanotubes with an inner diameter of 3.1 nm and with a larger interplanar distance than in h-BN. The electronic properties of the multiwall BN nanotubes as derived from the q-dependent dielectric function e(w,q) are dominated by the band structure of the hexagonal-like BN sheets, as revealed by the large degree of momentum dispersion observed for the p and s+p plasmons, in agreement with that previously reported for different graphitic allotropic forms. Moreover, a fast and highly efficient synthesis route to produce BN nanocapsules with a narrow size distribution was developed. This was achieved by an adapted substitution process using SWCNT as templates followed by a rapid cooling treatment. The IR responses reveal the strong dipole active fingerprint lines of h-BN with distinct differences, which are due to texturing effects and which highlight the BN nanocapsules potential application as a reference source when deriving the sp2 to sp3 ratio in BN species due to their random orientation Furthermore, the idea of substitution was used for the systematic studies of B-doped SWCNT. The experiments carried out have resulted in 1, 5, 10, and 15 % boron incorporated into the single wall carbon nanotubes. Core level excitation spectroscopy of the B1s and C1s edges revealed that the boron atoms substitute carbon atoms in the tube lattice keeping an sp2-like bond with their nearest C neighbour atoms. Our results show that a simple rigid band model as has been applied previously to intercalated SWCNT is not sufficient to explain the changes in the electronic properties of highly doped B-SWCNT and a new type of a highly defective BC3 SWNT with new electronic properties is obtained. Finally, different silicon carbide nanostructures were produced. The spectroscopic and microscopic data led to a good understanding of the formation process. NH3 acts as a source of hydrogen that plays a key role in the formation of the structures through its ability to decompose SiC at high temperature such that along with the stacking faults that arise from the many polytypes of SiC the produced SiC nanorods become porous then hollow and eventually are completely decomposed.

Multifunctional materials both with damping properties and strain sensing properties are very important. They promise to be more weight-efficient, and provide volume-efficient performance, flexibility and potentially, less maintenance than traditional multi-component brass-board systems. The goal of this dissertation work was to design, synthesize, investigate and apply polyaniline/Multiwall carbon nanotube (PANI/MWCNT) and polyurethane (PU) /MWCNT composites films for structural vibration control and strain sensors using free layer damping methods and static and dynamic strain sensing test methods. The PANI/MWCNT was made by in situ polymerization of PANI in the presence of MWCNT, then frit compression was used to make circular and rectangular PANI/MWCNT composite films. PU/MWCNT composites were made by the layer-by-layer method. Free end vibration test results showed both of PANI/MWCNT and PU/MWCNT have better damping ratios than each of their components. Static sensing test indicated that though there appears to be residual strain in both composite sensors after the load is removed, both the sensor and the foil strain gage react linearly when re-engaged. A drift test of the sensor showed that it is stable. The dynamic sensing test results showed that over the range of 10-1000 Hz, the PANI/MWCNT composite sensor was consistently superior to foil strain gage for sensing purposes since the highest peak consistently corresponded to the input frequency and was much higher, for example, at 20 Hz, 820 times higher than those of the strain gage. Using the same criterion, the PU/Buckypaper composite sensor was comparable to or superior to the foil strain gage for sensing purposes over the range of 10 Hz to 200 Hz. The relationship of loss factor, η, and beam coverage length, L1/L, is discussed for single sided and double sided attachment. For both PANI/MWCNT and PU/MWCNT, the loss factor, η, was found to increase as coverage length, L1/L, increases. The loss factor, η, was found to have a maximum as with coverage length, L1/L, as the coverage length continues to increase. The trend for double sided attachment was found to follow the trends discussed by Rao (2004) and Levy and Chen (1994) for viscoelastic material constrained damping.

The hybrid nanostructures exhibit excellent performances in various fields such as catalysis, sensing, and energy conversion as compared to their individual ones. The thesis deals with the new methods for the synthesis of different type of hybrids with doped/pristine carbon nanostructures in the form of graphene, multiwall carbon nanotubes (MWCNTs) as one component and metals nanostructures (Ag, Pd, Pt and Au), carbide (Fe3C), metal chalcogenides (Ni3S2 and Co9S8) and oxide (CoO) as the other components. Various synthesis techniques such as modified galvanic replacement reaction at room temperature, hydrothermal, microwave and pyrolysis have been explored for the synthesis of different hybrid nanostructures. Furthermore, various hybrid nanostructures have been explored for various catalytic activities such as oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and 4-nitrophenol (4-NP) reduction. It may be noted that the ORR and OER which are undoubtedly vital for their applications in fuel cells, metal-air batteries and water oxidation reaction. Interestingly, the catalytic activities of these hybrid nanostructures are comparable or better as compared to the commercial benchmark precious catalysts.