In the past two decades polymer/clay nanocomposites (PCNs) have emerged as promising materials that exhibit remarkably improved properties when compared to conventional composites and pristine polymers. Such improvements strongly depend on the dispersion of clay nanoparticles in the polymer matrix. In spite of great efforts expended in characterizing clay dispersion, effective, simple and quantitative techniques are still needed. This work addresses this challenge by presenting new aspects of 1H solid-state NMR for quantifying clay dispersion in PCNs filled with clay containing paramagnetic ions. Employing these 1H solid-state NMR methods, some structure-processing-deformation relationships of PCNs were derived, and basic insights into nuclear relaxation and spin diffusion in PCNs were gained as well. Detailed models and analyses were described for 1H spin-lattice relaxation in the presence of paramagnetic clays in PCNs. Relaxation recovery was analytically correlated to clay dispersion in two ways: one is the initial relaxation recovery which is related to clay surface area, and the other is the spin-lattice relaxation time which is related to interparticle spacing. These two NMR observables were employed to quantitatively observe the evolution of clay morphology in poly(propylene)/clay (PP/MMT) nanocomposites upon equibiaxial stretching, as well as upon in situ uniaxial deformation. The initial relaxation recovery was independently utilized to determine the polymer-clay interfacial surface area and the degree of clay exfoliation. We demonstrated the capabilities of our models in quantitatively characterizing several materials, including poly(vinyl alcohol), nylon 6, poly(å-caprolactone) (PCL), poly(lactic acid) (PLA) and PP nanocomposites. These results were used to examine the dependence of clay morphology upon processing (strain ratio, strain rate, temperature), deformation (extension), component characteristics (polymer molecular weight, clay surface modification) and clay content. Effects of paramagnetic Fe3+ concentration and external magnetic field strength on 1H spin-lattice relaxation in PCNs were also investigated and discussed. In particular, low field separates the initial relaxation recovery into two stages: one related to clay content and the other related to the polymer-clay interfacial surface area. The low field was observed to enhance the paramagnetic contribution to the spin-lattice relaxation rate, increasing its sensitivity to clay morphology. In addition, measurements of long-distance spin diffusion coefficients for a variety of polymers and paramagnetic characteristics of organically modified clay were explored. Overall, the utility of NMR relaxometry in characterizing PCNs has been significantly expanded and successfully demonstrated in this dissertation.

Thesis (M.S.)--Mississippi State University. Department of Physics and Astronomy. / Title from title screen. Includes bibliographical references.

Realizamos medidas de tempos de relaxação de centros F em cristais de KCN, pela técnica de saturação do sinal de absorção por pulsos de microonda. Observamos um comportamento não exponencial para a recuperação da magnetização da amostra ap6so pulso. Este fato deve-se ao efeito combinado de relaxação cruzada ou difusão da magnetização pelo espectro de absorção, juntamente com a relaxação spin-rede. Medidas à 4,2 °K e 1,8 °K fornecem indícios que, ap6s algum tempo, apenas a relaxação spin-rede sobrexiste. O modelo teórico baseado na modulação da interação hiperfina e no processo direto fornece tempos menores que os obtidos experimentalmente. Isto deve-se à formação de conglomerados de centros. Também elaboramos um modelo levando em conta processo Raman, para prever tempos de relaxação spin-rede a temperaturas mais elevadas. / We measure the spin-lattice relaxation time of F centers in KCN at 1.8 and 4.2 K using the saturation recovery technique. The observed recovery is non exponential. This result is interpreted in terms of the combined effect of cross-relaxation and spin lattice relaxation. The values obtained for T1 (- sec) are found to be shorter than those calculated theoretically. This discrepancy is throught to arise from the presence of clusters. The characteristic time found from the initial part of recovery is found to be -6 sec in agreement with that found in KC for the recovery of a hole burnt in the resonance line (45). Finally the value of T1 was calculated for the Raman processes at high temperature and compared with known results.

In this work I present a 23Na/51V-NMR study of sodium vanadate as pure compound, and the influence of very small amounts of Sodium substitution by Calcium and Lithium is reported and discussed. The measurements of spin-lattice relaxation for 23Na and 51V are also presented. The sodium vanadate is found to have a double phase transition. The two transitions are close together and take place around 34 K. Above the transition temperature there is one V site in the mixed oxidation state 4.5+ and there is one Na site. A consistency for a number of un-doped and very slightly doped samples of three vanadium valences is argued, confirming a charge ordering transition at transition temperature, in good qualitative agreement with Bernert’s model and as well in quantitative and qualitative agreement with Sawa’s monoclinic structure. Below the transition temperature sodium is found to have ten sites. The number of the Na site is continuously developed with decreasing the temperature below transition temperature. This continues development of the Na sites demonstrates that the second transition is continues. The detailed spin-lattice relaxation rate for 23Na in both, the pure and the doped samples, in transition region, provided evidence for a non-symmetric and complex transition peak structure which we relate to the onset of more than one transition occurring at slightly different temperatures. This scales with the transition temperature reduction provided by lithium and calcium doping. The two transitions (i.e. dimerization and charge ordering) are intimately related. We investigated the spin-gap by means of Vanadium and Sodium spin-lattice relaxation temperature dependence well below transition temperature. The analysis of the single crystal data reveals a significant anisotropy in the nature of the gap, which is sensitive to Calcium and Lithium doping, indicating that is constrained to the ladder plane.

The spin-lattice relaxation rates are calculated for a rigid magnetic spin cluster in an elastic medium in the presence of a magnetic eld using the latticerame method. This rate is then compared with both the rate calculated using the quantum mechanical densitymatrix method and with the Glauber dynamics. These calculation results are used in the contribution of various heat baths, such as a phonon bath in various dimensions or a fermionic bath, to transition rates that enter into dynamic Monte Carlo simulations of molecular magnets and nanomagnets.

A cinza obtida da queima controlada da casca de arroz é um material que apresenta propriedades pozzolânicas: reage na presença de água e dióxido de cálcio produzindo silicato de cálcio hidratado (C-S-H), o material que confere a resistência mecânica aos cimentos. Portanto, a cinza de casca de arroz é um material de potencial interesse para o desenvolvimento de cimentos não convencionais, baseados em subprodutos industriais ou agrícolas. Neste trabalho, os compostos presentes em cinzas de alta reatividade pozzolânica e os produtos obtidos de sua reação pozzolânica foram estudados através da Ressonância Magnética Nuclear (RMN) de alta resolução de 13C e 29Si. Na cinza não hidratada foram detectados domínios de sílica amorfa, o componente principal, e quantidades menores de sílica cristalina (cristobalita e quartzo), carbono amorfo e cadeias de siloxanos. Foi estudada a evolução da reação em pastas obtidas da hidratação da cinza na proporção água: cal: cinza O,47H20+O,53(O,1CCA+O,9Cal)=1 (entre 8 e 134 dias de idade). Mediante a RMN de 29Si foi possível caracterizar a formação de C-S-H e disposição dos grupos silicatos na estrutura. A estrutura do C-S-H obtido é comparável à observada em cimentos convencionais e cimentos de escoria de alto forno, e é compatível com os modelos propostos. A quantidade de C-S-H produzido e a velocidade da reação são menores quando comparadas com os outros cimentos. Efeitos da carbonatação de C-S-H foram observáveis em atmosfera ambiente. Foi detectado também o efeito da hidratação sobre os componentes minoritários da cinza. / The ashes obtained from burning rice husks have pozzolanic properties: in the presence of water and calcium dioxide the ashes react to produce calcium silicate hydrate (C-SH), the main binding agent in cementitiuos materials. Therefore, rice husk ashes are interesting materials in order to produce non-conventional cement, based in industrial or agricultural byproducts. The compounds present in a sample of rice husk ashes of high pozzolanic activity, and the products of hydration, were characterized using high resolution solid-state Nuclear Magnetic Resonance (NMR) of 13C and 29Si. Several compounds were detected in anhydrous ashes: amorphous silica (the main component), and minor quantities of crystalline silica (cristobalite and quartz), amorphous carbon and siloxane polymeric chains. Hardened pastes were prepared with a ratio water:calcium dioxide:ash O,47H20+O,53(O,1dioxide ash+O,9calcio)=1. The evolution of the hydration reaction was monitored at several ages between 8 to 134 days. The formation of C-S-H was detected by 29Si-NMR and the arrangement of the silicate groups was characterized. The structure of the C-S-H formed in these pastes agrees with the one observed in conventional cements and also b1ast furnace slag cements. Also, it is in agreement with the accepted structural models of C-S-H. The amount of C-S-H produced and the velocity of the reaction are minor than those observed in blast furnace slag cements. Carbonation effects were detected in ambient atmospheric conditions. Also, the effect of the hydration on the minority compounds was also detected.

A cinza obtida da queima controlada da casca de arroz é um material que apresenta propriedades pozzolânicas: reage na presença de água e dióxido de cálcio produzindo silicato de cálcio hidratado (C-S-H), o material que confere a resistência mecânica aos cimentos. Portanto, a cinza de casca de arroz é um material de potencial interesse para o desenvolvimento de cimentos não convencionais, baseados em subprodutos industriais ou agrícolas. Neste trabalho, os compostos presentes em cinzas de alta reatividade pozzolânica e os produtos obtidos de sua reação pozzolânica foram estudados através da Ressonância Magnética Nuclear (RMN) de alta resolução de 13C e 29Si. Na cinza não hidratada foram detectados domínios de sílica amorfa, o componente principal, e quantidades menores de sílica cristalina (cristobalita e quartzo), carbono amorfo e cadeias de siloxanos. Foi estudada a evolução da reação em pastas obtidas da hidratação da cinza na proporção água: cal: cinza O,47H20+O,53(O,1CCA+O,9Cal)=1 (entre 8 e 134 dias de idade). Mediante a RMN de 29Si foi possível caracterizar a formação de C-S-H e disposição dos grupos silicatos na estrutura. A estrutura do C-S-H obtido é comparável à observada em cimentos convencionais e cimentos de escoria de alto forno, e é compatível com os modelos propostos. A quantidade de C-S-H produzido e a velocidade da reação são menores quando comparadas com os outros cimentos. Efeitos da carbonatação de C-S-H foram observáveis em atmosfera ambiente. Foi detectado também o efeito da hidratação sobre os componentes minoritários da cinza. / The ashes obtained from burning rice husks have pozzolanic properties: in the presence of water and calcium dioxide the ashes react to produce calcium silicate hydrate (C-SH), the main binding agent in cementitiuos materials. Therefore, rice husk ashes are interesting materials in order to produce non-conventional cement, based in industrial or agricultural byproducts. The compounds present in a sample of rice husk ashes of high pozzolanic activity, and the products of hydration, were characterized using high resolution solid-state Nuclear Magnetic Resonance (NMR) of 13C and 29Si. Several compounds were detected in anhydrous ashes: amorphous silica (the main component), and minor quantities of crystalline silica (cristobalite and quartz), amorphous carbon and siloxane polymeric chains. Hardened pastes were prepared with a ratio water:calcium dioxide:ash O,47H20+O,53(O,1dioxide ash+O,9calcio)=1. The evolution of the hydration reaction was monitored at several ages between 8 to 134 days. The formation of C-S-H was detected by 29Si-NMR and the arrangement of the silicate groups was characterized. The structure of the C-S-H formed in these pastes agrees with the one observed in conventional cements and also b1ast furnace slag cements. Also, it is in agreement with the accepted structural models of C-S-H. The amount of C-S-H produced and the velocity of the reaction are minor than those observed in blast furnace slag cements. Carbonation effects were detected in ambient atmospheric conditions. Also, the effect of the hydration on the minority compounds was also detected.

Magnetic resonance imaging is a routine and powerful diagnostic technique capable of providing detailed information about the structure and composition of the tissues. This diploma thesis is concerned with the mechanisms of contrast origin and contrast modifications by molecular and nanoparticle contrast agents. First sections of the thesis summarize basic knowledge about pulse sequences and it aims to provide an overview on MRI contrast agent with a special emphasis on paramagnetic gadolinium contrast agents and superparamagnetic nanoparticles. The main purpose of this study is to develop the software called MRICalc, which is able to optimize contrast in MRI images. Based on analysis of signal formula of typical pulse sequences, MRICalc is able to propose the parameters of the pulse sequence for compartment-specific enhancement of the contrast. User chooses from the list of the samples and after calculation he obtains the values of echo time, repetition time and flip angle, all of which simultaneously seem to create the appropriate setting to enhance the contrast. MRICalc also allows to plot contrast function with respect to the chosen parameter. Software, including its graphical user interface, is designed in Python. The sample consists from solution of CuSO4 and distilled water was designed to verify the correct function of MRICalc. Sulphate represents a contrast agent. Preclinical MR system Bruker BioSpec 94/30 USR located at Institute of Scientific Instruments of the ASCR, v.v.i was used to measure contrast curve of FLASH pulse sequence, which is a typical representative of gradient echo. Results of the measurement were compared to the theoretical model provided by MRICalc.

In this work we studied magnetic properties of molecular magnets of the new heteropolyanion {Cu20}, dodecanuclear cluster {Ni12}, and the heterometallic {Cr7M} wheels, in which one of the CrIII ions of Cr8 has been replaced by a Fe, Cu, Zn, Ni, ion with this extra-spin acts as local probe for the spin dynamics.Such systems have been synthesized recently and they are well described using the Heisenberg spin Hamiltonian with a Zeeman term of an applied magnetic field along the z-axis. Using the numerical exact diagonalization method, we have calculated the energy spectrum and the eigenstates for different compounds,and we have used them for reexamining the available experimental susceptibility data to determine the values of exchange parameters.We have studied the thermodynamic properties such magnetization, susceptibility, heat-capacity. At low temperature regions molecular magnets act as individual quantum nanomagnets and can display super-paramagnetic phenomena like macroscopic quantum tunneling, ground state degeneracy, level-crossing. A crucial issue for understanding these phenomena is the coupling between magnetic molecular levels and the environment such as nuclear spins. We have modeled the behavior of the proton spin lattice relaxation rate as a function of applied magnetic field for low temperatures as it is measured in Nuclear Magnetic Resonance (NMR) experiments.

Conducting and semiconducting polymers, consisting of delocalized π-electrons, have been studied for the past three decades. These materials have shown novel physical properties with interesting applications in batteries, detectors, light emitting diodes, field effect transistors, solar cells, biosensors etc. Nevertheless the charge transport properties are yet to be understood in detail due to the complexity of the system, especially due to the interplay of quasi-one dimensionality (q-1D), disorder, localization and electron-electron interactions(EEI). A combined investigation of both conductivity and spin lattice relaxation time, especially at very low temperatures and high magnetic fields, is really lacking in conducting polymers. In this thesis a set of experiments – dc conductivity, magnetoresistance (MR), Nuclear Magnetic Resonance (NMR) spin lattice relaxation time (T1) measurements, magnetic susceptibility amd ac conductivity have been carried out in conducting polymers. NMR being a local probe it is possible to get the nanoscopic scale charge transport mechanism. Further, this helps to develop a consistent understanding among a wide range of the physical properties in conducting polymers. In this thesis author has reported the results of experiments at ultra low temperature (mk) and ultra high magnetic field which give more insight about the roles of electron-electron interaction(EEI) and disorderin charge transport properties. This thesis describes a detailed study of charge transport and NMR relaxation in three representative conducting polymers namely polypyrrole(PPy)., poly-3-methylthiophene(P3MT) and poly3-hexylthiophene(P3HT). The emphasis is to understand the charge transport phenomena and NMR relaxation, especially at ultra low temperatures (down to 20 mk) and high magnetic field (up to 23.4 T). The NMR T1 relaxation mechanisms are discussed in terms of (i) Korringa relaxation, (ii) relaxation due to spin diffusion to paramagnetic centers (SDPC) amd (iii) reorientation of symmetric groups, depending upon the temperature range.