Polymer-derived ceramics (PDCs) are exceptional ultra-high temperature and stable multifunctional class of materials that can be synthesized from a polymer precursor through thermal decomposition. The presented research focuses on 1-D nanofibers, 2-D films and 3-D bulk, carbon-rich silicon carbon nitride (SiCN) ceramics. 1-D nanofibers were prepared via electrospinning for light weight, flame retardant and conductive applications. The commercially available CerasetTM VL20, a liquid cyclosilazane pre-ceramic precursor, was mixed with polyacrylonitrile (PAN) in order to make the cyclosilazane electrospinnable. Carbon-rich PDC nanofibers were fabricated by electrospinning various ratios of PAN/cyclosilazane solutions followed by pyrolysis. Surface morphology of the electro spun nanofibers characterized by SEM show PDC nano?bers with diameters ranging from 100-300 nm. Also, thermal stability towards oxidation showed a 10% mass loss at 623°C. 2-D carbon/SiCN films were produced by drop-casting a mixture of PAN/cyclosilazane onto a glass slide followed by pyrolysis of the film. Samples ranging from 10:1 to 1:10 PAN:cyclosilazane were made by dissolving the solutes into DMF to produce solutions ranging from 1% to 12% by weight. Green, heat-stabilized, and pyrolyzed 8% films were examined with FTIR to monitor the change in chemical structure at each step of the ceramization. SEM shows that high PAN samples produced films with ceramic embedded spheroid components in a carbon matrix, while high cyclosilazane samples produced carbon embedded spheroid. Finally, this research focuses on the challenge of making fully dense, 3-D bulk PDCs materials. Here we present a composite of SiCN with reduced graphene oxide (rGO) aerogels as a route for fully dense bulk PDCs. Incorporation of the rGO aerogel matrix into the SiCN has its pros and cons. While it lowers the strength of the composite, it allows for fabrication of large bulk samples and an increase in the electrical conductivity of the PDC. The morphology, mechanical, electrical properties and thermal conductivity of graphene-SiCN composite with varying rGO aerogel loading (0.3-2.4%) is presented. The high temperature stability, high electrical conductivity and low thermal conductivity of these composites make them excellent candidates for thermoelectric applications. Generally, carbon-rich SiCN composites with improved thermal and electrical properties are of great importance to the aerospace and electronics industries due to their expected harsh operating environments.

The effects of in situ Ti0₂ whisker reinforcement on mechanical and thermal properties of glass-ceramics in the Li₂O-Al₂0₃-P₂0₆-Si0₂ system were investigated. When Ti0₂ whiskers, having an average aspect ratio of 28, are precipitated from the glass-ceramic matrix, (Li_0.4,Ca_0.05)AI(Si_0.75,P_0.5)_04.5, flexural strength is improved from 72 to 134 MPa. Fracture toughness, K_Ic, is increased from the 1.1 to 1.6 MPa·m^1/2 due to crack deflection by the Ti0₂ whiskers. In situ Ti0₂ whisker-reinforced glass-ceramic exhibits rising fracture resistance, K_R, with increasing crack extension. The fracture resistance, K_R, is increased from 1.89 to 2.5 MPa·m^1/2 over the crack extension range range of 40 to 200 μm. The composite shows a narrow failure strength distribution compared to the glass-ceramic without Ti0₂ whisker precipitation. The coefficient of thermal expansion (CTE) changes from -2.8x10⁻⁷/"C to -1.7xl0⁻⁷/°C due to the precipitation of Ti0₂ phase which has a positive CTE (7.3xl0⁻⁶/°C). With the matrix composition, (Li_0.41,Mg_0.035)AI(Si₀0.48</sub>,P_O.52)O₄, a three-fold increase in flexural strength was observed with a Ti0₂ content of 12 wt%. CTE value of the composite increases linearly from a negative to a positive value with increasing Ti0₂ content up to 12 wt%. The in situ composite containing 8-10 wt% Ti0₂ exhibits near zero CTE values up to l000°C. / Ph. D.

The first chapter introduces the basic principles governing the phenomenon like ferroelectricity, piezoelectricity and pyroelectricity, which influences the material properties for its device applications. An effort is made to examine the present status of material issues, measurement techniques and applications pertaining to the lead based PZT type systems. This chapter also highlights the objectives and the scope of work. The second chapter deals with the various basic experimental techniques and principles adopted for the synthesis and characterizations of materials which include phase and quantitative analysis by X-ray diffraction, density measurements, microstructures by scanning electron microscopy, electrical properties such as dielectric permittivity, dielectric loss, and piezoelectricity by impedance analyzer and piezometer etc. The materials were synthesized via two step solid state reaction by adopting a low temperature calcinations route. Further, hot processing was employed for densification and better control of microstructure of the ceramics. In the third chapter PZT1-x –PZNx (x=0, 0.1, 0.2 & 0.3) compositions prepared by the single step low temperature calcination method have been described. It is seen that the pyrochlore free perovskite phase could be obtained up to x=0.2 compositions. The effect of additives like Li and Mn on the structure, sinterability, microstructure, density and dielectric properties has been investigated. The improvement in densification and ferroelectric properties were observed for Li addition favor tetragonal phase while Mn addition compositions were inclined to pseudocubic phase. Further, the addition of Mn led to the significant decrease in Tc than the parent compositions compared to Li added compositions. In the fourth chapter, the X-ray diffraction data on pbzrx Ti1-x O3 (PZT) for x=0.48 to 0.52 are presented. High resolution x-ray studies for composition x=0.5 show the MPB which consists of monoclinic Zr rich studies and tetragonal Ti rich phase at room temperature. The refined structural parameters for MPB compositions have been obtained using least square Rietveld refinement program, FULLPROF 2006. The evolutions of lattice parameters of the system were also studied with respect to the temperature. The phase transformation in the system has been analyzed by x-ray diffraction pattern and dielectric measurements. The monoclinic phase transforms to tetragonal phase at 270oC after which the tetragonal phase transforms to paraelectric cubic phase at 370DoC. Dielectric properties show signature of the phase transformation. Hence, it is concluded to pole the MPB samples below 270o C to gain the advantage of increased ease of polarization reorientation for monoclinic phase. The fifth chapter deals with the systematic structural investigation on PZT1-y-PNZy (PZT-PNZ) and PZT1-y-PMNy (PZT-PMN) systems. In this chapter, an effort has been made to determine quantitatively the MPB phase contents and variation in Zr/Ti ratio of PZT-PZN and PZT-PMN systems. High resolution XRD data has been used for quantitative phase analysis using FULLPROF 2006. The correlation between the width of MPB and grain size has also been discussed for these systems. It is found that the addition of PMN and PZN to PZT system shifts the MPB towards pbZrO3 (PZ). The MPB can be regained by tuning the Zr/Ti ratio in the system. Further, there exists an inverse relation between the grain size and coexistence region in the system. It is seen that the MPB range is from x=0.48 to 0.58 and x=0.44 to 0.58 for 10% and 20% PZN concentration respectively. Similar trend has been obtained for the PZT-PMN system. The MPB ranges from x=0.46 to 0.53 and x=0.42 to 0.50 for 10% and 20% PMN respectively. The broadening of coexistence width is attributed to the lower grain size of our samples synthesized by adopting low temperature calcinations route. The sixth chapter deals with the hot pressing technique employed (adopting low temperature calcinations) for the synthesis of various PZT-PMN compositions with an intention of obtaining highly dense piezoceramics with fine, homogeneous and uniform microstructure. It also describes the dielectric, pyroelecrtic and pi ezoelectric properties were enhanced by hot processing technique. Li and Mn addition further improved the properties of the system. The seventh chapter investigates various nominal compositions of PZT-(Li, Nb) compositions based on certain assumptions. The attempt was made to introduce Li at A site and B site of ABO3 perovskite lattice. The ball milled, calcined powders were densified at<1000oC using hot pressing technique to prevent Li and Pb loss. High density ceramics have been studied for structural, dielectric, piezoelectric and pyroelectric properties. Through the clear cut evidence for the identification of Li site in the PZT system could not be established but the system which were synthesized under the assumption that Li substitutes A-site of the perovskite, favored the tetragonal phase and led to the enhancement in the dielectric, pyroelectric and piezoelectric properties. Further, their transition temperature was higher compared to the compositions where Li was tried to substitute B-site, which makes them promising candidates for transducer applications. The key finding in this thesis has been carried out by the candidate as part of the ph. D. programme. She hopes that this would constitute a worthwhile contribution towards the understanding of the behavior of lead based perovskites and in tailoring the properties of these ceramics towards device applications by the introduction of suitable additives in the system.

No description available.

The following investigations have been carried out in this thesis 1)Cordierite is already well known for its low thermal expansion behaviour. Chemical substitutions at various octahedral and tetrahedral sites have been done and their thermal expansion characteristics have been studied Synthesis of cordierite in more reactive environment provided by AlF3 used as sintering aid has been attempted 2) Diffuse ferroelectric phase transition of lead based perovskite materials leads to low expansion region. Solid solutions of lead iron niobate with lead titanate is investigated to increase the structural distortion and see it this low expansion region can be extended to wider temperature Preparation of materials with higher tetragonal distortion In PbTi03- BlFeO3 system is undertaken to study the thermal expansion anisotropy. 3) Composites between lead iron niobate(+(x) and lead titanate (-(x below Tc) has been undertaken to prepare low expansion hulk over a wide temperature range 4) Acoustic emission has been employed as a tool to detect the microcracking in solid solutions between PFN1-x, PTx, and PT1-x, ,BFx, It is hoped to understand relation between magnitude of lattice distortion transition temperature and microcracking in ceramics of the class of materials.

Bismuth layer-structured ferroelectrics have received significant attention recently due to their fairly high TC and good fatigue endurance which make them important candidates for non-volatile ferroelectric random access memories (Fe-RAMs) as well as for the piezoelectric device applications at high temperatures. Structure of these compounds is generally described as the pseudo-perovskite block (An-1BnO3n+1)2- sandwiched between the bismuth oxide layers (Bi2O2)2+ along the c-axis, where n represents the number of corner sharing BO6 octahedra forming the perovskite-like slabs. Only a few compounds belonging to this family show relaxor behavior (frequency dependent diffuse phase transition). Relaxor ferroelectrics are very attractive for a variety of applications, such as capacitors, sensors, actuators, and integrated electromechanical systems. The present work attempts to understand the mechanism of relaxor behavior in Aurivillius oxides as well as to improve the piezoelectric and ferroelectric properties of some of the known phases. Details pertaining to the fabrication and characterization of BaBi4Ti4O15 (n = 4 member of Aurivillius family of oxides) ceramics are presented. X-ray diffraction, Raman spectroscopy, Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) were employed to probe the structural and microstructural details. The contribution of irreversible domain wall movement to the room temperature dielectric constant and polarization was quantitatively evaluated using the nonlinear dielectric response. Dielectric dispersion and conduction mechanism of these ceramics are also explicated using the complex impedance spectroscopy. The effects of La3+ and Ca2+ doping on the phase transition behavior and other properties of BaBi4Ti4O15 are investigated. La3+ doping for Bi3+ was found to strengthen the relaxor behavior. New compounds such as CaNaBi2Nb3O12, SrNaBi2Nb3O12, Na0.5La0.5Bi4Ti4O12, etc. belonging to the Aurivillius family of oxides have been synthesized and investigations concerning their structural, dielectric and ferroelectric properties are presented. Rietveld refinement of room temperature X-ray powder data suggested that CaNaBi2Nb3O12 and SrNaBi2Nb3O12crystallize in the orthorhombic space group B2cb. SrNaBi2Nb3O12 ceramics exhibited frequency-dependent Tm which follows the Vogel-Fulcher relation implying a relaxor nature. No frequency dependence of Tm was observed for CaNaBi2Nb3O12 ceramics. Polarization - electric field hysteresis loops recorded well above Tm confirmed the coexistence of polar and non-polar domains in SrNaBi2Nb3O12 ceramics. Dielectric anomaly observed around 675 K for CNBN corresponds to the ferroelectric to paraelectric phase transition which is accompanied by the change in crystal structure from orthorhombic to tetragonal. Fe and Nb co-doped Bi4Ti3O12 ceramics were fabricated and characterized for their structural, electrical and magnetic properties.

Relaxor ferroelectrics have been a subject of intense research owing to their interesting physical properties such as high dielectric constant and giant electro-striction. Unlike the conventional lead based relaxors, the relaxors belonging to Aurivillius family of oxides have received much less attention because of the poor understanding of the origin of the relaxor behavior and high processing temperatures involved. In the present investigations, an attempt has been made to understand the origin of relaxor behavior of the materials belonging to Aurivillius family of oxides. The structure and relaxor behavior of BaBi2Nb2O9 (BBN) has been established via the XRD, electron diffraction and dielectric spectroscopy. The results are compared with that of a normal ferroelectric like SrBi2Nb2O9 belonging to the same family as well with that of a conventional relaxor like PMN. The results indicate that the dielectric behavior of BBN is significantly different from that of the conventional relaxors like BBN with very slow broadening of relaxation times and was attributed to the absence of significant polar ordering. To substantiate the existing understanding, studies have been carried out by adopting different strategies such as B-site and A-site cationic substitutions and texturing of the ceramics. Vanadium doping on B-site was found to decrease the sintering temperatures significantly. Aliovalent La3+ doping was found to affect the dielectric behavior strongly with substantial decrease of the freezing temperature and dielectric constants which shows that the relaxor behavior of BBN is highly sensitive to A-site order-disorder. The (00l) textured ceramic of pure and vanadium doped BBN was fabricated via a simple melt-quenching technique and was found to exhibit a significant dielectric and pyroelectric anisotropy. A new class of relaxor compositions (K0.5La0.5Bi2Nb2O9 & K0.5La0.5Bi2Ta2O9) have been synthesized and characterized. These new compounds exhibited interesting physical properties which are akin to that of the conventional lead based relaxors. The presence of superlattice reflections in the electron diffractin patterns recorded on these compounds establish the presence of polar nano regions of significant size. These relaxor crystallites at nano/micro level embedded in a glass matrix have been found to be very promising from their physical properties view point.

This thesis deals with the investigations on the dielectric properties of polycrystalline ceramics having uncommon substitutions in barium titanate and other related phases of BaTiO3-CaTiO3, MgTiO3-CaTiO3 and MgTiO3-BaTiO3 systems. After presenting a brief introduction on the ceramic materials studied in terms of their crystal structures, electrical properties, nonstoichiometry and microstructural characteristics. The thesis describes the synthesis of the ceramics and the methodology of different techniques utilized in characterizing the samples. Barium calcium titanate was synthesized through novel wet chemical techniques and the dielectric properties of calcium substituted barium titanate do not reveal multi-site occupancy whereas they are predominantly influenced by the A/B cationic ratio. The role of transition metals of the 3d series from vanadium (Z=23) to zinc (Z=30) in modifying the crystallographic phase content, microstructure and the dielectric properties of BaTiO3 ceramics containing 10 at% impurities were studied. All the transition metals brought about the phase conversion to hexagonal BaTiO3, although no systematics could be arrived at relating the hexagonal content to the 3d electronic configuration of the impurities. The relaxor dielectrics arising from the titanate solid solution with uncommon substitution and its interconversion to normal ferroelectrics is studied. The effects of cationic substitutions of iron and niobium for titanium in BaTiO3 pervoskite lattice in crystal symmetry and dielectric properties were investigated. The above dielectric characteristics are comparable in a converse way to those of the well known Pb(Mg1/3Nb2/3)O3-PbTiO3 system wherein the relaxor behaviour occurs within the lower lead titanate compositional limits. The modification in -T characteristics of positive temperature coefficient in resistance (PTCR) by the addition of segregative additives such as B2O3, Al2O3 etc in BaTiO3 and its conversion to grain boundary layer capacitance is studied. The presence of Al-related hole centers at the grain boundary regions resulted in charge redistribution across the modified phase transition temperatures due to symmetry-related vibronic interactions, which result in broad PTCR characteristics extending to higher temperatures. The processing of high permittivity ceramics by the manipulation of microstructural features in semiconducting BaTiO3 is studied wherein the grain boundary layer effect superimposed with the contributions from the barrier layers formed during electroding related to microstructure is proposed to be responsible for the unusual high permittivity in semiconducting BaTiO3. The influence of Mg2+ as a substituent in modifying the crystallographic phase contents, microstructure and the dielectric properties of (Ba1-xMgx)TiO3 ceramics, (x ranging from zero to 1.0 ) is studied. The results point to the dual occupancy of Mg2+ both in A and B sublattice and the role of oxygen vacancy as well as (Ti3+ –VO) defects in stabilization of hexagonal phase to lower temperatures. The microwave dielectrics of the BaMg6Ti6O19 phase formed in the compositional range of x=0.4 to 0.7 was investigated for suitable application in microwave dielectrics. Extensive miscibility between the ilmenite-type MgTiO3 and perovskite-type CaTiO3 over a wide compositional range is brought about by the simultaneous equivalent substitution of Al3+ and La3+. The resulting Mg1-(x+y)CaxLay)(Ti1-yAly)O3 ceramics exhibit improved microwave dielectric properties by way of high permittivity, low TCK and high quality factor. The elemental distribution reveals the complexity in the Mg/Ca distribution and its correlation with the solid state miscibility as well as dielectric properties. Microwave dielectric property of Mg4Al2Ti9O25 which is detected as secondary phase is studied in detail.

No description available.

Embrace the Suck is an important and widely experienced military colloquialism. The phrase is based on the undeniable fact that life is about to become very difficult and the only option is to embrace all that is horrible. I reimagine childhood toys, playing at war and subvert the monumental. Common heroic exploits are restructured into moments between action, the hurry up and wait, the busy work, the catharsis through self-destruction. Based on my personal experiences in the US Army and an arsenal of information and stories from fellow soldiers, I become a native informant.