Sodium oxalate is one of the many organics present in Bayer liquor. Due to its limited solubility, sodium oxalate can co-precipitate with alumina trihydrate during precipitation. This can have detrimental effects on the final product quality, especially if it occurs in the initial stages of precipitation.Quaternary amine type cationic surfactants can prevent sodium oxalate co-precipitation and increase the tolerable concentration of sodium oxalate in Bayer liquor. Their action is via the inhibition of nucleation or/and the inhibition of crystal growth. This study presents work detailing the effect of quaternary amines on sodium oxalate crystal growth in Bayer liquor.A series of quaternary amines were tested and classified as strong, medium or weak crystal growth inhibitors in plant liquor. The octadecyltrimethylammonium bromide was found to be the most effective under plant conditions.Results will show that while quaternary amines inhibit crystal growth in Bayer liquor, they have no effect on crystallization in synthetic liquor. It has been postulated that the presence of certain organic molecules is required for quaternary amines to crystallization and therefore stabilize the liquor. The inhibition of oxalate crystal growth in Bayer process liquors is due to the plant organics present, and the stabilizing effect of quaternary amines is the result of an interaction between quaternary amines and plant humic material on the oxalate surface. A series of organics, anionic macromolecules and anionic surfactants, have been tested to simulate the behaviour of plant humates, and their inhibitory effect on sodium oxalate crystal growth has been measured.A method for the analysis of the strongest quaternary amine has been adopted, improved and modified in order to fulfil experimental conditions.The CMC of quaternary amines has been determined in liquor. Surface tension ++ / measurements revealed relationships between certain liquor components and quaternary amines.Adsorption isotherms of quaternary amines have been successfully generated in Bayer liquor. Investigations with quaternary amines and plant humics reveal a synergy between the two. Co-adsorption of quaternary amines and plant humates onto the oxalate surface has been found, and the effect of the components on the adsorption behaviour will be discussed. The inhibitory effect and the adsorbed amount of components have been compared. Results revealed a relationship between the amount of plant humates on the surface and the crystal growth inhibition.The nature of the adsorption has been investigated with confocal laser scanning microscopy. These results will show that humic material adsorbs at the edges and in the corners of the crystals. In the presence of quaternary amines, the humic material occupies the main crystal faces as well. The nucleation of sodium oxalate from humic solution and from a mixture of humates and quaternary amine resulted in crystals with different morphology.Fourier Transform Infrared Attenuated Total Reflection Spectroscopy investigations will present the adsorption of quaternary amine on oxalate, and will indicate that the adsorption is pH dependent.

The modern insular shelf and slope of western Puerto Rico is characterized by reef carbonate and siliciclastic sedimentary environments controlled by the complex interplay of tectonic arching and faulting, vigorous erosion of the elevated island of Puerto Rico, fluvial incision and sedimentation pulses, reef growth, and rapid late Quaternary eustatic sea-level changes. For this study, I interpret 725 km of high-resolution, single-channel seismic lines that were collected over the western insular shelf and slope by the RV Isla Magueyes in 2000 to better understand tectonic, erosional, and eustatic controls on late Quaternary history. The seafloor geology of the western shelf and slope area of Puerto Rico has been well studied and mapped mainly from grab and short cores collected by geoscientists at the U.S. Geological Survey and at the University of Puerto Rico at Mayagü̈ez. Because of low tectonic uplift rates from the western coast of Puerto Rico, the onland late Quaternary sedimentary history is not recorded in Quaternary coastal outcrops. The results of my seismic interpretation and correlation with multi-channel seismic data collected in 1972, reveal four main units defined by characteristic stratal reflection terminations and seismic facies. These units include: Unit 1 (basement) - a gently folded and faulted basal section correlated to the Oligocene-early Pleistocene carbonate shelf of Puerto Rico; deeper penetration, industry multi-channel seismic lines show that these rocks are deformed in a broad east-west-trending arch; Unit 2 (lowstand systems tract, LST) - chaotic channel fill deposits filling deep (~ 30 meter) incisions formed during the Last Glacial Maximum about 20 ka; Unit 3 (transgressive system tract, TST) - poorly stratified deposits truncating the top of Unit 2 and deposited during early Holocene transgression of the shelf margin; Unit 4 (highstand system tract, HST) - late Holocene, highly stratified deposits related to aggradation as the Holocene transgression began to slow. The base of unit 4 is a downlap surface interpreted as a maximum flooding surface likely formed about 8 ka. East-northeast-striking faults are observed that offset the late Quaternary units in three separate zones off the west coast of Puerto Rico. Because of a lack of wells and long cores from the shelf and slope area, age estimates for the four units are based on correlations with sea-level curves derived from dated coral samples in the Caribbean and western Atlantic region. All four units are deformed by faulting that should be considered active and possibly hazardous for the rapidly developing west coast of Puerto Rico. In one area, a large, late Holocene-slump (~ 0.016 km³) is mapped using seismic, sidescan sonar and bathymetric data. Onland continuations of these faults are likely, but have not been identified due to cultural overprint of natural scarps on late Quaternary floodplains. / text

The neoidic sulphide mineralization located in tertiary sediments of Lom Bílina in Bílina's fault is of hydrothermal origin. The sulphidic mineralization is associated with fault systems of Eger rift and temperature of fluid crystallization was about 50řC. The mineralization of Bílina's fault is rather monotonous, the marcasite and pyrite is mostly found without a trace elements. In the crystals were also registered zones with the contents of trace elements, especially As and Ni. The contents of As enriched precipitation zones were fluctuating from 0,2 to 5,4 wt. %, Ni enriched zones were ranged from 1,6 to 5,9 wt. %. The precipitation zones with increased As and Ni content were very thin, there were very short time intervals of As and Ni enriched fluids precipitation. In the marcasite crystals were also found the porous zones of clay mineral microinclusions. These zones showed higher content of Al and Si. There is high abundance of Fe-disulfides at Bílina's fault-dispersed in coal bed, or bonded to tectonic zone of the Bílina's fault. Pyrite and marcasite are dispersed in the coal bed and genetially aren't related to sulphides bonded to Bílina's fault.

A Dissertation Submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, for the Degree of Master of Science Johannesburg, 1997 / The palaeoclimate of southern Africa for the last twenty thousand years is investigated through the production of palaeoclimate maps based on an analysis of literature and data from the ongoing PASH project. The trends from the maps are compared with published reviews and modelling studies of the region' s palaeoclimates, and are contextualised in terms of global palaeoceanographic and palaeoclimatic dynamics. The changes evident in the past climate of southern Africa tend to mirror global climate changes, however, evidence exists that the timing of climate changes between the two hemispheres are not quite synchronous, and may 110tfit present theories of global palaeoclimate dynamics,

This diploma thesis deals with the research of primary and secondary magnetic fabric of aeolian loess sediments and paleosols on the cross-section temporary cropping out during the construction work in Prague 6. Magnetic enrichment - and the formation of magnetic nanoparticles in soil horizons - occurs during pedogenesis in warmer interglacials periods. The aim of this work is the interpretation of the paleoenvironment, weathering and pedogenic processes, by measuring the magnetic properties of sediments. Magnetic susceptibility, frequency-dependent magnetic susceptibility, anhysteresis remanent magnetization and natural remanent magnetization are used to detect the increased occurrence of magnetic particles, which indicate these pedogenic processes. The most developed paleosol horizon within the cross-section was the horizon of black soil and subsoil brown soil. Small signs of pedogenesis were revealed in the upper and lower loess part of the section. The magnetic fabric of loess, measured by means of anisotropy of magnetic susceptibility, reflects secondary sedimentary processes. This involves the displacement of clastic particles by flowing water and the redeposition of the material along the slope. The direction of movement of these sediments corresponds to the current geomorphology of the...

This master's thesis deals with changes of work localization in Prague metropolitan region and concentrates on the suburbanisation of quarternary functions. Goal of the presented thesis is to analyze changes of work localization in different parts of Prague metropolitan region and discuss whether suburbanization of quarternary functions exists in Prague metropolitan region and evaluate its importance through the number of jobs in the new R&D institutions. Component goals include evaluation of the structure of jobs in new R&D institutions and evaluation of the potential for formation of cooperation with the private sector, which could lead to creation of new secondary economic centres in the periphery of the Prague metropolitan region. Other component goal finds out whether the existence of new R&D institutions can lead to changes in the social structure of the periphery and to the increased demand on social, technical and transportation infrastructure. For the purpose of analysis I used data on work commuting from 2001 and 2001 censuses, data on the number of employees in R&D institutions from the Central Bohemian innovation centre and questionnaire survey, which took place among the employees of new R&D institutions in the periphery of Prague metropolitan region. In the theoretical part I discuss...

Indiana University-Purdue University Indianapolis (IUPUI) / Both quaternary ammonium bromide (QAB) and furanone derivatives were synthesized, characterized and formulated into dental resin composites for improved antibacterial properties. Compressive strength (CS) and S. mutans viability were used to evaluate the mechanical strength and antibacterial activity of the restoratives. The effects of chain length, loading, saliva and aging on CS and S. mutans viability were investigated. Chapter 2 describes how we studied and evaluated the formulated antibacterial resin composites by incorporating the synthesized QAB-containing oligomers into the formulation. The results show that all the QAB-modified resin composites showed significant antibacterial activity and mechanical strength reduction. Increasing chain length and loading significantly enhanced the antibacterial activity but dramatically reduced the CS as well. The 30-day aging study showed that the incorporation of the QAB accelerated the degradation of the composite, suggesting that the QAB may not be well suitable for development of antibacterial dental resin composites or at least the QAB loading should be well controlled. Chapter 3 describes how we studied and evaluated the formulated antibacterial resin composite by incorporating the synthesized furanone derivative into the formulation. The results show that the modified resin composites showed a significant antibacterial activity without substantially decreasing the mechanical strengths. With 5 to 30% addition of the furanone derivative, the composite kept its original CS unchanged but showed a significant antibacterial activity with a 16-68% reduction in the S. mutans viability. Further, the antibacterial function of the new composite was found not to be affected by human saliva. The aging study indicates that the composite may have a long-lasting antibacterial function. In summary, we have developed a novel QAB- and furanone-containing antibacterial system for dental restoratives. Both QAB- and furanone-modified resin composites have demonstrated significant antibacterial activities. The QAS-modified experimental resin composite may not be well suitable for development of antibacterial dental resin composites due to its accelerated degradation in water unless the QAB loading is well controlled. The furanone-modified resin composite shows nearly no reduction in mechanical strength after incorporation of the antibacterial furanone derivative. It appears that the furanone-modified resin composite is a clinically attractive dental restorative that can be potentially used for long-lasting restorations due to its high mechanical strength and permanent antibacterial function.

This work describes the application of a variety of Lewis bases, encompassing predominantly N-heterocyclic carbenes (NHCs), but also the use of imidazoles, aminopyridines, amidines and isothioureas, as effective catalysts in the dearomatisation of heterocyclic carbonates, predominantly the rearrangement of oxazolyl carbonates to their C-carboxyazlactone isomers by means of the Steglich rearrangement. This rearrangement reaction has been investigated extensively, with the development of simplified reaction procedures and the invention of domino cascade protocols incorporating this transformation. In an attempt to understand the mechanism of this O- to C-carboxylation process, a number of interesting observations have been made. Firstly, the class of NHC has an important factor in promoting the rearrangement, with triazolinylidenes being the most effective. Secondly, an interesting chemoselectivity has been delineated using triazolium-derived NHCs, prepared using weak bases (typically Et₃N) or strong metallated bases; both alkyl and aryl oxazolyl carbonates undergo smooth rearrangement with triazolinylidenes derived from strong metallated bases such as KHMDS, while only aryl oxazolyl carbonates undergo rearrangement using Et₃N. Extensive effort has focused towards the development of asymmetric variants of these protocols, primarily towards the design, synthesis and evaluation of chiral NHC precatalysts. To this end, a number of chiral azolium salts have been prepared, encompassing a number of different NHC classes, including C₁- and C₂-imidazolinium salts, C₂-imidazolium salts and a range of triazolium salts. Efforts towards the asymmetric catalysis of the Steglich rearrangement of oxazolyl carbonate substrates have given an optimal 66% ee. Similar rearrangements have been demonstrated with the related furanyl heterocyclic substrate class, producing a mixture of α- and γ-carboxybutenolides. In contrast to the analogous oxazolyl carbonates, the regioselectivity of this rearrangement is dependent upon the nature of the Lewis base employed. Amidines and aminopyridines give a mixture of the α- and γ- regioisomers with generally the α-regioisomer being preferred, while a triazolium-derived NHC gives rise to predominantly the thermodynamically more stable γ-carboxybutenolide. Using amidines or aminopyridines, this rearrangement has been shown to proceed via an irreversible C-C bond-forming process, but in contrast, the rearrangement using the NHC proceeds via an equilibrium process with an optimised regioselectivity of >98:2 for the γ-carboxybutenolide regioisomer over the α-regioisomer. Whilst the asymmetric variant using chiral NHCs has proven unfruitful, rearrangements using a chiral isothiourea have given high levels of regioselectivity towards the α- regioisomer and with excellent levels of enantiodiscrimination (77–95% ee).

Molecular interaction among proteins drives the cellular processes through the formation of complexes that perform the requisite biochemical function. While some of the complexes are obligate (i.e., they fold together while complexation) others are non-obligate, and are formed through macromolecular recognition. Macromolecular recognition in proteins is highly specific, yet it can be both permanent and non permanent in nature. Hallmarks of permanent recognition complexes include large surface of interaction, stabilization by hydrophobic interaction and other noncovalent forces. Several amino acids which contribute critically to the free energy of binding at these interfaces are called as “hot spot” residues. The non permanent recognition complexes, on the other hand, usually show small interface of interaction, with limited stabilization from non covalent forces. For both the permanent and non permanent complexes, the specificity of molecular interaction is governed by the geometric compatibility of the interaction surface, and the noncovalent forces that anchor them. A great deal of studies has already been performed in understanding the basis of protein macromolecular recognition.1; 2 Based on these studies efforts have been made to develop protein-protein docking algorithms that can predict the geometric orientation of the interacting molecules from their individual unbound states. Despite advances in docking methodologies, several significant difficulties remain.1 Therefore, in this thesis, we start with literature review to understand the individual merits and demerits of the existing approaches (Chapter 1),3 and then, we attempt to address some of the problems by developing methods to infer protein quaternary structure from the crystalline state, and improve structural and chemical understanding of protein-protein interactions through biological complex prediction. The understanding of the interaction geometry is the first step in a protein-protein interaction study. Yet, no consistent method exists to assess the geometric compatibility of the interacting interface because of its highly rugged nature. This suggested that new sensitive measures and methods are needed to tackle the problem. We, therefore, developed two new and conceptually different measures using the Delaunay tessellation and interface slice selection to compute the surface complementarity and atom packing at the protein-protein interface (Chapter 2).4 We called these Normalized Surface Complementarity (NSc) and Normalized Interface Packing (NIP). We rigorously benchmarked the measures on the non redundant protein complexes available in the Protein Data Bank (PDB) and found that they efficiently segregate the biological protein-protein contacts from the non biological ones, especially those derived from X-ray crystallography. Sensitive surface packing/complementarity recognition algorithms are usually computationally expensive and thus limited in application to high-throughput screening. Therefore, special emphasis was given to make our measure compute-efficient as well. Our final evaluation showed that NSc, and NIP have very strong correlation among themselves, and with the interface area normalized values available from the Surface Complementarity program (CCP4 Suite: <http://smb.slac.stanford.edu/facilities/software/ccp4/html/sc.html>); but at a fraction of the computing cost. After building the geometry based surface complementarity and packing assessment methods to assess the rugged protein surface, we advanced our goal to determine the stabilities of the geometrically compatible interfaces formed. For doing so, we needed to survey the quaternary structure of proteins with various affinities. The emphasis on affinity arose due to its strong relationship with the permanent and non permanent life-time of the complex. We, therefore, set up data mining studies on two databases named PQS (Protein Quaternary structure database: http://pqs.ebi.ac.uk) and PISA (Protein Interfaces, Surfaces and Assemblies: www.ebi.ac.uk/pdbe/prot_int/pistart.html) that offered downloads on quaternary structure data on protein complexes derived from X-ray crystallographic methods. To our surprise, we found that above mentioned databases provided the valid quaternary structure mostly for moderate to strong affinity complexes. The limitation could be ascertained by browsing annotations from another curated database of protein quaternary structure (PiQSi:5 supfam.mrc-lmb.cam.ac.uk/elevy/piqsi/piqsi_home.cgi) and literature surveys. This necessitated that we at first develop a more robust method to infer quaternary structures of all affinity available from the PDB. We, therefore, developed a new scheme focused on covering all affinity category complexes, especially the weak/very weak ones, and heteromeric quaternary structures (Chapter 3).6 Our scheme combined the naïve Bayes classifier and point-group symmetry under a Boolean framework to detect all categories of protein quaternary structures in crystal lattice. We tested it on a standard benchmark consisting of 112 recognition heteromeric complexes, and obtained a correct recall in 95% cases, which are significantly better than 53% achieved by the PISA,7 a state-of-art quaternary structure detection method hosted at the European Bioinformatics Institute, Hinxton, UK. A few cases that failed correct detection through our scheme, offered interesting insights into the intriguing nature of protein contacts in the lattice. The findings have implications for accurate inference of quaternary states of proteins, especially weak affinity complexes, where biological protein contacts tend to be sacrificed for the energetically optimal ones that favor the formation/stabilization of the crystal lattice. We expect our method to be used widely by all researchers interested in protein quaternary structure and interaction. Having developed a method that allows us to sample all categories of quaternary structures in PDB, we set our goal in addressing the next problem that of accurately determining stabilities of the geometrically compatible protein surfaces involved in interaction. Reformulating the question in terms of protein-protein docking, we sought to ask how we could reliably infer the stabilities of any arbitrary interface that is formed when two protein molecules are brought sterically closer. In a real protein docking exercise this question is asked innumerable times during energy-based screening of thousands of decoys geometrically sampled (through rotation+translation) from the unbound subunits. The current docking methods face problems in two counts: (i), the number of interfaces from decoys to evaluate energies is rather large (64320 for a 9º rotation and translation for a dimeric complex), and (ii) the energy based screening is not quite efficient such that the decoys with native-like quaternary structure are rarely selected at high ranks. We addressed both the problems with interesting results. Intricate decoy filtering approaches have been developed, which are either applied during the search stage or the sampling stage, or both. For filtering, usually statistical information, such as 3D conservation information of the interfacial residues, or similar facts is used; more expensive approaches screen for orientation, shape complementarity and electrostatics. We developed an interface area based decoy filter for the sampling stage, exploiting an assumption that native-like decoys must have the largest, or close to the largest, interface (Chapter 4).8 Implementation of this assumption and standard benchmarking showed that in 91% of the cases, we could recover native-like decoys of bound and unbound binary docking-targets of both strong and weak affinity. This allowed us to propose that “native-like decoys must have the largest, or close to the largest, interface” can be used as a rule to exclude non native decoys efficiently during docking sampling. This rule can dramatically clip the needle-in-a-haystack problem faced in a docking study by reducing >95% of the decoy set available from sampling search. We incorporated the rule as a central part of our protein docking strategy. While addressing the question of energy based screening to rank the native-like decoys at high rank during docking, we came across a large volume of work already published. The mainstay of most of the energy based screenings that avoid statistical potential, involve some form of the Coulomb’s potential, Lennard Jones potential and solvation energy. Different flavors of the energy functions are used with diverse preferences and weights for individual terms. Interestingly, in all cases the energy functions were of the unnormalized form. Individual energy terms were simply added to arrive at a final score that was to be used for ranking. Proteins being large molecules, offer limited scope of applying semi-empirical or quantum mechanical methods for large scale evaluation of energy. We, therefore, developed a de novo empirical scoring function in the normalized form. As already stated, we found NSc and NIP to be highly discriminatory for segregating biological and non biological interface. We, therefore, incorporated them as parameters for our scoring function. Our data mining study revealed that there is a reasonable correlation of -0.73 between normalized solvation energy and normalized nonbonding energy (Coulombs + van der Waals) at the interface. Using the information, we extended our scoring function by combining the geometric measures and the normalized interaction energies. Tests on 30 unbound binary protein-protein complexes showed that in 16 cases we could identify at least one decoy in top three ranks with ≤10 Å backbone root-mean-square-deviation (RMSD) from true binding geometry. The scoring results were compared with other state-of-art methods, which returned inferior results. The salient feature of our scoring function was exclusion of any experiment guided restraints, evolutionary information, statistical propensities or modified interaction energy equations, commonly used by others. Tests on 118 less difficult bound binary protein-protein complexes with ≤35% sequence redundancy at the interface gave first rank in 77% cases, where the native like decoy was chosen among 1 in 10,000 and had ≤5 Å backbone RMSD from true geometry. The details about the scoring function, results and comparison with the other methods are extensively discussed in Chapter 5.9 The method has been implemented and made available for public use as a web server - PROBE (http://pallab.serc.iisc.ernet.in/probe). The development and use of PROBE has been elaborated in Chapter 7.10 On course of this work, we generated huge amounts of data, which is useful information that could be used by others, especially “protein dockers”. We, therefore, developed dockYard (http://pallab.serc.iisc.ernet.in/dockYard) - a repository for protein-protein docking decoys (Chapter 6).11 dockYard offers four categories of docking decoys derived from: Bound (native dimer co-crystallized), Unbound (individual subunits as well as the target are crystallized), Variants (match the previous two categories in at least one subunit with 100% sequence identity), and Interlogs (match the previous categories in at least one subunit with ≥90% or ≥50% sequence identity). There is facility for full or selective download based on search parameters. The portal also serves as a repository to modelers who may want to share their decoy sets with the community. In conclusion, although we made several contributions in development of algorithms for improved protein-protein docking and quaternary structure inference, a lot of challenges remain (Chapter 8). The principal challenge arises by considering proteins as flexible bodies, whose conformational states may change on quaternary structure formation. In addition, solvent plays a major role in the free energy of binding, but its exact contribution is not straightforward to estimate. Undoubtedly, the cost of computation is one of the limiting factors apart from good energy functions to evaluate the docking decoys. Therefore, the next generation of algorithms must focus on improved docking studies that realistically incorporate flexibility and solvent environment in all their evaluations.

Thermoelectric (TE) materials directly convert heat energy into electrical energy. The conversion efficiency of the TE devices depends on the performance of the materials. The conversion efficiency of available thermoelectric materials and devices is low. Therefore, the development of new materials for improving thermoelectric device performance is a highly essential. As the performance of the TE materials depends on TE figure of merit [zT=S2P T ] which consist of three material properties such as Seebeck coefficient (S), electrical resistivity ( ) and thermal conductivity ( ). Thermoelectric figure of merit can be improved by either increase of power factor or decreasing of thermal conductivity or by both. In the present thesis, Cu based chalcogenide compounds are chosen for the study of thermoelectric properties because of their complex crystal structure, which leads to lower values of thermal conductivity. Also, the power factor of these materials can be tuned by the partial substitution doping. In the present thesis, Cu based chalcogenide compounds quaternary chalcogenide compound (Cu2ZnSnSe4), ternary compounds (Cu2SnSe3 and Cu2GeSe3) and tetrahedrite materials (Cu12Sb4S13) have been prepared by solid state synthesis. The prepared compounds are characterized by XRD for the phase identification, Raman Spectroscopy used as complementary technique for XRD, SEM for surface morphology and EPMA for the phase purity and elemental composition analysis respectively. For the evaluation of zT, thermoelectric properties of all the samples have been studied by measuring Seebeck coefficient, resistivity and thermal diffusivity. In the chapter 1, a brief introduction about thermoelectricity and its effects is discussed. Thermoelectric materials parameters such as electrical resistivity, Seebeck coefficient and thermal conductivity for different class of materials are mentioned. The selection of thermoelectric materials and the motivation for choosing the Cu based chalcogenide compounds for thermoelectric applications are discussed. In chapter 2, the details of the experiments carried out for Cu based chalcogenide compounds are presented. In chapter 3, the effect on thermoelectric properties by the cation substitution on quaternary chalcogenide compound Cu2+xZnSn1 xSe4 (0, 0.025, 0.05, 0.075, 0.1, 0.125, and 0.15) is studied. The electrical resistivity of all the samples decreases with an increase in Cu content except for Cu21ZnSn09Se4, most likely due to a higher content of the ZnSe. All the samples showed positive Seebeck coefficients indicating that holes are the majority charge carriers. The thermal conductivity of doped samples was higher as compared to Cu2ZnSnSe4 and this may be due to the larger electronic contribution and the presence of the ZnSe phase in the doped samples. The maximum zT = 0.23 at 673 K is obtained for Cu205ZnSn095Se4. In chapter 4, the effect of multi{substitution of Cu21ZnSn1 xInxSe4 (0, 0.05, 0.075, and 0.1) on transport properties were studied. The Rietveld powder X-ray diffraction data accompanied by electron probe microanalysis (EPMA) and Raman spectra of all the samples con firmed the formation of a tetragonal kesterite structure. The electrical resistivity of all the samples exhibits metallic-like behavior. The positive values of the Seebeck coefficient and the Hall coefficient reveal that holes are the majority charge carriers. The co-doping of copper and indium leads to a significant increase of the electrical resistivity and the Seebeck coefficient as a function of temperature above 650 K. The thermal conductivity of all the samples decreases with increasing temperature. Lattice thermal conductivity is not significantly modified as the doping content may infer negligible mass fluctuation scattering for copper zinc and indium tin substitution. Even though, the power factors (S2 ) of indium-doped samples Cu21ZnSn1 xInxSe4 (x=0.05, 0.075) are almost the same, the maximum zT=0.45 at 773 K was obtained for Cu21Zn09Sn0925In0075Se4 due to its smaller value of thermal conductivity. In chapter 5, thermoelectric properties of Zn doped ternary compounds Cu2ZnxSn1 xSe3 (x = 0, 0.025, 0.05, 0.075) were studied. The undoped com\pound showed a monoclinic crystal structure as a major phase, while the doped compounds showed a cubic crystal structure confirmed by powder XRD (X-Ray Diffraction). The electrical resistivity decreased up to the samples with Zn content x=0.05 in Cu2ZnxSn1 xSe3, and slightly increased in the sample Cu2Zn0075Sn0925Se3 . This behavior is consistent with the changes in the carrier concentration confirmed by room temperature Hall coefficient data. Temperature dependent electrical resistivity of all samples showed heavily doped semiconductor behavior. All the samples exhibit positive Seebeck coefficient (S) and Hall coefficient indicating that the majority of the carriers are holes. A linear increase in Seebeck coefficient with increase in temperature indicates the degenerate semiconductor behavior. The total thermal conductivity of the doped samples increased with a higher amount of doping, due to the increase in the carrier contribution. The total and lattice thermal conductivity of all samples decreased with increasing of temperature, which points toward the dominance of phonon scattering at high temperatures. The maximum zT = 0.34 at 723 K is obtained for the sample Cu2SnSe3 due to a low thermal conductivity compared to the doped samples. In chapter 6, thermoelectric properties of Cu2Ge1 xInxSe3 (x = 0, 0.05, 0.1, 0.15) compounds is studied. The powder X-ray diffraction pattern of the undoped sample revealed an orthorhombic phase. The increase in doping content led to the appearance of additional peaks related to cubic and tetragonal phases along with the orthorhombic phase. This may be due to the substitutional disorder created by indium doping. The electrical resistivity ( ) systematically decreased with an increase in doping content, but increased with the temperature indicating a heavily doped semiconductor behavior. A positive Seebeck coefficient (S) of all samples in the entire temperature range reveal holes as predominant charge carriers. Positive Hall coefficient data for the compounds Cu2Ge1 xInxSe3 (x= 0, 0.1) at room temperature (RT) con rm the sign of Seebeck coefficient. The trend of as a function of doping content for the samples Cu2Ge1 xInxSe3 with x = 0 and 0.1 agrees with the measured charge carrier density calculated from Hall data. The total thermal conductivity increased with rising doping content, attributed to an increase in carrier thermal conductivity. The thermal conductivity decreases with increasing temperature, which indicates the dominance of Umklapp phonon scattering at elevated temperatures. The maximum thermoelectric figure of merit (zT) = 0.23 at 723 K was obtained for Cu2In01Ge09Se3. In chapter 7, thermoelectric properties of Cu12 xMn1 xSb4S13 (x = 0, 0.5, 1.0, 1.5, 2.0) samples were studied. The Rietveld powder XRD pattern and Electron Probe Micro Analysis revealed that all the Mn substituted samples showed a single tetrahedrite phase. The electrical resistivity increased with increasing Mn due to substitution of Mn2+ on the Cu1+ site. The positive Seebeck coefficient for all samples indicates that the dominant carriers are holes. Even though the thermal conductivity decreased as a function of increasing Mn, the thermoelectric figure of merit (zT) decreased, because the decrease of the power factor is stronger than the decrease of the thermal conductivity. The maximum zT = 0.76 at 623 K is obtained for Cu12Sb4S13. In chapter 8, the summary and conclusion of the present work is presented.