L’objectif de ce projet était de comprendre comment l’expression du génome influence les caractères de qualité du foie gras, tels que le poids de foie, le taux de fonte et les teneurs, en lipides et protéines, et d’identifier les mécanismes moléculaires sous-jacents. Afin de répondre à ces objectifs, nous avons dans un premier temps étudié l’expression différentielle de protéines selon les phénotypes des foies des canards mulards puis dans un second temps, nous avons entrepris d’identifier des QTL phénotypiques et protéiques (pQTL) à l’aide d’une nouvelle carte génétique composée de marqueurs SNP et microsatellites. Tout d’abord, une optimisation du dispositif expérimental a été entreprise : 3 famille F1, composées de 98 canes backcross et de leurs 294 fils mulards ont été sélectionnés pour leur contribution à des QTL existants liés à la qualité du foie gras. La première approche nous a permis de montrer que les foies ont des profils protéiques et métaboliques différents selon leur phénotype. Ainsi, les foies légers qui fondent peu, avec une faible teneur en lipides mais une forte teneur en protéines présentent un processus anabolique par la surexpression de protéines impliquées dans les métabolismes lipidiques, glucidiques, de synthèse. Au contraire, les foies lourds, fondant beaucoup, avec une forte teneur en lipides mais une faible teneur en protéines présentent des mécanismes de cytoprotection et de réponse au stress. La seconde approche nous a permis de mettre en évidence 30 QTL relatifs à des phénotypes de qualité du foie gras et 50 pQTL relatifs à différentes protéines. Sept chromosomes se démarquent par la ségrégation de plusieurs QTL et pQTL permettant d’émettre des hypothèses quant aux fonctions des gènes sous-jacents à ces QTL. Entre autres, le locus d’APL15 semble lié à la glycolyse et celui d’APL18 à des processus de survie cellulaire. L’ensemble de ces résultats permet ainsi non seulement d’identifier les voies métaboliques impliquées dans la qualité du foie, mais également d’établir un lien entre les caractères, les protéines et les loci des QTL suggérant un déterminisme génétique de ces voies métaboliques impliquées. Ces relations nécessitent d’être approfondies afin de préciser les processus et les gènes impliqués dans la qualité du foie gras. / The aim of this project was to understand how the genome expression influences liver quality traits such as liver weight, melting rate, lipid and protein rates, and to identify the molecular mechanisms underlying it. First, we studied the differential expression of proteins according to liver quality traits of mule ducks. Then we carried out detections of uni-trait and multi-traits phenotypic QTL and protein QTL using a new genetic map containing SNP and microsatellite markers. In preamble to the study, the optimization of the experimental disposal was necessary: 98 backcross dams and their 294 mule sons, composing 3 F1 families were selected because of their contribution to the likelihood of existing QTL related to foie gras quality. The first study showed that livers presented different protein and metabolic profiles according to their phenotypes. Indeed, light livers, with low melting rate, low lipid rate and high protein rate show an over-expression of proteins involved in lipid, glucid or in synthesis metabolism, suggesting an anabolism process. On the contrary, heavy livers, with high melting rate, high lipid rate and low protein rate show cytoprotection and response to stress mechanisms. The second study highlighted 30 QTL related to liver quality traits and 50 pQTL related to different proteins. In particular, 7 chromosomes segregated several QTL and pQTL, permitting to assess hypothesis on the functions of the genes underlying these QTL regions. As an example, the APL15 locus seems linked to glycolysis and the APL18 one seems linked to cell survival ones. All these results helped in identifying metabolic pathways implicated in liver quality as well as establishing a link between traits, proteins and the QTL loci, suggesting a genetic determinism of these pathways. These relationships need to be further studied in order to bring precision to the process and to determine more precisely the genes implicated in the foie gras quality traits.

Les données électromagnétiques imagent des zones du manteau plus conductrice que l’olivine sèche. Il y a peu d’ambiguïté sur le fait qu’un liquide est thermodynamiquement stable et présent au niveau de l’asthénosphère, mais son impact sur la conductivité électrique du manteau reste débattu. Les études pétrologiques réalisées ces 30 dernières années ont montré qu’une péridotite exposée aux conditions the P-T-fO₂ de l’asthénosphère produisait des liquides riches en H₂O and CO₂, mais les conductivités électriques de ces liquides sont mal connues. Pour cette raison, des expériences de conductivité électrique ont été réalisées en piston cylindre sur des liquides riches en H₂O and CO₂. Différentes compositions de liquides ont été explorées, des liquides carbonatés aux basaltes. Les effets de la composition chimique et des volatiles sur ces liquides ont été déterminés. Les mesures de conductivités électriques ont montré que les liquides hydratés et carbonatés sont très conducteurs, et que l’incorporation de basalte décroit la conductivité. Avec ces nouvelles données, un modèle semi-empirique calculant la conductivité en fonction des teneurs en H₂O and CO₂ a été produit. Sur la base de ce modèle et de la conductivité électrique de l’olivine, des profils 1D de conductivité ont été construits. Avec ces profils, l’effet des teneurs en volatiles (partagé entre le liquide et le solide), les fractions de liquides (loi de mélange et interconnexion du liquide) et les différents régimes de température sur la conductivité ont été discutés. Ces calculs ont été considérés en milieu océanique et continental pour différents âges. La conductivité électrique du manteau est donc un outil puissant pour suivre les processus fondamentaux de la fusion du manteau, qui est à son tour étroitement liée aux cycles de H₂O and CO₂ dans le manteau supérieur. / Electromagnetic data images mantle regions more conductive than that of dry olivine. There is no doubt that melt is thermodynamically stable and present in the asthenosphere, but how they can impact on mantle electrical conductivity remains debated. Petrological studies realized some 30 years ago have shown that peridotites exposed at the P-T-fO₂ conditions of the asthenosphere produced H₂O and CO₂ rich-melts, but electrical conductivities of these melts are poorly known. Therefore, electrical conductivity experiments have been performed in piston cylinder on H₂O-CO₂ rich melts. Different melt compositions have been explored, from carbonated melts to basalts. The effects of chemical compositions and volatiles on these melts have been determined. The electrical conductivity measurements have shown that hydrous carbonated melts are very conductive, and the incorporation of basalt decreases the conductivity. With these new data, a semi-empirical law predicting the conductivity as a function of H₂O and CO₂ contents has been produced. Based on this law and the electrical conductivity of olivine, 1D conductivity profiles were constructed. With these profiles, the effect of volatile contents (partitioned between the melt and in the solids), melt fractions (mixing law and interconnection of the melt) and different temperature regimes on conductivity are discussed. These calculations are conducted on oceanic and continental settings with different ages. The electrical conductivities of the mantle is thus a powerful tool to track the fundamental process of mantle partial melting, which is in turn narrowly associated to the cycling of H₂O and CO₂ in the upper mantle.

Made available in DSpace on 2014-06-11T19:30:54Z (GMT). No. of bitstreams: 0 Previous issue date: 2008-06-13Bitstream added on 2014-06-13T19:19:37Z : No. of bitstreams: 1 alves_fr_dr_sjrp.pdf: 2029517 bytes, checksum: f737742cea44bc8699abdd17def3823d (MD5) / Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) / Estudos de calorimetria diferencial de varredura (DSC) e fluorescência de estado estacionário da sonda Vermelho do Nilo indicam a formação de vesículas de DODAX (X = Cl- ou Br-) em concentrações de surfactantes tão baixas quanto 10 µM. Estas vesículas foram denominadas microvesículas (µV), cuja Tm diminui monotonicamente com a concentração de DODAX até valores de Tm das vesículas tradicionais preparadas em 1.0 mM do surfactante. O efeito do contra-íon (Br- e Cl-) no comportamento termotrópico de fase das vesículas mistas de DODAB-DODAC foi investigado por DSC, condutimetria e espalhamento dinâmico de luz (DLS). Observou-se que a Tm aumenta sigmoidalmente de 45.8 a 48.9 oC com a fração molar de DODAC (xDODAC), com um ponto de inflexão no ponto eqüimolar. A condutividade e o diâmetro hidrodinâmico das vesículas variam muito pouco com xDODAB, indicando que a densidade superficial de carga das vesículas de DODAX é semelhante entre si, e o efeito do contra íon na Tm de DODAX se deve a interações específicas desses contra-íons na interface das vesículas. Medidas de DSC, fluorescência e turbidez de misturas de DODAB-DDAB indicam que as vesículas de DODAB têm maior afinidade por DDAB do que o oposto, resultando na formação de duas populações de vesículas mistas de DDAB-DODAB, com propriedades distintas. Além disso, medidas de fluorescência mostraram que a presença de pequena quantia de DODAB incorporado nas vesículas de DDAB causa um efeito significante na emissão da sonda devido ao aumento do tamanho das vesículas, sugerido por medidas de turbidez. O estudo dos sistemas DODAB/CnTAB/água na concentração total de surfactante igual a 1,0 e 5,0 mM, variando a concentração de CnTAB, e também mantendo a concentração de DODAB fixa em 1,0 mM, revelou uma forte dependência do comprimento da cadeia de hidrocarbonetos... / Differential scanning calorimetry (DSC) and fluorescence of the probe Nile Red studies reveal the formation of DODAX vesicles (X = Br- and Cl-) at surfactant concentrations as low as 10 µM. These vesicles were referred to as microvesicles (mV), whose Tm decreases monotonically with increasing DODAX concentration to the value for the ordinary vesicles at 1 mM. The effect of counterion (Br- and Cl-) on the thermotropic phase behavior of mixed DODAB-DODAC vesicles were investigated by differential scanning calorimetry (DSC), conductimetry and dynamic light scattering (DLS). Tm increases sigmoidally from 45.8 to 48.9 oC with DODAC molar fraction (xDODAC), with an inflection point at the equimolarity. The conductivity and the apparent hydrodynamic diameter vary little with xDODAB, indicating that the surface charge density is similar for DODAX, evidencing that the effect of counterion on Tm is due to the counterion specific interactions. DSC, fluorescence and turbidity measurements indicate a higher affinity of DDAB for DODAB vesicles than the reverse, resulting in two populations of mixed DDAB-DODAB vesicles with different properties. Besides, fluorescence measurements show that the presence of a small amount of DODAB in DDAB vesicles causes a pronounced effect on the Nile Red emission, due to the increase in vesicle size, as suggested from turbidity results. The study of DODAB/CnTAB/água systems at 1.0 and 5.0 total surfactant concentration, and varying CnTAB concentrations with constant 1.0 mM DODAB revealed a strong dependence of the chain length n and relative concentration of the surfactante in the properties of mixed DODAB-CnTAB vesicles. This study allowed analyzing the thermotropic phase behavior containing different amount of DODAB, and the mechanism of vesicle-micelle transition with increasing CnTAB concentration, below and above CMC... (Complete abstract click electronic access below)

La fusion sélective par laser est un procédé de la technologie de fabrication rapide de plus en plus utilisé dans l’industrie automobile, aéronautique, médicale, etc. Selon le principe de la fabrication rapide, la pièce est fabriquée couche par couche en fusionnant et soudant les particules fines par laser. Actuellement, les principaux matériaux utilisés sont les métaux métalliques ou les polymères. Le faible ou modeste point de fusion de ces matériaux conduit à une mise en œuvre par laser relativement facile. Cependant, en raison de leur point de fusion élevé, de la forte résistance à haute température et de la faible conductivité thermique, l’utilisation de matériaux céramiques est limitée dans la technologie de fusion laser sélective. Cette étude explore la fusion laser sélective de zircone stabilisée par yttrine avec un laser à fibre de longueur d’onde d’environ 1 µm. L’influence de différentes puissances de laser et de différentes vitesses de balayage sur la microstructure et la déformation de l’échantillon a été étudiée, et la densité relative et la microdureté ont été mesurées. Notamment, l’effet de différentes températures de préchauffage sur la microstructure sera étudié. En même temps, la structure cristalline céramique et la transformation des phases pendant le procédé de prototypage rapide ont été analysées. Les résultats expérimentaux montrent qu’il est possible de fondre complètement de la poudre YSZ avec un laser à fibre NIR, et avec l’optimisation des paramètres de fabrication, la densité relative de l’échantillon peut atteindre 91 %. Il est inévitable de voir se former des fissures et des pores dans les pièces fabriquées du fait de l’hétérogénéité de la distribution de l’énergie du laser. Cette distribution de l’énergie peut être améliorée grâce à l’optimisation des paramètres ; les longueurs de fissure peuvent être contrôlées et maîtrisées par un préchauffage du lit de poudre. Notamment, à haute température (1500°C, 2000°C et 2500°C) de préchauffage, la fissure verticale continue devient désordonnée et courte. Une transformation de la structure monoclinique et cubique en structure tétragonale s’est produite pendant le processus de fabrication. / Selective laser melting is a rapid manufacturing process coming from the rapid prototyping technology, which is widely used in the automotive, aeronautical, medical industry etc. According to the principle of rapid manufacturing, the piece is manufactured layer by layer through the laser sintering or melting the fine powder. Currently, the main powder materials used are metal or polymer materials. The low melting point of these materials facilitates the melting process. However, duo to the high melting point, strong strength at high temperature and low thermal conductivity the application of ceramic materials is limited in the technology of selective laser melting. In this study, selective laser melting of the ceramic yttria stabilized zirconia by a 1μm wavelength fiber laser was explored. The influence of different laser powers and different scanning velocities on the microstructure and the deformation were analyzed, then the micro-hardness and relative density were measured. In particular, the effect of different preheat temperatures on microstructure was investigated. At the same time, the crystal structure and phase transformation during the fabrication were analyzed. Experimental results show that YSZ powder can be completely melted by the near IR fiber laser. With the optimization of the manufacturing parameters, the relative density of sample could reach 91 %. The forming of cracks and pores in the manufactured parts is rarely avoid due to the heterogeneity of distribution of energy. The energy distribution could be improved by optimizing the parameters and the crack lengths can be controlled by preheating the powder bed. In particular, the high temperature (1500 ℃, 2000 ℃ and 2500 ℃) lead the continuous vertical crack becomes messy and short. The transformation of monoclinic and cubic crystal to tetragonal crystal can be observed during the fabrication.

The reduction behaviour of the olivine iron ore pellet MPBOwas studied in laboratory scale at KTH as well as in the LKABexperimental blast furnace. Initially, a newreduction-under-load, or so-called reduction/softening/melting,test equipment was developed. Experiments using differentreducing conditions, corresponding to different radialpositions of the blast furnace, were conducted. The experimentsincluded different temperature profiles, reducing atmospheresand mechanical loads applied on the sample bed to simulate thevarying conditions in the blast furnace process. The progressof reduction was investigated, as well as the processes ofsintering and contraction during reduction. A model of thecarburisation (pick-up of carbon by the reduced iron) andmelt-down process during rapid contraction was presented. Laboratory testing of MPBO pellets was compared with resultsfrom the LKAB experimental blast furnace. The reduction of ironore pellets in the experimental blast furnace was surveyed by adissection of the furnace after quenching. The high temperaturephenomena occurring when reducing the MPBO pellet, with limitedsoftening and a short temperature range of the melting process,resulting in a thin cohesive zone, were found to be the same inlaboratorytests and in the experimental blast furnace. Thereduction down through the burden of the experimental blastfurnace was similar, but not identical to the results of theRUL experiments. The differences were found to be due todifferent reducing conditions. Therefore, it was concluded thata simulation of the reduction occurring in the blast furnacecan be performed in laboratory scale, provided the experimentalconditions are correctly chosen. Finally, a modification to further improve the properties ofthe MPBO pellets was examined. With the aim to improve theblast furnace process, coating of blast furnace pellets wasinvestigated in laboratory scale, as well as in the LKABexperimental blast furnace. Olivine, dolomite and quartzitewere used as coating agents. In laboratory scale the stickingprevention action of the different coating materials wasverified, in established test methods as well as in new testmethods, modified for blast furnace conditions. Testing of thecoated pellets in the experimental blast furnace revealedseveral advantages; significantly reduced blast furnace fluedust generation, improved gas utilisation and a smoother blastfurnace operation with a potential for a lowered fuel rate. <b>Keywords:</b>Olivine, pellets, pellet testing,reduction/softening/melting, MPBO, blast furnace, reduction,quenching, dissection, coating, sticking, coated pellets.

There is a high demand for quadruplex-specific compounds that not only bind preferentially to quadruplex DNA over duplex DNA, but also bind to one quadruplex motif over other motifs. Quadruplex structures are recognized as common occurrences in cancer cells, and if a compound could stabilize this structure, it may serve as an effective anti-cancer treatment with minimal side effects. In this study, cyanine dyes’ interactions with DNA were analyzed with fluorescence titrations, UV-Vis thermal studies, circular dichroism titrations, and surface plasmon resonance (SPR) analysis. With these techniques, binding affinity, DNA stabilization, and conformational shifts were analyzed to determine if cyanine dyes could act as quadruplex-specific binding compounds for possible cancer treatments.

The problem of inadequate measurement techniques for quantifying the isothermal solidification process during transient liquid phase sintering (TLPS) in binary isomorphous systems such as Ni-Cu, and the resulting uncertainty regarding the solidification mechanism and its sensitivity to important process parameters, has been investigated. A unique combination of differential scanning calorimetry (DSC), neutron diffraction (ND), and metallographic techniques has enabled the quantitative characterization of important TLPS stages (i.e., solid-state sintering, melting and dissolution, isothermal solidification, and homogenization) as well as verifying the re-melt behaviour of post-sintered specimens and measuring variable melting point (VMP) properties. This has resulted in the advancement of the fundamental understanding of liquid formation and its removal mechanism during isothermal, or diffusional, solidification. The Ni-Cu system was chosen for experimentation due to its commercial relevance as a braze filler material and also because it is an ideal model system (due to its isomorphous character) that is not well understood on a quantitative or phenomenological basis. Samples consisted of elemental Ni and Cu powder mixtures of varying particle size and composition. In DSC experiments, the progress of isothermal solidification was determined by measuring the enthalpy of melting and solidification after isothermal hold periods of varying length and comparing these to the measured enthalpy of pure Cu. The low melting enthalpies measured for all Ni/Cu mixtures heated just past the Cu melting point (1090°C) indicate that solid-state sintering and interdiffusion during heat-up significantly suppress initial liquid formation and densification from the wetting liquid. For samples heated well past the Cu melting point (1140°C), Ni dissolution causes increased initial liquid fractions and densification. It was found that significantly more time was required for complete liquid removal at 1140°C vs. 1090°C. This is attributed to the observed increase in initial liquid fractions formed at higher processing temperatures due to the dissolution of Ni. This effectively counteracts the increased diffusivities at these temperatures, and thus more time is required to completely remove the increased liquid content. TLP mixtures sintered at 1140°C using three different particle sizes revealed that fine base metal Ni particles cause high degrees of solid-state interdiffusion during heat-up, small initial liquid fractions, and accelerated liquid removal rates due to high surface area/volume ratios. A diffusion-based analytical model was developed to account for these effects (i.e., particle size, temperature, solid-state sintering, and dissolution). Comparison with experimental DSC results reveals that this model can accurately predict liquid removal given accurate diffusivities. Metallographic analysis of post-sintered DSC specimens via SEM and EDS indicates that isothermal liquid solidification leaves behind Ni-rich cores surrounded by Cu-rich matrix regions having compositions given by the Ni-Cu phase diagram solidus (CS) at a selected isothermal processing temperature (TP). ND experiments were used to investigate the melting event and interdiffusion during the isothermal hold segment by analyzing the evolution of the {200} FCC peaks of Ni and Cu. ND patterns were collected in situ at 1 minute intervals during prolonged sintering cycles for larger powder specimens. The Cu melting event was characterized by an abrupt decrease in Cu peak intensity at 1085°C as well as a shift towards higher 2 angles corresponding to lower Cu contents. This shifted residual peak (hereafter referred to as the CS peak) originates from regions of the specimen having compositions near solidus at TP. Immediately following the melting event, the evolution of ND patterns shows that these CS peaks grow rapidly, indicating the isothermal growth of a Cu-rich phase. These in situ findings confirmed the metallographic and DSC data and indicated that isothermal solidification of the liquid phase proceeds via the growth of a solute-rich solid solution layer surrounding the Ni particles. This occurs by the transient progression of the solid/liquid interface at compositions given by the liquidus and solidus (CS/CL). During sintering, diffraction intensities gradually increased at intermediate 2 angles between previous Ni and Cu peaks. ND patterns gradually evolved from initially having a broad double-peak profile to a sharper single-peak profile due to increased Ni-Cu interdiffusion. The 2position and width of the post-sintered peaks indicated very homogeneous sintered alloys. Metallographic analysis of post-sintered specimens having undergone prolonged sintering and homogenization revealed extensive Kirkendall pore formation from unequal diffusivities (DCu > DNi). In this study, the unique combination of diffusion-based modelling as well as DSC, ND, and supporting metallographic analysis has enabled the identification of characteristic sintering behaviour, important process parameters, and processing windows for TLPS in Ni-Cu systems. Quantitative and in situ information of this nature is absent in the previous TLPS literature.

The problem of inadequate measurement techniques for quantifying the isothermal solidification process during transient liquid phase sintering (TLPS) in binary isomorphous systems such as Ni-Cu, and the resulting uncertainty regarding the solidification mechanism and its sensitivity to important process parameters, has been investigated. A unique combination of differential scanning calorimetry (DSC), neutron diffraction (ND), and metallographic techniques has enabled the quantitative characterization of important TLPS stages (i.e., solid-state sintering, melting and dissolution, isothermal solidification, and homogenization) as well as verifying the re-melt behaviour of post-sintered specimens and measuring variable melting point (VMP) properties. This has resulted in the advancement of the fundamental understanding of liquid formation and its removal mechanism during isothermal, or diffusional, solidification. The Ni-Cu system was chosen for experimentation due to its commercial relevance as a braze filler material and also because it is an ideal model system (due to its isomorphous character) that is not well understood on a quantitative or phenomenological basis. Samples consisted of elemental Ni and Cu powder mixtures of varying particle size and composition. In DSC experiments, the progress of isothermal solidification was determined by measuring the enthalpy of melting and solidification after isothermal hold periods of varying length and comparing these to the measured enthalpy of pure Cu. The low melting enthalpies measured for all Ni/Cu mixtures heated just past the Cu melting point (1090°C) indicate that solid-state sintering and interdiffusion during heat-up significantly suppress initial liquid formation and densification from the wetting liquid. For samples heated well past the Cu melting point (1140°C), Ni dissolution causes increased initial liquid fractions and densification. It was found that significantly more time was required for complete liquid removal at 1140°C vs. 1090°C. This is attributed to the observed increase in initial liquid fractions formed at higher processing temperatures due to the dissolution of Ni. This effectively counteracts the increased diffusivities at these temperatures, and thus more time is required to completely remove the increased liquid content. TLP mixtures sintered at 1140°C using three different particle sizes revealed that fine base metal Ni particles cause high degrees of solid-state interdiffusion during heat-up, small initial liquid fractions, and accelerated liquid removal rates due to high surface area/volume ratios. A diffusion-based analytical model was developed to account for these effects (i.e., particle size, temperature, solid-state sintering, and dissolution). Comparison with experimental DSC results reveals that this model can accurately predict liquid removal given accurate diffusivities. Metallographic analysis of post-sintered DSC specimens via SEM and EDS indicates that isothermal liquid solidification leaves behind Ni-rich cores surrounded by Cu-rich matrix regions having compositions given by the Ni-Cu phase diagram solidus (CS) at a selected isothermal processing temperature (TP). ND experiments were used to investigate the melting event and interdiffusion during the isothermal hold segment by analyzing the evolution of the {200} FCC peaks of Ni and Cu. ND patterns were collected in situ at 1 minute intervals during prolonged sintering cycles for larger powder specimens. The Cu melting event was characterized by an abrupt decrease in Cu peak intensity at 1085°C as well as a shift towards higher 2 angles corresponding to lower Cu contents. This shifted residual peak (hereafter referred to as the CS peak) originates from regions of the specimen having compositions near solidus at TP. Immediately following the melting event, the evolution of ND patterns shows that these CS peaks grow rapidly, indicating the isothermal growth of a Cu-rich phase. These in situ findings confirmed the metallographic and DSC data and indicated that isothermal solidification of the liquid phase proceeds via the growth of a solute-rich solid solution layer surrounding the Ni particles. This occurs by the transient progression of the solid/liquid interface at compositions given by the liquidus and solidus (CS/CL). During sintering, diffraction intensities gradually increased at intermediate 2 angles between previous Ni and Cu peaks. ND patterns gradually evolved from initially having a broad double-peak profile to a sharper single-peak profile due to increased Ni-Cu interdiffusion. The 2position and width of the post-sintered peaks indicated very homogeneous sintered alloys. Metallographic analysis of post-sintered specimens having undergone prolonged sintering and homogenization revealed extensive Kirkendall pore formation from unequal diffusivities (DCu > DNi). In this study, the unique combination of diffusion-based modelling as well as DSC, ND, and supporting metallographic analysis has enabled the identification of characteristic sintering behaviour, important process parameters, and processing windows for TLPS in Ni-Cu systems. Quantitative and in situ information of this nature is absent in the previous TLPS literature.

Homogenous acid catalysts are prevalent throughout the chemical industry but all have the drawback of requiring post reaction neutralization and subsequent downstream removal of the product salt. The use of a base to neutralize the acid and the processing of the salt are ancillary to the process and the disposal of the salt is an environmental concern. The work presented here shows the use of alkylcarbonic acids, which form in situ with CO₂ pressure and neutralize on loss of CO₂ pressure rather than requiring a base. Thus CO₂ can be used to "switch" the acid on and off. The properties of alkylcarbonic acids are explored to gain understanding of the mechanisms by which they act. The acids are also used to catalyze the synthesis of α-pinene, methyl yellow, and benzyl iodide. These reactions are examples of common acid catalyzed reactions where this technology could be implemented. The second half of the work explores two other "switches". The first is using temperature to break an emulsion with a novel thermally cleavable surfactant. This technology has potential applications in a wide range of fields where surfactants are used including polymerization, oil recovery, and biosynthesis. The second is using CO₂ to liquefy a solid ionic compound to allow its use as a solvent. This would greatly increase the number of ionic species available for use in ionic liquid-CO₂ biphasic systems.

In this work, feasibility of utilizing municipal incinerator fly ash (MIFA) of different sources as a substitute of raw materials for steel-making in a mini-mill was studied. Also studied included the efficacy of this mode of melting treatment and recycling. Under the condition of adding 1 wt% MIFA to scrap iron/scrap steel for partial replacement of lime, the L9 orthogonal arrays of Taguchi methods were utilized to investigate the effects of MIFA melting treatment of different sources by an electric arc furnace (EAF). Four experimental factors (i.e., scrap iron mass, lime mass, coke mass, and MIFA mass) were selected to study their effects on Pb leaching of EAF dust and slag. Test results for MIFA obtained from Plants K1, K2, and K3 show that EAF dust remains hazardous as it is originally a listed waste. On the other hand, slag so generated remains nonhazardous based on the TCLP results. The experimental results of EAF dust and slag were further subjected to the analysis of variance (ANOVA) and regular analysis. Using this process, the optimal operating conditions with respect to the leached Pb concentration would be as follows: (1) Plant K1(injection mode operation)--87 tons of scrap iron, 1.4 tons of lime, 0.4 ton of coke, and 0.9 ton of MIFA; (2) Plant K2(injection mode operation)--90 tons of scrap iron, 1.4 tons of lime, 0.7 ton of coke, and 1.1 tons of MIFA; (3) Plant K2(one-time-charge mode operation)--90 tons of scrap iron, 1.4 tons of lime, 0.9 ton of coke, and 0.7 ton of MIFA; (4) Plant K3(injection mode operation)--85 tons of scrap iron, 1.4 tons of lime, 0.7 ton of coke, and 0.9 ton of MIFA; and (5) Plant K3(one-time-charge mode operation)--87 tons of scrap iron, 1.5 tons of lime, 0.4 ton of coke, and 0.7 ton of MIFA. In this study, using MIFA from Plant K2 as an example, it was found that it required 29-35 kg of lime per ton of steel billets produced when MIFA was added. Under a normal operation of EAF steel-making, however, it required 35-45 kg of lime per ton of steel billets produced based on the past experience. In average, when MIFA is added, it needs only 32 kg of lime per ton of steel billets produced as compared to 40 kg of lime for regular steel-making. In other words, it would result in a reduction of 8 kg of lime per ton of steel billets produced by using this novel process. Based on an average monthly production of 20,973 tons of steel billets and a unit cost of 2,200 NT$ per ton of lime, a monthly saving of lime cost would be 369,125 NT$. Namely, about 4.4 million NT$ per year. In addition, it was also found that using this novel process to melt MIFA would not deteriorate the quality of steel billets and bars produced.