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The present thesis deals with Nb-Si alloy composites in both bulk and multilayer forms. The work has been divided into two parts. First part (chapter 4-6) deals with Nb based silicides binary and ternary alloys with alloying additions like Ga and Al. These alloys are synthesized by vacuum arc melting and suction casting (non-equilibrium processing techniques). The studies on intermetallic coatings of Nb-Si alloys and Nb/Si multilayer synthesized by pulsed laser deposition technique have been presented in the second part (chapter7-8). Nb-Si alloys are one of the candidate materials for the advanced structural and microelectronic applications. There are few issues with these materials like poor oxidation resistance, low fracture toughness and brittleness which need to be solved. Microstructure plays a crucial role to control these properties. The main focus of this work is to understand the process of phase transformation and thereby control the microstructure in both bulk alloys and thin films. We have also investigated in a limited manner mechanical and environmental properties of bulk alloys. This thesis is subdivided into nine chapters. After a brief introduction in the first chapter, a brief overview on Nb-Si phase diagram and literature reviews on Nb-Si based alloys are presented with emphasis on the current work in the second chapter. Literature reviews on the phase formations sequence and stability in Nb-Si alloys thin films and Nb/Si multilayers are also discussed in the same chapter. In the third chapter different experimental techniques, processing parameters and characterization tools like XRD, SEM, TEM etc. are briefly discussed. Special emphasis is given on two non-equilibrium techniques: laser deposition technique to deposit the thin film/multilayer and vacuum suction casting to produce the 3 mm diameter rods of different Nb-Si alloys. The fourth chapter discusses the microstructural aspects of Nb-Si alloys prepared by suction casting and its mechanical behavior. The samples have the compositions hypoeutectic (Nb-10at.%Si and Nb-14at.%Si), eutectic (Nb-18.7at.%Si) and hypereutectic (Nb-22at.% Si and Nb-25at.% Si). SEM microstructural analyses of all the samples clearly show the enhancement in the volume fraction of eutectic and decease in the eutectic spacings in microstructure due to large undercooling. Rod eutectic is observed in most of places with irregular eutectic a few places in all samples. First check of phases has been done by XRD in all samples. Phase confirmation using TEM showed the eutectic between Nbss and Nb3Si phases in all samples. The primary phase for hypoeutectic alloys is Nbss (dendritic structure), Nb3Si phase for eutectic composition and β-Nb5Si3 phase for hypereutectic alloys. Compositional analysis using EDS and EPMA also supported the above results. No signature of eutectoid reaction (Nb3Si→Nb+α-Nb5Si3) is observed. Mechanical properties like hardness, strength, ductility and indentation fracture toughness have been determined for above mention alloy compositions. SEM micrographs showed that silicides fractured by cleavage and Nb phase in a ductile manner during the compression tests carried out at room temperature. We attempt to explain how the above mention mechanical properties change with alloy compositions and processing. Chapter five deals with the effect of Ga addition on the microstructure and mechanical properties of the Nb-Si alloy. The composition selected for this study is Nb-20.2at.%Si-2.7at.%Ga. The results of ternary alloy have been compared with the binary alloy composition Nb-18.7at.%Si. Phase analysis has been carried out using TEM and XRD. Ga addition has suppressed the formation of Nb3Si phase and promoted the formation of β-Nb5Si3 phase. Ga addition also established the eutectic between Nbss and β-Nb5Si3, which is a metastable eutectic. Ga added ternary alloy, on suction casting, yields ultrafine eutectic with nanometer length scale (50-100nm). From the compression tests, it is concluded that the combination of ultrafine eutectic (Nbss-β-Nb5Si3) and primary β-Nb5Si3 in ternary alloy results in a high compressive strength ~2.8±0.1 GPa with 4.3% plasticity. In contrast binary alloy under identical conditions shows the compressive strength ~1.35±0.1 GPa and 0.2% plasticity. Ga addition also enhances the indentation fracture toughness from 9.2±0.05 MPa√m (binary) to 24.11±0.5 MPa√m (ternary). Composite hardness values of the ternary and binary alloys are 1064±20 Hv and 1031±20 Hv respectively. Chapter six deals with Al added Nb-Si ternary alloy. Here we have discussed microstructural and mechanical properties like in chapter 5 along with oxidation behavior for the alloy composition Nb-12.7at.%Si-9at.%Al. SEM micrograph shows the presence of primary dendrites structure with ultra fine lamellar eutectic (50-100nm). Detailed TEM studies confirm the Nbss as primary phase present in form of dendrites. These dendrites contain the plate shape precipitates of δ-Nb11Si4 (body centered orthorhombic structure) phase in Nb matrix (primary dendrites). Eutectic phases are Nbss and β-Nb5Si3. The analysis of the results indicates that Al addition promote the formation of β-Nb5Si3 phase in the eutectic. The results of this ternary composition were also compared with the binary alloy composition Nb-18.7at.%Si. Compression tests have been carried out at room and elevated temperatures to measure the strength of the material. Al added ternary alloy yields the compressive strength value 1.6±0.01 GPa whereas binary alloy yields the compressive strength value 1.1±0.01 GPa. Enhancement in indentation fractured toughness is observed in Al added ternary alloy (20.4±0.5MPa√m) compare to binary alloy (9.2±0.05 MPa√m). Thermal analysis by TGA and DTA were used to see the oxidation behavior of Al added ternary alloy. Chapter seven deals with the deposition characteristics and the TEM studies on the laser deposited Nb-Si thin films. Films were deposited on the NaCl crystals and Si single crystal substrates. The compositions chosen in this case are Nb-25at.%Si, Nb-37.5at.%Si and Nb-66.7at.%Si. These compositions correspond to the equilibrium intermetallic compounds Nb3Si, Nb5Si3 and NbSi2 respectively. In this chapter we have briefly discussed the microstructural and phase evolutions in the intermetallic coatings. The smooth films quenched from the vapor and/or plasma state show amorphous structure. The sequence of crystallization was studied by hot stage TEM experiments as well as by cross sectional TEM in the films deposited at the elevated temperatures (600oC and 700oC) on Si substrates. During the hot stage experiment, crystallization is observed in Nb-25at.%Si film around 850oC with nucleation of metastable cubic Nb3Si phase. Occasionally metastable hexagonal Nb3Si3 phase has also been observed (close to Si substrate) along with cubic Nb3Si phase in the films at elevated temperatures. For Nb-37.5at.%Si film, crystallization is observed at 800oC with the nucleation of grains of metastable hexagonal Nb5Si3 phase. Cross-sectional TEM shows the presence of hexagonal Nb5Si3 phase along with few grains of NbSi3 (equilibrium) phase in the films deposited at elevated temperatures. Hot stage experiment of Nb-66.3at.%Si film showed the onset of crystallization much earlier at 400oC and complete crystallization at 600oC. This crystallization leads to the nucleation of grains of NbSi2 phase. Films of this composition deposited at elevated temperatures showed the presence of NbSi2 and metastable hexagonal Nb5Si3 phases (occasionally). The laser ablated films, besides the film matrix also contain the micron and submicron sized spherical droplets of different sizes. These droplets travel at very high velocities and impinge on the substrate resulting in a very high rate of heat transfer during solidification from liquid state. Therefore in this work we have also studied the microstructural evolution in the droplets for each composition. The phases observed in the droplets embedded in the matrix of Nb-25 at% Si alloy film are the bcc Nb and the cubic Nb3Si (metastable phase). The droplets in the matrix of Nb-37.5 at% Si alloy showed the bcc Nb and tetragonal β-Nb5Si3 phases. The phases observed in the droplets of in the Nb-66.3at.%Si alloy are the bcc Nb, tetragonal β-Nb5Si3 and the hexagonal NbSi2 (metastable phase). Chapter eight describes the synthesis and microstructural characterization using TEM of Nb/Si multilayers. The aim of this work is to check the stability and phase formation sequence in Nb/Si multilayer. Nb/Si multilayers were first annealed at different time intervals at 600oC and at different temperatures (for 2 hours) and then characterized by the cross-sectional transmission electron microscopy. As-deposited Nb layer is crystalline while Si layer is amorphous. Microstructural and compositional evidences suggest the intermixing between the Nb and Si layers at the interfaces. Nb/Si multilayer annealed at 600oC for 1 hour, NbSi2 was identified as the first crystalline nucleating phase. However amorphous silicide layers were also observed between Nb and NbSi2 layers. Metastable hexagonal Nb5Si3 was identified as the next crystalline phase that nucleated from the amorphous silicide layers at the interfaces of Nb and NbSi2 layers. Occasionally few grains of cubic Nb3Si phase were also observed after 8 hours of annealing at 600oC. In the chapter we have compared the results to the other reported works in Nb-Si bulk diffusion couples and also thin film couples. The final chapter summarizes the major conclusions of the present work and scope of future work.

This diploma thesis deals with the design of composition and the study of properties of the ternary binding system based on purposeful ettringite formation, which was subsequently used for the preparation of self-leveling floor materials, specifically self-levelling underlay and thin-layer floor screed. In the designed compositions of the mixtures is then focused attention on optimizing the dosage of two kinds of plasticizer agents, followed by assessing their impact on the technological properties of these materials.

Cancer is responsible for upward of 13% of human deaths. Contemporary chemotherapy of disseminated cancer is often thwarted by dose limiting systemic toxicity and by multi-drug resistance (MDR). Riminophenazines are a novel class of potential anticancer agents that possess a potent multi-mechanistic antineoplastic action. Apart from their broad action against intrinsic, non-classical resistance, Riminophenazines inhibit the action of Pgp and hypothetically all ABC transporters demonstrating their great utility against classical MDR. Considering that combination chemotherapy is the norm, the vision directing R&D efforts was that Riminophenazines could be used with benefit within many standard chemotherapeutic regimes. The strategic intent of this project was to attain improved therapeutic benefit for patients through gains in both pharmaco dynamic and pharmacokinetic specificity for cancer cells over what is currently available. Tactically, this was driven through the use of synergistic Fixed-Ratio Drug Combinations (FRDC) encapsulated within tumour-targeting Nanoparticulate Drug Delivery Systems (NDDS). Long-term aims of this R&D project were to: 1) Screen FRDC of clofazimine (B663) and the lead derivative (B4125) with etoposide, paclitaxel and vinblastine for synergistic drug interactions in vitro. 2) Design, assemble and characterize a novel nanoparticulate, synergistic, anticancer co-formulation. 3) Evaluate the in vivo safety and efficacy of the developed product/s in accordance with international regulatory guidelines. Using the median effect and combination index equations, impressive in vitro synergistic drug interactions (CI<1) were shown for various FRDC of the three standard chemotherapeutics tested (etoposide, paclitaxel and vinblastine) in combination with either B663 or B4125 against MDR neoplastic cell cultures. Considering in vitro results and with the view to advance quickly to clinical studies, the already approved clofazimine (B663) was elected as the combination partner for paclitaxel (PTX). Considering the potency and wide action of PTX, a novel coformulation (designed to circumvent drug resistance) has the potential to greatly impact upon virtually all cancer types, particularly if selectively delivered through innovative delivery systems and loco-regional administration. A passively tumour targeting, micellular NDDS system called Riminocelles™ that encapsulates a synergistic FRDC of B663 and PTX has been designed, assembled using thin film hydration methods and characterized in terms of drug loading, particle size, zeta potential, CMC and drug retention under sink conditions. An acute toxicity and a GLP repeat dose toxicity study confirmed Riminocelles to be well tolerated and safe at clinically relevant dosages whilst Taxol® (QDx7) produced statistically significant (P<0.05) weight loss within 14 days. The same study demonstrated statistically significant (P<0.05) tumour growth delays superior to that of Taxol at an equivalent PTX dosage of 10 mg/kg. Importantly, all components (amphiphiles and drugs) used in assembly of Riminocelles are already individually approved for medicinal use - this promotes accelerated development towards advanced clinical trials and successful registration. Although these results are very promising (outperforming Taxol), this system was however found in a pharmacokinetic study to suffer from in vivo thermodynamic instability due to the high concentration (abundance) of albumin present in plasma. For this reason, in vivo longevity within circulation, permitting passive tumour accumulation was not fully realized. A second NDDS called the RiminoPLUS™ imaging system was additionally developed. This lipopolymeric nanoemulsion system has successfully entrapped Lipiodol® Ultra fluid (an oil based contrast agent) within the hydrophobic core of a monodisperse particle population with a size of roughly 100 nm and a stability of one week. This formulation is therefore thought capable of CT imaging of tumour tissue and drug targeting after either intravenous or loco-regional injection. In vivo proof of the imaging concept is warranted. The results of this study serve to highlight the great potential of in vitro optimized synergistic FRDC against drug resistant cancers. Lipopolymeric micelles are an effective way to formulate multiple hydrophobic drugs for intravenous administration and present a means by which cancer can be readily targeted; provided that the delivery system possess the prerequisite in vivo stability and surface attributes. Further experiments exploring synergistic drug and biological combinations as well as “intelligent” NDDS actively guided through specific molecular recognition are called for. / Thesis (PhD)--University of Pretoria, 2012. / Pharmacology / unrestricted

In dieser Arbeit wird das neue Prinzip der „Selbstinkompatiblen Lösungsmittel“ vorgestellt. Es wird theoretisch abgeleitet, dass eine Mischung aus zwei Substanzen mit ungünstigen Wechselwirkungen bereitwillig eine weitere Substanz aufnehmen sollte, die diese ungünstigen Wechselwirkungen durch Verdünnen vermindert. Dies sollte umso stärker ausgeprägt sein, je ungünstiger die Wechselwirkungen zwischen den beiden ersten Substanzen sind. Da sich jedoch Substanzen mit sehr ungünstigen Wechselwirkungen physikalisch nicht mischen, entstand die Idee, diese Substanzen durch eine kovalente Bindung aneinander zu binden. Ein solches Molekül, das aus zwei inkompatiblen Hälften besteht, wird im Folgendem Selbstinkompatibles Lösungsmittel genannt. Die in dieser Arbeit gewählten Substanzen zeigen mäßige Inkompatibilität, deshalb ist ein Vergleich zwischen einfachen physikalischen Mischungen und kovalent verknüpften Molekülhälften noch möglich. Dieses Prinzip wird für binäre und ternäre Mischungen quantitativ berechnet und experimentell in drei Serien von Experimenten bestätigt: i) unter Verwendung von Lösungskalorimetrie und Bestimmung der Wechselwirkungsparameter zwischen Komponente 3 und einer bereits hergestellt physikalischen binären Mischung aus Komponente 1 und 2, ii) unter Verwendung von Lösungskalorimetrie und Bestimmung der Wechselwirkungsparameter zwischen Komponente 3 und den selbstinkompatiblen Losungsmitteln, die den in (i) gewählten Mischungen entsprechen und iii) aus der Sättigungslöslichkeit der Komponente 3 in den entsprechenden selbstinkompatiblen Lösungsmitteln. In diesen drei verschiedenen Messserien wird stets der gleichen Trend beobachtet: Die Selbstinkompatibilität eines Lösungsmittels begünstigt den Lösevorgang. / In this thesis a new principle of Self Incompatible Solvent is introduced. It is shown theoretically that a preexisting mixture of two substances (compound 1 and 2) with unfavorable interactions will readily dissolve a third compound because it diminishes the unfavorable interaction between the compound 1 and 2 by dilution. This behavior should be the stronger the more unfavorable the interactions between compound 1 and 2 are. However, substances with strong unfavorable interactions will not mix. Therefore the idea pursued here is to enforce the desired preexisting mixture for example by linking compound 1 covalently to compound 2. Such a molecule that is composed of two incompatible parts is called Self Incompatible Solvent in this work. In this thesis examples of incompatible compounds that show moderate incompatibility are chosen, therefore it was possible to do a comparison between simple physical mixtures and covalently linked incompatible molecules. The theoretical prediction of the theory is compared with experiments. This principle is calculated quantitatively for binary and ternary mixtures and compared with the experimental results in three distinct series of experiments: i) by using solution calorimetry and calculation of the interaction parameters between compounds 3 and the preexisting binary mixture of compound 1 and 2, ii) by using solution calorimetry and calculation of the interaction parameters between compound 3 and the Self Incompatible Solvent that correspond to the mixtures used in (i) and iii) from the saturation solubility of compound 3 in the Self Incompatible Solvent. The results obtained from the theoretical prediction and these obtained from the three different series of experiments show the same trend: the self incompatibility of the solvent improves the dissolution process.

This dissertation aims to provide a comprehensive understanding of the evolution of solid phase composition with ongoing hydration in OPC‒rich and CAC‒CsHx rich ternary binders. The work is based on a multi‒method approach including XRD, TGA, MAS NMR spectroscopy, calorimetry, microscopy and thermodynamic calculations. From the combinations of results obtained from the different analytical methods, a schematic representation of the phase evolution with ongoing hydration in OPC and CAC‒CsHx rich combinations was achieved, along with plots showing the distributing hydrate phases in the ternary diagram OPC‒CAC‒CsHx. C‒S‒H, portlandite, ettringite and AFm phases stand as main hydration products in the OPC‒rich combinations. C‒S‒H accounts for ~70% of the X‒ray amorphous fraction. In the CAC‒CsHx rich combinations ettringite along with AH3, monosulphoaluminate, strätlingite and hydrogranet phases precipitate. The high portions of X‒ray amorphous fractions in such combinations were mainly attributed to AH3 gel and AFm phases. Additionally, comparison of QXRD results with stoichiometric calculations, thermal analysis and 27Al NMR revealed that a portion of the formed ettringite and portlandite are in an X‒ray amorphous state during hydration. The variation of CAC type and water content strongly influences the hydration mechanism and phase assemblage in the ternary binders, whereas differences in mixtures with different sulphate sources are mainly related to the different dissolution kinetics of the sulphate.

The implementation of energy storage systems in the current electrical grid will increase the grid's reliability and e ciency. Room temperature sodium batteries are seen as potential technology, especially to assist renewable energy generation sources. Currently, suggested negative electrode materials, however, are still not satisfactory for practical use in terms of fabrication costs, gravimetric /volumetric energy densities, cyclability, and irreversible capacity losses occur at the rst cycle. The literature describes various strategies that enhance the specific capacity and/or the cyclability of negative electrode materials but all involve increasing the fabrication costs due to the chosen synthesis or the complexity of the electrode's design. Furthermore, strategies, that reduce the irreversible capacity loss at first cycle, are not discussed. In this present experimental research work, presodiating bulk metallic negative electrode materials prior to cycling, prepared via a simple, cheap and easy-to-scaleup synthesis route, is introduced as a new strategy to improve the cyclability and to effectively reduce the first cycle irreversible capacity loss. Electrochemical and structural experiments were carried out to investigate sodiumtin-antimony powders. Presodiating mechanically bulk Sn-Sb negative electrode materials e ectively reduces the irreversible capacity loss at first cycle and enhances the specific capacity when compared to the non-presodiated powder, while the proper choice of electrode composite and electrolyte formulation improves the cycle life of the electrodes. The enhancement of the electrochemical properties of the presodiated NaSnSb powder, composed of the ternary phase Na5Sb3Sn and an unknown ternary phase crystallising in a hexagonal setting P6, is associated with the stabilisation of the SnSb as desodiation product. Presodiating bulk SnSb negative electrode material is a viable strategy to reduce the first cycle irreversible capacity loss, alleviating the volume changes. With an optimised system, this approach may be extended to other negative electrode materials, reducing the fabrication costs of high capacity negative electrode materials for room temperature sodium batteries. Presodiated NaSnSb negative electrode material may be combined with non-sodiated positive electrode material, such as sulphur to develop competitive room temperature sodium-sulphur batteries. / Die Implementierung von Energiespeichersystemen im bereits bestehenden Stromnetz ist eine der Lösungen, um die Zuverlässigkeit und die Effizienz des Netzes zu nutzen. Raumtemperatur Natrium-Batterien gelten als erfolgsversprechende Technologie insbesondere zur Unterstützung erneuerbarer Energieerzeugungsquellen. Jedoch sind die naheliegenden negativen Elektrodenmaterialien für eine praktische Anwendung hinsichtlich Herstellungskosten, gravimetrischer oder volumetrischer Energiedichte, Zyklenfestigkeit und irreversiblen Kapazitätsverlusten im ersten Zyklus noch nicht zufriedenstellend. Die Literatur beschreibt verschiedene Strategien, die die spezifische Kapazität und / oder die Zyklenfestigkeit von negativen Elektrodenmaterialien verbessern. Diese führen jedoch alle zu einer Erhöhung der Herstellungskosten aufgrund der gewählten Synthese oder des Designs der komplexierten Elektrode. Darüber hinaus werden Strategien zur Reduzierung des irreversiblen Kapazitätsverlusts im ersten Zyklus nicht erörtert. Diese experimentelle Forschungsarbeit präsentiert mit Natrium angereicherte metallische negative Elektrodenmaterialien vor der Wechselbeanspruchung/dem periodischen Durchlaufen, die durch einen schlichten, billigen und einfach zu skalierenden Syntheseweg hergestellt wurden, als eine neue Strategie zur Verbesserung der Zyklenfestigkeit und zur wirksamen Verringerung des irreversiblen Kapazitätsverlusts im ersten Zyklus. Elektrochemische und strukturelle Experimente wurden durchgeführt, um mit Natrium angereichertes Zinn-Antimon-Pulver zu untersuchen. Die mechanischen mit Natrium angereichertes Sn-Sb-negativen Elektrodenmaterialien verringert effektiv den irreversiblen Kapazitätsverlust im ersten Zyklus und erhöht die spezische Kapazität im Vergleich zu dem ohne Natrium angereicherte Pulver, während die richtige Wahl der Elektrodenzusammensetzung und der Elektrolytformulierung die Lebenszyklus der Elektroden verbessert. Die Verbesserung der elektrochemischen Eigenschaften des mit Natrium angereicherten NaSnSb-Pulvers, bestehend aus der ternären Phase Na5Sb3Sn und einer unbekannten ternären Phase, die in einer hexagonalen Aufbau P6 kristallisiert, ist mit der Stabilisierung des Enddesodiationsproduktes beim periodischen Zyklus verbunden, wobei das intermetallische SnSb nach Rekristallisation vorliegt. Mit Natrium angereicherte SnSb negativen Elektrodenmaterialien sind eine tragfähige Strategie zur Verringerung des irreversiblen Kapazitätsverlustes im ersten Zyklus, die Volumenänderungen abschwächen. Mit einem optimierten System kann dieser Ansatz auf andere negative Elektrodenmaterialien erweitert werden um die Herstellungskosten von negativen Elektrodenmaterialien mit hoher Kapazität für Raumtemperatur-Natrium-Batterien zu verringern. Mit Natrium angereichertes NaSnSb-negatives Elektrodenmaterial kann mit nicht mit Natrium versetztem positivem Elektrodenmaterial wie Schwefel kombiniert werden, um realisierbare Raumtemperatur Natrium-Schwefel-Batterien zu entwickeln.

Die vorliegende Arbeit liefert einen Beitrag zum Verständnis der komplexen Wechselwirkungen zwischen Nanopartikeln und Polymeren in dünnen Schichtsystemen. Dazu wurden in einem geeignetem Modellsystem drei verschiedene Einflussparameter auf die Nanopartikelverteilung im Polymer und zwischen einer hydrophilen und einer hydrophoben Grenzfläche analysiert. Für eine erste Abschätzung der Verträglichkeit der einzelnen Komponenten wurden Wechselwirkungsparameter, binäre und ternäre Phasendiagramme ermittelt. Die experimentelle Charakterisierung der Nanopartikelverteilung erfolgte mittels Rasterkraftmikroskopie, Rasterelektronenmikroskopie und Transmissionselektronenmikroskopie. Die erhaltenen Ergebnisse wurden mit denen der theoretischen Vorbetrachtungen verglichen um herauszufinden, ob Vorhersagen zur Nanopartikelverteilung in einem Polymer möglich sind. In dieser Arbeit konnte gezeigt werden, dass die Nanopartikelverteilung im Polymer mit den untersuchten Parametern gezielt beeinflusst werden kann.

Long-term evolution of nature-society interactions can be studied by using data of land use change. In the thesis is used a detailed statistical database of Czechia (developed at Charles University in Prague, Faculty of Science). The database allows monitoring changes of eight categories of land use in the period 1845-2000. Attention is devoted to the growing differentiation of land use at different scale levels, the thesis is concentrated on functional specialization of czech regions. Deepening division of labour between regions is reflected by increasing territorial concentration of land use. This process is monitored by using three methods. Ternary plots present an overview of the differentiation trends of land use. Spatial autocorrelation methods present the general development and specific areas of functional specialization in Czechia. A review by territorial heterogeneity rate provides a detailed look at the change of territorial concentration of land use. The thesis operates with three territorial classifications (hydrological, geomorphological and administrative) at two regional levels and the level of Czechia. Results are interpreted using the driving forces (such as technological development, economics, historical events, society). The final part of the thesis compares the development of...

In the presented paper, the applicability of pressure-decay methods to determine the diffusivities of gases in hydraulic fluids is analysed. First, the method is described in detail and compared to other measurement methods. Secondly, the thermodynamics and the mass transfer process of the system are studied. This results in four different thermodynamic models of the gaseous phase in combination with two diffusion models. Thirdly, the influence of the models on the pressure-decay method is evaluated computationally by examining the diffusion process of air in water as all system parameters are available from literature. It is shown that ordinary pressure-decay methods are not applicable to gas mixtures like air and therefore a new method for calculating the diffusivities is suggested.