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Hydrogen storage in Ti-based coatings and Ti6Al4V alloyMazwi, Sive January 2016 (has links)
>Magister Scientiae - MSc / Hydrogen has been regarded as an ideal energy carrier for future, it can be stored as a liquid in cryogenic tanks, a gas in high pressure cylinders and as solid in metal hydrides. Hydrogen storage in metal hydrides is of research interest because hydrides often have high energy density than gas or liquid hydrogen and are relatively safe. Ti and Ti alloys are promising hydrogen storage material because they have high affinity for hydrogen, light in weight and react reversibly with hydrogen. This work aims to investigate the hydrogen storage capacity of CP- Ti and Ti6Al4V alloy and Pd/Ti6Al4V alloy, where Pd was deposited on Ti6Al4V alloy. Samples were hydrogenated from room temperature to 650 °C at atmospheric pressure in the vacuum furnace under the 15%H/Ar atmosphere. Hydrogenation was carried out for a period of 3 hours for all samples. Sample composition and layer thickness were determined using Rutherford backscattering spectrometry. The microstructure and phase transformation were investigated using optical microscopy and X-ray diffraction technique. Hydrogen storage capacity was determined using elastic recoil detection analysis and gravimetric method. It was found that hydrogenation temperature has an effect on hydrogen absorption, microstructure and phase transformation. Maximum hydrogen concentration was obtained at hydrogenation temperatures of 550 °C for all materials with 45.57 at.% in CP-Ti, 34.77 at.% in Ti6Al4V alloy and 39 at.% H in Pd/Ti6Al4V coated system. In CP-Ti it was found that hydrogen absorption begins at 550 °C and decreases at hydrogenation temperature of 650 °C and that hydrogenation at both temperatures leads to formation of titanium hydrides and needlelike microstructure. At temperatures below 550 °C no hydrides were formed. For Ti6Al4V alloy ERDA results showed that no significant hydrogen absorption occurred at temperatures below 550 °C and at hydrogenation temperature of 650 °C, hydrogen absorption decreased drastically. The δ- titanium hydride was detected in the sample hydrogenated at 550 °C. Fine needle like microstructure was observed in the sample hydrogenated at 550 °C, and at higher temperature (650 °C ) coarse needles were formed. Pd coatings on Ti6Al4V alloy was found to increase the absorption of hydrogen, and allowing hydrogen to be absorbed at low temperatures. / National Research Foundation (NRF)
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An investigation of ferromagnetic resonance in some transition group metalsRobertson, John A. January 1968 (has links)
No description available.
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Ligand-accelerated catalysis in palladium(II)-mediated C-H functionalisation ; Hydrogen bonding effects on the reactivity of fluoride anionEngle, Keary Mark January 2013 (has links)
No description available.
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Investigation of transition metal-carbon bondsGoodfellow, R. J. January 1965 (has links)
No description available.
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Synthesis and testing of palladium and platinum phosphine complexes with potential mitochondrial targeting anti-cancer propertiesGitari, Patricia Wanjiru 23 September 2009 (has links)
The main theme of this thesis focuses on the preparation of palladium and platinum phosphine complexes that possess the potential to act as anti-cancer agents. The design of the complexes was based on the known compound, [Au(dppe)2]Cl which was shown to have an anti-mitochondrial mode of action on cancer cells. Major problems were experienced in the synthesis of these novel palladium and platinum compounds as the five phosphine ligands required diverse reaction conditions. Instability was the major hindrance as decomposition occurred during purification. This led to the substitution of the counter-ion (Cl-) with PF6-. The complexes prepared in this study were varied in lipophilicity as the gold complex was found to be non-selective due to high lipophilicity. In total, six compounds were prepared, purified and tested for potency against a panel of cancer cell lines as well as normal cells. The most lipophilic compound, [Au(dppe)2]Cl, was non-selective as it exhibited the highest toxicity to both cancerous and normal cells. In general, in vitro studies showed that palladium complexes were more toxic than the platinum analogues. These novel compounds were also non-toxic to both resting and stimulated lymphocytes signifying high selectivity for cancer cells. Three compounds, Pg 3, Pg 4a and Pg 8 exhibited high toxicity and were hence tested as such on murine cancer cell lines. Pg 8, with intermediate lipophilicity, showed toxicity against a larger number of cancer cell lines and this led to further investigations in an attempt to determine its mode of action. Analysis of the effects of Pg 8 on the mitochodria showed that it did not depolarise the mitochondrial membrane potential. A seven day analysis showed that while it did not have any effect on the mitochondrial membrane potential, it depolarised the plasma membrane potential from day 4. In contrast, [Au(dppe)2]Cl depolarised the mitochondrial membrane potential as expected. Pg 8 was shown to induce apoptosis and necrosis on Jurkat cells after exposure for 48 h. It was also shown to induce cell cycle arrest (after 48 h) as it caused blockade in the S-phase. In contrast, [Au(dppe)2]Cl caused a blockade in the G0/G1 phase. Uptake studies with radiolabelled Pg 8, [103Pd(d2pyrpe)2][PF6]2, showed that it accumulated significantly in Jurkat cells. Biodistribution studies in Wistar rats demonstrated that it was mostly taken up in the spleen followed by the liver. However, it was excreted faster than [198Au(dppe)2]Cl as this latter compound accumulated significantly in the lungs followed by the spleen, small intestine and liver. Acute toxicity studies in Balb/c mice showed that Pg 8 was less toxic than [Au(dppe)2]Cl. The latter compound (at 3 and 6 ìM) caused a significant reduction of total body weight over a 5-day period. Toxicity was evident as it was also shown to cause elevation of liver enzymes (AST and GGT), contrary to the results obtained from the mice treated with Pg 8 (at 3, 6, 12 and 15 ìM). Preparation of a patent for the synthesis as well as anti-cancer properties of the novel compound, [Pd(d2pyrpe)2][PF6]2 (Pg 8) is currently in progress. Copyright / Thesis (PhD)--University of Pretoria, 2009. / Pharmacology / unrestricted
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Ruthenium and palladium assisted silver transport in silicon carbideO'Connell, Jacques Herman January 2012 (has links)
No description available.
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The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of HeteroaromaticsPetrov, Ivan January 2011 (has links)
The regioselectivity in Pd(0)-catalyzed direct arylation of pyrrole, thiophene, and indole can be improved by blocking some of the reactive sites with a chloride group, leading to increased yields of the desired regioisomers. Competition experiments and computational studies show that the blocking group also activates the substrates toward arylation. Due to the activated nature of chlorinated heteroaromatics, rare and sought after regioisomers, such as 3-arylthiophenes, can be obtained under mild conditions in good yields. Chlorine-bearing thiophenes arylated at C3 and C4 have the potential to undergo controlled regioregular polymerization under conditions developed in the field of polythiophene chemistry. Mechanistic studies support the hypothesis that the arylation of the substrates under investigation likely proceeds via the CMD transition state.
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Spectroscopic ellipsometry of Palladium thin filmsSullivan, Brian Thomas January 1987 (has links)
Spectroscopic ellipsometry is a nondestructive, ambient surface analysis technique for studying surfaces, interfaces and thin films. To take advantage of this method an automatic spectroscopic ellipsometer was designed and constructed for the microstructural characterization of thin films. This high precision instrument is capable of measuring in real-time the optical properties of bulk or thin film materials over the visible-UV region (1.5 - 6.0 eV). The microstructure of thin films can be determined from an effective medium theory analysis of the spectroellipsometric data to investigate how the film morphology evolves with varying preparation conditions and to determine the optimum deposition parameters.
In this thesis the pseudodielectric function of palladium films prepared by dc planar magnetron sputtering was measured while the substrate temperature, argon partial pressure and rf-induced substrate bias were varied independently during deposition. The film data are in excellent agreement with the effective medium theory of Sen, Scala, and Cohen, relevant for a random coated-particle microstructure where the grains are optically isolated from each other.
With increasing substrate temperature, the Pd volume fraction in the bulk was found to decrease slightly, while the rms microroughness of the film surface increased in magnitude. At 190° C, the rms microroughness was 80 ± 3 Awith the Pd volume fraction in the bulk region falling slightly to 97 ± 1% relative to the film deposited at 22° C.
For argon partial pressures below a transition pressure, Pt≃15 mTorr, the films consisted of densely packed grains, corresponding to the zone T in Thornton's structure zone model. Above this transition pressure, the films developed into a more voided columnar structure, characteristic of the zone 1 region. A microstructural analysis indicated a general trend towards increased porosity and microroughness of the films with higher argon pressures. The zone 1 region was best described optically by a random coated-particle microstructure and the electron microscopy confirmed that for thin films prepared at argon pressures higher than Pt, the grains became isolated by void boundaries. The optical data could not distinguish whether or not the films were 2- or 3-dimensionally isotropic.
With increasing rf-induced substrate biasing, the Pd film microstructure was modified in a manner similar to that obtained by varying the substrate temperature alone. Significant resputtering of the Pd films occurred, varying from 2 to 11 A/sec for bias voltages of -550 V to -1375 V, respectively. The measured deposition rate while bias sputtering was significantly higher than that expected upon the measured resputtering rate and several mechanisms were proposed to account for the enhancement in the deposition rate. The films were best characterized by a 2-dimensional isotropy which was supported by the columnar nature of the films observed by electron microscopy.
Finally, the dielectric function of the "best" palladium film is compared to optical constants of Pd previously reported in the literature for bulk and thin film specimens. While all the authors quote essentially the same values for the real part of the dielectric function, regardless of the preparation or measurement technique, the imaginary part differs up to a factor of two. Surface microroughness, bulk porosity and oxide layers are unable to account for the difference. A possible grain boundary scattering mechanism is suggested. / Science, Faculty of / Physics and Astronomy, Department of / Graduate
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Analýza výkonnosti investičních kovů a mincí / Analysis of performance of investment metals and coinsKabelková, Zuzana January 2012 (has links)
The thesis "Analysis of Performance of Investment Metals and Coins" deals with the evolution of prices of gold, silver, platinum and palladium. It analyzes factors which have an influence on the prices of these metals. It compares profitability and risk of the investment in gold with the index S&P 500. The strength of dependency is measured by coefficient of correlation between the variables gold and silver/ palladium/ platinum/ brent crude oil/ index S&P 500/prices of the mining company Randgold Resources Ltd. The third part of the thesis deals with the means of investing in the investment metals and it compares the advantages and disadvantages of each option.
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The reaction of 4-Vinylcyclohexene with palladium (II)Beeler, Kathy Ellen 01 January 1982 (has links)
This program of study was concerned with the elucidation of the causes(s) behind the inability of various workers to reproduce the work of Fyre and Kuljian on the rearrangement of 4-vinylcyclohexene to 1,5-cyclooctadiene by the action of palladium (II).
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