This study uses the combination of block copolymer and metal nanoparticles to array ordered structure and specific physical properties such as optics, electricity and magnetism. In this first part, 2-phenylethanethiol was used as the monolayer-protected gold nanoparticles (nps) and dispersed in block copolymer PS-b-PB-E thin film. Two different methods are compared, the first method was PS-b-PB-E thin film by partial crosslinked treatment then the 2-phenylethanethiol of monolayer-protected gold nanoparticles soaked into PS-b-PB-E thin film. The second method was blended gold nps within PS-b-PB-E directly. We found that the first method was better than second method which had arrangement dispersedly. The analyses of UV-VIS, TEM, and SAXS measurement are able to provide the positive evidence to characterize the dispersion of gold nps in diblock copolymer thin film. In the second part, we design to manufacture the multi-nanoholes golden electrode, which has many application in catalysis, selective transit function and fuel cell electrode. We use the PS-b-PB-E copolymer as the spherical micelle, which is the templates and then micelle surface reaction in mercaptane (S-H) function. Gold nps will use the exchange stabilizing ligands method in the micelle surface layer, and the porous gold electrode material by way of the heat treatment step.

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Although bacterial leaching of sulphidic minerals is a well-known phenomenon, it is only in the last ten years that full-scale bacterial leaching plants have been commissioned for gold processing. In order for bacterial leaching to compete successfully with other pretreatment processes for refractory ores, particularly with established technologies such as roasting and pressure leaching, it needs to be efficient. This requires the optimization of the parameters affecting the leaching reaction and the growth of bacteria. The entire biotreatment process is agitation leaching, carried out in stirred reactors or Pachuca type reactors. The bacterial oxidation is a complex reaction involving gaseous, liquid and solid phases. The interactions are highly complex, and analysis is complicated by the presence of solids in the leaching medium. Inspite of the amount of research that has been performed, kinetic and process models are underdeveloped. Since kinetic data varies widely with the type and source of concentrate, experimental data should be generated before doing the full-scale reactor design. In sizing reactors for a commercial scale process, it would be useful to have a mathematical model that one could use to predict the amount and rate of release of metal, as a function of the various operating parameters of the system. G.R.Halli arsenical gold sulphide concentrate obtained from Hutti Gold Mines Ltd., Karnataka, was chosen for our study, because of its high refractoriness. An indegenous strain of Thiobacillus ferrooxidans was used for biooxidation. The experiments were conducted in a well-agitated stirred tank reactor under controlled conditions. Sparged air was supplemented with carbon-dioxide for optimized growth. In this work, more than 90% gold and 95% silver could be recovered from the sulphidic gold concentrate when bioleaching was used ahead of cyanidation, compared to 40% and 50% by direct cyanidation. A generalized model, which accounts for both direct bacterial attack and indirect chemical leaching, has been proposed for the biooxidation of refractory gold concentrates. The bacterial balance, therefore, accounts for its growth both on solid substrate and in solution, and for the attachment to and detachment from the surface. The overall process is considered to consist of several sub-processes, each of which can be described in terms of a mechanism and related rate expressions. These sub-processes were studied seperately under kinetically controlled conditions. The key parameters appearing in the rate equations were evaluated using the experimental data. Since the refractory concentrate contains pyrite and arsenopyrite as the major leachable entities, leaching studies have been done on pure pyrite and arsenopyrite as test minerals and the key parameters in the rate equations are evaluated using this data. The model so developed is tested with the leaching kinetics of the concentrate. The growth of bacteria is dependent on the availability of the substrate, ferrous iron, and the dependence is modelled by the widely accepted Monod equation. The effect of carbon dioxide supplementation on the bacterial activity was studied and the optimal concentration for growth was found to be l%(v/v). Studies on indirect chemical leaching showed that the rate is sensitive to surface area of concentrate. Indirect rate constant of arsenopyrite was found to be greater than that of pyrite, since pyrite is more nobler than arsenopyrite. Conditions of direct leaching alone was obtained at high pulp density and using substrate adapted bacteria. The rate constant of arsenopyrite was found to be greater than that of pyrite. The parameters obtained were tested with the overall batch leaching data of the concentrate and favourable comparision was obtained. Thus, it has been possible to isolate the various simultaneous sub-processes occurring during the leaching and propose useful models to describe these processes in some detail. The model has been extended successfully to predict the continuous leaching behaviour using the parameters obtained from the batch data. Studies on the effect of residence time and pulp density on steady state behaviour showed that there is a critical residence time and pulp density below which washout conditions occur. The critical residence time at 10% pulp density was found to be 11 hrs. Operation at pulp densities lower than 5% and residence times lower than 72 hrs is not favourable for efficient leaching. Studies on the effect of initial ferric iron concentration showed that there exists an optimum concentration of ferric iron at which the time required to reach steady state is minimum.

Thesis (Ph.D.)--University of Nebraska-Lincoln, 2009. / Title from title screen (site viewed October 13, 2009). PDF text: 261 p. : ill. (some col.) ; 5 Mb. UMI publication number: AAT 3359063. Includes bibliographical references. Also available in microfilm and microfiche formats.

Gold has been considered catalytically inert due to its resistance to oxidation and corrosion. However, decades ago, it was discovered that gold nano-particles (<5nm) on metal oxides demonstrate superior chemical activity towards many reactions. These seminal findings spurred considerable interest in investigations of the mechanistic details of oxidative reactions on gold-based catalysts. However, the active site and structure of supported Au nanoclusters as well as the active oxygen species remains elusive. Achieving high selectivity toward partial oxidation products also remains a challenge. In this dissertation, an oxygen-covered Au(111) crystal under ultra vacuum conditions was used as a model system to gain insights into oxidative reactions in gold-based catalysis. I have been able to demonstrate that (i) surface-bound oxygen atoms are metastable at low temperature; (ii) the oxygen atoms participate in surface reactions as a Brønsted base or a nucleophilic base; and (iii) the acid-base reactions that have been observed on silver and copper may also occur on gold. Low temperature CO oxidation and the associated mechanistic aspects are investigated. CO reacts with hydroxyls formed from water-oxygen interactions to produce CO₂ on Au(111) populated with atomic oxygen at low temperatures. Directing an ¹⁶O beam toward C¹⁸O₂ pre-adsorbed Au(111), the formation of carbonate is significantly enhanced. This reaction is suggested to follow a hot-precursor-mediated mechanism. The identification of reaction pathways in oxidation of N-containing molecules such as ammonia and propylamine is presented. Abstraction of hydrogen from ammonia or propylamine by O atoms is the initial step in the surface decomposition of NHx (or RNHx-1) on Au(111). Atomic oxygen or hydroxyl-assisted dehydrogenation steps have lower barriers than the recombination steps under relevant conditions. 100% selectivity of N₂ or propionitrile can be obtained if the oxygen coverage is below the stoichiometric value. The surface oxidative chemistry of alcohols on Au(111) is also investigated. Except for methanol that is fully oxidized, alcohols initially undergo O-H bond cleavage (producing alcoxides) followed by selective β-C-H bond activation to form aldehydes or ketones. This finding reveals that the interaction of Au with the metal oxide support might not be essential to facilitate the reactions if active oxygen species are readily present, particularly at low temperatures. / text

The exploration of nanoparticles for applications in medicine has grown dramatically in recent years. Due to their size, nanoparticles provide an ideal platform for combining multiple functionalities and interfacing directly with the biological realm. Additionally, nanoparticles can have physical properties that don't naturally exist in biology. Metal nanoparticles in particular have unique optical and magnetic properties which have driven nanomaterials research. The optical properties of gold nanoparticles and the magnetic properties of iron nanoparticles make them suitable for use as contrast agents in diagnostics and for radiation enhancement in therapeutic applications. The strong optical absorption and scattering and the nature of the conduction electrons of gold particles makes them ideal contrast agents for two-photon microscopy, photoacoustic imaging, and photothermal therapy. The superparamagnetic nature of iron oxide nanoparticles is clearly visible in magnetic resonance imaging, rendering them suitable as whole-body imaging contrast agents. All nanoparticle types can serve as delivery vehicles for drugs consisting of small molecules, peptides, or nucleic acids. This multiplicity of characteristics renders nanoparticles suitable for use in combining diagnosis and therapy, such as using particles to first detect the spatial extent of a cancer, and then to enhance near-infrared radiation in the tissue optical window to induce localized heating of diseased tissue. This combined approach requires both a mechanism of enhanced imaging contrast and a localized therapeutic mechanism, and the studies presented in this dissertation present work both on these aspects. By coating iron oxide nanoparticle cores with gold shells, it is possible to obtain a nanoparticle with both magnetic and optical properties. While individual gold nanoparticles do not absorb light in the infrared, receptor-mediated aggregation and the plasmon coupling effect lead to enhanced optical absorption only in diseased tissue. In addition to exploring these advanced applications, this work presents a fundamental investigation into the stability of gold nanoparticles in biological media. A previously unknown mechanism of gold nanoparticle destabilization and opsonization is presented and supported, along with a technique for reducing this opsonization and greatly enhancing the stability of gold particles in biological applications. This work will provide guidance to future designs of nanoparticle systems. / text

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

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