Mercury (Hg) is a toxic heavy metal that poses significant human and environmental health risks. Mineral-associated Hg is the largest reservoir of Hg in the environment where it can account for nearly 60% of the global Hg mass inventory. A large fraction of this pool is comprised of mercury sulfide (HgS) minerals, including metacinnabar (beta-HgS). HgS minerals have long been considered insignificant sources of Hg to aqueous or atmospheric pools in all but severely acidic environments due to their low solubility and slow abiotic dissolution kinetics. Little previous work has been conducted investigating the bacterial colonization of HgS minerals and the potential role of these mineral-associated communities in impacting the mobility of mineral-hosted Hg. To address this gap in knowledge, the studies within this dissertation employed a combination of field- and laboratory-based methods. Using culture-independent techniques, this work revealed that sulfur-oxidizing bacteria can extensively colonize metacinnabar within aerobic, near neutral pH, creek sediments, suggesting a potential role for chemolithotrophic bacteria in metacinnabar weathering. Within laboratory incubations, the dominant bacterial colonizer (Thiobacillus thioparus), induced extensive release and volatilization of metacinnabar-hosted Hg. These findings expose a new pathway for metacinnabar dissolution and point to mineral-hosted Hg as an underappreciated source of elemental Hg that may contribute to global atmospheric Hg budgets. In addition, this work elucidates the importance of thiosulfate, a major intermediate sulfur species in the environment, in stimulating metacinnabar dissolution. Therefore, the work within this dissertation shows that authigenic HgS minerals are not merely a sink for Hg within non-acidic natural environments and instead are a source of dissolved and gaseous Hg. This work provides critical information for predicting the transport of Hg in the environment and for developing appropriate management and remediation strategies for Hg-contaminated systems. / Engineering and Applied Sciences

El presente trabajo de investigación obedece a la percepción de sensación de desprotección que siente una persona al tener un problema societario que debería de ser extirpado, la irregularidad de las sociedades; que puede traer consigo un drástico cambio en el contexto económico de cada persona. / Trabajo de investigación

Diploma paper describes the process of dissolution of a company without its liquidation. The main accent is put on transformation in a form of intrastate merger in accordance with the legal form of company, analysis of its legal regulation in force as compared with prior regulation forced until 30. 6. 2008.

abstract Aim of this Master's Thesis is to describe the process of liquidation to the reader step by step from winding-up of the company to its dissolution and focus on prospective problems that might arise in connection therewith. Based on the valid legislation the theoretical part deals with basic terms and explanation thereof with regards to anticipated effectiveness of the New Civil Code and Act on Business Corporation in January 2014 and changes related thereto. The practical part contains description of the liquidation process of the fictitious limited liability company. Key words: liquidation, liquidator, winding-up and dissolution of the company

The treatment of advanced nuclear fuels is relevant to the stabilisation of legacy spent fuels or nuclear materials and fuels from future nuclear reactors. Historically, spent fuel reprocessing has been driven to recover uranium and plutonium for reuse. Future fuel cycles may also recover the minor actinides neptunium, americium and perhaps curium. These actinides would be fabricated into new reactor fuel to produce energy and for transmutation of the minor actinides. This has the potential to reduce the long lived radioactivity of the spent fuel and reprocessing high level waste, whilst also maximising energy production. To achieve these aims there are a range of materials that could be used as advanced nuclear fuels, these include metals, oxides, carbides, nitrides and composite materials, and these fuels may also be alloyed. These advanced fuels may need to be reprocessed, and as head end is the first chemical treatment step in a reprocessing plant, the issues caused by treating these advanced fuels are faced primarily by head end. Changes to the overall reprocessing specification, such as reduction in discharge authorisations for volatile radionuclides, will have the greatest impact upon head end. All these factors may lead to the introduction of pre-treatment technologies (e.g. Voloxidation) or enhanced dissolution technologies, e.g. mediated dissolution using silver(II).Literature and experimental studies show that uranium dioxide and low plutonium content MOx dissolves in nitric acid via direct and indirect nitrate reduction. The indirect nitrous acid catalysed route is kinetically most significant. The kinetics for the dissolution of uranium dioxide and 5 % plutonium MOx have been derived experimentally. Studies of the dissolution of MOx pellets in concentrated nitric acid and near boiling conditions indicate that dissolution shows a degree of mass transfer limitation. Thermodynamic studies show that the pronounced reduction in the MOx dissolution extent at 30-40% plutonium is due to the thermodynamics of the key dissolution reactions. One technology that could be used to dissolve plutonium-rich residues that are generated from the reprocessing of MOx fuels is mediated dissolution. Inactive studies using linear staircase voltammetry (LSCV) and constant current bulk electrolysis (BE) have been used to optimise a 100 ml dissolution cell. The generation of silver(II) is dependent upon silver concentration, agitation and the size of the separator membrane. Whilst the stability of silver(II) is defined by the kinetics of water oxidation, this is dependent upon a number of factors including nitric acid concentration, silver(I):(II) ratio, temperature and the rate of migration from the catholyte into the anolyte. LSCV experiments have shown that Tafel analysis confirms there is a good relationship between potential and anode current density assuming oxygen evolution and silver(I) oxidation. Kinetic modelling of the BE experiments can be used to model the silver(II) generation, steady state and decomposition due to reaction with water. The dissolution cell has been demonstrated to be capable of dissolving plutonium dioxide to 200 g.l-1 in less than 2 hours with good faradaic efficiency.

In this study, the ability of pharmaceutical cocrystals on improving solubility and dissolution behaviour of poorly water soluble drug has been studied by a novel technique SDI300 UV imaging surface dissolution system. Pharmaceutical cocrystals of poorly water soluble drug carbamazepine (CBZ) were synthesized, which are 1: 1 carbamazepine - nicotinamide (CBZ-NIC) cocrystal, and 2:1 carbamazepine - succinic acid (CBZ-SUC) cocrystal. Firstly, dissolution and solution mediated phase transformation behaviour (SMPT) of CBZ-NIC cocrystal was studied by in situ techniques of UV imaging and Raman spectroscopy. This study has shown that in situ UV imaging and Raman spectroscopy with a complementary technique of SEM can provide an in depth understanding of cocrystal dissolution processes. It has been found that CBZ-NIC cocrystal including other polymorphs of CBZ III and I and mixture are converting to CBZ DH during dissolution. The influence of surfactants, SLS and Tween 80, on the solubility and dissolution behavior of the CBZ-NIC cocrystal has been studied. Results show that the SMPT of CBZ III and CBZ-NIC cocrystal can be altered by inclusion of a surfactant in dissolution medium. However, CBZ III and CBZ-NIC cocrystal have shown different transformation behavior with different surfactants. The solubility and dissolution behaviour of CBZ-NIC cocrystal, CBZ-SUC cocrystal in four biomedia (simulated gastric fluid, pH1.2 HCl buffer, simulated intestinal fluid, and pH 6.8 PBS buffer) were studied. Results have shown that equilibrium solubility of CBZ samples varied in different media. The two cocrystals dissolution rates show different trends as that of parent drug CBZ III. This can be explained by that the formation of cocrystal change the dissolution ability of CBZ III.

Magister Pharmaceuticae - MPharm / In conclusion, the results obtained firstly indicated that the BP, EMEA and WHO were in fairly good agreement on the criteria and specifications that can be used to assesses the pharmaceutical quality of a traditional plant medicine such as Phela. Secondly, the Phela plant powders were found to have acceptable pharmaceutical properties that did not complicate or adversely affected the capsule manufacture. Thirdly, the Phela capsules produced were generally of acceptable pharmacopoeial standard. Fourthly, HPLC fingerprinting and pattern recognition analysis proved useful to examine the chemical stability of selected marker compounds of Phela and indicated that the capsules had no practical shelf life under elevated temperature and humid conditions. Overall, the Phela capsules should thus be suitable for use in a short time clinical trial, but for use in a long period trial the long term stability of the Phela capsules under ambient conditions must still be confirmed. / South Africa

Mineral dust aerosols emitted from the Earth crust during various natural and anthropogenic processes continuously alter the chemical balance of the atmosphere via heterogeneous processes and thus, impact on the global climate. Understanding of heterogeneous chemistry and photochemistry on mineral dust has become vital to accurately predict the effect of mineral dust loading on the Earth's atmosphere. Here, laboratory measurements are coupled with model studies to understand heterogeneous chemistry and photochemistry in the atmosphere with the specific focus on reactions on mineral oxide surfaces. Heterogeneous uptake of gas phase HNO3 on well characterized metal oxides, oxyhydroxides and carbonates emphasized binding of nitric acid to these surfaces in different modes including monodentate, bidentate and bridging under dry conditions. It is becoming increasingly clear that the heterogeneous chemistry, including uptake of HNO3, is a function of relative humidity (RH) as water on the surface of these particles can enhance or inhibit its reactivity depending on the reaction. All the studied model systems showed a significant uptake of water with the highest uptake by CaCO3. Quantitative analysis of water uptake indicated formation of multilayers of water over these reactive surfaces. Under humid conditions, two water solvated nitrate coordination modes were observed that is inner-sphere and outer-sphere, which differ by nitrate proximity to the surface. Photochemical conversion of nitric acid to gas phase nitrous oxide, nitric oxide and nitrogen dioxide through an adsorbed nitrate intermediate under different atmospherically relevant conditions is shown using transmittance FTIR and XPS analysis. The relative ratio and product yields of these gas phase products change with relative humidity. Photochemistry of adsorbed nitrate on mineral aerosol dust may be influenced by the presence of other distinct gases in the atmosphere making it complicated to understand. This thesis converses formation of active nitrogen, NOx and N2O, and chlorine, ClOx, species in the presence of co-adsorbed trace gases, that could potentially regulate the peak concentration and geographical distribution of atmospheric ozone. Here we report formation of atmospheric N2O, from the photodecomposition of adsorbed nitrate in the presence of co-adsorbed NH3 via an abiotic mechanism that is favorable in the presence of light, relative humidity and a surface. Estimated annual production of N2O over the continental United States is 9.3+0.7/-5.3 Gg N2O, ~5% of total U.S. anthropogenic N2O emissions. Not only NH2 but also gaseous HCl react with adsorbed nitrate to activate "inert" N and Cl reservoir species, yielding NOCl, NOx, Cl and Cl2, through adsorbed nitrate under different atmospherically relevant conditions. Mineral dust aerosol is a major source of bioavailable iron to the ocean with an annual deposition of ~ 450 Tg of dust into the open ocean waters. In this study, we report enhanced Fe dissolution from nano scale Fe-containing minerals, i.e.alpha-FeOOH, beyond the surface area effects that can be attributed to the presence of more reactive sites on specific crystal planes exposed. We further report with clear evidence that aggregation impacts on dissolution. Proton-promoted dissolution of nanorods is nearly or completely quenched in the aggregated state. Acid type, presence of oxyanions and light are several other key factors responsible for regulating for iron dissolution. The work reported in this thesis provides insight into the heterogeneous chemistry and photochemistry of mineral dust aerosol under different atmospherically relevant conditions.

Understanding the size dependent dissolution of engineered nanoparticles is one important aspect in addressing the potential environmental and health impacts of these materials as well as their long-term stability. In this study, experimental measurements of size dependent dissolution of well-characterized zinc oxide (ZnO) nanoparticles with particle diameters in the range of 4 to 130 nm have been measured and compared at circumneutral pH (pH 7.5). Enhanced dissolution was found for the smaller particles with the largest enhancement observed in Zn2+(aq) concentrations for 4 nm diameter ZnO nanoparticles compared to larger-sized particles. Interestingly, size dependent dissolution was observed even though the nanoparticles aggregated with hydrodynamic diameters on the order of 1-3 m in diameter. Although these results are found to be in qualitative agreement with theoretical predictions used to predict the dissolution of solids, a linearized form of the Kelvin equation to calculate a bulk dissolution value for ZnO and a surface free energy yielded quantities inconsistent with known literature values. It is therefore concluded that deviations from solubility behavior from classical thermodynamics are due to a lack of the detailed knowledge of the surface free energy as well as its dependence on the details of the surface structure, surface properties, including the presence of different surface crystal facets and adsorbed ligands, as well of aggregation state. The presence of citric acid significantly enhances the extent of ZnO dissolution for all sizes such that no significant differences were observed for total Zn2+(aq) concentrations for nanoparticles between 4 to 130 nm. This can be attributed to ligand enhanced dissolution of ZnO nanoparticles where there is no dependence on size. Adsorption of citrates onto ZnO nanoparticles was observed using ATR-FTIR spectroscopy. A reversal of surface charge of ZnO nanoparticles was observed upon adsorption of citrates. Adsorption of negatively charged Cit3- onto ZnO nanoparticles make the surfaces negatively charged and this result in a repulsion between nanoparticles eventually leading to a lesser extent of aggregation. Formation of a stable suspension was also observed in the presence of citric acid. These trends observed in aggregation pattern are of great environmental and biological importance as citric acid is abandon in the environment as well as in human body.

<p>As amorphous solid dispersions (ASDs) are more widely employed as a formulation strategy for poorly water-soluble drugs, there is a pressing need to increase the drug loading in these formulations. The drug loading is typically kept low to obtain the desired drug release rate, but often results in large or even multiple dosage units, which is undesirable from a patient compliance perspective. We have identified the cause of this conundrum to be the drug loading dependent dissolution mechanism of ASDs. At low drug loadings, the dissolution rate of ASDs is polymer-controlled, while at high drug loadings, the dissolution rate is drug-controlled and considerably slower. This phenomenon is most pronounced for ASDs with hydrophilic polymers, such as poly (vinylpyrrolidone-co-vinyl acetate) (PVPVA) and the change in dissolution mechanism from being polymer-controlled to drug-controlled has been attributed to water-induced amorphous-amorphous phase separation (AAPS) in higher drug loading ASD matrices of hydrophilic polymers. The drug loading limit for this switch has been found to be dependent on drug properties as well as drug-polymer interactions. Interestingly, drug-polymer hydrogen bonding interaction has been found to be detrimental and decrease the drug loading limit for polymer-controlled release while drug log P did not have any impact on this limit. Variable dissolution temperature studies indicated a detrimental impact on the polymer-controlled drug loading limit when the drug-rich phase (of phase separated ASD matrix) exists in a glassy state. ASDs with relatively hydrophobic polymers, such as hypromellose acetate succinate (HPMCAS), have been found to be polymer-controlled up to higher drug loadings. The mechanistic understanding obtained in this body of work can thus be adopted to develop strategies enabling ASD formulations with optimized performance and improved drug loading.</p>