A espectrometria de absorção atômica (AAS) é consolidada como uma técnica robusta, cujas aplicações estendem-se a diversos analitos e matrizes. Sua limitação encontra-se na região do UV distante (~ 190 nm), por isso ela permaneceu exclusiva à determinação de metais durante vários anos: não-metais geralmente absorvem na região de UV de vácuo. Com o advento da AAS de alta resolução com fonte contínua, houve a implementação de uma terceira dimensão (comprimento de onda) nas análises: a visualização da região espectral da linha analítica. Esta nova característica permitiu um maior número de informações espectrais, principalmente em relação às bandas estruturadas de moléculas diatômicas, o que resultou na determinação de absorção molecular (HR CS MAS). Destarte, o objetivo deste trabalho foi a elaboração de novos procedimentos analíticos para determinação de não-metais por HR CS MAS, especificadamente Br, Cl e S, com atomizador de forno de grafite. O bromo foi avaliado via CaBr em componentes plásticos de amostras eletrônicas, extraído por extração Soxhlet com tolueno, e obteve limites de detecção (LD) e quantificação (LQ) de 4,3 e 14 ng de Br, respectivamente, com Pd como modificador químico. Duas matrizes foram estudadas para a quantificação de enxofre via CS: carvão e diesel. O carvão foi injetado em HR CS MAS como uma suspensão com Triton X-100 0,04 % m v-1, e (NH4)2SO4 foi empregado como padrão de enxofre. Os LD e LQ obtidos para o método foram 0,01 e 0,05 % m m-1, respectivamente. Para o diesel, dois métodos foram estudados: (i) emulsão alcoólica com etanol 50 % v v-1, a qual apresentou LD de 0,12 g kg-1 e LQ de 0,40 g kg-1, adequados para determinação de altos teores de S em diesel; e (ii) injeção direta de diesel no sistema de HR CS MAS, cujos LD e LQ foram 3 e 9 mg kg-1, respectivamente. Ambos empregaram nanopartículas de Pd como modificador químico, das quais a análise direta de diesel obteve melhores resultados. Finalmente, um novo conceito foi investigado em HR CS MAS: o deslocamento isotópico em moléculas diatômicas. Os estados vibracionais e rotacionais presentes na transição eletrônica observada em HR CS MAS confere esta propriedade. As moléculas de AlCl e CaBr, cujos isótopos de interesse foram 35Cl e 37Cl, e 79Br e 81Br, respectivamente, foram estudadas. Os deslocamentos isotópicos observados foram de 15,6 pm para AlCl e 41,6 pm para CaBr nos comprimentos de onda selecionados, suficientes para implementação de calibração por diluição isotópica, a qual apresentou LDs de 2,5 e 64 ng, respectivamente. Amostras de água natural e mineral foram empregadas para o Cl, enquanto o Br foi determinado em amostras de PVC e folhas de tomate, as quais foram introduzidas diretamente como sólidos. A diluição isotópica corrigiu adequadamente as interferências espectrais acarretadas pelas matrizes de ambos os analitos. / Atomic Absorption Spectrometry (AAS) is a robust analytical technique whose applications extend to many different analytes and matrices. Its limitation lies on the far UV region (~ 190 nm) and therefore it remained exclusive for metal determination as non-metals typically absorb within the vacuum-UV region. With the invention of the High-Resolution Continuum Source AAS (HR CS AAS), the AAS analysis has been upgraded and a new dimension (wavelength) was added: the visualization of the analytical lines vicinity. This new feature allowed improved spectral information, mainly related to the structured bands of diatomic molecules, giving rise to the HR CS Molecular Absorption Spectrometry (MAS). The goal of this thesis was the evaluation of new analytical procedures for non-metals determination by HR CS MAS, specifically Br, Cl, and S, using graphite furnace as the atomizer. Bromine in plastic electronic components was evaluated as CaBr after Soxhlet extraction with toluene. This method had limits of detection (LD) and quantification (LQ) of 4.3 and 14 -ng, respectively, using Pd as chemical modifier. Sulfur determination via CS molecule employed two distinct matrices: coal and diesel. Coal samples were prepared as a slurry with Triton X-100 0.04% m v1 for injection in the HR CS MAS and the external calibration employed was (NH4)2SO4as sulfur standard. The method LD and LQ were 0.01% m m1 and 0.05% m m1, respectively. Two methods were studied for diesel samples: (i) alcoholic emulsion with ethanol 50% v v1, with an LD of 0.12 g kg1 and an LQ of 0.40 g kg1, suitable for sulfur high concentration determination in diesel; and (ii) direct diesel injection in the HR CS MAS system, whose LD and LQ were 3 mg kg-1and 9 mg kg-1, respectively. Both methods employed Pd nanoparticles as chemical modifier, with better results for direct diesel analysis. Ultimately, a new concept was investigated in HR CS MAS: the isotopic shift of diatomic molecules. An absorption profile consisted of multiple peaks was due to vibrational and rotational energy couplings within the electronic transition observed by HR CS MAS, which provided the isotopic shift. This effect was detected on AlCl and CaBr molecules, whose target isotopes were, respectively, 35Cl &37Cl and 79Br &81Br. The observed isotopic shifts were 15.6 pm (AlCl) and 41.6 pm (CaBr) at the selected wavelengths, appropriate for isotopic dilution calibration, which featured LDs of 2.5 ng and 64 ng, respectively. Natural and mineral water samples were evaluated for Cl determination; and Br was found in PVC and tomato leaves samples, both introduced as solid samples in HR CS GFMAS. Isotopic dilution adequately corrected the spectral interferences derived from the matrices of both analytes.

Assessment of a significant number of water samples across South Africa by Casey and Meyer over a number of years, revealed that high concentrations (30- 32 mg/L) of bromine (Br) occur naturally within groundwater in South Africa, hence a potentially hazardous chemical constituent (PHCC). Br, the only liquid non-metallic element, is ubiquitous and an abundant trace element, but it has not been conclusively shown to perform essential functions in plants, micro organisms or animals (NRC, 2005). The recommended limit (maximum limit for no risk) for Br in drinking water was set at 1 mg/L by Kempster et al. (1980); Casey and Meyer (2001) recommend the relevant safety guideline for Br to be 0.01 mg/L. The aim of this project was to establish the effect of Br and iodine (I) in drinking water on the physiological parameters of broilers. This will contribute to verifying and refining water quality guidelines. The effect of six treatments administered as sodium bromide (NaBr) and potassium iodide (KI): 0 mg Br/L and 0 mg I/L; 1 mg Br/L; 1mg Br/L and 0.7 mg I/L; 0.7 mg I/L; 3 mg Br/L; 3 mg Br/L and 0.7 mg I/L, in the drinking water of 540 mixed Ross broiler chickens was investigated. The trial ran over a 42-day growth period from Day 1 post-hatching where mortalities, water and feed intakes were recorded daily. Chickens were weighed weekly and slaughtered at 4 and 6 weeks of age. Blood samples were taken before slaughter and free T3 and T4 hormone levels were quantified. Thyroid gland, liver and kidney samples were analysed for Br and I quantity. The different treatments of Br, irrespective of I, significantly decreased water intake (P=0.0232) and feed intake (P=0.0035) over the 42 days. The overall interaction of Br and I had no significant effect on water (P=0.0928) and feed (P=0.9593) intakes thus I did have an effective ameliorating effect on Br. FCR, weight gain and mortalities were not significantly affected by Br intake. This was also found for free T3 and T4 hormone levels. Br had an overall effect on the thyroid gland (P=0.0457), liver (P=0.0025) and kidney (P=0.0032) with accumulation of the PHCC within these three organs. It was apparent that 1 and 3 mg Br/L water administered to broilers or ingestion rates of 1.59 and 4.44 mg Br/L per bird per day, over a production period of 42 days did affect the production parameters of the birds sub-clinically. Another derivation to refine the water quality guidelines was that the administration of 0.7 mg I/L water or ingestion rates of 1.1 mg I/L per bird per day did alleviate the severe detrimental effect of the high PHCC. The 3 mg Br/L guideline is thus not too restrictive. Further research exposing the animals for a longer time period (exceeding 42 days) and exposing mature animals (producing nutritional products for human consumption) to these treatments would assist in quantifying these results. / Dissertation (MSc(Agric))--University of Pretoria, 2010. / Animal and Wildlife Sciences / unrestricted

No / The Raman and electron impact mass spectra of synthetic indigo and its four 6,6'-dihalogeno analogues are reported and discussed. The influence of varying the halogen on these Raman spectra is considered. Particular emphasis is laid on distinguishing indigo from 6,6'-dibromoindigo and differentiating between the dihalogenocompounds, so as to develop protocols for determining whether artefacts are coloured with dyes of marine or terrestrial origin and whether such artefacts are dyed with genuine Tyrian Purple or with dihalogenoindigo substitutes that do not contain bromine. The value of even low resolution electron impact mass spectrometry in a forensic context as a means of identifying authentic 6,6'-dibromoindigo and distinguishing it from its dihalogenoanalogues is emphasised.

Made available in DSpace on 2014-10-09T12:42:54Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:07:52Z (GMT). No. of bitstreams: 1 05403.pdf: 3608647 bytes, checksum: 066e3f6af2ef001c7431582e2ce35791 (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / Tese (Doutoramento) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP / FAPESP:96/01220-7

Made available in DSpace on 2014-10-09T12:42:54Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:07:52Z (GMT). No. of bitstreams: 1 05403.pdf: 3608647 bytes, checksum: 066e3f6af2ef001c7431582e2ce35791 (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / Tese (Doutoramento) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP / FAPESP:96/01220-7

No description available.

Organic frameworks with rigid backbones, such as acenaphthene, are highly suitable for the study of interatomic interactions. The short “natural” peri-distance (2.44 Å) and the rigidity of the aromatic system causes considerable steric strain between peri-substituted heteroatoms. As a consequence, substitution at both peri-positions leads to in- and out-of-plane distortions, which often result in buckling of the ring system. In order to relax this geometric strain, weak bonding interactions can also exist between the peri-substituents. This thesis focuses on the synthesis, structural characterisation and investigation of a range of sterically crowded peri-substituted acenaphthene compounds. This involves the study of the acenaphthene geometry, through X-ray crystallography when different peri-substituents occupy the close 5,6-positions; our main focus is to study weak non-bonded interactions that can occur across the peri-gap, for example weakly attractive three-centre four-electron (3c-4e) type interactions which are known to prevail in such compounds under the appropriate conditions. Repulsion within these systems, resulting from the steric crowding of the peri-space is also investigated, employing changes in bond lengths, bay-region angle splay, displacement of atoms from the mean plane and central acenaphthene torsion angles to help quantify the degree of acenaphthene distortion, which are all conveniently probed by the peri-distance. To this end we have synthesised a range of novel sterically crowded mixed bromo-tin acenaphthene derivatives (Chapter 3), chalcogen-tin acenaphthene molecules (Chapter 4), phosphorus–tin derivatives (Chapter 5) and a series of homologous tin-tin acenaphthenes (Chapter 6). All the compounds studied in this thesis were characterised by multinuclear NMR spectroscopy and X-ray crystallography in an effort to gain a greater understanding of the deformation that occurs when disparate functionalities are located in close proximity and explore the potential for weak non-covalent intramolecular interactions to occur.

<div>Halogen chemistry in the Arctic boundary layer catalytically destroys O3 and impacts the chemical lifetimes of hydrocarbons, the HOx-NOx cycle, and atmospheric mercury. While many advances have been made in the last several decades in understanding the sources, sinks, and recycling pathways of halogens in the Arctic there are still many unknowns. Previous studies have shown that Br2, BrCl and Cl2 are produced photochemically in the Arctic tundra snowpack, but the magnitude of this production is still poorly understood. Additionally, while there have been suggestions that the tundra snowpack should also produce I2, there have been no previous measurements of I2 in the Arctic. The lack of measurements of the halogen production capacity of Arctic snowpacks has left the community to rely on one-dimensional modeling to estimate the impact of snowpack-derived halogen chemistry on the Arctic atmosphere. Because modeling is inherently dependent on understanding recycling mechanisms, mixing processes, and sinks this leaves the effect of halogens on atmospheric chemistry in the Arctic highly uncertain.</div><div><br></div><div>This work describes efforts to address these uncertainties through measurements made during two field campaigns in Utqiaġvik (formerly Barrow), Alaska in January – February 2014, and February – May 2016. The first measurements of I2 in the Arctic, both in the snowpack interstitial air, and in the air above the snowpack demonstrate that iodine chemistry is active in the Arctic atmosphere, and that I2 is produced photochemically in the tundra snowpack. The effects of active iodine chemistry on both O3 and bromine chemistry is examined through zero- and one dimensional modeling. The first speciated measurements of snowpack phase iodine reveal that much like previous reports of iodine enriched aerosols, the Arctic snowpack is highly enriched in iodine. Vertical profiles of I- in the snowpack suggest that there is a consistent, non-radiation dependent source of iodine to the Arctic environment. It seems likely that this source is transport of iodine-enriched aerosols from the mid-latitudes. However, unlike the Antarctic, and previous</div><div>observations in the mid-latitudes, most Arctic snowpack phase iodine is inorganic, which may contradict transport from the mid-latitudes as a source. One-dimensional modeling was also utilized, in conjunction with the first vertical profile measurements of Br2 and Cl2 between 1 and</div><div>7 m above the snowpack surface to examine the community’s understanding of recycling mechanisms, mixing, sources, and sinks of halogens in the Arctic Atmosphere.</div>

Over the last decade our understanding of mercury cycling has dramatically changed. Evidence of rapid atmospheric oxidation has been observed in the Arctic, Antarctic, the MBL, coastal environments, saline lakes, and the upper troposphere/lower stratosphere. These results show that, Hg0, can undergo rapid gas-phase oxidation under standard atmospheric conditions. However, the mechanism and importance of this transformation is still unclear. The goal of this work was two-fold: to investigate of the kinetics of potential pathway for the gas phase oxidation of atmospheric mercury and to develop new laser based techniques, which can be employed for both laboratory and field studies of Hg(0) and the products of mercury oxidation. First and foremost, this work determined kinetic rate coefficients for the potentially important mercury reactions. Rate coefficients were determined using a Pulse Laser Photolysis - Laser Induced Fluorescence (PLP-LIF) technique monitoring one or more of the following species, Hg(0), Cl, Br, HgCl, and HgBr. The concentrations of these species were measured by LIF as the reaction occurred and a concentration vs. time profile was generated. From these profiles a rate coefficient for the reaction can be obtained. In the course of this work kinetic rate coefficients for the following mercury reactions were measured. Hg(0) + Cl + M --> HgCl + M Hg(0) + Br + M --> HgBr + M HgBr + M --> Hg(0) + Br + M HgBr + Br --> products HgCl + O2 --> products This work is the first direct measurement of a kinetic rate coefficient for these reactions, and the first work which employed one photon LIF to monitor the HgCl and HgBr products. The second aspect of this work was the development of new laser based techniques to detect atmospheric mercury and its oxidation products for both laboratory and field application. In this work a LIF technique was develop to detect HgCl and HgBr. In addition, a two photon LIF technique initially developed by Bauer et al., 2002 was verified and expanded. The two photon LIF technique was used to directly monitor Hg(0) atoms in-situ, to monitor Hg(0) evolving form a gold tube, and to monitor the Hg(0) evolving from the thermal decomposition of reactive gaseous mercury collected on a KCl coated or uncoated denuder. This work represents a significant advance in the development of a viable method the detect mercury and the mercury oxidation products in the laboratory and in the field and is the first study to observe clear differences in the characteristic desorption profiles of HgO and HgX2. This work has broad implications, it enhanced our current knowledge concerning the biogeochemical cycling of mercury, broadened our understanding of the mercury chemistry in high halogen environment, and provided new techniques which can be applied in future field and laboratory studies.

Antimony trioxide (Sb203) and halogenated additives are used together in flameretarded formulations due to their synergistic retardant properties. A study has been made to determine the effects of adding different grades of Sb203 (dSD particle sizes 0.11 um, 0.52um and 1.31 um) into ABS polymer either alone or with commercial brominated materials (BTBPE, TBBA, DBDPO) and an experimental bromine grade (sDBDPO). The Sb20 3 was added at 4wt% loadings and the bromines at 20wt% loadings. The results consider the influence of the additives on processing, mechanical, morphological and flame retardant properties. All compounds were produced using a twin-screw co-rotating extruder and then an injection moulder was used to mould notched impact (falling weight testing), flexural, LOI and UL-94 flame test bars. Samples of all the compounded formulations were titrated to determine Sb20 3 and Br contents. Fracture surface, morphology, size and dispersion analysis was carried out using both SEM and TEM equipment. Osmium tetroxide (OS04) staining was used to determine relative locations of filler particles and polybutadiene phase. Additions of the different antimony trioxide grades showed that the 0.52um and 1.31 um grades lowered impact energy absorption (-25 to -30%) when added at 4wt% loading. The use of a sub-micron size grade (0.1 um) did not significantly lower impact properties (-3%) and had similarly small effects on the flexural modulus and flexural strength. Additions of the brominated materials had much greater effects causing large reductions in impact properties (-20 to :70%). The presence of the bromines generally increased flexural modulus and lowered flexural strength with the exception of TB BA, which increased both modulus and strength. Compounds containing both 1.31 um Sb203 and bromines suffered a further reduction in impact energies, with the bromine properties dominating. Using the 0.1 um Sb20 3 grade again improved impact and flexural properties compared to the 1.31 um grade. The 0.1 um grade resulted in improvements in fire resistance as measured by the UL-94 properties when used with all bromine grades.