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The chemical reactivity of a solid is influenced to a marked degree by the presence of imperfections or defects in the solid. Bond strengths are considerably weaker at points of imperfection than elsewhere in the solid, and hence the initiation of reaction is favoured at these sites due to the relative ease of bond rupture. Line defects, such as edge or screw dislocations, jogs, Smekul cracks etc, are of prime importance in such changes. The surface of a solid or in intergranular boundaries, where a state of strain exists, are also favourable places for the initiation of a reaction, Point defects e.g. vacancies or interstitialions or atoms also play important roles in chemical change, often in conjuction with line defects.

The effects of 1 min 4 hr exposures to mercuric chloride (HgCl2), methyl mercuric chloride (CH3HgCl), p-chloromercuribenzoate (p-CMB) and ethylmercurithiosalicylate (TMS) on cell viability and kinetics of cell death, microtubules, F-actin, CD3 receptor expression, protein tyrosine phosphorylation (PTyr-P), intracellular calcium [Ca2+]i and responses to polarized signals in YAC-1 lymphoma cells were investigated. We hypothesized that immunotoxic effects of HgCl2 (Hg2+) are initiated by global receptor triggering, accompanied by increased protein tyrosine phosphorylation (PTyr-P) and down-regulation of the T-cell receptor (TCR). As a polychloride anion with poor lipid solubility, inorganic Hg2+ may produce effects at the outer cell membrane before significant intracellular accumulation, loss of microtubule integrity (a sensitive target) and activation of cell death through apoptotic pathways. The organomercurial compound p-CMB is likewise thought to penetrate membranes slowly as a result of ionization. In contrast, the highly lipid-soluble organomercurial compounds CH3HgCl and TMS were expected to reduce responses to polarized stimuli only in conjunction with and not prior to loss of microtubule integrity and the onset of necrotic cell death. <p>Two general patterns of effects were observed. In HgCl2-treated YAC-1 cells, inhibition of responses to polarized stimuli preceded loss of microtubules and onset of cell death. Effects on polarized stimuli were preceded by a transient Ca2+ signal; however, this Ca2+ signal appeared abortive, accompanied by a paradoxic decrease in PTyr-P and partial down-regulation of CD3 receptors. Responses to polarised stimuli were inhibited prior to extensive loss of microtubule staining, indicating effects preceded cytosolic Hg2+ accumulation. HgCl2 exposure was followed rapidly by necrotic cell death. <p>Similarly, p-CMB-treated YAC-1 cells failed to respond to polarized stimuli before effects on microtubules or loss of viability, and proceeded rapidly to late apoptosis; however, a transient Ca2+ signal and progressive loss of F-actin preceded effects in all other assays and may account for loss of polarized responses. <p>In CH3HgCl- and TMS-treated YAC-1 cells, CD3 receptor expression, [Ca2+] and PTyr-P were increased immediately, along with loss of microtubules. These reductions preceded inhibition of polarized signaling responses and seemed to indicate a general loss of cellular homeostasis not seen in HgCl2- and p-CMB-treated cells; loss of homeostasis did not necessarily produce simultaneous loss of viability, as TMS-treated cells remained viable for 30 min while CH3HgCl-treated cells became apoptotic within 1 min. Nonetheless, the YAC-1 cells proceeded to cell death more slowly, remaining early apoptotic after 4 hr, when almost all HgCl2- and p-CMB-treated cells were necrotic. These findings indicate the two groups of mercury compounds may alter responses to polarized stimuli and induce cell death by distinct pathways, one involving an apparently abortive signal and the other mediated by much more profound disruption of cellular homeostasis. Within the larger patterns there are further differences between the effects produced by each Hg compound, likely reflecting the combined influence of pharmacokinetic and dynamic factors governing access to and interactions with different cellular targets leading to cell death. These distinct targets may in turn be reflected in the different immune effects produced by these compounds <i>in vivo</i>.

The effects of 1 min 4 hr exposures to mercuric chloride (HgCl2), methyl mercuric chloride (CH3HgCl), p-chloromercuribenzoate (p-CMB) and ethylmercurithiosalicylate (TMS) on cell viability and kinetics of cell death, microtubules, F-actin, CD3 receptor expression, protein tyrosine phosphorylation (PTyr-P), intracellular calcium [Ca2+]i and responses to polarized signals in YAC-1 lymphoma cells were investigated. We hypothesized that immunotoxic effects of HgCl2 (Hg2+) are initiated by global receptor triggering, accompanied by increased protein tyrosine phosphorylation (PTyr-P) and down-regulation of the T-cell receptor (TCR). As a polychloride anion with poor lipid solubility, inorganic Hg2+ may produce effects at the outer cell membrane before significant intracellular accumulation, loss of microtubule integrity (a sensitive target) and activation of cell death through apoptotic pathways. The organomercurial compound p-CMB is likewise thought to penetrate membranes slowly as a result of ionization. In contrast, the highly lipid-soluble organomercurial compounds CH3HgCl and TMS were expected to reduce responses to polarized stimuli only in conjunction with and not prior to loss of microtubule integrity and the onset of necrotic cell death. <p>Two general patterns of effects were observed. In HgCl2-treated YAC-1 cells, inhibition of responses to polarized stimuli preceded loss of microtubules and onset of cell death. Effects on polarized stimuli were preceded by a transient Ca2+ signal; however, this Ca2+ signal appeared abortive, accompanied by a paradoxic decrease in PTyr-P and partial down-regulation of CD3 receptors. Responses to polarised stimuli were inhibited prior to extensive loss of microtubule staining, indicating effects preceded cytosolic Hg2+ accumulation. HgCl2 exposure was followed rapidly by necrotic cell death. <p>Similarly, p-CMB-treated YAC-1 cells failed to respond to polarized stimuli before effects on microtubules or loss of viability, and proceeded rapidly to late apoptosis; however, a transient Ca2+ signal and progressive loss of F-actin preceded effects in all other assays and may account for loss of polarized responses. <p>In CH3HgCl- and TMS-treated YAC-1 cells, CD3 receptor expression, [Ca2+] and PTyr-P were increased immediately, along with loss of microtubules. These reductions preceded inhibition of polarized signaling responses and seemed to indicate a general loss of cellular homeostasis not seen in HgCl2- and p-CMB-treated cells; loss of homeostasis did not necessarily produce simultaneous loss of viability, as TMS-treated cells remained viable for 30 min while CH3HgCl-treated cells became apoptotic within 1 min. Nonetheless, the YAC-1 cells proceeded to cell death more slowly, remaining early apoptotic after 4 hr, when almost all HgCl2- and p-CMB-treated cells were necrotic. These findings indicate the two groups of mercury compounds may alter responses to polarized stimuli and induce cell death by distinct pathways, one involving an apparently abortive signal and the other mediated by much more profound disruption of cellular homeostasis. Within the larger patterns there are further differences between the effects produced by each Hg compound, likely reflecting the combined influence of pharmacokinetic and dynamic factors governing access to and interactions with different cellular targets leading to cell death. These distinct targets may in turn be reflected in the different immune effects produced by these compounds <i>in vivo</i>.

Doctor of Philosophy / Department of Mechanical and Nuclear Engineering / Douglas McGregor / The effect of polyethylene addition on the growth of mercuric iodide (HgI[supscript]2) tetragonal prismatic crystals is examined. Three types of polyethylene powder are utilized: low molecular weight (¯Mw ~ 4 x 103), ultra high molecular weight (¯Mw ~ 3 x 6 106), and spectrophotometric grade polyethylenes. Among these types of polyethylene, the low molecular weight polyethylene produces the most significant change in HgI[supscript]2 morphology, with {110} being the most prominent crystal faces. Thermal desorption - gas chromatography/mass spectroscopy (TD-GC/MS) studies show that thermal desorption of the low molecular weight polyethylene at 100°C and 150°C produce isomers of alkynes, odd nalkanes, and methyl (even-n) alkyl ketones. HgI[supscript]2 growth runs with n-alkanes, with either neicosane, n-tetracosane, or n-hexatriacontane, cannot replicate the crystal shapes produced during growth with the low molecular weight polyethylene, whereas HgI[supscript]2 growth runs with ketones, with either 3-hexadecanone or 14-heptacosanone, produce HgI[supscript]2 tetragonal prismatic crystals, similar to the crystals grown with the low molecular weight polyethylene. C-O double bond contained in any ketone is a polar bond and this polar bond may be attracted to the mercury atoms on the top-most layer of the {110} faces through dipoledipole interaction. As a result, the growth of the {110} faces is impeded, with the crystals elongated in the [001] direction and bounded by the {001} faces along with large, prismatic {110} faces.

Os compostos semicondutores com alto número atômico e energia de banda proibida larga vêm sendo pesquisados como detectores de radiação X e gama, com alta resolução energética, operando à temperatura ambiente. O denominador comum dos materiais semicondutores, que operam à temperatura ambiente, é a dificuldade em crescer cristais com pureza química elevada e boa estequiometria. O desenvolvimento deste tipo de detectores semicondutores de radiação é ainda um desafio tecnológico e tem deparado com muitos fatores limitantes, tais como: material de partida com qualidade compatível para o uso no crescimento de cristal, baixa estabilidade do detector ao longo do tempo, oxidação superficial e outras dificuldades relatadas na literatura, que limitam o seu uso. Neste trabalho, estabeleceu-se a metodologia de transporte físico de vapor (PVT) para a purificação e crescimento do cristal semicondutor de Iodeto de Mercúrio (HgI2). Cristais de HgI2 com orientação cristalina, estequiometria e morfologia da superfície adequadas foram obtidos por essa técnica. Uma redução nítida de impurezas após a purificação pode ser observada e o nível de impureza presente nos cristais não interferiu nas suas estruturas cristalinas. Uma boa morfologia com uniformidade nas camadas da superfície foi encontrada nos cristais, indicando uma boa orientação na estrutura cristalina. Um estudo inédito foi realizado no Laboratório da University of Freiburg, sob a coordenação do Prof. Michael Fiederle, com o intuito de aumentar a estabilidade do detector de HgI2 ao longo do tempo. A aplicação de diferentes tipos de resina polimérica para encapsulamento dos detectores HgI2 foi realizada e estudada, no intuito de proteger o cristal de HgI2 das reações com os gases atmosféricos e isolar eletricamente a superfície dos cristais. Quatro resinas poliméricas foram analisadas, cujas composições são: Resina n 1: 50% - 100% de heptano, 10% - 25% metilcicloexano, <1% de ciclo-hexano; Resina n2: 25% - 50% de etanol, 25% - 50% de acetona, <2,5% de acetato de etilo; Resina n3: 50% - 100% de acetato de metilo, 5% - 10% de n-butilo e Resina 4: 50% - 100% de etil-2- cianoacrilato. A influência dos tipos de resina polimérica utilizada na espectroscopia de desempenho do detector semicondutor HgI2 é, claramente, demonstrada. O melhor resultado foi encontrado para o detector encapsulado com resina n3. Um aumento de até 26 vezes no tempo de estabilidade, como detector de radiação, foi observado para os detectores encapsulados com resina em comparação com o detector não encapsulado, exposto à atmosfera. / The semiconductor compounds with high atomic number and wide band gap energy have been investigated as X and gamma range radiation detectors, with high energy resolution, operating at room temperature. The common denominator of semiconductor materials, which operate at room temperature, is the difficulty to grow crystals with high chemical purity and good stoichiometry. The development of this type of radiation semiconductor detectors is still a technological challenge and it has faced many limiting factors, such as: starting material quality compatible for use in crystal growth, low stability of the detector over the time, surface oxidation and other difficulties reported in the literature, which limit their use. In this work, the Physical vapor transport (PVT) methodology for purification and growth of the Iodide Mercury (HgI2) semiconductor crystals was established. HgI2 crystals with crystalline orientation and suitable surface stoichiometry and morphology were obtained by this technique. A significant reduction of impurities after purification could be observed and the impurity levels present in crystals did not interfere in their crystal structures. A good morphology with uniformity in the surface layers of the crystals was found, indicating a good orientation in the crystal structure. A novel study was conducted at the Laboratory of the University of Freiburg, under the guidance of Prof. Michael Fiederle, in order to increase the stability of the HgI2 detector over the time. The application of different types of polymer resins for encapsulation of HgI2 detectors was carried out and studied, in order to protect the HgI2 crystal of reactions with the atmospheric gases and to isolate, electrically, the surface of these crystals. Four types of polymeric resins were evaluated, and each composition is : (a) Resin n1: 50% - 100% heptane 10% - 25% methyl cyclohexane, <1% cyclohexane; (b) Resin n2: 25% - 50% ethanol, 25% - 50% acetone <2.5% ethyl acetate; (c) Resin n3: 50% - 100% methyl acetate, 5% - 10% n-butyl and (d) Resin n 4: 50% - 100% ethyl-2- cyanoacrylate. The influence of the different types of polymer resins composition, used in the HgI2 detector encapsulation, is clearly demonstrated by the results of the gamma ray spectroscopy. The best results were found for the detector encapsulated with resin n3. An increase of up to 26 times in the stability period was observed for the detectors encapsulated with resin, compared to those which were not encapsulated and, therefore, had been exposed to the atmosphere.

O iodeto de mercúrio vermelho (?-HgI2 ou comumente conhecido na literatura como HgI2) vem sendo largamente estudado para utilização em detectores de radiação -X e -? por apresentar alta faixa de energia proibida (gap de energia = 2,13eV), alto número atômico (ZHg = 80; ZI = 53) e alta densidade (6,4 mg/ml), além de outras propriedades que auxiliam na absorção destes tipos de radiação. A obtenção de filmes e cristais usando uma técnica de baixo custo é abordada neste trabalho. A técnica que obtenção de cristais utilizada foi a evaporação de solvente, que consiste na evaporação de um solvente volátil de uma solução preparada com sal de HgI2. Os solventes voláteis utilizados foram etanol, tetrahidrofurano (THF) e algumas misturas de ambos. Duas principais condições de evaporação foram testadas: na presença de luz ambiente (claro) e na ausência desta (escuro) em temperatura ambiente. Somente para o etanol obteve-se cristais com controle de temperatura (temperatura de 40°C) dentro de estufa no escuro. Observou-se, como resultado geral, que os cristais apresentam um aumento da desorganização estrutural quando se adiciona THF. Como esperado, isso se refletiu nas propriedades elétricas, diminuindo a resistividade (?) e energia de ativação (Ea) destes materiais. Além disso, é observado para os cristais obtidos com etanol (claro, escuro e estufa a 40°) diferentes resultados estruturais, ópticos, elétricos e de fotocondutividade. Em relação aos resultados estruturais, as condições influenciaram três orientações distintas que se acredita ser devido a variações energéticas relacionadas a temperatura e excitação eletrônica promovida pela luz. Anisotropia também foi observada pela análise dos resultados do espalhamento Raman. Medidas ópticas destacaram a presença principal de contribuições referentes a transições de elétrons da banda de valência a banda de condução (transição excitônica). Os cristais obtidos no claro e estufa apresentam ainda contribuições de transições de elétrons relacionadas a desorganização estrutural e ligações pendentes. Quanto as medidas elétricas, observou-se que o cristal obtido no escuro com etanol (E100E) apresentou os maiores valores de ? e Ea (2,67x108 ? .cm e 1,13 eV) e resultados de fotocondutividade mostraram baixos valores da relação fotocorrente corrente de escuro. Os filmes híbridos de iodeto de mercúrio foram obtidos usando a mesma técnica com presença de polímeros isolantes que atuaram como matriz de sustentação dos cristais de HgI2. Os polímeros utilizados foram poliamida (PA), policarbonato (PC) e poliestireno (PS). Estes eram dissolvidos em THF e o sal de HgI2 era acrescido a esta solução. Filmes foram confeccionados variando a temperatura de evaporação do THF para todos os polímeros, e para PS (que apresenta maior resistência a radiação na faixa de radiodiagnóstico) foi realizado estudos de variação da concentração de polímero (de 20 a 200mg/ml) e da massa de iodeto de mercúrio (de 0,6 a 2,0g). Com o acréscimo dos polímeros isolantes nos filmes, nota-se que se tem um aumento de ?, ainda maior que o observado para os cristais. Também a relação entre fotocondutividade e corrente de escuro é aumentada. No entanto, não se observa uma formação homogênea no filme quando analisamos morfologicamente, sendo possível ver cristais dispersos. Por fim, estes filmes apresentaram um gap de energia de 2,1 eV, muito próximo do obtido para cristais HgI2 (2,13 eV) / Red mercuric iodide (?-HgI2 or known in literature as HgI2) has been widely studied for X- and ?- radiation detector applications because of the high gap energy (2.13 eV), high atomic number (ZHg = 80, ZI = 53), high density (6.4 mg/ml) and other properties that raise the absorption of these types of radiation. Films and crystals were obtained using a low-cost technique that is discussed in this work. The technique used was solvent evaporation, which is the evaporation of volatile solvent from solution prepared with HgI2 salt. The solvents were ethanol, tetrahydrofuran (THF) and some mixtures of both. Two main evaporation conditions were experimented: in (Light) or without (Dark) ambient light presence at room temperature. Only ethanol was obtained crystals with temperature control (constant temperature of 40o in dark oven. It was observed, as general result, that the crystals show an increase of structural disorder when it was added THF for initial solution. This reflects in electrical properties, decreasing resistivity (?) and activation energy (Ea) from this material. Furthermore, it is observed for ethanol crystals (Light, Dark, and Oven at 40o) different structural, optical, electrical and photoconductivity results. In relation to structure, the conditions influenced three distinct orientations that it is energetic variations related to temperature and light excitation. Anisotropy was also observed by Raman scattering analysis. Optical measurements present main contributions of electron transitions from valence to conduction band (excitonic transitions). The Light and Oven crystals show contributions related to structural disorder and dangling bounds. Electrical studies highlighted higher values of ? and Ea (2.67x10-8 ?.cm e 1.13 eV), and photoconductive curves has lower photocurrent-dark current relation. HgI2 hybrid films were obtained using the same technique (solvent evaporation) with insulator polymers forming a matrix to sustain the crystals. The polymers were polyamide (PA), polycarbonate (PC) and polystyrene (PS). These were dissolved in THF and HgI2 salt was added to this solution. Films were made varying the evaporation temperature, and for PS (whose shows the best resistance for diagnostic radiation) was varying polymer concentration (from 20 to 200mg/ml) and HgI2 mass (from 0.6 to 2.0). It was observed an increase of ? adding the polymers in relation of crystals. The photocurrent-dark current relation is also higher than crystals. However, it was not seen homogeneous surface, where it was seen dispersed crystals by SEM images. Finally, the films show energy gap of 2.1 eV, very close to single crystal of literature.

O perfil de concentração do soluto próximo à interface cristal/liquido foi estudado durante o processo de crescimento e dissolução de cristais de iodeto de mercúrio (\'ALFA\'-Hg\'I IND.2\') com a técnica óptica medida de fase par difração, denominada de \"diffrasor\". A técnica é simples, sensível a fenômenos hidrodinâmicos e pode ser usada tanto em macro com em micro-observações. Com essa técnica medimos, pela primeira vez, o perfil de concentração do soluto até 10 \'mu\'m da superfície do cristal. Os resultados mostram que o crescimento do \'ALFA\'-Hg\'I IND.2\' é fortemente afetado pela supersaturação da solução, a qualidade da superfície cristalina, a convecção da solução, a história do processo de crescimento e o número de faces vinculadas. A difusão do soluto e o fluxo interfacial são considerados os responsáveis pelo transporte de massa durante o processo de crescimento da face (001) do \'ALFA\'-Hg\'I IND.2\'. Uma anomalia no perfil de concentração próximo da interface foi detectada, pela primeira vez, durante a dissolução de um cristal de iodeto de mercúrio. Nós acreditamos QUe essa anomalia está diretamente associada aos fluxos de soluto. / The solute concentration profile near to the crystal/liquid inter-face was studied during mercuric iodide crystal growth and dissolution with phase measurement by diffraction optical technique - \"diffrasor\". It\'s simple, sensitive to hydrodynamics phenomena and may be used either in macro or in micro-observations. With this technique we measured, for the first time, the solute concentration profile up to 10 um from the a-Hg12 crystal surface- The state of the art results the us first that \'ALFA\'-Hg\'I IND.2\' is strongly affected by supersaturation, convenction in the solution, history of the growth process, surface quality and of the tied facets numbers- The solute diffusion and interfacial flow are considered responsible by mass transport during crystal growth. A anomaly in the concentration profile near interface was detected, for the first time, during the mercuric iodide crystal dissolution- We believe that this anomaly is directly associated with the solute flux during dissolution process.

Os compostos semicondutores com alto número atômico e energia de banda proibida larga vêm sendo pesquisados como detectores de radiação X e gama, com alta resolução energética, operando à temperatura ambiente. O denominador comum dos materiais semicondutores, que operam à temperatura ambiente, é a dificuldade em crescer cristais com pureza química elevada e boa estequiometria. O desenvolvimento deste tipo de detectores semicondutores de radiação é ainda um desafio tecnológico e tem deparado com muitos fatores limitantes, tais como: material de partida com qualidade compatível para o uso no crescimento de cristal, baixa estabilidade do detector ao longo do tempo, oxidação superficial e outras dificuldades relatadas na literatura, que limitam o seu uso. Neste trabalho, estabeleceu-se a metodologia de transporte físico de vapor (PVT) para a purificação e crescimento do cristal semicondutor de Iodeto de Mercúrio (HgI2). Cristais de HgI2 com orientação cristalina, estequiometria e morfologia da superfície adequadas foram obtidos por essa técnica. Uma redução nítida de impurezas após a purificação pode ser observada e o nível de impureza presente nos cristais não interferiu nas suas estruturas cristalinas. Uma boa morfologia com uniformidade nas camadas da superfície foi encontrada nos cristais, indicando uma boa orientação na estrutura cristalina. Um estudo inédito foi realizado no Laboratório da University of Freiburg, sob a coordenação do Prof. Michael Fiederle, com o intuito de aumentar a estabilidade do detector de HgI2 ao longo do tempo. A aplicação de diferentes tipos de resina polimérica para encapsulamento dos detectores HgI2 foi realizada e estudada, no intuito de proteger o cristal de HgI2 das reações com os gases atmosféricos e isolar eletricamente a superfície dos cristais. Quatro resinas poliméricas foram analisadas, cujas composições são: Resina n 1: 50% - 100% de heptano, 10% - 25% metilcicloexano, <1% de ciclo-hexano; Resina n2: 25% - 50% de etanol, 25% - 50% de acetona, <2,5% de acetato de etilo; Resina n3: 50% - 100% de acetato de metilo, 5% - 10% de n-butilo e Resina 4: 50% - 100% de etil-2- cianoacrilato. A influência dos tipos de resina polimérica utilizada na espectroscopia de desempenho do detector semicondutor HgI2 é, claramente, demonstrada. O melhor resultado foi encontrado para o detector encapsulado com resina n3. Um aumento de até 26 vezes no tempo de estabilidade, como detector de radiação, foi observado para os detectores encapsulados com resina em comparação com o detector não encapsulado, exposto à atmosfera. / The semiconductor compounds with high atomic number and wide band gap energy have been investigated as X and gamma range radiation detectors, with high energy resolution, operating at room temperature. The common denominator of semiconductor materials, which operate at room temperature, is the difficulty to grow crystals with high chemical purity and good stoichiometry. The development of this type of radiation semiconductor detectors is still a technological challenge and it has faced many limiting factors, such as: starting material quality compatible for use in crystal growth, low stability of the detector over the time, surface oxidation and other difficulties reported in the literature, which limit their use. In this work, the Physical vapor transport (PVT) methodology for purification and growth of the Iodide Mercury (HgI2) semiconductor crystals was established. HgI2 crystals with crystalline orientation and suitable surface stoichiometry and morphology were obtained by this technique. A significant reduction of impurities after purification could be observed and the impurity levels present in crystals did not interfere in their crystal structures. A good morphology with uniformity in the surface layers of the crystals was found, indicating a good orientation in the crystal structure. A novel study was conducted at the Laboratory of the University of Freiburg, under the guidance of Prof. Michael Fiederle, in order to increase the stability of the HgI2 detector over the time. The application of different types of polymer resins for encapsulation of HgI2 detectors was carried out and studied, in order to protect the HgI2 crystal of reactions with the atmospheric gases and to isolate, electrically, the surface of these crystals. Four types of polymeric resins were evaluated, and each composition is : (a) Resin n1: 50% - 100% heptane 10% - 25% methyl cyclohexane, <1% cyclohexane; (b) Resin n2: 25% - 50% ethanol, 25% - 50% acetone <2.5% ethyl acetate; (c) Resin n3: 50% - 100% methyl acetate, 5% - 10% n-butyl and (d) Resin n 4: 50% - 100% ethyl-2- cyanoacrylate. The influence of the different types of polymer resins composition, used in the HgI2 detector encapsulation, is clearly demonstrated by the results of the gamma ray spectroscopy. The best results were found for the detector encapsulated with resin n3. An increase of up to 26 times in the stability period was observed for the detectors encapsulated with resin, compared to those which were not encapsulated and, therefore, had been exposed to the atmosphere.

O iodeto de mercúrio(HgI2) vem sendo largamente estudado com o objetivo de utilizá-lo em detectores de radiação –X e –&#947;. Este material semicondutor apresenta propriedades interessantes que o tornam um grande candidato a esta aplicação em relação a outros materiais. Suas propriedades são gap óptico largo (2,13 eV), alto numero atômico (ZHg = 80; ZI = 53) e alto coeficiente de absorção para comprimentos de onda da ordem de energia do raios-X e -&#947;. Este, também, pode apresentar três fases quando sólido: fase vermelha (ou &#945;-HgI2), fase amarela (ou &#946;-HgI2) e fase laranja. Cada uma destas fases é associada com diferentes estruturas cristalinas. O &#945;-HgI2 é tetragonal, o HgI2 laranja é também tetragonal,diferindo da fase vermelha somente na posição dos átomos de mercúrio, e &#946;-HgI2 é ortorrômbico. Neste trabalho, estes materiais foram obtidos por duas técnicas: spray pyrolysis e evaporação de solvente. Nas duas técnicas os mais importantes parâmetros para a obtenção das diferentes estruturas são a temperatura e a taxa de evaporação do solvente. Através do método de spray pyrolysis foi possível obter filmes finos de HgI2 com duas estruturas diferentes, somente variando a temperatura do aquecedor de substratos e o solvente. Acima da temperatura de 100ºC com o solvente água foi possível obter filmes amarelados de HgI2. Por sua vez, a temperatura abaixo de 100ºC com o solvente etanol foi possível obter filmes avermelhados. Com a técnica de evaporação de solvente foi possível obter cristais e filmes laterais variando somente a taxa de evaporação de solvente. Variaram-se as taxas de evaporação entre rápida(~10ml/h), média(~0,5ml/h), lenta(~0,1ml/h) e super-lenta(~0,01ml/h). Para a taxa de evaporação média e lenta foram obtidos filmes laterais. Já para a taxa super-lenta foi possível obter cristais. Outro ponto estudado foi a influência da luz no crescimento dos cristais: no escuro obteve-se cristais maiores que os submetidos a luz ambiente. Todos os filmes foram caracterizados por difração de raios-X, microscopia eletrônica de varredura (MEV), e espectroscopia de dispersão de energia (EDS). Já os cristais foram caracterizados por difração de raios-X, MEV e espalhamento Raman. / Recently, attention has been devoted to the study of mercuric iodide (HgI2) because this material is a strong candidate for the development of X- and &#947; -ray detectors. This material has an optical gap of 2.13 eV, high atomic number (ZHg = 80; ZI = 53) and high absorption coefficient for radiation in the wavelength region of X- and &#947; –rays. When solid, three phases can be obtained: red (or &#945;-HgI2), yellow (or &#946;-HgI2) and orange. Each of these phases has a different crystalline structure: &#945;-HgI2 is tetragonal, as it is the orange- HgI 2 (the difference is that for the last one the mercury atoms sits in different positions), while the &#946;-HgI2 is orthorhombic. In this work we obtained these materials using two different techniques: spray pyrolysis and solvent evaporation. For both of them the most important parameters are the deposition temperature and solvent evaporation rate. Thin films with two different structures were obtained by spray pyrolysis varying the substrate temperature and the solvent. Using water as solvent and deposition temperature above 100ºC we obtained yellow HgI2. When the temperature is reduced below that value and the solvent is ethanol, red films were obtained. For the solvent evaporation technique, lateral films and millimeter-sized crystals were obtained by varying the solvent evaporation rate. For ethanol as solvent we used four evaporation rates named as fast(~10ml/h), medium (~0.5ml/h), slow (~0.1ml/h) and super-slow (~0.01ml/h). For the medium and slow evaporation rates lateral films were obtained on the wall of the reservoir. For the super-slow evaporation rate crystals were obtained at the bottom of the reservoir. We observed that light has a tremendous influence on crystal growth: bigger crystals are obtained in the dark than under ambient light illumination. As characterization techniques we used: X-rays diffraction, Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), and Raman Scattering.