Pt-aluminide (PtAl) coatings form an integral part of thermal barrier coating (TBC) systems that are applied on Ni-based superalloy components operating in the hot sections of gas turbine engines. These coatings serve as a bond coat between the superalloy substrate and the ceramic yttrium stabilized zirconia (YSZ) coating in the TBC system and provide oxidation resistance to the superalloy component during service at high temperatures. The PtAl coatings are formed by the diffusion aluminizing process and form an integral part of the superalloy substrate. The microstructure of the PtAl coatings is heavily graded in composition as well as phase constitution. The matrix phase of the coating is constituted of the B2-NiAl phase. Pt, in the coating, is present as a separate PtAl2 phase as well as in solid solution in B2-NiAl. The oxidation resistance of the PtAl bond coat is derived from the B2-NiAl phase. At high temperatures, Al from the B2-NiAl phase forms a regenerative layer of alumina on the coating surface which, thereby, lowers the overall oxidation rate of the superalloy substrate. The presence of Pt is beneficial in improving the adherence of the alumina scale to the surface and thereby enhancing the oxidation resistance of the coating. However, despite its excellent oxidation resistance, the B2-NiAl being an intermetallic phase, renders the PtAl coating brittle and imparts it with a high brittle-to-ductile-transition-temperature (BDTT). The PtAl coating, therefore, remains prone to cracking during service. The penetration of these cracks into the substrate is known to degrade the strain tolerance of the components. Evaluation of the mechanical behavior of these coatings, therefore, becomes important from the point of views of scientific understanding as well as application of these coatings in gas turbine engine components. Studies on the mechanical behavior of coatings have been mostly carried on coated bulk superalloy specimens. However, since the coating is brittle and the superalloy substrate more ductile when compared to the coating, the results obtained from these studies may not be representative of the coating. Therefore, it is imperative that the mechanical behavior of the coating in stand-alone condition, i.e. the free-standing coating specimen without any substrate attached to it, be evaluated for ascertaining the true mechanical response of the coating. Study of stand-alone bond coats involves complex specimen preparation techniques and challenging testing procedures. Therefore, reports on the evaluation of mechanical properties of stand-alone coatings are limited in open literature. Further, no systematic effort has so far been made to examine important aspects such as the effect of temperature and strain rate on the tensile behavior of these coatings. The deformation mechanisms associated with these bond coats have also not been reported in the literature. In light of the above, the present research study aims at evaluating the tensile behavior of free-standing PtAl coatings by the micro-tensile testing technique. The micro-tensile testing method was chosen for property evaluation because of its inherent ability to generate uniform strain in the specimen while testing, which makes the results easy to interpret. Further, since the technique offers the feasibility to test the entire graded PtAl coating in-situ, the results remain representative of the coating. Using the above testing technique, the tensile behavior of the PtAl coating has been evaluated at various temperatures and strain rates. The effect of strain rate on the BDTT of the coating has been ascertained. Further, the effect of Pt content on the tensile behavior of these coatings has also been evaluated. Attempts have been made to identify the mechanisms associated with tensile deformation and fracture in these coatings. The thesis is divided into nine chapters. Chapter 1 presents a brief introduction on the operating environment in gas turbine engines and the materials that are used in the hot sections of gas turbine engines. The degradation mechanisms taking place in the superalloy in gas turbine environments and the need for application of coatings has also been highlighted. The basic architecture of a typical thermal barrier coating (TBC) system applied on gas turbine engine components has been presented. The constituents of the TBC system, i.e. the ceramic YSZ coating, MCrAlY overlay as well as diffusion aluminide bond coats and, the various techniques adopted for the deposition of these coatings have been described in brief. Chapter 2 presents an overview of the literature relevant to this study. This chapter is divided into four sub-chapters. The formation of diffusion aluminide coatings on Ni-based superalloys has been described in the first sub-chapter. Emphasis has been laid on pack cementation process for the formation of the coatings. The fundamentals of pack aluminizing process, including the thermodynamic and kinetic aspects, have been mentioned in brief. The microstructural aspects of high activity and low activity plain aluminide and Pt-aluminide coatings have also been illustrated. The techniques applied for the mechanical testing of bond coats have been discussed in the second sub-chapter. The macro-scale testing techniques have been mentioned in brief. The small scale testing methods such as indentation, bend tests and micro-tensile testing have also been discussed in the context of evaluation of mechanical properties of bond coats. Since the matrix in the aluminide bond coats is constituted of the B2-NiAl phase, a description of the crystal structure and deformation characteristics of this phase including the flow behavior, ductility and fracture behavior has been mentioned in the third sub-chapter. In the fourth sub-chapter, reported literature on the tensile behavior and brittle-to-ductile-transition-temperature (BDTT) of diffusion aluminide bond coats has been discussed. In Chapter 3, details on experiments carried out for the formation of various coatings used in the present study and, their microstructural characterization, are provided. The method for extraction of stand-alone coating specimens and their testing is discussed. The microstructure and composition of the various coatings used in the present study are discussed in detail in Chapter 4. Unlike in case of bulk tensile testing, for which standards on the design of specimens exist, there are no standards available for the design of micro-tensile specimens. Therefore, as part of the present research work, a finite element method (FEM)-based study was carried out for ascertaining the dimensions of the specimens. The simulation studies predicted that failure of the specimens within the gage length can be ensured only when certain correlations between the dimensional parameters are satisfied. Further, the predictions from the simulation study were validated experimentally by carrying out actual testing of specimens of various dimensions. Details on the above mentioned aspects of specimen design are provided in Chapter 5. The PtAl coatings undergo brittle fracture at lower temperatures while ductile fracture occurs at higher temperatures. Further, the coatings exhibit a scatter in the yielding behavior at temperatures in the vicinity of BDTT. Therefore, the BDTT, determined as the temperature at which yielding is first observed in the stress-strain curves, may not be representative of the PtAl coatings. In Chapter 6, a method for the precise determination of BDTT of aluminide bond coats, based on the variation in the plastic strain to fracture with temperature, has been demonstrated. The BDTT determined by the above method correlated well with the variation in fracture surface features of the coating and was found representative of these coatings. In Chapter 7, the effect of temperature and strain rate on the tensile properties of a PtAl bond coat has been evaluated. The temperature and strain rate was varied between room temperature (RT)-1100°C and 10-5 s-1-10-1 s-1, respectively. The effect of strain rate on the BDTT of the PtAl bond coat has been examined. Further, the variation in fracture surface features and mechanism of fracture with temperature and strain rate are illustrated. The micro-mechanisms of deformation and fracture in the coating at different temperature regimes have also been discussed. The coating exhibited brittle-to-ductile transition with increase in temperature at all strain rates. The BDTT was strain rate sensitive and increased significantly at higher strain rates. Above BDTT, YS and UTS of the coating decreased and its ductility increased with increase in the test temperature at all strain rates. Brittle behavior occurring in the coating at temperatures below the BDTT has been attributed to the lack of operative slip systems in the B2-NiAl phase of the coating. The onset of ductility in the coating in the vicinity of BDTT has been ascribed to generation of additional slip systems caused by climb of dislocations onto high index planes. The coating exhibited two distinct mechanisms for plastic deformation as the temperature was increased from BDTT to 1100°C. For temperatures in the range BDTT to about 100°C above it, deformation was controlled by dislocations overcoming the Peierls-Nabarro barrier. Above this temperature range, non-conservative motion of jogs by jog dragging mechanism controlled the deformation. The transition temperature for change of deformation mechanism also increased with increase in strain rate. For all strain rates, fracture in the coating at test temperatures below the BDTT, occurred by initiation of cracks in the intermediate single phase B2-NiAl layer of the coating and subsequent inside-out propagation of the cracks across the coating thickness. Ductile fracture in the coating above the BDTT was associated with micro-void formation throughout the coating. The effect of Pt content on the tensile behavior of PtAl coating, evaluated at various temperatures ranging from room temperature (RT) to 1100°C and at a nominal strain rate of 10-3 s-1, is presented in Chapter 8. Irrespective of Pt content in the coating, the variation in tensile behavior of the coating with temperature remained similar. At temperatures below BDTT, the coatings exhibited linear stress-strain response (brittle behavior) while yielding (ductile behavior) was observed at temperatures above BDTT. At any given temperature, the elastic modulus decreased while the strength increased with increase in Pt content in the coating. On the other hand, the ductility of the coating remained unaffected with Pt content. The BDTT of the coating also increased with increase in Pt content in the coating. Addition of Pt did not affect the fracture mechanism in the coating. Fracture at temperatures below BDTT was caused by nucleation of cracks at the intermediate layer and their subsequent inside-out propagation. At high temperatures, fracture occurred in a ductile manner comprising void formation, void linkage and subsequent joining with cracks. The deformation sub-structure of the coating did not get affected with Pt incorporation. Short straight dislocations were observed at temperatures below BDTT, while, curved dislocations marked by jog formation were observed at temperatures above BDTT. The factors controlling fracture stress and strength in the PtAl coatings at various temperatures have also been assessed. The overall summary of the present research study and recommendations for future studies are presented in the last chapter, i.e. Chapter 9.

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<p>U disertaciji je izvršena karakterizacija mikrostrukture i mehaničkih osobina<br />nelegiranog austemperovanogi nodularnog liva (ADI materijala), kao i uticaja<br />mikrostrukture na prelaznu temperaturu u intervalu od -196 do +100&deg;C.<br />Utvrđeno je da mehaničke osobine ADI-ja zavise od morfologije ausferitne<br />mikrostrukture i količine zadržanog austenita, tj. parametara austemperovanja.<br />Na osnovu mehaničkih osobina utvrđen je i opseg procesiranja u skladu sa<br />standardima ASTM, ISO i EN. Zaključeno je da prelazna temperatura ADI<br />materijala zavisi od količine i stabilnosti zadržanog austenita. U višem<br />temperaturnom opsegu (iznad cca. -25&deg;C) dominantna je količina zadržanog<br />austenita, dok na nižim temperaturama, stabilnost. Visoka obogaćenost<br />ugljenikom, stabilnog zadržanog austenita sprečava stvaranje martenzita na<br />niskim temperaturama, a time i pojavu krtosti kod ADI-ja.</p> / <p>The object of this thesis was to characterize microstructure and mechanical properties<br />of the unalloyed ADI material (Austempered Ductile Iron). In addition, the influence of<br />microstructure on the ductile to brittle transition temperature (DBTT) by Charpy impact<br />test in temperature interval from 196 to +100&deg;C has been studied. The all properties<br />obtained depend on the morphology of microstructure and the amount of retained<br />austenite, i.e. on the austempering parameters. According to the mechanical properties<br />and standard requirements (ASTM, ISO and EN) the processing window has been<br />proposed, also. It was found that DBTT is influenced by amount and stability of retained<br />austenite. In upper temperature range (above cca. 25&deg;C) the most influence factor on<br />DBTT is amount of retained austenite, while at the lower temperatures the stability is<br />more prominent. Stability of high carbon retained austenite at lower temperatures<br />prevents transformation to martensite and thus the embrittlement of ADI.</p>

Farmaceutická fakulta, Katedra farmaceutické technologie, Hradec Králové, 2014 Vypracovala: Markéta Valentová Školitel: Doc. RNDr. Milan Dittrich, CSc. ABSTRACT STUDY OF POLYESTER DRUG CARRIERS DEGRADATION USING THE DSC METHOD The aim of this work was focused on the study of relations among various parameters of degradation process, such as time-dependent range of glass transition temperature, swelling, erosion, and molar weight decrease. Two model polyesters of two type architectures of polyester molecules were used and monitored during two-week period. In the theoretical part of this diploma thesis are in details described biopolymers with stimulus responsive activity and exploitation of these materials in various biomedical applications in the topic of tissue engineering. The experimental part of this work is directed into the study of molecule degradation parameters, eventually into simulated biodegradation in the in vitro conditions of two different in the type polyesters with the contrast polyester molecule constitution. It was demonstrated that parameter Mn decreases towards the limit values. Between the values of molar weight and glass transition temperature is not Flory-Fox relation in the advanced phase of degradation process. The erosion of the material begins after the lag-time in the dependency...

La grande majorité des résines époxy utilisées aujourd’hui sont issues ou dérivées du bisphénol-A (BPA). Cependant, le BPA est soumis à de très fortes régulations, notamment vis-à-vis de sa récente classification comme substance chimique extrêmement préoccupante par l’agence européenne des produits chimiques (ECHA). Dans un but d’anticiper les évolutions de régulation, ArianeGroup a décidé de remplacer cette substance chimique de ces formulations. Ces travaux de thèse portent donc sur l’élaboration de nouvelles résines époxy biosourcées ayant des propriétés similaires voire supérieures aux références dérivées du bisphénol-A. Pour cela, une bioplatforme de monomères polyépoxydés issus de la vanilline, du méthyl vanillate, du 2,6-diméthoxyphénol et de l’eugénol a été développée. Ces précurseurs biosourcés ont ensuite été utilisés comme précurseurs de réseaux époxyde par réticulation avec des amines. Les réseaux réticulés biosourcés ainsi obtenus ont démontré des propriétés thermomécaniques remarquables bien supérieures à la référence de type DGEBA, notamment en termes de température de transition vitreuse (>300 °C) et taux de coke (>50%). En parallèle de ces travaux, la synthèse de diamines biosourcées, dérivées de la divanilline, et pouvant être utilisées comme agents de réticulation de résines époxy, a été réalisée. Des réseaux époxyde entièrement biosourcés ont ainsi été synthétisés et présentent des propriétés thermomécaniques prometteuses. / Today, most of the epoxy resins produced are derived from bisphenol-A (BPA). However, BPA is subject to strong regulations, particularly because of its recent classification as chemical of very high concern by the European Chemicals Agency (ECHA). In order to anticipate new regulations, ArianeGroup has decided to replace this substance in its applications. The aim of this thesis is to develop new bio-based epoxy thermosets with comparable thermomechanical properties as the ones issued from bisphenol-A-based materials. For this purpose, a bio-platform of epoxy monomers from vanillin, methyl vanillate, 2,6-dimethoxyphenol and eugenol was developed. These precursors were cross-linked with amines used as curing agent to obtain bio-based epoxy networks. The latter demonstrated thermomechanical properties well above the DGEBA-type reference, especially in terms of glass transition temperature (> 300 °C) and char content (> 50%). Finally, the synthesis of bio-based diamines derived from divanillin was developed and enabled the synthesis of fully bio-based epoxy networks with promising thermomechanical properties.

Com o decorrer dos anos o consumo de petróleo e seus derivados aumentou significativamente e com isso houve a necessidade de se investir em pesquisas para descobertas de novas jazidas de petróleo como o pré-sal. Porém, não apenas a localização dessas jazidas deve ser estudada, mas, também, sua forma de exploração. Essa exploração e extração, na maioria das vezes, se dão em ambientes altamente corrosivos e o transporte do produto extraído é realizado através de tubulações de aço de alta resistência e baixa liga (ARBL). Aços ARBL expostos a ambientes contendo H2S e CO2 (sour gas) sofrem corrosão generalizada que promovem a entrada de hidrogênio atômico no metal, podendo diminuir sua tenacidade e causar falha induzida pela presença de hidrogênio (Hydrogen Induced Cracking HIC), gerando falhas graves no material. Tais falhas podem ser desastrosas para o meio ambiente e para a sociedade. O objetivo deste trabalho é estudar a tenacidade, utilizando ensaio Charpy, de um tubo API 5L X65 sour após diferentes tempos de imersão em uma solução saturada com H2S. O eletrólito empregado foi a solução A (ácido acético contendo cloreto de sódio) da norma NACE TM0284 (2011), fazendo-se desaeração com injeção de N2, seguida de injeções de H2S. Os materiais foram submetidos a: ensaios de resistência a HIC segundo a norma NACE TM0284 (2011) e exames em microscópio óptico e eletrônico de varredura para caracterização microestrutural, de inclusões e trincas. As amostras foram submetidas a imersão em solução A durante 96h e 360h, sendo que, após doze dias do término da imersão, foram realizados os ensaios Charpy e exames fractográficos. Foram aplicados dois métodos: o de energia absorvida e o da expansão lateral, conforme recomendações da norma ASTM E23 (2012). As curvas obtidas, em função da temperatura de impacto, foram ajustadas pelo método da tangente hiperbólica. Esses procedimentos foram realizados nas duas seções do tubo (transversal e longitudinal) e permitiram a obtenção dos seguintes parâmetros: energias absorvidas e expansão lateral nos patamares superior e inferior e temperaturas de transição dúctil-frágil (TTDF) em suas diferentes definições, ou seja, TTDFEA, TTDFEA-DN, TTDFEA-FN, TTDFEL, TTDFEL-DN e TTDFEL-FN (identificação no item Lista de Abreviaturas e Siglas). No exame fractográfico observou-se que o material comportou-se conforme o previsto, ou seja, em temperaturas mais altas ocorreu fratura dúctil, em temperaturas próximas a TTDF obteve-se fratura mista e nas temperaturas mais baixas observou-se o aparecimento de fratura frágil. Os resultados mostraram que quanto maior o tempo de imersão na solução A, menor é a energia absorvida e a expansão lateral no patamar superior, o que pode ser explicado pelo (esperado) aumento do teor de hidrogênio em solução sólida com o tempo de imersão. Por sua vez, os resultados mostraram que há tendência à diminuição da temperatura de transição dúctil-frágil com o aumento do tempo de imersão, particularmente, as TTDFEA-DN e TTDFEL-DN das duas seções do tubo (longitudinal e transversal). Esse comportamento controverso, que pode ser denominado de tenacificação com o decorrer do tempo de imersão na solução A, foi explicado pelo aparecimento de trincas secundárias durante o impacto (Charpy). Isso indica uma limitação do ensaio Charpy para a avaliação precisa de materiais hidrogenados. / Over the years the consumption of crude oil and its derivatives increased significantly, creating the necessity to invest in research to discover new sources of pre-salt crude oil. However, not only the location of these deposits should be studied, but also its extraction. This exploration and extraction, in most cases, occur in highly corrosive environments and the transport of the extracted product is performed by high strength low alloy steel pipes (HSLA). HSLA steels exposed to environments containing CO2 and H2S (sour gas) suffer general corrosion that promotes the diffusion of atomic hydrogen into the metal structure, which may decrease its toughness and induce cracks by the presence of hydrogen (Hydrogen Induced Cracking - HIC), leading the material to severe failures. Such events can be disastrous for the environment and the society. The objective of this work is to study the toughness using Charpy Impact Tests on an API 5L X65 sour service steel pipe, submitted to different immersion times in a H2S saturated solution. The used electrolyte was the NACE TM0284 (2011) solution A (acetic acid containing sodium chloride), with deaeration by N2 injection followed by H2S injection. The materials were submitted to HIC resistance tests according to NACE TM0284 (2011) standard and examination by optical microscopy and scanning electron microscopy for microstructural inclusions and cracks characterization. The samples were immersed in the solution for 96h and 360h and after twelve days of immersion, Charpy tests and fracture analysis were performed. Two analytical methods were applied to Charpy tests results: the energy absorbed and lateral expansion, as recommended by the ASTM E23 (2012). The obtained curves, that are a function of impact temperature, were adjusted by the hyperbolic tangent method. This procedure was performed in two different orientations in the pipe (transverse and longitudinal) and allowed the determination of the following parameters: energy absorbed and lateral expansion in the upper and lower levels and ductile-to-brittle transition temperatures (DBTT) in its different definitions: DBTTAE, DBTTAE-DN, DBTTAE-FN, DBTTLE, DBTTLE-DN e DBTTLE-FN. Fracture analysis revealed that the material behaved as expected, meaning that at higher temperatures ductile fracture occurred, at temperatures near DBTT it was obtained a mixed fracture and at lower temperatures it was observed the presence of brittle fracture. Results showed that when the immersion time in the solution was higher, the energy absorbed in upper shelf decreases, and also lateral expansion in upper shelf decreases, which may be explained by the (expected) increase of hydrogen level in solid solution, induced by the immersion time. It was found that there is a tendency of the ductile-to-brittle transition temperature to be lower with the increase of immersion time, particularly the DBTTAE-DN and DBTTLE-DN of the two pipe sections (longitudinal and transversal). This controversial behavior, which may be defined as the toughening by the increase of immersion time in the solution A, was explained by the appearance of secondary cracks during impact test (Charpy). This indicates a limitation of the Charpy test for the accurate characterization of hydrogenated materials, concerning toughness.

Em projetos de oleodutos e gasodutos utilizam-se aços de alta resistência e baixa liga (ARBL), como o aço API 5L X80. Na soldagem multipasse destas tubulações, a zona afetada pelo calor (ZAC) do passe de raiz é submetida a um novo ciclo térmico pelos passes de soldagem subsequentes. Isto resulta em alterações nos valores das propriedades físicas. Nos aços ARBL, a ZAC de grãos grosseiros reaquecida intercriticamente (IC-ZACGG) pode se tornar uma zona frágil localizada, isto é, uma zona com maior dureza. Consequentemente, falhas estruturais podem ocorrer, ocasionando paradas não desejadas no transporte de fluidos. O objetivo deste trabalho é desenvolver uma metodologia baseada no modelo de fontes de calor distribuídas de Mhyr e Gröng, para avaliar o fluxo de calor na soldagem considerando as propriedades físicas dependentes da temperatura. Estender a aplicação desta ferramenta em soldagens multipasses para identificar sub-regiões da ZAC de um passe anterior sendo afetada pela ZAC de passes subsequentes. As isotermas simuladas foram validadas através de medições realizadas em macrografias de juntas soldadas. Os ciclos térmicos simulados foram validados através das temperaturas máximas atingidas e pelos tempos de resfriamento de 800 a 500 ºC (?t8-5) dos ciclos térmicos experimentais. Ao aplicar a metodologia proposta, foi possível delimitar com acurácia as regiões reaquecidas da ZAC e analisar os efeitos dos passes subsequentes em cada uma das sub-regiões da ZAC do passe de raiz. A IC-ZACGG na região do passe de raiz foi localizada, mas não se comportou como zona frágil devido à boa soldabilidade do aço API 5L X80 comprovada pelos ensaios de dureza e de tenacidade ao impacto Charpy-V. / In pipelines projects, the high strength low alloy (HSLA) steels are used, such as the API 5L X80 steel. During the multipass welding of these pipes, the heat affected zone (HAZ) of the root pass is subjected to a new thermal cycle by the subsequent welding passes. This results in changes in the values of the physical properties. In the HSLA steels, the intercritical reheated coarse-grained heat-affected zone (IR-CGHAZ) can become a local brittle zone, that is, a region with greater hardness. Consequently, structural failures could happen, causing undesired shutdowns in fluid transportation. The objective of this work is to develop a methodology based on the distributed heat sources model of Mhyr and Gröng, to evaluate the heat flux in the welding considering the temperature-dependent physical properties. Extend the application of this tool in multipass welds to identify HAZ subregions of a previous pass being affected by the HAZ of subsequent passes. The simulated isotherms were validated through measurements made on macrographs of welded joints. The simulated thermal cycles were validated through the maximum temperatures reached and the cooling times from 800 °C to 500 ºC (?t8-5) of the experimental thermal cycles. By applying the proposed methodology, it was possible to accurately delimit reheated HAZ regions and analyze the effects of subsequent passes in each of the root pass HAZ subregions. The IRCGHAZ in the root pass region was localized, but it did not behave as a brittle zone due to the good weldability of the API 5L X80 steel as proven by the hardness and Charpy-V impact tests.

Esta tese apresenta os estudos realizados quanto à síntese e caracterização de microgéis termo-responsivos de N-isopropilacrilamida (NIPAM) e macromoléculas de origem amilácea em sua composição, sistemas ainda pouco explorados na literatura. Inicialmente, nanopartículas de amido (SNP) foram preparadas por nanoprecipitação para incorporação nos microgéis de interesse, através da dissolução dos grânulos do amido em DMSO/H2O, aplicação de ultrassom e precipitação em não-solvente. As SNPs preparadas foram utilizadas como copolímero para formação de microgéis híbridos do tipo SNP-co-p(NIPAM) através de polimerização em emulsão na presença e na ausência de surfactante. A influência das SNPs nas propriedades dos microgéis foi estudada por MEV, DLS, PZ e SAXS, onde foram observadas mudanças no comportamento físico-químico e estrutura supramolecular dos microgéis. No geral, observaram-se deslocamentos da temperatura de transição de fase para valores maiores (até 35 °C, cerca de 3 °C acima do valor determinado para sistemas contendo p(NIPAM) puro), aumento da estabilidade coloidal e organização dos polímeros presentes no microgel em uma arquitetura caroço-casca. As propriedades de inchamento dos microgéis também foram estudadas através da teoria de Flory-Rehner, onde a temperatura theta e o grau de polimerização entre dois pontos de reticulação foram determinados através do ajuste apropriado do parâmetro de interação (χ). Paralelamente, visando um sistema diferente do descrito acima, foi estudado um novo agente de reticulação baseado nos polímeros do amido, a amilose e a amilopectina. Para isso, os polímeros do amido que compõem as nanopartículas foram modificados para a utilização como agente de reticulação na síntese de microgéis de p(NIPAM). Nesta etapa, uma reação de substituição dos grupos hidroxila dos polímeros do amido foi realizada com o cloreto de acriloíla de forma a inserir insaturações na estrutura dos polímeros, para que estes fossem aplicados como reticulante. O sucesso da reação de modificação foi verificado através de RMN 1H e FTIR, no qual um maior grau de substituição foi obtido quando um tempo maior de reação foi empregado. Microgéis de p(NIPAM) foram então preparados através de polimerização em emulsão utilizando os reticulantes sintetizados. Observou-se a influência do grau de substituição e da concentração do reticulante nos microgéis, analisados por MEV, DLS e UV-Vis com controle de temperatura. As principais mudanças foram relativas à temperatura de transição de fase e tamanho dos microgéis. Utilizando o agente de reticulação com maior grau de substituição, foi possível deslocar a temperatura de transição de fase dos microgéis preparados para valores maiores (35 °C, cerca de 3 °C acima do valor determinado para sistemas contendo p(NIPAM) puro). Observou-se também uma resposta mecânica da rede do microgel, que refletiu no tamanho das partículas, influenciada pela concentração dos agentes de reticulação e do grau de substituição. Quanto maior a concentração e o grau de substituição do agente de reticulação, maior a resistência ao intumescimento observado no microgel. / This thesis presents the studies regarding the synthesis and characterization of thermoresponsive microgels of N-isopropylacrylamide (NIPAM) and amylaceous-based macromolecules, which are systems still little explored in the literature. At first, starch nanoparticles (SNP) were prepared by nanoprecipitation, through dissolution of starch granules in DMSO/H2O, ultrasound application and non-solvent precipitation. SNPs were then used as copolymer in SNP-co-p(NIPAM) hybrid microgels synthesized by emulsion polymerization in the presence and absence of surfactant. The influence of SNPs in microgel properties were studied by SEM, DLS, ZP, and SAXS, where changes in the physicalchemical behavior and supramolecular structure were observed. Summing up, shifts in the phase transition temperature up to 35 °C, increased colloidal stability, and microgel polymers organization into a core-shell structure were observed. Microgels swelling behaviour were also studied by the Flory-Rehner theory, where the theta-temperature and the degree of polymerization between two crosslinker points were determined through interaction parameter (χ) fitting. In parallel, a new starch-based crosslinker was studied. For this purpose, starch polymers (amylose and amylopectin within the SNPs) were modified in order to use them as crosslinker in p(NIPAM) microgel synthesis. In this step, a substitution reaction in hydroxyl groups of SNP was carried out with acryloyl chloride, where double bonds were attached in polymers structure, making it suitable as a crosslinker. Reaction performances were evaluated through 1H NMR and FTIR. Then, p(NIPAM) microgels were prepared by emulsion polymerization using the crosslinker synthesized. The degree of substitution and the crosslinker concentration influence were verified and analyzed by SEM, DLS and UV-Vis with temperature control. The main observed changes were related to the phase transition temperature e microgels size. Using the crosslinker with higher substitution degree, it was possible the shift of the phase transition temperature to higher values (~35 °C). A mechanical response, observed trough microgels size, was found, driven by the crosslinker concentration and substitution degree. As higher the concentration and substitution degree of the crosslinker, higher was the swelling resistance observed in microgel structure.

La mise en place, l'étalonnage et l'utilisation d'un nouveau banc expérimental basses températures basé sur une technique photothermique appelée photo pyroélectricité (PPE) sont décrits dans ce manuscrit. Les échantillons que nous avons étudiés en utilisant ce nouvel instrument sont le glycérol, le 1,2 propanediol et leurs mélanges binaires avec l'eau. Ce sont des cryoprotecteurs bien connus (CPAs) utilisés dans la cryoconservation, qui est une technique de préservation des cellules et tissus vivants en les refroidissant à des très basses températures. Le but ultime de la cryoconservation est d'éviter ou de maîtriser la formation de glace et d'atteindre un état vitreux ou amorphe. La vitesse de refroidissement, de chauffage et la concentration des CPAs utilisés sont les paramètres clés qui déterminent la formation de la glace. Par conséquent, l'étude des propriétés thermiques, en particulier près de la transition vitreuse (Tg) des solutions binaires des CPAs avec de l'eau est très importante pour comprendre leur comportement lors du refroidissement. La PPE a été utilisée pour étudier l'effusivité et le temps de relaxation ∝ caractéristique de la transition vitreuse. Le Tg et la fragilité (m) ont été déterminés à partir des données de la PPE en utilisant le modèle d'Havriliak Negami. L'état vitreux présente une très grande viscosité, de l'ordre de 10¹² Pa.s au voisinage du Tg. Le Tg et m peuvent être calculés à partir de l'évolution de la viscosité en fonction de la température ou par calorimétrie différentielle à balayage (DSC). Ainsi, des études à l'aide de ces deux techniques ont été menées et les résultats ont été comparés avec les données de la PPE. / The construction, calibration and application of a new low temperature instrument based on a photothermal technique called photo pyroelectricity (PPE) is described in this manuscript. The samples we studied using the new PPE instrument were glycerol, 1,2 propanediol and their binary mixtures with water. These liquids are well known cryoprotectants (CPAs) used in cryopreservation, which is a technique to preserve the living cells and tissues from biological degradation by cooling to sub zero temperatures. The ultimate goal in cryopreservation is to avoid or control the ice formation and attain a glassy or amorphous state.The rate of cooling and heating and the concentration of the CPAs used are the key parameters that determine the ice formation. Therefore, studying the temperature dependent thermal properties especially near their glass transition temperature (Tg) of the binary solutions of CPAs with water at different concentrations are highly important to understand their behavior while cooling. The PPE technique was used to study the effusity and the ∝ relaxation time near the glass transition phenomenon. The Tg and fragility (m) were determined from the PPE data using the Havriliak Negami model. The glassy state has a characteristic property of very high viscosity, of the order of 10¹² Pa.s at Tg. The Tg and m can be calculated from the temperature evolution of viscosity or from Differential Scanning Calorimetry (DSC) measurements. Therefore, viscosity and DSC studies were conducted on the samples and were compared with PPE data.