[pt] Nanofolhas de ferrititanato com estrutura tipo lepidocrocita foram sintetizadas a partir de um precursor de baixo custo (areia ilmenítica), via rota hidrotérmica alcalina. Dois tipos de nanofolhas com alto e baixo teor de sódio foram obtidos: a) nanofolhas sódicas (NaLTs) e b) nanofolhas protonizadas (pLTs), obtidas mediante uma reação rápida de troca-ácida à temperatura ambiente. As capacidades de troca catiônica de ambos os tipos de nanofolhas foram determinadas seguindo-se a norma C 837 da ASTM. Após a síntese desses dois nanomateriais com diferentes teores de sódio foi estudado o processo de esfoliação em camadas de espessura sub-nanométrica, sob agitação intensa à temperatura de 60 C, utilizando-se como o agente de esfoliação pela primeira vez numa estrutura lepidocrocítica o sal cloreto de dimetildioctadecilamônio (2C18), visando a posterior aplicação das nanofolhas esfoliadas como reforço em nanocompósitos de matriz polimérica. O intuito de aplicar estes reforços em uma matriz polimérica foi buscar uma dispersão mais homogênea das folhas esfoliadas, além do aumento da compatibilidade das nanocargas com a matriz polimérica pela presença dos grupos orgânicos do sal quimicamente ligados às nanofolhas e, consequentemente, o incremento das propriedades térmicas e mecânicas do material polimérico. Dependendo do teor de sódio, foram obtidas nanofolhas esfoliadas e/ou intercaladas que foram posteriormente caracterizadas por fotometria de chama, espetroscopia de infravermelho, área superficial específica por adsorção de N2, termogravimetria, difração de raios-X de alto ângulo, espalhamento de raios-X a baixo ângulo, microscopia de força atômica e microscopia eletrônica de transmissão. Para a fabricação dos nanocompósitos foram utilizadas duas matrizes: a) uma de PEAD puro e b) a outra de PEAD com adição de uma porcentagem baixa, e constante, de polietileno funcionalizado com anidrido maleico (PE-g-MA), sendo reforçadas com as nanocargas protonizadas virgens (pLTs) e esfoliadas (pLTs-o-2C18) nas concentrações de 1,0; 2,0 e 4,0 por cento p. Finalmente, foram avaliadas as propriedades mecânicas e térmicas dos nanocompósitos por meio de ensaios de tração, termogravimetria, calorimetria diferencial de varredura e dilatometria. Os nanocompósitos preparados com pLTs virgem e os fabricados com a adição de agente de acoplamento de PE-g-MA apresentaram um aumento no módulo de Young de aproximadamente 12,8 por cento e 5,1 por cento para cargas de 4 por cento e 2 por cento em peso de pLTs virgem, respectivamente. Os nanocompósitos, que apresentam o maior aumento no limite de escoamento foram os reforçados com 4 por cento p de nanofolhas esfoliada (pLTs-o-2C18). No entanto, estes materiais apresentam uma diminuição no módulo de Young de aproximadamente 12 por cento. Os nanocompósitos com o maior aumento no módulo de Young foram os preparados com 4 por cento p pLTs ( aproximadamente 12,8 por cento), enquanto sua tensão no escoamento também foi melhorada (um aumento de aproximadamente 4 por cento). A incorporação de nanofolhas não afetou significativamente as propriedades de estabilidade térmica da matriz e uma diminuição no coeficiente de expansão térmica de 4 a 5,5 por cento foi apenas observada para nanocompósitos preparados com pLTs virgens. O grau de cristalinidade diminuiu para todos os nanocompósitos fabricados, no qual variou de 2,17 até 26 por cento. / [en] Ferrititanate nanosheets with lepidocrocite-like structure were synthesized from a low cost precursor (ilmenite sand) through alkaline hydrothermal route. Two types of nanosheets with high and low-sodium content were obtained: a) sodium rich nanosheets (NaLTs) and b) protonated nanosheets (pLTs), obtained by a rapid acid-exchange reaction at room temperature. The cation exchange capacities of both types of nanosheets were determinated according ASTM C 837. After the synthesis of these two nanomaterials with different sodium levels, it was studied the exfoliation process to obtain monolayers of nanometric lateral dimensions under intensive stirring at 60 C, using dimethyldioctadecylammonium cloride (2C18) as the exfoliating agent of the lepidocrocite-like ferrititanate nanosheets for the first time, aiming the further application of the exfoliated nanosheets as reinforcement in polymer matrix nanocomposites. The purpose of the addition of these nanofillers within a polymer matrix is to obtain a more homogeneous dispersion of exfoliated nanosheets, as well as the improvement of the compatibility between nanofillers and the polymer matrix, due to the presence of the organic groups from 2C18, chemically attached to nanosheets and hence, to promote the an increase on mechanical and thermal properties of the polymeric matrix. Depending on the sodium content, it was obtained exfoliated and/or intercalated nanosheets that were further characterized by flame photometry, infrared spectroscopy, specific surface area by N2 adsorption, thermogravimetry, X-ray powder diffraction (XRPD) and of small angle X-ray scattering (SAXS), atomic force microscopy (AFM) and transmission electron microscopy (TEM). For the manufacturing of nanocomposites two types of matrices were used: a) neat high density polyethylene (HDPE) and b) HDPE with the addition of a low percentage of polyethylene-graft-maleic anhydride (PE-g-MA). Pristine nanosheets (pLTs) and exfoliated nanosheets (pLTs-O-2C18) were used as nanofillers at loadings of 1.0; 2.0 and 4.0 wt percent. Finally, we assessed the mechanical and thermal properties of the as-prepared nanocomposites through tensile tests, thermogravimetry analysis (TGA), differential scanning calorimetry (DSC) and dilatometry. Nanocomposites prepared with pristine pLTs and those manufactured with the addition of PE-g-MA coupling agent showed an increase on the Young modulus of about 12,8 percent and 5,1 percent for loadings of 4wt percent and 2 wt percent of pristine pLTs, respectively. The nanocomposites that present the highest increase on yield stress were reinforced with 4 wt percent of exfoliated nanosheets (pLTs-o-2C18). However, these materials presents a decrease in the Young modulus of about 12 percent. The nanocomposites with the highest increase on Young Modulus were those prepared with 4 wt percent of pristine ( about 12,8 percent), and the yield stress was also improved (increase of about 4 percent). The incorporation of nanosheets did not affect significantly the thermal stability properties of the matrix and a decrease on the coefficient of thermal expansion was solely observed for nanocomposites prepared with pristine pLTs. The degree of crystallinity decreased for all the manufactured nanocomposites, in the range of about 2,17 t-26 percent for nanocomposites prepared with pristine pLTs and those fabricated with the addition of PE-g-MA, respectively. up to about pLTs with the addition of PE-g-MA.

Made available in DSpace on 2016-12-08T17:19:19Z (GMT). No. of bitstreams: 1 Juliana Paz.pdf: 1684316 bytes, checksum: 5c2617141f2eaa7e6d38f5e9791c52b5 (MD5) Previous issue date: 2012-07-27 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Epoxy-clay nanocomposites has been widely studied with interests in their thermal, mechanical and structural. A major breakthrough in research can be no use of solvents when the clay dispersion in epoxy resin, which reduces the environmental impact, although epoxies can not be recycled. This paper presents a study of the thermal properties (by Thermogravimetry, Differential scanning calorimetry and Dilatometry), mechanical (for traction, flexion and K1c) and structural (by Fourier Transform Infrared Microscopy and scanning electron) of epoxy-clay nanocomposites and as a rheological analysis (for viscosity) of the solutions of pre-cured composite at the moment of the load as first dispersion parameter selection of samples for later analyzes mechanical, thermal and structural characteristics. In the analyzes were chosen viscosity samples that had higher values, wherein the cured samples were used in two dispersion conditions, with and without sonication, and variations in concentration of 2, 4, 6 and 8 wt% as a means of comparison to obtain clear results improvements or not the properties of these nanocomposites, which are related to the respective condition dispersion. It is understood that nanocomposites with good dispersion is intercalated / exfoliated since the clay used in this work is called montmorillonite and has lamellar structure with nanometer thickness and large surface area, which results in an interface adhesion between clay and epoxy resin. In this, it is also observed that the condition of non-sonicated dispersion nanocomposites showed improvements in their thermal properties, but structurally the dispersion appears to be more efficient in samples sonificadas. The analysis shows improvements in their mechanical properties in samples with intermediate concentration (mainly 4 wt% clay), depending on the destination of the nanocomposite can indicate these materials for various applications, such as coatings and objects that require low chemical reactivity. / Nanocompósitos epóxi-argila vem sendo largamente estudados com interesses em suas propriedades térmicas, mecânicas e estruturais. Um grande avanço nas pesquisas pode ser a não utilização de solventes no momento da dispersão da argila na resina epóxi, o que diminui o impacto ambiental, apesar de os compostos epoxídicos não poderem ser reciclados. Este trabalho apresenta um estudo das propriedades térmicas (por Termogravimetria, Dilatometria e Calorimetria diferencial exploratória), mecânicas (por Tração, Flexão e K1c) e estruturais (por Infravermelho por Transformada de Fourier e Microscopia eletrônica de varredura) de nanocompósitos epóxi-argila, bem como uma análise reológica (por viscosidade) das soluções pré-curadas dos compósitos no momento da dispersão da carga como primeiro parâmetro de seleção das amostras para posteriores análises mecânicas, térmicas e estruturais. Nas análises de viscosidade foram escolhidas amostras que apresentavam maiores valores, na qual foram utilizadas as amostras curadas em duas condições de dispersão, com e sem sonificação e, em variações de concentração de 2, 4, 6 e 8% em massa como via de comparação para obter-se resultados claros de melhorias ou não das propriedades desses nanocompósitos, sendo estes relacionados com a respectiva condição de dispersão. Entende-se que nanocompósitos com boa dispersão são intercalados/esfoliados, uma vez que a argila utilizada neste trabalho é chamada montmorillonita e apresenta estrutura lamelar com espessura nanométrica e grande área superficial, que resulta numa interface de adesão entre argila e resina epóxi. Neste, observa-se também que a condição de dispersão não-sonificada os nanocompósitos apresentavam melhorias em suas propriedades térmicas, porém, estruturalmente a dispersão parece ser mais eficiente em amostras sonificadas. As análises mecânicas mostras melhorias em suas propriedades em amostras com concentração intermediária (principalmente 4% em massa da argila); dependendo do destino do nanocompósito pode-se indicar esses materiais para diversas aplicações, tais como revestimentos e objetos que necessitem baixa reatividade química.

Made available in DSpace on 2016-03-15T19:36:55Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-08-18 / Fundo Mackenzie de Pesquisa / A two-dimensional structure with a thickness of one atom in a Bravais lattice in a "honeycomb". So it is known graphene, with interesting property both in basal plane as the edges of the material. Consisting of carbon atoms in its sp2 hybridization, graphene has applications to mechanical areas, electrical, optical, chemistry, biology. This requires mastered the techniques of obtaining graphene. This paper presents the study of obtaining exfoliated material, seeking to control the process as well as obtain graphene by electrochemical. The process of obtaining exfoliation is important because through it can obtain more control over the exfoliated material. The material obtained was analyzed by Raman spectroscopy. Our results show that it is possible to obtain exfoliated material, and as the spectra material by analyzing the intensity of the peaks. / Uma estrutura bidimensional com a espessura de um átomo, em uma rede de bravais em forma de favos de mel . Assim é conhecido o grafeno, com propriedade interessante tanto no plano basal como nas bordas do material. Constituído de átomos de carbono em sua hibridização sp2, o grafeno possui aplicações às áreas de mecânica, elétrica, ótica, química, biologia. Para isso é necessário dominar as técnicas de obtenção de grafeno. Este trabalho apresenta o estudo da obtenção de material esfoliado, buscando controle no processo, além de se obter grafeno por via eletroquímica. O processo de obtenção por esfoliação eletroquímica é importante, pois por meio dele pode-se adquirir mais controle sobre o material esfoliado. O material obtido foi analisado através da técnica de Espectroscopia Raman. Os resultados mostraram que é possível obter material esfoliado e a análise deste material através da intensidade das bandas de seu espectro Raman.

Nowadays, new approaches to fabricate high-performance electrode materials are of vital importance in the renewable energy field. Here, we present a facile synthesis procedure of 3D Ni(OH)2/graphene hybrids for supercapacitors via synchronous electrochemical-assisted exfoliation and assembly of graphene on 3D Ni(OH)2 networks. With the assistance of an electric field, the electrochemically exfoliated high-quality graphene can be readily, uniformly assembled on the surfaces of 3D Ni(OH)2. When serving as electrode materials for supercapacitors, the resulting 3D Ni(OH)2/graphene composites exhibited excellent specific capacitance (263 mF cm−2 at 2 mA cm−2), remarkable rate capability and super-long cycle life (retention of 94.1% even after 10 000 continuous charge–discharge cycles), which may be attributed to their highly porous, stable 3D architecture as well as uniform, firm anchoring of ultrathin graphene on their surfaces. Therefore, our approach provides a facile strategy for the large-scale synthesis of high-quality graphene based composites towards various applications.

Grafen v kombinaci s komplexy kovů by mohl poskytnout nové přísutpy v hybridních materiálech založených na grafenové bázi a v oblasti molekulárního magnetismu. Obě témata jsou velmi diskutovaná jako taková, nicméně, výzkumu vedoucího k možnosti jejich míchání není mnoho. Vzorky byly připraveny sonikací grafitu v kapalné fázi, což vedlo k exfoliaci grafenu. Následně byly nadeponovány pomocí modiikované Lagmuirovy– Schaeferovy depoziční metody různé komplexy kovů na substrát pokrytý grafenem. Klíčovým krokem bylo určení vlastností takto připraveného materiálu. Proto byly následně vlastnosti takového hybridního materiálu charakterizovány pomocí vysokofrekvenční elektronové paramagnetické rezonance (angl. HFEPR), rastrovacího elektronového mikroskopu, (angl. SEM), Ramanovou spektroskopií a čtyř bodovou metodou měření odporu. V této práci jsme potvrdili naši presumpci, že je možné vytvořit hybridní materiál smícháním exfoliovaného grafenu s molekulárními magnety pro získání nových magnetických a elektronických vlastností, které by mohly být využity v další generaci detektorů a elektroniky.

This diploma thesis deals with the preparation of the very thin films and their investigation by scanning probe microscopy methods. The ultrathin films of Pt on Pt(111) were created by pulsed laser deposition and the ultrathin films of Co on Pt(111) were deposited by thermal evaporation. The coverage of the substrate was much smaller than one monolayer (in order of hundredths of monolayer). The nucleation theory was verified by these experiments using so-called Onset method. Further graphene sheets were prepared on layer of Si/SiO2 by the mechanical exfoliation from the graphite crystal. The fabricated graphene sheets were studied by micro-Raman spectroscopy, microreflectometry, atomic force microscopy and similar techniques. These methods proved the thinnest graphite layers were consisted of two graphene monolayers.

<p>  </p> <p>Graphene is a two-dimensional (2-D) sheet of <em>sp2</em> hybridized carbon atoms with extraordinary thermal, electrical, and mechanical properties. Among numerous sophisticated and costly synthesis techniques including chemical vapor deposition (CVD), SiC and microwave plasma; liquid-phase exfoliation (LPE) has been one of the most widely used techniques for low-cost and large scale graphene synthesis since it was first reported in 2008. LPE involves the use of liquid media to exfoliate graphite precursors directly into mono- or few-layered graphene. Stable dispersions of few-layered graphene are desirable for thin-film deposition on a large scale but are limited by the use of polar organic solvents with high boiling points and unfavorable toxicity profiles. This limitation can be overcome by milling and exfoliation of graphene nanoplatelets (GrNPs) in ethyl acetate (EtOAc) and acetone, volatile solvents with low toxicity profiles and modest environmental impact. Solvent-assisted grinding of pristine GrNPs on a horizontal ball mill followed by sonication produces concentrated suspensions up to 356 µg/mL that remain stable at room temperature for a minimum of 6 weeks without the addition of surfactants. Exfoliated graphene layers have an average thickness of 4.5 nm which corresponds to 10–12 layers of graphene on Si/SiO2 substrates. EtOAc and acetone-based dispersions of exfoliated graphene can be deposited uniformly using conventional airbrush equipment as low-boiling point solvents evaporates instantaneously after deposition. This deposition method also provides freedom regarding to target substrate and overcomes any substrate related limitations observed in other techniques. Practical demonstrations of spray-coated graphene films include (i) conductive surfaces with sheet resistance as low as 1 kΩ/sq, and (ii) solid contacts for disposable and low-cost nitrate-selective electrodes, with high reproducibility in the voltage readouts across multiple sensors.</p>

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No description available.

Two-dimensional conjugated metal–organic frameworks (2D c-MOFs), possessing extended π–d conjugated planar structure, are emerging as a unique class of electronic materials due to their intrinsic electrical conductivities. Taking advantage of the large-area flat surface, 2D c-MOF thin films allow facile device integration with sufficient electrode contact, high device stability, and high charge transport, thereby emerging as appealing active layers for a broad range of electronic applications. Synthesis and device investigation of thin films are of great importance for their further development, which are systematically summarized in the current review. Here, the authors firstly introduce the molecular structures of representative 2D c-MOFs and present the fundamental understanding on structure–property relationships. After that, the state-of-art synthetic methodologies toward high-quality 2D c-MOF thin films are summarized, including exfoliation and reassembly (ERA), liquid-interface-assisted synthesis (LIAS), and chemical vapor deposition (CVD). By considering the advantages of 2D c-MOF films in device integration, remarkable progress in (opto-)electronic device applications are discussed, such as field-effect transistors (FETs), chemiresistive sensors, photodetectors, superconductors, and thermoelectrics. In the end, the remained challenges about the development of 2D c-MOF films for (opto-)electronics are highlighted and possible future directions are proposed to address these challenges.