Academic literature on the topic 'Zn(S,O,OH)'
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Journal articles on the topic "Zn(S,O,OH)":
Vallejo, William, Carlos Diaz-Uribe, and Cesar Quiñones. "Optical and Structural Characterization of Cd-Free Buffer Layers Fabricated by Chemical Bath Deposition." Coatings 11, no. 8 (July 27, 2021): 897. http://dx.doi.org/10.3390/coatings11080897.
Zhang, Shaoqing, Yanyan Liu, Jiqi Zheng, Yang Mu, Hanmei Jiang, Haoran Yan, Yanping Wang, Yifu Zhang, and Changgong Meng. "Rice-like and rose-like zinc silicates anchored on amorphous carbon derived from natural reed leaves for high-performance supercapacitors." Dalton Transactions 50, no. 27 (2021): 9438–49. http://dx.doi.org/10.1039/d1dt01381e.
Vallejo, W., C. Quiñones, and G. Gordillo. "A comparative study of thin films of Zn(O;OH)S and In(O;OH)S deposited on CuInS2 by chemical bath deposition method." Journal of Physics and Chemistry of Solids 73, no. 4 (April 2012): 573–78. http://dx.doi.org/10.1016/j.jpcs.2011.12.014.
Ernits, K., K. Muska, M. Danilson, J. Raudoja, T. Varema, O. Volobujeva, and M. Altosaar. "Anion Effect of Zinc Source on Chemically Deposited ZnS(O,OH) Films." Advances in Materials Science and Engineering 2009 (2009): 1–5. http://dx.doi.org/10.1155/2009/372708.
Bhattacharya, R. N., K. Ramanathan, L. Gedvilas, and B. Keyes. "Cu(In,Ga)Se2 thin-film solar cells with ZnS(O,OH), Zn–Cd–S(O,OH), and CdS buffer layers." Journal of Physics and Chemistry of Solids 66, no. 11 (November 2005): 1862–64. http://dx.doi.org/10.1016/j.jpcs.2005.09.006.
Hildebrandt, Thibaud, Nicolas Loones, Nathanaelle Schneider, Muriel Bouttemy, Jackie Vigneron, Arnaud Etcheberry, Daniel Lincot, and Negar Naghavi. "Effects of additives on the improved growth rate and morphology of Chemical Bath Deposited Zn(S,O,OH) buffer layer for Cu(In,Ga)Se2- based solar cells." MRS Proceedings 1538 (2013): 39–44. http://dx.doi.org/10.1557/opl.2013.976.
Piilonen, P. C., I. V. Pekov, M. Back, T. Steede, and R. A. Gault. "Crystal-structure refinement of a Zn-rich kupletskite from Mont Saint-Hilaire, Quebec, with contributions to the geochemistry of zinc in peralkaline environments." Mineralogical Magazine 70, no. 5 (October 2006): 565–78. http://dx.doi.org/10.1180/0026461067050350.
Vallejo, W., M. Hurtado, and G. Gordillo. "Kinetic study on Zn(O,OH)S thin films deposited by chemical bath deposition." Electrochimica Acta 55, no. 20 (August 2010): 5610–16. http://dx.doi.org/10.1016/j.electacta.2010.04.088.
Fan, Hong-Jie, Qian-Qian Xu, Tie-Zhen Ren, Xiang-Ying Xing, and Kirsten E. Christensen. "Zn/Mn–MOFs with `S-shaped' packing modes." Acta Crystallographica Section C Structural Chemistry 70, no. 5 (April 18, 2014): 502–7. http://dx.doi.org/10.1107/s2053229614005828.
Altahan, Mohammed A., Michael A. Beckett, Simon J. Coles, and Peter N. Horton. "Transition-metal complexes with oxidoborates. Synthesis and XRD characterization of [(H3NCH2CH2NH2)Zn{κ3O,O′,O′′-B12O18(OH)6-κ1O′′′}Zn(en)(NH2CH2CH2NH3)]·8H2O (en=1,2-diaminoethane): a neutral bimetallic zwiterionic polyborate system containing the ‘isolated’ dodecaborate(6−) anion." Pure and Applied Chemistry 90, no. 4 (March 28, 2018): 625–32. http://dx.doi.org/10.1515/pac-2017-0901.
Dissertations / Theses on the topic "Zn(S,O,OH)":
Moura, Alysson Elson Galv?o de. "S?ntese, sinteriza??o e caracteriza??o de ferritas ? base de Ni-Zn." Universidade Federal do Rio Grande do Norte, 2008. http://repositorio.ufrn.br:8080/jspui/handle/123456789/17599.
Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
Were synthesized different ferrites NixZn1-xFe2O4 (0,4 ≤ x ≤ 0,6) compositions by using citrate precursor method. Initially, the precursors citrates of iron, nickel and zinc were mixed and homogenized. The stoichiometric compositions were calcined at 350?C without atmosphere control and the calcined powders were pressed in pellets and toroids. The pressed material was sintered from 1100? up to 1200?C in argon atmosphere. The calcined powders were characterized by XRD, TGA/DTG, FTIR, SEM and vibrating sample magnetometer (VSM). All sintered samples were characterized using XRD, SEM, VSM and measurements of magnetic permeability and loss factor were obtained. It was formed pure ferromagnetic phase at all used temperatures. The Rietveld analyses allowed to calculate the cations level occupation and the crystallite size. The analyses obtained nanometric crystals (12-20 nm) to the calcined powder. By SEM, the sintered samples shows grains sizes from 1 to 10 μm. Sintered densities (ρ) were measured by the Archimedes method and with increasing Zn content, the bulk density decrease. The better magnetization results (105-110 emu/g) were obtained for x=0,6 at all sintering temperatures. The hysteresis shows characteristics of soft magnetic material. Two magnetization processes were considered, superparamagnetism at low temperature and the magnetic domains formation at high temperatures. The sintered toroids presents relative magnetic permeability (μr) from 7 to 32 and loss factor (tanδ) of about 1. The frequency response of toroids range from 0,3 kHz to 0,2 GHz. The composition x=0,5 presents both greater μr and tanδ values and x=0,6 the most broad range of frequency response. Various microstructural factors show influence on the behavior of μr and tanδ, such as: grain size, porosity across grain boundary and inside the grain, grain boundary content and domain walls movement during the process of magnetization at high frequency studies (0,3kKz 0,2 GHz)
Foram sintetizadas diferentes composi??es da ferrita Ni1-xZnxFe2O4 com 0,4 ≤ x ≤ 0,6 pelo uso do m?todo dos citratos precursores. Para se obter a fase estequiom?trica do sistema Ni1-xZnxFe2O4 foram misturados e homogeneizados os citratos precursores de ferro, n?quel e zinco. As composi??es estequiom?tricas foram calcinadas em atmosfera ambiente na temperatura de 350?C e depois prensadas em pastilhas e tor?ides. As amostras prensadas foram sinterizadas nas temperaturas de 1100?, 1150? e 1200?C em atmosfera de arg?nio. Os p?s calcinados foram caracterizados por DRX, TGA/DTG, FTIR, MEV e magnetometria de amostra vibrante (MAV) e as amostras sinterizadas por DRX, MEV, MAV, massa espec?fica e medidas de permeabilidade e perdas magn?ticas. Observou-se a forma??o de fase pura ferrimagn?tica em todas as temperaturas aplicadas. A an?lise pelo m?todo de Rietveld calculou o n?vel de ocupa??o dos c?tions e o tamanho de cristalito. Foram obtidos tamanhos de cristais nanom?tricos, de 12 a 20 nm para os p?s calcinados. Por MEV, as amostras sinterizadas apresentam tamanhos de gr?os na faixa de 1 a 10 μm. A massa espec?fica (ρ) do material sinterizado apresenta uma tend?ncia de diminui??o com a adi??o de Zn. Os melhores resultados de magnetiza??o foram obtidos para x=0,6 nas tr?s temperaturas de sinteriza??o, variando de 105 a 110 emu/g. As histereses mostram um perfil de materiais magn?ticos moles. Dois processos de magnetiza??o foram considerados, o superparamagnetismo a baixa temperatura (350?C) e a forma??o de dom?nios magn?ticos em altas temperaturas. Os materiais sinterizados apresentam permeabilidade (μ) de algumas unidades, de 7 a 30, e perdas magn?ticas (tanδ) por volta de 1. A resposta em freq??ncia dos n?cleos toroidais est? na faixa de 0,3 kHz a 0,2 GHz. Os maiores valores de μ e tanδ s?o para x=0,5 e a maior faixa de resposta em freq??ncia ? para x=0,6. V?rios fatores da microestrutura contribuem para o comportamento das grandezas μ e tanδ, tais como: os tamanhos dos gr?os, porosidade inter e intragranular, quantidade de contornos de gr?os e os aspectos da din?mica das paredes de dom?nios quando excitadas magneticamente sob alta freq??ncia
Hultqvist, Adam. "Cadmium Free Buffer Layers and the Influence of their Material Properties on the Performance of Cu(In,Ga)Se2 Solar Cells." Doctoral thesis, Uppsala universitet, Fasta tillståndets elektronik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-133112.
Felaktigt tryckt som Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 717
Hora, Paulo Henrique Almeida da. "S?ntese, caracteriza??o, propriedades e aplica??o dos sistemas Mg- Al, Zn-Al e Mg-Fe." Universidade Federal do Rio Grande do Norte, 2014. http://repositorio.ufrn.br:8080/jspui/handle/123456789/17758.
Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
The Layered Double Hydroxides has become extremely promising materials due to its range of applications, easily obtained in the laboratory and reusability after calcination, so the knowledge regarding their properties is of utmost importance. In this study were synthesized layered double hydroxides of two systems, Mg-Al and Zn-Al, and such materials were analyzed with X-ray diffraction and, from these data, we determined the volume density, planar atomic density, size crystallite, lattice parameters, interplanar spacing and interlayer space available. Such materials were also subjected to thermogravimetric analysis reasons for heating 5, 10, 20 and 25 ? C / min to determine kinetic parameters for the formation of metaphases HTD and HTB based on theoretical models Ozawa, Flynn-Wall Starink and Model Free Kinetics. In addition, the layered double hydroxides synthesized in this working ratios were calcined heating 2.5 ? C / min and 20 ? C / min, and tested for adsorption of nitrate anion in aqueous solution batch system at time intervals 5 min, 15 min, 30 min, 1h, 2h and 4h. Such calcined materials were also subjected to exposure to the atmosphere and at intervals of 1 week, 2 weeks and 1 month were analyzed by infrared spectroscopy to study the kinetics of regeneration determining structural called "memory effect"
Os Hidr?xidos Duplos Lamelares tem se tornado materiais extremamente promissores devido a sua gama de aplica??es, f?cil obten??o em laborat?rio e a possibilidade de reutiliza??o ap?s calcina??o, portanto o conhecimento referente ? suas propriedades ? de extrema relev?ncia. Neste estudo foram sintetizados hidr?xidos duplos lamelares de dois sistemas, Mg-Al e Zn-Al, e tais materiais foram submetidos a an?lise com difra??o de raios X e, a partir de tais dados, foram determinados a densidade volum?trica, densidade at?mica planar, tamanho do cristalito, par?metros de rede cristalina, dist?ncia interplanar e espa?o interlamelar dispon?vel. Tais materiais tamb?m foram submetidos ? an?lise termogravim?trica em raz?es de aquecimento de 5, 10, 20 e 25 ?C/min para determina??o de par?metros cin?ticos durante a forma??o das metafases HTD e HTB com base nos modelos te?ricos de Ozawa, Flynn-Wall, Starink e Model Free Kinetics. Al?m disso, os hidr?xidos duplos lamelares sintetizados neste trabalhado foram calcinados em raz?es de aquecimento de 2,5 ?C/min e 20 ?C/min e submetidos a ensaios de adsor??o de ?nion nitrato em solu??o aquosa em sistema de batelada em intervalos de tempo de 5 min, 15 min, 30 min, 1h, 2h e 4h. Tais materiais calcinados tamb?m foram submetidos ? exposi??o com a atmosfera e em intervalos de tempo de 1 semana e 2 semanas foram analisados atrav?s de difra??o de raios X para estudo determina??o da cin?tica de regenera??o estrutural denominada efeito mem?ria
Xavier, Camila Soares. "Estudo das propriedades fotoluminescentes de 'CA''ZN IND.2''(OH) IND.6'.2'H IND.2"O' obtidos a partir do método hidrometal-microondas /." Araraquara : [s.n.], 2010. http://hdl.handle.net/11449/105771.
Banca: Mário Cilense
Banca: Fenelon Martinho Lima Pontes
Banca: Máximo Siu Li
Banca: João Batista Baldo
Resumo: Neste trabalho, foi estudado a formação dos pós de hexahidroxodizincato de cálcio dihidratado, CaZn2(OH)6.2H2O (CZO) sobre condições hidrotermais-microondas (HM) e partindo de diferentes reagentes e surfactantes. Estes pós foram analisados por difração de raios X (DRX), microscopia eletrônica de varredura com canhão de elétrons por emissão de campo (FEG-MEV), espectroscopia de absorção na região do ultravioleta visível (UV-vis), espectroscopia na região do infravermelho (IV) e medidas de fotoluminescência (FL). Os padrões de DRX confirmaram que a fase CZO pura foi obtida após o processamento HM realizado a 130 ºC por 2 h com a síntese partindo de nitratos, enquanto que as demais apresentaram fases secundárias. As micrografias FEG-MEV indicaram que as modificações bem como o crescimento das micropartículas de CZO foram orientadas pelo mecanismo de coalescência e Ostwald-ripening. O espectro UV-vis ilustrou que este material tem um band gap óptico indireto. Os pós de CZO puros exibiram uma emissão amarela quando excitados por um comprimento de onda de 350 nm em temperatura ambiente, enquanto que os demais exibiram uma emissão na região do laranja
Abstract: In this work, it was studied the formation of calcium hexahydroxodizincate dehydrate, CaZn2(OH)6.2H2O (CZO) powders under microwave-hydrothermal (MH) conditions and using the different reagents and surfactants. These powders were analyzed by X-ray diffraction (XRD), Field-emission gum scanning electron microscopy (FEG-SEM), ultraviolet-visible (UV-vis) absorption spectroscopy, infra red spectroscopy (FTIR) and photoluminescence (PL) measurements. XRD patterns confirmed that the pure CZO phase was obtained after MH processing performed at 130 ºC for 2 h. FEG-SEM micrographs indicated that the morphological modifications as well as the growth of CZO microparticles are governed by Ostwal-ripening and coalescence mechanisms. UV-vis spectra showed that this material have an indirect optical band gap. The pure CZO powders exhibited an yellow PL emission when excited by 350 nm wavelength at room temperature, whereas the other powders exhibited the orange emission
Doutor
Gomes, Kalyanne Keyly Pereira. "S?ntese e caracteriza??o de aluminofosfato impregnado com molibd?nio/zinco visando a dessulfuriza??o por adsor??o." Universidade Federal do Rio Grande do Norte, 2011. http://repositorio.ufrn.br:8080/jspui/handle/123456789/15910.
Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
Discussions about pollution caused by vehicles emission are old and have been developed along the years. The search for cleaner technologies and frequent weather alterations have been inducing industries and government organizations to impose limits much more rigorous to the contaminant content in fuels, which have an direct impact in atmospheric emissions. Nowadays, the quality of fuels, in relation to the sulfur content, is carried out through the process of hydrodesulfurization. Adsorption processes also represent an interesting alternative route to the removal of sulfur content. Both processes are simpler and operate to atmospheric temperatures and pressures. This work studies the synthesis and characterization of aluminophosphate impregnate with zinc, molybdenum or both, and its application in the sulfur removal from the gasoline through the adsorption process, using a pattern gasoline containing isooctane and thiophene. The adsorbents were characterized by x-ray diffraction, differential thermal analysis (DTG), x-ray fluorescence and scanning electron microscopy (SEM). The specific area, volume and pore diameter were determined by BET (Brunauer- Emmet-Teller) and the t-plot method. The sulfur was quantified by elementary analysis using ANTEK 9000 NS. The adsorption process was evaluated as function of the temperature variation and initial sulfur content through the adsorption isotherm and its thermodynamic parameters. The parameters of entropy (ΔS), enthalpy variation (ΔH) and free Gibbs energy (ΔG) were calculated through the graph ln(Kd) versus 1/T. Langmuir, Freundlich and Langmuir-Freundlich models were adjusted to the experimental data, and the last one had presented better results. The thermodynamic tests were accomplished in different temperatures, such as 30, 40 and 50?C, where it was concluded the adsorption process is spontaneous and exothermic. The kinetic of adsorption was studied by 24 h and it showed that the capability adsorption to the adsorbents studied respect the following order: MoZnPO > MoPO > ZnPO > AlPO. The maximum adsorption capacity was 4.91 mg/g for MoZnPO with an adsorption efficiency of 49%.
As discuss?es sobre o problema da polui??o causada por emiss?es veiculares s?o antigas e v?m evoluindo com o passar do tempo. A procura por tecnologias mais limpas e as altera??es clim?ticas cada vez mais frequentes induziram as ind?strias e os ?rg?os governamentais a impor limites cada vez mais rigorosos para os teores de contaminantes nos combust?veis, os quais impactam diretamente nas emiss?es atmosf?ricas. Atualmente a forma de melhorar a qualidade dos combust?veis, quanto ao enxofre, ? atrav?s do processo de hidrodessulfuriza??o e recentemente, os processos de adsor??o tem se mostrado como uma alternativa bastante interessante ? remo??o de enxofre, pois tais processos s?o mais simples e operam a temperaturas e press?es atmosf?ricas. O presente trabalho contempla a s?ntese e caracteriza??o do aluminofosfato impregnado com zinco, molibd?nio ou ambos e sua aplica??o no estudo da remo??o de enxofre da gasolina atrav?s do processo de adsor??o, utilizando uma gasolina modelo contendo iso-octano e tiofeno. Os adsorventes foram caracterizados por difra??o de raios-X, an?lise termogravim?trica (ATG), fluoresc?ncia de raios-X e microscopia eletr?nica de varredura (MEV). A ?rea espec?fica, volume e di?metro de poros foram determinados pelo m?todo BET (Brunauer-Emmet-Teller) e m?todo t-plot. O enxofre foi quantificado por analise elementar atrav?s do ANTEK 9000 NS. O Processo de adsor??o foi avaliado em fun??o da varia??o da temperatura e da concentra??o inicial de enxofre atrav?s das isotermas de adsor??o e de seus par?metros termodin?micos. Os par?metros varia??o de entropia (ΔS), varia??o de entalpia (ΔH) e varia??o da energia livre de Gibbs (ΔG) foram calculados pelo gr?fico de ln(K) versus 1/T. Os modelos de Langmuir, Freundlich e Langmuir-Freundlich foram ajustados aos dados experimentais, tendo o ?ltimo apresentado os melhores resultados. Os testes termodin?micos foram realizados nas temperaturas de 30, 40, 50 ?C e constatou-se que o processo de adsor??o ? espont?neo e exot?rmico. A cin?tica da adsor??o foi estudada por 24 horas e mostrou que a capacidade de adsor??o para os adsorventes estudados segue a seguinte ordem: MoZnPO > MoPO > ZnPO > AlPO. A capacidade m?xima de adsor??o foi 4,91 mg/g para o MoZnPO com uma efici?ncia de adsor??o de 49%.
Platzer-Björkman, Charlotte. "Band Alignment Between ZnO-Based and Cu(In,Ga)Se2 Thin Films for High Efficiency Solar Cells." Doctoral thesis, Uppsala universitet, Fasta tillståndets elektronik, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6263.
Adler, Tobias [Verfasser], Andreas [Akademischer Betreuer] Klein, and Heinz von [Akademischer Betreuer] Seggern. "Zn(O,S) Puffer Eigenschaften in Cu(In,Ga)Se2 Solarzellen / Tobias Adler. Betreuer: Andreas Klein ; Heinz von Seggern." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2013. http://d-nb.info/1108094082/34.
Buffière, Marie. "Synthèse et caractérisation de couches minces de Zn (O,S) pour application au sein des cellules solaires à base de Cu (In, Ga) Se2." Nantes, 2011. http://www.theses.fr/2011NANT2057.
Thin film solar cell based on Cu(In,Ga)Se2 contain a thin, chemically deposited (CBD), cadmium sulfide (CdS) buffer layer. For environmental and industrial reasons, its replacement by a Cd-free material deposited under vacuum is among the challenges of the research community. In this work, co-sputtered (PVD)Zn(O,S) thin films have been studied as an alternative buffer layer. The properties of these layers have been compared to an optimized (CBD)Zn(O,S) reference. It is observed that the deposition technique has a strong impact on the optical and structural properties of the films for a given composition. As a result, the electrical behavior of the corresponding devices is also affected. The electrical characterization of (CBD)Zn(O,S)-buffered solar cells has shown that the absorber and the window layers properties strongly influence the performance of the cells. These progress together with the understanding of Zn(O,S) films properties makes it possible the realization of 16 % efficiency stable devices with a (CBD)Zn(O,S) buffer layer. Meanwhile, the tuning of the sulfur content has lead to the control of the conduction band offset in CIGSe/(PVD)Zn(O,S) devices and the achievement of similar Jsc than the one of (CBD)Zn(O,S)-buffered devices. Although the present structure of the (PVD)Zn(O,S) buffer layer is not suitable to obtain comparable Voc, these results offer many research perspectives in hetero-interface for a better understanding of Cu(In,Ga)Se2-based solar cells
Santos, Damilson Ferreira dos. "S?ntese e caracteriza??o de tensoativos e estudo de equil?brio de fase dos sistemas CnH2n+2/H2O/CnH2n+1COONa/But-OH." Universidade Federal do Rio Grande do Norte, 2014. http://repositorio.ufrn.br:8080/jspui/handle/123456789/15934.
Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior
The growing utilization of surfactants in several different areas of industry has led to an increase on the studies involving solutions containing this type of molecules. Due to its amphiphilic nature, its molecule presents one polar part and one nonpolar end, which easily interacts with other molecules, being able to modify the media properties. When the concentration in which its monomers are saturated, the airliquid system interface is reached, causing a decrease in interfacial tension. The surfactants from pure fatty acids containing C8, C12 and C16 carbonic chains were synthesized in an alcoholic media using sodium hydroxide. They were characterized via thermal analysis (DTA and DTG) and via infrared spectroscopy, with the intention of observing their purity. Physical and chemical properties such as superficial tension, critical micelle concentration (c.m.c), surfactant excess on surface and Gibbs free energy of micellization were determined in order to understand the behaviour of these molecules with an aqueous media. Pseudo-ternary phase diagrams were obtained aiming to limit the Windsor equilibria conditions so it could be possible to understand how the surfactants carbonic chain size contributes to the microemulsion region. Solutions with known concentrations were prepared to study how the surfactants can influence the dynamic light scattering spectroscopy (DLS) and how the diffusion coefficient is influenced when the media concentration is altered. The results showed the variation on the chain size of the studied surfactant lipophilic part allows the conception of surfactants with similar interfacial properties, but dependent on the size of the lipophilic part of the surfactant. This variation causes the surfactant to have less tendency of microemulsionate oil in water. Another observed result is that the n-alcanes molecule size promoted a decrease on the microemulsion region on the obtained phase diagrams
O crescente uso de tensoativos nas mais diferentes ?reas da ind?stria tem levado a um aumento nos estudos envolvendo solu??es contendo este tipo de mol?cula. Devido a sua natureza anfif?lica, sua mol?cula apresenta uma parte polar e outra apolar, que facilmente interage com outros tipos de mol?culas, podendo modificar as propriedades do meio. Quando a concentra??o, na qual seus mon?meros saturam, a interface do sistema ar-l?quido, ? atingida promovendo a redu??o da tens?o interfacial. Os tensoativos dos ?cidos graxos puros com cadeias carb?nicas C8, C12 e C16 foram sintetizados em meio alco?lico, utilizando hidr?xido de s?dio. Eles foram caracterizados por an?lise t?rmica (DTA e DTG) e espectroscopia de infravermelho com o objetivo de se observar a pureza dos mesmos. Foram determinadas algumas propriedades f?sicoqu?micas como: tens?o superficial, c.m.c. , excesso de tensoativo na interface e energia livre de Gibbs de miceliza??o a fim de se entender o comportamento das intera??es dessas mol?culas com meio aquoso. Foram elaborados diagramas de fase pseudotern?rios com o intuito de realizar as delimita??es do equil?brio de Winsor para compreender como o tamanho da cadeia carb?nica dos tensoativos contribui com a regi?o de microemuls?o. Preparou-se solu??es com concentra??es conhecidas para se estudar como os tensoativos podem influenciar a espectroscopia de espalhamento din?mico de luz (Dynamic Ligth Scattering - DLS) e como o coeficiente de difus?o ? influenciado quando a concentra??o do meio ? alterada. Os resultados mostraram que o aumento ou diminui??o do tamanho da cadeia da parte lipof?lica dos tensoativos estudados permite conceber tensoativos com propriedades interfaciais similares, mas tamb?m dependente do tamanho da parte lipof?lica do tensoativo. Esta varia??o deixa o tensoativo com menor tend?ncia a microemulsionar ?leo em ?gua. Outro resultado observado ? que o tamanho das mol?culas de n-alcanos promoveu uma redu??o da regi?o de microemuls?o dos diagramas de fases obtidos
Assis, Raimison Bezerra de. "S?ntese e caracteriza??o de ferrita ni-zn pelo m?todo dos precursores polim?ricos calcinada por energia de microondas." Universidade Federal do Rio Grande do Norte, 2013. http://repositorio.ufrn.br:8080/jspui/handle/123456789/12816.
Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior
Magnetic ceramics have been widely investigated, especially with respect to intrinsic and extrinsic characteristics of these materials. Among the magnetic ceramic materials of technological interest, there are the ferrites. On the other hand, the thermal treatment of ceramic materials by microwave energy has offered various advantages such as: optimization of production processes, high heat control, low consumption of time and energy among others. In this work were synthesized powders of Ni-Zn ferrite with compositions Ni1- xZnxFe2O4 (0.25 ≤ x ≤ 0.75 mols) by the polymeric precursor route in two heat treatment conditions, conventional oven and microwave energy at 500, 650, 800 and 950?C and its structural, and morphological imaging. The materials were characterized by thermal analysis (TG/ DSC), X-ray diffraction (XRD), absorption spectroscopy in the infrared (FTIR), scanning electron microscopy (SEM), X-ray spectroscopy and energy dispersive (EDS) and vibrating sample magnetometry (VSM). The results of X-ray diffraction confirmed the formation of ferrite with spinel-type cubic structure. The extrinsic characteristics of the powders obtained by microwave calcination and influence significantly the magnetic behavior of ferrites, showing particles ferrimagn?ticas characterized as soft magnetic materials (soft), is of great technological interest. The results obtained led the potential application of microwave energy for calcining powders of Ni-Zn ferrite
Cer?micas magn?ticas t?m sido amplamente investigadas, principalmente com rela??o as caracter?sticas intr?nsecas e extr?nsecas destes materiais. Dentre os materiais cer?micos magn?ticos de interesse tecnol?gico, destacam-se as ferritas. Por outro lado, o tratamento t?rmico de materiais cer?micos por energia de microondas tem oferecido diversas vantagens, tais como: otimiza??o dos processos de obten??o, alto controle de aquecimento, menor consumo de tempo e energia entre outras. Neste trabalho, foram sintetizados p?s de ferritas Ni-Zn com composi??es Ni1-xZnxFe2O4 (0,25 ≤ x ≤ 0,75 mols) pela rota dos precursores polim?ricos em duas condi??es de tratamento t?rmico, em forno convencional e por energia de microondas a 500, 650, 800 e 950?C, e sua caracteriza??o estrutural, morfol?gica e magn?tica. Os materiais obtidos foram caracterizados por an?lises t?rmicas (TG/DSC), difra??o de raios x (DRX), espectroscopia de absor??o na regi?o do infravermelho (FTIR), microscopia eletr?nica de varredura (MEV), espectroscopia de raios X por dispers?o de energia (EDS) e magnetometria de amostra vibrante (VSM). Os resultados da difra??o de raios X confirmaram a forma??o da ferrita com estrutura c?bica do tipo espin?lio. As caracter?sticas extr?nsecas dos p?s obtidos e a calcina??o por microondas influenciaram de forma significativa o comportamento magn?tico das ferritas, apresentando part?culas ferrimagn?ticas, caracterizadas como materiais magn?ticos moles (macias), sendo de grande interesse tecnol?gico. Os resultados obtidos induziram o potencial de aplica??o de energia de microondas para a calcina??o de p?s de ferritas Ni-Zn
Book chapters on the topic "Zn(S,O,OH)":
Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "(Zn,Cu)6Zn2(OH)13[(S,Si)(O,OH)4]2." In Structure Types. Part 9: Space Groups (148) R-3 - (141) I41/amd, 247. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02702-4_156.
Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "Na15Ca3(Mn,Fe)3Zr3(Zr,Na)3(Si,Nb)(S,Ti,Si)Si24O72(O,OH)5(Cl,F,H2O)." In Structure Types. Part 9: Space Groups (148) R-3 - (141) I41/amd, 442–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02702-4_311.
Chihara, H., and N. Nakamura. "NQRS Data for CoHO2 ; [Co(OH)O] ; (Subst. No. 1948)." In Substances Containing C10H16 … Zn, 813. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02943-1_683.
Fontboté, L., and H. Gorzawski. "Isotope (Sr, C. O, and S) Tracing of Diagenetic Ore Formation in Carbonate-Hosted Ore Deposits Illustrated on the F-(Pb-Zn) Deposits in the Alpujarrides, Spain and the San Vicente Zn-Pb Mine, Peru." In Mineral Deposits within the European Community, 465–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-51858-4_25.
"Systems with four chemical elements. Ac-H-O-P to B-O-S-Zn." In Handbook, 712–76. De Gruyter, 2011. http://dx.doi.org/10.1515/9783110268935.712.
West, Amy E., Sally M. Weinstein, and Mani N. Pavuluri. "Family Problem Solving." In RAINBOW, 77–80. Oxford University Press, 2017. http://dx.doi.org/10.1093/med-psych/9780190609139.003.0010.
Schweitzer, George K., and Lester L. Pesterfield. "The Oxygen Group." In The Aqueous Chemistry of the Elements. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195393354.003.0012.
"a) Hal/OH-Acetale." In Hal/O(S,N)-, S/S(N)-, N/N-Acetale : Hal/O-, O/O-Acetale als anomere Zentren von Kohlenhydraten, edited by Hermann Hagemann and Dieter Klamann. Stuttgart: Georg Thieme Verlag, 1992. http://dx.doi.org/10.1055/b-0035-111877.
Chemla, F., F. Ferreira, and B. Roy. "OH/SR Acetals." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00712.
Chemla, F., F. Ferreira, and B. Roy. "OH/SOR Acetals." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00754.
Conference papers on the topic "Zn(S,O,OH)":
Gonzalez-Chan, I. J., and A. I. Oliva. "Chemical bath deposited Zn(S, OH, O) films near room temperature: Physicochemical considerations." In 2016 13th International Conference on Electrical Engineering, Computing Science and Automatic Control (CCE). IEEE, 2016. http://dx.doi.org/10.1109/iceee.2016.7751191.
Oliveri, R. L., R. Inguanta, G. Ferrara, S. Piazza, C. Sunseri, A. Parisi, L. Curcio, G. Adamo, A. C. Cino, and A. C. Busacca. "CuInSe2/Zn(S,O,OH) junction on Mo foil by electrochemical and chemical route for photovoltaic applications." In 2014 Fotonica AEIT Italian Conference on Photonics Technologies (Fotonica AEIT). IEEE, 2014. http://dx.doi.org/10.1109/fotonica.2014.6843915.
Sozzi, Giovanna, Simone Di Napoli, Matteo Enna, Roberto Menozzi, Dimitrios Hariskos, and Wolfram Witte. "Numerical simulation of CIGS solar cells with Zn(O,S) or (Cd,Zn)S buffers and (Zn,Mg)O as high-resistive layer." In 2019 IEEE 46th Photovoltaic Specialists Conference (PVSC). IEEE, 2019. http://dx.doi.org/10.1109/pvsc40753.2019.8980882.
Tolstova, Yulia, Stefan T. Omelchenko, Raymond E. Blackwell, Amanda M. Shing, and Harry A. Atwater. "Cu2O photovoltaic devices incorporating Zn(O, S) buffer layers." In 2016 IEEE 43rd Photovoltaic Specialists Conference (PVSC). IEEE, 2016. http://dx.doi.org/10.1109/pvsc.2016.7750170.
Hildebrandt, Thibaud, Nicolas Loones, Muriel Bouttemy, Jackie Vigneron, Arnaud Etcheberry, Daniel Lincot, and Negar Naghavi. "Search for new bath formulations Of Zn(S, O, OH) buffer layer to outperform record performances Of CdS-based CIGSe solar cells." In 2013 IEEE 39th Photovoltaic Specialists Conference (PVSC). IEEE, 2013. http://dx.doi.org/10.1109/pvsc.2013.6744336.
Kushiya, Katsumi, Y. Tanaka, H. Hakuma, Y. Goushi, S. Kijima, T. Aramoto, Y. Fujiwara, et al. "Improvement of the Interface Quality Between Zn(O,S,OH)x Buffer and Cu(InGa)(SeS)2 Surface Layers to Enhance the Fill Factor over 0.700." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1123-p07-01.
Hildebrandt, T., N. Loones, M. Bouttemy, J. Vigneron, A. Etcheberry, D. Lincot, and N. Naghavi. "Towards a better understanding of the use of additives in Zn(S,O,OH) deposition bath for high efficiency Cu(In,Ga)Se2-based solar cells." In 2015 IEEE 42nd Photovoltaic Specialists Conference (PVSC). IEEE, 2015. http://dx.doi.org/10.1109/pvsc.2015.7355625.
Wiren, Z. Q., H. Kepa, C. M. Brown, J. Leao, S. Kolesnik, B. Dabrowski, J. K. Furdyna, and T. M. Giebultowicz. "Studies of intrinsic exchange interactions in Zn(Mn)O, Zn(Mn)S and Zn(Mn)Te at 4 kbar by inelastic neutron scattering." In PHYSICS OF SEMICONDUCTORS: 28th International Conference on the Physics of Semiconductors - ICPS 2006. AIP, 2007. http://dx.doi.org/10.1063/1.2730327.
Klenk, Reiner, Paul Gerhardt, Iver Lauermann, Alexander Steigert, Frederick Stober, Frank Hergert, Siegmund Zweigart, and Martha Ch Lux-Steiner. "Design, preparation and performance of Cu(In, Ga)(S, Se)2/Zn(O, S)/ZnO:Al solar cells." In 2013 IEEE 39th Photovoltaic Specialists Conference (PVSC). IEEE, 2013. http://dx.doi.org/10.1109/pvsc.2013.6744279.
Arredondo, Carlos Andres, William Vallejo, Johann Hernandez, and Gerardo Gordillo. "In(O,OH)S/AgInS2 absorbent layer/buffer layer system for thin film solar cells." In 2012 IEEE 38th Photovoltaic Specialists Conference (PVSC). IEEE, 2012. http://dx.doi.org/10.1109/pvsc.2012.6317986.
Reports on the topic "Zn(S,O,OH)":
Kidder, J. A., M. B. McClenaghan, M I Leybourne, M. W. McCurdy, P. Pelchat, D. Layton-Matthews, C. E. Beckett-Brown, and A. Voinot. Geochemical data for stream and groundwaters around the Casino Cu-Au-Mo porphyry deposit, Yukon (NTS 115 J/10 and 115 J/15). Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/328862.
Kontak, D. J., S. Paradis, Z. Waller, and M. Fayek. Petrographic, fluid inclusion, and secondary ion mass spectrometry stable isotopic (O, S) study of Mississippi Valley-type mineralization in British Columbia and Alberta. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/327994.