Academic literature on the topic 'Silicate glasse'
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Journal articles on the topic "Silicate glasse"
Pan, Qun, Bin Zhu, Xiao Huang, and Lin Liu. "Properties of Alkli-Activated Slag Cement Compounded with Soluble Glasses with a High Silicate Modulus." Advanced Materials Research 712-715 (June 2013): 905–8. http://dx.doi.org/10.4028/www.scientific.net/amr.712-715.905.
Full textMöncke, Doris, Brian Topper, and Alexis G. Clare. "Glass as a State of Matter—The “newer” Glass Families from Organic, Metallic, Ionic to Non-silicate Oxide and Non-oxide Glasses." Reviews in Mineralogy and Geochemistry 87, no. 1 (May 1, 2022): 1039–88. http://dx.doi.org/10.2138/rmg.2022.87.23.
Full textRamamurthy, Sundar, Brian C. Hebert, and C. Barry Carter. "Olivine-MgO interfaces produced by crystallization of glass fulms on single-crystal MgO substrates." Proceedings, annual meeting, Electron Microscopy Society of America 53 (August 13, 1995): 342–43. http://dx.doi.org/10.1017/s0424820100138087.
Full textYanina, Svetlana V., Matthew T. Johnson, Zhigang Mao, and C. Barry Carter. "On Devitrification of Monticellite (CaMgSiO4) Films Grown on (001)-Oriented Single-Crystal MgO." Microscopy and Microanalysis 4, S2 (July 1998): 590–91. http://dx.doi.org/10.1017/s1431927600023072.
Full textVaiborisut, Napaporn, Chanittha Chunwises, Dararat Boonbundit, Sirithan Jiemsirilers, and Apirat Theerapapvisetpong. "Effect of the Addition of ZrSiO4 on Alkali-Resistance and Liquidus Temperature of Basaltic Glass." Key Engineering Materials 766 (April 2018): 145–50. http://dx.doi.org/10.4028/www.scientific.net/kem.766.145.
Full textVaisman, Ya I., I. S. Glushankova, Yu A. Ketov, L. V. Rudakova, and M. P. Krasnovskikh. "Recovery of Sulfur-Alkaline Waste by Processing into Cellular Silicate Material." Ecology and Industry of Russia 22, no. 10 (October 5, 2018): 24–27. http://dx.doi.org/10.18412/1816-0395-2018-10-24-27.
Full textda Silva, Antônio Carlos, S. C. Santos, and Sonia Regina Homem de Mello-Castanho. "Transition Metals in Glass Formation." Materials Science Forum 727-728 (August 2012): 1496–501. http://dx.doi.org/10.4028/www.scientific.net/msf.727-728.1496.
Full textSaakyan, Emma, Artavazd Arzumanyan, and Gagik Galstyan. "New Energy Efficient Technology of Cellular Glass." Key Engineering Materials 828 (December 2019): 146–52. http://dx.doi.org/10.4028/www.scientific.net/kem.828.146.
Full textChen, Lu, and Ying Dai. "Effects of Iron Oxide on the Crystallization of Calcium Alumino-Silicate Glass." Key Engineering Materials 680 (February 2016): 293–96. http://dx.doi.org/10.4028/www.scientific.net/kem.680.293.
Full textLu, An Xian, S. J. Liu, X. D. Tang, and S. B. He. "Difference of Properties between Yb3+-Doped Silicate and Phosphate Laser Glasses." Advanced Materials Research 11-12 (February 2006): 213–16. http://dx.doi.org/10.4028/www.scientific.net/amr.11-12.213.
Full textDissertations / Theses on the topic "Silicate glasse"
Gaddam, Anuraag. "Structure and crystallization of multicomponent lithium silicate glasses." Doctoral thesis, Universidade de Aveiro, 2017. http://hdl.handle.net/10773/21819.
Full textA presente tese tem como objetivo adquirir uma compreensão aprofundada acerca do processo de cristalização de vidros à base de silicato de lítio com a adição de pequenas quantidades de outros componentes. Os principais componentes investigados neste estudo são os óxidos de Mn, Al, B e P. Estudaram-se os efeitos de cada um destes componentes na estrutura do vidro, na separação de fases líquido-líquido, nos processos de nucleação e crescimento de cristais, na microestrutura e no conjunto das fases cristalinas formadas. Os vitro-cerâmicos utilizados neste estudo são produzidos a partir de amostras tridimensionais de vidro fundido e vertido em moldes, ou a partir de pós de frita obtida por arrefecimento dos fundidos em água. A adição de óxidos de Mn aos vidros de silicato de lítio resulta na criação de entidades moleculares individuais de Mn. Por conseguinte, estas entidades moleculares dificultam o todo o processo de cristalização do vidro. Óxidos de Al e B são incorporados na rede de vidro como formadores de rede. Estes componentes, por conseguinte, também diminuem a tendência do vidro para a cristalização. O P2O5 também desempenha um papel de formador de rede do vidro. No entanto, ele aumenta a tendência do vidro para a cristalização. Dá-se uma ênfase especial ao estabelecimento de correlações entre a estrutura do vidro e seu comportamento na cristalização. Estes esforços levaram à introdução de um novo modelo matemático baseado na mecânica estatística para descrever a estrutura de vidro. O modelo foi desenvolvido principalmente para silicatos binários e mais tarde estendido para composições de silicatos multicomponentes.
The present thesis is aimed at gaining an in-depth understanding of the crystallization process in multicomponent lithium silicate based glasses when other components are added in small amounts. The added components investigated in this study are oxides of Mn, Al, B and P. The effects of each of these components on glass structure, liquid-liquid phase separation, crystal nucleation, crystal growth, microstructure and phase assemblage are studied. The glass ceramics used in this study are produced by both bulk glasses obtained by melt quenching as well as by powder methods from glass frits. Oxides of Mn when added to lithium silicate glasses result in creating individual Mn molecular entities. Consequently, these molecular entities hinder the overall crystallization ability of the glass. Oxides of Al and B are incorporated into glass network as network formers. These components consequently decrease the overall crystallization ability of the glass. P2O5 is also incorporated into glass network as network former. However, it increases the overall crystallization ability of the glass. Particular emphasis is given to establishing correlations between glass structure and its corresponding crystallization behaviour. These efforts led to introducing a new mathematical model based on statistical mechanics for describing the glass structure. The model was primarily developed for binary silicates and later on extended to multicomponent silicates.
Goel, Ashutosh. "Clinopyroxene based glasses and glass-ceramics for functional applications." Doctoral thesis, Universidade de Aveiro, 2009. http://hdl.handle.net/10773/2323.
Full textAs piroxenas são um vasto grupo de silicatos minerais encontrados em muitas rochas ígneas e metamórficas. Na sua forma mais simples, estes silicatos são constituídas por cadeias de SiO3 ligando grupos tetrahédricos de SiO4. A fórmula química geral das piroxenas é M2M1T2O6, onde M2 se refere a catiões geralmente em uma coordenação octaédrica distorcida (Mg2+, Fe2+, Mn2+, Li+, Ca2+, Na+), M1 refere-se a catiões numa coordenação octaédrica regular (Al3+, Fe3+, Ti4+, Cr3+, V3+, Ti3+, Zr4+, Sc3+, Zn2+, Mg2+, Fe2+, Mn2+), e T a catiões em coordenação tetrahédrica (Si4+, Al3+, Fe3+). As piroxenas com estrutura monoclínica são designadas de clinopiroxenes. A estabilidade das clinopyroxenes num espectro de composições químicas amplo, em conjugação com a possibilidade de ajustar as suas propriedades físicas e químicas e a durabilidade química, têm gerado um interesse mundial devido a suas aplicações em ciência e tecnologia de materiais. Este trabalho trata do desenvolvimento de vidros e de vitro-cerâmicos baseadas de clinopiroxenas para aplicações funcionais. O estudo teve objectivos científicos e tecnológicos; nomeadamente, adquirir conhecimentos fundamentais sobre a formação de fases cristalinas e soluções sólidas em determinados sistemas vitro-cerâmicos, e avaliar a viabilidade de aplicação dos novos materiais em diferentes áreas tecnológicas, com especial ênfase sobre a selagem em células de combustível de óxido sólido (SOFC). Com este intuito, prepararam-se vários vidros e materiais vitro-cerâmicos ao longo das juntas Enstatite (MgSiO3) - diopsídio (CaMgSi2O6) e diopsídio (CaMgSi2O6) - Ca - Tschermak (CaAlSi2O6), os quais foram caracterizados através de um vasto leque de técnicas. Todos os vidros foram preparados por fusão-arrefecimento enquanto os vitro-cerâmicos foram obtidos quer por sinterização e cristalização de fritas, quer por nucleação e cristalização de vidros monolíticos. Estudaram-se ainda os efeitos de várias substituições iónicas em composições de diopsídio contendo Al na estrutura, sinterização e no comportamento durante a cristalização de vidros e nas propriedades dos materiais vitro-cerâmicos, com relevância para a sua aplicação como selantes em SOFC. Verificou-se que Foi observado que os vidros/vitro-cerâmicos à base de enstatite não apresentavam as características necessárias para serem usados como materiais selantes em SOFC, enquanto as melhores propriedades apresentadas pelos vitro-cerâmicos à base de diopsídio qualificaram-nos para futuros estudos neste tipo de aplicações. Para além de investigar a adequação dos vitro-cerâmicos à base de clinopyroxene como selantes, esta tese tem também como objetivo estudar a influência dos agentes de nucleação na nucleação em volume dos vitro-cerâmicos resultantes á base de diopsídio, de modo a qualificá-los como potenciais materiais hopedeiros de resíduos nucleares radioactivos.
The pyroxenes are a wide spread group rock-forming silicate minerals found in many igneous and metamorphic rocks. They are silicates that, in their simplest form, contain single SiO3 chains of linked SiO4 tetrahedra. The general chemical formula for pyroxenes is M2M1T2O6, where M2 refers to cations in a generally distorted octahedral coordination (Mg2+, Fe2+, Mn+, Li+, Ca2+, Na+), M1 to cations in a regular octahedral coordination (Al3+, Fe3+, Ti4+, Cr3+, V3+, Ti3+, Zr4+, Sc3+, Zn2+, Mg2+, Fe2+, Mn2+), and T to tetrahedrally coordinated cations (Si4+, Al3+, Fe3+). Monoclinic pyroxenes are called clinopyroxenes. The stability of clinopyroxenes over a broad spectrum of chemical compositions, in conjunction with the possibility of achieving desired physical properties and high chemical durability, has generated a worldwide interest due to their applications in material science and technology. The present work deals with the development of clinopyroxene based glasses and glass-ceramics for functional applications. The objective of the study was dual, both scientific and technological; particularly to gain fundamental knowledge on the formation of crystalline phases and solid solutions in selected glass-ceramic systems, and to evaluate the feasibility for application of new materials in different technological areas with emphasis on sealing in solid oxide fuel cells (SOFC). In this pursuit, various glasses and glass-ceramics along Enstatite (MgSiO3) - Diopside (CaMgSi2O6) and Diopside (CaMgSi2O6) – Ca – Tschermak (CaAlSi2O6) joins have been prepared and characterized by a wide array of characterization techniques. All the glasses were prepared by melt-quenching technique while glass-ceramics were produced either by sintering and crystallization of glass powders or by nucleation and crystallization in monolithic glasses. Furthermore, influence of various ionic substitutions/additions in Alcontaining diopside on the structure, sintering and crystallization behaviour of glasses and properties of resultant glass-ceramics has been investigated, in relevance with final application as sealants in SOFC. It has been observed that enstatite based glasses/glass-ceramics do not exhibit requisite characteristics in order to qualify for the job of sealing in SOFC while the superior properties exhibited by diopside based glass-ceramics qualify them for further experimentation as SOFC sealants. Apart from investigating the suitability of clinopyroxene based glass-ceramics as sealants, this thesis also aims to study the influence of nucleating agents on the volume nucleation in the resultant diopside based glass-ceramics so as to qualify them for further experimentation as hosts for radioactive nuclear wastes.
Scannell, Garth. "Understanding the structure and deformation of titanium-containing silicate glasses from their elastic responses to external stimuli." Thesis, Rensselaer Polytechnic Institute, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10158591.
Full textThe responses of structure and properties to composition and temperature have been investigated for glasses in TiO2-SiO2 and Na2O-TiO2-SiO2 systems. Additionally, the response of Na2O-TiO2-SiO2 glasses to plastic deformation has been studied. (x)TiO2-(1-x)SiO2 glasses were prepared through the sol-gel process with compositions 0 ≤ x ≤ 10 mol% and compared to commercial glasses prepared through flame hydrolysis deposition with x = 0, 5.4, and 8.3 mol%. (x) Na2O - (y) TiO 2 - (1-x-y) SiO2 glasses were prepared with x = 10, 15, 20, and 25 mol% and y = 4, 7, and 10 mol% through a melt-quench process. Density and index of refraction of glasses was measured through the Archimedes's method and using a prism coupler, respectively. The glass transition temperature of Na2O-TiO2-SiO2 glasses was measured through differential thermal analysis.
The structure and elastic moduli have been studied through Raman spectroscopy and Brillouin light scattering, respectively, at room temperature and in-situ up to 1200 °C for TiO2-SiO2 glasses and up to 800 °C for Na2O-TiO2-SiO2 glasses. Young's modulus was observed to decrease from 72 GPa to 66 GPa with the addition of 8.3 mol% TiO2 in TiO2-SiO2 glasses and to increase from 65 GPa to 73 GPa with the addition of 10 mol% TiO2 in 10 Na2O - (0-10) TiO2-SiO2 glasses. The addition of TiO2 was observed to shift the 460, 490, and 600 cm-1 Raman peaks to lower frequencies in TiO2-SiO2 glasses, suggesting a more open and flexible network, and the 720, 800, and 840 cm -1 Raman peaks to higher frequencies in Na2O-TiO2 -SiO2 glasses, suggesting a lower free volume and stiffer network. The addition of TiO2 has little effect on the temperature response of the elastic moduli in either system, but decreases the thermal expansion and increases the frequency shifts in the 950 and 1100 cm -1 Raman peaks in the TiO2-SiO2 system while the thermal expansion increases with initial additions of TiO2 and then remains constant in the Na2O-TiO2-SiO 2 system.
Changes in structure and property with composition have been discussed, and structural models were proposed. The reduction of thermal expansion and elastic moduli in TiO2-SiO2 glasses occurs through the promotion of cooperative, inter-tetrahedral rotations facilitated by the longer and weaker Ti-O bonds. The increase in elastic moduli in the Na2O-TiO 2-SiO2 glasses occurs through the formation of small clusters with local, relatively high Ti and Na concentrations, promoted by Ti adopting a five-fold coordination in a square-pyramidal geometry. These clusters work to shield the silica network from non-bridging oxygens from the presence of Na while simultaneously increasing the volume bond density of the glass.
For Na2O-TiO2-SiO2 glasses, the response to mechanical damage and plastic deformation has been examined through Vickers indentation experiments at loads from 10 mN to 49 N. Fracture toughness was measured through the single-edge precracked beam method. The permanent deformation volumes around Vickers indents were investigated through atomic force microscopy. Critical loads for crack initiation and cracking patterns were systematically investigated and correlated with the elastic properties of glass. Vickers indents were observed to change from a mixture of radial/median and cone cracks to radial/median and lateral cracks as Poisson's ratio increases. As Poisson's ratio increases hardness decreases from 5.5 GPa to 4.5 GPa, the average radial/median crack length roughly doubles, and fracture toughness remains constant. A minimum in the critical crack initiation load was observed at ν = 0.21–0.22. The volume of glass deformed through shear flow during indentation increases gradually with increasing Poisson's ratio, becomes larger than the densified volume at ν = 0.237. The densified volume increases between ν = 0.18 and ν = 0.21 and decreases rapidly from 16.5 µm3 to 8.7 µm3 at ν = 0.235–0.237. A correlation between the minimum in crack initiation load and the change in deformation mechanisms over the same Poisson’s ratio range was observed.
Meng, Ji Xing. "Contribution to the modeling of densification in silicate glasses under very high pressures." Thesis, Rennes 1, 2013. http://www.theses.fr/2013REN1S116/document.
Full textHigh-pressure behavior of SiO2 glass has been studied extensively because it has attracted considerable attention in various fields of mechanical and physical sciences, such as non-linear mechanics, high-pressure physics, noncrystalline physics, applied physics, geophysics, etc. Permanent densification is the most fundamental property obtained from very high pressure. We discuss a constitutive model describing the permanent densification induced deformation mechanism of silica. The constitutive law is assumed to be pure hydrostatic pressure, and uses a yield function and a flow rule describing the evolution of permanent strains after initial densification, and three hardening rules discussing the dependence of the incremental densification on the levels of applied stresses. Ex-situ and in-situ experiments are both considered to evaluate our model. Implementing our model to a finite software Abaqus and a corotational framework software SiDoLo, inverse analysis is used to determine the threshold densification pressure, the saturate densification pressure and the saturate value of densification. Numerical results show an excellent agreement to experimental data. It should be noted that our model not only succeeding in determine the densification properties, but also in predicting the changes of elastic properties, such as Bulk modulus, Shear modulus, Young’s modulus and Poisson’s ratio, under hydrostatic pressure. Seen in perspective, our model provides a new rule to analyze the deformation behavior of silica under complex stress states
Medina, Francelys A. Lanagan Michael Thomas. "Impedance spectroscopy studies of silica-titania glasses and glass-ceramics." [University Park, Pa.] : Pennsylvania State University, 2009. http://etda.libraries.psu.edu/theses/approved/PSUonlyIndex/ETD-4566/index.html.
Full textBarker, Michael Francis. "Crystallization of lithium alumino-silicate glasses and the formation of photomachinable glass ceramics of controlled thermal expansion." Thesis, University of Sheffield, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362506.
Full textDamart, Tanguy. "Energy dissipation in oxide glasses." Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE1189/document.
Full textThe origin of sound attenuation at low and high frequency in glasses stays elusive mainly because of the complex temperature and frequency dependence of the phenomena at its root. Indeed, the presence of complex structures and multi-scale organizations in glasses induce the existence of relaxation time ranging from the second to the femto-second and of spatial correlation ranging from the Angström to a hundred nanometers. At low-frequency, a better understanding of the phenomena at the origin of dissipation would be beneficial to several applications. For example, the multi-layers coating the mirrors of gravitational waves detectors consists of a superposition of two oxide glasses: silicate (SiO2) and tantalum pentoxide (Ta2O5), are an important source of dissipation. At high frequency, the study of dissipation raises theoretical questions about the link between attenuation and dissipation as well as between loclt asymmetry and dissipation. In the present study, we conducted an analysis of the interaction between mechanical waves and the structure of two oxide glasses using simulation techniques such as non-equilibrium molecular dynamics. At high-frequencies, we implemented and used mechanical spectroscopy to measure dissipation numerically and performed in parallel an analytical development based on the projection of the atomic motion on the vibrational eigenmodes. At low-frequencies, we used molecular dynamics to gather sets of thermally activated events that we classed in three categories based on topologically distinct atomic motions and from which we predicted dissipation numerically using a refreshed TLS model
SILVA, ANTONIO C. da. "Incorporacao de residuo galvanico em vidro silicato obtido a partir de finos de silica." reponame:Repositório Institucional do IPEN, 2004. http://repositorio.ipen.br:8080/xmlui/handle/123456789/11223.
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Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP
Twyman, Helen Louise. "Structural characterisation of silicate and phosphate glasses." Thesis, University of Kent, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534329.
Full textReid, William B. "The electrical characteristics of lithium silicate glasses." Thesis, University of Aberdeen, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328008.
Full textBooks on the topic "Silicate glasse"
Mysen, B. O. Structure and properties of silicate melts. Amsterdam: Elsevier, 1988.
Find full textWebb, Sharon L. Silicate melts: With 33 figures. Berlin: Springer, 1997.
Find full textFarwell, Stebbins Jonathan, McMillan Paul Francis 1955-, and Dingwell D. B, eds. Structure, dynamics, and properties of silicate melts. Washington, D.C: Mineralogical Society of America, 1995.
Find full textMazurin, Oleg Vsevolodovich. Ternary non-silicate glasses. Amsterdam: Elsevier, 1991.
Find full textPascal, Richet, ed. Silicate glasses and melts: Properties and structure. Boston, Mass: Elsevier, 2005.
Find full textP, Ryan Michael. The viscosity of synthetic and natural silicate melts and glasses at high temperatures and 1 bar (10⁵ Pascals) pressure and at higher pressures. Washington, DC: U.S. Dept. of the Interior, 1987.
Find full textP, Ryan Michael. The viscosity of synthetic and natural silicate melts and glasses at high temperatures and 1 bar (10p5s. [Reston, Va.?]: Dept. of the Interior, U.S. Geological Survey, 1987.
Find full textP, Ryan Michael. The viscosity of synthetic and natural silicate melts and glasses at high temperatures and 1 bar (10⁵ Pascals) pressure and at higher pressures. [Washington]: U.S. G.P.O., 1987.
Find full textVladimirovna, Strelʹt͡s︡ina Marina, and Shvaĭko-Shvaĭkovskai͡a︡ Tatʹi͡a︡na Pavlovna, eds. Single-component and binary non-silicate oxide glasses. Amsterdam: Elsevier, 1985.
Find full textThe structure of binary alkali silicate melts. Åbo: Åbo akademi, 1985.
Find full textBook chapters on the topic "Silicate glasse"
James, Peter F. "Volume Nucleation in Silicate Glasses." In Glasses and Glass-Ceramics, 59–105. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0817-8_3.
Full textWallenberger, F. T. "Structural Silicate and Silica Glass Fibers." In Advanced Inorganic Fibers, 129–68. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4419-8722-8_6.
Full textLe Losq, Charles, Maria Rita Cicconi, G. Neville Greaves, and Daniel R. Neuville. "Silicate Glasses." In Springer Handbook of Glass, 441–503. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-93728-1_13.
Full textVogel, Werner. "Structural Elements of Silicates." In Glass Chemistry, 34–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78723-2_3.
Full textGarofalini, Stephen H. "5. Molecular Dynamics Simulations of Silicate Glasses and Glass Surfaces." In Molecular Modeling Theory, edited by Randall T. Cygan and James D. Kubicki, 131–68. Berlin, Boston: De Gruyter, 2001. http://dx.doi.org/10.1515/9781501508721-008.
Full textDe La Rocha, Christina, and Daniel J. Conley. "Glass Houses and Nanotechnology." In Silica Stories, 69–93. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-54054-2_5.
Full textDeCarlo, Keith J., Thomas F. Lam, and William M. Carty. "Dissolution of Alumina in Silicate Glasses and the Glass Formation Boundary." In Ceramic Transactions Series, 61–69. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470599730.ch7.
Full textHambardzumyan, A. G., G. A. Kraveckiy, and V. V. Rodionova. "Glass-Silicide Coverings." In Ceramic Transactions Series, 249–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118405949.ch23.
Full textDavila, Lilian P., Subhash H. Risbud, and James F. Shackelford. "Quartz and Silicas." In Ceramic and Glass Materials, 71–86. Boston, MA: Springer US, 2008. http://dx.doi.org/10.1007/978-0-387-73362-3_5.
Full textTulyaganov, Dilshat, and Francesco Baino. "Silicate Glasses and Glass–Ceramics: Types, Role of Composition and Processing Methods." In PoliTO Springer Series, 119–52. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-85776-9_4.
Full textConference papers on the topic "Silicate glasse"
Miniscalco, William J. "Materials for Erbium-Doped Fiber Amplifiers." In Optical Amplifiers and Their Applications. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oaa.1991.wd1.
Full textEssid, M., M. Verhaegen, L. B. Allard, J. L. Brebner, and J. Albert. "Ion Implantation Induced Photosensitivity in Silica and Ge-Doped Silica." In Photosensitivity and Quadratic Nonlinearity in Glass Waveguides. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/pqn.1995.sub.16.
Full textJacquier, B., and R. M. Macfarlane. "A Comparison of Spectral Holeburning in Fluoride and Silicate Glasses Doped With Nd3+." In Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.tub32.
Full textKulikov, S., J. P. Galaup, F. Chaput, and J. P. Boilot. "Hole-burning and site selection spectroscopy of porphyrins in various sol-gel matrices." In Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.mb15.
Full textKulikov, S., J. P. Galaup, F. Chaput, and J. P. Boilot. "Hole-burning and site selection spectroscopy of porphyrins in various sol-gel matrices." In Spectral Hole-Burning and Luminescence Line Narrowing: Science and Applications. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/shbl.1992.tub15.
Full textImai, Hiroaki, Suguru Horinouchi, Naoko Asakuma, Kazuhiro Fukao, Daizaburo Matsuki, Hiroshi Hiroshima, and Keisuke Sasaki. "Effects of doping of H2O and Na on second-order nonlinearity in poled silica glass." In Bragg Gratings, Photosensitivity, and Poling in Glass Fibers and Waveguides. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/bgppf.1997.bmg.6.
Full textBelostotsky, V. I. "Ion-exchange processes in silicate glasses: the role of oxygen." In Bragg Gratings, Photosensitivity, and Poling in Glass Fibers and Waveguides. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/bgppf.1997.jsue.40.
Full textHirao, K. "Writing Waveguides and Gratings in Silica and Related Materials by Femto-Second Laser." In Bragg Gratings, Photosensitivity, and Poling in Glass Fibers and Waveguides. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/bgppf.1997.btub.4.
Full textGlebov, L., L. Glebova, M. G. Moharam, K. Richardson, and V. Smirnov. "Volume grating recording in fluorinated silicate glasses." In Bragg Gratings, Photosensitivity, and Poling in Glass Fibers and Waveguides. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/bgppf.1997.jsue.11.
Full textJackel, J. L., A. Yi-Yan, E. M. Vogel, A. Von Lehmen, J. J. Johnson, E. Snitzer, and A. Nestorowicz. "Guided blue and green upconversion fluorescence in an erbium-and-ytterbium-containing silicate glass." In Integrated Photonics Research. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/ipr.1991.wc6.
Full textReports on the topic "Silicate glasse"
Adelstein, N., and V. Lordi. Comparison of Atomic and Electronic Structures of Silica and Sodium Silicate Glasses. Office of Scientific and Technical Information (OSTI), October 2014. http://dx.doi.org/10.2172/1178383.
Full textMueller, H., and L. M. Perle. Long lifetime silicate laser glass compositions. Office of Scientific and Technical Information (OSTI), August 1985. http://dx.doi.org/10.2172/6730599.
Full textSwarts, E. L. Glass science tutorial lecture {number_sign}6: The melting of silicate glasses, a review of selected topics. Office of Scientific and Technical Information (OSTI), March 1995. http://dx.doi.org/10.2172/52749.
Full textStolper, Edward. Infrared Spectroscopy and Stable Isotope Geochemistry of Hydrous Silicate Glasses. Office of Scientific and Technical Information (OSTI), March 2007. http://dx.doi.org/10.2172/900289.
Full textEpstein, S., and E. Stolper. Infrared spectroscopy and hydrogen isotope geochemistry of hydrous silicate glasses. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/5676215.
Full textTrifumcac, Alexander D. Radiation Effects on Transport and Bubble Formation in silicate Glasses. Office of Scientific and Technical Information (OSTI), June 1999. http://dx.doi.org/10.2172/829924.
Full textTrifunac, A. D., I. A. Shkrob, and D. W. Werst. Radiation Effects on Transport and Bubble Formation in Silicate Glasses. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/829925.
Full textTrifunac, A. D., I. A. Shkrob, and D. W. Werst. Radiation Effects on Transport and Bubble Formation in Silicate Glasses. Office of Scientific and Technical Information (OSTI), December 2001. http://dx.doi.org/10.2172/829926.
Full textWereszczak, Andrew A., Ethan E. Fox, Timothy G. Morrissey, and Daniel J. Vuono. Low Velocity Sphere Impact of a Soda Lime Silicate Glass. Office of Scientific and Technical Information (OSTI), October 2011. http://dx.doi.org/10.2172/1026738.
Full textEpstein, S., and E. Stolper. Infrared spectroscopy and hydrogen isotope geochemistry of hydrous silicate glasses. Progress report. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/10125268.
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