118 research outputs found
Thermal strengthening of lowâexpansion glasses and thinâwalled glass products by ultraâfast heat extraction
Thermal strengthening remains the primary method for enhancing the practical strength of commodity glass products, however, the process is limited in terms of applicable glass thickness and coefficient of thermal expansion. The primary reasons for this limitation are the achievable heat transfer coefficient when using conventional gas cooling, and the occurrence of transient surface tension in the early stages of rapid quenching. We revisit this problem for the case of thin borosilicate glass sheet. Using liquid gallium as the cooling medium, ultraâfast heat extraction is achieved, with a heat transfer coefficient exceeding 5000 Wm â2 K â1 . The low vapor pressure of gallium even at high temperatures enables preheating to a wide range of sheet entrant temperatures. We demonstrate thermal strengthening of lowâexpansion borosilicate glass with persistent surface compression of up to 85 MPa, and quenching to a fictive temperature of ~190 K above the glass transition temperature. Glass sheet obtained in this way exhibits notably enhanced surface defect resistance to sharp indentation. In addition to thermal strengthening, the extraordinarily high heat extraction rates achieved by liquid metal immersion enable exploitation of highâ T f glass properties beyond small and thin sample geometry
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Mid-infrared laser sensors for mapping environment and combustions
[no abstract available
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Controlling Growth of Poly (Triethylene Glycol Acrylate-Co-Spiropyran Acrylate) Copolymer Liquid Films on a Hydrophilic Surface by Light and Temperature
A quartz crystal microbalance with dissipation monitoring (QCM-D) was employed for in situ investigations of the effect of temperature and light on the conformational changes of a poly (triethylene glycol acrylate-co-spiropyran acrylate) (P (TEGA-co-SPA)) copolymer containing 12â14% of spiropyran at the silicaâwater interface. By monitoring shifts in resonance frequency and in acoustic dissipation as a function of temperature and illumination conditions, we investigated the evolution of viscoelastic properties of the P (TEGA-co-SPA)-rich wetting layer growing on the sensor, from which we deduced the characteristic coil-to-globule transition temperature, corresponding to the lower critical solution temperature (LCST) of the PTEGA part. We show that the coil-to-globule transition of the adsorbed copolymer being exposed to visible or UV light shifts to lower LCST as compared to the bulk solution: the transition temperature determined acoustically on the surface is 4 to 8 K lower than the cloud point temperature reported by UV/VIS spectroscopy in aqueous solution. We attribute our findings to non-equilibrium effects caused by confinement of the copolymer chains on the surface. Thermal stimuli and light can be used to manipulate the film formation process and the filmâs conformational state, which affects its subsequent response behavior
Strain-rate sensitivity of glasses
AbstractWe report on the loading-rate dependence of localized plastic deformation in inorganic covalent, metallic, ionic and superionic glasses. For this, the strain-rate sensitivity is determined through instrumented nanoindentation in a load-controlled strain-rate jump test. Through relating the strain-rate sensitivity to the reduced temperature, the packing density, the network dimensionality and the average single bond strength of the system, a qualitative mechanistic description of the strain-mediating process is possible. A strong variability of strain-rate sensitivity is obtained only at intermediate values of packing density, network connectivity or bond strength, when other parameters such as chemical composition and specific structural arrangement are dominating the deformation process. On the other side, for high bond strength and connectivity or for high packing density, the strain-rate sensitivity of the considered glasses is always low, which is also confirmed through the dependence of strain-rate sensitivity on Poisson ratio. Here, only for glasses with a Poisson ratio of ~0.3â0.4 we observe a wide variability of the loading-rate dependence of local deformation. For higher or lower Poisson ratio, the observed dependence is always low: when the limiting factor in deformation is primarily network connectivity and bond strength or packing density, respectively, once an activation barrier is overcome, deformation is only weakly loading-rate-dependent. This is regardless of the height of the activation barrier. When approaching the glass transition temperature, high strain-rate sensitivity is observed only in glasses where non-Newtonian flow is expected also in the corresponding liquid
Angular scattering pattern of femtosecond laserâinduced refractive index modifications in optical fibers
Abstract Focused femtosecond laser irradiation is used to induce light scattering modifications in the core of an optical fiber. This turns the fiber into a diffuse, lineâshaped light source. The scattering is investigated by imaging almost the full solid angle farâfield pattern for the first time. Additionally, an electromagnetic scattering model is developed to explain the observations. The findings herein change how the relationship between light scattering and the refractive index fluctuations is perceived by showing that the farâfield scattering pattern is the power spectral density of the polarization current inside the scattering center. Further, the authors contribute to a better estimation of the scattering process by showing that the total scattering power scales quadratically with the laserâinduced refractive index change and its volume
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Boson peak, heterogeneity and intermediate-range order in binary SiO2-Al2O3 glasses
In binary aluminosilicate liquids and glasses, heterogeneity on intermediate length scale is a crucial factor for optical fiber performance, determining the lower limit of optical attenuation and Rayleigh scattering, but also clustering and precipitation of optically active dopants, for example, in the fabrication of high-power laser gain media. Here, we consider the low-frequency vibrational modes of such materials for assessing structural heterogeneity on molecular scale. We determine the vibrational density of states VDoS g(Ï) using low-temperature heat capacity data. From correlation with low-frequency Raman spectroscopy, we obtain the Raman coupling coefficient. Both experiments allow for the extraction of the average dynamic correlation length as a function of alumina content. We find that this value decreases from about 3.9ânm to 3.3ânm when mildly increasing the alumina content from zero (vitreous silica) to 7âmol%. At the same time, the average inter-particle distance increases slightly due to the presence of oxygen tricluster species. In accordance with Loewensteinian dynamics, this proves that mild alumina doping increases structural homogeneity on molecular scale
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Mid-infrared laser absorption spectroscopy for process and emission control in the glass melting industry : Part 2. Difference frequency generation based MIR laser spectrometer for glass melting furnaces
Emerging techniques of mid-infrared absorption spectroscopy offer potentially great sensitivity and selectivity for combustion control and emission monitoring. Beeause of that, a differenee frequency based mid-infrared absorption spectrometer has been considered for application in the glass industry.
Based on preliminary tests within laboratory conditions, a spectrometer which operates at wavelengths around 5 ÎŒm was applied to online monitoring of the atmosphere of a gas fired glass melting furnace. The CO concentration was measured in order to demonstrate the feasibility of a mid-infrared absorption spectrometer for process control in the glass industry. Î series of measurements was performed in situ as well as crossing the recuperator entry, resulting in general advice on the construction of a prototype device
Controlled formation of gold nanoparticles with tunable plasmonic properties in tellurite glass
Silicate glasses with metallic nanoparticles (NPs) have been of intense interest in art, science and technology as the plasmonic properties of these NPs equip glass with light modulation capability. The so-called striking technique has enabled precise control of the in situ formation of metallic NPs in silicate glasses for applications from coloured glasses to photonic devices. Since tellurite glasses exhibit the unique combination of comparably easy fabrication, low phonon energy, wide transmission window and high solubility of luminescent rare earth ions, there has been a significant amount of work over the past two decades to adapt the striking technique to form gold or silver NPs in tellurite glasses. Despite this effort, the striking technique has remained insufficient for tellurite glasses to form metal NPs suitable for photonic applications. Here, we first uncover the challenges of the traditional striking technique to create gold NPs in tellurite glass. Then, we demonstrate precise control of the size and concentration of gold NPs in tellurite glass by developing new approaches to both steps of the striking technique: a controlled gold crucible corrosion technique to incorporate gold ions in tellurite glass and a glass powder reheating technique to subsequently transform the gold ions to gold NPs. Using the Mie theory, the size, size distribution and concentration of the gold NPs formed in tellurite glass are determined from the plasmonic properties of the NPs. This fundamental research provides guidance for designing and manipulating the plasmonic properties in tellurite glass for photonics research and applications
Lateral deformation and defect resistance of compacted silica glass: Quantification of the scratching hardness of brittle glasses
Human interaction with multimedia devices occurs predominantly over inorganic glass surfaces. Scratch-induced damage is a primary limitation in the suitability of brittle glasses for this purpose. However, neither truly quantitative data nor a topo-chemical understanding of the underlying deformation process which would allow for the development of improved materials is presently available. Here, we present lateral nano-indentation experiments for determining the work of deformation which is involved in the process of glass scratching. Using a series of hot-compressed vitreous silica with mild degrees of structural densification, we derive relations between quantitative scratch hardness and the underlying glass structure. We show that Young's modulus provides a clear rational for the observed variations in scratching hardness. In the specific case of silica, the energy needed to generate a certain scratch volume corresponds to roughly one tenth of Young's modulus. This relationship formally indicates that only about one tenth of the bonds which are involved in the deformation process are broken in its course. However, comparison with a more complex glass material with a certain fraction of two dimensional structural units and a strong ability for topological adaption to local stress clearly indicates a deviation from this behavior. This opens a pathway to topo-chemical engineering of scratch-resistant glasses
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