Thermoluminescent response of gamma irradiated Na^(+)–Cu^(+) ionexchanged silicate glass in large dose range

The introduction of metals into vitreous matrices is the origin of various interesting phenomena;in particular,the presence of copper ions in glass has been the subject of considerable research because of its numerous applications.The ion-exchange process is primarily used to introduce copper ions into glass matrices.The thermoluminescence(TL)of silicate glass was studied to evaluate its potential as gamma-sensitive material for dosimetric applications;the effect of copper doping on the thermoluminescent sensitivity was investigated using the Cu-Na ion-exchange technique for different concentrations and doping conditions,over a wide dose range of 10 mGy to 100 kGy.The results showed that Cu doping significantly improved the sensitivity of the glasses to gamma radiation.After the ion-exchange,two peaks appeared in the glow curves at approximately 175 and 230°C,respectively,which possibly originated from the Cu^(+) centers,along with a weak TL peak at around 320℃.We also attempted to explain the origin of the observed thermoluminescence by exploiting the Electron paramagnetic resonance(EPR)spectra.The results clearly show quenching of the TL emission with increasing copper concentrations.The present work indicates that the thermoluminescence response of these glasses to gamma rays can be reasonably measured in the range of 0.001-100 kGy.This study also facilitates the understanding of the basic TL mechanism in this glass system.

Properties of Local Structure Surrounding Eu^(3+)Ion in Various Niobate-Silicate Glasses

A Series of niobate silicate glasses doped with Eu 3+ ions were prepared. The emission, phonon side band spectra, fluorescence line narrowing spectroscopy and fluorescence lifetimes in these glasses were studied. The intensity parameters and crystal field parameter of Eu 3+ were obtained. The results indicate that the intensity ratio of the electric dipole to magnetic dipole transition and the intensity parameter Ω 2 increase with the increasing concentration of Nb 2O 5, indicating that the symmetry becomes lower, the Eu O bonds become stronger and the covalency of Eu O bond increases. The value of B 20 decreases with the increasing concentration of Nb 2O 5, indicating that the distance between the Eu 3+ ion and oxygen decreases and the Eu O bond becomes strong, corresponding to the results of the former. As the concentration of Nb 2O 5 increases, the electron phonon coupling becomes stronger, thus the nonradiative transition rate of 5D 0 becomes larger and the lifetime of 5D 0 becomes shorter.

NMR Study on Structural Characteristics of Rare Earth Doped Boro-Alumino-Silicate Glasses

The structural characteristics of Re2O3 doped B2O3-Al2O3-SiO2 glasses and factors such as the component and heat-treating conditions affecting the glass structure were investigated by magic angle spin nuclear magnetic resonance （MAS NMR） spectroscopy and differential thermal analysis （DTA）. It is found that, in B2O3-Al2O3-SiO2 glass, the boron （4）, and Al（5）, Al（6） changes to Al（4）. On the other hand, compared with Ba^2＋ , RE^3＋ can accumulate the boron network because of its higher field strength, which results in a large network structure. With the increase of samarium oxide, the silicate coordination Qa（3T） will have predominance gradually. Heat-treatment has little effect on the boron and aluminum coordination sites in the glass structure.

Trace element partitioning between amphibole and hydrous silicate glasses at 0.6–2.6 GPa

Partitioning behavior between amphibole and silicate glass of thirty-three minor and trace elements(Sc,Ti, V, Cr, Co, Rb, Sr, P, Y, Zr, Nb, Cs, Ba, K, La, Ce, Pr,Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, Pb,Th, and U) have been determined experimentally. Products of crystallization of hydrous basalt melts from 0.6 GPa/860 °C up to 2.6 GPa/970 °C were obtained in a multianvil apparatus. Major and trace element compositions of amphibole and glass were determined with a combination of electron microprobe and laser ablation inductively coupled plasma mass spectrometry. The main mineral phase is calcic amphibole, and the coexisting glass compositions are tonalite, granodiorite, and granite. The compatibility of rare earth elements increase at 915 °C and then decrease at 970 °C, but the compatibility of most of these elements shows a continued, significant increase with increasing pressure. For high-field strength elements, large ion lithophile elements, actinide compatibility decrease with increasing temperature or pressure, but transition metals show a continued increase in compatibility within the temperature–pressure conditions. From mathematical and graphical fitting, we determined best-fit values for the ideal ionic radius(r_0, 1.01–1.04 ?), the strain-free partitioncoefficient(D_0, 1.18–1.58), and apparent Young's modulus(E, 142–370 GPa) for the M4 site in amphibole according to the lattice strain model. The D_0^(M4) for rare earth elements rises at 915 °C and then drops at 970 °C at 0.6 GPa.However, the D_0^(M4) values are positively proportional to the pressure for rare earth elements in the amphibole-glass pairs at 0.6–2.6 GPa and 970 °C. Furthermore, the derived best-fit values for r_0^(M4) and E^(M4) are almost constant and trend to increase with rising temperature and pressure,respectively. The partition coefficient is distinctly different for different melt compositions. The rare earth elements become more enriched in amphibole if the quenched glass is granodiorite or granite compared to the tonalitic glasses.

Space-selective Precipitation and Dissolution of Ag and Au Nanoparticles in Silicate Glasses by Femtosecond Laser Irradiation

In Ag^＋ and Au^3＋ co-doped silicate glass sample, we realized controllable precipitation and dissolution of Ag and Au nanoparticles. A new method was proposed for separate precipitation of Ag and Au nanoparticles in different areas of the same sample through femtosecond laser irradiation and further annealing; different colors were obtained in the same glass. We also studied the laser dissolution of Ag and Au nanoparticles in the Ag^＋ and Au^3＋co-doped silicate glass. The mechanism of the phenomena we observed was discussed briefly.

Spectroscopic Properties and Effect of Radiation Trapping of a New Er^(3+)/Yb^(3+) Co-Doped Tellurite-Silicate Glasses

A new serials of Er^3＋/Yb^3＋ co-doped tellurite-silicate glasses were prepared by the technique of high-temperature mehing. The thermal stability, absorption spectra, emission spectra and upconversion spectra were measured and investigated. It is found that these kinds of glasses have good thermal stability, broad FWHM and large stimulated emission cross-section. The three upconversion emission at 525, 546, 658 nm, corresponding to the ^2H11/2→^4Ⅰ15/2, ^4S3/2→4^Ⅰ15/2 and ^F9/2→^4Ⅰ15/2 transitions of Dr^3＋ ions,

Spectroscopic Properties and Judd-Ofelt Theory Analysis of Er^(3+)-Doped Heavy Metal Oxyfluoride Silicate Glass

Er^(3+)-doped heavy metal oxyfluoride silicate glass was fabricated and characterized, and the absorption spectrum and fluorescence spectrum of the glass were studied. The Judd-Ofelt intensity parameters Ω_t (t =2, 4, 6), spontaneous transition probability, fluorescence branching ratio and radiative lifetime of each energy levels for Er^(3+) were calculated by Judd-Ofelt theory, and stimulated emission cross-section of (()~4I_(13/2))→(()~4I_(15/2)) transition was calculated by McCumber theory. The results show that fluorescence full width at half maximum and stimulated emission cross-section of Er^(3+)-doped heavy metal oxyfluoride silicate glass are broad and large, respectively. Compared with other host glasses, the gain bandwidth property of Er^(3+)-doped heavy metal oxyfluoride silicate glass is close to those of tellurite and bismuth glasses, and has advantage over those of silicate, phosphate and germante glasses.

Green and red up-conversion emissions and thermometric application of Er^(3+) -doped silicate glass

The green and red up-conversion emissions centred at about 534, 549 and 663 nm of wavelength, corresponding respectively to the ^2H11/2 → ^4I15/2, ^4S3/2 → ^4I15/2 and ^4F9/2 → ^4I15/2 transitions of Er^3＋ ions, have been observed for the Er^3＋-doped silicate glass excited by a 978 nm semiconductor laser beam. Excitation power dependent behaviour of the up-conversion emission intensity indicates that a two-photon absorption up-conversion process is responsible for the green and red up-conversion emissions. The temperature dependence of the green up-conversion emissions is also studied in a temperature range of 296-673 K, which shows that Er^3＋-doped silicate glass can be used as a sensor in high-temperature measurement.

Broadband Near-Infrared Emission from Transparent Ni^2＋ -Doped Sodium Aluminosilicate Glass Ceramics

Broadband near-infrared emission from transparent Ni^2＋-doped sodium aluminosilicate glass-ceramics is observed. The broad emission is centred at 1290nm and covers the whole telecommunication wavelength region （1100- 1700hm） with full width at half maximum of about 340hm. The observed infrared emission could be attributed to the 3T2（F） → 3A2（F） transition of octahedral Ni^2＋ ions that occupy high-field sites in nanocrystals. The product of the lifetime and the stimulated emission cross section is 2.15 × 10^-24 cm^2s. It is suggested that Ni^2＋- doped sodium aluminosilicate glass ceramics have potential applications in tunable broadband light sources and broadband amplifiers.

Corrosion mechanism of HVOF silicate glass coating in 5% NaCl solution

On the basis of good anticorrosion capability of silicate glass,silicate glass coating was sprayed by high velocity oxygen fuel (HVOF) and the corrosion mechanism in 5% NaCl solution was studied. Scanning electron microscope (SEM) ,energy dispersive X-ray analysis (EDX) ,X-ray diffraction (XRD) and potentiom- eter were used to study the coating composition and corrosion process. The result shows that silicate glass coating is entirely noncrystallizable. Silicate glass coating has very low incidence of hole with compact structure. Electric double-layer can form at coating/solution interface and corrosive solution performs as a lead connecting the coating surface and substrate after permeating through glass coating. The corrosion mechanism of silicate glass coating is similar to that of glass and the entire corrosion process can be divided into some states. The whole corrosion process happens in glass coating without substrate basically. The fluctuation of the self-corrosion potential about glass coating in corrosion solution can help to research the corrosion process.

Crystallinity and crystallization mechanism of lithium aluminosilicate glass by X-ray diffractometry

The crystallinity of lithium aluminosilicate(LAS) glass after crystallization were studied at different temperatures by X-ray diffractometry and the crystallinity of the standard glass ceramic with known crystal and glass phases was examined. The crystallization mechanism of LAS glass was analyzed by the crystallinity, with a formula relating the crystallinity (X) and temperature (T). The results show that the calculated crystallinity of LAS glass by XRD increases with the crystallization temperature, in the range of 40%?50%, which is close to the calculated ones of standard samples with spodumene quartz ratio of 40%?70%. The activation energy of LAS glass is different within different temperature ranges; nEc is 125.44 kJ/mol at 710?810 ℃ and nEc is 17.42 kJ/mol at 810?980 ℃, which indicates different crystallization mechanisms. It has been proved that the required energy for crystallization of glass in the lower temperature range includes the interfacial energy between glass and crystalline phase and the free energy difference of atoms in structures of glass and crystal, and in the higher temperature ranges only the interfacial energy between glass and crystalline phase is considered.

XPS and Raman studies of electron irradiated sodium silicate glass

The microstructure modifications of sodium silicate glass induced by 1.2-MeV electron irradiation are studied by x-ray photoelectron spectroscopy and Raman spectroscopy. Depth profile analyses are also performed on the irradiated glass at 109 Gy. A sodium-depleted layer with a thickness of a few tens of nanometers and the corresponding increase of network polymerization on the top surface are observed after electron bombardment, while the polymerization in the subsurface region has a negligible variation with the irradiation dose. Moreover, the formation of molecular oxygen after electron irradiation is evidenced, which is mainly aggregated in the first two-micron-thick irradiated glass surface. These modifications are correlated to the network relaxation process as a consequence of the diffusion and desorption of sodium species during electron irradiation.

Dissolution behavior of calcium-magnesium-silicate glass fiber

The dissolution behavior of CaO-MgO-SiO2 glass fiber was investigated by scanning electron microscopy (SEM), Fourier-transform infrared spectrometer (FTIR) and inductively coupled plasma atomic emission spectroscopy (ICP-AES) using in-vitro tests. The results show that the soaked fiber is surrounded by an outer calcium-magnesium silicate hydrated layer, and there exists a balancing function between the formation and abscission of the hydrated layer during the dissolution process. The concentrations of leached ions increase constantly, and the mass loss of the fibers and pH changes of the solution are found to rise rapidly during the initial dissolution process, then their increasing rates are controlled by the balancing function of the hydrated layer at the subsequent dissolution stages. The dissolution rate constant and time for complete dissolution are estimated to be 274 ng/(cm2·h) and 15.2 d, respectively, presenting preferable biosolubilities.

Recycling water glass from wet reclamation sewage of waste sodium silicate-bonded sand

Wet reclamation of waste sodium silicate-bonded sand produces much alkaline sewage and causes pollution. Recycling water glass from wet reclamation sewage of the waste sodium silicate-bonded sand can solve pollution issues and generate economic benefits. In this work, the wet reclamation sewage was filtered, and the filtrate was causticized with a quicklime powder to produce a lye. The effects of causticization temperature, causticization time, and the amount of quicklime powder on the causticization rate were studied. The lye was used to dissolve the silica in the filtration residue to prepare a sodium silicate solution. The effects of the mass of filtration residue, dissolution temperature, and dissolution time on sodium silicate modulus were studied. Finally, the recycled water glass was obtained by concentrating the sodium silicate solution, and the bonding strength of the recycled water glass was tested. The results showed that the causticization rate could be improved by increasing the amount of quicklime powder, causticization temperature, and causticization time, and the highest causticization rate was above 92%. Amorphous silica in the filtration residue dissolved in the lye. Increasing the amount of the filtration residue, dissolution temperature, and dissolution time could improve the sodium silicate modulus. The bonding strength of the recycled water glass was close to that of commercial water glass. The recycled water glass could be used as a substitute for the commercial water glass.

STUDY ON THE POLYMERIZATION DEGREE OF SILICATE ANIONS IN THE SILICATE GLASS BY TRIMETHYLSILYLATION METHOD

In the present paper,a mixed solvent method is applied to the trimethylsilylation of silicate glass,and the polymerization degree and its distribution of silicate anions in the silicate glass are measured by means of the analyses of gas chromatography-mass spectrography.

Formation of Na_(1+x)V_3O_8 Nanoribbon Thin Film from V_2O_5 Xerogel on Sodium Silicate Glass Substrate

Na1＋xV3O8 nanoribbon thin film was successfully fabricated by annealing the V2O5 xerogel film on sodium sili-cate glass substrate at 450℃. It has been identified that the amount of sodium ions diffused into the V2O5 xerogel film increases with the high temperature of annealing treatment. The sodium glass substrate serves as a limited sodium source to induce the transformation from V2O5 to Na1＋xV3O8.

Interaction of RuO₂and Lead-Silicate Glass in Thick-Film Resistors

Results of investigation of X-ray diffraction, infrared and optical spectra of powders of the ruthenium dioxide, lead-silicate glass as well as their mixture before and after sintering are reported. Sintering conditions typical for thick film resistors were used. Intensity of main lines of RuO2 in X-ray diffraction patterns of sintered mixtures decreases and they slightly shift towards small angles. No new reflexes appear in these patterns. Absorbance of RuO2 in the range of 2.5-100 μm is proportional to and featureless. Infrared spectrum of lead-silicate glass has absorption bands of [SiO4]4- tetrahedra and Pb-O bonds only. Optical spectrum of RuO2 has wide absorption bands at 950 and 370 nm. Spectra of the mixture of RuO2 and glass powders before and after sintering are different indicating that there is interaction between them during the sintering process. Concentration of free charge carriers estimated from the optical spectra is about 1021 cm-3.

Effect of Pb Ions on the Ionic Conductivity of Some Silicate Glass Systems

Conductivity of glasses in the systems SiO2.PbO.RO, (where R=Ca, Sr or Ba) was investigated between room temperature and 530 K. The dependence of log resistivity as well as the activation energy on the PbO content has been studied. Based on the present experimental results, the possible different conduction mechanisms in such glasses are discussed. It was postulated that Pb2+ ions may represent the major charge carrying species in these glasses. This assumption was confirmed by the calculations of the mean distance between the interstitial Pb2+ ions and the effective center of the O2- ions in the glass networks. The variation in the values of the density and the molar volume with PbO content is also discussed in view of the obtained activation energies for the studied glass-systems.

Development of Kaolin and Glass Fiber Reinforced Composites for Thermal Insulating Panels

In our modern world, where conserving energy is highly valued, thermal insulation panels play a crucial role in reducing heat transfer between two spaces, surfaces, or materials. They are used to enhance the energy efficiency of various industrial applications by minimizing heat loss and temperature control. These panels function as silent protectors, aiding in reducing energy consumption and making things more sustainable and better for the environment. This is where composite materials come in;they are known for their lightweight nature, high strength-to-weight ratio, and excellent thermal insulation properties and have gained significant attention. Researchers are actively engaged in various studies aimed at enhancing these materials further. This research project focuses on the development of kaolin and glass fiber-reinforced composites for thermally insulating panels, to which natural strengthening materials like corn husk and bamboo fibers are added. The aim is to create cost-effective and efficient composite materials for thermal insulation applications by incorporating these components with a binder consisting of potassium silicate, hydroxide, and distilled water. This project involves conducting compression tests, bending tests, impact tests, thermal conductivity measurements, and microscopic analysis to evaluate the mechanical and thermal properties of the developed composites. The profound impact of these engineered composites on thermal insulation panels stands to revolutionize energy conservation efforts, offering a potent avenue to minimize heat loss and enhance overall energy efficiency across an array of industrial sectors.