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Borosilicate glass is an ideal material for microfluidic chip substrates due to its excellent light transmittance and stable chemical properties. However, it is also prone to brittle fracture during processing, making it a typical difficult-to-machine material. As an emerging processing technology, longitudinal torsional ultrasonic assistant milling (LTUVAM) can effectively reduce the surface damage of glass materials and improve the proportion of plastic removal of materials. The mechanism of LTUVAM of borosilicate glass was studied in this paper. Critical undeformed chip thickness (h c) is a key factor in achieving plastic material removal. At present, the influence of LTUVAM on the h c is not clear. Therefore, in this paper, the material-specific cutting energy model in the LTUVAM process was established to predict the h c. Firstly, the motion path of LTUVAM was analyzed, and the undeformed chip thickness model and the tool-workpiece separation rate model were established. Then, based on the above model, the material-specific cutting energy model was established according to the material removal principle. Finally, an LTUVAM orthogonal experiment was carried out to study the surface quality of the material. The experimental results showed that with the increase of ultrasonic power, the roughness and side damage area increased first and then decreased. With the increase of spindle speed, it showed that the roughness and side damage area decreased first and then increased. With the increase of feed per tooth, it showed that the roughness increased first and then decreased, and then increased, and the side damage area increased first and then decreased. Through the analysis of the experimental and model results, the increase of the separation rate between the tool and the workpiece contributes to the increase of the h c and the improvement of the processing quality. [ABSTRACT FROM AUTHOR]

Cesium lead halide perovskite (CsPbX 3) quantum dots (QDs) are recognized as viable substitutes for conventional fluorescent powder color converters, which can improve the color gamut and reproducibility of liquid crystal displays (LCDs). Encapsulating QDs in glass can effectively solve the water oxygen stability of QDs, but the glass matrix impedes the nucleation of QDs and the precipitation of QDs requires secondary heating. In our research, we successfully accomplished the self-crystallization of CsPbBr 3 QDs facilitated by LiF within a B 2 O 3 -SiO 2 -ZnO borosilicate glass matrix. The results indicate that the self crystallization of CsPbBr 3 QDs induced by LiF in borosilicate glass matrix has a synergistic effect. The Li + ions can break the glass network structure and facilitate ionic migration and transport, while F− ions have good electronegativity due to ion aggregation, and can strongly attract Cs+ and Pb2+ ions with larger atomic radii, thereby promoting the rapid nucleation and growth of CsPbBr 3 QDs, ultimately synthesizing QDs with uniform particle size, narrow half peak width, good optical properties, and thermal stability. [ABSTRACT FROM AUTHOR]

The use of ultrashort pulse lasers opens up a wide range of possibilities for processing dielectric materials. The present study focuses on the investigation of the ablation‐free microscopic surface modification of borosilicate glass using femtosecond laser radiation (350 fs at 515 nm wavelength) in a scanning machining process. Furthermore, its aim is to analyze the relationship between the laser process parameters and the microscopic changes in the surface topography observed. The characteristic of the generated surface structure, which takes place below the ablation threshold, shows both elevations and depressions within the irradiated field (2 × 2 mm2). The realized structures reach a profile height Peak‐to‐Valley (PV) of up to 10 µm. The amount of surface deformation depends on the selected parameters such as laser fluence, number of passes, and scanning strategy. The microdeformation is detected on both the top and bottom sides of the processed glass material with a thickness ≤1 mm. The influence of the temporal and spatial energy distribution on the material modification is discussed, demonstrating the possibilities of microforming of silicate glasses using ultrashort pulsed laser radiation. [ABSTRACT FROM AUTHOR]

Thanks to their exceptional thermal and electrical properties, borosilicate glasses are widely used in chip packaging and electronic pastes. Nonetheless, borosilicate glass powders suffer from the phenomenon of foaming and expansion during sintering process, which greatly affects the sintering densities of the powders and poses limitations to their applications. Herein, we explored the foaming mechanism of borosilicate glasses by ball milling. The foaming of borosilicate glass is due to the adsorption of CO 2 from the atmosphere by the glass powder during ball milling. The CO 2 forms carbonates on the surface of the glass powder and is released during the sintering process, leading to foaming. Additionally, as the specific surface area of the glass powder increases, its corrosion resistance decreases while its foaming strength increases. The foaming strength of the four glass powders, listed in ascending order, is: SrO-B 2 O 3 -SiO 2, ZnO-B 2 O 3 -SiO 2 , BaO-B 2 O 3 -SiO 2 and CaO-B 2 O 3 -SiO 2. Meanwhile, it was found that the foaming strength could be weakened better by ball milling organic modification method. These findings contribute to a deeper understanding of the glass foaming phenomenon. Furthermore, they offer practical strategies to reduce the foaming and optimize the performance of borosilicate glass-based materials in applications of chip packaging and electronic pastes. [ABSTRACT FROM AUTHOR]

MnO has been used for the decoloration of glasses containing iron oxide impurity since ancient times, based on the oxidation-reduction of Fe-Mn redox pairs (Fe2++Mn3+→Fe3++Mn2+). In this work, it was evidenced that a combinative addition of Fe 2 O 3 and MnO into borosilicate glasses for pharmaceutical packaging application induced the above reaction and improved the water resistance of glass. As a comparative study, the structure of glasses with the inclusion of either MnO or Fe 2 O 3 and both of them as well as the valence, coordination of Fe and Mn ions in the glasses were fully investigated by using FTIR, Raman, NMR, EPR, PL and UV–Vis–NIR spectroscopy. It was concluded that the single addition of Fe 2 O 3 or MnO had a similar depolymerization effect on the glass structure, while the co-addition of Fe 2 O 3 and MnO exhibited a synergistic effect, which led to the increase of glass network connectivity due to oxidation-reduction of Fe/Mn redox pairs and consequently the improvement of water resistance of the glasses. [ABSTRACT FROM AUTHOR]

Radiation shielding glass is an interesting material in the field of radiation shielding due to its remarkable features. In the present paper, we investigated the physical properties of radiation-shielding glass materials that consist of sodium oxide (Na 2 O), cerium oxide (CeO 2), and iron oxide (Fe 2 O 3) incorporated into borosilicate glasses with the formula 90SiO 2 -(70-x)B 2 O 3 + 20Na 2 O–1Fe 2 O 3 -xCeO 2 (CeFeNaBS-glasses). One of the distinguishing characteristics of this glass system is its enhanced radiation shielding capabilities. The structural studies indicated a gradual rise in glass density from 1.954 to 2.658 g/cm with further CeO 2 doping. Optical studies showed that the optical band gaps went down from 3.41 eV to 3.33 eV as the amount of CeO 2 in the CeFeNaBS-glass matrix rose. The decrease in optical band gap has been correlated with the rising basicity. Also, the increased basicity behavior induces more conversion of Ce3+ to Ce4+ ions by losing a 4f electron. Moreover, with further CeO 2 additions, the glass color changed from light brown to dark brown. The presence of Ce4+ ions with further CeO 2 additions is responsible for this color transformation. The linear and non-linear refractive indices exhibit enhanced behaviors with higher CeO 2 concentrations. We used declining basicity and polarizability behaviors to describe this behavior. The incorporation of larger CeO 2 concentrations enhances the ability to improve radiation shielding properties, as demonstrated by the increased values of the mass attenuation coefficient and half-value layer, especially in the energy ranges of soft tissues X-ray and hard tissues X-ray. Hence, the investigated CeFeNaBS-glasses exhibit enhanced transparency and radiation shielding capabilities, rendering them highly suitable for implementation in this domain. [ABSTRACT FROM AUTHOR]

The recent COVID-19 emergency has led to an impressive increase in the production of pharmaceutical vials. This has led to a parallel increase in the amounts of waste glass; manufacturers typically recover material from faulty containers by crushing, giving origin to an unrecyclable fraction. Coarse fragments are effectively reused as feedstock for glass melting; on the contrary, fine powders (<100 microns), contaminated by metal and ceramic particles due to the same crushing operations, are landfilled. Landfilling is also suggested for pharmaceutical containers after medical use. This study aims at proposing new opportunities for the recycling of fine glass particles, according to recent findings concerning alkali activation of pharmaceutical glass, combined with novel processing, i.e., binder jetting printing. It has already been shown that pharmaceutical glass, immersed in low-molarity alkaline solution (not exceeding 2.5 M NaOH), undergoes surface dissolution and hydration; cold consolidation is later achieved, upon drying at 40–60 °C, by a condensation reaction occurring at hydrated layers of adjacent particles. Binder jetting printing does not realize a full liquid immersion of the glass powders, as the attacking solution is selectively sprayed on a powder bed. Here, we discuss the tuning of key parameters, such as the molarity of the attacking solution (from 2.5 to 10 M) and the granulometry of the waste glass, to obtain stable printed blocks. In particular, the stability depends on the formation of bridges between adjacent particles consisting of strong T-O bonds (Si-O-Si, Al-O-Si, B-O-Si), while degradation products (concentrating Na ions) remain as a secondary phase, solubilized by immersion in boiling water. Such stability is achieved by operating at 5 M NaOH. [ABSTRACT FROM AUTHOR]

One major factor impeding the design of nuclear waste glasses with enhanced waste loadings is our insufficient understanding of their composition–structure–durability relationships, specifically in the environments the waste form is expected to encounter in a geological repository. In particular, the high field‐strength cations (HFSCs) are an integral component of most waste streams. However, their impact on the long‐term performance of the glassy waste form remains mostly undeciphered. In this context, the present study aims to understand the impact of some HFSCs (i.e., Nb5+, Zr4+, Ti4+, and La3+) on the dissolution behavior of alkali/alkaline‐earth aluminoborosilicate‐based model nuclear waste glasses in hyper‐alkaline media. At pH = 13, the studied glasses dissolve through the dissolution–reprecipitation mechanism, with Ca precipitation being the most vital step to passivation. In Ca‐free glasses, although the HFSCs slow down the forward rate, they do not seem to impact the residual rate behavior of glasses. The presence of Ca2+, however, initiates the rapid precipitation of network polymerizing HFSCs (i.e., Nb5+, Zr4+, and Ti4+) into a Ca2+/HFSCs‐based passivating layer, thus suggesting a synergy between Ca2+ and HFSCs that contributes to the enhanced long‐term durability of the glasses. Such synergy is not strongly evident for La3+, but instead, a potential La/Si affinity is observed upon the formation of the alteration layer. [ABSTRACT FROM AUTHOR]

To address the issues of low processing efficiency, poor forming accuracy, and internal damage in glass material processing, this study proposes the use of flame jet forming. However, the mechanism of flame jet processing requires further elucidation. This research investigates the relationship between the indentation morphology on the glass surface and the inlet velocity of the flame jet. A theoretical model was established through mathematical analysis to reflect this relationship. The model's accuracy was validated using numerical simulation methods. By comparing experimental data with theoretical model results, surface tension was incorporated, and the model was iteratively optimized using MATLAB R2024a. The final optimized model demonstrated an absolute error range of 0.009 to 0.069 mm. This study confirms the feasibility of flame jet processing and enriches the understanding of its mechanism, providing a novel, efficient, and precise method for processing glass materials. [ABSTRACT FROM AUTHOR]

The sonication method was used to prepare a new set of CuO and CuO/Ag nanocomposites. The particle size was estimated using XRD and HR-TEM while the morphology of the nanoparticles was investigated with SEM. The average particle sizes of CuO and Ag falls in the 29.32–35.80 nm and 35.13–45.95 nm ranges, respectively. XRD declared that CuO has the space groups C 1 c 1 (9) and C 1 2/c 1 (15), while silver has space group F m -3 m (225). XPS analysis indicated the presence of Ag as Ag0 and Cu as Cu2+. Nano-oxide and nanocomposites were used to synthesis CuO and CuO/Ag doped lithium–zinc borosilicate glass. Physical parameters of the glass samples were calculated including density, V m , V o , V m B , OPD, d B - B , n b , and N, R p , and R i depending on Ag and CuO mole fractions. The physical properties of glass indicated an increase in density and an initial expansion in glass structural network with the addition of silver metal due to its larger size followed by a compression as its molar ratio increase due to its higher C no . XRD measurements were reported for the glass samples doped with nanoparticles, proving the amorphous phase. ESR measurements were determined for all glass samples to detect the nature of the doped nanoparticles when incorporated inside a glassy matrix where CuO was found as tetragonal in octahedral sites and silver can be transformed after melting inside the glass matrix into Ag+ to form more stable Ag y x + clusters.The fabricated sample of CuAgB-4 with significant nano silver doping (7.32% mol) has the maximum LAc and effective atomic number. Nano silver content increases the γ -RdSg in the lithium–zinc borosilicate glasses. [ABSTRACT FROM AUTHOR]

Due to the adoption of fluorescent powder encapsulated by organic resin, commercial light emitting diodes (LEDs) suffer from low thermal stability and poor light quality under high temperature, and luminescent glass is one of the effective ways to solve this problem. A series of borosilicate (B 2 O 3 –SiO 2 –Al 2 O 3 –PbO-Dy 2 O 3 –Eu 2 O 3 , marked as BSAP: DyEu) was prepared by the gas suspension technique. The basic characterization test indicate that the prepared glass has excellent thermal stability and stable structure. The optical properties of the luminescent glass were investigated in detail. By changing the Eu3+ doping amount, the Dy3+/Eu3+ co-doped glass can realize warm white light emission. The temperature-variable fluorescence spectra of BASP: Dy1.25Eu1.0 were analyzed, and the glass can produce strong warm white light emission in a wide temperature range. At 700 K, the luminous intensity of the glass remains above 38.49 % of the room temperature, and the chroma shift ΔC = 8.57 × 10−3. In addition, the w- LED device based on commercial GaN chip and BSAP: DyEu glass realizes warm white light output with excellent correlated color temperature (3063 K) and high color rendering index (90.3). The analysis shows that Dy3+/Eu3+ co-doped borosilicate glass can be used as a candidate material for w- LED applications. [ABSTRACT FROM AUTHOR]

Halide perovskite quantum dots (QDs) glass has attracted much attention in the field of optoelectronics, but its photoluminescence (PL) properties and water stability still need further improvement. In this work, the melt-quenching method is used to successfully precipitate CsPbBr 3 QDs in borosilicate glass. By increasing the concentration of ZnO, the photoluminescence quantum yield (PLQY) of CsPbBr 3 QDs glass is enhanced up to 30 times from 1.91 % to 65.87 %. The results demonstrate that the introduction of ZnO loosens the glass network structure, which contributes to the QDs to precipitate. In addition, it can be found that the PL intensity maintains 91.68 % of the initial PL intensity after 30 days of immersion, which is attributed to ZnO delays the corrosion of borosilicate glass by water. The effect of ZnO-modified borosilicate glass structure on PL and stability provides a certain reference value for further research on QDs glass, and the good PLQY and water stability make ZnO-modified CsPbBr 3 QDs glass a potential material in the field of WLEDs. [ABSTRACT FROM AUTHOR]

Abstract The sonication method was used to prepare a new set of CuO and CuO/Ag nanocomposites. The particle size was estimated using XRD and HR-TEM while the morphology of the nanoparticles was investigated with SEM. The average particle sizes of CuO and Ag falls in the 29.32–35.80 nm and 35.13–45.95 nm ranges, respectively. XRD declared that CuO has the space groups C 1 c 1 (9) and C 1 2/c 1 (15), while silver has space group F m -3 m (225). XPS analysis indicated the presence of Ag as Ag0 and Cu as Cu2+. Nano-oxide and nanocomposites were used to synthesis CuO and CuO/Ag doped lithium–zinc borosilicate glass. Physical parameters of the glass samples were calculated including density, $$\hbox {V}_{m}$$ V m , $$\hbox {V}_{o}$$ V o , $$\hbox {V}_{m}^{B}$$ V m B , OPD, $$\hbox {d}_{B-B}$$ d B - B , $$\hbox {n}_{b}$$ n b , and N, $$\hbox {R}_{p}$$ R p , and $$\hbox {R}_{i}$$ R i depending on Ag and CuO mole fractions. The physical properties of glass indicated an increase in density and an initial expansion in glass structural network with the addition of silver metal due to its larger size followed by a compression as its molar ratio increase due to its higher $$\hbox {C}_{no}$$ C no . XRD measurements were reported for the glass samples doped with nanoparticles, proving the amorphous phase. ESR measurements were determined for all glass samples to detect the nature of the doped nanoparticles when incorporated inside a glassy matrix where CuO was found as tetragonal in octahedral sites and silver can be transformed after melting inside the glass matrix into Ag+ to form more stable $$\hbox {Ag}^{x+}_{y}$$ Ag y x + clusters.The fabricated sample of CuAgB-4 with significant nano silver doping (7.32% mol) has the maximum LAc and effective atomic number. Nano silver content increases the $$\gamma$$ γ -RdSg in the lithium–zinc borosilicate glasses.

In this study, the results of the investigation of the influence of Al atoms on the structural characteristics of ZnO films obtained by the sol-gel method are presented. It has been determined that the glass substrates consist of subcrystallites with dimensions of 28.6 nm, having cubic unit cells with lattice parameters a = 0.3336 nm, and their surfaces belong to the crystallographic orientation (111). It has been identified that the grown thin ZnO films consist of subcrystallites with dimensions of 39.5 nm, having a wurtzite structure with lattice parameters a = b = 0.3265 nm and c = 0.5212 nm, respectively. It has been determined that at the boundaries of the division of these subcrystallites, polycrystalline regions with sizes of 12.6 nm, 28.3 nm, 30 nm, and 33 nm are formed. Additionally, nanocrystallites with sizes of 56.8 nm self-assemble on the surface areas of the deposited films. The increase in the values of the “c”axis of the hexagonal crystal lattice of ZnO films by 0.0009 nm when doping Al atoms from 1% to 5% is explained by the shift of the main structural line (002) at small angles (Δθ=0.12°). It has been established that nanocrystallites with lattice parameters аn = 0.5791 nm, belonging to the spatial group Fd3m, self-assemble on the surface areas of ZnO:Al films. the curve due to the presence of a monoenergetic level of fast surface states at the heterojunction.

To decipher the effects of replacing alkali with zinc on thermo-mechanical properties, a series of borosilicate glasses with the molar compositions of 70.65SiO 2 ·21.09B 2 O 3 ·1.88Al 2 O 3 ·1Li 2 O·(5.38- x)R 2 O· x ZnO (x = 0, 0.34, 0.67, 1, 1.34, 2.69, 4.04, and 5.38) were prepared. Upon adding a slight quantity of ZnO, a local extreme point for glass transition temperature (T g) appears. This behavior is deciphered to be originated from two opposite factors. On one hand, T g reduces as a characteristic of the colligative properties for a dilute solution; in addition, T g rises due to the higher field strength, bond energy and covalent characteristic of zinc cations compared to that of alkali ions. Otherwise, based on the evolution of intermediate-range clusters revealed by infrared, Raman and NMR spectra, we elucidate the atomic-scale structural origin, which leads to the nonlinear evolution of elastic moduli and coefficient of thermal expansion with the molar ratio of [ZnO]/([R 2 O]+[ZnO]). [ABSTRACT FROM AUTHOR]

This article uses a high-temperature sintering imaging instrument to test the flowability of borosilicate glass melt doped with Cr 2 O 3 , and establishes a mathematical model for high-temperature glass melt spreading. Discuss the glass melt from a thermodynamic perspective by combining model interpretation with experimental characterization. The results indicate that the thermodynamic judgment formula for high-temperature flow spreading of borosilicate glass is: Q ≥ ρ [ A 0 exp (− T / k 0) + S 0 ] − M · δ [ A 0 exp (− T / k 0) + S 0 ] 1 / 2 . To improve the high-temperature flow ability of borosilicate glass, it is necessary to increase the spreading activation energy Q. On the other hand, it is necessary to reduce the spreading coefficients A 0 、 k 0 and S 0. As a refractory metal oxide and active oxide, Cr 2 O 3 plays a role in reducing the spreading coefficient of glass systems. [ABSTRACT FROM AUTHOR]

The gamma shielding parameters of an admixture of waste borosilicate glass (BS) and geopolymer (GP) made from activated metakaolin are presented in the present study. The influence of the BS quantity on the density and different gamma shielding quantities is investigated over a wide gamma energy range. Four batches of the G-BS composite were prepared using the solid-state diffusion method, containing 0 (G), 10 % (G-10BS), 20 % (G-20BS), and 30 % (G-30BS) by weight of BS, respectively. The chemical compositions of the G-xBS samples were determined through X-ray fluorescence spectrometry. In addition, the density of the BS-doped geopolymers was determined using the liquid displacement method using deionized water as the displacement fluid. The theoretical determination of estimating shielding parameters began by estimating the mass (μ ρ) and linear (μ) attenuation coefficients of the geopolymers for photon energies in the range of 15 keV to 15 MeV using the XCOM data library. The B and Si content and density of the geopolymer samples increased as the BS weight proportion increased in the geopolymer. The values of the attenuation coefficients (ACs) decreased with energy. For μ, the decrease was from 9.1533 to 0.0355 cm−1, 6.7486 to 0.0374 cm−1, 10.2964 to 0.0396 cm−1, and 10.7722 to 0.0414 cm−1, while for μ ρ , it was 5.3217 to 0.0206 cm2 g-1, 5.3860 to 0.0206 cm2 g-1, 5.3627 to 0.0206 cm2 g-1, and 5.3594 to 0.0206 cm2 g-1, for G, G-10BS, G-20BS, and G-30BS, respectively. There are no significant differences between the photon energy absorption capacity of the geopolymers, especially at energies greater than 1 MeV. The photon buildup factors of the G-xBS samples have very close relative values with no clear order. The introduction of waste borosilicate glass is therefore a way of improving the photon attenuation capacity of geopolymer and, therefore, the potential of shielding applications of geopolymer-based concrete. [ABSTRACT FROM AUTHOR]

The present study investigates in-vitro biomineralization, mechanical, and tribological properties of bioactive borosilicate glass composed of 31B 2 O 3 –20SiO 2 -(24.5-x)Na 2 O-24.5CaO and xCuO (mol%). Glass was manufactured using conventional melt-quench technique, utilizing chemicals partially derived from bio-waste, with varying copper oxide (CuO) content (x = 0, 1, 3, and 5). In-vitro study was conducted by immersing the specimens in simulated body fluid for 21 days. The formation of apatite layer was confirmed using FTIR, XRD and FESEM-EDS. Vicker's micro hardness tester and a universal testing machine measured hardness and compressive strength, while a pin-on-disc tribometer assessed wear. MTT assay was performed for all the specimens using osteosarcoma MG63 cell line. The study revealed that substituting copper in place of sodium increased the ion dissolution and improved the formation of the apatite layer hence, enhanced the bioactivity, however, accompanied by a gradual decrease in hardness and compressive strength. BSG-0 exhibited the highest hardness (6.64 GPa) and compressive strength (86.81 MPa), while wear resistance weakened with higher CuO content, notably in BSG-5 with the highest specific wear rate (0.072 mm³/N-m) under a 5 N load. Although MTT assay showed non-toxicity for all specimens, except BSG-5, the compounds demonstrated cell tolerance and growth stimulation. In conclusion, the study suggests that CuO-doped borosilicate glasses exhibit superior bioactivity, making them potentially effective for bone filling, wound healing, and dental applications, despite a compromise in mechanical strength and wear resistance. [Display omitted] [ABSTRACT FROM AUTHOR]

Microstructural evolution of borosilicate glass–sulfate (BaSO4 or Na2SO4) mixture was observed in situ using a high‐temperature confocal scanning laser microscope. The phase compositions and sulfate retention of the mixture at different temperatures were also examined. The results indicate that for the glass–BaSO4 sample (abbreviated as BS), the borosilicate glass begins to melt at about 900°C, and the triangular BaSO4 crystals grow obviously between 900°C and 1100°C. At temperatures above 1100°C, the BaSO4 crystals gradually melt and decompose. For the glass–Na2SO4 sample (abbreviated as NS), strip‐shaped BaSO4 crystals begin to form at about 820°C after the borosilicate glass melting, and then gradually melt with further increasing temperature. When the temperature increases to 1000°C, the upper layer of the NS sample possesses Na2SO4, LiNaSO4, and BaSO4 phases, while the lower layer possesses an amorphous phase. Moreover, the SO3 retention in the BS sample remains almost unchanged with temperature increases from 900°C to 1100°C, and then decreases with further increasing temperature. The SO3 retention retained in the NS sample decreases rapidly at temperatures above 900°C. These findings can provide a guidance for vitrifying sulfur‐rich high‐level liquid waste. [ABSTRACT FROM AUTHOR]

Progress in glass science has given rise to innovative functional glasses, unlocking significant applications for creating cutting-edge materials such as solid-state batteries, solar cells, optical reinforcement, and medical technologies. In this study, rice husk silica, Bismuth (Bi) and Tin (Sn) oxide ores were used to fabricate a novel glass series. The electrical conductivity (i.e., dielectric constant) of the glasses increased with the dopant's gravimetric levels. The novel glass series also possesses good optical non-linearity with metallisation criteria ranging from 0.35 to 0.40, which points to a novel non-linear optical material. The non-bridging oxygen content in the new glasses exceeds the bridging oxygen, indicating high polarisation. The transmission coefficient decreased with increasing dopant concentration from 0.76 to 0.75, while the reflection loss decreased from 0.37 to 0.38. For the Caesium-137 energy, GS6 has a minimum HVL of ∼5.02 cm, which is ∼20 % lower than that of commercial Pb/Ba glass. For the two energies, GS6 has the least MFP, suggesting that the addition of dopants improved the efficiency of the glass attenuation. Process capability analysis based on Caesium-137 (661.7 keV) and overall performance analysis of the fabricated glass series revealed that GS3 glass (15 wt% dopant) is the optimal material, even outperforming the commercial Pb/Ba glass. Although Cobalt-60 (1253 keV) yielded comparable outcomes, concentrations beyond 15 wt% in GS3 showed marginal enhancements in the photon attenuation parameters of the glasses. Hence, the fabricated GS3 and the circular synthesis method of the glasses are cost-effective for low-energy gamma/X-ray shielding. The percentage deviation between the experimental data for MAC and that of Monte Carlo simulations for Cs-137 and Co-60 energies are both within 10 %, which validates the methods of this paper. [ABSTRACT FROM AUTHOR]

In this study, the results of the investigation of the influence of Al atoms on the structural characteristics of ZnO films obtained by the sol- gel method are presented. It has been determined that the glass substrates consist of subcrystallites with dimensions of 28.6 nm, having cubic unit cells with lattice parameters a = 0.3336 nm, and their surfaces belong to the crystallographic orientation (111). It has been identified that the grown thin ZnO films consist of subcrystallites with dimensions of 39.5 nm, having a wurtzite structure with lattice parameters a = b = 0.3265 nm and c = 0.5212 nm, respectively. It has been determined that at the boundaries of the division of these subcrystallites, polycrystalline regions with sizes of 12.6 nm, 28.3 nm, 30 nm, and 33 nm are formed. Additionally, nanocrystallites with sizes of 56.8 nm self-assemble on the surface areas of the deposited films. The increase in the values of the "c"axis of the hexagonal crystal lattice of ZnO films by 0.0009 nm when doping Al atoms from 1% to 5% is explained by the shift of the main structural line (002) at small angles (40-0.12°). It has been established that nanocrystallites with lattice parameters an = 0.5791 nm, belonging to the spatial group Fd3m, self-assemble on the surface areas of ZnO:Al films. the curve due to the presence of a monoenergetic level of fast surface states at the heterojunction. [ABSTRACT FROM AUTHOR]

The stress distribution in sealing glass is one of the most concerning issues for glass‐to‐metal (GtM) seals. In this study, photoluminescence spectroscopy was applied by exploiting the piezospectroscopic effect of Cr‐doped α‐Al2O3 (ruby), and the overall stress distribution along the radius of a concentric seal was detected and analyzed. It was discovered that the compressive stress first increased and then decreased at the edge of the seal. The maximum compressive stress of 91 MPa was detected at ∼20 µm from the interface and was ascribed to the interaction between the glass and surface oxide film of the metal. Stress distributions in pore regions were also investigated and obvious stress fluctuations were observed clustering around pores. A circle of compressive stress was observed around the pores in a single glass without a metal housing; for the pores in the center of the concentric seal, the stress distribution was dominated by the inner contraction of the metal housing; and for the pores near the edge of the seal, the concentration of tensile stress located perpendicular to that of the compressive stress. This study demonstrates a high‐resolved and nondestructive method to detect the stress field and explores the potential for future tailorability of stress distribution in GtM seals. [ABSTRACT FROM AUTHOR]

Knowledge of the structural organization of nuclear waste glasses at the atomic scale is the basis for further studies of macroscopic properties (e.g., fracture toughness, chemical durability, and leaching rate). Recent studies have focused on the iodine dissolution mechanism in oxide‐based glasses synthesized under high‐pressure conditions, but there is still a lack of key information on the extent of the modifications caused by iodine entering the glass network. We therefore decided to conduct an in‐depth study by nuclear magnetic resonance on two series of aluminoborosilicate glasses synthetized under high pressure conditions and doped with either I2 or I2O5. The obtained 11B, 23Na, and 27Al nuclear magnetic resonance (NMR) spectra were fitted and correlated with the iodine content in order to find possible relationships with the local environment change for the probed cations. These data showed that iodine has no effect on the coordination of aluminum and very little effects on that of boron. In contrast, we found an expected relationship of the I content with the 23Na NMR parameters. In comparison with previous studies on the non‐bridging oxygen (NBO) distribution in aluminoborosilicate, we suggest that Na+ is mainly scavenged from silica tetrahedra with one or two NBO (Q3${Q}^3$ or Q2${Q}^2$) as no boron planar triangles with one NBO are expected for such compositions. From those information, we establish a model for iodine dissolution in nuclear waste glass that is consistent with previous studies. [ABSTRACT FROM AUTHOR]

Borosilicate glass has good light transmittance and stable chemical property, which is an ideal material for microfluidic chip matrix, However, brittle fracture is easy to occur during processing, which is a typical material difficult to process. This limits the surface accuracy. In recent years, longitudinal torsional ultrasonic vibration–assisted milling (LTUVAM) has been proposed as an effective way to machine hard and brittle materials. To elucidate the mechanism of material removal methods and elaborate the material removal mechanism during longitudinal torsional ultrasonic vibration–assisted milling process, this paper established a 3D morphology prediction model to investigate the material removal method. Firstly, the three-dimensional surface morphology model was created by describing the intricate tool path and the workpiece surface morphology reconstruction process under ultrasonic conditions while also considering the tool run-out effect. The model exhibited a certain degree of scalability, enabling the acquisition of various process morphology prediction models by altering the tool coordinates via matrix manipulation. Secondly, the accuracy of the model was verified by longitudinal torsional ultrasonic processing experiments. Thirdly, longitudinal torsional ultrasonic vibration–assisted milling experiments and longitudinal ultrasonic vibration–assisted milling experiments were conducted, and the surface roughness of the machined workpieces was measured. The experimental results show that LTUVAM further reduces the roughness compared with LUVAM, indicating that the reduction ratio reaches a maximum value of 61.06% at the spindle speed of 16,000 RPM, and then, the reduction ratio decreases to 42.88% with the increase of spindle speed. Combining modeling and experimental results, we concluded that LTUVAM was more advantageous in achieving plastic material removal and enhancing the surface quality of the machined surface compared to LUVAM. And under the same process conditions, as the spindle speed increases, the surface roughness of the workpiece increases first and then decreases. [ABSTRACT FROM AUTHOR]

New borosilicate glass (BSG) systems doped with different rare earth (RE) ions; Dy, Y, Nd and Ho, were molten by the common melting-quenching technique. XRD analysis exhibited the amorphous glassy states of the samples. Some optical, physical, and spectral features of the glasses were inspected within the influence of progressive gamma irradiation doses up to 300 kGy. FTIR spectra displayed the large structural stability against 200 kGy of gamma radiation which is correlated to the dual contribution of silicate (SiO 4), and borate (BO 3 and BO 4) vibrational bands. Optical UV–visible spectra revealed common peaks in the range 215–340 nm owing to the various valence states of the present transition metal (TM) ions e.g., Fe2+/Fe3+, Cu+/Cu2+, Ti3+/Ti4+, Zn2+ and the introduced RE ions. By following the dosimetric characteristics of the glasses up to 300 kGy, only Nd-BSG and Ho-BSG were sensitive to gamma rays, and a systematic obvious increase was detected for the characteristic peaks of Nd- BSG at 582 nm and Ho-BSG at 450 nm, however, the remaining samples (BSG, Dy-BSG, and Y-BSG) did not achieve a systematic change. Both Nd-BCG and Ho-BSG response curves showed a linear part extended up to 150 kGy. Nd-BCG and Ho-BSG are humidity-independent with satisfactory stability through 30 days of storage. Many optical and physical parameters for Nd- and Ho- BSGs were studied at the whole dose range up to 300 kGy e.g, optical band gap energy (Eopt), density (ρ), refractive index values (n Eopt , n k-s , n m and n R–S), electronegativity (χ), electron polarizability (∝°) and optical basicity (⋀), all revealed either a gradual increase or decrease with the progressive irradiation doses. The study recommends the hopeful usage of the prepared Nd and Ho- BSGs as high-dose radiation dosimeters in a useful high-dose range up to 300 kGy of gamma radiation. [ABSTRACT FROM AUTHOR]

Researchers have extensively studied borate bioactive glass (BBG) for bone regeneration and wound healing applications. In the current study, 13-93B3 (54.6% B2O3, 22.1% CaO, 7.9% K2O, 7.7% MgO, 6.0% Na2O, and 1.7% P2O5) was synthesized using a sol–gel technique and doped with different molar concentrations of Cu (0.01, 0.05, and 0.25 M) into BBG for possible biomedical applications. Then, the antibacterial activity was tested against E. coli and S. aureus. The maximum zone of inhibition against S. aureus was achieved at 100 μg/mL of 0.25 M Cu-doped BBG. At 50 μg/mL of 0.25 molar copper concentration, E. coli showed a significant reduction in colony-forming units. Hydroxyl radical production, influenced by the BBG powder, was most effective against S. aureus, followed by E. coli. Protein leakage studies demonstrated significant leakage after treatment with BBG powder, demonstrating a strong effect on bacterial strains. This shows a change in protein synthesis, which is essential for central metabolism and gene transcription, affecting proteins in the periplasm and inner and outer membranes. Furthermore, carbohydrate leakage studies showed that BBG is effective against all three categories of cellular carbohydrate, namely membrane-bound, transmembrane, and intracellular carbs. This study focuses on the diverse antibacterial processes of Cu-doped BBG, which has emerged as a promising contender for biological applications that require strong antibacterial characteristics. [ABSTRACT FROM AUTHOR]

Abstract The use of ultrashort pulse lasers opens up a wide range of possibilities for processing dielectric materials. The present study focuses on the investigation of the ablation‐free microscopic surface modification of borosilicate glass using femtosecond laser radiation (350 fs at 515 nm wavelength) in a scanning machining process. Furthermore, its aim is to analyze the relationship between the laser process parameters and the microscopic changes in the surface topography observed. The characteristic of the generated surface structure, which takes place below the ablation threshold, shows both elevations and depressions within the irradiated field (2 × 2 mm2). The realized structures reach a profile height Peak‐to‐Valley (PV) of up to 10 µm. The amount of surface deformation depends on the selected parameters such as laser fluence, number of passes, and scanning strategy. The microdeformation is detected on both the top and bottom sides of the processed glass material with a thickness ≤1 mm. The influence of the temporal and spatial energy distribution on the material modification is discussed, demonstrating the possibilities of microforming of silicate glasses using ultrashort pulsed laser radiation.

Three borosilicate glass samples of 25 % Si 2 O – 30 % Na 2 O – 45 % B 2 O 3 doped with x Dy 2 O 3 (where x = 0, 2, and 4 mol %) were prepared using the melt quenching technique. Photoluminescence spectra for glass samples were studied when excited by 350 nm in the 400–800 nm range, where emission sharply increases for samples doped with 2 % Dy 2 O 3 (BSNDy2) at 580 nm after exposed to 30 kGy. Also, glass containing 2 % Dy photoluminescence constants, such as decay curves CIE chromaticity, was measured for all samples that gave three decay behaviors: slow, intermediate, and fast. Experimental lifetime (τ exp.), color coordination (X, Y), and yellow/blue intensity ratio (y/b) beside the color correlated temperature (CCT) were determined before and after being irradiated by 30 and 60 kGy from γ ray source where the y/b ratio of BSNDy2 increase by increasing exposure to gamma doses and were >1. In addition, electrical conductivity at different temperatures was investigated as the BSNDy2 sample gave the highest conductivity and decreased by BSNDy4. Moreover, shielding parameters such as the tenth value layer, half value layer, mean free path and mass attenuation coefficient values were calculated at different gamma-ray energies via the Phy-X program, showing the highest values for MAC, Z eff , N eff, and C eff for BSNDy4 sample. The findings showed that adding Dy 2 O 3 to the glass gave a fortified shielding character. [ABSTRACT FROM AUTHOR]

The immobilization of high-level nuclear waste (HLW) in glass waste matrices provides the key safety function of slowing down radionuclide emissions from an underground disposal site. This study examines the leaching behavior of two major elements, Na and Si, in HLW borosilicate glass simulated from waste of a 1000 MWe class pressurized water reactor (PWR) using response surface methodology and Box-Behnken Design. The design of the experiment was carried out considering three independent variables: the pH of the solution, the contact time, and the leaching temperature, leading to 17 leaching runs performed using the static product consistency test (PCT). The results of statistical analysis (ANOVA: analysis of variance) indicated that the effects of the individual variables and the interactions between them were statistically significant, and the relative consistency of the data further confirmed the model's applicability. Data obtained from the PCT experiments revealed that the leaching behavior of Na and Si in the evaluated waste glass exhibited similar behavior to previously researched glasses for each condition tested. [ABSTRACT FROM AUTHOR]

This article presents the results of studies of 15 low-melting borosilicate glasses of different compositions using the simplex-based method of mathematical planning. For each glass, the melting temperature and uniformity, as well as the rate and degree of leaching are determined in accordance with GOST (State Standard) R 52126–2003 [1] and NP-019-2015 [2]. Mathematical models are built based on the data obtained. As a result of the research, the most promising area for further research and development of the composition of borosilicate glass for a removable small-sized melter designed by Mayak Production Association is identified. [ABSTRACT FROM AUTHOR]

At present, doping of different alkaline-earth metal ions is mainly used to tune the emission peak of europium (Eu) ions in glasses. However, the optimization of Eu-doped glasses is hindered due to limited discussion on the relationship between local glass network structure, concentration of Eu ion dopants, and visible light emission by Eu ions. In this study,we prepared two series of borosilicate glasses doped with Eu ions, by varying the ratio of SiO2 to B2O3 and adjusting the concentration of Eu ion dopants to obtain cyan emission. The optical properties, structure, and differential scanning calorimetry (DSC) of the investigated glasses were systematically studied. With gradual increase in the content of SiO2, red shifting from 471 nm to 492 nm was observed under excitation at 410 nm, with the introduction of Eu2O3 also causing a redshift from 471 nm to 488 nm. The spectral results also revealed that under excitation at 410 nm all the glass samples exhibited cyan emission, with the optimal cyan peak at 492 nm (Si-45) and the strongest cyan emission at Eu-0.4 (480 nm). By adjusting the concentration ratios of Si to B in europium-doped borosilicate glass, it was observed that by altering the [SiO4] tetrahedra, [BO4] tetrahedra, and [BO3] triangles within the glass ultimately cyan emission can be achieved. By varying the doping concentration of Eu ion to change the degree of local Eu ion clustering in the glass system, cyan emission can be achieved by tuning the emission peak. [ABSTRACT FROM AUTHOR]

Lanthanide borosilicate glasses containing Pu and the nonradioactive analog element Ce were subjects of an x-ray absorption spectroscopy investigation to quantify the +3/+4 ratio of these redox-sensitive elements. The data show that the dominant oxidation states are +4 for Pu and +3 for Ce. The data also indicate that the reductive potential of glasses can be quantified from a solution chemistry method adapted to glass chemistry, although allowances must be made for glass composition. These data can therefore be used to formulate glass compositions and processing schedules that lead to a controlled oxidation state of Pu in melts. Furthermore, the data show that Ce is a poor analog for Pu behavior in melts and that the suitability of surrogates can be assessed by the evaluation approach presented here. The method demonstrated in this paper can be used to estimate the oxidation states of a range of multi-valent elements as functions of temperature and composition with data from only a single redox couple.

To address the issues of low processing efficiency, poor forming accuracy, and internal damage in glass material processing, this study proposes the use of flame jet forming. However, the mechanism of flame jet processing requires further elucidation. This research investigates the relationship between the indentation morphology on the glass surface and the inlet velocity of the flame jet. A theoretical model was established through mathematical analysis to reflect this relationship. The model’s accuracy was validated using numerical simulation methods. By comparing experimental data with theoretical model results, surface tension was incorporated, and the model was iteratively optimized using MATLAB R2024a. The final optimized model demonstrated an absolute error range of 0.009 to 0.069 mm. This study confirms the feasibility of flame jet processing and enriches the understanding of its mechanism, providing a novel, efficient, and precise method for processing glass materials.

Evaluating the corrosion behavior of borosilicate glass after irradiation holds vital importance for the safe geological disposal of high‐level radioactive waste. This study examined the leaching properties of three kinds of sodium‐borosilicate (RNa2O‒B2O3‒KSiO2, denoted as "NBS") glasses with the same R but varying K under 5 MeV Xe‐ion radiation to decipher the correlation between the corrosion mechanism and glass composition. After Xe‐ion radiation, an increase in [BO3] units was observed, indicative of the glass network depolymerization. Irradiated glasses exhibited a more significant change in [BO3] units over the leaching time compared to their pristine counterparts. There is a strong correlation between the initial dissolution rates of pristine glasses, the K value, and the proportion of Na. Additionally, the initial Si dissolution rate of the NBS glasses has been accelerated by heavy ion irradiation. For the same R value over the glass series, the initial Si dissolution rates in ternary borosilicate glasses change at similar rates after irradiation. This study concluded that the variation trend in the initial dissolution rate of Si and Na differs under ion radiation. [ABSTRACT FROM AUTHOR]

The development of matrix with high capacity and stability immobilization of nuclear waste is highly desirable. Herein, new type of zircon-based borosilicate glass-ceramics (ZBGC) with high immobilization capacity and excellent aqueous stability was prepared and applied to immobilize simulated trivalent actinide (Nd). The effects of Nd doping and sintering temperature on the microstructure and phase composition of the obtained ZBGC were researched. The experimental suggested that high ZrSiO 4 formation rate (97.49 wt%) was obtained by tuning the Nd content and sintering temperature. The record high immobilization capacity of Nd in ZGBC (18 at%) was achieved owing to the synergistic effect between the crystal lattice and glass network immobilization. Additionally, the obtained Nd-doped ZBGC exhibited excellent aqueous stability (∼10−6 g m−2 d−1) due to the high compactness. The results demonstrated that ZBGC with high immobilization capacity and aqueous stability could be potential matrix for actinides immobilization. [ABSTRACT FROM AUTHOR]

The borosilicate glass was used to join reaction bonded silicon carbide through two steps, namely: laser cladding and low-temperature heat treatment. The wettability and microstructure of the laser cladding glass layer were examined, while joint microstructure and strength were analyzed at various temperatures and times. The results show that the laser cladding layer improved the wetting of glass on the substrate, formed a good interfacial bond, and reduced the joining temperature. The joints primarily consist of the glass phase, the boron-rich phase, and a few crystals. The high-strength joints obtained after heating the joint interface at 950 °C for 30 min had a flexural strength of 250 ± 20 MPa, a 68% improvement compared with direct connection under the same conditions. The joints also exhibit good thermal shock resistance and high-temperature strength. At 400 °C (thermal shock temperature) and 600 °C (test temperature), the residual flexural strengths were 122 ± 25 and 152 ± 12 MPa, respectively.

Relevance. The need to obtain experimental data on dependence of thermoviscosimetric properties of the examined borosilicate glasses on temperature, in order to solve the problem of developing a low-melting composition of borosilicate glass for a small-scale melter designed by Mayak Production Association. Aim. To get the most complete characterization of the glasses under study using thermoviscometric measurements. Methods. Mathematical modelling, simplex-lattice design. Results and conclusions. One of the most effective methods of experiment planning, which allows, with a relatively small number of experiments, obtaining a mathematical model reflecting the dependence of the studied property of the mixture on the content of components in it, is the simplex experiment planning method. To simplify the solution of such a task, a group or groups of components are usually distinguished, in which the ratio of the mass fraction of the components does not change. In this article, three groups of components are taken – simulators of high-level radioactive waste, sodium and boron oxides, and glass frit. The authors have identified the most promising area, where the mass fraction of glass frit is from 67.5 to 75%, the mass fraction of sodium and boron is from 25 to 32.5% and the mass fraction of high-level waste components is from 0 to 20%. The paper presents the results of thermoviscometric measurements of 15 melts of low-melting borosilicate glasses of different compositions at temperatures ranging from 700 to 1,200°C. Using simplex-based mathematical models of experiment planning, domains of dependence of thermoviscosimetric characteristics of glass melts on their compositions were created. The authors identified the compositions of glass melts that are found within the viscosity limits determined as allowable for glass melt discharge during operation of the removable small-scale melter of Mayak Production Association design.

The immobilization of high-level nuclear waste (HLW) in glass waste matrices provides the key safety function of slowing down radionuclide emissions from an underground disposal site. This study examines the leaching behavior of two major elements, Na and Si, in HLW borosilicate glass simulated from waste of a 1000 MWe class pressurized water reactor (PWR) using response surface methodology and Box-Behnken Design. The design of the experiment was carried out considering three independent variables: the pH of the solution, the contact time, and the leaching temperature, leading to 17 leaching runs performed using the static product consistency test (PCT). The results of statistical analysis (ANOVA: analysis of variance) indicated that the effects of the individual variables and the interactions between them were statistically significant, and the relative consistency of the data further confirmed the model’s applicability. Data obtained from the PCT experiments revealed that the leaching behavior of Na and Si in the evaluated waste glass exhibited similar behavior to previously researched glasses for each condition tested.

The supply consumption of ladle furnace slag (LFS) is a prominence of recent researches and is extensively considered. In this work LFS has the potential to be utilized as the main raw material for producing glass and glass-ceramics because of its chemical compositions similarities to the silicate glass materials. Three borosilicate glass samples were produced via melting – quenching technique. The three samples contained 10, 20, 30 wt % of slag waste materials, respectively. The second sample was heat treated at 625 °C, guiding by DTA studies, for 2, 6, 10, or 15 h. XRD studies showed traces precipitation of Ca(Mg,Al) (Si,Al) 2 O 6 (diopside), Sodium Aluminum Silicate (NaAlSiO 4), Sodium Aluminum Borate (Na 2 Al 2 B 2 O 7) and Clinoenstatite (MgSiO 3) phases. FTIR analysis demonstrated the same functional groups through glass and glass ceramics sample confirming that all prepared samples had the same structure. Ferrimagnetism property of a glass sample and its glass ceramic sample derivative was confirmed by vibrating sample magnetometer (VSM) analysis. Vickers microhardness and fracture toughness results indicated noticeable rising in toughness value and decreasing of hardness after using 100 g load by increasing slag percent in glass samples. The glass ceramic sample had little change, in hardness and toughness values, rather than its corresponding glass sample due to its lower crystallization behavior. The low dielectric constant values are very good indication for the availability of using these type of glass for electronic applications. X-ray photoelectron spectroscopy (XPS) studies indicate that manganese ions are found as MnO in both glass and glass ceramic samples. [ABSTRACT FROM AUTHOR]

A new method for molecular dynamics (MD) modeling of the glass structure using a crystal structural template is proposed. The template is based on the unit cell of the crystalline phase, whose composition is qualitatively similar to the modeled glass. Using this approach and multistage MD simulation, the model of the spatial structure of grade E borosilicate glass, reproducing its physicochemical characteristics, is obtained. The proposed method enables to model the glass structure using classical MD methods with greater productivity and stability. [ABSTRACT FROM AUTHOR]

In this work, we fabricated a new series of borosilicate glass doped with different concentrations of Gd 2 O 3. Then the glass samples were converted to glass ceramics using heat treatment at 500 °C for 2 h, and then the temperature was raised to 700 °C for 3 h. The X-ray diffraction (XRD) affirmed the amorphous nature of glass samples and the crystalline phase of glass-ceramic samples, which is related to SiO 2 (cristobalite). The Fourier transform infrared displayed many peaks related to functional groups for B 2 O 3 and SiO 2 , with a slight difference between glass and glass ceramic samples. The band gap (E g) for glass samples is 3.69, 3.64, 3.65, and 3.67 eV for BSTSGd0.5, BSTSGd1, BSTSGd1.5, and BSTSGd2, respectively. At the same time, the E g for glass ceramics is 3.61, 3.64, 3.64, and 3.64 eV for GCBSTSGd0.5, GCBSTSGd1, GCBSTSGd1.5, and GCBSTSGd2, respectively. The mechanical properties of glass samples align with packing density (V t) and compactness results, which indicated the superiority of BSTSGd1 glass samples over other glass systems. For example, the V t values are 0.674, 0.688, 0.683, and 0.680 for BSTSGd0.5, BSTSGD1, BSTSGd1.5, and BSTSGD2, respectively. On the other hand, we compared the linear attenuation coefficient (μ) between glass and glass ceramics which showed high compatibility due to the low difference in density for glass and glass ceramics. The μ values for BSTSGd0.5, BSTSGD1, BSTSGd1.5, and BSTSGD2 glasses at 0.600 are 0.088, 0.092, 0.093, and 0.095 cm−1, which showed enhancement when adding Gd 2 O 3 to the glass system. It can be concluded that adding Gd 2 O 3 slightly reduced the particle range for proton and alpha particles and enhanced the neutron and gamma shielding properties, which indicates the possibility of using the current samples in the radiation shielding field. [ABSTRACT FROM AUTHOR]

Fe 2 O 3 and TiO 2 were used as colorants in borosilicate glass, aimed to form amber-colored pharmaceutical glass. The status of the Fe and Ti ions and their influences on the glass structure were analyzed by FTIR, Raman and Mössbauer spectroscopic technique. The large addition of Fe 2 O 3 led to the decrease of connectivity of silica network and the increase of [BO 3 ]. TiO 2 showed even larger depolymerization effect. Fe3+ coordinated with the bridging oxygen in [SiO 4 ] increasing the aggregation of silica network and the [Fe2+O 6 ] filled the voids of glass network. Both types of iron ions helped to restrain the mobility of Na+ and improved the water resistance of the glass, while TiO 2 as a network modifier did the opposite. Either Fe 2 O 3 - or TiO 2 -containing samples exhibited enhanced UV-absorption capacity. The glass sample containing both Fe 2 O 3 and TiO 2 as colorants completely blocked the UV light, and exhibited the best water resistance. The results obtained herein enriched the understanding of the effects of colorants on borosilicate glasses and could provide useful information for the production of amber glasses used in pharmaceutical packing. [ABSTRACT FROM AUTHOR]

Here, we report on core–clad bioactive borosilicate fibers, that we have prepared both with round and rectangular cross‐section profile. The exposed approach, which relies on the stacking and drawing of glass slabs, demonstrates our ability to develop bioactive‐based glass fibers with tailored cross‐section profiles. Tens‐of‐meters‐long fibers were successfully drawn, although suffering from elevated losses in the case of the rectangular ones. The response of the fibers in simulated body fluid was studied for both geometries. We found that a round cladding can act as protective layer, tempering effects of the corrosion. We also noticed that rectangular fibers are more prone to degradation, the enhanced corrosion beginning from their sharp corners as they accumulated residual tensile stress during drawing. To the best of our knowledge, this is the first report on the effect of residual tensile stresses from surface tension deformations applied to the corrosion of rectangular fibers. As geometry plays a critical role on the biodegradation behavior of the fiberglass, we believe the enclosed results could lead to the design of fiber devices with tailored cross‐section profile in order to tune their rate of degradation on solely based geometrical effects. [ABSTRACT FROM AUTHOR]

We examine the impact of the glass network‐modifier cation field strength (CFS) on ion irradiation‐induced mechanical property changes in borosilicate (BS) glasses for the ternary M2O–B2O3–SiO2 systems with M = {Na, K, Rb} and the quaternary [0.5M(2)O–0.5Na2O]–B2O3–SiO2 systems with M = {Li, Na, K, Rb Mg, Ca, Sr, Ba}. 11B nuclear magnetic resonance (NMR) experiments on the as‐prepared BS glasses yielded the fractional population of four‐coordinated B species (B[4]) out of all {B[3], B[4]} groups in the glass network, along with the fraction of B[4]–O–Si linkages out of all B[4]–O–Si/B bonds. Both parameters correlated linearly with the (average) CFS of the M+ and/or {M(2)+, Na+} cations. Both the nanoindentation‐derived hardness and Young's modulus values of the glasses reduced upon their irradiation by Si2+ ions, with the property deterioration decreasing linearly with increasing Mz+ CFS, that is, for higher Mz+⋅⋅⋅O interaction strength. The irradiation damage of the glass network also increased linearly with the fraction of B[4]–O–Si linkages, which are the second weakest in the structure after the Mz+⋅⋅⋅O bonds. Our results underscore the advantages of employing BS glasses with high‐CFS cations for enhancing the radiation resistance for nuclear waste storage. [ABSTRACT FROM AUTHOR]

In the current study, crystallization and phase separation of a borosillicate glass composition in the system Na2O–CaO–Al2O3–B2O3–SiO2 used for nuclear waste immobilization have been investigated. At first, base glass composition was prepared by mixing and homogenizing of pure raw materials, melting in an alumina crucible and then casting in a stainless steel mold. Mo2O3 was added in constant values of 0.5, 1.5, 2.5 and 3.5 %mole. XRD analysis was carried out to ensure no crystalline phases were formed. Heat treatment was performed at temperature intervals of 620, 650, 680 and 710°C. To study phase separation creation, SEM analysis was carried out. In the next step, acid leaching of phase separated glasses was performed. Porosity analysis and measurement of specific surface area by BET were performed on acid-leached samples. The results show that all samples show different amounts of phase separation. Also, the highest specific surface area was related to the sample containing 1.5 %mole Mo2O3 with two acid washing steps.

Borosilicate glass is currently the best comprehensive solidified material for deep disposal of high-level radioactive waste. The stability of borosilicate glass under irradiation is an important factor affecting the leakage of radioactive isotopes into the biosphere. In this study, three-component borosilicate glass (NBS) was irradiated by γ-rays at doses of 8 kGy and 800 kGy, respectively. The leaching behaviors of the irradiated samples at different absorbed doses were studied. The surface morphologies of the samples were analyzed using optical microscopy and scanning electron microscopy (SEM). The distributions of elements were analyzed using energy dispersive X-ray spectroscopy (EDS), and the elements in solution were characterized using inductively coupled plasma-optical emission spectroscopy (ICP-OES). The results indicate that the irradiation effects on the leaching behavior of borosilicate glass occurs at certain thresholds. When the corrosion time is prolonged, the corrosion effect gradually covers the irradiation effect of the glass. Compared with 8 kGy irradiation, NBS glass samples exhibit more significant changes in elemental behavior under 800 kGy irradiation. After high-dose irradiation, the effect of corrosion on surface morphology is more significant than at low doses, and the element leaching rate of NBS glass is higher after 7 days of corrosion.

Classical molecular dynamics simulations have been used to investigate the structural role of Mg and its effect when it is incorporated in sodium aluminoborosilicate glasses. The simulations have been performed using three interatomic potentials; one is based on the rigid ionic model parameterized by Wang et al. (2018) and two slightly different parameterization of the core–shell model provided by Stevensson et al. (2018) and Pedone et al. (2020) The accuracies of these models have been assessed by detailed structural analysis and comparing the simulated nuclear magnetic resonance (NMR) spectra for spin active nuclei (29Si, 27Al, 11B, 17O, 25Mg, and 23Na) with the experimental counterparts collected in a previous work. Our simulations reveal that the core–shell parameterizations provide better structural models. In fact, they better reproduce the NMR spectra of all the investigated nuclei and give better agreement with known experimental data. Magnesium is found to be five coordinated on average with distances with oxygen in between a network modifier (like Na) and an intermediate network formed (like Al). It prefers to lay closer to three‐coordinated B atoms, forming B–NBO bonds, with respect to Si and especially Al. This can explain the formation of AlO5 and AlO6 units in the investigated Na‐free glass, together with a Si clusterization. [ABSTRACT FROM AUTHOR]

Glass containing chromium is a promising material for use in various modern fields of application (laser technology, optoelectronic devices, and luminescent resources). Chromium oxides are well-known nucleating agents that can cause crystallization. One of the most commonly observed crystalline phases in silicate glasses is cristobalite, which lowers their mechanical strength, leading to the destruction of the material. The objective of this investigation was to study in detail the crystallization of cristobalite in sodium borosilicate glass in the presence of 2 mol% Cr2O3, depending on the thermal history of the glass. The glass was studied using XRD, SEM, EPR, FTIR-spectroscopy, XPS, and solid-state NMR. Eskolaite, α-Cr2O3, which had crystallized in this glass, stimulated the bulk crystallization of cristobalite at 550 °C after isothermally treating it for 72 h, due to the phase-separated structure of the glass with its interpenetrating phase morphology. Polytypism, resulting in the incorporation of alkalis into the cristobalite structure, was observed. Cr2O3 causes the catalytic crystallization of cristobalite at an extremely low temperature, which is at lower concentrations and temperatures than in glass containing Fe2O3 with a similar composition. The crystal growth rate and the incubation time for the crystallization of cristobalite were roughly estimated. [ABSTRACT FROM AUTHOR]

This paper investigates the wettability of Kovar alloys with high-borosilicate glass and microscopically analyses the mechanism of wettability and diffusion between Kovar and borosilicate glass. First, Kovar was oxidised at 800 °C for 5, 15, 25, 35, and 60 min to observe the oxide morphology of the Kovar surface layer and to analyse the composition of the oxide layer. To investigate the wetting pattern formations of Kovar and high-borosilicate glass under different wetting temperatures, times, and preoxidation conditions, Kovar and high-borosilicate glass obtained from different oxidation treatments were held at 1060 °C for 20 min for wetting experiments, and the glass–metal wetting interface morphology and elemental distribution were observed using SEM and EDS. The elemental diffusion at the wetting interface between the borosilicate glass and the Kovar with different preoxidation and at the glass spreading boundary was investigated. The longitudinal diffusion of the liquid glass in the metal oxide layer formed a new tight chemical bond of Fe2SiO4, and the lateral diffusion of the liquid glass in the Kovar surface layer formed a black halo. [ABSTRACT FROM AUTHOR]