Search Results (20)

Glass curators often question how their treatments affect the long-term stability of historical glass. While damp cotton swabs are commonly used to remove surface salts and dust, the use of water remains controversial, particularly for heavily altered glass, due to concerns about worsening hydration. This study investigates the effect of water rinsing on an unstable soda-lime glass altered for six months (monoliths) and fifteen months (powders) at 35 °C and 85% relative humidity. Samples were then rinsed with Milli-Q water at 20 °C or 50 °C, and the monolithic glass was subsequently subjected to an additional 15 months of alteration under the same conditions. The glass surface was characterized by optical and scanning electron microscopy (SEM) as well as Raman spectroscopy to identify the nature of the salts. The evolution of the hydrated layer was assessed using transmission FTIR, Raman and solid-state NMR spectroscopies, ToF-SIMS, and thermogravimetric analysis (TGA). The results show that rinsing effectively removes surface salts—primarily sodium carbonate—and induces structural changes in the hydrated layer, promoting silicate network polymerization. Upon resuming alteration, rinsed monolithic samples exhibit no further degradation after the additional 15 months of alteration. These findings offer promising insights for conservation practices and may help curators refining their treatment strategies for altered glass. Full article

The present investigation introduces a novel approach, using As-Zn-Fe mining tailings (MT) and recycled bottle glass (cullet) to enable the manufacturing of a new glass for ornamental articles, with characteristics similar to those of soda–lime–silicate glass (SLS), and at the same time, immobilizing potentially toxic elements (PTEs) from mining tailings, which cause environmental pollution with severe risks to human health. The glass used was obtained from transparent glass bottles collected from urban waste, which were later washed to remove impurities and then crushed until they reached No. 70 mesh (212 μm) level; in the case of mining tailings, the sample used comes from the ore benefit process, with 96.8% of particles below the No. 50 mesh level (300 μm). Six mixtures were made by varying the composition of the mining tailings and glass, K₂CO₃ and H₃BO₃ as fluxes were also used in constant proportion. The mixtures were melted at 1370 °C, and later, the glass samples were cast on a steel plate at room temperature. The characteristics of the glasses were studied using thermal analysis (TA), X-ray diffraction (XRD), Fourier transform infrared (FTIR), and scanning electron microscopy (SEM). Likewise, their chemical resistance in acid and basic media and density were evaluated. The results unequivocally demonstrate the feasibility of manufacturing glasses with a light green color, the increase in the content of mining tailings increased the apparent T_g from 625 to 831 °C. Glasses with 17 and 21.3% MT presented lower density values due to a better-polymerized glass structure, attributed to the increase in SiO₂ and Al₂O₃ and the decrease in alkaline oxides, which allowed for the retention of PTEs in their structure. Full article

This paper presents an experimental approach to the study of the compressive strength, isothermal calorimetry and life cycle assessment (LCA) of alkali-activated pastes based on soda–lime–silica glass, established to investigate the effect of the nature and proportion of the activator. Four different activators are compared: Portland cement, sodium silicate, sodium carbonate (at four percentages by weight: 5, 10, 15 and 25 wt% relative to glass) and sodium hydroxide (3.5 wt%). Portland cement and sodium carbonate were added in dry form (powder), while sodium hydroxide (pellets) and silicate were used in solution. At room temperature, glass exhibited slow reaction kinetics, with mechanical performance increasing significantly beyond 28 days of curing. The nature of the activator had a direct impact on the mechanical performance of the activated glass. Cement-activated pastes and those containing 25 wt% of sodium carbonate developed strength at an early age (0–7 days). The other activators showed lower strength development before 28 days of reaction. While a higher activator content improved short-term performance, it also increased the environmental impact, primarily due to the activator. The LCA, conducted on 11 indicators, revealed that the environmental impact was largely driven by the type and amount of activator used. A performance impact indicator (PII) related to global warming was introduced to compare pastes with different performance values. At an early age (0–28 days), the PII was lower when the activator level was high but decreased over time as the strength improved. In terms of long-term performance (360 days), hydroxide and sodium carbonate (10 wt%) achieved compressive strengths of 91 and 74 MPa, respectively. These systems offered a balance between high performance and a reduced environmental impact, making them of interest for sustainable applications. Full article

This article analyses the combined effect of a mixture of natural zeolite and ground soda lime silicate glass on the durability properties of concrete. The specimens were prepared by replacing 25% of the cement with a mixture of zeolite and glass at different proportions with zeolite particles of two different sizes and cured for 28 and 90 days. Chloride migration, the depth of water penetration under pressure, and freeze–thaw cycle tests were performed, and compressive strength was determined. The combined effect of the mixture on the composition and microstructure of the cement matrix was studied by analysing the results of XRD, TGA, SEM-BSE, and porosity tests. The test results showed that irrespective of the cement “dilution” effect, the mixture of additives had a beneficial combined effect: increased durability of concrete, a denser structure of the cement matrix, the formation of calcium aluminate hydrates, faster rate, and higher degree of hydration. Full article

Architectural soda-lime silicate glass (SLS) is increasingly taking on complex shapes that require more detailed numerical analysis. Glass modeling is a thoroughly described topic with validated constitutive models. However, these models require a number of precise material parameters for SLS glass, and these are very sensitive to changes in glass composition. The currently available information is based on SLS glass tested in the late 1990s. As a result, most current publications are based on the above data. The object of this work was to analyze the available sources and update the information on selected key parameters for modeling. Using the currently utilized SLS glass in construction, the coefficient of thermal expansion (CTE), glass transition temperature, and the Young’s modulus have been experimentally investigated. The updated material parameters will allow for more accurate modeling of the SLS glass currently used in construction, and in consequence will make the prototyping process for glass with complex geometries possible to be transferred from the production stage to the design stage, resulting in shorter production times. Full article

Fireproof inorganic coatings based on sodium silicate solution with intumescent additions were prepared and tested to assess their ability to limit the negative effect of a fire. The intumescent materials were obtained by the alkali activation of waste glass powder (obtained by the grinding of recycled soda-lime culet) and slag (waste resulting from the metallurgical industry). The replacement of talc (used as filler in paint formulation) with the intumescent materials obtained by the alkaline activation of waste glass powder (WGP), determined an increase in the intumescence coefficient (up to 65%) and decreased the activation temperature of this process. To evaluate these coatings’ abilities to prevent or delay the temperature increase in metal structures, the paints were applied on steel plates and tested in direct contact with the flame of a butane burner for 60 min. The coatings prevented the increase in the steel substrate temperature over one considered critical (500°C) for steel mechanical properties; the combination of two coatings, with different intumescence activation temperatures, correlated with the increase in the coating’s thickness, sensibly reduced the rate of temperature increase (up to 75%) in the steel substrate. Full article

TiO₂ is an important oxide for property modifications in the conventional soda lime silicate glass family. It offers interesting optical and mechanical properties, for instance, by substituting heavy metals such as lead in consumer glasses. The compositional effects on the hardness, reduced elastic modulus and crack resistance as determined by indentation of chemically strengthened (CS) TiO₂-doped soda lime silicate glass was studied in the current paper. The CS, which was performed by a K⁺ for Na⁺ ion exchange in a molten KNO₃ salt bath at 450 °C for 15 h, yielded significant changes in the indentation mechanical properties. The hardness of the glass samples increased, and this was notably dependent on the SiO₂, CaO and TiO₂ content. The reduced elastic modulus was less affected by the CS but showed decrease for most samples. The crack resistance, an important property in many applications where glasses are subjected to contact damage, showed very different behaviors among the series. Only one of the series did significantly improve the crack resistance where low CaO content, high TiO₂ content, high molar volume and increased elastic deformation favored an increased crack resistance. Full article

Aluminium dross is a hazardous industrial waste generated during aluminium production. It contains metallic oxides of aluminium and magnesium, other phases (aluminum nitride), and residues of fluxes and salts from the melting process of aluminium. Discarding this by-product is considered an environmental and economic challenge due to the high reactivity of dross with water or even air humidity. After removing the hazardous components from the as-received dross, one of the optional approaches is to incorporate the treated dross into construction materials. Dross is applied in several types of research as a secondary raw material source for alumina, clinker, cement or glass-ceramic production, but only a few papers focus on the usage of dross as a foaming agent for foams. Even fewer research are reported where dross was applied as a basic component of foam glasses. In this work, foam glasses were produced completely from waste materials: Aluminium dross, container (SLS) glass, and cathode ray tube (CRT) glass. The research holds several specificities, i.e., combining two industrial waste materials (CRT glass and dross), and adding an increased amount from the wastes. The physical and mechanical characteristics were examined with a special focus on the effect of the foam glass components on the microstructure, density, thermal conductivity, and compressive strength. Full article

It is shown for the first time that the vacuum poling of soda-lime silicate glass and the subsequent processing of the glass in a melt containing silver ions results in the formation of silver nanoparticles buried in the subanodic region of the glass at a depth of 800–1700 nm. We associate the formation of nanoparticles with the transfer of electrons from negatively charged non-bridging oxygen atoms to silver ions, their reduction as well as their clustering. The nanoparticles do not form in the ion-depleted area just beneath the glass surface, which indicates the absence of a spatial charge (negatively charged oxygen atoms) in this region of the vacuum-poled glass. In consequence, the neutralization of the glass via switching of non-bridging oxygen bonds to bridging ones, which leads to the release of oxygen, should occur in parallel with the shift of calcium, magnesium, and sodium ions into the depth of the glass. Full article

Evolution of spectroscopic properties of a soda–lime silicate glass with different thermal history and under applied uniaxial stress was investigated using Raman and Brillouin spectroscopies as well as Nd³⁺ photoluminescence techniques. Samples of soda–lime silicate with a cooling rate from 6 × 10⁻⁴ to 650 K/min were prepared either by controlled cooling from the melt using a differential scanning calorimeter or by a conventional annealing procedure. Uniaxial stress effects in a range from 0 to −1.3 GPa were investigated in situ by compression of the glass cylinders. The spectroscopic observations of rearrangements in the network structure were related to the set cooling rates or the applied uniaxial stress to calculate an interrelated set of calibrations. Comparing the results from Raman and Brillouin spectroscopy with Nd³⁺ photoluminescence analysis, we find a linear dependence that can be used to identify uniaxial stress and cooling rate in any given combination concurrently. The interrelated calibrations and linear dependence models are established and evaluated, and equations relating the change of glass network due to effects of cooling rate or uniaxial stress are given. Full article

A set of 14 glass fragments and production remains dated to the 16th and 17th centuries was collected during rescue archaeological works conducted in Granada, Spain, and was characterised by µ-PIXE. This preliminary study constitutes the first analytical approach to glass manufacturing remains from a Spanish production dated to the early-modern period. µ-PIXE allowed for the quantification of major, minor and some trace elements of the glass fragments. It also allowed mapping the elemental distribution on the fragments that were identified as an interface of crucible/glass. This analysis constitutes an evaluation of the ionic exchange between glass and crucible. The glass colours vary from the natural green and blue hues to completely colourless samples. The results show that the majority of the glass samples are of soda-lime-silicate composition, and only one proved to be of a potassium-rich composition. From this, one can hypothesise that glass rich in sodium (following the Mediterranean tradition) and potassium-rich glass (following a central and north European tradition) were both locally produced. Since this location was known as la Calle Horno del Vidrio (Glass Furnace Street) and several production evidences were found, it is highly probable that an artisanal glass production existed in this area. Full article

The need for sustainable solutions to reduce the carbon footprint of the ceramics and glass industry leads towards the development of new electric current-assisted technologies. Flash sintering-like processes in glasses allow a reduction of the softening temperature and could pave the way for new shaping technologies. Herein, we investigated the flash transition in soda-lime silicate glass using two different electrode materials, silver, and platinum. The high dielectric strength registered on samples tested with platinum electrodes undergoes a significant reduction when silver is used. In other words, in the case of silver electrodes, the flash ignition takes place at a lower onset field. Moreover, the Joule heating developed during the process can be turned from being highly inhomogeneous with Pt electrodes to homogeneous when Ag electrodes are used. Full article

Glass ionomer cement (GIC) is a well-known restorative material applied in dentistry. The present work aims to study the effect of hydroxyapatite (HA) addition into GIC based on physical, mechanical and structural properties. The utilization of waste materials namely clam shell (CS) and soda lime silica (SLS) glass as replacements for the respective CaO and SiO₂ sources in the fabrication of alumino-silicate-fluoride (ASF) glass ceramics powder. GIC was formulated based on ASF glass ceramics, polyacrylic acid (PAA) and deionized water, while 1 wt.% of HA powder was added to enhance the properties of the cement samples. The cement samples were subjected to four different ageing times before being analyzed. In this study, the addition of HA caused an increment in density and compressive strength results along with ageing time. Besides, X-ray Diffraction (XRD) revealed the formation of fluorohydroxyapatite (FHA) phase in HA-added GIC samples and it was confirmed by Fourier Transform Infrared (FTIR) analysis which detected OH‒F vibration mode. In addition, needle-like and agglomeration of spherical shapes owned by apatite crystals were observed from Field Emission Scanning Electron Microscopy (FESEM). Based on Energy Dispersive X-ray (EDX) analysis, the detection of chemical elements in the cement samples were originated from chemical compounds used in the preparation of glass ceramics powder and also the polyacid utilized in initiating the reaction of GIC. Full article

Both vitrified bottom ashes (VBAs) and waste glasses are forms of inorganic waste material that are widely landfilled, despite having some economic potential. Building on previous studies, we prepared glass-ceramic foams by the combination of VBA with either soda-lime glass (SLG) or borosilicate glass (BSG). Suspensions of fine powders in weakly alkaline solution underwent gelation, followed by frothing at nearly room temperature. Hardened “green” foams were sintered, with concurrent crystallization, at 850–1000 °C. All foams were highly porous (>70%), with mostly open porosity. The glass addition was fundamental in both gelation (promoting the formation of carbonate and silicate hydrated phases) and firing steps. While SLG addition enhanced the viscous flow sintering, without a significant impact on the crystallization of gehlenite, the main crystalline phase from the devitrification of VBA, BSG addition caused a reactive sintering, with remarkable changes in the phase assemblage. The glass addition generally also allowed lower sintering temperatures and yielded products with excellent crushing strength. However, only specific conditions resulted in the complete immobilization of pollutants (e.g., Cr³⁺ ions). Full article

Mineral wools—a general term for stone wool and glass wool—are the most common insulation materials in the world. Consequently, 2.5 million tons of mineral wool waste is generated globally which is mainly landfilled. Recently, it was found that mineral wool waste can be used as cementitious material by alkali activation. In alkali activation, dissolution is the primary process as it involves the breakage of bonds and release of ionic species from the surface of the material upon interaction with the reacting solution. Dissolution plays a significant role in the strength development and micro/nano-structural morphology of the final cementitious material. Here, we study the dissolution of stone wool (depicting chemistry of Al-Ca-Mg-Fe silicate glass) and glass wool (depicting chemistry of soda lime silicate glass) in sodium hydroxide solution to provide a better understanding of their reactivity under alkali activation.
Experimental studies were carried out at two different liquid to solid ratio (L/S) conditions: high L/S (1000) and low L/S (50) in an N₂ glove box. High L/S conditions give information on the early stages of the dissolution whereas low L/S provides later stages of the process.
The ICP results show that under both L/S conditions glass wool releases increasing amount of Si, Al and B reaching 39–45 wt.%, 23–26 wt.% and 34–44 wt.% extent of dissolution with time respectively. However, in stone wool the release rate of Si and Al increases initially but becomes constant after certain time period. In both mineral wools, release rate of Ca and Mg varied with time. These changes in the release rate was observed to be due to precipitation of dissolved species. XRD results revealed that three crystalline phases-hydrotalcite, calcite, and calcium silicate were present on both glass and stone wool fibers after 25 days of dissolution. SEM results revealed that the morphology varies at different dissolution times and experimental conditions for both the mineral wools depicting the change in the reaction path. From these studies, we conclude that the dissolution rate and mechanism are controlled by both chemical composition of the fiber and the reacting solution conditions. Full article