Abstract:Crystallization proceeds through high-temperature and non-stoichiometric phases which recrystallize to become sanbornite (BaSi2O5) during heating or through time.
“…The primitive cell of sanbornite (Pmcn) contains 32 atoms and therefore, 96 normal modes including the three acoustic translations (B1u, B2u & B3u) ( Figure 2). The correlation method [41] allows for the determination of the vibrational modes at the center of the Brillouin There is no known published evaluation of the vibrational spectra despite the multiple Raman studies involving sanbornite [27,28,42]. However, theoretical results reproduce the experimental vibrational modes with an absolute mean deviation of <6 cm -1 , and the high degree of overlap in the measured peaks and the displacement from unity in the calculated frequencies yields a small potential for ambiguity.…”
Section: Low-basi2o5mentioning
confidence: 99%
“…When doped with rare-earth elements, these materials can be used as light emitting diode materials [23,24]. Although interesting behaviors have been shown, there is a lack of clarity regarding the origin and significance of the vibrational modes and their transitions during crystallization processes [21,[25][26][27][28].…”
We report here the analysis of vibrational properties of the sanbornite (low-BaSi2O5) and Ba5Si8O21 using theoretical and experimental approaches, as well as results of high temperature experiments up to 1100-1150˚C. The crystal parameters derived from Rietveld refinement and calculations show excellent agreement, within 4%, while the absolute mean difference between the theoretical and experimental results for the IR and Raman vibrational frequencies was <6 cm-1. The temperature-dependent Raman study renders that both sanbornite and Ba5Si8O21 display specific Ba and Si sites and their Ba-O and Si-O bonds. In the case of the stretching modes assigned to specific Si sites, the frequency dependence on the Si-O bond length exhibited very strong correlations. Both phases showed that for a change of 0.01 Å, the vibrational mode shifted 10 ± 2 cm-1. These results are promising for using Raman spectroscopy to track in situ reactions under a wide variety of conditions, especially during crystallization.
“…The primitive cell of sanbornite (Pmcn) contains 32 atoms and therefore, 96 normal modes including the three acoustic translations (B1u, B2u & B3u) ( Figure 2). The correlation method [41] allows for the determination of the vibrational modes at the center of the Brillouin There is no known published evaluation of the vibrational spectra despite the multiple Raman studies involving sanbornite [27,28,42]. However, theoretical results reproduce the experimental vibrational modes with an absolute mean deviation of <6 cm -1 , and the high degree of overlap in the measured peaks and the displacement from unity in the calculated frequencies yields a small potential for ambiguity.…”
Section: Low-basi2o5mentioning
confidence: 99%
“…When doped with rare-earth elements, these materials can be used as light emitting diode materials [23,24]. Although interesting behaviors have been shown, there is a lack of clarity regarding the origin and significance of the vibrational modes and their transitions during crystallization processes [21,[25][26][27][28].…”
We report here the analysis of vibrational properties of the sanbornite (low-BaSi2O5) and Ba5Si8O21 using theoretical and experimental approaches, as well as results of high temperature experiments up to 1100-1150˚C. The crystal parameters derived from Rietveld refinement and calculations show excellent agreement, within 4%, while the absolute mean difference between the theoretical and experimental results for the IR and Raman vibrational frequencies was <6 cm-1. The temperature-dependent Raman study renders that both sanbornite and Ba5Si8O21 display specific Ba and Si sites and their Ba-O and Si-O bonds. In the case of the stretching modes assigned to specific Si sites, the frequency dependence on the Si-O bond length exhibited very strong correlations. Both phases showed that for a change of 0.01 Å, the vibrational mode shifted 10 ± 2 cm-1. These results are promising for using Raman spectroscopy to track in situ reactions under a wide variety of conditions, especially during crystallization.
“…X-ray diffraction was performed using a Shimadzu XRD6000 (CuKα, 40kV/30mA). All the experiments were performed at room temperature, with a goniometer speed of 2 • /min, an angular step of 0.02, and a counting time 0.6 s [46][47][48]. The granulometric analysis was performed by low-angle laser light scattering (Cilas, 1064LD, Orléans, France), where the clays were scattered in 250 mL of distilled water in a Hamilton Beach N5000 stirrer at a speed of 17,000 rpm for 10 min; then, the scatterings were inserted in the equipment in wet mode until they reached the optimal concentration of 150 units of diffraction/incidence area [49,50].…”
The efficiency of acid treatment on natural calcium bentonite (natural bentonite) for anionic dye adsorption was investigated using methyl orange (MO) as a probe. Additionally, adsorption experiments were accomplished between the natural bentonite, acidified bentonite, and a cationic dye (methylene blue, MB). Acid functionalization in natural bentonite (RF) was carried out with HCl and H2SO4 acids (RF1 and RF2, respectively). The samples were characterized by chemical analysis, mineralogy, particle size, and thermal behavior with the associated mass losses. The adsorption efficiency of MO and MB dyes was investigated by the effects of the initial concentration of adsorbate (Ci) and the contact time (tc). The acid treatment was efficient for increasing the adsorption capacity of the anionic dye, and the Qmaxexp values measured were 2.2 mg/g, 67.4 mg/g e 47.8 mg/g to RF, RF1 e RF2, respectively. On the other hand, the acid functionalization of bentonite did not significantly modify the MB dye adsorption. The Sips equation was the best fit for the adsorption isotherms. Thus, we found that the acid-functionalized bentonite increases the anionic dye adsorption by up to 8000%. The increased adsorptive capacity of acidified bentonite was explained in terms of electrostatic attraction between the clay surface and the dye molecule.
“…The presence of a small amorphous halo was also noticed between 15 ° and 25 ° (2θ), which is related to the glass phase. This glassy phase is probably formed due to excess SiO 2 in the ceramic formulations [ 29 ]. The amorphous halo area reduced with the increasing sintering temperature, which may be directly related to the formation of mullite and, consequently, a decrease in the glass phase.…”
Section: Resultsmentioning
confidence: 99%
“…The mullite crystal growth is probably attenuated in the C 0 sample due to a less viscous liquid phase, which does not favor the dissolution of silica and alumina [ 37 ]. Anorthite crystals were not observed because they have isometric round morphology with a size smaller than those of mullite [ 29 ] and probably are immersed in the vitreous phase.…”
New ceramic formulations based on scheelite tailing were developed, and their potential in the ceramic industry was evaluated. Green bodies with different contents of scheelite tailing (0–8 wt%) were sintered (1150 °C, 1200 °C, and 1250 °C) and characterized in terms of the main mineralogical phases, microstructure, and physico-mechanical properties. The mullite was the main phase identified in all sintered temperatures. This result was also ratified with the aid of scanning electron microscope (SEM) images, in which small needles of the mullite were detected. The presence of mullite is required because it contributes to increasing the mechanical resistance of the material. The physico-mechanical properties measured (water absorption, linear shrinkage, apparent porosity, and flexural strength) were compared to the ISO 13006, and the samples sintered at 1150 °C presented potential to be used as semi-stoneware, while those sintered at 1200 °C and 1250 °C can be employed stoneware and porcelain tiles, respectively.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.