Increasing Calcination Temperature Research Articles

Facile preparation of vanadium oxide films under varied calcination temperature and their multicolor electrochromic behaviors

A vanadium oxide (VO) film was prepared on indium tin oxide (ITO) glass using a simple electrophoretic method and the VO film and its device demonstrated multicolor electrochromic properties of yellow, green, orange-red, and their intermediate colors. The X-ray diffraction (XRD) and X-ray photoelectron spectra (XPS) were employed to characterize the composition of the as-prepared films. The ratio of V5+/V4+ in the XPS is significantly different in the yellow, green, and orange-red states and this ratio can be adjusted by applied voltages. The detailed effect of calcination temperature as a post-treatment method on the electrochromic performance of VO film was explored. With the increase of calcination temperature, the optical modulation ability of the films was enhanced, and the color change contrast of the films was most obvious at 200 °C. Meanwhile, the cyclic stability of the VO films was also enhanced. The cyclic voltammetry (CV) curves show that the prepared V2O5 films have high cyclic stability at a calcination temperature of 300 °C. The color efficiency (CE) values of the VO devices were 3.4 cm2C-1 (from initial yellow to green) and 21.6 cm2C-1 (from green to orange-red) at 700 nm, and the coloring time (Tc) and bleaching time (Tb) of the VO devices were 6 s and 10 s, respectively. This work develops a simple and environmentally friendly method to prepare VO films and their devices with multicolor electrochromic properties.

Study of Pure and Mixed-Phase TiO2 Nanomaterials Synthesized via a Modified Solvothermal Method and Their Optical Properties

The modified-solvothermal method has been used to synthesize pure anatase and anatase-rutile mixed-phase TiO2 nanomaterials using titanium isopropoxide, sodium hydroxide, and triethylamine as primary sources with different calcination temperatures (500 °C and 700 °C). The effect of the precipitating agent, capping agent, and calcination temperatures on the properties, such as structural, morphological, and optical of the resultant nanomaterials has been investigated through several techniques including X-ray diffraction (XRD), Raman spectroscopy, Transmission electron microscopy (TEM), UV–Vis absorption spectroscopy, Scanning electron microscopy (SEM), selected area electron diffraction (SAED), and high-resolution transmission electron microscopy (HRTEM). XRD and Raman spectra confirmed the pure anatase and anatase-rutile mixed structures of the prepared nanomaterials at 500 °C and 700 °C. Furthermore, the Raman active modes confirmed the formation of TiO2. It is noticed that the crystallite size of the nanomaterials increased with increasing calcination temperature of the XRD pattern. The morphologies of the prepared samples were displayed using SEM and TEM micrographs, which are almost the same in shape (cubic and cubic rod mixed). The particle size increased with an increase in calcination temperature and was found to be between 10 and 20 nm, which is similar to the crystallite size. The lattice fringes (d) from HRTEM images are assigned to the XRD plane (101) and (110) plane of anatase and anatase-rutile TiO2, respectively. The SAED exhibited well crystalline nature and confirmed the polycrystalline nature of the prepared nanomaterials by the bright points and the ring patterns. The optical band gap decreased with an increase in temperature and the optical properties are affected by calcination temperature and triethylamine.

Microstructural characteristics of aluminosilicate minerals in cement clinker prepared from coal gangue, carbide slag, and desulfurization gypsum

Utilizing solid waste to prepare cement clinker with low-calcium minerals is crucial for the low-carbon evolution of cementitious materials. In this study, a belite-ye’elimite-ternesite cement clinker was prepared using coal gangue, carbide slag, and desulfurization gypsum instead of non-renewable resources. The evolution law of the silica-alumina mineral phase in cement clinker under different calcining temperatures was tested and analysed. The results show that the predominant mineral phases in cement clinker consist of belite, ye’elimite, and ternesite at 1200 °C to 1250 °C. The composition of cement clinker transforms into belite and ye’elimite as the calcination temperature increases to 1300–1400 °C. At 1400 ℃, the content of belite in cement clinker reaches a remarkable 85 %. The results of XPS and NMR spectra showed that the chemical binding energy and chemical shift of Al in the cement clinker changed after calcination, representing the transformation of the aluminate in kaolinite, with [AlO6], to ye’elimite, with [AlO4]. The peak fitting results of 29Si NMR spectra semi-quantitatively describe the transition process of the silicate mineral phase from kaolinite to ternesite and then to belite. Morphologically, the increase in calcination temperature leads to a significant enlargement of the grain size of belite in cement clinker. This study can provide a basis for research on the phase regulation of cement clinker composed mainly of low-calcium minerals.

Mitigation of Fluoride Contamination in Drinking Water Supply Sources by Adsorption Using Bone Char: Effects of Mineral and Organic Matrix

This study focused on fluoride (F−) contamination of water sources in Bahimi village, Cameroon. After the first investigation, results revealed that all water samples collected had elevated concentrations of fluoride ions (2.3 ± 0.1) mg/L to (4.5 ± 0.2) mg/L above the WHO guidelines (less than 1.5 mg/L). To mitigate the F− levels, the use of bone char (BC) as an adsorbent material was proposed and its performance was tested. BC was prepared from bovine bones at different calcination temperatures (350 °C, 450 °C, 550 °C and 650 °C) and residence times (1 h and 2 h). The prepared materials were characterized in detail by SEM/EDS, BET, FTIR, and XRD. The BET findings indicated that the surface area of BC samples decreased with increasing calcination temperature and residence time. At a lower heating temperature and holding time (350 °C, 1 h), the prepared BC exhibited a higher specific surface area (112.3 ± 0.3) m2/g and adsorption capacity for F− in the sampled water. Also, the batch adsorption experiments showed that the optimized adsorbent dose of 8 g/L facilitates the reduction in the F− level of the sampled water below the acceptable limit level (1.5 mg/L) within 5 min of treatment. The presence of Ca2+ and Mg2+ in natural water has a positive effect on the removal of F− in BC resulting in a high adsorption performance range of (72.5 ± 1.4)% to (80.3 ± 0.6)%. It was found that the adsorption of Ca2+ on the BC surface occurs via cation exchange with Na+. However, an increase in dissolved organic carbon (DOC) in the treated water limited the application of BC. Overall, the study presented a cost-effective adsorbent for the removal of this recalcitrant ion in the water source.

Investigating and correlating the photocatalytic activity of synthesised strontium titanate nanopowder with calcination temperature

In this study, SrTiO3 nanoparticles were synthesised in high yield using a simple and low-cost method, followed by calcination. The effect of the calcination temperature in the range from 700 to 1100 °C on the morphology, phase structure, crystallite size, and photocatalytic activity of SrTiO3 nanoparticles was investigated. Analysis of the morphology and structure of the synthesised samples revealed an increase in the average particle size from 70.4 to 361.72 nm as well as crystallite growth with increasing calcination temperature (from 800 to 1100 °C), likely due to the fusion of smaller crystallites into larger ones. A possible pathway for the growth mechanism of strontium titanate grains was also proposed. The SrTiO3 sample calcined at 800 °C exhibited the highest methylene blue (MB) photodegradation efficiency, achieving 100 % degradation within 30 min of irradiation. The pseudo-first-order reaction rate constant k for this sample was determined to be 0.156 min−1, which is almost 1.8 and 14.19 times higher compared to those of commercial P25 and SrTiO3, respectively. The analysis indicated that the high photoactivity of this sample was due to its high crystallinity, relatively small particle size, and optimal light absorption, which enhanced the separation and transport of the photogenerated charges and increased the number of active sites, thereby positively affecting the photocatalytic properties. Additionally, the effects of the initial dye concentration and amount of photocatalyst loaded on the photodegradation efficiency were investigated.

Electric Properties Change during Morphological Evolution of CeO2 Nanostructures: Synergy between Bulk and Surface Defects.

CeO2 samples were synthesized via the polymeric precursor method at different calcination temperatures. Electric properties were investigated using positron annihilation lifetime spectroscopy, electron paramagnetic resonance spectroscopy, and complex impedance spectroscopy. Reduction in the specific surface area of the particles with increasing calcination temperature along with morphological changes were observed. PALS depicted doubly ionized oxygen vacancies surrounded by two Ce3+ atoms, while the EPR spectroscopy showed a singly ionized oxygen vacancy surrounded by Ce3+ and Ce4+ ions. Impedance measurements unraveled the presence of polarons, while thermal treatments led to a lower electrical conductance, as the calcination temperature increased.

Cr-MIL-101 derived nano Cr2O3 for highly efficient dehydrogenation of n-hexane

Nano Cr2O3 (n-Cr2O3) was prepared by the thermolysis of the mesoporous Cr-MIL-101, and its catalytic performance for n-hexane dehydrogenation was investigated and compared with Cr2O3 obtained by traditional method. It is found that dehydrogenation of n-hexane on n-Cr2O3 catalyst can produce n-hexenes and benzene efficiently, and the catalytic performance is related to the calcination temperature. The optimal n-hexane conversion can be obtained on n-Cr2O3 calcinated under 600 °C, is 40.6%, and the selectivities to n-hexenes and benzene are 20.1% and 69.3%, respectively. The conversion of n-hexane for n-Cr2O3 catalyst is decreased with calcination temperature increase, while the catalyst stability in dehydrogenation reaction is enhanced. n-Hexane conversion of p-Cr2O3-1 (obtained by precipitation method) and p-Cr2O3-2 (calcinating Cr(NO3)·9H2O directly) catalysts are very low (<7.5%), and their specific activity for n-hexane dehydrogenation are 1.5 and 1.7 g/(m2·h) respectively, lower than that of n-Cr2O3-600 (2.0 g/(m2·h)). The results of BET, XRD, TEM and FT-IR reveal that n-Cr2O3 is the nanoparticles with large specific surface area that more dehydrogenation active sites are exposed, while p-Cr2O3 is the large particles with extremely low surface area that few dehydrogenation active sites are presented. By contrast, industrial Cr2O3/Al2O3 catalyst possesses the highest specific activity of 2.4 g/(m2·h) due to the dispersion effect of Al2O3. Therefore, highly catalytic activity of n-Cr2O3 for n-hexane dehydrogenation is attributed to the unique properties of small particle, large specific surface area and more exposed active sites. This work not only explains the high dehydrogenation activity of nano-Cr2O3 derived by Cr-MIL-101, but also provides guidance for the precise design and synthesis of high-performance CrOx-based catalyst for the dehydrogenation of alkanes.

Early hydration and mechanical performance of composited cementitious system prepared from high temperature calcined molybdenum tailings

To improve the recycling of solid waste and achieve the secondary utilization of waste resources, this study investigates the preparation of molybdenum tailings composited binders by high temperature calcination using molybdenum tailings, limestone, bauxite, and iron concentrate powder. Besides, to explore the mechanical properties of the new molybdenum tailings composited binders, a molybdenum tailings composited mortar was prepared. The mechanical properties, micro performance and hydration mechanism of the new molybdenum tailings composited binders were studied. Finally, the carbon dioxide emission of green molybdenum tailings composited binders/molybdenum tailings composited mortar was evaluated by the life cycle assessment method. The results show that the compressive strength of molybdenum tailings composited binders gradually increases with the increase of calcination temperature. When the calcination temperature is 1350 °C, the compressive strength and flexural strength at 28 days are 44.17 MPa and 7.56 MPa, respectively, which are 3.65 % and 4.63 % higher than control group made by P·O 42.5 cement. The early strength of molybdenum tailings composited binders increases slowly, and the later strength increases rapidly. In addition, there is more C2S in the matrix, resulting in a slow hydration heat rate and low cumulative hydration heat. Compared with other groups, the hydration kinetic parameters and hydration rate of molybdenum tailings composited binders under 1350 °C were the lowest. The main hydration prodcuts of molybdenum tailings composited binders are C-S-H, calcium hydroxide, and Aft gels. Compared with P·O 42.5 cement paste and mortar, the carbon dioxide emission of molybdenum tailings composited binders/molybdenum tailings composited mortar is reduced by 42.82 % and 29.08 %, respectively, which can indicate that the new binders can produce less carbon dioxide. Overall, this study can provide new ways for the development of the new binder mixed with plenty of molybdenum tailings, and offer a novel way for recycling the molybdenum tailings, and also present some valuable experimental results for the application of molybdenum tailings in infrastructures.

SnO2QDs: Photophysical properties, photocatalytic activity, mineralization financial cost and recycling process during industrial effluent treatment

This study investigates the synthesis, characterization, and photocatalytic performance of pure and titanium-doped tin dioxide quantum dots (SnO2QDs) prepared via a sonochemical method. The structural and morphological properties were thoroughly examined using XRD, FTIR, SEM-EDX, HRTEM, UV-DRS, and BET surface area analysis. XRD confirmed the formation of tetragonal SnO2 with high phase purity and average crystallite sizes of 2.95 nm for SnO2QD1 (calcined at 270 °C) and 8.36 nm for SnO2QD2 (calcined at 480 °C). Titanium doping was achieved without altering the SnO2 crystalline structure, as evidenced by FTIR spectra showing characteristic vibrational modes and hydroxyl groups. HRTEM images revealed spherical nanoparticles with diameters of 3.2 nm for SnO2QD1 and 9.7 nm for SnO2QD2, supported by SAED patterns confirming their polycrystalline nature. The photocatalytic efficiency was evaluated through the degradation of Reactive Yellow 145 dye under Xenon lamp irradiation. SnO2QD1 exhibited superior photocatalytic activity with a rate constant (k) of 6.94 × 10−3 s−1, achieving 80 % dye degradation in 105 min, compared to SnO2QD2 with a k of 4.50 × 10−3 s−1 and 83 % degradation in 120 min. Titanium doping further enhanced the photocatalytic performance, with SnO2QDT1 (1 % Ti) showing a k of 9.89 × 10−3 s−1 and 80 % degradation in just 90 min, three times more efficient than SnO2QDT2 (9 % Ti). BET analysis indicated a significant reduction in surface area with increased calcination temperature, from 154 m2/g for SnO2QD1 to 86 m2/g for SnO2QD2. The bandgap energies, determined via UV-DRS, were 3.30 eV for SnO2QD1 and 3.34 eV for SnO2QD2, slightly reduced in Ti-doped samples, enhancing visible light absorption. The SnO2QDs demonstrated excellent recyclability, maintaining photocatalytic activity over eight reuse cycles. Economic analysis based on Saudi Arabian electricity tariffs highlighted the cost-effectiveness of SnO2QD1, offering a 5.2 % reduction in energy consumption compared to SnO2QD2. These findings position SnO2QDs as highly efficient and sustainable photocatalysts for industrial wastewater treatment applications.

Research on the Influence of Thermal Decomposition of Magnesium Chloride Hexahydrate on the Preparation of Magnesium Oxide and Hydrated Magnesium Hydroxide

Magnesium chloride hexahydrate is an important intermediate product in magnesite processing. In order to promote the efficient utilization of magnesite resources, based on the pyrolysis interval of magnesium chloride hexahydrate, the relationship between magnesium oxide with different physicochemical properties and the apparent properties of hydrated magnesium hydroxide was studied. The results show that the effect of temperature on magnesium oxide sintering is stronger than that of holding time. With the increase of calcination temperature and the extension of holding time of magnesium chloride hexahydrate, the calcined product magnesium oxide was sintered into large particle size with the characteristic particle size D&lt;sub&gt;50&lt;/sub&gt; of 33.89 μm. The crystal was distorted, the chemical activity deteriorated, and the color development time was up to 407 s. When hexahydrate magnesium chloride was calcined at 480 °C with 2 h, it decomposed almost completely. The product, magnesium oxide, consisted of uniformly distributed small coral rod-like particles with strong chemical reactivity and a color development time of 115 s. The particles were small and evenly distributed, with a characteristic particle size D50 of 1.36 μm, and the highest specific surface area reached 7.292 m&lt;sup&gt;2&lt;/sup&gt;/g. The hydrated magnesium hydroxide particles had well-defined edges and corners, with a characteristic particle size D50 of 1.59 μm and a uniform particle size distribution.

Fabrication of temperature-regulated sorbitol/mannitol-doped copper oxides derived from a Cu complex and their photocatalytic properties

In this study, a series of composites containing copper oxide (CuxO) particles doped with sorbitol/mannitol, namely Cu/CuxO@C (x = 1 or 2), was successfully derived from a novel copper complex ([Cu(IPZ)2Cl2] (Cu-Complex), where IPZ = 4-Iodopyrazole) by pyrolysis method and exploiting the stability and modulation of the coordination sites of sorbitol/mannitol, which exhibited excellent photocatalytic properties. The results showed that Cu/CuxO@C possessed high efficiency in degrading rhodamine B (RhB), gentian violet (GV), methyl orange (MO) and Congo red (CR) dyes under UV irradiation, and the degradation effect was gradually enhanced with the increase of calcination temperature. The structural and chemical states of the materials were characterised in detail. Furthermore, the effects of experimental factors such as catalyst dose, solution pH, and inorganic anions on dye degradation efficiency were investigated. The photocatalytic mechanism study demonstrated that the primary oxygen-active substance was superoxide radical (·O2-). The electron transport hypothesis explains the effective separation of electrons and holes within a substance. The Cu/CuxO@C composite was regarded as a potential photocatalyst for dye wastewater treatment due to its high photocatalytic efficiency, reusability, and universality, offering a novel solution to environmental and energy issues.

Experimental investigation on mechanical property and hydration process of sintered sludge cement paste at different water‐binder ratios and curing ages

AbstractThis research investigated the mechanical property and hydration process of sintered sludge cement (SSC) paste, focusing on the effects of calcination temperature of sludge, sintered sludge ash (SSA) content, curing age, and water‐binder ratio using isothermal calorimetry, X‐ray diffraction, scanning electron microscopy, and multiple regression. Increasing calcination temperature enhanced the compressive strength of SSC paste due to the decomposition of minerals like Clinochlore and Muscovite. The compressive strength decreased by 2.4%–49.4% when the SSA content increased from 0% to 50%, with more significant declines noted at higher water‐binder ratios. Notably, the 7‐day compressive strength of the cement paste with 10% SSA showed little change, and the 28‐day compressive strength actually increased at a water‐binder ratio of 0.4. SSA slowed down the hydration rate of cement and induced more Monocarbonate to form in the early stage. A multiple linear regression model was developed to predict SSC compressive strength with a 12% error margin.

Interface enhanced magnetoelectric coupling effect of multiferroic liquids based on CoFe2O4@BaTiO3 core shell particles

A new type CoFe2O4@BaTiO3 (CFO@BTO) multiferroic liquid with different CoFe2O4 (CFO) particle sizes was constructed, and its magnetic properties, electrical properties, and magnetoelectric coupling effects were systematically studied. XRD results show that the CFO phase has a spinel structure, whereas the BaTiO3 (BTO) phase has a perovskite structure, with no obvious heterophase formation. It can be seen from the SEM diagram that the CFO powder has a cuboid shape, and the CFO particle size (1.56 × 0.58 × 0.48 µm, 3.16 × 1.04 × 0.66 µm, 6.47 × 1.53 × 1.40 µm, and 11.19 × 2.64 × 2.28 µm) gradually increased with increasing calcination temperature(T = 450 ℃, 550 ℃, 650 ℃, 750 ℃). TEM results show that the composite particles have obvious core-shell structure. From the hysteresis loop, it can be seen that the saturation magnetization (Ms) of the CFO@BTO powder gradually increases with increasing CFO size. The sedimentation stability of the multiferroic liquid gradually decreases, the dielectric constant and residual polarization (Pr) decrease first and then increase, and the magnetoelectric coefficient and magnetoelectric coupling coefficient increase first and then decrease. When the particle size of the CFO is 6.47 × 1.53 × 1.40 µm, the maximum magnetoelectric coupling coefficient is 210.76 V/(cm·Oe) under an applied magnetic field of 50 Oe, which realizes a strong magnetoelectric coupling effect at room temperature.

Lithium extraction from a clay-type lithium ore using a mixed solution of sulfuric acid and ferric chloride

The demand for lithium resources continues to grow owing to the extensive application of lithium-ion batteries in the clean energy industry, and in consequence the development of lithium extraction technologies is significant. In this study, the mixed solution of H2SO4 and FeCl3 was found to have a synergistic effect on the lithium extraction from a clay lithium ore. Upon calcination at 600 °C for 60 min, followed by leaching with a mixture of 10.5 w% H2SO4 and 2 w% FeCl3 at a liquid-to-solid ratio of 5 mL/g for 90 min at 80 °C, a lithium leaching efficiency of 96.18 % was obtained, better than using individual H2SO4 and FeCl3 at higher concentrations. The TG-DTG-DSC, FTIR, BET and XRD results showed that with the increase of calcination temperature the structures of partial minerals such as kaolinite and cookeite became collapsed, amorphous, unstable and activated, which favored for the release of lithium. With the further increase of calcination temperature, the mineral structure continued to collapse and tends to be stable, making the interlayer lithium tightly fixed and difficult to be released. The XRD and SEM results indicated that the lithium extraction is an ion exchange process rather than mineral dissolution. The synergistic effect of H2SO4 and FeCl3 on the lithium extraction was attributed to the fact that the entry of Fe3+ into the interlayer of the layered structure of clay minerals not only released Li+, but also increased the interlayer spacing, conducive to the access of H+ to the interlayer, and consequently facilitated the ion exchange of H+ and Li+.

Hydrothermal Synthesis of a Valence State Constant High-Entropy Perovskite Sr(TiZrHfVNb)O3 with Improved Photoresponsiveness.

A vanadium ion valence state constant high-entropy perovskite system was synthesized using the hydrothermal method with a trivalent vanadium ion as the vanadium source. The B-site of the perovskite crystal lattice was loaded with five atoms in equal proportions. We tried to synthesize the Sr(TiZrHfVNb)O3 high-entropy system using different methods. However, the valence state of the vanadium ion could only be kept constant using the hydrothermal process in the valence balanced high-entropy composition system. There was significant vanadium element segregation and second phase in the Sr(TiZrHfVNb)O3 system prepared using the solid-state reaction process. Also, obvious vanadium ion valence state ascending from V3+ to V5+ appeared in this high-entropy system with an increase in calcination temperature. Inconspicuous vanadium element segregation appeared at 900 °C, the significant segregation phenomenon and second phase appeared at 1200 °C, and the particle size increased with the temperature. This meant that the high-entropy value could not only stabilize the crystal phase, but also stabilize the ionic valence state. Moreover, the constant trivalent vanadium ion valence state could provide coordinated performance with a wide optical response range and a low band gap for the high-entropy system. This suggests that the system might grow a potential ceramic material for optical applications.

Molecular Crystal Structure Simulations and Structure-Magnetic Properties of LiFePO4 Composite Particles Optimized by La.

In this study LiFePO4/C composite particles were synthesized using five different carbon sources via a one-step sol-gel method. La-doped LiFePO4 was also synthesized using the sol-gel method. The XRD pattern of LixLayFePO4 (x = 0.9~1.0, y = 0~0.1) after being calcined at 700 °C for 10 h indicates that as the doping ratio increased, the sample's cell volume first increased then decreased, reaching a maximum value of 293.36 Å3 (x = 0.94, y = 0.06). The XRD patterns of Li0.92La0.08FePO4 after being calcined at different temperatures for 10 h indicate that with increasing calcination temperature, the (311) diffraction peak drifted toward a smaller diffraction angle. Similarly, the XRD patterns of Li0.92La0.08FePO4 after being calcined at 700 °C for different durations indicate that with increasing calcination times, the (311) diffraction peak drifted toward a larger diffraction angle. The infrared spectrum pattern of LixLayFePO4 (x = 0.9~1.0, y = 0~0.1) after being calcined at 700 °C for 10 h shows absorption peaks corresponding to the vibrations of the Li-O bond and PO43- group. An SEM analysis of LixLayFePO4 (x = 1, y = 0; x = 0.96, y = 0.04; x = 0.92, y = 0.08) after being calcined at 700 °C for 10 h indicates that the particles were irregular in shape and of uniform size. The hysteresis loops of Li0.92La0.08FePO4 after being calcined at 600 °C, 700 °C, or 800 °C for 10 h indicate that with increasing calcination temperature, the Ms gradually increased, while the Mr and Hc decreased, with minimum values of 0.08 emu/g and 58.21 Oe, respectively. The Mössbauer spectra of LixLayFePO4 (x = 1, y = 0; x = 0.96, y = 0.04; x = 0.92, y = 0.08) after being calcined at 700 °C for 10 h indicate that all samples contained Doublet(1) and Doublet(2) peaks, dominated by Fe2+ compounds. The proportions of Fe2+ were 85.5% (x = 1, y = 0), 89.9% (x = 0.96, y = 0.04), and 96.0% (x = 0.92, y = 0.08). The maximum IS and QS of Doublet(1) for the three samples were 1.224 mm/s and 2.956 mm/s, respectively.

Fabrication, physicochemical properties, and cytocompatibility of 3D-printed Sr2MgSi2O7 bioceramic scaffolds calcined at different temperature for bone repair

3D-printed bioactive ceramic scaffolds hold significant promise for addressing critical-size bone defects, owing to their biodegradable and osteogenic properties. Numerous 3D-printed silicate-based (e.g., Sr2MgSi2O7) ceramic scaffolds have been developed, but the rapid degradation and insufficient mechanical properties of which impede their application efficacy. Despite recognizing the pivotal role of calcination temperature in shaping the physicochemical and biological attributes of 3D-printed scaffolds, its specific influence on Sr2MgSi2O7 bioceramics remains ambiguous. This study elucidated the fabrication, physicochemical properties, and cytocompatibility of 3D-printed Sr2MgSi2O7 ceramic scaffolds calcined at different temperatures. The findings revealed a significant enhancement in compressive strength (up to 19.9 MPa) and a decrease in degradation rate with increasing calcination temperature. Compared to conventional tricalcium phosphate scaffolds, Sr2MgSi2O7 scaffold demonstrated superior osteogenic potential, particularly when calcined at 1250°C. With commendable mechanical strength and remarkable osteogenic capabilities, the Sr2MgSi2O7 scaffold emerges a promising avenue for repairing critical-size bone defects.

Utilization of Sintered Sludge Ash with Different Mechanical-Thermal Activation Parameters as a Supplementary Cementitious Material: Mechanical Properties and Life Cycle Assessment of Cement-Based Paste.

The proposal of sintered sludge cement (SSC) paste aligns with the low-carbon development goals of building materials. However, there is a lack of scientific guidance for the preparation of sintered sludge ash (SSA). Herein, this study systematically investigates the influence mechanism of mechanical-thermal activation parameters of SSA on the mechanical properties and life cycle assessment (LCA) of SSC paste, and conducts a comprehensive evaluation using a radar chart and the TOPSIS method. The results show that with the increase in calcination temperature and duration, the compressive and flexural strengths of the SSC paste are improved, especially at 600 °C and above, increasing by 57.92% and 62.52%, respectively. The longer calcination time at 1000 °C results in a decrease in its mechanical properties. The addition of SSA significantly reduces the LCA indicators of cement paste. Specifically, 30% SSA only contributes 8.1% to the global warming potential. Compared to calcination, the LCA indicators have less sensitivity to ball milling, and prolonging the time hardly increases them. Based on performance and environmental impact, the optimal SSA is obtained by calcining at 800 °C for 2 h and ball milling for 10 min. This study can provide theoretical guidance for efficient building material utilization of dredged sludge.

Effect of calcination on the structural, morphological and optical properties of earth abundant Cu2FeSnS4 powders prepared by solid-state reaction

In this paper, we investigate the effect of calcination on the properties of Cu2FeSnS4 (CFTS) prepared by solid-state reaction. As fabricated, the polycrystalline sample was crushed and the powders was calcined at different temperatures (TC = 800, 900 and 1000 °C). A Rietveld analysis shows that the calcined powders have predominately the stannite phase with a nearly stoichiometric composition, with the presence of a small amount of SnS, supported by Raman scattering. Energy dispersive spectroscopy confirms the homogeneity of the CFTS materials. Moreover, the analysis of the surfaces of CFTS pellets using scanning electron microscopy showed a more compact and dense morphology as the calcination temperature increases, thus enhanced photosensitivity. From optical studies, we found that the bandgap energy decreases from 1.40 to 1.18 eV with increasing calcination temperature. Calcination can be a tool to engineer the optical band gap.

Photoacoustic Spectroscopy of Titanium Dioxide, Niobium Pentoxide, Titanium:Niobium, and Ruthenium-Modified Oxides Synthesized Using Sol-Gel Methodology.

The aim of this work was the development and morphological/chemical, spectroscopic, and structural characterization of titanium dioxide, niobium pentoxide, and titanium:niobium (Ti:Nb) oxides, as well as materials modified with ruthenium (Ru) with the purpose of providing improvement in photoactivation capacity with visible sunlight radiation. The new materials synthesized using the sol-gel methodology were characterized using the following techniques: scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), photoacoustic spectroscopy (PAS), and X-ray diffraction (XRD). The SEM-EDS analyses showed the high purity of the bases, and the modified samples showed the adsorption of ruthenium on the surface with the crystals' formation and visible agglomerates for higher calcination temperature. The nondestructive characterization of PAS in the ultraviolet visible region suggested that increasing calcination temperature promoted changes in chemical structures and an apparent decrease in gap energy. The separation of superimposed absorption bands referring to charge transfers from the ligand to the metal and the nanodomains of the transition metals suggested the possible absorption centers present at the absorption threshold of the analyzed oxides. Through the XRD analysis, the formation of stable phases such as T-Nb16.8O42, o-Nb12O29, and rutile was observed at a lower temperature level, suggesting pore induction and an increase in surface area for the oxides studied, at a calcination temperature below that expected by the related literature. In addition, the synthesis with a higher temperature level altered the previously existing morphologies of the Ti:Nb, base and modified with Ru, forming the new mixed crystallographic phases Ti2Nb10O29 and TiNb2O7, respectively. As several semiconductor oxide applications aim to reduce costs with photoexcitation under visible light, the modified Ti:Ru oxide calcined at a temperature of 800 °C and synthesized according to the sol-gel methodology used in this work is suggested as the optimum preparation point. This study presented the formation of a stable crystallographic phase (rutile), a significant decrease in gap energy (2.01 eV), and a visible absorption threshold (620 nm).