2010
DOI: 10.1016/j.jallcom.2010.01.012
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Sol–gel synthesis and characterization of Al2O3–CeO2 composite nanopowder

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Cited by 27 publications
(11 citation statements)
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“…The results indicated that the obvious weight losses began at 80 • C and all chemical reactions involving weight losses, such as decomposition of the organic polymeric network with evolution of CO 2 and H 2 O, were completed below 531.6 • C. The total weight loss was about 80%, which occurred in three steps: (i) initial weight loss (about 10%) below 250 • C, resulting from the evaporation of residual solvent and water, with wide and weak endothermic peaks from about 100 • C, (ii) a second significant weight loss (about 60% caused by the decomposition of the organic polymeric network with evolution of CO 2 and H 2 O, with endothermic peaks ranging from 250 • C to 400 • C, and (iii) a third weight loss (about 10-20%) in the TG curves, combined with an exothermal peak at the temperature region of 400-531.6 • C, which was attributed to the oxidation of metal-organic groups. The similar TG results of MN xerogel were also reported in other microwave dielectric ceramics with citrate sol-gel method [14][15][16][17]. No further significant weight loss and thermometric peaks were observed above 531.6 • C in the TG-DTA curves, indicating the minimum firing temperature to synthesize the magnesium niobate phases.…”
Section: Methodssupporting
confidence: 85%
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“…The results indicated that the obvious weight losses began at 80 • C and all chemical reactions involving weight losses, such as decomposition of the organic polymeric network with evolution of CO 2 and H 2 O, were completed below 531.6 • C. The total weight loss was about 80%, which occurred in three steps: (i) initial weight loss (about 10%) below 250 • C, resulting from the evaporation of residual solvent and water, with wide and weak endothermic peaks from about 100 • C, (ii) a second significant weight loss (about 60% caused by the decomposition of the organic polymeric network with evolution of CO 2 and H 2 O, with endothermic peaks ranging from 250 • C to 400 • C, and (iii) a third weight loss (about 10-20%) in the TG curves, combined with an exothermal peak at the temperature region of 400-531.6 • C, which was attributed to the oxidation of metal-organic groups. The similar TG results of MN xerogel were also reported in other microwave dielectric ceramics with citrate sol-gel method [14][15][16][17]. No further significant weight loss and thermometric peaks were observed above 531.6 • C in the TG-DTA curves, indicating the minimum firing temperature to synthesize the magnesium niobate phases.…”
Section: Methodssupporting
confidence: 85%
“…According to the sintering equation of initial stage [24], the use of MN nanopowders as the starting materials was effective in preparing high density MN ceramics through low-temperature sintering and short sintering time. Therefore, the sol-gel process showed significant advantages of sintering the ceramics at relatively low temperatures, which were demonstrated by other reports elsewhere [14][15][16][17].…”
Section: Phase Formation and Characterization Of Mn Powderssupporting
confidence: 52%
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“…In vapor phase methods there are some disadvantages such as high cost equipment and low efficiency. Among these methods, sol-gel is a simple and economical route with high efficiency and specific properties at low temperature like high surface area in volume ratio, fine particle size distribution, and so on [10].…”
Section: Introductionmentioning
confidence: 99%
“…The precursor solution was stirred at 100°C for 3 h and was aged at 60°C until the batch set to a rigid gel. It was then dried at 80°C for 48 h. More details about the processing of nanopowder are mentioned elsewhere . The resultant synthesis product (gel) has been calcined at 900°C for 30 min to remove volatile components.…”
Section: Methodsmentioning
confidence: 99%