2014
DOI: 10.1016/j.jnoncrysol.2013.06.023
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Influence of amorphous phase separation on the crystallization behavior of glass-ceramics in the BaO–TiO2–SiO2 system

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Cited by 13 publications
(14 citation statements)
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“…750 ± 5 °C. 12 Furthermore, various crystal growth mechanisms of fresnoites have been reported ranging from polygon growth in stoichiometric BTS-glass 12,24 to dendritic growth in BT0.75S and a mechanism proposed to be viscose fingering in a glass of the composition ST0.75S where Sr-fresnoite crystallized from the surface. 25 The growth of the hexagonal phase Sr 0.75 Al 1.5 -Si 0.5 O 4 in a glass of that same composition 20 remarkable similarities to the growth of Sr-fresnoite in the ST0.75S-glass.…”
Section: ■ Introductionmentioning
confidence: 99%
“…750 ± 5 °C. 12 Furthermore, various crystal growth mechanisms of fresnoites have been reported ranging from polygon growth in stoichiometric BTS-glass 12,24 to dendritic growth in BT0.75S and a mechanism proposed to be viscose fingering in a glass of the composition ST0.75S where Sr-fresnoite crystallized from the surface. 25 The growth of the hexagonal phase Sr 0.75 Al 1.5 -Si 0.5 O 4 in a glass of that same composition 20 remarkable similarities to the growth of Sr-fresnoite in the ST0.75S-glass.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Additionally, nucleating agents may be added to increase bulk crystallization. Phase-separation could also be used deliberately to nucleate crystallization such as has been proposed for oxide systems precipitating cordierite [15], spinel [16,65], fresnoite [66], and fluorides [67]. This method is likely to result in a reasonably low to moderate total crystal fraction, perhaps at b 50 vol.%.…”
Section: Discussionmentioning
confidence: 99%
“…The powders were prepared in a mole ratio of 70 BaCO 3 : 30 TiO 2 and thoroughly mixed in acetone inside an ultrasonic bath. This composition was chosen because of its effectiveness to form a BTS glass-ceramic structure, as reported in the literature [13,[31][32][33][34]. The mixed power was inserted into the preform and the preform was then heated up to~1900 • C in a tube furnace under a nitrogen environment, while the inside of the tube was kept in a low vacuum (~0.1 bar).…”
Section: Introductionmentioning
confidence: 99%
“…The drawn fiber was then isothermally heat treated at 850 • C for 10 h with a heating rate of 10 • C/min to form a glass-ceramic core. This specific thermal heat treatment was chosen based on the composition analysis of the fiber (which will be discussed in the Section 3) and its corresponding crystallization temperature, reported in the literature [13,[31][32][33][34]. has an eutectic point of ~1260 °C and a melting point of ~1445 °C [13].…”
Section: Introductionmentioning
confidence: 99%