TY - JOUR
T1 - Microstructural characterization and crystallization behaviour of (1 - x)TeO2 - xWO3 (x = 0.15, 0.25, 0.3 mol) glasses
AU - Öveçoǧlu, M. L.
AU - Özen, G.
AU - Cenk, S.
PY - 2006
Y1 - 2006
N2 - DTA, XRD and SEM investigations were conducted on the (1 - x)TeO2-xWO3 glasses (where x=0.15, 0.25 and 0.3). Whereas the 0.75TeO2-0.25WO3 and 0.7TeO2-0.3WO3 glasses show no exothermic peaks, an indication of no crystallization in their glassy matrices, two crystallization peaks were observed on the DTA plot of the 0.85TeO2-0.15WO3 glass. On the basis of the XRD measurements of the 0.85TeO2-0.15WO3 glass samples heated to 510 °C and 550 °C (above the peak crystallization temperatures), α-TeO2 (paratellurite), γ-TeO2 and WO3 phases were detected in the sample heated to 510 °C and the α-TeO2 and WO3 phases were present in the sample heated to 550 °C. SEM micrographs taken from the 0.85TeO2-0.15WO3 glass heated to 510 °C showed that centrosymmetrical crystals were formed as a result of surface crystallization and were between 3 μm and 15 μm in width and 12 μm and 30 μm in length. On the other hand, SEM investigations of the 0.85TeO2-0.15WO3 glass heated to 550 °C revealed the evidence of bulk massive crystallization resulting in lamellar crystals between 1 μm and 3 μm in width and 5 μm and 30 μm in length. DTA analyses were carried out at different heating rates and the Avrami constants for the 0.85TeO2-0.15WO3 glass heated to 510 °C and 550 °C were calculated as 1.2 and 3.9, respectively. Using the modified Kissinger equation, activation energies for crystallization were determined as 265.5 kJ/mol and 258.6 kJ/mol for the 0.85TeO2-0.15WO3 glass heated to 510 °C and 550 °C, respectively.
AB - DTA, XRD and SEM investigations were conducted on the (1 - x)TeO2-xWO3 glasses (where x=0.15, 0.25 and 0.3). Whereas the 0.75TeO2-0.25WO3 and 0.7TeO2-0.3WO3 glasses show no exothermic peaks, an indication of no crystallization in their glassy matrices, two crystallization peaks were observed on the DTA plot of the 0.85TeO2-0.15WO3 glass. On the basis of the XRD measurements of the 0.85TeO2-0.15WO3 glass samples heated to 510 °C and 550 °C (above the peak crystallization temperatures), α-TeO2 (paratellurite), γ-TeO2 and WO3 phases were detected in the sample heated to 510 °C and the α-TeO2 and WO3 phases were present in the sample heated to 550 °C. SEM micrographs taken from the 0.85TeO2-0.15WO3 glass heated to 510 °C showed that centrosymmetrical crystals were formed as a result of surface crystallization and were between 3 μm and 15 μm in width and 12 μm and 30 μm in length. On the other hand, SEM investigations of the 0.85TeO2-0.15WO3 glass heated to 550 °C revealed the evidence of bulk massive crystallization resulting in lamellar crystals between 1 μm and 3 μm in width and 5 μm and 30 μm in length. DTA analyses were carried out at different heating rates and the Avrami constants for the 0.85TeO2-0.15WO3 glass heated to 510 °C and 550 °C were calculated as 1.2 and 3.9, respectively. Using the modified Kissinger equation, activation energies for crystallization were determined as 265.5 kJ/mol and 258.6 kJ/mol for the 0.85TeO2-0.15WO3 glass heated to 510 °C and 550 °C, respectively.
KW - Crystallization
KW - Glasses
KW - Microstructure-final
KW - TeO
KW - WO
UR - http://www.scopus.com/inward/record.url?scp=31744451549&partnerID=8YFLogxK
U2 - 10.1016/j.jeurceramsoc.2005.01.039
DO - 10.1016/j.jeurceramsoc.2005.01.039
M3 - Article
AN - SCOPUS:31744451549
SN - 0955-2219
VL - 26
SP - 1149
EP - 1158
JO - Journal of the European Ceramic Society
JF - Journal of the European Ceramic Society
IS - 7
ER -