Nonepitaxial heterogeneous nucleation of α-sialon in the Ca-doped system

2001 ◽  
Vol 16 (2) ◽  
pp. 578-582 ◽  
Author(s):  
Ya-Wen Li ◽  
Pei-Ling Wang ◽  
Wei-Wu Chen ◽  
Jing-Wei Feng ◽  
Yi-Bing Cheng ◽  
...  

Ca-α-sialon compacts pressureless-sintered to intermediate temperatures, which consisted of both α-sialon and unreacted α–Si3N4 grains, were investigated with transmission electron microscopy for an overall composition Ca1.8Si6.6Al5.4O1.8N14.2. Special attention was paid to identification of the possible crystallographic orientation between a-sialon and the α–Si3N4 particles. In contrast to the frequently occurring heteroepitaxial nucleation of α-sialon in rare-earth-doped samples with low x values, this study showed that most of the newly formed α-sialon grains had no epitaxial orientation relationship with the α–Si3N4 particles, suggesting nonepitaxial heterogeneous nucleation to be a more probable mechanism for the Ca–α-sialon phase with high Ca concentrations.

1998 ◽  
Vol 13 (4) ◽  
pp. 974-978 ◽  
Author(s):  
Seong-Hyeon Hong ◽  
Naesung Lee ◽  
Altaf H. Carim ◽  
Gary L. Messing

Interfacial precipitation in sol-gel derived, titania-doped diphasic mullite gels was investigated using conventional and high resolution transmission electron microscopy. Rutile, anatase, and brookite precipitated on the interface between {110} planes of mullite and glass pockets in the sintered body. The formation of brookite may be attributable to the Si- and Al-rich environment during precipitation. Each polymorph of titania has a unique morphology and orientation relationship with mullite. Brookite exhibits a truncated pill box shape, and anatase displays a vermicular morphology. Quenching experiments suggest that the precipitates grow and undergo phase transformations during cooling.


2003 ◽  
Vol 18 (2) ◽  
pp. 475-481 ◽  
Author(s):  
Karfa Traoré ◽  
Philippe Blanchart

Kaolinite mixed with calcite was sintered at low temperature (1100 °C; 5 °C/min). The successive phase transformations are metakaolinite to gehlenite and then anorthite, although the available phase diagram indicates a direct anorthite recrystallization. Transmission electron microscopy and electron diffraction studies of nanocrystallites revealed that the transformation path is favored by the structural similarities of phases. In particular, the pseudolayers of gehlenite have a major orientation relationship with the initial metakaolinite layers. The gehlenite axis, [001]G, is parallel to the metakaolinite axis, [001]A. This direct transition is favored by the existence of Si tetrahedral units and 4–fold–coordinated Al in both structures. Ca atoms, initially in the interlayer spacing of metakaolinite, remain in the interlayers of gehlenite. During the second transformation step, anorthite recrystallizes from gehlenite with axis [020]A parallel to [210]G. It is proposed that this orientation relationship is favored by the orientation and shape of Ca-atom channels through both structures, along [001]G and [100]A axes.


2015 ◽  
Vol 33 (6) ◽  
pp. 395-401 ◽  
Author(s):  
Ramasis Goswami

AbstractTransmission electron microscopy (TEM) was employed to investigate the dissolution behavior of nanocrystalline grain boundary T1 precipitates in Al-3Cu-2Li. These grain boundary T1 plates exhibit an orientation relation with matrix, with the (1-11)α-Al parallel to (0001)T1 and [022]α-Al parallel to [10-10]T1, which is similar to the orientation relationship of T1 plates formed within grains. TEM studies showed that these grain boundary T1 plates react readily in moist air. As a result of the localized dissolution, the Cu-rich clusters form onto T1, which is consistent with the localized dissolution behavior observed in nanocrystalline S phase in Al-Cu-Mg.


2006 ◽  
Vol 21 (12) ◽  
pp. 3047-3057 ◽  
Author(s):  
A. Vlad ◽  
A. Stierle ◽  
N. Kasper ◽  
H. Dosch ◽  
M. Rühle

The oxidation in air of NiAl(110) was investigated in the temperature range from 870 °C–1200 °C by in situ x-ray diffraction and transmission electron microscopy. Oxidation at 870 °C and 1 bar oxygen leads to the formation of an epitaxial layer of γ-alumina showing an R30° orientation relationship with respect to the underlying substrate. At oxidation temperatures between 950 °C and 1025 °C, we observed a coexistence of epitaxial γ- and polycrystalline δ-Al2O3. The α-Al2O3 starts to form at 1025 °C and the complete transformation of metastable phases to the stable α-alumina phase takes place at 1100 °C. The fcc-hcp martensitic-like transformation of the initial γ-Al2O3 to epitaxial α-Al2O3 was observed. X-ray diffraction and cross-section transmission electron microscopy proved the existence of a continuous epitaxial α-Al2O3 layer between the substrate and the polycrystalline oxide scale, having a thickness of about 150 nm. The relative orientation relationship between the epitaxial alumina and the underlying substrate was found to be NiAl(110) || α-Al2O3 (0001) and [110] NiAl || [1120].


2009 ◽  
Vol 24 (1) ◽  
pp. 192-197 ◽  
Author(s):  
G.M. Cheng ◽  
Y.X. Tian ◽  
L.L. He

The orientation relationship (OR) and the interfacial structure between Nb solid solution (Nbss) precipitates and α-Nb5Si3 intermetallics have been investigated by transmission electron microscopy (TEM). The OR between Nbss and α-Nb5Si3 was determined by selected-area electron diffraction analyses as (222)Nb//(002)α and . High-resolution TEM images of the Nbss/α-Nb5Si3 interface were presented. Steps existed at the interface that acted as centers of stress concentration and released the distortion of lattices to decrease the interfacial energy. In addition, the interfacial models were proposed based on the observed OR to describe the atomic matching of the interface. The distribution of alloying elements at the Nbss/α-Nb5Si3 interface has also been investigated, and Hf was enriched at the interface to strengthen the grain boundary.


Author(s):  
P. Gu ◽  
G. Yang ◽  
R.F. Klie

Cerium oxide doped with various rare earth metals is often used as a support for nano-sized gold particles, and demonstrates to be a promising catalyst for the water gas shift reaction at low temperatures. Many factors are hypothesized to affect the activity of this heterogeneous catalyst, including its loading with gold, the rare-earth dopant, the support and Au particle size, and leaching of the sample. In this study, we examined several Au/CeO2-based catalyst samples, including 2.4% Au/(Ce,Gd)O2, 1.8% Au/(Ce,La)O2 leached, 0.5% Au/(Ce,Gd)O2 leached, and 0.75% Au/CeO2 utilizing analytical transmission electron microscopy. The effects of Au and rare-earth doping on the ceria lattice parameter were investigated, and it was determined that there are no significant variations in the particle's structure or lattice-spacing. Furthermore, the particle sizes of each of the four samples were investigated concluding that although the 1.8% Au/(Ce,La)O2 leached sample has a slightly larger particle size, and the 2.4% Au/(Ce,Gd)O2 sample has a slightly smaller particle size, the differentiation is not adequate to be accountable for the radical distinction in catalytic activity.


Sign in / Sign up

Export Citation Format

Share Document