TEXTURES OF PHASES IN AIzO - ZrO (Y O3)

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Textures and Microstructures, 1995, Vol. 25, pp. 25-32 Reprints available directly from the publisher Photocopying permitted by license only (C) 1995 OPA (Overseas Publishers Association) Amsterdam B.V. Published in The Netherlands under license by Gordon and Breach Science Publishers SA Printed in Malaysia TEXTURES OF PHASES IN AIzO - ZrO (Y O3) EUTECTIC COMPOSITES B. A. GNESIN and M. YU. STAROSTIN Institute of Solid State Physics, Russian Academy of Sciences, 142432, Chernogolovka, Moscow district, Russia (Received 20 June 1995) Crystallograhic textures of phases in eutectics AO + ZrO (Y203) were investigated by means of X-ray diffraction. In all studied eutectic polycrystalls (grown from the melt by EFG technique) a preferred orientation [0001] of A1203 along the growth direction in all the samples was revealed for both initial orientations of A120 seeding crystal: <0001> and <1011>. For a cubic ZrO there were two types of a preferred orientations: sharp ones, close to <123> with a 6-fold symmetry and more spread <110>. Such a 6-fold symmetry for a cubic phase appears in eutectic due to a joint crystallization. KEY WORDS: Directional crystallization, macroscopic symmetry, eutectic, alumina, zirconia. INTRODUCTION Directional solidification of eutectic composites is of a great interest since it allows to obtain highly anisotropic multyphase structures with regularly arranged components. Such materials are attractive because of their properties but up to date many features of eutectic crystallization and the resulting structures are not clear. "Crystals" of Al20 ZrO (Y203) eutectics are of an interest first of all because of their high-temperature mechanical properties and corrosion resistance. In the present investigation the crystallographic texture of a directionaly crystallized Al20 ZrO (Y203) eutectics is studied. EXPERIMENTAL PROCEDURE Powders of pure (99.9%) A1203; Zr02; Y203; were dried, weighted (52.9%, 42.7% and 4.4%, respectively) and mixed. Compacted pellets were melted in a molybdenum crucible in vacuum. The rate of directional solidification by EFG (edge-defmed film-fed growth) was about 40 mm/h. Seed crystals in these experiments were sapphire single crystals of <0001> or (1011) direction along growth direction. Rods 6 mm in diameter and up to 200 mm in length were obtained. Samples were sectioned and polished at 25, 100 and 200 mm from the seeding crystal. The structure was investigated with the help of SEM and light microscopy. Textures were measured at a computer controlled diffractometer with monochromatisated MoK radiation. Angular steps of 3 and 5 degrees were used both for tp and 25

26 B.A. GNES1N AND M. YU. STAROSTIN PHASES AND STRUCTURES Only two phases AI203 and cubic ZrO2(Y203) were found in all investigated samples and a presence of well defined texture was clear from the diffraction data. Phases are well detrmed (Figure 1, ZrO looks white) and 48-58% of the volume are phases in eutectic colonies. Crystallites dimensions are about x 10 gm of ZrO2(Y203) in eutectic colonies with an average dimensions of these colonies about 60 x 100 /.tm. Both phases are aligned in the direction of growth, Al203 crystallites being often connected with each other forming a binding matrix for eutectic colonies. This colony structure corresponds to a steady-state process and does not change with changing of seed crystal orientation. The presence of ZrO crystalites in two different forms (whiskers in colonies and almost isometrical in intercolony space) is connected with the amount of yttria 1 ]. It may be assumed that solidification in this case proceeds in two stages: at the first one eutectic colonies consisting of zirconia whiskers in the alumina matrix are formed from the melt similar to primary crystal formation and at the second stage solidification of the melt in the intercolony space occurs resulting in the isometrical form of coarse zirconia cyrstallites in the binding alumina matrix. Besides, the difference in yttria content in zirconia crystallites inside the colonies and within them confirms the two stage model of crystallization. TEXTURE INVESTIGATIONS A 2 mm slit before a counter used in a present experiments permits to resolve a distance between diffraction peaks about 0.65. Measurements with a slit 0.25 mm have shown, that peaks 111 13.74; 200 15.98; 220 22.51 o; 311 26.48 for ZrO and {0112}- 11.71; {1120}- 17.15; {.1123}- 19.59; {0224}- 23.53; {1126} 25.59; {0118} 27.15 for Al203 may be well resolved in our investigation (Figure 2). Defocusing was estimated in a powder sample, but due to the small diameter of the sample and not ideal adjustement of the sample position under X-ray beam these data were not too reliable. After defocusing and background corrections only peaks positions on pole figures (PF) were well defined within angular step accuracy, errors of their intensity could be about 20-50%, or even more for a larger O. For our purposes we have used only levels on PF in 0.1; 0.3, 0.5 etc. of a maximum corrected intensity for a given PF. The size of the irradiated region on a sample was about 3 x 5 mm, depending on the diffraction and tilting angles, therefore exposure time was 2.5 seconds in every point of a PF, diffraction from dozens of thousands of eutectic crystallites was measured. In all samples in this investigation, for Al203 a main texture component was an orientation (Figure 3) close to [0001] aligned to the growth direction (GD). In the case of a seed crystal with the same orientation this may be regarded as an inheritance of the orientation of a seed crystal by the alumina phase. But for [1011] seeding crystals we also found the same orientation of the alumina phase already at a distance of 25 mm from the seed crystal and it was the same on all other samples. Therefore, this preferential orientation is stable for Al203 in eutectics obtained in our process of directional crystallization and is independent of the seed orientation. The character of corresponding peaks is similar to that from a single crystal, showing a good perfection of the matrix phase in these eutectic samples.

TEXTURES OF PHASES IN Al203 ZrO (Y203) Figure 1 Longitudinal (a) and transverse (b) sections of a sample, x200. 27

28 B.A. GNESIN AND M. YU. STAROSTIN Figure 2 Vicinities of a diffraction peak of {200} ZrO corresponding to a maximum on the. pole figure, tilting angle of the texture goniometer 0 35.

TEXTURES OF PHASES IN AlEO ZrO (Y203) 29 / Figure 3 Pole figure {1123} of AlE0, levels corresponding to 0.1, 0.3 and 0.5 of the maximum corrected intensity for a given pole figure are drawn. On {200} PF for ZrO (Figure 4) one can see an evident presence of six-fold symmetry in the arrangement of peaks. These peaks alternate through 60 at the circles t 35 and t9 55 degrees on PF. Such an arrangement of peaks was found for all investigated samples. It was a possibility to "suspect" that such a surprising symmetry of PF for ZrO was caused by superposition of Al203 diffraction peaks. To clear this question we have measured the intensity near the peak with 35 on the {200} PF (Figure 2). A little discrepancy in the position of the peak and ASTM data was due to tilting of the texture goniometer at 35 and to the presence of Y203 in the stabilized cubic phase. Also the nearest peak of {1120} AI203 must be located near t9 90 because Al203 has [0001] orientation. In the Figure 5 only the positions of local extremums on the experimental PF 111, {200} and {220 of the ZrO phase are indicated and the presence of six-fold symmetry is evident from all the PF. All peaks are distinctly positioned on circles y const. There are 3 such circles within an area t < 65 for {111} PF, 2 for {200} and 4 for {220}. Because of the fact that all these PF correspond to axes of symmetry in a cubic crystal, one can conclude that in our case ZrO is oriented with <uvw> II GD with u v w.

30 B.A. GNESIN AND M. YU. STAROSTIN Figure 4 Pole figure {200} of the ZrO phase in eutectic, levels 0.07, 0.14 and 0.21 of the maximum corrected intensity for a given pole figure are drawn. Indexes <uvw> of such directions were obtained by the following procedure. Starting from <123> direction we have calculated the sum of discrepancies Sh for every PF {hkl as follows: E ( caln=l where #cal and tgex p are calculated and experimental values of t for peaks on PF {hkl}. Then the sum S was calculated: s + S oo + After a simple procedure it was established, that the best fit with experimental data corresponds to <123> II GD. After this it wasn t difficult to determine a direction in ZrO parallel to 1120] direction in Al203 because both phases were investigated without changing initial sample orientation. Possible orientation relations between phases are: [12311110001]; [15311111010]; [0110]; [1100]; [1010]; [0110] and [1100]; [30111111120]; [1210]; [2110]; [1120]; [1210] and [2110]. For ZrO there are 3 indexes and for A1203-4. With the help of these relations peak positions for {111}; {200} and {220} PF of zirconia were calculated. As it is clear from Figure 5, positions of peaks are quite similar to that for all 3 experimental PF, average error may be estimated as 7.

TEXTURES OF PHASES IN AlEO ZrO (Y203) 31 (d) " Figure 5 Experimental (a,b,c) and calculated (d,e,f) positions of maximums on a pole figure 111 (a,d), 200 (b,e), 220 (c,f) for the ZrO phase.

32 B.A. GNESIN AND M. YU. STAROSTIN The six-fold macroscopic symmetry in the texture of zirconia was forming during the eutectic solidification process under the influence of alumina which was the first phase to nucleate and which controls the solidification of ZrO 2. The leading role of alumina was established earlier, [2]. The results of the present investigation show that the nucleating phase can determine the texture symmetry of the second phase. Therefore, by analyzing the phase symmetry, one can find what particular phase is the nucleating one in the case that the eutectic comprises phases of the different of crystallographic symmetry. Also the presence of broad and weaker (about 10 times) peaks was found for both phases. These peaks for zirconia are more significant and they corresponds to <110> II GD. The intensity of these peaks increases from the seed to the end of the eutectic rods. It is noteworthy that, <1011> seed crystal orientation strongly affects the intensity of the broad peaks for zirconia in a sample cut from the beginning of the crystal. The presence of two types of ZrO preferred orientations can be related to the duplex eutectic structure of this phase. Sharp six-fold symmetry peaks can be attributed to the whiskers in colonies, whereas broad peaks can be attributed to the coarse crystallites in intercolony space. In order to prove this fact a local orientation technique must be used. References Eshigoya, J., Takabayashi, Y., Suto, H. and Ishigame, M. (1986). J. Materials Science Letters, 5, p. 150-152. Schmid, F. and Viechnicki, D. (1970). J. Materials Science, 5, p. 470-473.