Method for preparing spherical alpha-phase alumina
A technology of spherical alumina and phase alumina, which is applied in the preparation of alumina/hydroxide, etc., can solve the problems of limitation and difficulty in preparing α-phase alumina, and achieve high filling capacity, short preparation time and high fluidity  Effect
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Embodiment 1
[0017] Commercially available α-alumina was crushed to an average particle size of 10 μm. As a raw material, the raw material was put into a triple tube burner and the temperature was controlled at 2100°C to 2300°C for melting and spheroidization to obtain Test Sample 1-1. The test sample 1-1 was put into the burner again and the flame temperature was controlled at 1800°C to 2000°C for heat treatment to obtain the test sample 1-2. The obtained samples were measured by XRD, and the content of each crystal phase was calculated from the intensity of each crystal characteristic peak and listed in Table 1.
Embodiment 2
[0019] Commercially available γ-alumina was crushed to an average particle size of 10 μm. As a raw material, the raw material was put into a triple tube burner and the temperature was controlled at 2100°C to 2300°C for melting and spheroidization to obtain test sample 2-1. The test sample 2-1 was put into the burner again, and the flame temperature was controlled at 1800°C to 2000°C for heat treatment to obtain the test sample 2-2. The obtained samples were measured by XRD, and the content of each crystal phase was calculated from the intensity of each crystal characteristic peak and listed in Table 1.
Embodiment 3
[0021] Commercially available α-alumina was crushed to an average particle size of 5 μm. As a raw material, the raw material was put into a triple tube burner and the temperature was controlled at 2100°C to 2300°C for melting and spheroidization to obtain test sample 3-1. The test sample 3-1 was put into the burner again and the flame temperature was controlled at 1800°C to 2000°C for heat treatment to obtain the test sample 3-2. The obtained samples were measured by XRD, and the content of each crystal phase was calculated from the intensity of each crystal characteristic peak and listed in Table 1.
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