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Article

Fabrication of the Li2TiO3 tritium breeder pebbles by a capillary-based microfluidic wet process

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Pages 250-257 | Received 26 Dec 2014, Accepted 31 Mar 2015, Published online: 27 Apr 2015

Figures & data

Figure 1. (a) Schematic diagram of the capillary-based microfluidic device; (b1)–(b7) snapshots of the droplet formation at the outlet of the capillary tube (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 5 µL min−1).

Figure 1. (a) Schematic diagram of the capillary-based microfluidic device; (b1)–(b7) snapshots of the droplet formation at the outlet of the capillary tube (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 5 µL min−1).

Figure 2. Procedure for fabricating Li2TiO3 pebbles.

Figure 2. Procedure for fabricating Li2TiO3 pebbles.

Table 1. Composition of the solution used in this study.

Figure 3. Optical micrographs of the microspheres: (a) Li2TiO3 droplets produced by the capillary-based microfluidic device (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 5 µL min−1); (b) the biggest Li2TiO3 droplet (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 10 µL min−1) and smallest droplet (flow rate of continuous phase: 180 µL min−1, flow rate of dispersed phase: 1 µL min−1); (c) small Li2TiO3 pebbles after sintering at 950 °C for 3 hours; (d) big Li2TiO3 pebbles after sintering at 950 °C for 3 hours.

Figure 3. Optical micrographs of the microspheres: (a) Li2TiO3 droplets produced by the capillary-based microfluidic device (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 5 µL min−1); (b) the biggest Li2TiO3 droplet (flow rate of continuous phase: 150 µL min−1, flow rate of dispersed phase: 10 µL min−1) and smallest droplet (flow rate of continuous phase: 180 µL min−1, flow rate of dispersed phase: 1 µL min−1); (c) small Li2TiO3 pebbles after sintering at 950 °C for 3 hours; (d) big Li2TiO3 pebbles after sintering at 950 °C for 3 hours.

Figure 4. TG-DSC curves of the dried Li2TiO3 green pebble in air atmosphere.

Figure 4. TG-DSC curves of the dried Li2TiO3 green pebble in air atmosphere.

Figure 5. Relationship between sintering temperature (a) and sintering time (b) (the sintering temperature was 950 °C) with Li2TiO3 pebbles density.

Figure 5. Relationship between sintering temperature (a) and sintering time (b) (the sintering temperature was 950 °C) with Li2TiO3 pebbles density.

Figure 6. Effect of solid content of slurry on the density of Li2TiO3 pebbles (the sintering temperature was 950 °C and the sintering time was 3 hours).

Figure 6. Effect of solid content of slurry on the density of Li2TiO3 pebbles (the sintering temperature was 950 °C and the sintering time was 3 hours).

Figure 7. Relationship between particle size of Li2TiO3 powder with Li2TiO3 pebbles density (the sintering temperature was 950 °C, the sintering time was 3 hours and the content of Li2TiO3 powder was 35 wt%).

Figure 7. Relationship between particle size of Li2TiO3 powder with Li2TiO3 pebbles density (the sintering temperature was 950 °C, the sintering time was 3 hours and the content of Li2TiO3 powder was 35 wt%).

Figure 8. XRD pattern of the prepared Li2TiO3 pebbles.

Figure 8. XRD pattern of the prepared Li2TiO3 pebbles.

Figure 9. SEM micrographs of sintered Li2TiO3 pebbles: (a) surface of Li2TiO3 pebbles sintered at 950 °C; scale bar is 200 µm; (b)--(d) cross section of Li2TiO3 pebbles sintered at 950 °C, 1050 °C and 1150 °C; scale bar is 30 µm.

Figure 9. SEM micrographs of sintered Li2TiO3 pebbles: (a) surface of Li2TiO3 pebbles sintered at 950 °C; scale bar is 200 µm; (b)--(d) cross section of Li2TiO3 pebbles sintered at 950 °C, 1050 °C and 1150 °C; scale bar is 30 µm.

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