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Reactive yttrium aluminate garnet powder via coprecipitation using ammonium hydrogen carbonate as the precipitant

Published online by Cambridge University Press:  31 January 2011

Ji Guang Li
Affiliation:
National Institute for Research in Inorganic Materials, Namiki 1–1, Tsukuba, Ibaraki 305–0044, Japan
Takayasu Ikegami
Affiliation:
National Institute for Research in Inorganic Materials, Namiki 1–1, Tsukuba, Ibaraki 305–0044, Japan
Jong-Heun Lee
Affiliation:
National Institute for Research in Inorganic Materials, Namiki 1–1, Tsukuba, Ibaraki 305–0044, Japan
Toshiyuki Mori
Affiliation:
National Institute for Research in Inorganic Materials, Namiki 1–1, Tsukuba, Ibaraki 305–0044, Japan
Yoshiyuki Yajima
Affiliation:
National Institute for Research in Inorganic Materials, Namiki 1–1, Tsukuba, Ibaraki 305–0044, Japan
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Abstract

Ammonium hydrogen carbonate was used as the precipitant to synthesize yttrium aluminate garnet (YAG) precursors from a mixed solution of aluminum and yttrium nitrates via coprecipitation. The carbonate precursor, with an approximate composition of NH4AlY0.6(CO3)1.9(OH)2 · 0.8H2O, transformed to pure YAG at 900 °C without the formation of intermediate phases. Reactive YAG powder was produced by calcining the precursor at 1100 °C. The YAG powder densified to 99.8% of the theoretical density by vacuum sintering at 1500 °C for 2 h, and the sintered body showed transparency. Less agglomeration of the precursor and good dispersity of the resultant YAG powder were responsible for the excellent sinterability.

Type
Rapid Communications
Copyright
Copyright © Materials Research Society 2000

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