TY - JOUR
T1 - Crystallization behavior of cubic boron nitride from an amorphous BN precursor via high-pressure, high-temperature treatment with controlled water addition
AU - Mochizuki, Takahiro
AU - Yamamoto, Yusuke
AU - Idota, Naokazu
AU - Kawamura, Fumio
AU - Taniguchi, Takashi
AU - Sugahara, Yoshiyuki
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Crystallization behavior of cubic boron nitride (c-BN) from amorphous boron nitride (a-BN) by high-pressure, high-temperature (HP-HT) treatment with the intentional addition of a controlled amount of water was studied. The a-BN precursor was prepared by pyrolysis of a boric acid-urea complex with urea/boric acid = 2 at 1000 °C for 3 h under an ammonia atmosphere. Hexagonal BN (h-BN) were initially crystallized from a-BN containing 2 mass% of water after HP-HT treatment at 7.7 GPa and 1200 °C, and the formation of c-BN was observed after 5 min. The crystallization of c-BN from a-BN containing 8 mass% of water after HP-HT treatment at 7.7 GPa and 1200 °C was observed even after 1 min, indicating that the crystallization of c-BN was promoted by increasing the amount of water added. In addition, since neither h-BN nor c-BN was crystallized from a-BN without intentional water addition after the same HP-HT treatment, the addition of water promoted the crystallization of both h-BN and c-BN from a-BN. Since no transformation from h-BN to c-BN was observed during HP-HT treatment at 7.7 GPa and 1200 °C, it was concluded that c-BN was directly crystallized from a-BN. After HP-HT treatment at 7.7 GPa and 1650 °C for 1 min, both h-BN and c-BN were crystallized from a-BN containing 8 mass% of water. These results clearly indicate that the addition of water has a positive effect on crystallization of c-BN from a-BN.
AB - Crystallization behavior of cubic boron nitride (c-BN) from amorphous boron nitride (a-BN) by high-pressure, high-temperature (HP-HT) treatment with the intentional addition of a controlled amount of water was studied. The a-BN precursor was prepared by pyrolysis of a boric acid-urea complex with urea/boric acid = 2 at 1000 °C for 3 h under an ammonia atmosphere. Hexagonal BN (h-BN) were initially crystallized from a-BN containing 2 mass% of water after HP-HT treatment at 7.7 GPa and 1200 °C, and the formation of c-BN was observed after 5 min. The crystallization of c-BN from a-BN containing 8 mass% of water after HP-HT treatment at 7.7 GPa and 1200 °C was observed even after 1 min, indicating that the crystallization of c-BN was promoted by increasing the amount of water added. In addition, since neither h-BN nor c-BN was crystallized from a-BN without intentional water addition after the same HP-HT treatment, the addition of water promoted the crystallization of both h-BN and c-BN from a-BN. Since no transformation from h-BN to c-BN was observed during HP-HT treatment at 7.7 GPa and 1200 °C, it was concluded that c-BN was directly crystallized from a-BN. After HP-HT treatment at 7.7 GPa and 1650 °C for 1 min, both h-BN and c-BN were crystallized from a-BN containing 8 mass% of water. These results clearly indicate that the addition of water has a positive effect on crystallization of c-BN from a-BN.
KW - Amorphous boron nitride
KW - Cubic boron nitride
KW - High-pressure
KW - High-temperature treatment
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U2 - 10.1016/j.jeurceramsoc.2016.06.027
DO - 10.1016/j.jeurceramsoc.2016.06.027
M3 - Article
AN - SCOPUS:84977085505
SN - 0955-2219
VL - 36
SP - 3565
EP - 3569
JO - Journal of the European Ceramic Society
JF - Journal of the European Ceramic Society
IS - 15
ER -