A COEXISTENCE OF BORON-NITRIDE AND BORIC OXIDE

被引:69
作者
HUBACEK, M [1 ]
SATO, T [1 ]
ISHII, T [1 ]
机构
[1] NATL INST RES INORGAN MAT,SAKURA,IBARAKI 305,JAPAN
关键词
D O I
10.1006/jssc.1994.1117
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Crystallization of turbostratic boron nitride, prepared from a mixture with varying ratios of boric acid and urea, was studied by heating from 220 to 1100-degrees-C. Formation of boron nitride layers was observed at temperatures as low as 220-degrees-C. Two ways to crystallization were revealed by further heating depending on the urea ratio in the starting mixture. Above 70%, the system remained monophasic and consisted of only one turbostratic phase. Below this ratio the system split into three phases at temperatures above 700-degrees-C. These were assigned as turbostratic boron nitride, boron oxynitride, and crystalline boric oxide. Boron oxynitride has been interpreted as an interfacial zone between turbostratic boron nitride crystallites and residual boric oxide resulting from an imperfect nitriding of starting oxidic precursors. Existence of this transition zone promotes the crystallization when heated at elevated temperatures. (C) 1994 Academic Press, Inc.
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页码:384 / 390
页数:7
相关论文
共 13 条
[1]   An X-ray study of carbon black [J].
Biscoe, J ;
Warren, BE .
JOURNAL OF APPLIED PHYSICS, 1942, 13 (06) :364-371
[2]   A CONTRIBUTION TO THE CRYSTALLOCHEMISTRY OF BORON-NITRIDE [J].
BROZEK, V ;
HUBACEK, M .
JOURNAL OF SOLID STATE CHEMISTRY, 1992, 100 (01) :120-129
[3]  
BROZEK V, 1978, CHEM PRUM, V37, P632
[4]   A NEW ROUTE TO BORON NITRIDE [J].
ECONOMY, J ;
ANDERSON, R .
INORGANIC CHEMISTRY, 1966, 5 (06) :989-&
[5]  
INGLES TA, 1960, SPECIAL CERAMICS, P114
[6]  
KUTOLIN SA, 1972, METODY POLUTSHENIYA, P223
[7]   THERMODYNAMIC ANALYSIS OF THE REFINING OF TECHNICAL BORON-NITRIDE [J].
LEITNER, J ;
VONKA, P ;
BROZEK, V ;
HUBACEK, M .
JOURNAL OF MATERIALS SCIENCE, 1988, 23 (10) :3594-3599
[8]   SYNTHESIS OF BORON NITRIDE [J].
OCONNOR, TE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1962, 84 (09) :1753-&
[9]  
OCONNOR TE, 1966, Patent No. 3241919
[10]  
PEASE RS, 1952, ACTA CRYSTALLOGR, V5, P536