The Post-treatments of Aluminum Oxynitride(AlON) Powders Synthesized by the Carbothermal Reduction and Nitriding Process

Author(s):  
Yingying Chen ◽  
◽  
Qinggang Li ◽  
Zhi Wang ◽  
Guopu Shi ◽  
...  
2010 ◽  
Vol 25 (7) ◽  
pp. 678-682 ◽  
Author(s):  
Xue-Jian LIU ◽  
Xian-Yang YUAN ◽  
Fang ZHANG ◽  
Zheng-Ren HUANG ◽  
Shi-Wei WANG

2007 ◽  
Vol 115 (1337) ◽  
pp. 42-46 ◽  
Author(s):  
Wenbin DAI ◽  
Wei LIN ◽  
Akira YAMAGUCHI ◽  
Jyunji OMMYOJI ◽  
Jingkun YU ◽  
...  

2010 ◽  
Vol 105-106 ◽  
pp. 791-793
Author(s):  
Ting Yan Tian ◽  
Hong Bing Du ◽  
Feng Sun ◽  
Hua Wei Jiang

γ-aluminum oxynitride (γ-ALON) powder was prepared by carbothermal reduction method using γ-Al2O3 and activated carbon as raw materials. Effects of activated carbon content, synthesizing temperature, holding time and carbon impurity on ALON powder were studied. It was found a ‘two-step’ procedure, first sintering at about 1550°C-1650°C then at about 1750°C-1850°C, was effective to prepare high-purity ALON powder. The removal of carbon impurity was crucial for the preparation of ALON powder, which effectively improved the purity of ALON powder. The prepared powder was characterized by XRD and SEM, which indicated that pure ALON powder prepared by a ‘two-step’ procedure had well-developed crystalline and homogenous granularity. Transparent ALON ceramics were prepared by hot-press sintering at 1850~1900°C for up to 2~4h using ALON powder and some sintering additive, the transmission of sample with thickness of 1mm was 81% at infrared wave.


2009 ◽  
Vol 66 ◽  
pp. 73-76
Author(s):  
Ding Peng ◽  
Hao Wang ◽  
Wei Min Wang ◽  
Yu Cheng Wang ◽  
Zheng Yi Fu

In this paper, a carbothermal reduction and nitridation (CRN) synthesis for cubic aluminum oxynitride (γ-AlON) powders is reported. The CRN reaction was conducted via a two-step synthesis procedure at a heating rate of 100 °C/min. In the first step, the mixture of fine γ-Al2O3 and soluble starch was annealed at 1550~1580 °C for different duration. It is found that the mixture of α-Al2O3 and AlN with an appropriate ratio can be obtained by CRN reaction. The content of AlN in mixture is closely related with the reaction condition. In the second step, the as-received mixture of α-Al2O3 and AlN was heat-treated at 1700 °C for 10 min. The single phase γ-AlON powders with particle size less than 3 µm were obtained.


2008 ◽  
Vol 368-372 ◽  
pp. 438-440
Author(s):  
Hai Ping Wang ◽  
Deng Xue Wu ◽  
Wei Pang ◽  
Jian Qi Qi ◽  
Ji Cheng Zhou ◽  
...  

Aluminum oxynitride powders were synthesized by carbothermal reduction, using nano-sized alpha-alumina, gamma-alumina and carbon as raw materials. Effects of the weight percentages of alpha-alumina in alumina (R) and synthesizing temperatures (T) on the preparation of single-phase AlON powders have been studied. The results showed that proper R can reduce the shrinkage and increase the formation rate of AlON phase, but a high R will reduce the formation rate of AlON phase, because the activity of alpha-alumina was lower than that of gamma-alumina. Single-phase AlON powder with excellent properties can be obtained under the condition of R=0.15, T=1700°C. Moreover, this single-phase AlON powder was well-dispersed with an average size of about 2 μm.


1984 ◽  
Vol 49 (4) ◽  
pp. 936-943 ◽  
Author(s):  
Bohumil Hájek ◽  
Pavel Karen ◽  
Vlastimil Brožek

For the investigation of the products of reaction of yttrium oxide with carbon mixed in various proportions, the chemical and X-ray diffraction methods of analysis were combined with the gas chromatographic analysis of the mixture of hydrocarbons and hydrogen formed on the sample decomposition with water. The carboreduction of Y2O3 was examined at relatively low temperatures, convenient for obtaining the reaction intermediates in higher yields. At 1 600 °C and pressures of 10-3 Pa the reduction of a mixture of Y2O3 with carbon in a stoichiometric ratio of 1 : 7 yields YC2 in equilibrium with 20% of Y2OC phase. At lower carbon contents (down to the Y2O3 : C ratio of 1 : 2) tha fraction of the Y2OC phase increases up to approximately 30%. In addition to Y2O3, the reaction mixture contains also Y2C, Y2OC and a phase giving propyne on hydrolysis. The presence of traces of C3 hydrocarbons and small amounts of methane in the product of hydrolysis of the carbide sample prepared by the carbothermal reduction of the oxide can be explained in terms of the occurrence of the Y15C19 phase, probably substituted in part by oxygen, and of the Y2OC phase. The results are compared with those obtained previously for the Sc2O3 + C system.


2021 ◽  
Vol 10 (1) ◽  
pp. 157-168
Author(s):  
Biwei Luo ◽  
Pengfei Li ◽  
Yan Li ◽  
Jun Ji ◽  
Dongsheng He ◽  
...  

Abstract The feasibility of industrial waste fly ash as an alternative fluxing agent for silica in carbothermal reduction of medium-low-grade phosphate ore was studied in this paper. With a series of single-factor experiments, the reduction rate of phosphate rock under different reaction temperature, reaction time, particle size, carbon excess coefficient, and silicon–calcium molar ratio was investigated with silica and fly ash as fluxing agents. Higher reduction rates were obtained with fly ash fluxing instead of silica. The optimal conditions were derived as: reaction temperature 1,300°C, reaction time 75 min, particle size 48–75 µm, carbon excess coefficient 1.2, and silicon–calcium molar ratio 1.2. The optimized process condition was verified with other two different phosphate rocks and it was proved universally. The apparent kinetics analyses demonstrated that the activation energy of fly ash fluxing is reduced by 31.57 kJ/mol as compared with that of silica. The mechanism of better fluxing effect by fly ash may be ascribed to the fact that the products formed within fly ash increase the amount of liquid phase in the reaction system and promote reduction reaction. Preliminary feasibility about the recycling of industrial waste fly ash in thermal phosphoric acid industry was elucidated in the paper.


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