检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:FENG Yue-bin YANG Bin DAI Yong-nian 冯月斌;杨斌;戴永年(昆明理工大学理学院,昆明650500;昆明理工大学冶金与能源工程学院,真空冶金国家工程实验室,昆明650093)
机构地区:[1]Faculty of Science,Kunming University of Science and Technology,Kunming 650500,China [2]National Engineering Laboratory of Vacuum Metallurgy,Faculty of Metallurgy and Energy Engineering,Kunrning University of Science and Technology,Ktmming 650093,China
出 处:《Transactions of Nonferrous Metals Society of China》2012年第1期215-221,共7页中国有色金属学报(英文版)
基 金:Project (u0837604) supported by the Joint Funds of the National Natural Science Foundation of China and Yunnan Province
摘 要:The carbothermal reduction-chlorination-disproportionation of alumina in vacuum was investigated by XRD and thermodynamic analysis. The experiments on alumina and graphite at 1643-1843 K in vacuum were carried out. The results demonstrate that AlCl3(g) reacts with Al2O(g) or Al(g) generated from the carbothermal reduction of alumina to form AlCl(g), and the AlCl(g) disproportionates to aluminum and AlCl3(g) at a lower temperature and the reaction rate of AlCl(g) reaches 90% at 980 K and 100 Pa. The aluminum can absorb CO to catalyze its disproportionation to C and CO2, and react backward with CO to form Al4C3, Al2O3, C and CO2, resulting in the aluminum product containing C, Al4C3 and Al2O3. The impurities in the aluminum product decrease as the AlCl(g) disproportionation temperature decreases. AlCl3 condenses at a temperature approximated to the room temperature.通过XRD物相分析和热力学分析研究氧化铝的真空碳热还原—氯化—歧化反应。以氧化铝和石墨为原料,在真空下、1643-1843K的温度范围内进行实验。结果表明,AlCl3(g)与氧化铝碳热还原产生的Al2O(g)或Al(g)反应生成AlCl(g),该AlCl(g)在较低温度下歧化分解为金属铝和AlCl3(g);当压力为100Pa、温度为980K时,AlCl(g)的歧化反应率达到90%。生成的金属铝可以吸附催化CO歧化为C和CO2,并可以与CO二次反应形成Al4C3、Al2O3、C和CO2,导致铝产物中含有C、Al4C3和Al2O3。产物铝中所含的这些杂质随着AlCl(g)歧化反应温度的降低而减少。AlCl3(g)在接近室温的温度下冷凝下来。
关 键 词:carbothermal reduction AL2O3 AlCl VACUUM DISPROPORTIONATION
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222