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作 者:张建明[1] 张晓彤[1] 宋丽娟[1] 孙兆林[1] 刘丽莉[1]
机构地区:[1]辽宁石油化工大学辽宁省石油化工重点实验室,辽宁抚顺113001
出 处:《当代化工》2011年第6期580-582,共3页Contemporary Chemical Industry
摘 要:钼酸铵焙烧制备碳化钼前驱体MoO3,以MoO3为钼源、V(H2)/V(CH4)混合气体为碳化介质采用程序升温反应法制备Mo2C催化剂;考察钼酸铵制备MoO3适宜的温度,以及程序升温反应法制备Mo2C的最适V(H2)/V(CH4)比和碳化终温,用XRD表征分析产物。得出制备Mo2C催化剂的最佳工艺条件是:钼酸铵焙烧温度为450℃、V(H2)/V(CH4)为2︰1~4︰1、碳化终温为700℃;其反应机理是:MoO3先被还原为MoO2,MoO2需经历过渡态的单质Mo才能碳化生成Mo2C。Molybdenum trioxide as precursor was prepared by roasting ammonium molybdate.Then using molybdenum trioxide and the gas mixture of H2 and CH4 as raw materials,molybdenum carbide was prepared by the temperature-programmed reaction method.The best temperature of preparing molybdenum trioxide from ammonium molybdate was investigated as well as the best ratio of H2 to CH4 and terminal temperature in the temperature-programmed reaction;the final product was characterized by X-ray diffraction.The results show that the optimum process conditions for the reaction: roasting temperature is at 450 ℃,V(H2)/V(CH4) is in the range of 2︰1~4︰1,the final temperature of carbonization is at 700 ℃;the reaction mechanism: firstly,MoO3 is reduced to MoO2,then MoO2 must be reduced to transition state Mo,finally Mo2C is gained.
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