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机构地区:[1]中国矿业大学江苏省煤基CO2捕集与地质储存重点实验室,江苏徐州221006 [2]太原理工大学煤科学与技术教育部及山西省重点实验室,山西太原030024
出 处:《燃料化学学报》2015年第10期1245-1251,共7页Journal of Fuel Chemistry and Technology
基 金:国家自然科学基金(21506249);江苏省博士后基金(1401096c);中央高校基本科研业务费(中国矿业大学;2014QNA19)资助项目~~
摘 要:将醋酸铜热解制备的Cu2O/AC(活性炭)催化剂,在氧化(O2/N2)和还原(H2/N2、CO/N2)气氛下进行预处理。350℃下预处理4 h,氧化气氛中Cu2O完全被氧化为Cu O,还原气氛中Cu2O被还原为单质铜。经CO/N2预处理的催化剂表面Cu0分散性好,催化活性显著升高。在常压固定床微型反应装置上测试,在140℃的反应温度下,碳酸二甲酯的时空收率和选择性分别达到了261.9 mg/(g·h)和74.7%。反应后,还原气氛(H2/N2、CO/N2)预处理的催化剂与Cu2O/AC催化剂中铜物种价态组成趋于一致,催化活性亦趋于一致。关联反应前后催化剂表面铜物种的变化和催化活性的差异,可以认为Cu0具有较高的初始催化活性,Cu2O活性和价态均较为稳定,Cu O活性较低。The Cu2O/AC catalyst prepared by pyrolysis of copper acetate supported on activatede carbon was pretreated under oxidative (Oz/N2 ) or reductive (HJN2 and CO/N2 ) atmospheres. The oxidation/reduction of Cu20 was completed through pretreatment at 350 ℃ for 4 h, the Cu20 in catalyst could be completely oxidized to CuO by oxidative atmosphere, or reduced to metallic copper by reductive atmosphere. The catalyst activities were evaluated in a continuous fixed-bed tubular micro reactor under atmospheric pressure at 140 ℃. The catalyst pretreated by CO/N2 had good Cu~ dispersion on its surface and exhibited the highest activity. The space-time yield and selectivity of DMC reached 261.9 mg/( g. h) and 74.7%, respectively. After 58 h reaction, the valence state of copper species and the catalytic activity of catalysts pretreated by reductive atmosphere were found to be close to that of the Cu20/AC catalyst. Comparing the catalytic performance, the characterization o( surface and bulk copper species before and after reaction, it was obvious that metallic copper exhibited a high initial activity, while Cu:O was stable in catalytic activity and valence state, and CuO was low in activity.
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