催化作用
煅烧
选择性
化学
钼
无机化学
酒
空间速度
碳酸钾
钾
解吸
吸附
硝酸钾
程序升温还原
有机化学
作者
Takashi Toyoda,T. Minami,Eika Weihua QIAN
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2013-06-03
卷期号:27 (7): 3769-3777
被引量:54
摘要
Several alumina-supported molybdenum-based catalysts were prepared by impregnation. The prepared catalysts were characterized using N 2 adsorption, X-ray diffraction, temperature-programmed desorption of ammonia, and temperature-programmed reduction with hydrogen. The catalytic activity in mixed alcohol synthesis was evaluated using a fixed-bed pressurized flow reaction system under conditions of 250–320 °C, 3.5–5 MPa, gas hourly space velocity of 280–5000 h –1, and H 2 /CO ratio of 0.5–1. Effects of reaction conditions, alumina supports, and the addition of potassium were elucidated. The CO conversion and selectivity of the catalysts changed depending upon the calcination temperature of alumina supports that influenced the acid amount of the catalysts. The selectivity of C 2+ alcohols eventually reached ca. 40% in the case of calcination temperatures higher than 1000 °C. The selectivity of C 2+ alcohols was almost proportional to the addition of potassium that promoted the formation of C 2+ alcohols. The selectivity of C 2+ alcohols and the chain growth probability of alcohols with potassium carbonate were higher than those with nitrate.
科研通智能强力驱动
Strongly Powered by AbleSci AI