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作 者:李鹏[1] 田志坚[1] 曲炜[1] 王炳春[1] 徐云鹏[1] 徐竹生[1]
机构地区:[1]中国科学院大连化学物理研究所,辽宁大连116023
出 处:《精细化工》2013年第11期1229-1233,共5页Fine Chemicals
基 金:中国石油天然气股份有限公司基金项目~~
摘 要:采用等体积浸渍法制备了3%MoO3-x%Re2O7,/y-A12O3(负载量均为质量分数,下同)双金属催化剂(z=0~1),以混合丁烯[n(1-丁烯)/n(2.丁烯)=3]为原料,在固定床反应器上考察了不同Re含量对Re—Mo双金属催化剂在丁烯自歧化反应中的催化性能,并采用XRD、NH3-TPD、H2-TPR和N2物理吸附对催化剂进行了表征。结果表明,与3%MoO,/T.A12O3催化剂相比,双金属催化剂增加了催化剂的酸量,抑制了在反应初期的“诱导期”,提高了催化剂在丁烯自歧化反应中的活性和稳定性。在80oC、1.0MPa、混合丁烯WHSV=1.2h“的条件下,3%MoO,-1%Re2O7,/A12O3,催化剂(Re207负载量1%,M003负载量3%)上丁烯自歧化反应在70h内可维持60%以上的丁烯转化率和约25%的丙烯收率。Abstract :3% MoO3-x% ReaO7/T-A1203 bimetallic catalysts( x = 0 - 1 ) were prepared via conventional incipient-wetness impregnation method. Mixed butene self-metathesis reactions over these catalysts were investigated in a fixed-bed reactor,where mixed butene [ n (1-butene)/n (2-butene) = 3 ] was chosen as reactant. The catalysts were characterized by means of XRD, NH3-TPD, n2-TPR and N2-adsorption. The results indicate that, compared to 3% MoO3/T-A1203 catalyst, molybdenum-rhenium bimetallic catalyst increased the acid amount, inhibited the induction period in the initial stage of the reaction, and enhanced the activity and stability of catalysts in mixed butene self-metathesis reaction. Under the reaction conditions of 80 ℃, 1.0 MPa, WHSV = 1.2 h-1,3 % MoO3-1% Re20T/T-A1203 catalyst gave butene conversion of above 60% ,and propene yield remained at about 25% during 70 h on stream.
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