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作 者:郑斌[1] 张安峰[1] 刘民[1] 丁凡舒[1] 代成义[1] 宋春山[1,2] 郭新闻[1]
机构地区:[1]大连理工大学化工学院工业催化系,精细化工国家重点实验室,辽宁大连116024 [2]宾夕法尼亚州立大学能源研究所,能源与矿物工程系,美国宾夕法尼亚州大学城16802
出 处:《物理化学学报》2012年第8期1943-1950,共8页Acta Physico-Chimica Sinica
摘 要:使用尿素沉淀凝胶、机械混合和等体积浸渍相结合的方法, 制备了一系列的纳米尺寸FeK-M/γ-Al2O3(M=Cd,Cu)催化剂, 采用扫描电镜(SEM)、透射电镜(TEM)、N2物理吸附、X射线衍射(XRD)光谱和H2程序升温还原(H2-TPR)仪对催化剂进行表征, 并在小型固定床反应器上考察其对 CO2加氢反应的催化性能. 结果表明:3 MPa, 400℃, 3600 h-1, H2/CO2摩尔比为3的条件下, 15%(w, 下同)Fe10%K/γ-Al2O3催化剂可稳定运行100h 以上, CO2转化率为51.3%, C2+烃类的选择性达62.6%. Fe含量降至2.5%时, C2+烃类的选择性仍能达到60.0%. 随着 K 含量由 0%增加至 10%, 低碳烯烃选择性增加, 烯烷比增加至 3.6. Cd 和 Cu 助剂可促进 Fe 物种的还原, 改善目的产物的分布, 其中Cu的加入使低碳产物烯烷比增至5.4, Cd的加入使C5+产物选择性增加了12%.Combining co-precipitation-gelation, mechanical mixing and impregnation methods, a series of catalysts of FeK-M/γ-Al2O3(M=Cd or Cu) have been attained. The catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 physisorption, X-ray diffraction (XRD) and temperature-programmed reduction of hydrogen (H2-TPR). The hydrogenation of carbon dioxide over these catalysts was also investigated in a fixed bed. Given a reaction time of 100 h, CO2 conversion over a 15%Fe/10%K/γ-Al2O3 catalyst reached 51.3 %, with a selectivity towards C2+ of 62.6 % at 3 MPa, 673 K, a space velocity of 3600 h-1 and at a molar ratio of H2/CO2 of 3. At the lower Fe content of 2.5%, the selectivity towards C2+ was still greater than 60.0%. Increasing the potassium content from 0% to 10%, increased the selectivity towards C2-C4= and the molar ratio of C2-C4= /C2-C40 increased to 3.6. The addition of Cd and Cu improved the reduction and catalytic activities. Specifically, Cu improved the molar ratio of C2-C4= /C2-C40 from 3.6 to 5.4, and the Cd increased the selectivity of C5+ by 12%.
关 键 词:二氧化碳:加氢转化:铁基催化剂:沉淀:低碳烃类
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