首页> 外文期刊>Catalysis Letters >CoMo Hydrotreating Catalysts Supported on Al2O3, SiO2 and SBA-15 Prepared from Single Co2Mo10-Heteropolyacid: In Search of Self-Promotion Effect
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CoMo Hydrotreating Catalysts Supported on Al2O3, SiO2 and SBA-15 Prepared from Single Co2Mo10-Heteropolyacid: In Search of Self-Promotion Effect

机译:由单CO 2MO10-杂多酸制备的Al 2 O 3,SiO 2和SBA-15负载的COMO加氢处理催化剂:寻找自我促进效果

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摘要

CoMo hydrotreating catalysts with varied metal loading (1-4 Mo at nm(- 2)) based on Co2Mo10 heteropolyacid (HPA) and different supports (gamma-Al2O3, SBA-15, SiO2) were prepared by incipient wetness impregnation. The catalysts were characterized by N-2 physisorption, high resolution transmission electron microscopy (HRTEM), Raman and X-ray photoelectron spectroscopy (XPS). Catalytic activity was evaluated in co-hydrotreating (HDT) of the model feed containing dibenzothiophene (DBT) and naphthalene. The catalytic properties of CoMo catalysts were shown to depend on the morphological characteristics of CoMoS species, its promotion degree, and metal loading. The sulfidation degree of the initial precursor and effective cobalt amount in the CoMoS species increased with the Mo loading increase from 1 to 4 at nm(- 2) in all studied catalysts. The DBT conversion maximum was achieved over CoMo/Al2O3 and CoMo/SBA-15 with 4 Mo at nm(- 2). CoMo/SBA-15 catalysts had higher TOF numbers both in DBT HDS and in naphthalene hydrogenation (HYD) at the surface concentration of Mo same as in the other samples. These results can be attributed to optimal morphology of sulfide particles and the Co/Mo promotion degree due to a more suitable interaction between the active phase and support in mesoporous silica channels.
机译:通过初期湿润浸渍制备具有多种金属负载(1-4mE)的多元金属负载(1-4mO)的COMO加氢处理催化剂(NM( - 2))和不同的载体(γ-Al2O3,SBA-15,SiO 2)。催化剂的特征在于N-2物理吸附,高分辨率透射电子显微镜(HRTEM),拉曼和X射线光电子谱(XPS)。在含有二苯并噻吩(DBT)和萘的模型饲料的共加氢处理(HDT)中评价催化活性。显示COMO催化剂的催化性质取决于COMOS物种的形态特征,其促进度和金属负载。在所有研究催化剂中,COMOS物种中初始前体和有效钴量的硫化程度随Mo加载量的增加量增加到4-4)。在NM( - 2)时,通过COM / AL2O3和COMO / SBA-15实现DBT转化最大值。 COMO / SBA-15催化剂在DBT HDS中具有更高的TOF编号和在与其他样品中的M0的表面浓度下的萘氢化(HYD)。这些结果可归因于硫化物颗粒的最佳形态和CO / MO促进度,因为在中孔二氧化硅通道中的活性相和载体之间更合适的相互作用。

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