首页> 外文OA文献 >Unsupported trimetallic Ni(Co)-Mo-W sulphide catalysts prepared from mixed oxides: characterisation and catalytic tests for simultaneous tetralin HDA and dibenzothiophene HDS reactions
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Unsupported trimetallic Ni(Co)-Mo-W sulphide catalysts prepared from mixed oxides: characterisation and catalytic tests for simultaneous tetralin HDA and dibenzothiophene HDS reactions

机译:由混合氧化物制备的无载体三金属Ni(Co)-Mo-W硫化物催化剂:并发四氢化萘HDA和二苯并噻吩HDS反应的表征和催化测试

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摘要

Unsupported A-Mo-W (A = Ni or Co) sulphide catalysts were obtained from mixed oxides containing different W:Mo ratios. An in situ liquid-phase sulphidation of the mixed oxides in a batch reactor was followed by catalytic tests in a liquid-phase reaction (at 613 K and 70 bar), using a mixture of dibenzotiophene (DBT) and tetralin (THN) as the feed. After the catalytic tests, the bulk sulphide catalysts were characterised by nitrogen physical adsorption, XANES/EXAFS, SEM and HR-(S)TEM. The HR-TEM images showed randomly oriented, stacked-layer particles typical of Mo (W) sulphides and an elemental HR-STEM mapping evidenced Mo/W homogeneous distribution in the trimetallic sulphides. The EXAFS results for the trimetallic catalysts are consistent with the presence of nickel or cobalt sulphide domains, and Mo1-xWxS2 solid solutions. The intralayer Mo:W solid solutions were confirmed to be thermodynamically stable with respect to phase separation by DFT calculations, which were also used to aid in the interpretation of the EXAFS results. The effect of the W:Mo ratio on the catalytic properties of the Ni- and Co-containing series was found to be different. For the Ni series, increasing the W content caused an activity increase in THN hydrodearomatization (HDA) relative to DBT hydrodesulphurization (HDS), while it had little influence on the relative contribution of the direct desulphurisation (DDS) route with respect to the previous hydrogenation (HYD) route for DBT HDS. In contrast, for the Co series, the activities and selectivities were essentially insensitive to the W content. Both the Ni and Co series of unsupported sulphides were more selective for the HYD route in DBT HDS than a supported NiMo/Al2O3 catalyst.
机译:从包含不同W:Mo比的混合氧化物中获得了无载体的A-Mo-W(A = Ni或Co)硫化物催化剂。在间歇反应器中对混合氧化物进行原位液相硫化,然后在液相反应中(613 K和70 bar)进行催化测试,使用二苯并噻吩(DBT)和四氢化萘(THN)的混合物作为催化剂。饲料。催化测试后,通过氮物理吸附,XANES / EXAFS,SEM和HR-(S)TEM表征了大部分硫化物催化剂。 HR-TEM图像显示了典型的Mo(W)硫化物的随机取向的堆积层颗粒,元素HR-STEM映射证明​​了Mo / W在三金属硫化物中的均匀分布。三金属催化剂的EXAFS结果与镍或钴硫化物域以及Mo1-xWxS2固溶体的存在一致。通过DFT计算,证实了层内Mo:W固溶体在相分离方面是热力学稳定的,这也可用于帮助解释EXAFS结果。发现W∶Mo比对含Ni和Co的系列的催化性能的影响是不同的。对于Ni系列,相对于DBT加氢脱硫(HDS),增加W含量会导致THN加氢脱芳香化(HDA)的活性增加,而对直接脱硫(DDS)路线相对于先前加氢的相对贡献影响很小(HYD)路线用于DBT HDS。相反,对于Co系列,活性和选择性对W含量基本不敏感。对于DBT HDS中的HYD路线,Ni和Co系列无载体硫化物的选择性都比负载NiMo / Al2O3催化剂高。

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