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Synthesis of ZSM-5/KIT-6 with a tunable pore structure and its catalytic application in the hydrodesulfurization of dibenzothiophene and diesel oil

机译:具有可调孔结构的ZSM-5 / KIT-6的合成及其在二苯并噻吩和柴油加氢脱硫中的催化应用

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Porous support materials were prepared by assembling primary and secondary ZSM-5 structural units into a well-ordered mesoporous framework. The materials possessed both ZSM-5 microporous building units and mesoporous structure were used as supports for the preparation of hydrodesulfurization (HDS) catalysts. The materials and their corresponding catalysts were characterized by XRD, FTIR, ~(27) Al MAS NMR, TEM, N _(2) adsorption–desorption, Py-FTIR, H _(2) -TPR, Raman, and HRTEM techniques. The pore structures of the composite materials were modulated by adjusting the molar ratio of butanol/P123 (BuOH/P123) and then, the influences of BuOH/P123 on the catalytic performance in the HDS of dibenzothiophene (DBT) and diesel oil were systematically studied. The results showed that butanol has a big influence on the structure of the micro–mesoporous material, whereby different micro–mesoporous structures, such as the p 6 mm hexagonal structure or Ia d cubic structure, were formed with different butanol addition amounts. The composite ZK-3 (BuOH/P123 = 100) possessed the best surface area and pore structure. Therefore, the NiMo/ZK-3 catalyst showed the highest catalytic activity in the HDS of DBT with a BP selectivity of 72.1% due to its excellent textural property, moderate MSI, relatively high B/L ratios, and highly dispersed NiMoS active phases. Moreover, the NiMo/AZK-3 catalyst exhibited excellent catalytic performance in the HDS of diesel oil.
机译:通过将一级和二级ZSM-5结构单元组装到有序的介孔框架中来制备多孔支撑材料。该材料同时具有ZSM-5微孔结构单元和中孔结构,用作制备加氢脱硫(HDS)催化剂的载体。通过XRD,FTIR,〜(27)Al MAS NMR,TEM,N_(2)吸附-脱附,Py-FTIR,H_(2)-TPR,拉曼和HRTEM技术对材料及其相应的催化剂进行了表征。通过调节丁醇/ P123(BuOH / P123)的摩尔比调节复合材料的孔结构,然后系统研究了BuOH / P123对二苯并噻吩(DBT)和柴油HDS催化性能的影响。 。结果表明,丁醇对微介孔材料的结构影响很大,从而形成了不同的微介孔结构,如p 6 mm六角形结构或Ia d立方结构,其丁醇添加量不同。 ZK-3复合材料(BuOH / P123 = 100)具有最佳的表面积和孔结构。因此,NiMo / ZK-3催化剂在DBT的HDS中显示出最高的催化活性,其BP选择性为72.1%,这归因于其优异的质构性质,中等的MSI,相对较高的B / L比和高度分散的NiMoS活性相。此外,NiMo / AZK-3催化剂在柴油的HDS中表现出优异的催化性能。

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