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Nickel-Exchanged Zincosilicate Catalysts for the Oligomerization of Propylene

机译:用于丙烯低聚反应的镍交换锌硅酸盐催化剂

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摘要

Two nickel-containing zincosilicates (Ni-CIT-6 and Ni-Zn-MCM-41) and two nickel-containing aluminosilicates (Ni- HiAl-BEA and Ni-USY) are synthesized and used as catalysts to oligomerize propylene into C_(3n) (C6 and C9) products. Both Ni- CIT-6 and Ni-HiAl-BEA have the *BEA topology and are investigated to assess the effects of framework zinc versus aluminum because the former gives two framework charges per atom, whereas the latter, only one. Ni-CIT-6 and Ni-Zn-MCM-41 enable the comparison of a microporous to a mesoporous zincosilicate. Ni2+ ion-exchanged into zeolite Y has been previously reported to oligomerize propylene and is used here for comparison. Reaction data are obtained at 180 and 250 °C, atmospheric pressure, and WHSV = 1.0 h-1 in a feed stream of 85 mol % propylene (in inert). At these conditions, all catalysts are capable of oligomerizing propylene with steady-state conversions ranging from 3 to 16%. With the exception of Ni-HiAl-BEA, all catalysts have higher propylene conversions at 250 °C than at 180 °C. Both *BEA materials exhibit similar propylene conversions at each temperature, but Ni-HiAl-BEA is not as selective to C_(3n) products as Ni-CIT-6. Zincosilicates demonstrate higher average selectivities to C_(3n) products than the aluminosilicates at both reaction temperatures tested. Hexene products other than those expected by simple oligomerization are present, likely formed by double-bond isomerization catalyzed at acid sites. Additionally, both of the aluminosilicate materials catalyzed cracking reactions, forming non-C_(3n) products. The reduced acidity of the zincosilicates relative to the aluminosilicates likely accounts for higher C_(3n) product selectivity of the zincosilicates. Zincosilicates also exhibited higher linear-to-branched hexene isomer ratios (typically 1.0-1.5) when compared with the aluminosilicates, which had ratios on the order of 0.3. The mesoporous zincosilicate shows the best reaction behavior (including C_(3n) product selectivity: ~99% at both temperatures for Ni-Zn-MCM-41) of the catalytic materials tested here.
机译:合成了两种含镍的硅酸锌(Ni-CIT-6和Ni-Zn-MCM-41)和两种含镍的硅铝酸盐(Ni-HiAl-BEA和Ni-USY),并用作催化剂将丙烯低聚为C_(3n )(C6和C9)产品。 Ni-CIT-6和Ni-HiAl-BEA都具有* BEA拓扑结构,并且进行了研究以评估骨架锌与铝的作用,因为前者每个原子给出两个骨架电荷,而后者仅给出一个原子。 Ni-CIT-6和Ni-Zn-MCM-41可以比较微孔与中孔硅酸锌。先前已经报道了将离子交换为沸石Y的Ni2 +可以使丙烯低聚,并将其用于比较。在85和mol%丙烯(惰性)进料流中,在180和250°C,大气压和WHSV = 1.0 h-1下获得反应数据。在这些条件下,所有催化剂均能够以3%至16%的稳态转化率低聚丙烯。除了Ni-HiAl-BEA,所有催化剂在250°C时的丙烯转化率都比180°C高。两种* BEA材料在每个温度下均表现出相似的丙烯转化率,但Ni-HiAl-BEA对C_(3n)产物的选择性不如Ni-CIT-6。在两个测试温度下,锌硅酸盐均比铝硅酸盐具有更高的对C_(3n)产物的平均选择性。存在除通过简单的低聚反应所期望的那些之外的己烯产物,其可能是由在酸性位点催化的双键异构化形成的。另外,两种硅铝酸盐材料均催化裂化反应,形成非C_(3n)产物。相对于铝硅酸盐而言,硅酸锌的酸度降低可能解释了硅酸锌的较高的C_(3n)产物选择性。与具有约0.3的比率的铝硅酸盐相比,锌硅酸盐还显示出较高的直链与支链己烯异构体比率(通常为1.0-1.5)。在此测试的催化材料中,介孔硅酸锌显示出最佳的反应行为(包括C_(3n)产物选择性:在两个温度下,对于Ni-Zn-MCM-41约为99%)。

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