首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >MoO3 on zeolites MCM-22 MCM-56 and 2D-MFI as catalysts for 1-octene metathesis
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MoO3 on zeolites MCM-22 MCM-56 and 2D-MFI as catalysts for 1-octene metathesis

机译:MOC-22MCM-56和2D-MFI沸石上的MoO3作为1-辛烯复分解的催化剂

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摘要

Highly active olefin metathesis catalysts were prepared by thermal spreading MoO3 and/or MoO2(acac)2 on MWW zeolites (MCM-22, delaminated MCM-56) and on two-dimensional MFI (all in NH4 + form). The catalysts‘ activities were tested in the metathesis of neat 1-octene (as an example of a longer chain olefin) at 40 °C. Catalysts with 6 wt % or 5 wt % of Mo were used. The acidic character of the supports had an important effect on both the catalyst activity and selectivity. The catalyst activity increases in the order 6MoO3/HZSM-5(25) (Si/Al = 25) << 6MoO2(acac)2/MCM-22(70) < 6MoO3/2D-MFI(26) < 6MoO3/MCM-56(13) < 6MoO3/MCM-22(28) reflecting both the enhancing effect of the supports‘ acidity and accessibility of the catalytic species on the surface. On the other hand the supports‘ acidity decreases the selectivity to the main metathesis product C14 due to an acid-catalyzed double bond isomerization (followed by cross metathesis) and oligomerization. 6MoO3/2D-MFI(26) with a lower concentration of the acidic centres resulting in catalysts of moderate activity but with the highest selectivity.
机译:通过将MoO3和/或MoO2(acac)2热分散在MWW沸石(MCM-22,分层MCM-56)和二维MFI(均在NH4中, + )中制备高活性烯烃复分解催化剂形成)。在40°C下,在纯净的1-辛烯(作为长链烯烃的一个例子)的复分解中测试了催化剂的活性。使用具有6重量%或5重量%的Mo的催化剂。载体的酸性对催化剂活性和选择性都具有重要影响。催化剂活性按以下顺序增加6MoO3 / HZSM-5(25)(Si / Al = 25) 6MoO2(acac)2 / MCM-22(70)<6MoO3 / 2D-MFI(26)<6MoO3 / MCM- 56(13)<6MoO3 / MCM-22(28)反映了载体酸度的增强作用和表面上催化物种的可及性。另一方面,由于酸催化的双键异构化(随后发生交叉易位)和低聚,载体的酸性降低了对主要易位产物C14的选择性。具有较低浓度的酸性中心的6MoO3 / 2D-MFI(26)导致活性中等但选择性最高的催化剂。

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