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首页> 外文期刊>Journal of Catalysis >Continuous acylation of anisole by acetic anhydride in mesoporous solid acid catalysts:Reaction media effects on catalyst deactivation
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Continuous acylation of anisole by acetic anhydride in mesoporous solid acid catalysts:Reaction media effects on catalyst deactivation

机译:介孔固体酸催化剂中乙酸酐对苯甲醚的连续酰化作用:反应介质对催化剂失活的影响

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摘要

The acylation of anisole with acetic anhydride was carried out in a continuous slurry reactor over mesoporous supported Nafion(SAC-13)and heteropolyacid(HPA)catalysts.At 70 deg C,using an anisole-rich feed molar ratio of 5:1 and a space velocity of 1.6 gacetic anhydride g_(cat)~(-1)h~(-1),acetic anhydride conversions of 40-50% with excellent selectivity(>95%)toward the primary product,p-methoxyacetophenone(p-MOAP),were observed at time on stream(TOS)of a few hours.However,all the catalysts deactivated completely during liquid-phase operation in less than 24 h.It was observed that the Keggin ions from the supported HPA-based catalyst(70% HPA/SiC>2)leached out into the solution,as confirmed by elemental analysis.The 50% Cs_(2.5)-HPA/SiO_2 catalyst,on the other hand,was more leach-resistant,yet deactivated rapidly during liquid-phase operation.SAC-13-type catalysts,which displayed the best combination of stability and leach resistance during liquid-phase operation,were evaluated in CO_2-expanded liquids(CXLs)to better enhance the transport properties and potentially mitigate deactivation.It is observed that the CXL media gave lower conversion and surprisingly,faster deactivation compared with liquid-phase operation,indicating that CO_2 had a detrimental effect despite the use of polar cosolvents like nitromethane.The spent catalysts were subjected to Soxhlet extraction with polar solvents like nitromethane.Such treatment did not restore catalyst activity.BET surface area,pore volume of the fresh and spent catalysts,GC/MS analysis of the Soxhlet extract,and IR analysis of the spent catalyst(before and after Soxhlet extraction)indicate that the deactivation could be caused by the primary product,p-MOAP and/or multiply acetylated products in the micropores of Nafion~R catalyst aggregates.Treating the spent catalyst with boiling HNO_3 solution restored complete activity of the SAC-13-type catalysts.The high TON(approx 400)achieved with these catalysts before deactivation and their ability to regain complete activity for acylation reactions indicate that Nafion~R catalysts are promising alternatives to the conventional homogeneous Lewis acids like AlCl_3.
机译:在连续淤浆反应器中,在介孔负载的Nafion(SAC-13)和杂多酸(HPA)催化剂上,在连续淤浆反应器中对苯甲醚进行酰化反应。在70摄氏度下,使用富苯甲醚进料摩尔比为5:1和1.6 g醋酐g_(cat)〜(-1)h〜(-1)的空速,醋酸酐转化率40-50%,对初级产物对甲氧基苯乙酮(p-MOAP)的选择性极佳(> 95%) ),在运行时间(TOS)上观察到了几个小时。然而,所有催化剂在液相操作中在不到24小时的时间内就完全失活了。观察到负载型HPA基催化剂的Keggin离子(70)经元素分析证实,%HPA / SiC> 2)浸出到溶液中。另一方面,50%Cs_(2.5)-HPA / SiO_2催化剂具有更高的耐浸出性,但在液相过程中迅速失活在CO_2-e中评估了SAC-13型催化剂,该催化剂在液相操作过程中表现出稳定性和耐溶出性的最佳组合xpanded液体(CXLs)可以更好地提高传输性能并潜在地减缓失活。观察到,与液相操作相比,CXL介质的转化率较低,并且失活速度更快,这表明尽管使用了极性,CO_2仍具有有害作用用硝基甲烷等极性溶剂对用过的催化剂进行索氏提取。这种处理不能恢复催化剂的活性.BET表面积,新鲜和用过的催化剂的孔体积,索氏提取物的GC / MS分析和红外光谱索氏提取前后的废催化剂分析表明,失活可能是由Nafion〜R催化剂聚集体的微孔中的初级产物,p-MOAP和/或多乙酰化产物引起的。用沸腾的HNO_3处理废催化剂溶液恢复了SAC-13型催化剂的完全活性。在失活之前,这些催化剂可实现高TON(约400)并且其恢复完全活性以进行酰化反应的能力表明,Nafion-R催化剂是常规均质路易斯酸(如AlCl_3)的有前途的替代品。

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