Centre for Research and Technology Hellas, Chemical Process and Energy Resources Institute, 6th km Charilaou-Thermi Road, Thessaloniki 57001, Greece.
Aristotle University of Thessaloniki, Department of Chemistry, University Campus, Thessaloniki 54124, Greece.
Molecules. 2017 Oct 21;22(10):1784. doi: 10.3390/molecules22101784.
ZSM-5-containing catalytic additives are widely used in oil refineries to boost light olefin production and improve gasoline octanes in the Fluid Catalytic Cracking (FCC) process. Under the hydrothermal conditions present in the FCC regenerator (typically >700 °C and >8% steam), FCC catalysts and additives are subject to deactivation. Zeolites (e.g., Rare Earth USY in the base catalyst and ZSM-5 in Olefins boosting additives) are prone to dealumination and partial structural collapse, thereby losing activity, micropore surface area, and undergoing changes in selectivity. Fresh catalyst and additives are added at appropriate respective levels to the FCC unit on a daily basis to maintain overall targeted steady-state (equilibrated) activity and selectivity. To mimic this process under accelerated laboratory conditions, a commercial P/ZSM-5 additive was hydrothermally equilibrated via a steaming process at two temperatures: 788 °C and 815 °C to simulate moderate and more severe equilibration industrial conditions, respectively. -Dodecane was used as probe molecule and feed for micro-activity cracking testing at 560 °C to determine the activity and product selectivity of fresh and equilibrated P-doped ZSM-5 additives. The fresh/calcined P/ZSM-5 additive was very active in C cracking while steaming limited its activity, i.e., at catalyst-to-feed (C/F) ratio of 1, about 70% and 30% conversion was obtained with the fresh and steamed additives, respectively. A greater activity drop was observed upon increasing the hydrothermal deactivation severity due to gradual decrease of total acidity and microporosity of the additives. However, this change in severity did not result in any selectivity changes for the LPG (liquefied petroleum gas) olefins as the nature (Brønsted-to-Lewis ratio) of the acid/active sites was not significantly altered upon steaming. Steam deactivation of ZSM-5 had also no significant effect on aromatics formation which was enhanced at higher conversion levels. Coke remained low with both fresh and steam-deactivated P/ZSM-5 additives.
ZSM-5 含催化添加剂广泛应用于炼油厂,以提高轻烯烃产量并改善流化催化裂化 (FCC) 过程中的汽油辛烷值。在 FCC 再生器中存在的水热条件下(通常 >700°C 和 >8%蒸汽),FCC 催化剂和添加剂会失活。沸石(例如基础催化剂中的稀土 USY 和烯烃增产添加剂中的 ZSM-5)容易脱铝和部分结构坍塌,从而失去活性、微孔表面积,并发生选择性变化。新鲜催化剂和添加剂每天以适当的水平添加到 FCC 装置中,以维持整体目标稳态(平衡)活性和选择性。为了在加速的实验室条件下模拟此过程,一种商业 P/ZSM-5 添加剂通过在两个温度下进行蒸汽处理来进行水热平衡:788°C 和 815°C,分别模拟中等和更严重的工业平衡条件。-十二烷用作探针分子和进料,用于在 560°C 下进行微活性裂化测试,以确定新鲜和平衡的 P 掺杂 ZSM-5 添加剂的活性和产物选择性。新鲜/煅烧的 P/ZSM-5 添加剂在 C 裂解中非常活跃,而蒸汽处理限制了其活性,即在催化剂与进料(C/F)比为 1 的情况下,新鲜和蒸汽处理的添加剂分别获得了约 70%和 30%的转化率。由于添加剂的总酸度和微孔率逐渐降低,水热失活严重程度增加时,观察到活性下降更大。然而,由于酸性/活性位的性质(Brønsted-Lewis 比)没有因蒸汽处理而发生显著变化,因此这种严重程度的变化并没有导致 LPG(液化石油气)烯烃的选择性发生任何变化。ZSM-5 的蒸汽失活也没有对芳烃的形成产生显著影响,芳烃的形成在更高的转化率水平下得到增强。新鲜和蒸汽失活的 P/ZSM-5 添加剂的焦炭含量均保持较低。