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首页> 外文期刊>Applied Surface Science >Catalytic fast co-pyrolysis of organosolv lignin and polypropylene over in- situ red mud and ex-situ HZSM-5 in two-step catalytic micro reactor
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Catalytic fast co-pyrolysis of organosolv lignin and polypropylene over in- situ red mud and ex-situ HZSM-5 in two-step catalytic micro reactor

机译:两步催化微反应器中原位赤泥和原位HZSM-5催化有机溶剂木质素和聚丙烯快速共热解

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摘要

The additional use of red mud (RM) on the catalytic fast co-pyrolysis (CFCP) of organosolv lignin (OL) and polypropylene (PP) over ex-situ HZSM-5 was investigated using a tandem micro reactor system. Non-catalytic fast co-pyrolysis of OL and PP increased their decomposition efficiency owing to the effective interactions. The in-situ catalytic fast pyrolysis (CFP) of OL over RM led to the enhanced conversion of large molecular OL pyrolyzates with the additional production of aromatic hydrocarbons. The in-situ CFCP of OL/PP over RM resulted in a further increase in the cracking efficiency of OL/PP pyrolyzates as well as an increase in the aromatics formation efficiency owing to the effective interactions between their CFP intermediates. Furthermore, the application of RM in 1st in-situ catalytic reactor was found to be the optimal catalyst system because the in-situ CFCP of OL/PP over RM can enhance the formation of the proper hydrocarbons precursors for the production of aromatics over ex-situ HZSM-5 in 2nd reactor. Compared to the one-step CFCP of OL/PP over ex-situ HZSM-5, two-step CFCP of OL/PP over in-situ RM and ex-situ ZSM-5 maintained the higher aromatics formation during the 7 times sequential reaction due to the slow deactivation of ex-situ HZSM-5.
机译:使用串联微反应器系统研究了赤泥(RM)在非原位HZSM-5上对有机溶剂木质素(OL)和聚丙烯(PP)的催化快速共热解(CFCP)的额外使用。由于有效的相互作用,OL和PP的非催化快速共热解提高了它们的分解效率。相对于RM的OL的原位催化快速热解(CFP)导致大分子OL热解产物的转化率提高,同时芳烃的产量增加。 OL / PP超过RM的原位CFCP导致OL / PP热解产物的裂化效率进一步提高,并且由于其CFP中间体之间的有效相互作用,芳烃形成效率也有所提高。此外,发现RM在第一个原位催化反应器中的应用是最佳的催化剂体系,因为与RM相比,OL / PP的原位CFCP可以增强形成适当的烃前体的生成,而芳烃的生产要比原先的HZSM-5在第二反应器中原位。与原位HZSM-5上的OL / PP一步CFCP相比,原位RM和原位ZSM-5的OL / PP两步CFCP在7次连续反应中保持较高的芳烃形成由于异位HZSM-5缓慢失活。

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