4.7 Article

In-situ and ex-situ catalytic pyrolysis/co-pyrolysis of empty fruit bunches using mesostructured aluminosilicate catalysts

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 366, Issue -, Pages 330-338

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.02.055

Keywords

In-situ/ex-situ catalytic pyrolysis; Co-pyrolysis; Biomass; Bio-oil; Aromatic hydrocarbons

Funding

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2018R1A2B2001121]
  2. National Research Foundation of Korea [2018R1A2B2001121] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Mesostructured aluminosilicates of Al-MSU-F (commercial), Al-SBA-15 (home-made), and mesoMFI (a mesoporous aluminosilicate with MFI structure, home-made), with a silica-to-alumina ratio of 40, were used as catalyst for the in-situ catalytic pyrolysis (CP) of empty fruit bunches (EFB) at 600 degrees C. The highest selectivity to aromatic hydrocarbons in bio-oil was obtained over mesoMFI due to its higher acidity than Al-SBA-15 and AlMSU- F. In addition, ex-situ CP of EFB using mesoMFI was compared with in-situ CP; the ex-situ configuration produced higher aromatic hydrocarbons than the in-situ configuration. Meanwhile, in-situ and ex-situ catalytic copyrolysis (CCP) of EFB (with a H/C-eff ratio less than 0.3) and polypropylene (PP) (with a high H/C(ef)f ratio about 2) were carried out using the mesoMFI at 600 degrees C to investigate the supplementary effect of PP on the deoxygenation of EFB-derived pyrolyzates for producing aromatic hydrocarbons. Ex-situ CCP of EFB/PP (with the mass ratios of 75/25, 50/50, and 25/75) resulted in a lower formation of aromatic hydrocarbons than the in-situ CCP. In addition, the thermal decomposition behavior of EFB, PP, and EFB/PP in non-catalytic and catalytic (mesoMFI) pyrolysis/co-pyrolysis was investigated using thermogravimetric analysis (TGA); use of catalyst reduced the temperature of PP thermal degradation, but did not change the maximum reactivity temperature of EFB degradation.

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