4.7 Article

Continuous hydroprocessing of microalgae biodiesel to jet fuel range hydrocarbons promoted by Ni/hierarchical mesoporous Y zeolite catalyst

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 44, Issue 23, Pages 11765-11773

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.03.073

Keywords

Continuous hydroprocessing; Hierarchical mesoporous zeolite; Jet fuel range hydrocarbons; Microalgae

Funding

  1. National Key Research and Development Program-China [2017YFE0122800]
  2. National Natural Science Foundation of China [51476141]

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To simulate the industrial production of jet fuel range hydrocarbons, the hydroprocessing of Nannochloropsis oceanica microalgae biodiesel over a nickel-based hierarchical mesoporous Y (meso-Y) zeolite catalyst in a continuous process was investigated. The goal was to optimize two of the key parameters involved in hydroprocessing process, i.e., the reaction temperature and feedstock injection rate, to improve the biodiesel conversion and product selectivity, especially to iso-alkanes. A microalgae biodiesel conversion of 91.5% with a selectivity to jet fuel range hydrocarbons of 56.2% was obtained for a feedstock injection rate of 0.02 mL/min at 275 degrees C over Ni/meso-Y zeolite catalyst (total acid density = 3.08 mmol/g and BET surface area = 599.57 m(2)/g) in a fixed bed continuous hydroprocessing system. In addition, an isomerization ratio of 46.4% was achieved and attributed to the optimized reaction conditions, as well as to the shape selectivity exhibited by the catalyst. XRD performed for the used catalyst revealed unchanged crystallinity of the zeolite while a sintering process was noted for Ni nanoparticles whose crystallite size increased from 25 to 54 nm during hydroprocessing at 275 degrees C. FTIR detected functional groups of -CH2- (final saturated hydrocarbons), -CHO (intermediate aldehydes), and C=C (intermediate olefins), which were generated over catalyst after reactions. SEM and EDS showed that carbon element (22.9 wt%) uniformly distributed over catalyst after reaction at 275 degrees C due to efficient conversion. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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