Please use this identifier to cite or link to this item: https://cuir.car.chula.ac.th/handle/123456789/61794
Title: Green diesel production through simultaneous deoxygenation of palmitic acid and desulfurization of 4,6-Dimethyl-dibenzothiophene over commercial CoMo/Al2O3
Authors: Sunya Boonyasuwat
Jirdsak Tscheikuna
Email: No information provided
Jirdsak.T@Chula.ac.th
Other author: Chulalongkorn University. Faculty of Engineering
Issue Date: 1-Jun-2018
Publisher: Green Wave Publishing of Canada
Citation: Biofuel Research Journal. Vol.2, Issue 2 (Spring, 2018), p. 821-826
Abstract: This study investigated the deoxygenation of palmitic acid as a model compound of palm fatty acid distillate (PFAD), in the presence of 4,6- di-methyl-di-benzothiophene as a sulfur-containing light gas oil (LGO). Reactions were performed at the pressure of 25 barg, liquid hourly space velocity (LHSV) of 1.7 h-1, and H2/oil of 630 NL/L over CoMo/Al2O3 as catalyst. The effect of temperature was studied in the range of 275-300 oC. Both deoxygenation and desulfurization led to approximately 100% conversions at 300 oC, while at 275 oC, palmitic acid deoxygenation was recorded at a higher conversion rate compared with that of the desulfurization of 4,6- di-methyl-di-benzothiophene. The presence of 4,6- di-methyl-di-benzothiophene during the deoxygenation of palmitic acid resulted in high conversions (>95%). Pressure drop studies showed that the formation of heavy products caused a gradual pressure drop throughout the reactor over time. The catalyst was deactivated during 10 d. Two different sulfur-containing reagents were used for catalyst reactivation including dimethyl-disulfide in n-C18 and LGO containing 484 ppmw of sulfur. Reactivation with 2 wt.% of dimethyl-disulfide in n-C18 at 320 oC for 36 h led to more favrable performance recovery vs. the sulfur-containing LGO.
URI: http://cuir.car.chula.ac.th/handle/123456789/61794
URI: http://doi.org/10.18331/BRJ2018.5.2.6
https://www.biofueljournal.com/article_63204.html
ISSN: 2292-8782
metadata.dc.identifier.DOI: 10.18331/BRJ2018.5.2.6
Type: Article
Appears in Collections:Foreign Journal Article

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