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Biodiesel synthesis from bio-heavy oil through thermally induced transesterification

Authors
Jung, SungyupKim, MinyoungLin, Kun-Yi AndrewPark, Young-KwonKwon, Eilhann E.
Issue Date
Apr-2021
Publisher
ELSEVIER SCI LTD
Keywords
Waste-to-energy; Biofuel; Biodiesel; Bioalcohol; Lipids; Fatty acids
Citation
JOURNAL OF CLEANER PRODUCTION, v.294
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CLEANER PRODUCTION
Volume
294
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190175
DOI
10.1016/j.jclepro.2021.126347
ISSN
0959-6526
Abstract
A huge amount of a mixture of unreacted fatty acids and mono/di/triglycerides, namely bio-heavy oil, is generated as a waste from biodiesel industry. Considering that the lipid (i.e., triglycerides) accounts for 80% of the total biodiesel production cost, valorization of bio-heavy oil into biodiesel can be a viable route for enhancing the economic/environmental benefits. Nonetheless, the high contents of free fatty acids and impurities have restricted practical valorization of bio-heavy oil into biodiesel because conventional acid/base catalyzed transesterification suffers from the presence of the impurities. To overcome the technical challenge, this study suggested a direct valorization platform for the conversion of bio-heavy oil into biodiesel via thermally induced transesterification. Prior to biodiesel production, the properties of bio-heavy oil, such as acid value (105 mg KOH g(-1) bio-heavy oil), its elemental compositions and thermal stability were characterized. Acid-catalyzed transesterification with a H2SO4 catalyst showed the 31.1 wt % of biodiesel yield after 24 h of reaction at 60 degrees C. However, thermally induced transesterification exhibited 59.3 wt% of biodiesel yield after 1 min of reaction at 400 degrees C using a porous medium (SiO2) with no presence of a catalyst. The porous SiO2 (pore size: 6 nm) provided confined spaces for lipids and methanol, allowing the rapid transesterification reactions between them at high temperature. The biodiesel yield from thermally induced transesterification was proportionate to reaction temperature by 360 degrees C, but it decreased at > 400 degrees C due to the chemical bond scissions of unsaturated hydrocarbons. C6-22 fatty acid methyl esters (FAMEs) were produced from thermally induced (non-catalytic) transesterifications, and weight fractions of each FAMEs were constant, regardless of the reaction conditions at <= 400 degrees C. All experimental findings offer a new recycle platform for BHO into biodiesel.
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Kwon, Eilhann E.
COLLEGE OF ENGINEERING (DEPARTMENT OF EARTH RESOURCES AND ENVIRONMENTAL ENGINEERING)
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