Kinetics and reusability of Zr/CaO as heterogeneous catalyst for the ethanolysis and methanolysis of Jatropha crucas oil

Zirconium impregnated (5-20 wt.%) calcium oxide (Zr/CaO) was prepared by a simple wet chemical method followed by calcination up to 900 [degrees]C. The prepared Zr/CaO was employed as a heterogeneous catalyst for the transesterification of Jatropha crucas oil with ethanol and methanol for the produc...

Full description

Saved in:
Bibliographic Details
Published in:Fuel processing technology Vol. 119; pp. 173 - 184
Main Authors: KAUR, Navjot, ALI, Amjad
Format: Journal Article
Language:English
Published: Amsterdam Elsevier 01-03-2014
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Zirconium impregnated (5-20 wt.%) calcium oxide (Zr/CaO) was prepared by a simple wet chemical method followed by calcination up to 900 [degrees]C. The prepared Zr/CaO was employed as a heterogeneous catalyst for the transesterification of Jatropha crucas oil with ethanol and methanol for the production of fatty acid ethyl and methyl esters, respectively. The catalysts were characterized by powder X-ray diffraction, Fourier transform-infrared spectroscopy, Brunauer-Emmett-Teller surface area measurement, scanning electron microscopy, transmission electron microscopy techniques and basic strength of the catalyst were established by acid-base titration. The catalytic activity was found to be a function of basic sites which in turn depend on calcination temperature and zirconium concentration. The catalyst with 15 wt.% zirconium concentration and calcined at 700 [degrees]C, showed the highest catalytic activity among the prepared catalysts. A pseudo first order kinetic equation was applied to evaluate the kinetic parameters of Zr/CaO catalyzed transesterification. The activation energy (E sub(a)) for the Zr/CaO catalyzed methanolysis and ethanolysis was found to be 29.8 kJ mol super(1) and 42.5 kJ mol super(1) respectively. The Koras-Nowak test was performed to demonstrate that catalytic activity was independent from the mass transport phenomenon and follows the kinetic regime.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0378-3820
1873-7188
DOI:10.1016/j.fuproc.2013.11.002