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Gasoline-like hydrocarbons by catalytic cracking of soap phase residue of neutralization process of palm oil (Elaeis guineensis Jacq).

Authors :
Santos, M.C.
Lourenço, R.M.
de Abreu, D.H.
Pereira, A.M.
de Castro, D.A.R.
Pereira, M.S.
Almeida, H.S.
Mâncio, A.A.
Lhamas, D.E.L.
da Mota, S.A.P.
da Silva Souza, J.A.
Júnior, S.D.
Araújo, M.E.
Borges, L.E.P.
Machado, N.T.
Source :
Journal of the Taiwan Institute of Chemical Engineers; Feb2017, Vol. 71, p106-119, 14p
Publication Year :
2017

Abstract

In this work, the soap phase residue of neutralization process of palm oil ( Elaeis guineensis Jacq) submitted to catalytic cracking to produce gasoline-like hydrocarbons fuels. The cracking reaction carried out in a stirred tank reactor of 143 L, operating in batch mode at 440 °C and 1.0 atmosphere, using 15% (wt.) Na 2 CO 3 as catalyst. The organic liquid products (OLP) yield 71.34% (wt.) with an acid value of 1.07 mg KOH/g and kinematic viscosity of 1.90 mm 2 s − 1 , matching sulfur content, copper strip corrosion, flash point, viscosity and density of ANP (Brazilian Petroleum Agency) N° 65 for diesel S10. The distillation of OLP carried out in laboratory scale according to the boiling temperature range of fossil fuels, yielding 6.69% (wt.) gasoline, 12.77% (wt.) kerosene, 15.52% (wt.) light diesel, and 38.02% heavy diesel-like hydrocarbons fuels, showing that Na 2 CO 3 was more selective to convert salts of carboxylic acids into diesel-like hydrocarbons fuels. The GC–MS analysis showed that OLP is composed by 91.59% (wt.) hydrocarbons and 8.41% (wt.) oxygenates. The gasoline-like hydrocarbons fraction composed by 100% hydrocarbons with an acid value of 1.69 mg KOH/g and kinematic viscosity of 0.83 mm 2 s −1 , matches many physicochemical parameters of ANP N° 40 for gasoline A, proving the technical feasibility of catalytic cracking process. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18761070
Volume :
71
Database :
Supplemental Index
Journal :
Journal of the Taiwan Institute of Chemical Engineers
Publication Type :
Academic Journal
Accession number :
121103722
Full Text :
https://doi.org/10.1016/j.jtice.2016.11.016