Matecconf Rsce2018 06007
Matecconf Rsce2018 06007
Matecconf Rsce2018 06007
https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
Abstract. Since long time ago, petroleum oil has been used as a lubricant in motor vehicles. But,
the uses of lubricants petroleum can pollute the environment and disrupt marine ecosystems and
terrestrial. On the other hand, the use of lubricants in the world in 2008 reached 46 million
kiloliters/year and increased by 2% every year. The future prospect the uses of lubricant
petroleum on the vehicle’s engine is predicted to have a bad prospect. Thus began research to
identify suitable materials to replace petroleum based lubricants. It can produce from vegetable
oils and animals oils by chemical modification. But, bio-lubricant properties are easily damaged
so we need more research to improve the shelf life of the bio-lubricant. The research must be
done to improve the characteristics by adding a bio-lubricant additive.
*
Corresponding author: ariantinuura@gmail.com
© The Authors, published by EDP Sciences. This is an open access article distributed under the terms of the Creative Commons Attribution
License 4.0 (http://creativecommons.org/licenses/by/4.0/).
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
content in vegetable oil. The fatty acid composition of vegetable oils were listed in Table 1.
Table 1. Fatty acids composition of vegetable oils [15-16]
Viscosity Oxidative
Lubricant Viscosity Viscosity Pour point Flash Coefficient Wear scar
100°C stability
requirement 40°C (cSt) index (°C) point (°C) of friction (mm)
(cSt) (min)
ISO VG32 >28.8 >4.1 >90 -6 204 - - -
ISO VG46 >41.4 >4.1 >90 -6 220 - - -
ISO VG68 >61.4 >4.1 >198 -6 226 - - -
ISO VG100 >90.0 >4.1 >216 -6 246 1670.26 - -
Paraffin 95 10 102 - - - - -
VG95
Paraffin 461 31 97 - - - - -
VG460
R150 150.04 - - - 195 931.16 - -
SAE20W40 105 13.9 132 -21 200 - 0.117 0.549
AG100 216 19.6 103 -18 244 - - -
75W-90 120 15.9 140 -48 205 - - -
75W-140 175 24.7 174 -54 228 - - -
80W-140 310 31.2 139 -36 210 - - -
Vegetable oil
Soybean 28.86 7.55 246 -9 325 - - -
Sunflower 40.05 8.65 206 -12 252 - - -
Passion fruit 31.78 - - - 228 7.5 - -
Moringa 44.88 - - - 204 28.27 - -
Castor 220.6 19.72 220 -27 250 - - -
Rapeseed 45.60 10.07 180 -12 240 - - -
Jatropha 35.4 7.9 205 -6 186 5 - -
Coconut 24.8 5.5 169 21 325 - 0.101 0.601
Rice bran 40.6 8.7 169 -13 318 - 0.073 0.585
Palm 52.4 10.2 186 -5 - - - -
Lesquerella 119.8 14.7 125 -21 - - 0.045 0.857
Pennycress 40.0 9.3 226 -21 - - 0.054 0.769
2
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
Modification Catalyst
Modification of Carboxyl Groups
- Esterification/transesterification Acids, Bases
- Estolides HClO4
Modification of fatty acid chains
- Selective hydrogenation Copper catalysts
- Dimerisation/oligomerisation Aluminosilicates
- Diels-Alder cycloaddition -
- Telomerisation H2O vapor
- Co-oligomerisation RhCl3.3H2O
- Hydroformylation (oxo-synthesis) Rh(Ph3P)3
- Friedel-Crafts alkylation Et3Al2Cl3
- Aminoalkylation [Rh(COD)Cl]2
- Friedel-Crafts acylation EtAlCl2
- Ene-reaction EtAlCl2, SnO4
- Radical addition Mn(OAc)3, Cu
- Acyloxylation Nafion/SiO2
- Cyclopropanation CH2I2, Zn(Cu), Et2Zn
- Metathesis Grubbs catalyst
- Epoxidation Peracids, chemo-enzymatic
- Ozonation -
- Oxidative cleavage Pb3O4
CH2OCOR CH2OCOR
2 ME + 2 RCOOH CH3CH2C CH2OH + CH3CH2C CH2OCOR + 2H2O
CH2OCOR CH2OH
Diester (DE)
CH2OCOR
2 DE + 2 RCOOH 2CH3CH2C CH2OCOR + 2H2O
CH2OCOR
Triester (TE)
Fig. 1. Esterification of fatty acids [20]
3
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
alcohol octavalen, using a base catalyst. The transesterification reaction is shown in Figure 2.
mechanism of the production biopelumas
CH2OH – C – R
CH2O
O
H
CH3 – CH2 – C – CH2OH + 3 RCOOCH3 CH3 – CH2 – C – CH2O – C – R + 3 CH3OH
CH2O CH2OH – C – R
H
O
polyol metyl ester polyol-triester methanol
Glycerol
OH
H 2C – O – C – R Glycerol
O O O
H 2C – O – C – R HO – C – R O–C–R
O Biolubricant
OH
H 2C – O – C – R
Fig. 3. Esterification Process Scheme (A) and transesterification (B) Bio-lubricant Production [22]
4
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
4.2 Transesterification using oscillatory flow Reeves et al. [31] conduct research on the effect of
reactor and sodium methoxide catalyst fatty acid composition of the viscosity index contained
in the avocado seed oil, canola oil, corn oil, olive oil,
Koh et al., [28] undertake the production of bio- peanut oil, safflower oil, sesame oil and soy oil. The
lubricant of palm methyl ester (PME) and result showed that the fatty acid composition affects
trimethylolpropane (TMP) using sodium methoxide the viscosity grades, with the highest viscosity in
catalyst (NaOCH3). Then do the transesterification peanut oil for 70.24 cP. Based on Zubaidah et al. [32]
reaction in the oscillatory flow reactor at 110°C to research used palm oil derivative compounds
150°C. An optimal reaction condition was obtained at a (trimetylolpropane) as bio-lubricant raw material.
temperature of 140°C to be reacted for 25 minutes. Production trimetylolpropane performed using a
Bio-lubricant obtained 94.6% by the concentration vacuum reactor with transesterification reaction. From
diesters 14.7% and 79.9% trimesters. However, the this study showed that the highest conversions were
lower yield obtained from the research Yunus et al. achieved by 66% at a temperature operating conditions
[29] 2003) with a concentration of 4.6% diesters and 120°C for 2 hours. Syaima et al. [33] produce bio-
trimesters 93.2%. lubricant from palm oil mill effluent (POME).
Although the results of a study by Koh et al., [28] Production of bio-lubricant performed using enzymatic
obtained a high yield, kinematic viscosity and viscosity hydrolysis and esterification. From the research,
index which is not accordance with ISO. Bio-lubricant optimum reaction conditions reached at 40°C, pH 7,
produced has a kinematic viscosity 47.1 cSt at 40°C, stirring speed of 650 rpm, the composition of the
9.0 cSt at 100°C and a viscosity index of 176. enzyme 20 U/ml and 50% (v/v) POME.
Meanwhile, based on ISO VG100 [30] lubricant should The research results bio-lubricant using processes
have a kinematic viscosity >90 cSt at 40°C, >4.1 cSt at esterification/transesterification is shown in Table 4.
100°C and a viscosity index >216.
Table 4. Characteristics of Bio-lubricant using esterification/transesterification process [17]
Pour Oxidative/
Reaction Viscosity Viscosity Viscosity Yield
Reactants Product Catalyst point Thermal
conditions 40°C (cSt) 100°C (cSt) index (%)
(°C) stability
Jatropha and TMP Sodium 150°C, 43.90 8.71 180 -6 - >80
TMP triesters methoxide 10mbar, 3 h
Jatropha ME TMP Sodium 150°C, 55 42.57 9.37 183 -6 325°C -
and TMP triesters methoxide min Degradation
temp
High oleic TMP Sodium 120-150°C, 45.5 – 50.7 9.2 - 10 183 - 200 (-37) to - -
palm ME triesters methoxide 0,3 mbar, 45 (-9)
and TMP min
Palm ME TMP Sodium 140°C, 25 47.1 9.0 176 -2 355°C 94.6
and TMP triesters methoxide mbar, 25 Degradation
min, temp
oscillatory
flow reactor
at 1,5 Hz
with 20 mm
amplitude
Palm ME TMP Calcium 180°C, 50 - - - - - 92,38
and TMP triesters methoxide mbar, 8 h
Canola TMP Sodium 110°C,1 40.5 7.8 204 -66 Induction time: 90.9
biodiesel triester methoxide mbar, 5 h 0.74 h
ME and
TMP
Castor TMP Dibutyltin 170°C, 0.01 287.2 26.13 119 -27 RPVOT: 43 min 89.7
biodiesel and triester dilaurate bar (Butylated
TMP hydroxytoluene
added)
Castor TMP Amberlyst 120°C, 0.01 20.94 4.467 127 - - -
biodiesel and triester 15 ionic bar
TMP exchange
resin
Castor TMP Sodium 120°C, 0.01 11.28 3.100 141 - RPVOT: 150 -
biodiesel and triester methoxide bar min (Butylated
TMP hydroxytoluene
added)
WCO ME TMP KOH 128°C, 200 38.60 8.44 204 -8 FP: 240°C 85.7
and TMP triester Pa, 1.5 h
5
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017
Soybean oil n- Sulfated 140°C, 4 h 10.3 – 432.7 3.0 – 34.4 45 - 195 - - >80
and various alcohol- zirconia
alcohols esters catalysts
Sunflower FA-n- Fe-Zn 170°C, 8 h 7.93 2.74 226 -3 23 min (RBOT) 98
oil and octyl double-
octanol esters metal
cyanide
(DMC)
complexes
Pentaerythrit Pentaeryt Ion 110°C, 6 h 63.08 12.00 190 -24 - -
ol and oleic hritol exchange toluene
acid tetraoleta resin, solvent
e ester Indion-
130
Valeric acid Valeric Silica- 70°C molar 9.5 2.5 80 -75 - -
TMP acid TMP sulphuric ratio of 3:1,
ester acid toluene
Rubber ME NPG/TM p- 135-140°C, 23,1-62,6 5.9-12.6 206-222 (-15) to 10-15 min 94.5-
and P/PE Toluensul until (-3) (RBOT) 96.5
NPG/TMP/P triesters phonic theoretical FP: 266 - 308°C
E acid reaction
complete
Rapeseed NPG/TM C 150, 200, 50 7.8 – 38.2 2.7-8.4 205-224 (-31.3) ∆v: 90.1-147.1 98
ME and P/PE Antarctica h to (-18) ∆Ac: 2.9-7.7
NPG/TMP/P triesters lipase
E
Thumba NPG/TM p- 135-140°C, 20.65-60.26 5.45-11.89 209-220 (-12) to 10-15 min 89-95
ME, xylene P/PE Toluensul until (-3) (RBOT)
and triesters phonic complete FP: 270-318°C
NPG/TMP/P acid
E
6
MATEC Web of Conferences 156, 06007 (2018) https://doi.org/10.1051/matecconf/201815606007
RSCE 2017