Research Article
Biofuel additive production from glycerol and determination of its
effect on some fuel properties
Abdülvahap Çakmak1
· Hakan Özcan2
Received: 13 February 2020 / Accepted: 6 August 2020 / Published online: 6 September 2020
© Springer Nature Switzerland AG 2020
Abstract
In this study, the effects of glycerol ethers as a biobased additive on some important fuel properties of the diesel–biodiesel blend are investigated. For this, firstly, glycerol ethers are synthesized by the etherification reaction of glycerol with
tert-butyl alcohol with the presence of Amberlyst-15 as an acidic catalyst. The process of synthesis is followed by analyzing product composition through Fourier-transform infrared spectroscopy and gas chromatography-mass spectroscopy.
Lastly, synthesized glycerol tert-butyl ethers are mixed with a diesel–biodiesel blend, and the effects of glycerol ethers on
the fuel properties are determined. The analysis results show that glycerol tert-butyl ether mixture consists of mono- and
di-ethers of glycerol. Due to the dehydration reaction and hindrance effect, the tri-ether of glycerol is not generated. The
outcomes of determination of fuel properties reveal that glycerol ethers can be blended with a biodiesel-diesel mixture
without any significant change in the fuel properties by fully meeting the ASTM D7467 standard, indicating glycerol
ethers could serve as a biobased additive to diesel–biodiesel blend.
Keywords Biodiesel · Biofuel additive · Glycerol · Glycerol ethers
1 Introduction
Internal combustion engines that convert the fuel chemical energy through combustion into mechanical energy
are the main power supply machines most commonly
used in transportation, agricultural, and construction facilities. An internal combustion engine generates mechanical power by burning the fuel inside the cylinders. This
process produces exhaust emissions that contain many
substances responsible for air pollution that cause serious environmental and health problems. Vehicles used in
transportation are the major air pollution producers [1].
They emit a significant amount of carbon monoxide (CO),
unburned hydrocarbon (UHC), nitrogen oxides (NOX), particulate matter (PM), carbon oxide (CO2), and unregulated
emissions such as formaldehyde, acetaldehyde, benzene,
toluene, and xylene [2, 3]. Each of these emissions has
extreme hazards on human health and the environment.
Also, currently, pollution from vehicles is responsible for
about two-thirds of air pollution in the urban area [4, 5].
In order to mitigate the risk of pollutants on health and
environment, emissions standards have been enforcing in most countries over the world. As a result of more
fuel-efficient engines, after-treatment devices, and fuel
processing technologies, the emissions have been substantially reduced [6]. However, increasing the number of
vehicles, resulting in no overall reduction in exhaust emissions. Therefore, to mitigate this problem, it is necessary
to utilize renewable biofuels instead of petroleum fuels.
Among the biofuels, biodiesel has emerged as an alternative renewable fuel to petroleum diesel. Biodiesel is an
oxygenated renewable fuel produced from vegetable oils,
* Abdülvahap Çakmak, abdulvahap.cakmak@samsun.edu.tr | 1Department of Motor Vehicles and Transportation Technologies, Kavak
Vocational School, Samsun University, 55850 Samsun, Turkey. 2Department of Mechanical Engineering, Ondokuz Mayıs University,
55139 Samsun, Turkey.
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animal fats, or waste oil/fats by a simple chemical process.
Biodiesel has numerous advantages over petroleum diesel
fuel; (1) it is biodegradable, non-toxic and environmentally friendly fuel, (2) it is a carbon–neutral fuel since the
carbon released by burning biodiesel will be absorbed by
plants in the photosynthesis process [7], (3) it can play a
significant role in reducing exhaust emissions such as carbon monoxide (CO), unburned hydrocarbon (UHC), and
particulate matter (PM) [8, 9], (4) it has a high flash point
and auto-ignition temperature that makes it safe for transportation, storage, and distribution; and thus it reduces
the risk of fire and explosion, (5) biodiesel is compatible
with the existing diesel engine technology and fuel storage and distribution infrastructure. The characteristics
mentioned above of biodiesel have led biodiesel to be an
attractive alternative fuel to petroleum-based diesel fuel.
Hence, its consumption has greatly increased in the last
two decades. In the period 2000–2018, world biodiesel
production has increased about 46 times, from 0.78 billion liters to 36.1 billion liters [10]. Moreover, as seen in
Fig. 1, the global biodiesel production will experience
sustainable growth in the next years, increasing up to 39
billion liters in 2027 [11]. However, global biodiesel production is foreseen to decrease in the next 3 years mainly
because of less favorable export opportunities, reduction
in mineral oil prices, and an increase in biofuel feedstock
price [12]. Although currently, the major energy source
used in diesel engines is from petroleum-diesel fuel,
there is an effort to increase the share of biodiesel in total
fuel. In 2018, total biodiesel blending with fossil diesel in
Europe was 5.8% [13]. Besides, the European Union (EU)
has set a 12% renewable fuel blending target on energy
bases for the transportation sector by 2030 [14]. Likewise,
other countries such as Turkey, the United States, Brazil,
Argentina, and Indonesia have developed a project to
increase biofuel use in transportation [15, 16]. As a consequence of the increased biodiesel production worldwide,
it is inevitable that glycerol production also will increase
since glycerol is a by-product in the biodiesel production
World biodiesel production
(billion liters)
39.50
39.27
39.03
39.00
39.03
38.79
38.86
38.70
38.50
38.00
2020
38.52
2021
2022
38.57
2023
2024
Year
Fig. 1 Global biodiesel production forecast [11]
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2025
2026
2027
process. The glycerol produced during this process is
approximately 10 wt% of total biodiesel [17, 18]. If the
estimated amount of biodiesel production of 34 million
tons is in 2024, approximately 3.4 million tons of glycerol
would be generated. This will create a surplus of glycerol
that cannot be evaluated related industries, and it may
cause a drop in glycerol prices and environmental concerns [17, 19, 20]. Therefore, it is necessary to find a way
of recovering the excess of glycerol. In fact, glycerol cannot be directly used as a fuel in diesel engines owing to
its improper fuel properties such as high viscosity, high
density, high boiling temperature, and immiscibility with
diesel fuel. Hence, the use of glycerol in new applications
is essential for both environment and sustainable biodiesel
production. However, the transformation of glycerol into
oxygenated fuel by chemical methods is possible, and it
has drawn the interest of many researchers due to its economic benefits [21]. The utilization of glycerol ethers as
a fuel additive would increase the percentage of biofuel
input in the internal combustion engines, and it makes it
easy to reach the biofuel blending target.
Glycerol conversion into oxygenated fuel can be easily
accomplished by the etherification reaction [22, 23]. This
reaction occurs between glycerol (G) and tert-butyl alcohol
(TBA) or isobutylene (IB) in the presence of a heterogeneous acid catalyst, giving the glycerol ethers that can be
used as a fuel additive [20, 24]. The reaction scheme that
shows the equilibrium reactions involved in the etherification of glycerol with TBA is presented in Fig. 2. As seen
in reaction scheme, a mixture of five tert-butyl ethers of
glycerol, namely mono-tert-butyl glycerol ether 1 (MTBG1),
mono-tert-butyl glycerol ether 2 (MTBG2), di-tert-butyl
glycerol ether 1 (DTBG1), di-tert-butyl glycerol ether 2
(DTBG2) and tri-tert-butyl glycerol ether (TTBG) are produced. [17, 25, 26]. Also, a small amount of IB is formed by
the dehydration of the TBA [27].
Glycerol ethers are a mixture of mono-, di-, and tri-tertbutyl glycerol ethers, however, di-ethers and tri-ether of
glycerol are potential oxygenated fuel additive to diesel,
biodiesel, or their mixture [28]. Also, these ethers can
improve fuel quality and reduce emissions [20, 28, 29].
Glycerol ethers could also be substitute MTBE (methyl tertbutyl ether) and ETBE (ethyl tert-butyl ether) that lead to
contamination of underground water [30].
The etherification reaction of glycerol by TBA has
numerous advantages over isobutylene. TBA is a by-product of polypropylene production. Also, TBA is cheaper than
isobutylene, and while the latter is petroleum originated
component. Moreover, TBA is a biobased product, and it
can also be produced from lignocellulosic biomass [31].
The etherification of glycerol with TBA occurs in a liquid
phase, and thus it does not require high pressure and
temperature, which increases the chemical processes risk
SN Applied Sciences (2020) 2:1637 | https://doi.org/10.1007/s42452-020-03308-7
Research Article
Fig. 2 Reaction pathway for
the etherification of glycerol
with TBA. Adapted from Ref.
[17] and Ref. [26]
and cost. Besides, there is no need to use a solvent in the
reaction medium for increasing solubility of reactants [25].
Amberlyst-15, as a heterogeneous acidic catalyst, has been
widely used in the etherification reaction due to its activity
and high ethers selectivity [19, 22, 32]. Moreover, Amberlyst-15 has a solid form that facilitates its separation from
reaction products, and its reusability also contributes to
decreasing processing costs [26, 32, 33]. Therefore, in this
study, TBA and Amberlyst-15 as a catalyst were chosen for
the etherification of glycerol.
Although glycerol ethers are proposed as a potential oxygenated fuel additive, limited studies dealing
with the effects glycerol ethers on fuel properties are
available in the existing scientific literature [24, 34, 35].
In this regard, the objective of this research is to study
the effect of the addition of glycerol ethers in the diesel–biodiesel blend on some important fuel properties and also is to determine whether the quality of the
fuel was in agreement with the ASTM D7467 standard.
Since glycerol ethers are not commercially available,
production and characterization of glycerol tert-butyl
ethers were also performed. This presented paper provides some outcomes about how glycerol ethers influence some significant fuel properties, and the authors
believe that the outcomes of this study could make a
noteworthy contribution to the biofuel research area.
This paper is organized into four parts. After a brief information about biofuels and current interest in biodiesel,
the importance and conversion process of glycerol into
biofuel additive is presented in the introduction part. In
the material and method section, the methods adopted
for the synthesis and characterization of glycerol ethers
are described. The findings from spectroscopic studies
and the outcomes from the measurement of fuel properties are discussed in the results and discussion section.
In the conclusion section, the key findings of this study
are summarized. Also, possible future research on the
glycerol ethers is suggested.
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2 Materials and methods
In this study, glycerol ethers were synthesized by the
etherification reaction of glycerol with TBA at the presence of Amberlyst-15 in a stainless steel batch reactor.
For this purpose, a stainless steel batch reactor with
500 cm3 volume was designed and manufactured. Glycerol (purity ≥ 99%, TEKKİM: a local chemical company
in İstanbul, Turkey), TBA (purity ≥ 99.5%, Merck), and
Amberlyst-15 (dry form, Dow Chemical Company) were
the chemicals for the production of glycerol ethers at
laboratory scale. The etherification reaction conditions
Fig. 3 The photographic view of the experimental procedure: a
synthesis of glycerol ethers in the batch reactor, b vacuum filtration
of Amberlyst-15 from the liquid phase, c separation of TBA from
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such as alcohol/glycerol molar ratio, amount of catalyst,
reaction time, reaction temperature, and stirring speed,
which gives high glycerol conversion and high ether
selectivity were determined from the previously published studies [31, 32, 36]. The conditions of the etherification reaction selected for this study are as follows:
•
•
•
•
•
TBA/Glycerol molar ratio: 4:1
Amount of Amberlyst-15: 7.5 wt%/glycerol
Reaction temperature: 90 °C
Reaction time: 3 h
Stirring speed: 1200 rpm
products by rotary type evaporator, d purification of glycerol ethers
by the distillation process
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The reaction procedure was the following: a defined
amount of glycerol, TBA, and Amberlyst-15 were loaded
into the reactor, and the reactor was purged with nitrogen gas to obtain an inert environment. Then, the reactor
was heated up to reaction temperature, and the reaction
started immediately by running magnetic stirring. Since
reaction temperature was set to 90 °C, and TBA boils at
82.5 °C, the pressure in the reactor increased up to 8 bar.
During the reaction, the reactor temperature and pressure continuously was measured by a digital thermometer and an analog pressure gauge, respectively. At the
end of the reaction, the reactor was cooled down to room
temperature to collect products in the liquid phase. The
Amberlyst-15 catalyst was removed from the product by
the vacuum filtration method. A two-stage distillation process was performed for purifying the products. Sufficient
amounts of glycerol ethers were produced with the same
method by repeating experiments. The detailed view of
the experimental procedure was given in Fig. 3.
Characterization of produced glycerol tert-butyl ethers
was performed by Fourier-transform infrared spectroscopy (FTIR) and Gas Chromatography-Mass Spectrometer
(GC–MS). Synthesized glycerol ethers were analyzed by
FTIR (Perkin Elmer, Spectrum-Two, USA) in the range of
400–4000 cm−1 with the resolution of 1 cm−1 and GC–MC
(Agilent GC–MSD, Model: 7890B GC-5977MSD) analysis.
The DB-WAX column (60 m × 250 μm × 0.25 μm) was used
for analyzing glycerol ethers. Selected chromatographic
conditions for GC–MS analysis were given in Table 1.
To investigate the effects of glycerol ethers on some
basic fuel properties, produced glycerol ethers were
blended with corn oil biodiesel. If all glycerol obtained
from biodiesel production were incorporated into glycerol ethers synthesis, a roughly blending ratio of 10%
would occur [37]. Therefore, a blending ratio of 10 vol%
was chosen in this study. This blending ratio might contribute to sustainable and economic biodiesel production.
Produced glycerol ethers were blended with corn oil biodiesel in 10 vol%, and this resulted in a biodiesel–glycerol
ethers mixture (10 vol% glycerol ethers + 90 vol% corn oil
Table 1 Selected
chromatographic conditions
for GC–MS analysis
Column
Air flow rate
H2 flow rate
He flow rate
Split ratio
Injection volume
Oven temperature program
Research Article
Table 2 Test methods used to determine fuel properties
Property
Test method
Density@15 °C
Dynamic viscosity
Cloud point
Cold filter plugging point (CFPP)
Cetane index
Distillation temperature
TS EN ISO 12185
DIN 53015
TS 2834 EN 23015
TS EN ISO 116
TS EN ISO 4264
TS EN ISO 3405
biodiesel). Firstly, this blend was mixed with a magnetic
stirrer, and then, to further increase blend homogeneity, an ultrasonic mixing process was applied at 40 kHz
for the time duration of 30 min. After that, the glycerol
ethers-biodiesel blend was mixed with diesel fuel in the
concentration of 20 vol% and this blended fuel designated
as B20_GTBEs. At the final stage, B20_GTBEs was obtained
with the 20 vol% renewable fraction, containing 80 vol%
diesel fuel, 18 vol% corn oil biodiesel, and 2 vol% glycerol tert-butyl ethers. B20 (20 vol%corn oil biodiesel was
blended with 80 vol% diesel), and pure diesel (D) were
selected as reference fuel for comparison. The biodiesel
utilized in this study is corn oil biodiesel because of the
high volume of corn oil in Turkey. The details of corn oil
biodiesel production and its fuel properties that meet
standard specifications of EN 14214 and ASTM D 6751 can
be found elsewhere [38].
It should be highlighted that fuel quality is an essential
factor in reducing harmful exhaust emissions and being
compatible with the existing engine technology. Therefore, before its commercialization, fuel specifications of
fuel produced must comply with the international fuel
standards. Although most of the countries have their fuel
standards, EN and ASTM standards widely accepted. In
this study, some essential fuel properties of the fuel samples measured according to international test methods.
The test methods used to determine fuel properties were
given in Table 2.
DB-WAX (60 m × 250 μm × 0.25 μm) (20–250 °C) max. 260 °C
300 ml/min
30 ml/min
1.4 ml/min
20:1
0.5 μL
Rate (°C/min)
Value (°C)
Hold time Run time (min)
(min)
Initial
–
50
10
10
Ramp 1
4
115
2
28.25
Ramp 2
15
250
2
39.25
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3 Results and discussion
Fig. 4 FTIR spectra of reactants and products
Fig. 5 The chromatogram of the reaction products
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The FTIR spectra of reactants and products were presented in Fig. 4, and the GC–MS chromatogram of the
products was shown in Fig. 5. As can be seen in FTIR
spectra, a total of 12 peaks appeared in the reactant,
while a total of 10 peaks observed in the products. From
the FTIR spectra, it can be seen that both reactants
and products have peaks that occurred in the range of
3500–3200 cm−1. The observed peak for reactants can
be attributed to O–H stretching vibration in alcohol, and
the peak appeared in products that can be attributed to
Research Article
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O–H bending vibration of water molecules formed by
dehydration of tert-butanol. The peaks in the range of
3000–2850 cm−1 indicate C–H stretching of the alkane
group. The peaks at the 1680–1640 cm−1 region can be
attributed to the C=C stretching vibration of the alkane
group. Peaks in the range of 1300–1000 cm−1 represent
the stretching vibration of C–O, which exists in the alcohols and ethers [39]. In addition, the peaks appeared at
3340.57, 2971.78, 1472.78, 1364.54, 1239.38, 1197.68,
1043.67, 910.70, and 749.11 cm−1 in the reactants were
shifted to 3370.34, 2973.33, 1472.78, 1366.10, 1240.59,
1196.41, 1023.73, 907.95, and 748.63 cm −1 in the products, respectively. Therefore, disappearing of the peaks
from the spectrum of reactants at 1380.56, 1112.30,
and 674.60 cm −1, and the formation of a new peak at
1647.23 cm−1 in the products spectrum confirm the conversion of glycerol into glycerol ethers. The results of the
FTIR spectrum are similar to those obtained by Jamróz
et al. [40].
The GC–MS analysis was utilized to identify the substances within the reaction products. MS spectra of
glycerol tert-butyl ethers are unavailable in Masshunter
libraries. Therefore, the products were confirmed by the
retention time and mass fragmentation pattern with the
previously published papers, wherein a detailed spectroscopic study on tert-butyl ethers of glycerol is carried
out [40, 41]. It can be easily seen in Fig. 5 that eight peaks
appeared in the chromatogram. The observed peaks
belong to IB, diisobutene (DIB), TBA, DTBG1, DTBG2,
MTBG1, MTBG2, and G, respectively. No peak was observed
for TTBG and indicating that TTBG did not form. This result
is in agreement with earlier reported results [26, 32, 41].
The reason for this is attributed to the steric hindrance [17,
32]. Besides, the formed of water from tert-butyl alcohol by
dehydration has an inhibition effect on the Amberlyst-15
catalyst, which decreases the formation of high ethers of
glycerol [25, 28, 31]. GC–MS results are in close agreement
with those obtained by Jamróz et al. [40], Özbay [42], and
Paula et al. [41].
EN 14214 and ASTM D 6751 standards are the most
referred standards for pure biodiesel. Biodiesel blends
Table 3 The properties of
B20_GTBEs, B20 fuel, and D
with ASTM D 7467 standard
up to 5 vol% must meet the ASTM D957 diesel standard. Diesel–biodiesel blends containing 6–20 vol% biodiesel should meet the ASTM D 7467 that is adopted for
diesel–biodiesel blends (greater than 5 vol% and up to
20 vol% biodiesel) quality [43]. Measured fuel properties
of B20_GTBEs, B20, and D and the minimum–maximum
limit fixed by ASTM D 7467 standard presented in Table 3.
Density is one of the critical fuel properties since it
directly affects fuel atomization, fuel consumption, and
hence engine performance and emissions. The density of
B20_GTBEs is lower than that of B20. However, B20_GTBEs
and B20 fuels have a higher density than diesel fuel due
to the high density of biodiesel, as expected. Moreover,
under the ASTM D7467 standard, the density of the fuel
is not limited.
The most important property of the fuel used in diesel
engines is the viscosity. Since viscosity has a significant
impact on fuel injection and combustion, it directly affects
engine performance and exhaust emissions. High viscosity
leads to problems with fuel atomization and the air–fuel
mixture formation, which results in incomplete combustion and poor engine performance. Also, high viscosity can
cause carbon deposits on cylinder walls and can damage
fuel injectors and fuel pumps. Dynamic viscosities of the
samples at 40 °C were determined by Falling ball viscosimetry (HAAKE™), water bath (HAAKE™), and stopwatch
according to DIN 53015 standard. More detail of dynamic
viscosity measurement can be found in Refs. [44, 45]. The
kinematic viscosity of each sample was determined by
dividing dynamic viscosity to the density at the temperature of 40 °C. As seen in Table 3, the kinematic viscosity
of the diesel–biodiesel blend was decreased by the addition of glycerol tert-butyl ethers. This result is in agreement with the study of Noureddini et al. [35] that showed
20 wt% a blend of glycerol ethers with methyl esters
resulted in an 8% reduction in kinematic viscosity. In this
study, 2 vol% fraction of glycerol tert-butyl ethers in the
final fuel (B20_GTBEs) resulted in a decrease in kinematic
viscosity from 3.27 to 3.15 mm2/s, which corresponding to
a decline in viscosity by 3.7% compared to B20. In addition,
Property
Unit
Uncertainty
B20_GTBEs
B20
D
ASTM D 7467
Density@15 °C
Kinematic viscosity@40 °C
Cloud point
Cold filter plugging point
Cetane index
Distillation temperature
kg/m3
mm2/s
°C
°C
–
T10 (°C)
T50 (°C)
T90 (°C)
± 0.2
± 0.002
± 0.1
± 0.5
–
± 0.1
± 0.1
± 0.1
846.0
3.15
− 4.0
− 14.0
52.5
204.0
302.3
342.4
847.9
836.3
3.27
2.86
− 4.0
− 6.0
− 14.0 − 19.0
52.0
53.3
217.1
210.0
294.0
274.9
342.8
340.3
–
1.9–4.1
–
–
40.0 min.
–
–
343 °C max.
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all fuels’ kinematic viscosity was found within the ASTM D
7467 standard.
Cloud point (CP) and Cold filter plugging point (CFPP)
are the low-temperature properties that affect the fuel
system functionality of a diesel engine. CP temperature is
the temperature below which wax in fuel forms a cloudy
appearance, and it indicates the onset of fuel solidification
[46]. CFPP is a cold flow property used to determine the
lowest temperature at which a fuel will freely flow through
fuel filters in a diesel fuel system. The cold flow properties
of B20 fuel was not affected by the addition of glycerol
ethers in the fuel. This was due to low glycerol ethers concentration. However, it has been shown that 20 wt% the
blend of ethers of glycerol with methyl esters results in a
5 °C reduction in cloud point temperature [29]. Nevertheless, diesel fuel exhibited the lowest CP and CFPP temperature among the fuels. Besides, the limit of cold flow
properties is not specified in ASTM D7467 standard.
Cetane number is an indication of a self-burning characteristic of diesel fuel, and it governs the fuel combustion
process inside the cylinder. The higher the cetane number,
the better the fuel ignitions within the cylinder that leads
to higher performance and lower emissions [6]. Measurement of the cetane number is carried out by a standard
test using a particular engine. However, it is difficult and
costly. Therefore, the cetane index is used as an alternative
to the cetane number due to the complexity of the cetane
number test, and it is calculated based on fuel density and
distillation temperature. It was found that the cetane index
of B20_GTBEs increased by 0.5 points when compared to
B20. Although both B20_GTBEs and B20 have a lower
cetane index than that of diesel fuel, the cetane number
all fuels are full compliance with ASTM D7467.
The evaporation characteristic is one of the critical
fuel features that directly affect the fuel economy, engine
performance, and emissions of an internal combustion
engine. Petroleum-based diesel fuel is a blend of many
hydrocarbons, each hydrocarbon has different chemical
and physical properties and hence a wide range of boiling
temperatures. This is a desired behavior of fuel to obtain
controlled and efficient combustion inside the cylinder. To
determine the fuel evaporation characteristic, the distillation test is used as a basic test, and extensive information about the fuel can be extracted from the distillation
results. The distillation test is performed by measuring the
recovery percentage of vaporized fuel as the temperature
increases [47]. The test result is a distillation profile temperature versus percentage volume of the evaporated
fuel, allow us to interpret the volatility behaviors of the
sample fuel. The point of T10, T50, and T90 are temperatures at which 10 vol%, 50 vol%, and 90 vol% of fuel is
vaporized, respectively. T10 represents the light hydrocarbons fraction in the fuel, and it is a critical parameter
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for cold start engine performance. Still, a low T10 value
is not desirable at all engines running conditions since it
adversely affects fuel economy and evaporative emissions
[48]. T50 is medium distillation temperature representing
the medium hydrocarbons fraction in the fuel, and it influences the engine warm-up, the vehicle acceleration performance, and fuel economy. T90 temperature is the high
distillation temperature that represents heavy hydrocarbons fraction in the fuel, and it has a significant effect on
lubrication oil dilution, the formation of carbon deposits,
and particulate matter (PM). The most important impact
of glycerol ethers on fuel properties was determined on
distillation temperature. It was measured that the low
distillation temperature (T10) of the B20 was decreased
from 217.1 to 204.0 °C when 10 vol% glycerol ethers
incorporated in the biodiesel. The reason for this could be
the low boiling point temperature of glycerol ethers. As
mentioned above, this could facilitate the cold start performance of the engine, but it could lead to an increase
in fuel consumption. However, B20_GTBEs resulted in a
slightly higher T50 temperature and nearly the same T90
temperature compared to B20. As a consequence, from
the distillation temperatures, it could be inferred that
glycerol ethers can improve the cold start performance of
the engine, however, due to the low T10 temperature of
B20_GTBEs the fuel economy could be deteriorated with
the use of glycerol ethers. Also, the T10, T50, and T90 temperature of B20_GTBEs were in line with the limit fixed by
the ASTM D7467.
4 Conclusions
In this research, glycerol tert-butyl ethers were synthesized by the etherification reaction of glycerol with TBA
at the presence of an acidic catalyst, and the produced
glycerol ethers were blended with a diesel–biodiesel blend
to determine the effects on glycerol ethers on some fuel
properties. It was revealed that measured fuel properties
of B20 slightly changed except for T10 temperature with
the addition of glycerol ethers, and they were full compliance with ASTM D7467. The significant effect of glycerol
ethers on determined fuel properties was observed as a
decrease in the T10 distillation temperature. All of the findings indicate that glycerol ethers could serve as a renewable oxygenated fuel additive to biodiesel-diesel blends.
Evaluation of the biodiesel-based glycerol in oxygenated
fuel production could be the solution to the problems that
arise from excess glycerol. Also, in this way, biofuel share
in transportation can be more easily increased, and this
may facilitate reaching a 12 vol% biofuel blending target.
Besides, air pollution and other environmental hazards
caused by petroleum fuels could be minimized by using
SN Applied Sciences (2020) 2:1637 | https://doi.org/10.1007/s42452-020-03308-7
glycerol ethers. As a consequence, the use of glycerol
ethers as a fuel additive has a great significance in terms of
environmental perspective and sustainable biodiesel production. However, the effects of glycerol ethers on other
fuel properties, engine performance, exhaust emissions,
and fuel economy should be extensively investigated in
future works.
Acknowledgements The authors thank Assoc.Prof. Selim CEYLAN
(Chemical Engineering Department, Ondokuz Mayıs University,
TURKEY) who provided expertise that greatly assisted the research.
The authors also thank Res. Assist. Agah YILDIZ (Chemical Engineering Department, Ondokuz Mayıs University, TURKEY) for experimental assistance. This study was financially supported by the Project
Management Office of Ondokuz Mayis University (Project ID: PYO.
MUH.1904.19.016).
Compliance with ethical standards
Conflict of interest The authors declare that they have no conflict of
interest.
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