[Dasin et. al., Vol.6 (Iss.6): June 2019]
ISSN: 2454-1907
DOI: 10.5281/zenodo.3252416
THE PHYSICOCHEMICAL ANALYSIS OF BIODIESEL PRODUCED
FROM AFRICAN SWEET ORANGE (Citrus Sinensis) SEEDS OIL
M. H. Ibrahim 1, D. Y. Dasin *2, I. Yahuza 3
1
Department of Mechanical/Production Engineering, Abubakar Tafawa Balewa University
Bauchi, Nigeria
*2
Department of Mechanical Engineering, Modibbo Adama University of Technology Yola,
Nigeria.
3
Department of Mechanical Engineering, Nigerian Army University, Biu, Borno State Nigeria
Abstract:
The research presents experimental study and investigation on the production of biodiesel from
African sweet orange seeds oil. The seeds were obtained, sundried, crushed and weighed.
Chemical extraction method was used to extract oil from the crushed seeds using soxhlet
extractor with n-hexane as a solvent. The physicochemical properties of the oil determined were;
flash 1510C, fire point 1730C, acid value 82%, product percentage yield 40% and specific
gravity 0.920 at 150C. The production of Biodiesel was carried out through transesterification
process from the extracted oil using methanol as catalyst. The results of the physicochemical
properties of the produced biodiesel are; Cloud point 60C, Pour point 20C, Flash point 1400C,
Density 0.86g/cm and Kinematic viscosity 1.938 mm2/s. The effect of methanol on the yielding
of biodiesel at constant ratios of oil and catalyst was determined to be 68% at 10ml, 77% at 9ml
and 72% at 7ml. The results obtained are in conformity when compared with ASTM standard
D6571 and imply that the African sweet orange seeds oil can be used to produce biodiesel.
Keywords: Physicochemical; Biodiesel; Sweet Orange; Transesterification; Oil; Characterization.
Cite This Article: M. H. Ibrahim, D. Y. Dasin, and I. Yahuza. (2019). “THE
PHYSICOCHEMICAL ANALYSIS OF BIODIESEL PRODUCED FROM AFRICAN SWEET
ORANGE (CITRUS SINENSIS) SEEDS OIL.” International Journal of Engineering
Technologies and Management Research, 6(6), 82-91. DOI: 10.5281/zenodo.3252416.
1. Introduction
The increase in the global energy demand particularly those that are petroleum based, coupled with
the depletion of the world’s petroleum reserves and increased interest in saving the environment
from pollution, geared up interest in the search for alternative sources of petroleum-based fuel,
including diesel and gasoline fuels. The search for a viable, sustainable and preferably, renewable
energy source led to the renewed interest in biofuels. First generation biofuels where produced
primarily from agricultural crops grown for food and animal feed purposes and led to unhealthy
competition [1]. The second-generation biofuels addressed the problem of competition with food
crops primarily produced for consumption using non edible oil like castor oil and neem oil, as
source material for fuel production.
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The African sweet orange fruit is a specialized berry known as Citrus Sinensis, which belongs to
the race variety sinensis, the fruit size varies base on the plant cultivation that has been produced
by selective breeding and crop load, but mostly are measure between 2.5–4 inches in diameter.
The shape of the fruit is spherical to oblong (having rectangular shape), with a peel thickness
between that of grape fruit and tangerine, and is either smooth or roughly pebbly. It is usually very
closely adhered to the flesh of the fruit. Its colour tints from green to light orange, depending on
the cultivation variety used in the production of the orange fruit. The presence and amount of seed,
depends also on cultivation variety.
Vegetable oils are promising feed stocks for biodiesel production since they are renewable in
nature, and can be produced on a large scale. Vegetable oils include edible and non-edible oils.
More than 95% of biodiesel production feed stocks come from edible oils, since they are mainly
produced in many regions of the world and the properties of biodiesel produced from these oils
are very much suitable as substitute for diesel fuel. Some of the oils used in biodiesel production
include; soybean oil, palm oil, groundnut oil, palm kernel oil, neem seed oil, castor oil etc. Some
of the approaches adopted for processing oils with high moisture and/or free fatty acid contents
include; the use of supercritical methanol to convert the oil at high temperature [2], a simultaneous
esterification/transesterification of the FFAs and triglyceride contents of the oil using acid catalyst,
and a two-step sulfuric acid-catalyzed pre-esterification before base-catalyzed transesterification
[3].
Biodiesel is a non-toxic, biodegradable, non-flammable diesel product which has fewer emissions
than the conventional petro-diesel [4]. Biodiesel is a renewable fuel consisting of fatty acid methyl
esters (FAME) derived through transesterification of vegetable oils, animal fat and also recycled
oil from the food industry with methanol, it must meet the special requirements such as the ASTM
and the European standards.
Biodiesel is recognized as “green fuel” with several advantages including: safety in operation, nontoxicity and biodegradability compared to petroleum diesel. It is oxygenated and essentially free
of Sulphur and aromatics making it a cleaner burning fuel with reduced emission of SOx, CO, unburnt hydrocarbons and particulate matter [5].
A number of studies have shown that triglycerides hold promise as alternative diesel engine fuel
[6]. The high viscosity, carbon deposits, acid composition, free fatty acid content of such oils, gum
formation due to oxidation and polymerization during storage and combustion, oil ring sticking,
lubricating problems, cooking and trumpet formation on the injectors to such an extent that fuel
atomization does not occur properly or is even prevented as a result of plugged orifices, thickening
and gelling of the lubricating oil as a result of contamination by vegetable oils, lower volatilities
content which causes formation of deposits in engines due to incomplete combustion and incorrect
vaporization characteristics are some of the more obvious problems [7].
Consequently, considerable effort has gone into developing vegetable oil derivatives that
approximate the properties and performance of hydrocarbon-based diesel fuels. Problems
encountered in substituting triglycerides for diesel fuels are mostly associated with high viscosity,
low volatility and polyunsaturated character [7]. The following processes have been used in
attempts to overcome these drawbacks and allow vegetable oils and oil waste to be utilized as a
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viable alternative fuel; Pyrolysis, Microemulsions, Dilution, Transesterification, Acid Catalyzed
Process, Base Catalyzed Process and Enzymatic Process.
Transesterification
Transesterification also called alcoholysis is the displacement of alcohol from an ester by another
alcohol [8]. It is the most used method of conversion and refers to the reaction of a vegetable oil
or animal fat with an alcohol in the presence of a catalyst to produce alkyl esters and glycerol. The
alkyl esters are what are called biodiesel.
Acid Catalyzed Process
The transesterification process is catalyzed by Bronsted acids, preferably by sulphonic and
sulphuric acids. These catalysts give very high yields in alkyl esters, but the reactions are slow,
requiring, typically, temperatures above 100 °C and more than 3 hr to reach complete conversion.
[6] Showed that the methanolysis of soybean oil, in the presence of 1 mol% of H2SO4, with an
alcohol/oil molar ratio of 30:1 at 65 °C, takes 50 h to reach complete conversion of the vegetable
oil. The alcohol/vegetable oil molar ratio is one of the main factors that influence the
transesterification. An excess of the alcohol favours the formation of the products. On the other
hand, an excessive amount of alcohol makes the recovery of the glycerol difficult, so that the ideal
alcohol/oil ratio has to be established empirically, considering each individual process. The
mechanism of the acid-catalyzed transesterification of vegetable oils is shown below for a
monoglyceride. However, it can be extended to di- and triglycerides [9].
Base Catalyzed Process
The base-catalyzed transesterification of vegetable oils proceeds faster than the acid-catalyzed
reactions. Due to the fact that the alkaline catalysts are less corrosive than acidic compounds,
industrial processes usually favour base catalysts, such as alkaline metal alkoxides and hydroxides
as well as sodium or potassium carbonates.
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The mechanism of the base-catalyzed transesterification of vegetable oils is as shown [9].
Fuel Quality
The primary criterion for biodiesel quality is the adherence to the appropriate standard. The
standard utilized in this project is the ASTM D6751-02 standard specification biodiesel fuel
(B100) blend for distillate fuels.
The table 1 shows the property values for a mixture of methyl esters to be considered. When these
limits are met, the biodiesels can be used in most diesel engines without modifications while
maintaining the engine’s durability and reliability.
Table 1: ASTM 6751-02 Biodiesel Specification
Property
Method Limit
Flash point, closed cup.
D93
130 min
Water and sediment
D2709
0.050 max
Kinematic Viscosity
D445
1.9-6.0
Sulfated Ash
D874
0.020 max
Total sulfur
D5453
0.05 max
Copper Strip Corrosion
D130
No.3 max
Cetane Number
D613
47 min
Cloud Point
D2500
Report to customer
Carbon Residue
D4530
0.05 max
Acid Number
D664
0.8 max
Free Glycerine
D6584
0.02 max
Total Glycerine
D6584
0.24 max
Phosphorus
D4951
0.001 max
Vacuum Distillation end Point D1160
360 max
Specification for Biodiesel (B100) – ASTM D6751-07b, March 2007
Unit
0
C
%Vol
mm2/s
Wt.%
Wt.%
0
C
Wt.%
Mg KOH/g
Wt.%
Wt.%
Ppm
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2. Materials and Method
2.1. Materials and Equipment
N-hexane, Potassium hydroxide, Methanol, Methanolic potassium hydroxide, Crusher, Beaker,
Glass rod, Soxhlet extractor, Conical flask, Rotary evaporator, Heating mantle, Oven, Separating,
funnel, Filter paper, Water bath and Weighing Balance.
2.2. Sample Collection and Preparation
The African sweet orange fruit (Citrus Sinensis) seeds were procured from discards of fruits at
Muda lawan Market Bauchi, Nigeria. After collection, the seeds were sun dried to remove moisture
content, de-coated and were crushed using a crusher in order to be prepared for the extraction. NHexane, potassium hydroxide, Methanol, Filter paper were purchased from Department of
Chemistry, Abubakar Tafawa Balewa University (ATBU) Bauchi.
2.3. Oil Extraction
The oil was extracted from the seeds using n-hexane as the solvent in a Soxhlet extractor. The
crushed African sweet orange seed sample was weighed and placed in the soxhlet extraction
chamber. Normal n-hexane was poured into the conical flask; the soxhlet extractor was connected
to the power source so as to extract the oil from the seed. The n-hexane in the flask was heated to
its boiling point until it starts evaporating. The condensation chamber above the extraction
chamber condenses the n-hexane which in turn pours on the sample in the extraction chamber. The
final mixture was allowed to stand overnight for proper extraction of the oil. The solvent-oil
mixture was poured into round bottom flask and the solvent was dissolved off at 450C using a
rotary evaporator.
2.4. Base Catalyzed Transesterification
The transesterification reaction was performed in a lab scale biodiesel reactor consisted of 1 L
round-bottomed flask, fitted with mechanical stirrer, thermostat and condensation systems. The
African sweet orange seed oil was preheated to 400C on a heating mantle before starting the
reaction. Freshly prepared methanolic solution of KOH was separately added to the oil and mixed.
In order to ensure complete transformation of the African sweet orange seed oil into fatty acid
methyl esters (FAMEs), the experiment was conducted for 45 min. As soon as the reaction was
completed, the contents of the reactor were transferred into a separating funnel and allowed to cool
and equilibrate for the partitioning of two distinct phases. Of the two separated phases, the upper
layer consisted of methyl esters with small amounts of impurities such as residual alcohol, glycerol
and partial glycerides, while the lower phase contained glycerol with other materials such as
unused methanol, catalyst, soaps derived during the reaction, some suspended methyl esters and
partial glycerides. The upper layer consisting of methyl esters was collected and further purified
by distilling off residual methanol at 650C (external bath temperature). The traces of the remaining
catalyst, methanol and glycerol were removed by repeated washings with distilled water. Any left
over water was then removed by drying esters with sodium chloride. The process was repeated 3
times to determine the ratio of oil/methanol which gives the high yield.
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2.5. Characterization of the Oil
The physical and chemical properties of the extracted oil and the biodiesel produced were carried
out in the chemistry laboratory of Abubakar Tafawa Balewa University, Bauchi.
Physical Properties
The physical properties determined are the kinematic viscosity, density, Flash point, pour point
and cloud point using ASTM: D445, D1298, D93, D97 and D2500 standard test procedure
respectively.
Determination of the Cloud Point
A portion of the biodiesel was poured into a test tube and the mercury point of the thermometer
with calibration below 1 0C was inserted in the test tube. The set up was inserted in a beaker
containing ice. The biodiesel was observed closely. After some time, the biodiesel was observed
to form a cloud of gel. The temperature was taken as the cloud point was recorded.
Determination of the Pour Point
The same set up as in the cloud point test was immersed in the ice and left to solidify. When the
solidification was confirmed, the test tube was removed and tilted and closely observed till it
started to flow. The instant temperature taken on observing the flow of solidified biodiesel was
recorded as the pour point temperature.
Determination of the Flash Point
Another portion of the biodiesel was poured into a flask with a branch opening and a cork with an
opening to allow the entrance of the thermometer was fitted into the flask and the thermometer put
in place. The tip of the thermometer was immersed in such a way that it does not touch the bottom
of the flask. This was done at every rise in temperature to increase the precision of valve. The flash
point temperature was taken to be the temperature at which the fume got ignited by the lighted
match stick. The value was recorded.
Kinematic Viscosity Test
The viscosity of biodiesel taken using the old oil glass viscometer, using the mouth the biodiesel
in the lower bulb was sucked to a point above the top white ring mark which of the second bulb of
the old glass viscometer. The biodiesel meniscus was adjusted by releasing the thumb till it is at
the same level with white ring mark on top of viscometer second bulb. The biodiesel was allowed
to flow and a stop watch was used to take the time interval of the flow. The time for the biodiesel
to pass the second ring mark was recorded. Similar procedure was repeated for water and the time
recorded. The viscometer is calculated from the results obtained.
Determination of Density
To determine the density, the mass of an empty container was weighed using an electric weighing
balance and the mass of the empty container was recorded. 5 ml of the produced biodiesel was
poured into the already weighed container and weighed again with the electric weighing balance.
The mass of the empty container was subtracted from the mass of the container plus biodiesel so
as to obtain the mass of the biodiesel. The density was then determined by dividing the mass of
the biodiesel by the volume.
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Chemical Properties
The chemical properties were determined using the standard test procedure as follows:
Determination of Saponification Value (S.V.)
The method that was used for the determination of the saponification value is that of the British
standards institute 1995. Two grams of oil was placed in a 250 ml conical flask and 25 ml of 0.5
M methanol potassium hydroxide solution added.
A reflux condenser was attached and the flask content refluxed for 30 minutes on a water bath with
continuous swirling until it simmered. The excess potassium hydroxide was titrated with 0.5 M
hydrochloric acid using phenolphthalein indicator while still hot. A blank determination was
carried out under the same condition and the S.V. calculated.
Where,
B = Blank titre
R = Real titre value
𝑆. 𝑉. =
(𝐵 − 𝑅) × 28.05
𝑊𝑒𝑖𝑔ℎ𝑡 𝑜𝑓 𝑆𝑎𝑚𝑝𝑙𝑒
(1)
Peroxide Value (P.V.)
The method used is that of British standards institute No. 684. One gram of oil was placed in a 250
ml conical flask and 30 ml glacial acetic acid/chloroform (3.2 v/v) added. The contents were
shaken until they dissolved. Saturated potassium iodide solution (1 ml) was added followed by the
addition of 0.5 ml starch indicator solution. This was titrated with 0.1 m Na2S2O3 until the dark
blue color just disappeared. A blank determination was carried out under the same condition and
the P.V. calculated.
𝑃. 𝑉. = (𝑅 × 𝐵) ×
𝑀𝑜𝑙𝑎𝑟𝑖𝑡𝑦 𝑜𝑓 𝑁𝑎2 𝑆2 𝑂3
𝑊𝑒𝑖𝑔ℎ𝑡 𝑜𝑓 𝑆𝑎𝑚𝑝𝑙𝑒
Where,
R = Real titre value determined
B = Blank titre value
(2)
Determination of Iodine Value (I.V.)
One gram of oil was placed in a 250 ml conical flask flowed by 30 ml of Hanus solution and the
flask stopped, and the contents mixed and placed in the drawer for exactly 30 minutes. Potassium
iodide solution (10 ml of 15% w/v) was added to the flask washing down any iodide that may be
found on the stopper. This was titrated against 0.14 m Na2S2O3 until the solution became light
yellow. Starch indicator (1%, 2 ml) was added and the titration continued until the blue colors just
disappeared. A blank determination was carried out under the same conditions. The titre value was
recorded and used to calculate the I.V.
𝐼. 𝑉. =
(𝐵 − 𝑅) × 𝑀𝑜𝑙𝑎𝑟𝑖𝑡𝑦 𝑜𝑓 𝑁𝑎2 𝑆2 𝑂3 × 12.69
𝑊𝑒𝑖𝑔ℎ𝑡 𝑜𝑓 𝑆𝑎𝑚𝑝𝑙𝑒
Where,
B = Blank titre value
R = Titre value of real determinants
(3)
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Cetane Number (CN)
The calculated saponification value (SV) and iodine value (IV) were used to calculate the cetane
number (CN) which is the ability of fatty acid methyl esters as a fuel to ignite quickly after being
injected. Empirical formula was proposed by [11] and was used in the work. The higher its value,
the better is its ignition quality. This is one of the most important parameter which is considered
during the selection of fatty acid methyl esters for use as a biodiesel. The cetane number was
determined using the relation provided by [12].
𝐶𝑒𝑡𝑎𝑛𝑒 𝑁𝑢𝑚𝑏𝑒𝑟 (𝐶𝑁) = 46.3 +
3. Results and Discussions
5458
𝑆𝑉 − 0.225 × 𝐼𝑉
(4)
3.1. Physicochemical Properties of the Oil
The oil was extracted chemically from the African sweet orange seeds, in which n-hexane was
used as solvent because it is the solvent that gives the highest yielding from the literature review.
The biodiesel produced was characterized to determine its physicochemical properties which are
shown in table 2.
Table 2: Physicochemical Properties of the Biodiesel
Test
Result
Specific Gravity
0.920 at 150C
Smoke Point
1490C
Flash Point
1510C
Fire Point
1730C
Product % yield
40%
Acid Value
82%
Saponification Value 292
Iodine Value
108
Peroxide Value
92.84
The biodiesel was produced using methanol and potassium hydroxide as a catalyst as shown in
table 3. Three different ratios of oil/methanol/catalyst were used in the production of the biodiesel
to check for the effect of methanol that gives the best yielding while the temperature, time and the
catalyst are kept constant. The ratios of oil /methanol/catalyst used were 1:10:0.3, 1:7:0.3 and
1:9:0.3. It was discovered that for the three ratios used, 1:9:0.3 has the highest percentage yield.
Table 3: Determination of the Effect of Methanol on the Yielding of Biodiesel at Constant Ratios
of Oil and Catalyst
Oil (ml) KOH (g) Methanol (ml) % Yield (%) Temp. (0C) Time (mins)
Ratio 1
0.3
10
68
45
40
Ratio 1
0.3
9
77
45
40
Ratio 1
0.3
7
72
45
40
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The physicochemical properties of the oil were determined. These are; flash point, which is 1510C
as shown in table 2 and within the range provided by ASTM standard as obtained in table 4. The
fire point, smoke point and percentage yield of oil is determined to 1730C, 1490C and 40%
respectively. The specific gravity obtained at 150C is 0.92; this is in agreement with the ASTM
D6751 values. The flash point, saponification value and iodine value determined was 1510C, 292
and 108 respectively, and is within the range obtained by standard values as shown in table 4. This
shows that the oil can be used to produce biodiesel according to ASTM standard which says that
oil must have a flash point of 130 0C to 1700C (from table 4), fire point of 140 0C, and yielding
of more than 30%.
Table 4: Results for the Physicochemical Properties of biodiesel produced from African Sweet
Orange (Citrus Sinensis) Seeds
Fuel property
Diesel
Biodiesel
Units
Fuel Standard
ASTM D975 ASTM D6751
Lower Heating Value
~129,050
~118,170
Btu/gal
0
Kinematic Viscosity @ 40 C 1.3 – 4.1
1.9 – 6.0
mm2/s
Specific Gravity @ 600C
0.85
0.88
kg/l
Density
7.079
0.88
g/cm3
Water and Sediment
0.05 max
0.05 max
% volume
Carbon
87
77
wt. %
Hydrogen
13
12
wt. %
Oxygen
0
11
Sulfur
0.0015
0.0 to 0.0024 wt. %
0
Boiling Point
180 to 340
315 to 350
C
0
Flash Point
60 to 80
130 to 170
C
0
C
Cloud Point
-15 to 5
-3 to 12
0
C
Pour Point
-35 to -15
-15 to 10
Cetane Number
40 to 55
47 to 65
Lubricity SLBOCLE
2,000 to 5,000 >7,000
Grams
Lubricity HFRR
300 to 600
<300
Microns
It was shown that the properties determined from the biodiesel were within the range of the
properties of biodiesel required according to ASTM standard as shown in the tables 2 and 4.
4. Conclusion
This study has shown that most of the properties evaluated from the biodiesel produced conform
to the ASTM standard values. It can be concluded from this study that the biodiesel produced from
African sweet orange can be among the potential replacements of fossil fuel while the production
and effective usage of biodiesel will help to reduce the cost of protecting the atmosphere from the
hazards in using fossil fuels, waste from the environment and hence will boost the economy of the
country.
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*Corresponding author.
E-mail address: dahirudasin @yahoo.com
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