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OPTIMIZATION OF BIODIESEL PRODUCTION USING

ASPEN PLUS

A Thesis submitted in partial fulfillment of the requirements for the degree of

Bachelor of Technology

in

Chemical Engineering

by

K.VIVEK RAJA

(111CH0482)

Under the supervision of

Prof. Arvind Kumar

DEPARTMENT OF CHEMICAL ENGINEERING

NATIONAL INSTITUTE OF TECHNOLOGY ROURKELA

2015

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 CERTIFICATE

This is to certify that the thesis entitled "Optimization of biodiesel production using Aspen Plus"

submitted by K. Vivek Raja (111CH0482) as a scholastic venture in partial fulfillment of the

requirements for the award of BACHELOR OF TECHNOLOGY degree in the Department of

Chemical Engineering, National Institute of Technology, Rourkela is an authentic record of bona

fide work completed by him under my direction and supervision.

Place: Rourkela Prof. Arvind Kumar

Date: 08/05/2015 Assistant Professor

Dept. of Chemical Engineering

NIT Rourkela

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 ACKNOWLEDGEMENT

I take this opportunity to express my sincere thanks and deep gratefulness to my project guide

Prof. Arvind Kumar, Department of Chemical Engineering, NIT Rourkela for suggesting me the

topic, giving me this opportunity to work under his esteemed supervision and providing me the

guidance, support and motivation throughout the course of the project.

I am also thankful to Prof.P.Rath (HOD), and Prof.H.M.Jena (Project Coordinator) of the

Department of Chemical Engineering, National Institute of Technology, Rourkela, for their

valuable supervision, for all the facilities provided and timely suggestions during the entire

duration of my project, without which this work would not have been possible.

K. Vivek Raja

111CH0482
 ABSTRACT

With the continuous increase in energy demand and also simultaneously depletion of

fossil fuels made it necessary to research of other alternative sustainable sources of energy. The

most promising alternatives include biofuels, especially biodiesel. Here ASPEN Plus software is

utilized for a better understanding of models, procedures associated with producing biodiesel.

Analyses were also conducted by varying operating parameters to find out how they affect

separation throughout the process.

In this project, different models and configurations for producing biodiesel are

considered. Models for both trans-esterification and esterification process are designed. In each

model, parametric study is done to find optimum parameters at which maximum conversion is

obtained and also process is modeled such that heat duty is minimized. Sensitivity analyses are also

carried to analyze behavior of all components.

Keywords: Biodiesel, Process simulation, Trans-esterification, Esterification, Optimization

 TABLE OF CONTENTS

Contents

COVER PAGE ................................................................................................................................... 1

CERTIFICATE ................................................................................................................................... 2

ACKNOWLEDGEMENT .................................................................................................................. 3

ABSTRACT ....................................................................................................................................... 4

TABLE OF CONTENTS ................................................................................................................... 4

LIST OF TABLES ............................................................................................................................. 7

LIST OF FIGURES ............................................................................................................................ 8

NOMENCLATURE ........................................................................................................................... 9

1. INTRODUCTION ........................................................................................................................ 10

2. LITERATURE REVIEW ............................................................................................................. 16

2.1 Biodiesel Production Process ............................................................................................................... 17

2.1.1 Biodiesel Production from Triglyceride ............................................................................ 17

2.1.2 Trans-esterification Reaction ............................................................................................. 17

2.2 Biodiesel Production by Trans-esterification......................................................................................... 18

 2.2.1 Biodiesel Production from Free Fatty Acid ........................................................................ 19

2.2.2 Esterification Reaction ........................................................................................................ 19

2.3 Biodiesel Production by Esterification ................................................................................................... 20

2.4 American and European Biodiesel Quality Standards (ASTM D-6751) ................................................ 20

3. ASPEN PLUS SIMULATION ..................................................................................................... 23

3.1 Model 1: (using Distillation column) ...................................................................................................... 24

3.2 Model 2: (without using distillation column) ......................................................................................... 26

3.3 Model for Esterification: ......................................................................................................................... 28

4. RESULTS AND DISSCUSION ................................................................................................... 30

4.1 For Model 1: (Stream Results)................................................................................................................ 30

4.2 Model 2: (Stream Results) ...................................................................................................................... 32

4.3 Esterification process (Stream Results): ................................................................................................. 40

5. CONCLUSION............................................................................................................................. 45

6. REFERENCES ............................................................................................................................. 46
 LIST OF TABLES

CHAPTER-2:
Table 2-1. Free fatty acid content in biodiesel feed stocks………………………………………16

Table 2-2. Fatty acid composition of different oils……………………………………………..17

CHAPTER-3:

Table 3-1. Operating conditions of Distillation Columns………………………………………25

CHAPTER-4:

Table 4-1. Product Configuration of model 1……………………………………………………31

Table 4-2. Heat duty Calculation of model 1…………………………………………………...32

Table 4-3. Product Configuration of model 2…………………………………………………..34

Table 4.4 Heat duty Calculation of model 2…………………………………………………….34

Table 4-5. Operating conditions and configurations for reactive distillation column………….41

Table 4-6. Product Configuration of Esterification model……………………………………..41

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 LIST OF FIGURES

Fig 1.1 Transesterification reaction of triglyceride molecule to form FAAEs (biodiesel)………..11

Fig 2.1 Trans-esterification Reaction.……………………………………………………………...18

Fig. 2-2. Biodiesel production by trans-esterification……………………………………………...19

Fig 2.3 Esterification reaction……………………………………………………………………...20

Fig. 2.4 Biodiesel production by esterification…………………………………………………….20

Fig. 3-1. Process flow diagram for trans-esterification process model 1…………………………24

Fig 3.2: Biodiesel production process flow sheet of model 2……………………………………...27

Fig 3.3 Process flow sheet for esterification process………………………………………………28

Fig 4.1 Stream Results of model 1…………………………………………………………………31

Fig 4.2 Change of conversion with feed ratio……………………………………………………...31

Fig 4.3 Stream Results of model 2…………………………………………………………………33

Fig 4.4 Temperature profiles with change in mole fraction of oil…………………………………35

Fig 4.5 Pressure profiles with change in mole fraction of oil……………………………………...35

Fig 4.6 Change of Y with X……………………………………………………………………….36

Fig 4.7: Dependence of temperature of conversion in the reactors at 1 bar……………………….37

Fig 4.8: Dependence of pressure of conversion in the reactor at 60oC…………………………….37

Fig 4.9: Dependence of temperature of separation in the flash at 1 bar……………………………38

Fig 4.10: Dependence of temperature of separation in the flash at 1 bar…………………………..39

Fig 4.11: Dependence of pressure of separation in the flash at 60oC……………………………...39

Fig 4.12: Dependence of pressure of separation in flash at 60oC…………………………………..40

Fig 4.13 Stream results for esterification process………………………………………………….41

Fig 4.14 Change in conversion with feed ratio for model 3………………………………………42
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Fig 4.15 Change in Heat duty with increasing methanol flow rate……………………………….43

Fig 4.16 Temperature profiles with changing mole fractions of oil………………………………43

Fig 4.17 Pressure profiles with changing mole fractions of oil…………………………………...44

Fig 4.18 Change of Y with X at 1atm pressure……………………………………………………44

Nomenclature

D Distillate flow rate, kmol/h

ex Molar exergy, kW/kmol

Ex Total exergy, kW

F Feed flow rate, kmol/h

h Enthalpy, kJ/kmol
H Total enthalpy, kJ
Q Heat flow (heat transfer rate), kW

L Liquid flow rate, kmol/h

n Molar flow rate, kmol/h
QC Condenser duty, kW

QR Reboiler duty, kW
R Reflux ratio
s Molar entropy, kJ/kmol K
T Temperature, K
x Liquid mole fraction
y Vapor mole fraction
V Vapor flow rate, kmol/h
W Work, kW

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 CHAPTER- 1

INTRODUCTION

The requirement to meet the world's developing energy requests in an economical way is a key

worldwide need, requiring escalated innovative work of cutting edge renewable energy

frameworks for oil-based energy and other fossil powers. Energy security, ecological concerns,

outside trade reserve funds, and financial issues have made clean biofuels gotten from biomass or

organic sources an interesting issue. Among the different option fuel choices, biodiesel has

spurned much intrigue and fame. Synthetically, biodiesel is a mixture of unsaturated fatty alkyl-

esters (FAAEs), got from triglyceride particles. Triglycerides and liquor are changed over to alkyl

esters (biodiesel) through a catalyzed trans-esterification process, as showed in Figure.1 (Nghi

Nguyen, 2012)

Fig 1.1 Transesterification reaction of triglyceride molecule to form biodiesel.

Glycerol and FAAEs are then differentiated and refined. Rapeseed and soybean oils are the main

vegetable oils for biodiesel generation. The ordinary catalysts for the trans-esterification reaction

of these vegetable oils are dominatingly fundamental generally antacid or basic earth oxides or

alkoxides. Biodiesel is exceptionally appealing as a renewable and naturally agreeable fuel

alternative for residential motors, aside from being nontoxic and biodegradable, biodiesel brings

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about lesser air pollution and gives energy more than diesel and an expected 93% more energy

than the energy put resources into delivering it. Biodiesel likewise has a higher flash point

temperature of 150 °C, making its taking care of, utilization, and transport more secure than

petroleum diesel and better greasing up properties that minimize motor wear and tear. A

promising different option for petroleum, biodiesel utilization and production is subsequently

anticipated that would rise fundamentally significantly.

The world's oil supply is foreseen to drain by 2060 because of the increment in interest

for energy coupled with exhaustion of petroleum oil. Accordingly, looking for a feasible energy

pathway to meet the energy needs without bounds era is attractive. Biodiesel is renewable,

nontoxic, biodegradable, and basically free of sulfur and aromatics may be a standout amongst the

most suitable contender for future bio fuel. Alongside, U.S. Branch of Energy life cycle

examination on biodiesel demonstrates that biodiesel produces 78.5% less net carbon dioxide

outflows contrasted with petroleum diesel. In 2011, the United States delivered pretty nearly 1.1

billion gallons of biodiesel and the volume of production is required to increment to 1.9 billion

gallons in 2015. Significant downsides of biodiesel production utilizing vegetable oil are the

expense of assembling and the high cost of oil since it contends with nourishment. As of now,

biodiesel production plants rely on upon government appropriations to keep their plants in

operation. Accordingly, looking for a more financial biodiesel generation methodology to lessen

the reliance of government appropriations and advance extension of biodiesel industry is desired.

Distillation is considered as an adult innovation and it is utilized for the

partition of numerous mixtures; on the other hand, a few enhancements are being made with a

specific end goal to decrease the energy and cooling water requests, since it is no doubt

understood its high energy prerequisites. These days, the tricky related to the energy prerequisites

is more extreme on account of the decreases in fossil powers and strategies in nursery gasses
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 outflows. Therefore, vital advancements have been completed in biofuels, for example,

bioethanol, biodiesel, bio turbo sine and others. On account of the biodiesel production, reactive

distillation and responsive retention have been considered to accomplish higher transformations

and lower prerequisites of energy and cooling water.

Process Overview:

Since straight vegetable oil (SVO), a triglyceride, is excessively gooey and does not have

other needed properties to proficiently fuel cutting edge diesel motors without decreasing motor

life, the SVO must experience a methodology of trans-esterification whereby one of its R-

gatherings is supplanted by the R-gathering of a liquor, normally methanol, consequently shaping

alkyl esters, or biodiesel. A basic catalyst, normally NaOH, is utilized to deprotonate the methanol

making it a stronger nucleophile that wills all the more openly responds with the triglyceride.

Through this process, the breaking point of the recently created biodiesel is much lower, as it

stands its thickness and propensity to polymerize. All things considered, it can be utilized as a part

of customary diesel motors without gambling motor wellbeing. It is additionally frequently

blended with ordinarily extricated diesel because of its predominant lubricity. Given the

undeniably strict laws on sulfur content in traditional diesel for ecological reasons, the expansion

of biodiesel gives a significant advantage in supplanting the ointment. Glycerol is additionally

framed through the procedure and is effortlessly tapped. It can then be refined and sold for

utilization in the production of cleansers and other nonessential and pharmaceutical items. In a run

of the mill persistent procedure biodiesel plant, the reaction happens in two stages and the general

methodology can be compressed in the accompanying steps:

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Vegetable Oil Pretreatment

Waste oil is gotten into capacity. Water is emptied and sent to waste water stockpiling or

treatment. The oil is gone through a coarse channel to uproot polluting influences and sent to a

dryer to evacuate further overabundance water. In the wake of drying, the oil is for the most part

gone through extra channels to guarantee the evacuation of all particulate matter.

Trans-esterification

Vegetable oil, methanol and an antacid catalyst are bolstered into the reactor with

methanol in sums reasonably higher than the stoichiometric proportion (more than 3 moles

methanol to 1 mole triglycerides) furthermore, the reaction happens at a generally low temperature

and weight.

Settling

The stream leaves the reactor into a settling tank where the glycerol is emptied and further

decontaminated. The remaining results of methanol, triglycerides, biodiesel and different

contaminations are killed, generally with hydrochloric acid, and are then bolstered to a distillation

section.

Distillation

The stream leaves the reactor into a distillation column. Unreacted methanol is dissipated

and recycled back to capacity or straightforwardly into the second reactor. The remaining mixture

is bolstered to a second reactor.

Trans-esterification II

Methanol and the unreacted triglycerides are sustained into a second reactor and the reaction

is again base catalyzed. The settling and balance steps are rehashed with items from the second

reactor.

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Distillation II

The items from the second balance tank are refined and the dissipated methanol is once

more recycled back to capacity. The biodiesel is gathered and put away and for the most part has a

change rate of 80-95% (Hillion, Delfort, le Pennec, Bournay, & Chodorge, 2003). It ought to be

noticed that a acid catalyst can likewise be utilized. Its utilization would help avoid undesirable

reactions from happening between the hydroxyl radical and alkyl esters (saponification). On the

other hand, the reaction can occur without a catalyst by any means, wherein the triglyceride is

responded with methanol in a supercritical state, at a high temperature and weight such that the two

reactants are in a solitary stage and the reaction continues suddenly. With the end goal of

improving the methodology in Aspen, and catalyst was excluded simultaneously.

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 CHAPTER 2

LITERATURE REVIEW

According to (Nghi Nguyen, 2012), these days, biodiesel generation methodologies use

waste vegetable oil (WVO), creature fats, and virgin oil as feedstock. When in doubt, the higher the

nature of the feedstock, the more lavish it will be. Refined soybean, palm, assault and canola oils,

contain more than 99% of triglycerides, are samples of probably the most costly oils. WVO and

creature fats are the least expensive feedstock yet the expense of generation may be most

astounding because of high substance of free unsaturated fats and contaminants (water, particles,

phospholipids, and so forth.) in triglycerides. Table 2-1 gives the rough centralization of free

unsaturated fat in refined vegetable oils, unrefined vegetable oils, eatery waste oil, creature fat, and

trap oil. In the United States, soybean oil is most usually utilized for biodiesel production.

Presently, roughly 90% of biodiesel in the United States is gotten from soybean oil. The present

cost of oil is about $60.0/barrel and it is records for more than 50% of the expense of biodiesel

production.

Table 2-1. Free fatty acid content in biodiesel feed stocks. [ 8]

Feedstock Free fatty acid content (%)
Refined vegetable oils <0.05
Crude vegetable oils 0.3-0.7
Restaurant waste grease 2-7
Animal fat 5-30
Trap grease 10-100

Table 2-2 gives the unsaturated fat synthesis of some usually utilize oils. As indicated by the

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 United States Department of Agriculture (USDA), 6.18 million metric huge amounts of coconut

oil is created worldwide in 2011. At present, coconut oil is being utilized to create biodiesel in

Philippines. Biodiesel delivered from coconut oil gel point is around 10oC, accordingly, utilization

of immaculate biodiesel is conceivable just in calm atmospheres. Cool stream improvers, for

example, poly homo polymer, ethanol, and olefin-ester copolymers, can be mixed to enhance the

chilly stream properties of biodiesel.

Table 2-2. Fatty acid composition of different oils [7]

Crude Food Waste Crude Crude Crude Crude

Fatty acid soybean grade cookin palm algae oil corn oil coconu
component oil (%) soybean g oil oil (%) (%) from t oil
sC 12:0 0 oil 0(%) (%)
0 0 0 DDGs
0 (%)
49.13
(%)
C 14:0 0.27 0 0 0.21 2.72 0 19.63
C 16:0 13.05 11.07 11.58 41.92 20.91 11.50 10.12
C 16:1 0.39 0.09 0.18 0.23 10.62 0 1.79
C 18:0 4.17 3.62 4.26 3.85 6.95 4.77 2.83
C 18:1 22.75 20.26 24.84 42.44 33.33 26.26 7.59
C 18:2 52.78 57.60 53.55 11.30 18.45 56.20 2.75
C 18:3 6.59 7.36 5.60 0.04 1.16 1.27 0.15
Others 0 0 0 0 6.86 00 6.01

2.1 Biodiesel Production Process [1]

2.1.1 Biodiesel Production from Triglyceride

Triolein is utilized to speak to triglyceride in this study for reproduction purposes. Every one of the

three unsaturated fat chains of triolein are oleic acid. The atomic weight of triolein is 885.46 g/mol,

which is like the sub-atomic weight of soybean oil.

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2.1.2 Trans-esterification Reaction

The trans-esterification reaction component comprises of three back to back and reversible

reactions [2]. Notwithstanding, the disentangled manifestation of the trans-esterification reaction

can be depicted by

Fig 2.1 Trans-esterification Reaction (Nghi Nguyen, 2012)

Here R1, R2, and R3 are the unsaturated fat chains, which makes out of carbon and hydrogen

particles. Most biodiesel production methods use sodium hydroxide (NaOH) or potassium

hydroxide (KOH) as a catalyst to launch the trans-esterification reaction. The catalyst is obliged

essentially to enhance the dissolvability of methanol in the oil stage. A solid mineral acid is utilized

to kill the base catalyst after the reaction.

2.2 Biodiesel Production by Trans-esterification

Presently, most biodiesel production plants use triglyceride, methanol and NaOH or KOH as the

three essential crude materials. Fig. 2-1 demonstrates the least difficult biodiesel production

prepare by trans-esterification. The trans-esterification reaction generally continues at 6:1 methanol

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to oil molar proportion, 65oC and utilize 0.3% to 1.5% of sodium hydroxide. Free unsaturated fats

respond with a base catalyst and structure cleanser and water, in this manner, it focus must be kept

underneath 1% so as to keep the cleanser and water impacts. The reactor outlet is sent to the

decanter for stage division in the middle of glycerol and biodiesel. Both stages contain liquor,

hence, an evaporator or a flash unit is utilized to expel liquor from both the glycerol and ester.

Water is utilized to kill and wash the glycerol stream. Water is additionally used to wash and kill

the ester stream to evacuate salts and lingering methanol. A dryer unit is utilized to expel water

from biodiesel.

Fig. 2-2. Biodiesel production by trans-esterification.(Nghi Nguyen, 2012)

2.2.1 Biodiesel Production from Free Fatty Acid[3]

Oleic acid, a soaked medium chain unsaturated fat with 12-carbon particle chain, is utilized to

speak to free unsaturated fats in this study for reproduction purposes in light of the fact that the

reaction active information is promptly accessible in writing. Oleic acid is the significant part of

soya bean oil as demonstrated in Table 2-2.

2.2.2 Esterification Reaction

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Esterification of free unsaturated fat with methanol is given by

Fig 2.3 Esterification reaction (Nghi Nguyen, 2012)

Here, water is delivered as the by-item rather than glycerol. A solid homogeneous acid catalyst,

for example, sulfuric acid (H2SO4) or sulfonic acid, is ordinarily used to catalyze the

esterification reaction since base catalysts respond with free unsaturated fats to frame cleanser and

water.

2.3 Biodiesel Production by Esterification

Some biodiesel plants e.g. BTK&S Biodiesel utilize almost unadulterated free unsaturated fat,

methanol and a solid acid catalyst as crude materials for biodiesel generation. A basic

methodology stream graph of biodiesel production by esterification is displayed in Fig. 2-3. A

solid base is utilized to kill the acid catalyst after the reaction. The item stream is then sent to the

methanol division unit to recuperation methanol. Further, water and different debasements are

evacuated by utilizing a dryer unit.

Fig. 2.4 Biodiesel production by esterification.(Nghi Nguyen, 2012)

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 2.4 American and European Biodiesel Quality Standards (ASTM D-6751) (Nghi Nguyen,
2012)

Parameters that must be met to acquire ASTM D6751 biodiesel quality standard are:

1. Flash point must be greater than 93oC.

2. Water and sediment must be under 0.05% by volume.

3. Kinematic viscosity at 40oC is between 1.9 - 6.0 mm2/s.

4. Sulfated ash must be under 0.02% by mass.

5. Total sulfur must be under 0.05 wt%.

6. Copper strip erosion must be less than No. 3.

7. Methanol content must be under 0.20% by volume.

8. Cetane number must be more than 47.

9. Cloud point must report in oC to client.

10. Carbon residue must be under 0.50% by mass.

11. Acid number must be lower than 0.50 mg KOH/g.

12. Free glycerine must be under 0.02% by mass.

13. Total glycerin must be under 0.24% by mass.

14. Phosphorus must be under 0.001 wt%.

15. Vacuum distillation end point must be under 360oC.

16. Oxidatione stability must be more than 3 hours.

ASTM Internationl has complete duplicates of ASTM g

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 CHAPTER -3

ASPEN PLUS SIMULATION

Aspen Plus reproduction utilizes fundamental building connections, for example, mass and

energy offsets, to gauge the conduct of a compound procedure. Aspen Plus reenactment permits

methodology specialists to outline and test a synthetic process in brief time of time. Likewise, it

can be utilized to explore the impacts of diverse configuration parameters of the synthetic

process and give comes about that are hard to acquire in research center. By utilizing test

thermodynamic information and practical working conditions, the real process conduct can be

reenacted. Also, transform reenactment empowers methodology architects grow better

methodologies by utilizing devices, for example, affectability investigation, adding machine

square, enhancement piece, benefit examination and outline particular. Aspen Plus methodology

reproduction can be utilized by the accompanying steps: [4]

Step 1: Identify the unit operations and the procedure streams that stream to and from them in the

process flow sheet. Name all streams and associate them to the unit operation models.

Step 2: Identify the substance columns from the Aspen Plus databanks or characterize them all

the while.

Step 3: Identify thermodynamic models incorporated with Aspen Plus to gauge the physical

properties of the parts and mixtures simultaneously.

Step 4: Identify the thermodynamic conditions and the part stream rates of the info streams.

Step 5: Identify the working conditions for the unit operation models.

Users can change the majority of the above information details to dissect option

forms. Besides, Aspen Plus can be utilized to fit plant information to reproduction models,

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 foresee and relapse physical properties, create even yield results, and interface results to

spreadsheets. In this undertaking, different models are contrasted with produce biodiesel and

parameters are improved such that greatest transformation and least warmth obligation is gotten.

Now, for trans-esterification reaction, let us consider different models to study.

3.1 Model 1: (using Distillation column)

This model is designed with reference to (Nghi T. Nguyen, 2012) with considerable

modifications.

Fig. 3-1. Process flow diagram for trans-esterification process model 1

Stiochiometric Equation for reaction taking place:

C57H104O6 + 3CH3OH 3C19H36O2 + C3H8O3

(Triolein) (methanol) (Biodiesel) (Glycerol)

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 Table 3.1 Operating conditions of Distillation Columns
Conditions & Design
Configuration
s of stages
No. 4
Feed stage 2
o
Feed temperature, C 60
Pressure, bar 0.08
Reflux ratio 1
Condenser duty, kW -4081.06
Distillate rate, kmol/hr 37.09
o
Condenser temperature, C 49.98
Reboiler duty, kW 4135.89
Boil up rate, kmol/hr 127.79
Bottoms rate, kmol/hr 0.87
Reboiler temperature, oC 297.70

Fig. 3.1 demonstrates the procedure flow diagram (PFD) of a routine biodiesel plant with

retrofitted distillation sections. The biodiesel plant uses methanol, oil, NaOH and hexane as the

essential food streams, and produces 2,175.40 kg/h and 96.3% pure unsaturated fat methyl ester

(FAME). The byproducts are 94.7% pure 134.55 kg/h glycerol. Recycle and new methanol and

oil are blended in blender M2 before sending to the RStoic reactor, R1, as indicated in Fig.3.1.

The FAME synthesis happens in an RStoic reactor by trans-esterification reaction catalyzed by

NaOH at 60oC with a byproduct of glycerol. The methanol/oil molar proportion is 6:1 and 95%

percent oil transformation was assumed. The reactor outlet contains FAME, methanol, oil,

hexane, NaOH, and glycerol is pumped into the extractor EX1 that uses hexane as a solvent to in

part extricate polar parts from the mixture. The top item is encouraged to distillation column T1

at stage 2 where the FAME is cleaned. This section works with four stages, a fractional vapor-

fluid condenser and a pot reboiler. The base item containing some FAME and basically oil is

recycled to the reactor. The vapor stage stream containing little measures of hexane/methanol is a
23 | P a g e
 waste stream while the distillate is the item FAME. Tables 4-1 demonstrate the stream results of

the above plant as shown in Fig. 3.1.

The bottom stream of the extractor EX1 and phosphoric acid (H3PO4) are

fed to the separator where biodiesel separates from other components. The top stream contains

about immaculate glycerol while the distillate is cooled to 80oC and encouraged to stage 9 of

distillation column T2 for filtration of methanol. Column T2 has 12 stages, an aggregate

condenser and a pot re boiler. The base item is basically hexane and other impurities and the

distillate methanol is recycled through blender M1.

3.2 Model 2: (without using distillation column)

This model is designed with reference to (David Houghton et al., 2014). The methodology was

demonstrated in Aspen to focus ideal conditions to expand the change of vegetable oil to biodiesel.

Vegetable oil is an intricate arrangement which was spoken to as triolein in the reproduction.

Biodiesel was spoken to as methyl oleate. Triolein is responded with methanol to create methyl

oleate and glycerol as per the reaction underneath.

Stiochiometric Equation for reaction taking place:

C57H104O6 + 3CH3OH 3C19H36O2 + C3H8O3

(Triolein) (Methanol) (Biodiesel) (Glycerol)

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 Figure 3.2: Biodiesel production process flow sheet of model 2

The process model included two RStoic reactors worked in arrangement, as indicated in the process

stream sheet above. Triolein (FEED-OIL) of 100lbmol/hr and methanol (FEED-MET) 300lbmol/hr

were fed into the first RStoic reactor (R1) in stoichiometric sums. The outlet of this reactor (R1-

OUT) was divided in a flash drum (R1-FLASH) to uproot unreacted methanol (METOH-R1) to be

gone to the second reactor. The two stage fluid leaving the first flash drum (PROD1) was then

divided in a decanter into glycerol (GLYC1) and a mixture of the unreacted triolein and biodiesel

(R2-FEED). The triolein-biodiesel mixture then entered the second RStoic minister (R2) with

recycled methanol (REC-MET). The second reactor item stream (R2-OUT) was then flashed to

uproot and recycle methanol (METOH-R2), this stream was part (RECSPLIT) to permit a cleanse

stream (PURGE). The bottoms fluid (PROD2) was emptied (DECANT2) to split the (BIODIESEL)

of around 299lbmol/hr and glycerol (GLYC-2). The glycerol streams were consolidated (GLYC-

MIX) to create the last glycerol item as a procedure yield.

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For the Esterification reaction, only one simple model is considered:

3.3 Model:

Fig 3.3 Process flow sheet for esterification process

Esterification of oleic acid with methanol may be described by

Methanol + oleic Acid Ester (Biodiesel) + Water

The reactive distillation column uses methanol and oleic acid as essential feedstock to

deliver methyl oleate and water. The section comprises of 30 stages with two partition zones at

every end and a reaction zone in the center, and works with an aggregate condenser and a pot

reboiler. Stream oleic comprises of 100 kmol/hr of oleic acid, which is warmed to 100oC preceding

entering top of the reaction zone of the column at stage 3. Stream METH comprises of 199 kmol/hr

of methanol and 1 kmol/hr of water, which is warmed up near to methanol's immersion point and

encouraged into the base of the reaction zone of the section at stage 29. The ester with a 104

kmol/hr stream rate is the base item, while the distillate is the mixture of water and methanol with a

stream rate 196 kmol/hr. The action coefficient model UNIQUAC is utilized to gauge the stage

balance in the section.

26 | P a g e
The test system of Aspen Plus is utilized to perform the reproduction esterification of oleic acid

with methanol. Oleic acid originates from soya bean oil. The main period of this work is to

diminish the centralization of water in the reaction zone by conforming the reflux proportion and

obligation of a side warmer in a balance plan. The outcomes are then utilized as starting data values

for the non-harmony plan. Under indistinguishable setups and conditions, non-balance

configuration has yielded lower transformation because of complex warmth and mass exchange

rates between the vapor and fluid stages. Accordingly, number of stages and weight expected to be

balanced keeping in mind the end goal to attain to the same level of change.

27 | P a g e
 CHAPTER 4

RESULTS AND DISSCUSION

4.1 For Model 1: (Stream Results)

OIL METH R1 R2 R3 S1 S2 S3 S4
Mass Flow
kg/hr
METHANO 0.00 1125.92 0.00 0.00 1045.33 0.00 2171.25 1139.91 1139.91
L
OIL 9639.09 0.00 360.92 360.91 0.00 10000.00 10000.00 500.00 500.00
METHY-01 0.00 0.00 140.00 140.00 0.00 140.00 140.00 9683.26 9683.26
GLYCEROL 0.00 0.00 0.00 0.00 0.00 0.00 0.00 988.09 988.09
NAOH 0.00 0.00 0.00 0.00 0.00 0.00 95.99 95.99 95.99
HEXANE 0.00 0.00 0.00 0.00 8.40 0.00 8.40 8.40 8.40

Mass Frac 0.0918

METHANO 0.0000 1.0000 0.0000 0.0000 0.9920 0.0000 0.1749 0.0918 0.0403
L
OIL 1.0000 0.0000 0.7205 0.7205 0.0000 0.9862 0.8054 0.0403 0.7799
METHY-01 0.0000 0.0000 0.2795 0.2795 0.0000 0.0138 0.0113 0.7799 0.0796
GLYCEROL 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0796 0.0077
NAOH 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0077 0.0077 0.0007
HEXANE 0.0000 0.0000 0.0000 0.0000 0.0080 0.0000 0.0007 0.0007 0.0000
Total Flow 9639.09 1125.92 500.92 500.91 1053.73 10140.00 12415.64 12415.64 60.11
kg/hr
Temperature 25.00 25.00 297.91 25.00 64.53 25.00 29.46 60.00 1
C
Pressure bar 1 1 0.18 1 1 1 1 4

HEXAN S5 S6 VAPOR BIODIES S7 BIODIES BIODIES

E 1 2 E
Mass Flow
kg/hr
METHANOL 0.00 88.73 1051.18 70.50 0.00 1051.18 1051.18 1045.40
OIL 0.00 500.00 0.00 0.16 0.00 0.00 0.00 0.00
METHY-01 0.00 9682.11 1.14 0.00 0.00 1.14 1.14 1.12
GLYCEROL 0.00 0.00 988.09 0.00 0.00 988.09 988.09 16.12
NAOH 0.00 0.00 95.99 0.00 0.00 0.00 0.00 0.00
HEXANE 0.00 33.50 124.90 27.37 0.00 168.13 168.13 167.36

Mass Frac
METHANOL 0.0086 0.4649 0.7191 0.0000 0.4493 0.4760 0.8499
OIL 0.0000 0.0485 0.0000 0.0016 0.0000 0.0000 0.0000 0.0000
METHY-01 0.0000 0.9396 0.0005 0.0000 0.0000 0.0005 0.0005 0.0009
GLYCEROL 0.0000 0.0000 0.4370 0.0000 0.0000 0.4223 0.4474 0.0131
NAOH 0.0000 0.0000 0.0424 0.0000 0.0000 0.0000 0.0000 0.0000

28 | P a g e
 HEXANE 0.0000 0.0033 0.0552 0.2792 0.0000 0.0719 0.0761 0.1361
Total Flow 0.0000 10304.35 2261.29 98.03 131.15 2339.69 2208.54 1230.00
kg/hr
Temperature C 78.40 60.40 60.19 53.67 50.00 50.00 50.00 100.00
Pressure bar 25.00 1 1 0.08 1 1 1 0.05
1

Fig 4.1 Stream Results of model 1

The biodiesel plant uses methanol, oil, NaOH and hexane as the essential food streams, and

produces 2,175.40 kg/h and 96.3% pure unsaturated fat methyl ester (FAME). The byproducts are

94.7% pure 134.55 kg/h glycerol. Recycle and new methanol and oil are blended in blender M2

before sending to the RStoic reactor, R1, as indicated in Fig.3.1. The FAME synthesis happens in

an RStoic reactor by trans-esterification reaction catalyzed by NaOH at 60oC with a byproduct of

glycerol. The methanol/oil molar proportion is 6:1 and 95% percent oil transformation was

assumed.

Feed Ratio vs % Conversion

120
99.24 99.24 99.24 99.24
100
77.72
% Conversion

80

60
44.39
40

20

0
0 1 2 3 4 5 6 7
Feed Ratio(Methanol : Oil)

Fig 4.2 Change of conversion with feed ratio

Table 3-1 shows the base case design (Model 1) operating conditions and design parameters for

distillation column T1, which operates with four equilibrium stages. Here we can observe that

after obtaining a feed ratio of 3 i.e. ratio of methanol to oil in feed to 3, there is no significant
29 | P a g e
 increase in conversion rate. Hence 3:1 is considered as optimum feed ratio.

Table 4.1 Product Configuration

Composition (Mol %)
Key Stream Total Hexane Methyl- Glycerol Methanol Triolein
Product Flow Oleate
(kmol/hr)
Biodiesel BIODIESEL 4.829 0.24 85.5 14.06 0.323 0.006
(Methyl-
oleate)
Glycerol GLYCEROL 1.252 1.09 0.013 94.53 2.168 2.199
Hexane VAPOR 0.02 96.88 0.005 0.0003 3.11 0.002

Table 4.2 Heat duty Calculation

Process Block Duty (kW)
Reactor 1 R1 -128.681
Distillation Column 1 T1 -338.208
Separator 1 SEP1 0.1127
Cooler E1 -17.781
Distillation Column 2 T2 334.557
TOTAL -150.16

In above table, we can observe that biodiesel of purity 94% is produced with a heat duty of 150KW

30 | P a g e
 4.2 Model 2: (Stream Results)

Feed Ratio vs % Conversion

120
98.64 98.73 98.74 98.74
100
% Conversion

80 66.67
60
33.33
40
20
0
0 1 2 3 4 5 6 7
Feed Ratio (Methanol:Triolein)

Fig 4.4 Change in conversion with feed ratio

31 | P a g e
 Fig 4.3 Stream Results of model 2

From above figures we can observe that an optimum feed ratio of 3:1 is maintained to obtain

98.7% conversion and 99% purity. From Tables 4.3 and 4.4, we can also observe that a minimum

heat duty of 75KW is consumed for the process to run.

Table 4.3 Product Configuration of model 1

Composition (Mol %)
Key Stream Total Flow Methyl- Glycerol Methanol Triolein
Product (Kmol/hr) Oleate
Biodiesel BIODIESEL 2.96 99 0.1 0.7 0.2
(Methyl-
oleate)
Glycerol GLYCEROL 1.04 0.01 94.9 3.8 1.18
32 | P a g e
Methanol PURGE 0.06 0.03 0.25 99.7 0.02

Table 4.4 Heat duty Calculation of model 1

Process Block Duty(kW)

Reactor 1 R1 -167.495
Reactor 1 Flash Drum R1-FLASH 100.513
Reactor 1 Decanter DECANT 1 0
Reactor 2 R2 -364.199
Reactor 2 Flash Drum R2-FLASH 356.537
Reactor 2 Separator SEPERATR -0.292
Total -74.936

T-xy for TRIOL-01/METHA-01

1200

T-x 1.0 atm

T-y 1.0 atm
950
Temperature K
700 450

0 0.2 0.4 0.6 0.8 1

Liquid/Vapor Molefrac TRIOL-01
Fig 4.4 Temperature profiles with change in mole fraction of oil

From above fig 4.4, varying of liquid and vapor mole fractions of oil with increasing temperature

is observed and analyzed.

33 | P a g e
 P-xy for TRIOL-01/METHA-01
0.2
P-x 25.0 C
P-y 25.0 C
0.15
Pressure atm
0.10.05

0 0.2 0.4 0.6 0.8 1

Liquid/Vapor Molefrac TRIOL-01
Fig 4.5 Pressure profiles with change in mole fraction of oil
Y-x for TRIOL-01/METHA-01
1

1.0 atm
Vapor Molefrac TRIOL-01
0.25 0.5 0.75

0 0.25 0.5 0.75 1

Liquid Molefrac TRIOL-01
Fig 4.6 Change of Y with X

From above figures 4.5, 4.6 we can observe and analyze the variation of mole fractions of oil with

change in pressure.

34 | P a g e
Parameter Optimization:

Reactor Temperature and Pressure vs Conversion

The beginning quality for the temperature of both reactors was chosen taking into account

writing survey and thusly examined with an affectability investigation. The reaction of triolein

to methyl oleate was investigated to expand change while making the methodology as gainful

as could be expected under the circumstances. An affectability examination was led on the

transformation proportion with changing minister temperatures and the outcomes are shown in

Fig 4.7. As can be seen, the change does not expand essentially up to 100oC. The minimal

increment in change was insufficient to legitimize the additional warmth obligation, equal to

cost, for the reactors. This investigation was done at 1 bar which is the working weight of the

reactor.

150
145
Biodiesel Flowrate (kmol/hr)

140
135
130
125
120
115
110
105
100
0 20 40 60 80 100
Reactor Temperature (oC)

Fig 4.7: Dependence of temperature of conversion in the reactors at 1 bar. Blue line is the molar
flow rate of methyl oleate in the R1-OUT stream measured on the outside vertical axis.

From above fig 4.7, we can observe that flow rate of product is slightly increasing with

35 | P a g e
increase in temperature of reactor. The weight of both reactors was picked in view of methanol's

vapor weight at the reactor temperature. Methanol's vapor weight at 60oC is 0.85 bar so a higher

weight is obliged to keep up methanol in the fluid stage. An affectability examination was

completed to focus the impact of weight on transformation of triolein to methyl oleate; the

outcomes are demonstrated in Fig 4.8. The diagram demonstrates no adjustment in transformation

at weights somewhere around 0 and 5 bars. A reactor weight of 1 bar was chosen to minimize cost

and augment security.

150
Biodiesel Flowrate(kmol/hr)

140

130

120

110

100
0 1 2 3 4 5 6
Pressure (in bar)

Fig 4.8: Dependence of pressure of conversion in the reactor at 60oC. Blue line is the molar flow
rate of methyl oleate in the R1-OUT stream.

From above fig 4.8, we can observe that there is no change in flow rate of biodiesel with variation

of pressure.

Flash Temperature and Pressure vs Product Purity

The flash drums were at first worked at a temperature of 60 C and a weight of 0.5 bar which is

beneath the vapor weight of methanol at 60 C (0.85 bar). An affectability examination was done to

figure out whether an adjustment in temperature and/or weight could enhance the virtue of the

flash items by uprooting more of methanol. The aftereffects of the affectability investigation are

demonstrated in Figure 6 to Figure 9. Methanol flow rate increases with increasing temperature

36 | P a g e
 and diminishing weight while the methanol mole fraction stays at 1. Consequently, more of

methanol can be differentiated while keeping up recycle stream virtue by increasing temperature

and diminishing the weight. The flash drums were worked at 0.1 bar and 100o C.

150
145
Methanol Flowrate(kmol/hr)

140
135
130
125
120
115
110
105
100
75 80 85 90 95 100
Flash Temperature(oC)

Fig 4.9: Dependence of temperature of separation in the flash at 1 bar. Blue line is the molar flow
rate of methanol in the METOH-R1 stream.

From above fig 4.9, we can observe that at 1 bar pressure, with increase in temperature flow rate

of methanol vapor flashing out of flash drum increases after remaining constant for a small

temperature increase.

37 | P a g e
 150
Methanol Flowrate(kmol/hr)

145

140

135

130

125
60 65 70 75 80 85 90 95 100
Flash Temperature (oC)

Fig 4.10: Dependence of temperature of separation in the flash at 0.3 bar. Blue line is the molar
flow rate of methanol in the METOH-R1 stream.

From above fig 4.10, we can observe that at 0.3 bar pressure, with increase in temperature flow

rate of methanol vapor flashing out of flash drum increases exponentially.

139.582
Methanol Flowrate(kmol/hr)

129.582

119.582

109.582

99.582

89.582
0.04 0.09 0.14 0.19 0.24 0.29
Flash Pressure (in bar)

Fig 4.11: Dependence of pressure of separation in the flash at 60oC. Blue line is the molar flow rate
of methanol in the METOH-R1 stream.

38 | P a g e
From above fig 4.11, we can observe that flow rate of methanol vapor flashing out increases with

decrease in pressure at 60oC after remaining constant for some pressure drop.

144

142
Methanol Flowrate (kmol/hr)

140

138

136

134

132

130
0.04 0.09 0.14 0.19 0.24 0.29
Flash Pressure (in bar)

Fig 4.12: Dependence of pressure of separation in flash at 100oC. Blue line is the molar flow rate
of methanol in the METOH-R1 stream measured on the outside vertical axis.

From above fig 4.12, we can observe that flow rate of methanol vapor flashing out increases

linearly with decrease in pressure at 100oC.

39 | P a g e
 4.3 Esterification process (Stream Results):

Esterfication
Stream ID BIODIESE M ETHANOL OLEIC WAT+M ET
From B1 B1
To B1 B1
Phase LIQUID VAPOR LIQUID VAPOR
Substream: M IXED
M ole Flow lbmol/hr
OLEIC-01 1.3592E-20 0.0 100.0000 1.0447E-31
M ETHA-01 3.04983E-5 190.0000 0.0 89.99997
M ETHY-01 93.99997 0.0 0.0 6.000031
WAT ER 1.4515E-20 0.0 0.0 100.0000
M ole Frac
OLEIC-01 1.4459E-22 0.0 1.000000 5.3302E-34
M ETHA-01 3.24450E-7 1.000000 0.0 .4591835
M ETHY-01 .9999997 0.0 0.0 .0306124
WAT ER 1.5441E-22 0.0 0.0 .5102041
T otal Flow lbmol/hr 94.00000 190.0000 100.0000 196.0000
T otal Flow lb/hr 27870.39 6088.010 28246.68 6464.292
T otal Flow cuft/hr 753.7443 62126.56 543.8935 88772.66
T emperature F 684.9740 212.0000 230.0000 458.5333
Pressure p si 21.75566 22.04392 22.04392 21.75566
Vap or Frac 0.0 1.000000 0.0 1.000000
Liquid Frac 1.000000 0.0 1.000000 0.0
Solid Frac 0.0 0.0 0.0 0.0
Enthalp y Btu/lbmol -2.0450E+5 -84883.50 -3.3242E+5 -95600.72
Enthalp y Btu/lb -689.7221 -2649.119 -1176.864 -2898.653
Enthalp y Btu/hr -1.9223E+7 -1.6128E+7 -3.3242E+7 -1.8738E+7
Entrop y Btu/lbmol-R -322.1902 -29.24725 -400.4338 -23.83184
Entrop y Btu/lb-R -1.086668 -.9127739 -1.417632 -.7225912
Density lbmol/cuft .1247107 3.05827E-3 .1838595 2.20789E-3
Density lb/cuft 36.97593 .0979936 51.93421 .0728185
Average M W 296.4936 32.04216 282.4668 32.98108
Liq Vol 60F cuft/hr 513.0190 122.7587 512.0718 119.8082

40 | P a g e
 Fig 4.13 Stream results for esterification process

Table 4-5. Operating conditions and configurations for reactive distillation column
Conditions & Configurations Equilibrium-1
Number of stages 30
Oleic acid feed stage 3
Methanol feed stage 29
Side reboiler stage
Side reboiler duty, kW 0

Oleic feed temperature, oC 100

Methanol feed temperature, oC 90
Molar reflux ratio 1.5
Reaction stages 3-29
Distillate rate, kmol/hr 196
Bottom rate, kmol/hr 104
Bottom ester mass percent 90.23

Liquid holdup, cm3 0.043

Condenser duty, kW -5014.33
Condenser temperature, oC 107.92
Condenser pressure, bar 3.5
Reboiler duty, kW 7029.99

Reboiler temperature, oC 224.36

Reboiler pressure, bar 4.0
Total Conversion, kmol/hr 90.19
Exergy loss, kW 1385.5

Table 4.6 Product Configuration

Composition (Mol %)
Key Product Stream Total Methyl- Water Methanol Triolein
Flow Oleate
(Kmol/hr)
Biodiesel BIODIESEL 42.64 99.9 0.01 0.03 0.06
(Methyl-oleate)
Water+Methanol WAT+MET 88.9 3.06 51 45.9 0.04
41 | P a g e
 Conversion vs Methanol Flow Rate 94
98.997
100
90 84
80 74
70 64
Conversion(in %)

60 54
50 44
40 34
30 24
20 14
10 4
0
100 120 140 160 180 200
Methanol Flow rate(in lbmol/hr)

Fig 4.14 Change in conversion with feed ratio for model 3

Methanol Flow Rate vs Heat Duty

Methanol Flow Rate(in lbmol/hr)
0
0 50 100 150 200
-1000

-2000
Heat Duty(in KW)

-3000

-4000

-5000

-6000

-7000

Fig 4.15 Change in Heat duty with increasing methanol flow rate

Analysis with respect to reflux ratio, numbers of stages are also done but there is no significant

change in product flow rate.

42 | P a g e
 300

T-xy for OLEIC-01/METHA-01

T-x 0.0698 bar

250

T-y 0.0698 bar

200
Temperature C
150
100
50

0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4 0.45 0.5 0.55 0.6 0.65 0.7 0.75 0.8 0.85 0.9 0.95 1
Liquid/Vapor Molefrac OLEIC-01

Fig 4.16 Temperature profiles with changing mole fractions of oil

P-xy for OLEIC-01/METHA-01

0.2

P-x 25.0 C
P-y 25.0 C
0.15
Pressure bar
0.05 0.1

0 0.2 0.4 0.6 0.8 1

Liquid/Vapor Molefrac OLEIC-01

Fig 4.17 Pressure profiles with changing mole fractions of oil

43 | P a g e
 Y-x for OLEIC-01/METHA-01

1
1.013 bar

Vapor Molefrac OLEIC-01

0.25 0.5 0.75

0 0.25 0.5 0.75 1

Liquid Molefrac OLEIC-01

Fig 4.18 Change of Y with X at 1atm pressure

From above fig 4.16,17,18 we can observe variation of mole fractions of oil with temperature and

pressure changes.

44 | P a g e
 CHAPTER- 6

CONCLUSIONS AND FUTURE SCOPE

Several optimizations were made to improve the conversion of triolein and the purity of the

methyl oleate. Sensitivity analyses were conducted on reactor temperature, reactor pressure, flash

drum temperature, and flash drum pressure to determine the effect on triolein conversion and

methanol removal which controls product purity. The model 1 produces a triolein conversion of

99% and a biodiesel purity of 94% at 60oC and 1 bar pressure with a heat duty of 150KW required

for process to run.

Similarly, in model 2 triolein conversion of 98.74% and biodiesel of purity 99% is obtained

at 60oC and 1 bar pressure with a net heat duty of 75KW requirement.

For the process of esterification, a reactive distillation column is used to convert all free

fatty acid content to methyl esters at 100oC and 1.5 bar pressure

For better and accurate results one should try to run non-equilibrium models with data

from literature and get results that are practically accurate. The optimum parameters obtained in

above models do not contribute to any deviations or errors theoretically but practically these may

not be the optimum parameters. But from these results we can minimize heat duty and maximize

conversion.

Future Scope:

As distillation columns require higher heat duties, energy integration methods should be used like

thermally coupled distillation columns etc.

Non-equilibrium models should be used for accurate results that does not deviate much than

practical values, i.e. rate based models with data.

45 | P a g e
 REFERENCES
1. Nguyen, Nghi T., "Change of Biodiesel Production Plants" (2012). Chemical &
Biomolecular Engineering Theses and Student Research. Paper.

2. Noureddini, H., Zhu, D. 1997. Energy of transesterification of soybean oil. JAOCS 74,
1457-1463.

3. Kiss, A.A. 2011. Warmth incorporated responsive refining procedure for combination of
greasy esters. Fuel Process Technol 92.

4. Aspen Technology, Inc. 2009. Beginning building and running a procedure model

5. Aashish Gaurav, et al., Department of Chemical Engineering, University of Waterloo,

Waterloo, Ontario, N2L 3G1 Canada.

6. Okullo, S.J., Reynes, F. 2011. Can spare additions in experienced grungy petroleum
districts decrease peak oil. Imperativeness.

7. Yan, S., Kim, M., Salley, S.O., et al. 2009. Oil transesterification over calcium oxides
altered with lanthanum. Appl Catal A Gen.

8. Gerpen, J.V., Shanks, B., Pruszko, R. 2004. Biodiesel generation innovation. National
Renewable Energy Laboratory, Colorado

9. Kapilakarn, K., Peugtong, A. 2007.A relationship of cost of biodiesel creation from trans-
esterification. Int Energy J 8.

10. Bandyopadhyay, S., et al., U.V. 1998. Temperature-enthalpy twist for essentialness
centering of refining segments. Comput Chem Eng 22.

11. Demirel, Y. 2006. Retrofit of refining sections using thermodynamic examination. Sep Sci
Technol 41.

12. Dhole V.R., Linnhoff, B. 1993. Refining section targets. Comp Chem Eng 17, 549-560.

13. Nguyen, N., Demirel, Y. 2011. Responsive refining segment for esterification of lauric
destructive with methanol: Equilibrium versus nonequilibrium approaches. AIChE Annual.
Meeting. Conf. Proc. Nov 7-12, Salt Lake City, Utah.

14. Dhar, B., & Kirtania, K. (2009). Plenitude Methanol Recovery in Biodiesel Production
Process Using a Distillation Column: A Simulation Study. Blend Engineering Research
Bulletin, V.13 No.2.

15. Hillion, G.,et al.,.-A. (2003). Biodiesel Production by a Continuous Process Using a
Heterogenous Catalyst. France: Institut Français du Pétrol

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