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International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 1
ISSN 2250-3153
www.ijsrp.org
Extraction of Pyrolytic Fuel from Non-biodegradable
Solid Wastes
Md. Nizam UDDIN
Department of Mechanical Engineering
Khulna University of Engineering & Technology (KUET)
Khulna-9203, Bangladesh
Md. Rasedul Islam
Department of Mechanical Engineering
Khulna University of Engineering & Technology (KUET)
Khulna-9203, Bangladesh
Md. Amzad Hossain
Department of Mechanical Engineering
Khulna University of Engineering & Technology (KUET)
Khulna-9203, Bangladesh
Md.Nashin Sobhani
Department of Mechanical Engineering
Khulna University of Engineering & Technology (KUET)
Khulna-9203, Bangladesh
Mohammad Mashud
Department of Mechanical Engineering
Khulna University of Engineering & Technology (KUET)
Khulna-9203, Bangladesh
Abstract- Leather and Styrofoam are very common figures in
our day to day life, as a result a large amount of worn leather
and used Styrofoam are thrown away as wastes. These wastes
take a long time to biodegrade. So these play a vital role in
environmental pollution. But if these wastes are further
processed by pyrolysis, valuable energy such as pyrolytic oil,
char and gas can be obtained which can meet the crisis of
energy. In this project a simple pyrolysis system is introduced
with a fixed bed reactor, two condensers, and two outlet pipes,
in which the waste leather and Styrofoam are processed to
obtain fuels. The shredded leathers and Styrofoam are fed into
the reactor and heated up to a fixed temperature. The
condensation process is carried out during the passage of the
gas (volatile material) formed due to heating the shredded
wastes to form pyrolytic fuel. Further different properties of
the fuel such as density, viscosity, Calorific Value, boiling
point and flash point are determined and a comparison
between leather and Styrofoam with diesel and gasoline were
made. From the observations it has noticed that, the properties
of the pyrolytic oils obtained from leather and Styrofoam
don’t fully match with the properties of diesel and gasoline.
The Styrofoam can be used as a fuel by further processing but
the oil from leather cannot be used as a fuel but can be used as
lubricant in the engine.
Index Terms— Non biodegradable solid waste (NBDSW),
Pyrolysis, Leather, Styrofoam, Fixed bed, Char.
INTRODUCTION
The energy crisis and environmental degradation are the
main problems mankind is facing today. These problems owe
their origin to a growing population, rapid industrialization and
huge quantities of non biodegradable solid wastes (NBSW),
which are generated daily. NBSW are those which biodegrades
slowly, such as plastics, leather, styrofoams, tire etc. Every
year a huge amount of waste leather and Styrofoam cups,
plates are disposed in the environment. From an appendix
worldwide an estimated 60 billion kilo of leather is lost
(burning, landfill etc.) every year [1]. The estimation of leather
wastes in world basis is given bellow.
TABLE-1 ESTIMATION OF THE WASTES GENERATED BY LEATHER
MANUFACTURING - WORLDWIDE BASIS
Countries
Leather wastes
(tons/year)
China 105198
Asia 195319
Middle east 37521
Eastern Europe 18264
Western Europe 186834
South America 87225
North and central
America
60018
International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 2
ISSN 2250-3153
www.ijsrp.org
Rest of the world 115277
total 805606
On the other hand, Styrofoam is mostly uneconomical to
recycle or otherwise to process. As waste material, it exists in
massive quantities, is environmentally useless and can be lethal
to any bird or sea creature that swallows significant amounts.
Weight based the volume of Styrofoam is approximately 50
times that of municipal solid waste. U.S. Environmental
Protection Agency (EPA) states: each year Americans throw
away 25,000,000,000 Styrofoam cups. Even 500 years from
now, the foam coffee cup one used this morning will be sitting
in a landfill [2].So if the worn leather and Styrofoam can be
converted into useful energy sources by appropriate
technologies, the energy crisis as well as the environment
pollution will be sorted to some manner. Thermal conversion
involves the use of a wide range of thermal decomposition
processes Such as pyrolysis and gasification to decompose
waste materials into smaller molecules that can be used as
energy source or inputs for the synthesis of new materials, e.g.
Hydrocarbon wastes are decomposed to produce syngas
(H2+CO); the syngas can be used as a fuel directly. [3] In
pyrolysis process waste materials are heated and cracked in the
absence of oxygen into smaller molecules. While thermal
conversion shows advantages in dealing with a wide variety of
wastes of a hydrocarbon nature (e.g. used tires [4] and plastic
wastes [5]), and recovering both the energy and chemical value
of the wastes [6]. Although thermal conversion techniques
have recently shown potential as an environmentally friendly
waste disposal method [7], such practice is yet to become
popular.
PYROLYSIS
Pyrolysis liquefaction is a non-combustion heat treatment
that catalytically (chemically) decomposes waste material by
applying heat, directly or indirectly to the waste material in an
oxygen free environment. It is an endothermic reaction which
requires an input of energy that is typically applied indirectly
through the walls of the reactor in which the waste material is
fed into. Pyrolysis liquefaction occurs under pressure and at
operating temperature of about 400ºc to 900ºc The basic
phenomena that take place during pyrolysis are [8]:
 Heat transfer from a heat source, leading to an
increase in temperature inside the fuel
 Initiation of pyrolysis reactions due to this increased
temperature, leading to the release of volatiles and the
formation of char;
 Out flow of volatiles, resulting in heat transfer
between the hot volatiles and cooler unpyrolysed
fuel;
 Condensation of some of the volatiles in the cooler
parts of the fuel to produce tar
 Auto- catalytic secondary pyrolysis reactions due to
these interactions.
Fig. 1 shows the simple pyrolysis system where leather and Styrofoam can be pyrolysed easily, and the volatile material easily
condensed in the condenser
Figure 1.0 Simple pyrolysis system
Pyrolysis oil is a complex mixture of chemicals resulting
from the thermal decomposition of biomass. The types and
amounts of each chemical may vary widely depending on the
thermal process used. Pyrolysis oil is also known as bio-crude,
bio-oil or bio-leum. [9]. Typical industrial applications of
pyrolysis oil as a fuel is in boilers, furnaces, hot water
generators, hot air generators, thermal fluid heater, electric
generators, diesel pumps etc. The gas product is termed
synthesis gas, shortened to syngas. It is generally composed of
carbon dioxide, carbon monoxide, methane, hydrogen and two-
carbon hydrocarbons in varying proportions. In this report it is
often referred to as the gas product and generally re-used in
plant [10-11].Char is the solid material that remains after light
gases (e.g. coal gas) and tar have been driven out or released
from a carbonaceous material during the initial stage of
combustion i.e. Pyrolysis [12]. Generally char is used in rubber
industry, plastic industry, paints, inks etc. Figure 2.0 shows the
as prepared pyrolysis system.
Here,
A: Outer Cylinder
B: Inner Cylinder
C and D: Condensers
E and F: Outlet Pipes
International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 3
ISSN 2250-3153
www.ijsrp.org
Figure 2.0 As prepared pyrolysis system
EXPERIMENTAL
3.1 Pyrolysis of Leather
In leather pyrolysis process worn leathers were collected
from different places and after removing dust they were
shredded into small rectangular pieces of about 0.5 inch. Those
shredded leathers were placed into the reactor and then the
system was ready for the pyrolysis process. The total system
was placed on the kerosene stove and heat was supplied to the
reactor. For a fixed feed volume of 250 gm of shredded leather,
the experiment was carried out up to a temperature of about
800 ºc. In each experiment the flaring of the white vapor from
the condenser pipe started at a temperature of about 250ºc. So
the volatile material began to form at this temperature. At a
certain fixed temperature the white vapor with high volatile
content was passed through the condensers and get condensed
into liquid oil in the collector by means of gravitational force.
The uncondensed gases were passed through the condenser
flared to the atmosphere. But as the temperature increased
from 450ºc to 600ºc, the precedence time of the condensed oil
decreased i.e. as the temperature increases the more pyrolytic
oil from leather condensed can be obtained within a decreasing
time. At a temperature of about 700 ºc the white vapor stopped
to flare. The heating process was carried out for an hour or
more. The absence of white vapor indicates that the reaction
was over and the worn leather totally converted into pyrolytic
oil, char and gas. So the stove was turned off and the oil from
the collector was collected in the beaker and weighed. After
cooling down the system the char from the reactor was
collected and then weighed. The weight of the gas flared to the
atmosphere was found by subtracting the weight of the char
and oil from the total weight of the worn leather.
Figure 3.0 Pyrolysis of leather; (A) shredded leather wastes, (B) pyrolytic oil
from leather, (C) char
3.2 Pyrolysis of Styrofoam
At first the used plates, cups etc of Styrofoam were
collected from different places and then after removing dust
shredded them into small pieces of about 0.25 inch. The
shredded Styrofoam of about 50 gm then placed into the rector
and the reactor placed on the stove. The reactor temperature
was increased up to 500o
c. About 10 minutes the Styrofoam
started to melt down. The Temperature of the reactor was
measured with a temperature recorder to be 250 o
c. After about
15 minutes the Styrofoam started to evaporate when the
temperature of the reactor was at 330 o
c. Five minutes later the
reactor temperature was 360 o
c and the first drop of condensed
vapor was collected at 60 ºc. The temperature of the condensed
vapor increased quickly from 60ºc to 131 ºc. The pyrolysis
system continued for 80 minutes and stopped when the
temperature of the condensing vapor dropped to 70 ºc while the
reactor temperature was above 450o
c. Thus the liquid obtained
from pyrolysis process was 37 gm, which was a 70% yield to
liquid. The volatile material that was not condensing by a water
cooling condenser at room pressure was not collected. The
leftover was 8 gm of a high viscous dark material in the bottom
of the reactor. So the amount of volatile material that was not
condensed was 6 gm.
Figure 4.0 Pyrolysis of Styrofoam waste; (a) Shredded Styrofoam plates, (b)
pyrolytic oil from Styrofoam
RESULTS AND DISCUSSION
Table 2.0 shows the different product produced during the
pyrolysis of leather:
International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 4
ISSN 2250-3153
www.ijsrp.org
TABLE 2.0 PRODUCT OF PYROLYSIS OF LEATHER
The amount of liquid, solid and uncondensed vapor produced during pyrolytic conversion of waste Styrofoam is shown in table
3.0.
TABLE 3.0 PRODUCT OF PYROLYSIS OF STYROFOAM
Observation
no
Product yield
Residence
time
(min)
Liqud
(oil)
(gm)
Solid
(char)
(gm)
Gas
(gm)
01 42 3 5 55
02 45 2 3 62
03 39 5 6 57
04 42 2 6 66
TABLE 4.0 PHYSICAL PROPERTIES OF PYROLYTIC OIL DERIVED FROM LEATHER & STYROFOAM
Extracted Oil
Diesel Gasoline
Leather Styrofoam
Density (ρ) 1010.6 854 820-850 719-780
Kinematic
Viscosity (cSt)
1.69 4.63 2- 4.5 1.95-3.3
Gross Calorific
value (MJ/kg)
28.63 39.38 44-46 43.2
Boiling point
(°C)
102 148 180-360 100-400
Flash point
(°C)
36 52 53- 80 N/A
Different properties of pyrolytic oil extracted from leather
and Styrofoam like Kinematic viscosity, Gross calorific value,
boiling point, flash point etc were determined in the laboratory.
The oil produced from the leather was brown in colour with an
acidic smell. It reacts with skin and acrid smell for a few days.
It stored in an air tight bottle but its colour or physical
properties didn’t change. The oil produced from the Styrofoam
was less dense than the oil from leather. It also posses acidic
odor and react with human skin.
CONCLUSION
Leather and Styrofoam is an important new alternative
transportation fuel. It can be produced from any kind of waste
leather and Styrofoam. This technique has extended to allow
pyrolytic fuel production from different non bio degradable
solid wastes. Adherence to a quality standard is essential for
proper performance of the fuel in the engine and will be
necessary for widespread use of these fuels, obtained from
leather and Styrofoam. But between these two the fuel from
Styrofoam is better than the fuel from leather. Because it
possesses good calorific value which ranges between the diesel
Observation no
Product yield
Residence time
(min)
Liquid (oil)
(gm)
Solid (char)
(gm)
Gas
(gm)
01 203 29 18 83
02 195 32 23 80
03 216 22 12 73
04 207 31 12 78
International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 5
ISSN 2250-3153
www.ijsrp.org
and its other properties are near to the properties of diesel and
gasoline.
This report investigates parameters of pyrolytic fuel from
leather and Styrofoam. The results of this work can be
summarized as follows:
 The production of the pyrolytic fuel from non
biodegradable solid wastes (leather & Styrofoam) was
done by heating them in inert atmosphere in a fixed bed
reactor and condensing them in an optimum temperature.
 The optimum temperature for extracting oil from pyrolysis
process was observed 600°C for leather and 250°C for
Styrofoam.
 The optimum reaction time was observed to be 40 min for
leather and 25 min for Styrofoam.
 The fuel properties of leather and styrofoam is determined
and shown in this report
 From the comparison of fuel properties between leather
and Styrofoam, Styrofoam showed better properties than
leather.
 There are some impurities in the produced pyrolytic oil. so
if refinement is done then the properties of the oil can be
changed and can make these oils more valuable and more
suitable.
REFERENCES
[1] Sinag, A.; Gulbay, S.; Uskan, B.; Uҫar, S.; Ozgurler, s.b.
Production and Characterization of pyrolytic oils by pyrolysis of
waste machinery oil. J. Hazard. Mater. 2010, 173, 420-426.
[2] FAO, World statistical compendium for raw hides and skins,
leather and leather footwear 1979-1997, 1998
[3] Dry, M.E. High quality diesel via the Fischer-tropsch process- A
review. J. Chem. Technol. Biotechnol. 2002, 77, 43-50.
[4] Uҫar, S.; Karagӧz, S.; Yanik, J,; Saglam, M.; Yuksel, M.
copyrolysis of scrap tires with waste lubricant oil. Fuel process.
Technol. 2005, 87, 53-58.
[5] Scheirs, J.; kaminsky, W. Feedstock Recycling and Pyrolysis of
Waste Plastics: Converting Waste Plastics into Diesel and Other
Fuels; Wiley: Chichester, UK, 2006; Volume 27, pp. 2-785.
[6] Ludlow-Palafox, C.; Chase, H.A. Microwave induced pyrolysis
of plastic wastes. Ind. Eng. Chem. Res. 2001,40, 4749-4756.
[7] Song, G.-J.; Seo, Y.-C.; Pudasainee, D.; Kim, I.-T.
characteristics of gas and residues produced from electric arc
pyrolysis of waste lubricating oil. Waste Manag. 2010, 30,
1230-1237.
[8] Dr. T. Muraleedharan Nair, “The Settling up of Pyrolysis Plant
for Plastic Wastes Conversion into Industrial Diesel (Pyrolysis
oil), Gaseous fuel & Carbon Black”; CSFC Manjeri, Industries
Dept., Govt. of Kerala.
[9] B.V. Babu *, A.S. Chaurasia; “Modeling, simulation and
estimation of optimum parameters in pyrolysis of biomass”;
Energy Conversion and Management 44 (2003) 2135–2158,
Department of Chemical Engineering, Birla Institute of
Technology and Science, Pilani 333031, Rajasthan, India.
[10] Peter Alexander Brownsort, “Biomass pyrolysis processes:
performance parameters and their influence on biochar system
benefits”, University of Edinburgh, 2009.
[11] Bandyopadhyay A, Basak GC. Studies on photocatalytic
degradation of polystyrene, Materials Science & Technology.
2007;23(3):307-314.
[12] Friend D. Conserving natural resources in illinois. University of
Illinois extension, College of Agricultural, Consumer and
Environmental Sciences; 200

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Extraction of fuels from waste leather and Styrofoam via pyrolysis

  • 1. International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 1 ISSN 2250-3153 www.ijsrp.org Extraction of Pyrolytic Fuel from Non-biodegradable Solid Wastes Md. Nizam UDDIN Department of Mechanical Engineering Khulna University of Engineering & Technology (KUET) Khulna-9203, Bangladesh Md. Rasedul Islam Department of Mechanical Engineering Khulna University of Engineering & Technology (KUET) Khulna-9203, Bangladesh Md. Amzad Hossain Department of Mechanical Engineering Khulna University of Engineering & Technology (KUET) Khulna-9203, Bangladesh Md.Nashin Sobhani Department of Mechanical Engineering Khulna University of Engineering & Technology (KUET) Khulna-9203, Bangladesh Mohammad Mashud Department of Mechanical Engineering Khulna University of Engineering & Technology (KUET) Khulna-9203, Bangladesh Abstract- Leather and Styrofoam are very common figures in our day to day life, as a result a large amount of worn leather and used Styrofoam are thrown away as wastes. These wastes take a long time to biodegrade. So these play a vital role in environmental pollution. But if these wastes are further processed by pyrolysis, valuable energy such as pyrolytic oil, char and gas can be obtained which can meet the crisis of energy. In this project a simple pyrolysis system is introduced with a fixed bed reactor, two condensers, and two outlet pipes, in which the waste leather and Styrofoam are processed to obtain fuels. The shredded leathers and Styrofoam are fed into the reactor and heated up to a fixed temperature. The condensation process is carried out during the passage of the gas (volatile material) formed due to heating the shredded wastes to form pyrolytic fuel. Further different properties of the fuel such as density, viscosity, Calorific Value, boiling point and flash point are determined and a comparison between leather and Styrofoam with diesel and gasoline were made. From the observations it has noticed that, the properties of the pyrolytic oils obtained from leather and Styrofoam don’t fully match with the properties of diesel and gasoline. The Styrofoam can be used as a fuel by further processing but the oil from leather cannot be used as a fuel but can be used as lubricant in the engine. Index Terms— Non biodegradable solid waste (NBDSW), Pyrolysis, Leather, Styrofoam, Fixed bed, Char. INTRODUCTION The energy crisis and environmental degradation are the main problems mankind is facing today. These problems owe their origin to a growing population, rapid industrialization and huge quantities of non biodegradable solid wastes (NBSW), which are generated daily. NBSW are those which biodegrades slowly, such as plastics, leather, styrofoams, tire etc. Every year a huge amount of waste leather and Styrofoam cups, plates are disposed in the environment. From an appendix worldwide an estimated 60 billion kilo of leather is lost (burning, landfill etc.) every year [1]. The estimation of leather wastes in world basis is given bellow. TABLE-1 ESTIMATION OF THE WASTES GENERATED BY LEATHER MANUFACTURING - WORLDWIDE BASIS Countries Leather wastes (tons/year) China 105198 Asia 195319 Middle east 37521 Eastern Europe 18264 Western Europe 186834 South America 87225 North and central America 60018
  • 2. International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 2 ISSN 2250-3153 www.ijsrp.org Rest of the world 115277 total 805606 On the other hand, Styrofoam is mostly uneconomical to recycle or otherwise to process. As waste material, it exists in massive quantities, is environmentally useless and can be lethal to any bird or sea creature that swallows significant amounts. Weight based the volume of Styrofoam is approximately 50 times that of municipal solid waste. U.S. Environmental Protection Agency (EPA) states: each year Americans throw away 25,000,000,000 Styrofoam cups. Even 500 years from now, the foam coffee cup one used this morning will be sitting in a landfill [2].So if the worn leather and Styrofoam can be converted into useful energy sources by appropriate technologies, the energy crisis as well as the environment pollution will be sorted to some manner. Thermal conversion involves the use of a wide range of thermal decomposition processes Such as pyrolysis and gasification to decompose waste materials into smaller molecules that can be used as energy source or inputs for the synthesis of new materials, e.g. Hydrocarbon wastes are decomposed to produce syngas (H2+CO); the syngas can be used as a fuel directly. [3] In pyrolysis process waste materials are heated and cracked in the absence of oxygen into smaller molecules. While thermal conversion shows advantages in dealing with a wide variety of wastes of a hydrocarbon nature (e.g. used tires [4] and plastic wastes [5]), and recovering both the energy and chemical value of the wastes [6]. Although thermal conversion techniques have recently shown potential as an environmentally friendly waste disposal method [7], such practice is yet to become popular. PYROLYSIS Pyrolysis liquefaction is a non-combustion heat treatment that catalytically (chemically) decomposes waste material by applying heat, directly or indirectly to the waste material in an oxygen free environment. It is an endothermic reaction which requires an input of energy that is typically applied indirectly through the walls of the reactor in which the waste material is fed into. Pyrolysis liquefaction occurs under pressure and at operating temperature of about 400ºc to 900ºc The basic phenomena that take place during pyrolysis are [8]:  Heat transfer from a heat source, leading to an increase in temperature inside the fuel  Initiation of pyrolysis reactions due to this increased temperature, leading to the release of volatiles and the formation of char;  Out flow of volatiles, resulting in heat transfer between the hot volatiles and cooler unpyrolysed fuel;  Condensation of some of the volatiles in the cooler parts of the fuel to produce tar  Auto- catalytic secondary pyrolysis reactions due to these interactions. Fig. 1 shows the simple pyrolysis system where leather and Styrofoam can be pyrolysed easily, and the volatile material easily condensed in the condenser Figure 1.0 Simple pyrolysis system Pyrolysis oil is a complex mixture of chemicals resulting from the thermal decomposition of biomass. The types and amounts of each chemical may vary widely depending on the thermal process used. Pyrolysis oil is also known as bio-crude, bio-oil or bio-leum. [9]. Typical industrial applications of pyrolysis oil as a fuel is in boilers, furnaces, hot water generators, hot air generators, thermal fluid heater, electric generators, diesel pumps etc. The gas product is termed synthesis gas, shortened to syngas. It is generally composed of carbon dioxide, carbon monoxide, methane, hydrogen and two- carbon hydrocarbons in varying proportions. In this report it is often referred to as the gas product and generally re-used in plant [10-11].Char is the solid material that remains after light gases (e.g. coal gas) and tar have been driven out or released from a carbonaceous material during the initial stage of combustion i.e. Pyrolysis [12]. Generally char is used in rubber industry, plastic industry, paints, inks etc. Figure 2.0 shows the as prepared pyrolysis system. Here, A: Outer Cylinder B: Inner Cylinder C and D: Condensers E and F: Outlet Pipes
  • 3. International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 3 ISSN 2250-3153 www.ijsrp.org Figure 2.0 As prepared pyrolysis system EXPERIMENTAL 3.1 Pyrolysis of Leather In leather pyrolysis process worn leathers were collected from different places and after removing dust they were shredded into small rectangular pieces of about 0.5 inch. Those shredded leathers were placed into the reactor and then the system was ready for the pyrolysis process. The total system was placed on the kerosene stove and heat was supplied to the reactor. For a fixed feed volume of 250 gm of shredded leather, the experiment was carried out up to a temperature of about 800 ºc. In each experiment the flaring of the white vapor from the condenser pipe started at a temperature of about 250ºc. So the volatile material began to form at this temperature. At a certain fixed temperature the white vapor with high volatile content was passed through the condensers and get condensed into liquid oil in the collector by means of gravitational force. The uncondensed gases were passed through the condenser flared to the atmosphere. But as the temperature increased from 450ºc to 600ºc, the precedence time of the condensed oil decreased i.e. as the temperature increases the more pyrolytic oil from leather condensed can be obtained within a decreasing time. At a temperature of about 700 ºc the white vapor stopped to flare. The heating process was carried out for an hour or more. The absence of white vapor indicates that the reaction was over and the worn leather totally converted into pyrolytic oil, char and gas. So the stove was turned off and the oil from the collector was collected in the beaker and weighed. After cooling down the system the char from the reactor was collected and then weighed. The weight of the gas flared to the atmosphere was found by subtracting the weight of the char and oil from the total weight of the worn leather. Figure 3.0 Pyrolysis of leather; (A) shredded leather wastes, (B) pyrolytic oil from leather, (C) char 3.2 Pyrolysis of Styrofoam At first the used plates, cups etc of Styrofoam were collected from different places and then after removing dust shredded them into small pieces of about 0.25 inch. The shredded Styrofoam of about 50 gm then placed into the rector and the reactor placed on the stove. The reactor temperature was increased up to 500o c. About 10 minutes the Styrofoam started to melt down. The Temperature of the reactor was measured with a temperature recorder to be 250 o c. After about 15 minutes the Styrofoam started to evaporate when the temperature of the reactor was at 330 o c. Five minutes later the reactor temperature was 360 o c and the first drop of condensed vapor was collected at 60 ºc. The temperature of the condensed vapor increased quickly from 60ºc to 131 ºc. The pyrolysis system continued for 80 minutes and stopped when the temperature of the condensing vapor dropped to 70 ºc while the reactor temperature was above 450o c. Thus the liquid obtained from pyrolysis process was 37 gm, which was a 70% yield to liquid. The volatile material that was not condensing by a water cooling condenser at room pressure was not collected. The leftover was 8 gm of a high viscous dark material in the bottom of the reactor. So the amount of volatile material that was not condensed was 6 gm. Figure 4.0 Pyrolysis of Styrofoam waste; (a) Shredded Styrofoam plates, (b) pyrolytic oil from Styrofoam RESULTS AND DISCUSSION Table 2.0 shows the different product produced during the pyrolysis of leather:
  • 4. International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 4 ISSN 2250-3153 www.ijsrp.org TABLE 2.0 PRODUCT OF PYROLYSIS OF LEATHER The amount of liquid, solid and uncondensed vapor produced during pyrolytic conversion of waste Styrofoam is shown in table 3.0. TABLE 3.0 PRODUCT OF PYROLYSIS OF STYROFOAM Observation no Product yield Residence time (min) Liqud (oil) (gm) Solid (char) (gm) Gas (gm) 01 42 3 5 55 02 45 2 3 62 03 39 5 6 57 04 42 2 6 66 TABLE 4.0 PHYSICAL PROPERTIES OF PYROLYTIC OIL DERIVED FROM LEATHER & STYROFOAM Extracted Oil Diesel Gasoline Leather Styrofoam Density (ρ) 1010.6 854 820-850 719-780 Kinematic Viscosity (cSt) 1.69 4.63 2- 4.5 1.95-3.3 Gross Calorific value (MJ/kg) 28.63 39.38 44-46 43.2 Boiling point (°C) 102 148 180-360 100-400 Flash point (°C) 36 52 53- 80 N/A Different properties of pyrolytic oil extracted from leather and Styrofoam like Kinematic viscosity, Gross calorific value, boiling point, flash point etc were determined in the laboratory. The oil produced from the leather was brown in colour with an acidic smell. It reacts with skin and acrid smell for a few days. It stored in an air tight bottle but its colour or physical properties didn’t change. The oil produced from the Styrofoam was less dense than the oil from leather. It also posses acidic odor and react with human skin. CONCLUSION Leather and Styrofoam is an important new alternative transportation fuel. It can be produced from any kind of waste leather and Styrofoam. This technique has extended to allow pyrolytic fuel production from different non bio degradable solid wastes. Adherence to a quality standard is essential for proper performance of the fuel in the engine and will be necessary for widespread use of these fuels, obtained from leather and Styrofoam. But between these two the fuel from Styrofoam is better than the fuel from leather. Because it possesses good calorific value which ranges between the diesel Observation no Product yield Residence time (min) Liquid (oil) (gm) Solid (char) (gm) Gas (gm) 01 203 29 18 83 02 195 32 23 80 03 216 22 12 73 04 207 31 12 78
  • 5. International Journal of Scientific and Research Publications, Volume 5, Issue 1, January 2015 5 ISSN 2250-3153 www.ijsrp.org and its other properties are near to the properties of diesel and gasoline. This report investigates parameters of pyrolytic fuel from leather and Styrofoam. The results of this work can be summarized as follows:  The production of the pyrolytic fuel from non biodegradable solid wastes (leather & Styrofoam) was done by heating them in inert atmosphere in a fixed bed reactor and condensing them in an optimum temperature.  The optimum temperature for extracting oil from pyrolysis process was observed 600°C for leather and 250°C for Styrofoam.  The optimum reaction time was observed to be 40 min for leather and 25 min for Styrofoam.  The fuel properties of leather and styrofoam is determined and shown in this report  From the comparison of fuel properties between leather and Styrofoam, Styrofoam showed better properties than leather.  There are some impurities in the produced pyrolytic oil. so if refinement is done then the properties of the oil can be changed and can make these oils more valuable and more suitable. REFERENCES [1] Sinag, A.; Gulbay, S.; Uskan, B.; Uҫar, S.; Ozgurler, s.b. Production and Characterization of pyrolytic oils by pyrolysis of waste machinery oil. J. Hazard. Mater. 2010, 173, 420-426. [2] FAO, World statistical compendium for raw hides and skins, leather and leather footwear 1979-1997, 1998 [3] Dry, M.E. High quality diesel via the Fischer-tropsch process- A review. J. Chem. Technol. Biotechnol. 2002, 77, 43-50. [4] Uҫar, S.; Karagӧz, S.; Yanik, J,; Saglam, M.; Yuksel, M. copyrolysis of scrap tires with waste lubricant oil. Fuel process. Technol. 2005, 87, 53-58. [5] Scheirs, J.; kaminsky, W. Feedstock Recycling and Pyrolysis of Waste Plastics: Converting Waste Plastics into Diesel and Other Fuels; Wiley: Chichester, UK, 2006; Volume 27, pp. 2-785. [6] Ludlow-Palafox, C.; Chase, H.A. Microwave induced pyrolysis of plastic wastes. Ind. Eng. Chem. Res. 2001,40, 4749-4756. [7] Song, G.-J.; Seo, Y.-C.; Pudasainee, D.; Kim, I.-T. characteristics of gas and residues produced from electric arc pyrolysis of waste lubricating oil. Waste Manag. 2010, 30, 1230-1237. [8] Dr. T. Muraleedharan Nair, “The Settling up of Pyrolysis Plant for Plastic Wastes Conversion into Industrial Diesel (Pyrolysis oil), Gaseous fuel & Carbon Black”; CSFC Manjeri, Industries Dept., Govt. of Kerala. [9] B.V. Babu *, A.S. Chaurasia; “Modeling, simulation and estimation of optimum parameters in pyrolysis of biomass”; Energy Conversion and Management 44 (2003) 2135–2158, Department of Chemical Engineering, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India. [10] Peter Alexander Brownsort, “Biomass pyrolysis processes: performance parameters and their influence on biochar system benefits”, University of Edinburgh, 2009. [11] Bandyopadhyay A, Basak GC. Studies on photocatalytic degradation of polystyrene, Materials Science & Technology. 2007;23(3):307-314. [12] Friend D. Conserving natural resources in illinois. University of Illinois extension, College of Agricultural, Consumer and Environmental Sciences; 200