CM17214 Project Report Polystyrene
CM17214 Project Report Polystyrene
By
Mridul
Bhawa CM
17214
CERTIFICATE
Signature
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Production Of
Polystyrene
ACKNOWLEDGEMENT
MRIDUL BHAWA
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Production Of
Polystyrene
Index
Topic Page No.
1. Introduction 5
2. Properties and Uses 6
3. Different processes used 10
4. Selection Of Process 12
5. Process Flow Diagram 14
6. Material Balance 15
7. Energy Balance 21
8. Equipment Design 26
i. Design of Reactor
ii. Design of Rotary Dryer
9. Pollution Control and safety 43
10. Instrumentation 46
11. Plant Layout 48
12. Plant location 51
13. Cost estimation and economics 54
14. Bibliography 60
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Polystyrene
SECTION I
INTRODUCTION
Ostromislensky of the Naugatuck chemical company first introduced polystyrene via a
pioneering parent in 1925. At about the same time, work by I.C. Farbenindustrie began that
resulted in the commercialization of polystyrene in Europe. The Dow Chemical Company also
began development of the polystyrene product and process in 1930.
The commercial production of polystyrene first took place at about the same time in Germany
and the US during the early 1930’s; it was manufactured primarily for its good electrical
properties. The polymer was produced in the UK at about the time of the beginning of the
Second World War, when it was used not only as an electrical insulant but also as a glass
replacement in optical instruments after lenses and prisms were no longer available from
Germany.
The major stimulus to the production of styrene monomer came in 1942 in the US with the
large-scale installation of manufacturing facilities for the styrene-butadiene rubber, which was
required to replace natural rubber after the cessation of suppliers from the Far East. After the
war when natural rubber became available again, there was a large surplus production for
styrene monomer, and polystyrene became available to help meet the demand for materials,
which could be used to satisfy the shortage of consumer goods. The polymer has good
mouldability, high transparency and rigidity, which made it suitable for wide range of
applications.
Crystal polystyrene was the initial polystyrene produced was a homopolymer. It is also known
as general-purpose polystyrene and exhibits exceptional clarity with heat resistance above that
of other commodity thermoplastics. A further development was rubber modified or impact
polystyrene. Impact polystyrene is opaque and exhibits increased toughness and ease of
processing versus other commodity thermoplastics.
Another major type of polystyrene application is expandable polystyrene, which is used
mainly in lightweight insulating applications.
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Production Of
Polystyrene
lower "greenhouse" emissions. As insulation, polystyrene foam enables enormous energy
savings in commercial installations such as cool stores.
PROPERTIES AND USES.
Properties
A] Processing properties:
Flow properties may be the most important properties of polystyrene processes. There are
two widely accepted industry methods for the measurement of processing properties. These
include the melt flow index and the solution viscosity.
The melt flow index is measured by ASTM method as a measure of the melt viscosity at 2000
C and a 5kg load. The melt flow index of polystyrene is generally controlled by adjustment of
the molecular weight of the material and by the addition of such lubricants as mineral oil.
Polystyrenes are commercially produced with melt flow ranges of less than 1 to greater than
50, although the most widely available grades generally have melt flows between 2.0 and 20g
per 10min.
Solution viscosity is another method for measuring the molecular structure of the polystyrene.
Solution viscosity can be measured as an 8% solution in toluene and increases with
increasing molecular weight.
B] Rheological properties:
Polystyrene is a non-Newtonian fluid with viscoelastic properties. The viscosity of polystyrene
melts or solutions is defined as the ratio of shear stress to shear rate. Generally, as the
molecular weight of the polymer is increased or mineral oil is decreased, melt viscosity
increases.
C] Mechanical properties:
Crystal polystyrenes have very low impact strengths of less than 0.5ft-lb. commercially
available impact polystyrene grades can be obtained with values of 1.0 -4.0ft-lb. Generally,
polystyrenes are not produced with greater than 15% total rubber because of polymerization
processing constraints. Nevertheless, impact properties can be increased substantially without
additional rubber by the proper control of rubber particle size, percentage of grafting, cross-
linking, and percentage of gel.
Tensile and flexural properties are also important representation of the strength of
polystyrenes. Increasing the rubber modification of polystyrene generally leads to lower
tensile strength, crystal grades being stiff and brittle. Tensile strength is also decreased by the
addition of lubricants, such as mineral oil. Flexural strengths for polystyrenes can be obtained
from 5000 to 18000psi and are also decreased by the addition of rubber and other additives to
the polystyrene. Elongations can be obtained from 1% for crystal polystyrene to 100% for
some impact polystyrene grades.
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D] Thermal properties:
Annealed heat distortion is one popular method for measuring he resistance to deformation
under heat for polystyrenes. The heat distortion temperature is decreased by the addition of
rubber, mineral oil, or other additives to polystyrene.
The glass transition temperature for unmodified polystyrene is 373 K, and the glass transition
temperatures for polybutadienes are 161-205 K, subject to the cis, Trans, and vinyl content.
E] Chemical properties:
Solvent crazing of polystyrene is a commercially important phenomenon. High impact
polystyrenes are susceptible to solvent crazing at the interface between the rubber particles
and the polystyrene phase. The resistance of polystyrene to this crazing is referred to as
environmental stress crack resistance (ESCR). For food-packaging applications, such as
butter tubs and deli containers, polystyrenes with high ESCR properties are desirable.
Increasing the percentage of gel, percentage grafting, and rubber particle size can increase
stress crack resistance.
Residual levels of low molecular weight materials are also important to polystyrene
performance. Some of the chemical impurities in the polystyrene are styrene monomer and
ethyl benzene solvent. Residual levels of styrene below 200 ppm and ethyl benzene levels
below 30 ppm are obtainable for very specialized applications.
F] Optical properties:
Crystal polystyrene is a transparent and colorless polymer; high impact polystyrene is generally
opaque as a result of the rubber particles. Developmental grades of translucent impact
polystyrenes have been produced but have not gained wide acceptance. The major optical;
property for high impact polystyrene is gloss. Gloss is a measure of the percentage of light
reflected is generally controlled by the size of the rubber particle. In general, the smaller rubber
particle gives higher gloss. Values from 20 to 95% reflectance are commercially available.
High impact polystyrene is naturally white and crystal polystyrene is naturally clear, but both
can be readily colored.
Applications
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Polystyrene
1. Extruded foam sheet of polystyrene can be thermoformed into such parts as egg
cartons or carryout food containers. Foam grade polystyrene is generally a high- heat
crystal polystyrene with a high molecular weight.
Typical applications include envelope windows, cap layers for glossy sheet, or
thermoforming into food packaging applications.
2. Solid or liquid pigments and dies color high impact and crystal polystyrenes. This can
be accomplished in both extrusion and injection molding processes. These colorants
are added and mixed during the melting stage of both the processes. Also, polystyrene
parts are amenable to high quality printing. Labels can be printed directly on the
polystyrene part to produce attractive containers.
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Polystyrene
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Production Of
Polystyrene
polymerization is carried out similarly to suspension polymerization except that the monomer
droplets are microscopic in size.
Suspension polymerization:
This is also called pearl polymerization. It has proved highly efficient for large- scale
production of polymers of high average molecular weight. By variation of the polymerization
condition it is possible to produce a range of polymers with different properties and
processing characteristics so that a number of grades are offered by the manufacturers to
meet the differing requirements of the conversion process and the final product.
There are many different ways of making polystyrene using suspension process. Most
producers use a batch process, although there are no technical reasons why a continuous
process could not work. In the suspension process a number of small styrene drops 0.15-
0.50mm in diameter are suspended in water. The reaction occurs within these drops. To aid
in the formation of proper size drops a suspending agent is used, and to keep them at that size
a stabilizing agent is added. A catalyst is used to control the reaction rate.
Suspension polymerization offers considerable advantages over the single-phase
techniques in so far that heat removal control is no longer a problem but there are
disadvantages such as the need to use a dispersing agent.
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Selection Of Process
I have selected suspension polymerisation process due to its wide usage in the
industry for the production of polystyrene. This is due to the fact that it has the
highest efficiency of conversion (between 90-95%).
Process Description
Suspension polymerization is a batch system popular for specialty grades of
polystyrene. It can be used to produce either crystal or high impact grades. In impact
production, the styrene and rubber solution are bulk polymerized beyond phase inversion and
is then suspended in water to create oil in water suspension utilizing soaps and suspending
agents. The suspended droplets are then polymerized to completion, utilizing initiator and a
staged heating profile. The water phase is used as a heat sink and heat transfer medium to a
temperature-controlled jacket. For the production of crystal polystyrene, the styrene monomer
itself is suspended and polymerized via the same mechanism.
Initiators: The initiators generally used are benzoyl peroxide and t-butyl hydroperoxide.
Suspending agent: To aid in the formation of the proper size drops a suspending agent is added.
Some typical suspending agents are methylcellulose, ethyl cellulose and polyacrylic acids. Their
concentration in the suspension is between 0.01-0.5% of monomer charged.
Stabilizing agent: To keep the drops at proper size, a stabilizing agent is added. The
stabilizing agents are often insoluble inorganic such as calcium carbonate, calcium phosphates
or bentonite clay. They are present in small amount than the suspending agents.
Catalyst: A catalyst is used to control the reaction rate. The catalysts are usually peroxides.
The most common ones are benzoyl, diacetyl, lauroyl, caproyl and tert-butyl. Their
concentration varies from 0.1-0.5% of the monomer charged. The ratio of
monomer to dispersing medium is between 10 and 40%. Polymerization temperature:
Polymerization of styrene occurs at temperature range of 90- 950C.
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Production Of
Polystyrene
Process description: The suspension method is carried out in large reactors equipped with
agitators, the styrene monomer being maintained in the aqueous phase as droplets with a
diameter varying between 0.4-1mm by use of a dispersing agent such as partially hydrolyzed
polyvinyl acetate, inorganic phosphates or magnesium silicates. To reduce the cycle time of
the reactors, the entering water and styrene will be preheated. The temperatures of the input
streams will be sent so as to obtain the desired reaction temperature. The water entering the
reactor will be heated to 950C. The bulk of the styrene is to be heated to 850C before being
charged. This is done in a vertical double pipe heat exchanger, which is directly above the
reactor. To prevent the polymerization from occurring in the heat exchanger or piping system,
there are to be no obstructions between this heat exchanger and the reactor. The catalyst,
rubber stabilizer, and suspending agent are premixed in styrene and discharged by gravity into
the reactor. This mixture will not be preheated, since it might polymerize. Typical water to
monomer ratios is 1:1 to 3:1. A combination of two or more initiators is used with a
programmed reaction temperature to reduce the polymerization time to a minimum for a
given amount of residual styrene.
Purification steps and Extrusion: If the water can be removed using physical separation
processes, then the styrene and the other impurities dissolved in it will also be discharged
A centrifuge with a washing step will be used to do this. The material leaving the centrifuge
has 1-5% water.
The final purification step is drying. The polystyrene leaving this unit must meet the
specifications set. (0.03% water). Then it is passed through a devolatisation extruder to
remove the volatile residues and to convert the polymer into pellets.
It was assumed that 3% of polystyrene would be removed from the process in drying,
centrifuging, transferring, or as bad as bad product. At least 95% of that which is lost in
processing must be intercepted before it leaves the plant. Most of it can be removed and sold
as off-grade material. This waste is split among the various streams leaving the processing
area.
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Section II
Material Balance
Reactor:
Input to the reactor:( unit ratios are obtained from literature):
Styrene = 1.032 kg styrene/kg polystyrene = 1.032*4166.67
= 4300 kg.
Water = 2.0 kg water/kg polystyrene = 2.0*4166.67
= 8333.34 kg.
Tricalcium phosphate = 0.005 kg tricalcium phosphate/kg polystyrene
= 0.005*4166.67
= 20.83 kg.
Dodecylbenzene sulphonate= 0.00006 kg dodecylbenzene sulphonate/kg polystyrene
= 0.00006*4166.67
= .25 kg.
Benzoyl peroxide = 0.0025 kg benzoyl peroxide/kg polystyrene
= 0.0025*4166.67
= 10.41 kg.
Miscellaneous = 0.004(styrene 99.6% pure)(unit ratio) = 0.004*4166.67
= 16.67 kg.
Total input to reactor = 12,681.50 kg.
Output from the rector:(unit ratios are obtained from literature: Baasel)
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Polystyrene =1.030 kg polystyrene / kg of polystyrene = 1.030*4166.67
= 4291.67 kg.
Styrene = 0.002 kg styrene/kg polystyrene = 0.002*4166.67
= 8.334 kg
Water = 2.0 kg water/kg polystyrene = 2.0*4166.67
= 8333.34 kg.
Miscellaneous = 0.0116 kg /kg polystyrene = 0.0116*4166.67
=48.337 kg.
Total output from reactor = 12,681.68 kg.
Wash tank:
Output from reactor
0.004 kg HCl/kg
1.030 polystyrene (unit ratio)
0.002 styrene (unit ratio)
4.0 water, 0.0156 miscellaneous
= 12,681.676 kg.
Centrifuge:
Output from wash tank
kg PS/kg PS
kg styrene/kg
PS
CENTRIFUGE
1.0 kg water/k g PS
4.95 kg water/kg PS
0.0155 misc.
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Output from centrifuge:
The output from centrifuge comprises of two layers. One is the desired and
the other is bad product.
Dryer:
0.0499 Kg Water/kg PS
1 kg PS/Ks PS
kg water /kg polystyrene
Input to the dryer:
Output from the centrifuge = 4,459.16 kg
2. Product with;
Polystyrene = 0.005 kg/kg polystyrene
= 0.005*4166.67
= 20.835kg
Water = 0.0499kg/kg polystyrene
= 0.0499*4166.67
= 207.92 kg
3. Bad product obtained has a composition;
Polystyrene = 0.015 kg/kg polystyrene
= 0.015*4166.67
= 62.50 kg
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Production Of Polystyrene
Extruder:
Output from dryer
EXTRUDER
Energy Balance
HEAT BALANCE
The additive feed tank must be large enough to handle all additive plus a carrier
solution of styrene. The amount of dodecylbenzene sulfonate, tricalcium phosphate and
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Production Of Polystyrene
Assume 2kg of styrene are to be used to carry each kg of additive into the reactor.
i.e. 52.39*2 = 104.79kg.
When GPPS is made, all but 104.79kg of styrene are heated to 93C. For the other
products less is used. The time to charge the reactor is set as 5min. Steam at 150psi will be
used as heating medium.
Qs = msCpsTs. = Us.A. Tss
(1)
Where,
Qs = rate of heat transfer.
ms = flow rate of styrene through exchanger.
= (1.032)*4166.67*5.5/4 – 104.79
(5/60)
= 69692.57 kg/hr.
Qs = 69692.57*1.799*63 = 7898.75*103kJ/hr.
7898.75*103 = 851.7*117.7*A
A = 78.80 m2.
One of the heat exchanger is needed for each reactor, because they must be positioned
vertically above the reactor. This is to prevent any hot styrene from remaining in the
exchanger or the piping where it might polymerize.
The average steam rate = msCpsTs/
= 4191.86*1.799*63 = 238.02 kg/hr.
1995.98
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Production Of Polystyrene
Where,
= 3927.33 kg/hr.
Where,
ma = flow rate of air.
= 5611 kg/hr.
Ua = 1 .
1/ho+1/hi
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Production Of Polystyrene
= mw.Cp. T.
Therefore,
mw= 2.085 kg/s in each reactor
Therefore amount of water required in total for 4 reactors= 2.085*4 = 8.34 kg/s.
Dryer:
Inlet Outlet
Temperatures:
Polystyrene 30C 80C.
.
Air 150 85C.
C.
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Production Of Polystyrene
= 2.849*105 + 0.44186*105W.
= 3.29*105W.
Tm = (150-30)-(85-80) =36.186C.
Ln(150-30)/(85-80)
The minimum air velocity is set by the particle size. A flow rate of 1000lb/hr.ft2 is
adequate for 420-micron particle. This will be used. The minimum velocity is used since it
gives the smaller dryer.
The amount of air required is determined by amount of energy the 150C. air
must supply to remove the moisture from the polystyrene.
m = Qt /( Cp.T)
Where,
Cp = heat capacity of air = 0.237 BTU/lb.C.
T = difference in air temperature entering and leaving dryer,C. Qt = heat
transferred in dryer =3.29*105W.
m = mass flow rate of air.
m= 3.29*105 = 5100.81kg/hr.
(0.9923*(150-85))
The amount of air is adequate. Add 10% to account for possible heat losses.
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Production Of Polystyrene
Design Of Equipments:
Process Design:
Reactor
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Production Of Polystyrene
= D 2L (2)
4
Where D = diameter of reactor L
= length of reactor.
It will be assumed that the reactor is generally 90% full and the height is twice
the diameter.
i.e. L = 2D
Therefore equation (1) becomes,
Weight of styrene in the reactor = 0.9*929.086*0.3390**2*D3
4
3
= 445.26D kg.
However, the reaction rate is not uniform. The maximum reaction rate must be known
to calculate the area needed for heat exchange. It will be assumed that maximum
conversion rate is assumed twice the average rate.
i.e. The maximum heat produced per hour = 2* average energy produced/hr.
= 2*77.674*103*D3 kJ/hr
= 155*106D3 J/s
3600
= 42152.778D3 J/s ------------- (3)
From literature, for cycle time of 5hrs, the overall heat transfer co-efficient between
reaction mixture and the cooling water in jacket is equal to 50 Btu/hr.ft2.K.=
283.9w/m2K
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Production Of Polystyrene
Since 95% of the time, the air temperature is below 30C. It will be assumed that inlet
cooling water temperature never exceeds 30C.
The reaction temperature = 93C.
It is assumed the maximum cooling water temperature rise is 5C. Therefore outlet
temperature of cooling water =35 C.
Therefore the average temperature of cooling water =(30+35)/2= 32.5C.
Therefore,
T= 93-32.5 = 60.5C.
The area of heat transfer is the area covered by the suspension. This can be estimated
to be the bottom plus 90% of the sides. ( because the reactor is 90% filled).
A = 0.9DL + D2
4
= 6.44D2
Substituting values of A, T and U in equation (4), we get,
= 2.563m.
Also,
L = 2D
= 2*2.563 = 5.127m.
And,
V = D2L
4
= 26.45m3
= 6987.35 gal.
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Production Of Polystyrene
T= 93 – 49 = 44C.
Also a ‘U’ of 60 BTU/ hr.ft2.F or a maximum reaction rate of 1.8 times the average
would be better estimates.
Taking maximum heat released per hour = 1.8 times average value.
= 1.8*77.674D3*106
3600
= 38837D3 J/s
Then,
And , 38837D3 = 60*5.687*6.44D2*44
L = 2*2.486 = 4.97m
V = 24.124m3
= 0.9*24.124*929.086*1.032
5.5*3.044
= 1243.43 kg/hr.
Number of GPPS reactors required is:
= 4166.67*1.032
1243.43
= 3.458 rectors.
An 5th reactor will be installed as a spare. This will allow full production to continue if
cleaning out the reactors becomes more of a problem than expected.
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Production Of Polystyrene
Mechanical design:
Data from literature:
Design pressure for the reactor = 220psi = 16.47 kg/cm2.
Design pressure for jacket = 75psi = 6.27 kg/cm2.
Permissible stress of reactor = 950kg/cm2.
Shell internal diameter = 2.486m.
Agitator horse power for 5000gal = 50hp
Diameter of agitator = 1035mm.
Speed = 200rpm.
Agitator blades (flat) =6
Width of blade =75mm.
Thickness of blades =8mm. Shaft
material – commercial cold rolled steel.
Permissible shear stress in shaft = 550kg/cm2.
Elastic limit in tension = 2460kg/cm2.
Modulus of elasticity =19.5*105kg/cm2.
Permissible stresses for key (carbon steel)
Shear = 650kg/cm2.
Crushing = 1300kg/cm2.
Stuffing box (carbon steel)
Permissible stress = 950kg/cm2.
Studs and bolts (hot rolled carbon steel)
Permissible stress = 587kg/cm2.
Joint efficiency = 0.85.
Poisons ratio = 0.3.
1. Shell thickness:
a) Internal pressure:
t= pi*Di + C
2ft*J-pi
Where, pi =16.47kg/cm2.
Di = diameter of reactor = 2486mm. ft
= permissible stress = 950kg/cm2. J =
joint efficiency = 0.85.
C = corrosion allowance =3mm.
Therefore,
t= 16.47*2486 +3
(2*950*0.85)-16.47
=28.0mm.
b) External pressure:
Let t =22mm.
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Production Of Polystyrene
2. Jacket thickness:
Jacket diameter = 1.04 – 1.05 times shell outer diameter.
= 1.045 * (2486+48) = 2623mm.
Therefore
t= pi*di +C
2ft*J-p
= 6.27 * 2623 + 2
2*950*.85 – 6.27
=11.7mm
Take 12mm as thickness of jacket.
3. Stiffening ring:
Required moment of inertia of stiffening ring is as per equation:
I=pcDo3L
24Epc= 4pe = 4*6.27 = 25.08kg/cm2.
I = 25.08 * (2486)2 4.97 = 4.619*104 mm4.
24 * 1900*103
Value of I is reduced by 30% to take into account the resistance of the steel.
I = 4.916*104 – 0.3*4.916*104 = 3.441*104mm4.
Use equal angle IS 2020 (size 20*20mm thickness = 3mm).
Ixx=Iyy = 0.4cm4.
4. Head thickness:
(a) Internal pressure:
t b = pRcW
2fJ
W = 1 * ( 3 + (Rc/Rl)0.5) 4
= 1 * (3 + (2486/128)0.5)
4
= 1.85
t b = 16.47 * 2486 *1.85 = 46.90mm.
2*950*0.85
(b)External pressure:
t b = 4.4*2486*(3(1-0.32)0.25*(6.27/(2*1900*103))0.5) = 43.179mm.
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Production Of Polystyrene
5. Shaft design:
= 179.049kgm.
d 3 = 49.013.
16
d = 6.296cm.
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Production Of Polystyrene
A = D2
4
0.0134 = D2 *2
4
D = 0.0134*4/2
= 0.0924m
= 92.4mm From
IS 803,
Thickness = 10mm.
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Production Of Polystyrene
A = 2.085*10-3m2. D =51.5mm.
From IS 803,
b = d + d
b = 10 +10
= 13.16 cm.
t = Pb*b + c
2f
= 16.47*13.16*10 + 3
2*950
= 4.14mm.
a = b + 2t
= 13.16 + 2* 4.14
= 13.988cm. 14.cm.
Load on gland:
F = * 16.47*(13.162 – 102) = 946.69kg.
4
Size of stud:
d 2 = 946.69*4 = 0.5137
*4*587
do = 7.16mm.
11. Coupling:
A clamp coupling is suggested. It is made of cast iron.
= 2*269.57*100
*0.25*10*4
= 1716.14kg.
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Production Of Polystyrene
= 2.824cm2.
Process design:
An air drier removes the excess water remaining in the polystyrene. A rotary drier will
be specified. Care must be taken that polymer does not exceed 85C, or its heat
distortion properties will be affected. Therefore this will be chosen as the exit
temperature of the air and the airflow will be parallel with the polymer flow. The air
will enter at 150C. It will be assumed that the solids will enter at room temperature
i.e. 30C and leave at 80C.
To estimate the size the following equations will be used,
Where,
Qt = Total energy transferred, kJ/hr.
Ua = Volumetric heat transfer coefficient, kJ/hr.m2. C.
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Production Of Polystyrene
= 2.849*105 + 0.44186*105W.
= 3.29*105W.
The minimum air velocity is set by the particle size. A flow rate of 1000lb/hr.ft2 is
adequate for 420-micron particle. This will be used. The minimum velocity is used
since it gives the smaller dryer.
The amount of air required is determined by amount of energy the 150C. air
must supply to remove the moisture from the polystyrene.
m = Qt /( Cp.T).
Where,
Cp = heat capacity of air = 0.237 BTU/lb.C.
T = difference in air temperature entering and leaving dryer,C.
Qt = heat transferred in dryer =3.29*105W.
m = mass flow rate of air.
m= 3.29*105 = 5100.81kg/hr.
(0.9923*(150-85))
Maximum amount of water that can be in air = 5100.814(kg/hr)* 0.7(kg water/kg dry
air)
= 3570.57kg water/hr.
Amount of water to be removed = 4166.67* 0.0497
= 207.083 kg water/hr.
The amount of air is adequate. Add 10% to account for possible heat losses.
Then,
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Production Of Polystyrene
= 1.20m.
From equation (2),
Ua = 20*(1000)0.16
(3.93)
= 15.36BTU/(hr.ft3.F).
V= 7.80778*105
15.36*97.1348
= 523.31ft3
= 14.81m3
Therefore,
L = V*4
D2
= 14.81*4
*(1.202)
= 13.10m.
Mechanical design:
1. Flight design:
Number of flights = 3*D.
= 3*3.93
=11.79 12 flights are required using lip angle of 45.
Radial height is taken as 1/8 of diameter, Radial
height =1.2 /8 = 0.15m.
2. Thickness of dryer:
Let x be the thickness of drier.
Mild steel can be used since it can withstand temperature up to 200C.
Density = 7688.86kg/m3.
D2 – D1 = 2x.
Volume of mild steel =(D22/4 - D12/4)*L
=((D1+2x)2/4 - D12/4)*L
= DLx.
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Production Of Polystyrene
M = (565.89x/8 + 7389.98/9)*12.24
= 865.81*103x + 11306.7
We know that,
M = f*Z. (1a).
f = 1800psi.
Take factor of safety = 5.
f = 3.6*105lb/ft3.
= 1.75767*104kg/m2.
3. Thickness of insulation:
Insulation material = asbestos.
Density of asbestos = 36lb/ft3.
Thermal conductivity of asbestos = 0.12BTU/hr.ft2.oF.
= 0.2077w/mK.
Material of dryer = mild steel.
Thermal conductivity = k = 26BTU/hr.ft2.oF.
Convective heat transfer coefficient from dryer surface = 56.78W/m2K.
Heat loss from the dryer = 3.31*105 BTU/hr = 3.492*105kJ.
A1 = (D1 + D2)L/2
= 75.83m2
A2 = (D2 + D3)L/2
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Production Of Polystyrene
= 78.2 + 38.45X
A3 = D3L
= 78.2 + 76.9X
T1 = 150C
T2 = 85C
= 18199.7kg
= 40123.47lb.
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Production Of Polystyrene
=0.000157*6021.8*10
= 9.45hp.
7. Horse power of exhaust fan:
Outlet temperature of air from dryer = 85C.
Humidity of outlet air = 0.00726
Total quantity of air going out = 212.8kg/min.
Volume of this air = 212.8*22.4*368.62
29*298
= 203.09m3/min.
= 7172.06ft3/min.
Air horsepower of exhaust fan for developed head of 10” water,
= 0.000157*7172.06*10
= 11.26 HP.
8. To find diameter of inlet and outlet:
At inlet conditions of 150C and humidity of 0.002,
Volume of air handled = 170.52*423/303
= 238.02m3/min.
= 3.967m3/s.
Assume an air velocity = 10m/s.
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Production Of Polystyrene
At outlet conditions,
Volume of air = 170.5*(273+85)/303
= 201.45m3/min.
= 3.357m3/s.
Cross section area of outlet pipe = 0.3357m2.
Diameter of outlet pipe = (0.3357*4/)0.5
= 0.6538m.
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Production Of Polystyrene
Ease of disposal:
According to the U.S. Environmental Protection Agency (EPA) in the 1999 update of the
"Characterization of Municipal Solid Waste in the U.S." report, less than one percent
(about 0.6 percent) of solid waste disposed of in the U.S. is polystyrene packaging -
including both food service packaging (cups, plates, bowls, trays, clamshells, meat trays,
egg cartons, yogurt and cottage cheese containers, and cutlery) and protective packaging
(shaped end pieces used to ship electronic goods and loose fill "peanuts").
The disposal of polystyrene is managed safely and effectively through the integrated system
advocated by the U.S. EPA, which includes: Source Reduction, Reuse, Recycling, Waste-to-
Energy Recovery, and Landfilling.
For more than 40 years, polystyrene has been in widespread use as a hygienic
material for protecting and preserving food. In fact, one-reason polystyrene single use food
containers are so widely used in hospitals and another sensitive environment is that
they are significantly more hygienic than the alternatives. Polystyrene does not harbour
bacteria, which is a major concern among health specialists.
A recent American study shows that 1 in 7 reusable dishes harbour a level of bacteria
which exceeds US health standards. In contrast, no disposable food service items exceeded
the standard.
Extruded foam polystyrene produced in for meat, chicken and vegetable trays and
takeaway food containers, does not use CFC blowing agents. Producers converted away
from CFC's in 1989 and now operate on recycled carbon dioxide or hydrocarbon gases.
Expandable or bead polystyrene (EPS) such as in produce boxes has always used a
hydrocarbon blowing agent.
Reuse:
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Production Of Polystyrene
Reuse, the practice of utilizing polystyrene products in the same form, is important not only
because it delays the final disposal of a product, but also because it reduces the manufacture
and purchase of new products. As a result, reuse prevents waste. Nearly 30 percent of
polystyrene loose fill (sometimes called "peanuts" because of its shape) is used again,
making it one of the most commonly reused packaging materials in some retail locations.
For mailing services, the reuse rate of loose fill is as high as 50 percent. The successful
application of reused loose fill polystyrene reduced the demand for virgin polystyrene by 25
percent in 1997 alone and, to this day, continues to directly reduce waste.
Other packaging and disposables commonly reused by the polystyrene industry include:
pallets, insulated shipping boxes, test tube trays, auto part trays, ice chests and coolers.
Recycling:
Some companies that make protective packaging are collecting it back for recycling
through the Alliance of Foam Packaging Recyclers. In addition, some makers of loose fill
"peanuts" have set up a network of collection sites for reuse and recycling of their
polystyrene products.
Waste-to-Energy Recovery:
In many overseas country’s polystyrene is recycled through incineration of municipal
waste for energy recovery. The burning of polystyrene is no more hazardous than
combustion of many natural organic materials. Polystyrene consists solely of carbon and
hydrogen. When combustion is complete, water and carbon dioxide are given off, leaving
trace levels of ash, the same combustion products as from paper or wood. While some
polystyrene in medical a municipal wastes is currently incinerated in Australia, the energy
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Production Of Polystyrene
Land filling:
While recycling and reuse continue to grow in popularity, most of the waste in this country
still goes to landfills. People assume the waste inside a landfill biodegrades. But the fact is
that very little - not paper, not polystyrene, not even food waste - degrades in a meaningful
way.
Polystyrene is effectively and safely disposed of in landfills. Modern landfills are designed
to protect the environment from the liquids and gases produced during the very slow
breakdown by reducing the exposure of garbage to air, water and sunlight - conditions
needed for degradation. Therefore, by design, modern landfills greatly retard the
degradation process to reduce the by-products that might otherwise contaminate
groundwater and the air.
Preventing Litter:
The polystyrene industry cares about the environment. A widely held misconception is that
litter is a problem caused by specific materials themselves rather than aberrant consumer
behavior. The reality is that some people improperly dispose of materials by littering.
Littering is a matter of behavior; people who discard materials into the environment usually
do so because they don't think or don't care. Attributing the litter issue to one particular
packaging material does not solve the problem because another type of packaging will take
its place as litter unless behavior changes. To address concerns effectively, the polystyrene
industry supports organizations such as Keep America Beautiful, that work to prevent litter
across the country.
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Production Of Polystyrene
Temperature Control
Temperature control is important for separation and reaction processes, and
temperature must be maintained within limits to ensure safe and reliable
operation of process equipment.
1. Thermo couple
2. Resistance Thermometers
3. Thermistors
4. Mercury in glass Thermometer
Flow Measurement
Flows throughout the process should the regulated near their desired values with
small variability; in these applications, good reproducibility is usually
sufficient. Flowing systems require energy, typically provided by pumps and
compressors, to produce a pressure difference as the driving force, and flow
sensors should introduce a small flow resistance, increasing the process energy
consumption as little as possible.
Commonly used devices are
1. Orifice
2. Venturi meter
3. Elbow meter
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Production Of Polystyrene
4. Pitot tube
Pressure Measurement
Most liquid and all gaseous materials in the process industries are contained
within closed vessels. For the safety of plant personnel and protection of the
vessel, pressure in the vessel is controlled. In addition, pressured is controlled
because it influences key process operations like vapor-liquid equilibrium,
chemical reaction rate, and fluid flow.
Commonly used devices are
1. Bourdon Gauges
2. Bellows
3. Diaphragm
4. Resistive/Strain Gauges
Level Measurement
Level of liquid in a vessel should be maintained above the exit pipe because if
the vessel empties the exit flow will become zero, a situation that would upset
downstream processes and could damage pumping equipment that requires
liquid. In addition, level can influence the performance of a process; the most
common example is a liquid phase chemical reactor.
Commonly used devices are
1. Float
2. Displacer level sensors
3. Manometers
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Availability Of Labour
Labour Will Be Needed For Construction Of The Plant And Its Operation. Skilled
Construction Workers Will Usually Be Brought In From Outside The Site, But There Should
Be An Adequate Pool Of Unskilled Labour Available Locally; And Labour Suitable For
Training To Operate The Plant. Skilled Tradesmen Will Be Needed For Plant Maintenance.
Local Trade Union Customs And Restrictive Practices Will Have To Be Considered When
Assessing The Availability And Suitability Of The Labour For Recruitment And Training.
Utilities (Services)
The Word “Utilities” Is Now Generally Used For The Ancillary Services Needed In The
Operation Of Any Production Process. These Services Will Normally Be Supplied From A
Central Facility; And Will Include:
• Electricity: - Power Required For Electrochemical Processes, Motors,
Lightings, And General Use
• Steam For Process Heating: - The Steams Required For The Process Are
Generated In The Tube Boilers Using Most Economic Fuel.
• Cooling Water: - Natural And Forced Draft Cooling Towers Are Generally
Used To Provide The Cooling Water Required On Site.
• Water For General Use: - The Water Required For The General Purpose Will
Be Taken From Local Water Supplies Like Rivers, Lakes And Seas. Because
Of This Reason All The Plants Located On The Banks OfRiver.
• Dematerialized Water: - Dematerialized Water, From Which All The Minerals
Have Been Removed By Ion-Exchange Is Used Where Pure Water Is
Needed For The Process Use, In Boiler Feed Water.
• Refrigeration: - Refrigeration Is Needed For The Processes, Which Require
Temperatures Below That Are Provided By The Cooling Water.
• Inert-Gas Supplies.
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Production Of Polystyrene
Sufficient Suitable Land Must Be Available For The Proposed Plant And Future
Expansion. The Land Should Be Ideally Flat, Well Drained And Have Load-Bearing
Characteristics. A Full Site Evaluation Should Be Made To Determine The Need For Piling
Or Other Foundations.
Climate
Adverse Climatic Conditions At Site Will Increase Costs. Abnormally Low Temperatures
Will Require The Provision Of Additional Insulation And Special Heating For Equipment
And Piping. Stronger Locations Will Be Needed At Locations Subject To High Wind Loads
Or Earthquakes.
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Production Of Polystyrene
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Production Of Polystyrene
future requirements.
Modular construction
In recent years there has been a move to assemble sections of plant at the plant
manufacturer’s site. These modules will include the equipment, structural steel, piping and
instrumentation. The modules are then transported to the plant site, by road or sea. The
advantages of modular construction are:
• Improved quality control.
• Reduced construction cost.
• Less need for skilled labour on site.
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Production Of Polystyrene
• Administration buildings, canteens are located near the entrance of the industry
where they will not interfere with production and it is convenient to contact the people
outside the industry.
• Location of services like power plant, cooling water, pump house, and switch
house is done such that their usage is not hindered and they are easily accessible in
case of fire.
• Pipelines laid are minimal and human safety is taken into account.
insulation & special heating for equipment & pipe runs. Stronger
earthquakes.
• Storage layout:
storage facilities for raw materials and products may be located in isolated areas or
in adjoining areas.
Hazardous materials become a decided menace to life and should be isolated when
stored. Storage tanks must be separated to facilitate suitable quantity. Process water
may be drawn from river, wells or purchased from local authority. Electrical power
will be needed at all sites. So plant should be located close to a cheap source of
power.
• Effluent disposal:
Effluent disposal should be according to the Indian standards. The appropriate authorities
must be consulted during the initial site survey to determine the standards that must be met.
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= 0.12×25.2375x107
= Rs. 6.357x107
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Production Of Polystyrene
A. Distribution and Selling costs: (2-20% of total product cost); includes costs for
sales offices, salesmen, shipping, and advertising.
Consider the Distribution and selling costs = 15% of total product cost
ÖDistribution and sellingcosts = 15% of 353.17x107 Ö
Distribution and selling costs = 0.15 × 353.17x107 Ö
Distribution and Selling costs = Rs 52.976x107
B. Research and Development costs: (about 5% of total product cost)
Consider the Research and development costs = 5% of total product cost
Research and Development costs = 5% of 353.175x107
Ö Research and development costs = 0.05 × 353.175x107
Ö Research and Development costs = Rs. 17.65x107
Thus,
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Production Of Polystyrene
V. Gross Earnings/Income:
Wholesale Selling Price of Polystyrene per ton = $ 1400 (USD)
Let 1 USD = Rs. 70.00
Hence Wholesale Selling Price of Polystyrene per ton. = 1400 ×70 = Rs 98000
Total Income = Selling price × Quantity of product manufactured
= 98000 × (100 T/day) × (325days/year)
Total Income = Rs.7.962x109
Gross income = Total Income – Total Product Cost
= (7.962x109) – (486.00x107)
Gross Income = Rs. 310.25×107
Let the Tax rate be 45% (common)
Taxes = 40% of Gross income
= 40% of 310.25×107= 0.40×310.25×107
Taxes = Rs. 124.10 x107
Net Profit = Gross income - Taxes = Gross income× (1- Tax rate)
Net profit = (310.25×107) – (124.10x107) = Rs. 186.15×106
Rate of Return:
Rate of return = Net profit×100/Total Capital Investment
Rate of Return = 186.15×107×100/ (770.165x107)
Rate of Return = 24.178%
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