Design For The Production of Soap PDF
Design For The Production of Soap PDF
INTRODUCTION:
Non-toilet soaps
Toilet soaps
Soaps are key components of most lubricating greases and thickeners.
Greases are usually emulsions of calcium soap or lithium soap and mineral oil.
Many other metallic soaps are also useful, including those of aluminium, sodium,
and mixtures thereof. Such soaps are also used as thickeners to increase the
viscosity of oils.
The insoluble oil/fat molecules become associated inside micelles, tiny
spheres formed from soap molecules with polar hydrophilic groups on the outside
and encasing a lipophilic pocket, which shields the oil/fat molecules from the water
making it soluble.
2.HISTORY:
The earliest recorded evidence of the production of soap-like materials dates
back to around 2800 BC in ancient Babylon. A formula for soap consisting of water,
alkali, and cassia oil was written on a Babylonian clay tablet around 2200 BC. The
Ebers papyrus (Egypt, 1550 BC) indicates the ancient Egyptians bathed regularly
and combined animal and vegetable oils with alkaline salts to create a soap-like
substance. In ancient Israel, the ashes from barilla plants, such as species of Salsola,
saltwort and Anabasis, were used in soap production, known as potash. The word
soap, Latin for soap, likely was borrowed from an early Germanic
language and is cognate with Latin sebum, “tallow”.
Zosimos of Panopolis, circa 300 AD, describes soap and soap making.
The use of soap for personal cleanliness became increasingly common in the second
century AD. A detergent similar to soap was manufactured in ancient China from
the seeds of Gleditsia sinensis. Hard toilet soap with a pleasant smell was produced
in the Middle East during the Islamic Golden Age, when soap-making became an
established industry. In the Middle East, soap was produced from the interaction of
fatty oils and fats with alkali.
A 12th century Islamic document describes the process of soap
production. In Europe, soap in the 9th century was produced from animal fats and
had an unpleasing smell. Finer soaps were later produced in Europe from the 16 th
century, using vegetable oils (such as olive oil) as opposed to animal fats.
Industrially manufactured bar soaps became available in the late 18th century. Until
the Industrial Revolution, soap making was conducted on a small scale and the
product was rough. William Gossage produced low-priced, good quality soaps from
the 1850s. Robert Spear Hudson began manufacturing a soap powder in 1837,
initially by grinding the soap with a mortar and pestle. In 1865, William Shepphard
patented a liquid version of soap.
3.PHYSICAL PROPERTIES OF COCONUT OIL:
Property Information
Acidity 13-14 pH
Corrosive High
Reactivity Medium
Solubility 110 g/L
• Caustic soda
• Lye
• Ascarite
• White caustic
• Sodium hydrate
8.METHODS OF PRODUCTION:
9.PROCESS DESCRIPTION:
In hot process, hot oils and lye are combined to begin saponification, and
then introduced to heat. The additional heat speeds up the saponification process
and cooks the soap before it goes into the mould.
Melt and pour soap is a ready-made soap base composed of fatty acids,
glycerine, and other natural ingredients. The base is produced through the
saponification process.
9.3 REBATCHING
Rebatching is taking soap that has already been made and giving it new
life by grating it, melting it, and then adding any additional colours, fragrances or
additives.
9.4 COLD PROCESS METHOD
9.4.1 Saponification
9.4.2 Emulsification
The lye is dissolved in water. Then oils are heated, or melted if they are
solid at room temperature. Once the oils are liquefied and the lye is fully dissolved
in water, they are combined. This lye-fat mixture is mixed until the two phases are
fully emulsified.
9.4.3 Moulding
The batch is then poured into moulds, kept warm with towels or blankets,
and left to continue saponification for 12 to 48 hours. During this time, it is normal
for the soap to go through a “gel phase”, wherein the opaque soap will turn
somewhat transparent for several hours, before once again turning opaque.
9.4.4 Cutting
After the insulation period, the soap is firm enough to be removed from
the mould and cut into bars. At this time, it is safe to use the soap, since
saponification is in essence complete. However, cold-process soaps are typically
cured and hardened on a drying rack for 2-6 weeks.
9.4.5 Curing
During the curing process, some molecules in the outer layer of the solid
soap react with the carbon dioxide of the air and produce a dusty sheet of sodium
carbonate.
10.JUSTIFICATION:
In the cold process, the essential oils or fragrances can be added to the soap
if needed during trace which is not possible in the other methods. Soap heats from
the inside out while in the hot process the external heat is required to bring the soap
to the gel phase before it is placed in a soap mould.
Cold process gives more flexibility to do swirls and embeds, designs within
the soap batter before pouring into the mould. Cold process soap batter is much
thinner when it is poured into the mould but the thick texture of hot process soap
makes swirls and techniques, such as layering, very difficult. Cold process soap will
appear to look shiny and polished while the hot process soap appears rustic.
11.CHEMICAL REACTIONS:
a) Fat splitting
b) Saponification
Sodium Soap
hydroxide
12.FLOW SHEET OF SOAP MANUFACTURING PROCESS:
14.MAJOR PLANTS:
Companies City
Vasa Global Company Mumbai
Twasa Cosmetics Ahmedabad
Baldha Industries Pvt Ltd Surat
Ivory Soap Works Ltd Nashik
Hindustan Unilever Ltd Hosur
Kavit Soap Industries Ahmedabad
Spice Herbals and Pitampura
Aminities Pvt Ltd
Karnataka Soaps and Mysore and Bangalore
Detergents Ltd
The Himalaya Drug Chennai
Company
ITC Ltd Chennai
15.USES OF COCONUT OIL SOAP:
• Coconut oil soap is an excellent moisturizer for both the skin and the
hair.
• It helps remove dead skin cells and dirt away from the body.
To avoid cavitation in centrifugal pumps, the pressure of the fluid at all points
within the pump must remain above saturation pressure.The quantity used to
determine if the pressure of the liquid being pumped is adequate to avoid cavitation is
the net positive suction head(NPSH).The net positive suction head available(NPSHA)
is the difference between the pressure at the suction of the pump and the saturation
pressure for the liquid being pumped. The net positive suction head required(NPSHR)
is the minimum net positive suction head necessary to avoid cavitation.
NPSHA=Pa+Pst - hf –Psat
NPSHA=net positive suction head available
Pa= absolute pressure on the surface of the liquid
Pst=pressure due to elevation between liquid surface and pump suction
hf=head losses in the pump suction piping
Psat=saturation pressure of the liquid being pumped
18.CAVITATION:
Cavitation is a phenomenon in which rapid changes of pressure in a liquid lead
to the formation of small vapour-filled cavities, in places where the pressure is
relatively low.
19. CENTRIFUGAL PUMP CHARACTERISTIC CURVE:
20.1Basis:
20.2 Assumptions:
= 200+200+600
Mass out= Mass of Soap+ Mass of Water+ Mass of Glycerin+ Mass of Lye
= 218.2+727.3+36.4+18.1
=1000 kg/hr
=1000 kg/hr
Crude soap
Washed soap
Mass in=218.2+185.4861+33.5+9.8377
=447.0238 kg/hr
Mass out=218.03+33.4696+185.5+9.4759
=447.02 kg/hr
218.03 kg/hr of soap
Wet soap
218.03 kg/hr of soap
183.3129 kg/hr of lye
8.4696 kg /hr of water
9.4759 kg/hr of glycerin
20.7 Recycle:
Assume the value recycled and purged to be x and y. The balance for
water content is
15.0483+x = 8.4696+x+y
y = 6.5787
6.5787 kg/hr of water is purged.
Assume the water content from centrifuge to be 25 kg/hr.
x+y = 25
x = 25-6.5787
= 18.4213
The amount of water recycled is 18.4213 kg/hr. The amount of lye purged is 0.4281
kg/hr. The amount of lye recycled is 1.199 kg/hr.
20.8 Neutralizer:
Mass in=218.03+183.3129+8.4696+9.4759+61.1+0.8819
=481.2703 kg/hr
20.9 Dryer:
= 335.4307 kg/hr
Mass in=218.03+88.0506+9.4591+19.89
Mass out=218.03+88.0411+9.4693+19.8903=335.43kg/hr
Solid soap
21.ENERGY BALANCE:
Reactor in:
T=322 K
Monolaurin, ∆H=200*1.6316*(27-25)
=652.64 KJ/hr
Water, ∆H=600*(27-25)*4.1833
=5019.96 KJ/hr
Lye, ∆H=200*1.4881*(27-25) = 595.24 KJ/hr
Reactor out:
Soap,∆H=2*218.2*(49-25)
=10473.6 KJ/hr
Water,∆H=727.3*4.1833*(49-25)
=73020.34 KJ/hr
=2107.04 KJ/hr
= -13465179.81 KJ/hr
= -12734680 KJ/hr
= -730499.81 KJ/hr
Amount of Heat,Q = H0 – Hi + Hr
= 6220.16 KJ/hr
Soap,∆H = 2*(49-25)*218.2
= 10473.6 KJ/hr
Lye,∆H = 1.4881*(49-25)*200
= 7142.88 KJ/hr
Glycerin,∆H = 17.5563*(49-25)*2.4119
= 1016.26 KJ/hr
Water,∆H = 4.1833*(49-25)*33.4696
= 3360.32 KJ/hr
Total enthalpy in,Hi = 3360.32 + 7142.88 + 1016.26 + 10473.6
= 21993.06 KJ/hr
Soap,∆H = 2*(60-25)*218.03
= 15262.1 KJ/hr
Water,∆H = 4.1833*(60-25)*33.4696
= 4900.47 KJ/hr
= 32051.95 KJ/hr
21.4 Centrifuge:
21.5 Neutralizer:
=-48789.99 + 7285.13
=-41504.86 KJ/hr
=-61.42-31937.4
=-31998.82 KJ/hr
Hr = -41504.86+31998.82
= -9506.04 KJ/hr
21.6 Dryer:
Dryer in:
Soap,∆H=2*218.03*(60-25)
=15262.1KJ/hr
Water in,∆H=4.1833*35*88.0506
=12891.97KJ/hr
Salt in,∆H=35*19.8910*0.4692
=326.65KJ/hr
=798.50KJ/hr
=29279.22KJ/hr
Dryer out:
Soap out,∆H=218.03*2*(100-25)
=32704.5KJ/hr
Glycerin out,∆H=2.4119*9.4571
=1710.72KJ/hr
=(4.1833*75*77.4107+77.4107*2260)+(4.1833*75*10.6304)
=199235.59+3335.26
=202570.85KJ/hr
Salt out,∆H=0.4692*75*19.8903
=699.94KJ/hr
=237686.01KJ/hr
Amount of Heat,Q=237686.01-29279.22
=208406.79KJ/h
21.7 Condenser:
Condenser in:
Steam,∆H=(77.4107*(100-25)*1.996) + (77.4107*2676)
Water,∆H=(77.4107*(49-25)*4.1833)
= 7771.97 KJ/hr
Q = 7771.97 + 218739.42
= -210967.44 KJ/hr
210967.44 = m*4.1833*(50-20)
m = 1681.03 Kg/hr
22. ZERO DISCHARGE:
The glycerin is produced as a by-product of soap production. This glycerin
is purified and bleached. The purified glycerin is used as a main ingredient in the
cosmetics and lotions producing industries. Waste water from the soap production is
treated by several methods like dissolved air flotation or chemical coagulation-
sedimentation. The treated water is then discharged into the municipal sewage system.
29.1.2 Head:
Shallow dished head
th =PRcW/2Fj
W = 1/4 (3+(√ Rc/R1)
Rc = Crown radius
Rc = 3.6619 m
R1 = Knuckle radius
R1 = 0.2197 m
W = 1/4 ( 3+ (√ 3.6619/0.2197)
= 1.7706
th =0.1115*3.6619*103*1.7706/(2*0.85*115.14)
= 722.9393/195.738
th = 3.69 mm
29.2 DRYER:
Inlet conditions:
Temperature of soap = 60⁰C
Temperature of hot air = 160⁰C
Outlet conditions:
Temperature of soap = 100⁰C
Temperature of cold air = 90⁰C
Air stream temperature difference = ∆tG= 160-90 = 70⁰C
Avg temperature difference = ∆tm= (Air out- solid in)+(Air in- solid out)/2
= (90-60)+(160-100)/2
= 45⁰C
Number of transfer units based on air stream NtOG =∆tG/∆tm = 70/45 =1.56
For drum diameter D = 1.2 m
Area of drum = 3.14 /4 * (1.2)2
= 1.1304 m2
Feed = 335.4307 kg/hr
Dry solid = 258.02 kg/hr
Moisture content at inlet = 26.3%
X1=0.263
Moisture content at outlet = 4.1%
X2= 0.041
Inlet temperature of feed = 60⁰C = Ts1
Outlet temperature of feed = 100⁰C= Ts2
Humidity of inlet air Y2 = 0.04
Humidity of outlet Y1
Inlet air temperature = 150⁰C
Outlet air temperature= 90⁰C
Relative humidity = Actual vapor pressure/Saturation vapor pressure
Air flow rate =G
ms (X1-X2)=G(Y1-Y2)
258.02( 0.263-0.0410=G(Y1-0.04)
ms(Hs1-Hs2)=G(HG1-HG2)+Q
Hs1 = (Cpsolid *dT)+(Cpwater*X1*dT)
=( 2.496*(60-0))+(4.183.0.263*(60-0))
= 149.76+66.008
= 215.768
Hs2 = (Cpsolid*dT)+(CPwater*X2*dT)
= (2.496*(100-0))+(4.183*0.0418*(100-0)
= 249.6+17.1503 = 266.75
HG1= (Cs*dT)+(Y1*λ0)
= ((1.005+(Y1*1.884))*(90-0))+(Y1-2502.3)
= 90.45+2671.86Y1
HG2 =(Cs*dT)+(Y2*λ0)
=(1.005+(0.04*1.884))(150-0)+(0.04*2502.3)
=(1.005+0.075)*150+100.092
= 150.75+ 11.25+ 100.092
= 262.092
258.02(215.768-266.75)=G(90.45+2671.86Y1-262.092)+Q
Q = 0.1*HG2*G
= 0.1*262.092*G
Q = 26.2092G
-13154.38=G(90.45+2761.86Y1-262.092)+(26.2092G)
-13154.38= -145.43G+ 2671.86Y1
57.28= GY1-0.04G
G= 4310.62 kg/hr of air
GY1= 229.7
Y1=229.7/4310.62=0.053
Air mass flux Gs =G/3600*A
= 4310.62/(3600*1.1304)
= 1.0593 kg/m2s
Solid mass flux Ss= ms/3600*A
= 258.02/3600*1.1304
= 0.0634 kg/m2s
Y2= 0.04 kg of water/kg of dry air
Y1 = 0.053 kg of water /kg of dry air
Average humidity Yavg= (1/1+1/2)/2
= 0.0465
Average air mass flux Gavg=Gs(1+Yavg)
= 1.0593(1+0.0465)
= 1.1086 kg/m2s
Heat transfer coefficient of the dryer Ua=237*(Gavg)0.67/D
Ua = 237*(1.1086)0.67/1.2 =211.62 W/m2k
Average humid heat Cs= Cs1+Cs2/2
Cs1= 1.005+1.884(Y2)
= 1.0804
Cs2= 1.005+1.884(Y1)
= 1.1049
Cs= 1.0804+1.1049/2
= 1.0927 KJ/kg K
HtOG= CsGs/Ua
= 1.0593*1.0927/211.62
= 5.4697m
Z = HtOG*NtOG
= 5.469*1
Z = 5.5 = 6 m
Power requirement = 0.3*π/4*D2*Z
= 0.3*3.14*(1.2)2*6/2
= 4.07 KW
Hold up ϕD = 0.05
k = 0.6085/ρsdP1/2
ρs= 976.4 kg/m3
Diameter of pellets,dP = 5mm
Correction factor k= 0.6085/(5*10-3)1/2*976.4
= 0.6085/69.0419
= 0.0088
Hold up with no flow ϕDO= ϕD-(k*Gavg)
= 0.05 –(0.0088*1.1086)
= 0.0402
Speed of dryer, N= 10 rpm
= 0.1667r/s
29.2.1 Shell Thickness:
ts= PDs/2Fj-P
Working pressure P= 0.05atm
Design pressure = 1.1*0.05
= 0.0051 N/mm2
Material of construction : Stainless steel
f = 115.14 N/mm2
Ds=1.2 m
J=0.85
ts = 0.0051*1.2*103/(2*115.14*0.85-0.0051)
= 0.031 mm
PITCH ANGLE:
Angle for pinion,Ө = tan-1(1/Velocity ratio)
= tan-1 (1/ 2.14)
= 25.05
Angle for gear,Ө = 90-25.05
= 64.95
29.3 CONDENSER:
29.3.1 Shell side:
Material of construction = carbon steel
Corrosion allowance = 3mm
Number of shells = 1
Number of pass = 1
Working pressure = 0.1 N/mm2
Design pressure = 1.5 * working pressure
= 0.1*1.5
= 0.15 N/mm2
Temperature inlet = 20⁰C
Temperature outlet = 50⁰C
29.3.2 Head:
Crown radius = 566.96 mm
Gasket= flat metal jacketed asbestos filled
Bolts = Steel
29.3.3 Nozzle:
Inlet & outlet =75 mm
Vent = 25 mm
Opening for relief values = 50 mm
Permissible stress for carbon steel = 95 N/mm2
Permissible stress for steel = 140.6 N/mm2
29.3.6 Nozzle:
Thickness of nozzle = (PD/2fJ-P) + C
= 0.15*75/(2*0.85*95-0.15)+3
= 3.07 mm
= 4 mm
29.3.7 Head:
Torispherical head
Head Thickness ,th = PRcW/2fJ +C
Stress intensification factor ,W =1/4 (3+√Rc/R1)
Rc = 566.96 mm
R1 = 5* ts= 5*8
= 40 mm
W = 1/4(3+√566.96/40)
= 1.69
th = (0.15*566.96*1.69/2*95*0.85)+3
= 3.89 mm
Head thickness = 8 mm
29.3.8 Baffles:
Baffle type = Transverse
Baffle spacing = Ds/5 = 566.96/5
= 113.4 mm
Assuming baffle thickness = 6mm
Baffle cut = 45%
Baffle length = 0.55*566.96
= 311.83 mm
Number of baffles = 8
Flange thickness
tf = G√(P/kf)+C
k = 1/(0.3+(1.5*WmhG/HG))
Wm = 4.15*105N
hG = 525-380/2
= 72.5 mm
H = π G2P/4
= 3.14*380*380*0.5/4
= 0.57*105 N
G = 380 mm
k = 1/(0.3+(1.5*4.15*105 *72.5/380*56677)
= 380*0.1088
= 41.34 mm
tf = 42 mm
29.4.1 Shell:
P = ρ (H-0.3)*9.807*10-6 N/mm2
= 1000( 5- 0.3)*9.807*10-6
= 0.0461 N/mm2
t =( PD/2fJ)+C
= (0.0461*10000/(2*165*0.85))+1.5
= (461/280.5)+1.5
t = 3.14 mm
Assume thickness to be 1 mm
P = 2tfJ/D
= 2*1*165*0.85/10*103
= 0.0281 N/mm2
H = (P/ρwater*9.807*10-6)+ 0.3
= (0.0281/1000*9.807*10-6)+ 0.3
H =3.17 m
Assumed thickness to be 0.5 mm
P =2*0.5*165*0.85/(10*103)
P = 0.014 N/mm2
H = (0.014/(1000*9.807*10-6))+0.3
= 1.73 m
Assume thickness to be 0.2 mm
P = 2*0.2*165*0.85/(10*103)
= 0.0056 N/mm2
H = (0.0056/1000*9.807*10-6)+0.3
= 0.87 m
The slope is within acceptable limit for a thickness of 12 mm. Hence self-supporting roof
is not recommended to use.
In this case,a column support type roof is used.
PRINCIPLE:
The centrifugal pump works on the principle of forced vortex flow which means that
when a certain mass of liquid is rotated by an external torque,the rise in pressure head of
the rotating liquid takes place.The rise in pressure head at any point of the rotating
liquid is proportional to the square of tangential velocity of the liquid at the point.
WORKING:
If the mechanical energy is converted into pressure energy by means of centrifugal force
acting on the fluid,then the hydraulic machine is called “Centrifugal Pump”.
The Centrifugal Pump acts as a reversed of an inward radial flow reaction turbine.This
means that the flow in centrifugal pumps is in the radial outward directions.
At outlet of the impeller the radius is more,the rise in pressure head will be more and the
liquid will be discharged at the outlet with a high pressure head.Due to this high pressure
head,the liquid can be lifted to a high level. There are large quantities of centrifugal
pumps associated with the catalytic cracker,most of them being conventional single-stage
and multistage units in cold and hot service.
CONSTRUCTION:
Type-Vertically split overhung or between bearing pumps,flow serve type.
Head-Since the pressure differential between the fractionator and reactor is low.
Operating Speed- 1180 to 1750 RPM range to reduce erosion of the catalyst in the slurry .
Furnishing-With chrome cases and impellers-Because of the temperature and sulfide
environment.
In addition,clean flushing oil is supplied to the wear rings,throat bushingsand
packing,through specially designed connection,to reduce erosion in wearing parts.
APPLICATION:
One special application that mertis consideration is the fractionator bottoms pumps,which
recycle the slurry oil form the fractionator back to the reactor feed system.
The slurry oil consists of a mixture of the heavy oil in the bottom of the fractionator and
catalyst particles that carry over from the reactor into the fractionator.
The slurry oil pumps are special units built to withstand the erosive action of the catalyst
powder suspended in the air.
They usually handle large quantities of 600 to 700⁰F oil – quantities in the range of 500 to
1000 gpm and are the vertically split overhung or between bearing pumps,Flowserve
type.
The fractionator gas oil pumps and light, heavy and extra-heavy gas oil, are all heavy-
duty
Refinery type units with low NPSH requirements, high temperature and high head
applications.
30.2 ROTARY LOBE PUMP:
WORKING:
Lobe pumps are similar to external gear pumps in operation in that fluid flows around the
interior of the casing.Unlike external gear pumps,however,the lobes do not make
contact.Pump shaft support bearing are out of the pumped liquid,pressure is limited by
bearing location and shaft deflection.
1)As the lobes come out of mesh,they create expanding volume on the inlet side of the
pump.Liquid flows into the cavity and is trapped by the lobes as they rotate.
2)Liquid travels around the interior of the casing in the pockets around the interior of the
casing in the pockets between the lobes and the casing-it does not pass between the lobes.
3)Finally the meshing of the lobes forces liquid through the outlet port under pressure.
MATERIALS OF CONSTRUCTION/CONFIGURATION OPTIONS:
Externals (head,casing) – Typically 316 or 316L stainless steel head and casing
Internals (rotors,shaft) – Typically 316 or 316L stain less steel, non-galling stainless steel
APPLICATIONS:
➢ Polymers
➢ Paper coatings
➢ Food application
ADVANTAGES:
➢ No metal-to-metal contact
DISADVANTAGES:
31.1 CENTRIFUGE:
2)Pipe
rupture
3)Pipe 2)Maintenance
leakage of pipes
31.2 REACTOR:
3) Control
valves fail to 3) Diminished
respond cooling
31.3 CONDENSER:
Table 31.3.1 HAZOP Analysis of Condenser
Improper mixing
Failure in
timer Less power
supply
Failure in temperature
Measuring device Improper supply of
cooling water