Chapter-1 Natural Products Industries: (In Cognitive Domain)

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NATURAL PRODUCT INDUSTRIES 2018-2019

CHAPTER-1

NATURAL PRODUCTS INDUSTRIES

Unit-no Major Learning Outcomes Topics and Sub-topics


and (in cognitive domain)
Name

1a. Define oil and fat 1.1 Basics of oil and fat

1b. Describe physical properties of oil 1.2 Physical properties of oil

1c. Describe carbohydrates 1.3 Introduction to Carbohydrates

1d. Draw flow diagram explain


Chapter-1 manufacturing process of 1.4 Manufacturing Process of
Natural (i)Vegetable oil (i) Vegetable oil
Product (ii) Hydrogenated products of oil (ii) Hydrogenated products of oil
Industries (iii) Sugar from sugar-cane (iii) Sugar from sugar-cane
(iv) Starch from maize (iv) Starch from maize
(v) Dextrin from starch (v) Dextrin from starch
1e. Distinguish chemicals available from 1.5 Chemicals from sea
the sea

1f. Draw flow diagram describes 1.6 Production of bromine from sea
manufacturing process of bromine from water
sea water.

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Oil and Fat:


Define:
 Oils and fats are organic molecule of carbon, hydrogen, oxygen and sometimes nitrogen
and sulphur.
 Fats and oils are called triglycerides because they are esters composed of three fatty
acid units joined to glycerol (tri-hydroxy alcohol)

 Fat: A triglyceride is called a fat if it is solid at room temperature 25°C


 Oil: A triglyceride is called a Oil if it is liquid at room temperature 25°C
 The main difference between fats and oils are that composed of high amount of
saturated fatty acids which will take a solid from at room temperature where oils are
composed of mainly unsaturated fatty acids which will take a liquid form at room
temperature.

Physical Properties:
1. Oils and fats are liquids or solids having a greasy feel. When pure, they are colourless,
odourless and tasteless.
2. They are insoluble in water but soluble in organic solvents such as ether, chloroform and
benzene.
3. They have a lower density than water and consequently float on the surface when mixed
with water.
4. Do not pass through membranes.

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Difference between fats and Oils:


Fats Oils
Fats are solid at room temperature. Oils are liquid at room temperature.
Fats are saturated compounds. Oils are unsaturated compounds.
Fats have high boiling point and high Oils have lower boiling point
melting point
Fats are obtained from animals Oils are obtained from Plants & Marine animals
No double bond Have double bond

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Q- Manufacturing Process of Vegetable oil.


 Raw material
 Seeds of oilseed plant

 Process Flow Sheet

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 Functional Role of Various Processes

(a) Cleaner and Dehulling:

 Mechanical cleaning is done to remove stones and other undesirable material.

 Dehulling remove hulls, dry outer covering of seed.

(b) Cracking rolls:

 Crushing rolls crush the oil seeds and gets flacked seeds.
(c) Digester:

 100 parts of flaked seeds are thoroughly mixed with 5-10 parts of water by rotating
blades.

 Softening by means of heat and moisture is done here.

 Steam is added for heating purpose.

 Acid is formed by hydrolysis of ester.

 The seeds get swollen up.

(d) Expeller:

 The swollen seeds are crushed under great pressure.

 Cells of seeds get ruptured and oil is released.

 The tapering shape ensures more application of pressure on the seeds

 The oil depleted cake is either sent for solvent extraction or used as animal feed.

 Oil is sent for purification.

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(e) Mix tank:

 The extracted oil is treated with alkali like NaOH or Na2CO3 to remove fatty acids.

 It also removes heavy metals, which can start oxidation of oil.

(f) Centrifuge:

 Acids are separated in centrifuge separator.

 These separated acids are used as foots for soap manufacturing.

(g) Rotary filter:

 The clear oil is treated with some bleaching agent like”Fullers Earth Carbon” in filter aid
before rotary filter.

 Rotary drum filter is used for removal of seed particles which may be present.

 This finished oil is produced.

 From this process around 1-2% oil content remains in the meal.
(h) Extractor:

 The flaked seeds or oil extracted seeds from crushing rolls are fed on a moving bed.

 Oil depleted cake is also added in extractor.

 The solvent extracts oil from the seeds.

 The wet meal (the left seed part) is collected in the middle and is sent for solvent
removal.

(i) Solvent removal:

 Steam is used to extract solvent carried by the oil seeds.

 The rotating blades ensure better exposure to steam.

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 The solvent free meal is sent to dryer and then used as animal feed.

 Solvent is collected from top and is recycled after cooling it in heat exchanger.

(j) Flash film evaporator:

 The solvent is preheated by steam.

 Oil is concentrated here by evaporating the more volatile component (hexane).

 The hexane is recycled back to extractor after heat recovery.

 The use of flash evaporator reduces the cost of vacuum stripping column.

(k) Vacuum stripping column:

 The oil from flash evaporator is fed here.

 The stripping is done by steam i.e. steam carries away the hexane.

 And it is under vacuum for the reason that the boiling point of hexane and oil are close
to each other.

 Jet ejector is used here to generate vacuum.

 The hexane is recycled again.

 Oil produced here is either directly used or sent for purification.

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Q- Hydrogenated Products of Oil


 Hydrogenation process is used to remove double bonds and to make fats and oil
saturated.
 Hydrogenation also raises its melting point and improves its resistance to rancid
oxidation.
 The most common end product of hydrogenation is Vanaspati ghee.
 Other products include vegetable ghee, hardened industrial oils and partially
hydrogenated liquid oil.

 Raw material:
 Oils which is to be saturated and pure hydrogen.

 Chemical Reactions: (* indicates activated catalytic state) Ni* catalyst


(a) Hydrogenation process

R1(C=C)x R2 + (x-y)H2 → R1(C=C)y R2


(b) Nickel catalyst preparation: 190˚C

Ni(HCOO)2.2H2O Ni* + 2CO2 + H2 + 2H2O

 This produces a finely divided catalyst which is preferred for well-stirred hydrogenation
reactors.
(c) Nickel catalyst preparation (reduced Ni on inert catalyst support) \

Ni(OH)2 + H2 → Ni* + 2H2O


NiCO3 + H2 →Ni* + H2O + CO2
 Nickel salts are precipitated on inert porous carrier such as kieselguhr or diatomaceous
earth and reduced at high temperature in a hydrogen atmosphere.

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(d) Nickel catalyst preparation

2Al.Ni + 6NaOH Ni* + 2NaAlO 3 + 3H2


 Alloy Raney nickel Produces spongy, high-surface area catalyst when the sodium
aluminate is washed with water.

 Process Flow Sheet

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 Functional Role of Various Processes

(a) Hydrogenator:

 Oil is fed to the hydrogenator.

 Hydrogen, and steam is introduced in it.

 The catalyst oil slurry of concentration 5 to 15 kg per ton of oil is also put.

 The reaction is slightly exothermic so steam is sometimes turned off.

(b) Deodorizer:

 The hydrogenated oil is now fed to vacuum steam deodorizer.

 It operates in continuous basis.

(c) Finishing

 Oil colour is removed by treating with fuller’s earth or carbon.

 It is then filtered, mixed with some vitamins.

 Now the finished oil is sent for packaging and storage.

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Q- Manufacturing Process Sugar from Sugar-Cane


 Introduction
 Sucrose is a disaccharide that occurs naturally in most fruits and vegetables. Sugar
occurs in greatest quantities in sugarcane and sugar beets from which sugar is separated
economically and commercially.
 Chemical formula – C 12H22O11.
 Sucrose is soluble in water but slightly soluble in methyl alcohol and ethyl alcohol.
 Raw material:
 Sugar cane , Water, SO 2 , Lime, CaHPO 4

 Functional Role of Various Processes


(A). Cutter

 The cutter consists of knives on a cylindrical shaft which rotate at a velocity of 400 to
500 rpm.

 The knives cut the canes into small pieces.

(B) Crusher

 Canes are shredded here.

 It consists of two rollers rotating in opposite direction.

(C) Series of Pressure mills

 Crushed canes are passed through four pressure mills to extract juice.

 Each pressure mill is made up of cast iron rolls.

 Rolls are grooved and the width decreases from first roll to the last.

 Make up water added in the third and fourth mill is recycled back to the first two mills.

 About 85-90% of juice present in cane is extracted.

 Bagasses are produced as byproduct.

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 Process Flow Sheet:

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(D) Clarifier

 In general two methods of clarification are available for the manufacture of white sugar,
namely, Sulfitation process and Carbonation process.

 The juice now comes to thickener.

 To precipitate the colloids, calcium phosphate(CaHPO4) is added followed by milk of


lime.

 The milk of lime used has 9 to 10% strength and about 400mg CaO/litre alkalinity.

 Apart from maintaining pH about 7, SO2 gas also acts as a bleaching agent.

 Phosphoric acid or CO2 can also be substituted as acidifying agent depending upon the
type of extracted juice.

 At the bottom of clarifier, mud (impurities) are settled and drained.

 Steam is used to slightly heat the juice.

(E) Rotary filter

 The underflow mud from the bottom of thickener is passed to a continuous rotary filter
press to recover sugar solution.

 This sugar solution if it is clear, is passed to multieffect evaporator or otherwise recycled


back to clarifier.

 The filter cake produced is used for fertilizer.


(F) Multieffect evaporator

 The clarified liquor overflows to the 3-4 forward feed Multieffect evaporator.

 Here juice is concentrated from 80-85% H2O to 40% H2O to make juice ready for
crystallization.

 A vacuum of 63cm is maintained in the last effect.

(G)Crystallizer

 The clarified concentrated sugar solution comes to crystallizer.

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 The sugar solution is further boiled in vacuum pans at vapor temperature of 57˚C until
fine cloud of crystals is seen.

 Crystallization is completed in vacuum pan unit.

(H) Centrifuge

 The mixture of crystals and syrup is called masscuite.

 The masscuite from crystallizer is centrifuged in basket type centrifuged to basket type
to centrifuge remove mother liquor (molasses) which is a by-product.

 The high grade sugar crystals are obtained here.

 The centrifuge speed is maintained at 800 to 1000 rpm.

Q- Manufacturing Process Starch from maize


 Introduction
 Starch consists of a chain of D-glucopyranosyl units.
 It is used in the manufacture of textiles, paper, adhesives, insecticides, paints, soaps,
explosives, and derivatives as dextrins, nitro starch and corn sugar. Chemical
formula- C 6H10O5
 Starch gets hydrolysed by acids, alkalis and enzymes giving dextrin, dextrose. Starch
forms gels with water within several minutes at 60-80˚C.
 The major source of starch is maize kernels.

 Raw Materials

 Maize, Air, Water

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Process Flow Sheet:

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 Functional Role of Various Processes


(a) Air cleaner:-

 At first, maize kernel containing 60-65% starch is introduced in air cleaner.

 Air is passed through the bottom of cleaner.

(b) Steeped tank:-

 Air cleaned maize kernel is passed to steeped tank to make it soft.

 50-55˚C water and 0.15-0.3% SO2 is added.

 Here SO2 acts as a bacteriostatic.

 Steeping is done to yield high production and quality of starch.

 The residence time is 40-50 hours.

(c) Grinding mill:-

 The soft grains are passed through coarse grinding mill to rupture the cells.

 The floating germ oil from the tank is removed.

(d) Buhrstone mill:-

 The kernel is then wet ground in buhrstone mill.

 This mill completely disrupts the cells of endosperm and release starch granules.

(e) Nylon screen:

 The wet ground kernel is then passed through nylon cloth.

 Water washes the starch through the screens.

 The fibre and hulls is left over on the nylon screen.

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(f) Two stage centrifuge:

 The gluten is water insoluble protein.

 Gluten is a light fraction which is separated in two-stage centrifuge.

(g) Rotary filter:

 Water starch mixture is then passed then passed to continuous rotary filter.

 Starch is separated as filter cake which is of yellow colored and contains high amounts
of protein.

 Other products can also be made by hydrolysis of starch.

(h) Dryer:

 Starch as filter cake is dried and powdered in dryer with the introduction of steam in
dryer and produced as pearl starch.

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Q- Manufacturing Process Dextrin from Starch


 Introduction
 Heating and acid depolymerisation of starch yields a water soluble carbohydrate gum
which is known as dextrin used in adhesives and gum.

 Raw Materials
1. Starch 2. HCL Vapour 3. Air

 Chemical Reaction
(C 6H10O5 )n (C6H10O5 )x

 Process flow sheet:

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 Process Description
 A batch operation charges 5-10 µ starch to an air suspended fluidizer.
 Heat is added via rectangular-shaped plate coils, using steam,in the upper section of
fluidizer.
 The charges reaches 65-170 °C, depending on the degree of hydrolysis desired, within
30 minutes.
 HCL vapour is introduced into the recirculating air stream and depolymerisation
continued for 1-8 hours.
 The reaction can be stopped by ammonia addition and/or by using H2O in plate- coil
exchangers.
 Starch agglomerates during hydrolysis, so allowing fluidisation without excessive carry
over of fines.

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Chemicals from Sea


 Ocean covers over 70% of the earth surface.
 The sea is still our important source of food but it is also a dumping ground for sewage,
radioactive wastes and a supplier of raw materials for a host of chemical industries.
 The oceans contains on an average about 35 parts per 1000 dissolved salts.
 Major salts can be found from sea are
1. Chlorine,
2. Sodium
3. Magnesium,
4. Sulfur,
5. Calcium,
6. Potassium,
7. Bromine,
8. Carbon,
9. Oxygen,
10. Strontium,
11. Boron,
12. Silicon,
13. Flourine,
14. Nitrogen, P
15. Phosphorous,
16. Iodine.
 The important commercial products obtained from sea water are common salt,
magnesium compounds, potassium compounds and bromine are extracted from sea
beaches.
 Phosphorite and calcareous deposits from the continental shelves.
 Oil, gas, sulphur, coal and iron are extracted from the subsea floor rocks.
 While clays, manganese, and calcareous oozes extracted from the deep sea floor.

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Q- Production of Bromine from Sea Water

 Bromine is a dark red, low boiling and high density liquid.


 It have intensely irritating odour and it is very reactive chemical.
 It belongs to halogen group of elements.
 In sea water bromine occurs in concentrations between 60-70 ppm.
 Most of bromine is converted into inorganic and organic compounds.
Uses:
 Bromine is used in many area such as Agricultural chemicals, Dye stuffs, Insecticides,
Pharmaceuticals and chemical intermediates
 Ethylene di-bromide and methyl bromide are used for fumigation of food grains, fruits,
seeds, and soil.
 They also used as anti knock fluids in aviation petrol.
 Bromine is also used in the preparation of fire extinguishing compounds and fire
proofing agents and dyes.
 Bromine Compound can be used as flame retardants.
 Bromine in small dosage (1 ppm) sterilizes water in swimming pools.

 Raw Materials
Sea water, Cl2, Air, SO 2, H2O

 Chemical Reactions

Cl2 + 2 Br- → 2Cl- + Br2

SO2 + Br2 + H2O → 2HBr + H2SO4

2HBr + Cl2 → 2HCl + Br2

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 Process Flow Sheet:

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 Process Description

1. Blow Out Tower


 The process involves oxidation of bromine ions of or brine to free elemental bromine .
 This bromine is vaporised by air or steam.
 When sea water is used bromine is first concentrated by vaporising chlorinated sea
water with air.
2. HBr Absorption Tower
 SO2 is introduced into dilute bromine laden air and is sent to absorption tower counter
current to water.
3. Steaming Out Tower
 The resulting hydrobromic acid solution from HBr absorption tower is chlorinated and is
steamed to vaporise Br2 .
 By products HCl & H2SO4 are used to acidify the incoming sea water.

4. Condenser
 Br2 vapour from Steaming out tower is condensed to liquid bromine.

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