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Commercial Production of Nitric Acid
By
Mr. Muhammad Ullah Afridi
Institute of Chemical Sciences, University of Peshawar.
INTRODUCTION
 Nitric acid (HNO3). A colorless liquid that is used in the
manufacture of inorganic and organic nitrates and nitro
compounds for fertilizers, dye intermediates, explosives,
and many different organic chemicals. Continued
exposure to vapor may cause chronic bronchitis;
chemical pneumonitis may occur.
 NITRIC ACID, RED FUMING is a pale yellow to
reddish brown liquid generating red-brown fumes and
having a suffocating odor. Very toxic by inhalation.
Corrosive to metals and tissues.
PHYSICAL PROPERTIES
 Appearance: Colorless, yellow or red
 Odor:
 Density
:
Acrid, suffocating
1.5129 g cm−3
 Melting point:
 Boiling point:
 Solubility :
 Vapor pressure:
−42 °C (231 K)
83 °C (356 K)
Completely miscible in water
48 mmHg (20 °C)
STRUCTURE
CHEMICAL PROPERTIES
 Stability : Pure nitric acid is not very stable. Even at ordinary temp. in presence of
sunlight it undergoes slight decomposition.
4 HNO3 → 2 H2O + 4 NO2 + O2.
 Oxidizing properties: Nitric acid is a strong oxidizing agent as shown
by its large positive E◦ values.
NO3- (aq) + 2H+ (aq) e- → NO2 (g) + H2O (l) E◦ = 0.79 V
NO3- (aq) + 4H+ + 3e- → NO (g) 2H2 (l) E◦ = 0.96 V
CHEMICAL PROPERTIES
 Reactions with metals: Nitric acid dissolves most metals including iron, copper,
and silver, with generally the liberation of lower oxides of nitrogen rather than
hydrogen. It can also dissolve the noble metals with the addition of hydrochloric
acid.
Cu + 4HNO3 → Cu(NO3)2 + 2NO2 + 2H2O
 Reactions with nonmetals: Reaction with non-metallic elements, with the
exception of silicon and halogen, usually oxidizes them to their highest oxidation
states as acids with the formation of nitrogen dioxide for concentrated acid and
nitrogen oxide for dilute acid.
C + 4HNO3 → CO2 + 4NO2 + 2H2O
MANUFACTURING OF NITRIC ACID
INDUSTRIALLY NITRIC ACID IS PREPARED BY
FOLLOWING THREE (3) METHODS:
 CHILE SALTPETRE METHOD BY NANO3
 BRIKLAND EYDE’S METHOD BY USINGAIR
 OSTWALD’S METHOD BY AMMONIA SOLVEY PROCESS
CHILE SALTPETRE METHOD (BY NANO3)
 It is the first commercial process of manufacture of nitric acid from sodium
nitrate extracted
 from Chile saltpeter. The process is now become obsolete since second decade
of nineteenth century.
 Raw Materials:
 Sodium Nitrate
 Sulfuric acid
 Process:
Equal weight of sodium nitrate (or potassium nitrate) and sulfuric
acid is charged to cast iron retort having outlet provided at bottom to
take out solution of sodium bisulfate.
The reactants are heated to about 2000 0C by the hot furnace gases.
The furnace gases are produced by combustion of coal in the
furnace.
Then the vapors of nitric acid are cooled and condensed in water
cooled silica pipes.
Process:
 The cooled acid is collected in stoneware receiver. The un-condensed vapours are
scrubbed with water in absorption tower which is packed with stone ware balls and
cooled by cold water.
 The dilute acid is re-circulated till it becomes concentrated. The residual sodium
bisulfate is removed by outlet provided at the bottom of retort.
Reaction:
NaNO3 + H2SO4 → NaHSO4 + HNO3
BRIKLAND EYDE’S METHOD (ARC PROCESS)
 Raw materials
o Air
o Water
o Carbon dioxide
BRIKLAND EYDE’S METHOD (ARC PROCESS)
 Process:
 CO2 and dust free air is heated in an arc furnace at 3000 o C.
 Nitric oxide is formed. Gases coming out from the furnace are
cooled at 1000 oC by passing through cooler then gases are passed
in a boiler and cooled at 150o C.
 Cold water is circulated around the boiler to cool the gases.
Gaseous mixture is now passed through aluminum tubes. The
temperature of gaseous mixture becomes 50oC.
 Gaseous mixture is passed in oxidizing tower where NO is oxidized into
No2.
2NO + O2 ——–> 2NO2
 NO2 is absorbed in water in absorption tower then dilute HNO3 is obtained.
3NO2 + H2O ——-> 2 HNO3 + NO
 Now HNO3 is not manufactured by this method because consumption of electricity
is very high to maintain the temperature 3000 o C. Even at this temperature 1%
NO is formed (Disadvantage).
OSTWALD’S METHOD
Principle:
 NH3 is oxidized into NO by air at 800 oC in the presence of Pt (Platinum)
catalyst.
 Raw Materials:
 Ammonia
 Air
 Platinum
 Water
 Steam
 Power
PROCESS
 Mixture of NH3 and O2 in the ratio of 1:9 is passed through catalyst chamber
containing Pt- gauge. Temperature of the catalyst is kept at 800 oC.About 95 % NH3
is converted into NO.
4NH3 + 5 O2 ——–> 4NO + 6 H2O + 21.6 K.Calorie
 Heat liberated maintains the temperature of the catalyst. The gases coming outare
cooled to about 50 oC and mixed with more O2. This gaseous mixture is passed in
oxidizing tower where NO is oxidized to NO2.
2NO + O2 ——> 2NO2
 NO2 is passed in absorption tower. The dilute solution of HNO3 is obtained.
3NO2 + H2O ——> 2HNO3 + NO
NITRIC ACID SAFETY AND
HANDLING:
Nitric Acid is an extremely corrosive acid capable of causing
severe chemical burns very rapidly.
When handling Nitric Acid in the workplace, it is highly
recommended to wear:
 Chemical Safety Glasses.
 Face shield.
 Gloves
As an added safety precaution, eyewash station and
washing stations should be easily accessible incase of
exposure to nitric acid.
APPLICATIONS
 As a starting material in the manufacture of nitrogen fertilizers such as
ammonium nitrate & ammonium etc. Large amounts are reacted with ammonia to
yield ammonium nitrate.
 It is commonly used in science laboratories at schools for experimenting when
specifically testing for chloride
 As a nitrating agent in the preparation of explosives such as TNT, nitroglycerine,
cellulose poly-nitrate, ammonium picrate.
 It is used as a medicine to remove chancres and warts.
 Used in fibers, plastics and dyestuffs industries
 Used in metallurgy and in rocket fuel production.
 It is used in calorimetric test to distinguish between heroin andmorphine.
THANK YOU
FOR
PAYING ATTENTION

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Nitric acid preparation

  • 1.
  • 2. Commercial Production of Nitric Acid By Mr. Muhammad Ullah Afridi Institute of Chemical Sciences, University of Peshawar.
  • 3. INTRODUCTION  Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur.  NITRIC ACID, RED FUMING is a pale yellow to reddish brown liquid generating red-brown fumes and having a suffocating odor. Very toxic by inhalation. Corrosive to metals and tissues.
  • 4. PHYSICAL PROPERTIES  Appearance: Colorless, yellow or red  Odor:  Density : Acrid, suffocating 1.5129 g cm−3  Melting point:  Boiling point:  Solubility :  Vapor pressure: −42 °C (231 K) 83 °C (356 K) Completely miscible in water 48 mmHg (20 °C) STRUCTURE
  • 5. CHEMICAL PROPERTIES  Stability : Pure nitric acid is not very stable. Even at ordinary temp. in presence of sunlight it undergoes slight decomposition. 4 HNO3 → 2 H2O + 4 NO2 + O2.  Oxidizing properties: Nitric acid is a strong oxidizing agent as shown by its large positive E◦ values. NO3- (aq) + 2H+ (aq) e- → NO2 (g) + H2O (l) E◦ = 0.79 V NO3- (aq) + 4H+ + 3e- → NO (g) 2H2 (l) E◦ = 0.96 V
  • 6. CHEMICAL PROPERTIES  Reactions with metals: Nitric acid dissolves most metals including iron, copper, and silver, with generally the liberation of lower oxides of nitrogen rather than hydrogen. It can also dissolve the noble metals with the addition of hydrochloric acid. Cu + 4HNO3 → Cu(NO3)2 + 2NO2 + 2H2O  Reactions with nonmetals: Reaction with non-metallic elements, with the exception of silicon and halogen, usually oxidizes them to their highest oxidation states as acids with the formation of nitrogen dioxide for concentrated acid and nitrogen oxide for dilute acid. C + 4HNO3 → CO2 + 4NO2 + 2H2O
  • 7. MANUFACTURING OF NITRIC ACID INDUSTRIALLY NITRIC ACID IS PREPARED BY FOLLOWING THREE (3) METHODS:  CHILE SALTPETRE METHOD BY NANO3  BRIKLAND EYDE’S METHOD BY USINGAIR  OSTWALD’S METHOD BY AMMONIA SOLVEY PROCESS
  • 8. CHILE SALTPETRE METHOD (BY NANO3)  It is the first commercial process of manufacture of nitric acid from sodium nitrate extracted  from Chile saltpeter. The process is now become obsolete since second decade of nineteenth century.  Raw Materials:  Sodium Nitrate  Sulfuric acid
  • 9.  Process: Equal weight of sodium nitrate (or potassium nitrate) and sulfuric acid is charged to cast iron retort having outlet provided at bottom to take out solution of sodium bisulfate. The reactants are heated to about 2000 0C by the hot furnace gases. The furnace gases are produced by combustion of coal in the furnace. Then the vapors of nitric acid are cooled and condensed in water cooled silica pipes.
  • 10. Process:  The cooled acid is collected in stoneware receiver. The un-condensed vapours are scrubbed with water in absorption tower which is packed with stone ware balls and cooled by cold water.  The dilute acid is re-circulated till it becomes concentrated. The residual sodium bisulfate is removed by outlet provided at the bottom of retort. Reaction: NaNO3 + H2SO4 → NaHSO4 + HNO3
  • 11.
  • 12. BRIKLAND EYDE’S METHOD (ARC PROCESS)  Raw materials o Air o Water o Carbon dioxide
  • 13. BRIKLAND EYDE’S METHOD (ARC PROCESS)  Process:  CO2 and dust free air is heated in an arc furnace at 3000 o C.  Nitric oxide is formed. Gases coming out from the furnace are cooled at 1000 oC by passing through cooler then gases are passed in a boiler and cooled at 150o C.  Cold water is circulated around the boiler to cool the gases. Gaseous mixture is now passed through aluminum tubes. The temperature of gaseous mixture becomes 50oC.
  • 14.  Gaseous mixture is passed in oxidizing tower where NO is oxidized into No2. 2NO + O2 ——–> 2NO2  NO2 is absorbed in water in absorption tower then dilute HNO3 is obtained. 3NO2 + H2O ——-> 2 HNO3 + NO  Now HNO3 is not manufactured by this method because consumption of electricity is very high to maintain the temperature 3000 o C. Even at this temperature 1% NO is formed (Disadvantage).
  • 15.
  • 16. OSTWALD’S METHOD Principle:  NH3 is oxidized into NO by air at 800 oC in the presence of Pt (Platinum) catalyst.  Raw Materials:  Ammonia  Air  Platinum  Water  Steam  Power
  • 17. PROCESS  Mixture of NH3 and O2 in the ratio of 1:9 is passed through catalyst chamber containing Pt- gauge. Temperature of the catalyst is kept at 800 oC.About 95 % NH3 is converted into NO. 4NH3 + 5 O2 ——–> 4NO + 6 H2O + 21.6 K.Calorie  Heat liberated maintains the temperature of the catalyst. The gases coming outare cooled to about 50 oC and mixed with more O2. This gaseous mixture is passed in oxidizing tower where NO is oxidized to NO2. 2NO + O2 ——> 2NO2  NO2 is passed in absorption tower. The dilute solution of HNO3 is obtained. 3NO2 + H2O ——> 2HNO3 + NO
  • 18.
  • 19. NITRIC ACID SAFETY AND HANDLING: Nitric Acid is an extremely corrosive acid capable of causing severe chemical burns very rapidly. When handling Nitric Acid in the workplace, it is highly recommended to wear:  Chemical Safety Glasses.  Face shield.  Gloves As an added safety precaution, eyewash station and washing stations should be easily accessible incase of exposure to nitric acid.
  • 20. APPLICATIONS  As a starting material in the manufacture of nitrogen fertilizers such as ammonium nitrate & ammonium etc. Large amounts are reacted with ammonia to yield ammonium nitrate.  It is commonly used in science laboratories at schools for experimenting when specifically testing for chloride  As a nitrating agent in the preparation of explosives such as TNT, nitroglycerine, cellulose poly-nitrate, ammonium picrate.  It is used as a medicine to remove chancres and warts.  Used in fibers, plastics and dyestuffs industries  Used in metallurgy and in rocket fuel production.  It is used in calorimetric test to distinguish between heroin andmorphine.