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 INTRODUCTION
 PRODUCTION
 PROPERTIES
 USES
 MANUFATURING PROCESS
 ADVANTAGES DISADVANTAGES
 WASTE MANAGEMENT
 SAFTEY
 sulphuric acid is a colourless dense oily corrosive
liquid produced by the reaction of sulphur trioxide
with water and used in accumulators and in the
manufacture of fertilizers, dyes, and explosives.
Formula: H2SO4
9th century: Islamic physician and alchemsit Ibn Zakariya
al-Razi – discovered dry distillation of vitriol (al-zajat), and
alcohol(ethanol).
17th century: German-Dutch chemist Johann
Glauber – burned sulphur with
saltpeter (potassium nitrate - KNO3)
18th century: Joseph Gay-Lussac, John Glover –
lead chamber process
19th century: Peregrine Phillips – contact process
Geometrical Shape : Tetrahedral
Bond angle : 109.5
 King of compounds
 Oil of vitriol
 Dipping acid
 Battery acid
 Electrolyte acid
 Mattling acid
 Dihydrogen sulphate
Sulphuric acid acts as a catalyst in the
following reactions:
C1 2H22O11 + H2SO4 12C + 11H2O
The dehydrating ability of sulfuric acid is
often utilised in laboratories to dry gas
mixtures that are being prepared or
analysed.
75% of the SulfuricAcid that is produced is used to make
fertilizers such as
 Superphosphate
 Ammonium sulphate and
 Ammonium phosphate.
 Rock phosphate contains insoluble Calcium Phosphate .To
be made available to plants it needs to be converted to a
soluble form:
 Ca3(PO4)2, (s) + 2H2SO4 (l) + 4H2O
 Ca(H2PO4)2 (s) + 2CaSO4 • 2H2O
(s)
superphosphate
There are three industrial processes for
manufacturing of sulphuric acid.
 Contact process
 Lead chamber process
 Wet Sulfuric Acid Process (WSA)
 Sulphur (source sulphide ore .etc )
 Water
 Air
 • Sulfur burning
 • Pyrites roasting
 • Metal sulfide roasting and smelting
 • Metal sulfate roasting
 • Combustion of H2S or other sulfur-
containing gases
H = -296.7 kJ/mole
 Sulphurdioxide burner gas contains impurities like
CO2 , As , F , N2 , Cl2 and dust.
 Also contain moisture which can cause corrosion to
equipment.
 To remove all these impurities the burner gas is
passed through dust filter chamber ,washing tower
and then drying tower
Dust filter chamber Washing tower Drying tower
V2O5
 The conversion of SO2 into SO3 is and exothermic
reaction .
 It releases -197 kj per mole energy
 To remove this extra heat coolers or heat
exchangers are adjusted on the outlets of reaction
bed
 The temperature in the converter is maintained
between 400°C and 500°C and the pressure is close
to 1 atm.
 Using Le Chatelier’s principal, the equilibrium
yield of sulfur trioxide will increase:
▪ As temperature decrease. Since the reaction is
exothermic a decrease in temperature will favour
the forward reaction.
▪ As pressure increases. Since there are more gas
particles on the reactants the forward reaction will
result in a decreased pressure.
▪ If excess reactants are added.
 Direct reaction of SO3 with water is very exothermic which results
in the formation of steam .sulphuric acid as gas is very difficult to
collect .
 SO3(g) + H2O(l) H2SO4(l) H= -103kjper mole
 Due to this SO3 is absorbed in H2SO4 to produce oleum
 SO3 (g)+ H2O (l ) H2S2O7(l)
 Oleum is mixed with water to form sulphuric
acid
 H2S2O7 + H2O 2H2SO4
ADVANTAGES
 Larger amount of sulphuric acid is manufactured
 High concentraion of sulphuric acid is obtained as compared
to all other processes
 Widely used
DISADVANTAGES
 The biggest problem is that the catalyst can be poisoned if
the sulfur dioxide is not fairly pure. Also it could be faster.
Advantages
 There are little or no waste by-products produced by this
process. It is also the most economic way to get rid of
sulfurous waste gases.
Disadvantages
 This process produces an acid with low concentration
instead of the high concentrations that the Contact Process
yields.
Advantages
 The original acid to be used can be obtained at any
concentration.
Disadvantages
 The acid in the chamber is between 62% and 68% sulfuric
acid.
 This process is not used as widely as the Contact Process is
today mainly because this process produces a more dilute
acid than the Contact Process which yields pure sulfuric acid.
The Contact Process also produces a much larger amount of
sulfuric acid than the Lead Chamber Process.
 Sulfuric acid plants use sulfur or sulfur dioxide that is a
by-product from other industries.
 To maximise their conversion of sulfur dioxide to sulfur
trioxide most plants now use a double absorption
process.
 Any unreacted gas from the absorption tower is
passed over the catalytic beds again and re passed
through the absorption tower.
 This improves the percentage of sulfur dioxide
converted from 98% to better than 99.6%
 Improvements in conversion have also been
made by adding small amounts of caesium
to the vanadium oxide catalyst to increase
its efficiency and allow it to operate at lower
temperatures
 There is relatively little solid waste produced
from sulfuric acid manufacturing.
 The catalyst is dumped in landfill after
recovering the mildly toxic vanadium.
 The cooling water is recycled.
 Most sulfuric acid plants are located near
smelting and refining industries that produce
waste sulfur dioxide, a raw material for the
production of sulfuric acid
 All three processes are exothermic, meaning energy is
produced.The heat released is bring to boilers to produce
steamThis energy is used to generate its electricity or as a
source to produce other chemicals.
 Monitoring of Mist Emissions in the Stack
 Emissions from S.A. plants generally consist of some
unconverted SO2, unabsorbed
 SO3, and acid mist escaping from demisters installed in final
absorption tower.
 These are minimized by the following techniques:
 • Providing a continuously operating alkali scrubber for SCSA
plants.
 • Using a DCDA process instead of SCSA and cesium
promoted catalyst in the last
 pass of the converter.
 • Strict control of process temperatures and SO2
percentages in gases at the inlet to the converter.
 • Use of efficient hot gas filters and sulfur filters to
minimize the deposition of ash
 on the catalyst surfaces.
 • Automatic adjustment of dilution water addition
to control the strength of the
 circulating acid at optimum level (98.0–98.5%).
 • Control of temperatures of acid and gas at the
inlet to the absorption towers.
 • Sufficient flow of acid in all towers.
 The SO3 vapors generated by the oleum boiler should be
condensed or absorbed
 into a suitable medium.Apart from well designed,
fabricated, tested, and maintained
 storage and condenser plant, operators will find the
following practical suggestions
 useful for safe operation:
 1. Use only pureTeflon PTFE gaskets in SO3 vapor and liquid
lines. Conventional
 acid resistant gaskets may not be able to withstand attack by
SO3.
 2. Provide steam tracing lines, i.e., another steam line in
contact with or in the near
 vicinity of the liquid SO3 pipeline instead of a steam jacket.
 3. Maintain a temperature of between 28 and 33 °C in the
storage tanks for SO3.
 4. Provide a dual pressure gauge on the SO3 condenser,
which can indicate pressures
 below and above atmospheric.
 5. Use a falling film condenser instead of a shell and tube
type condenser wherein
 cooling water flows under pressure in the tubes.
 In the case of a tube leak, no water should enter the SO3
side.The tubes in the
 falling film condenser are open to the sky and, in the case of
a leak, the pressure
 gets released to the top opening.
 6. Safety vents, rupture discs, and air vents will form
standard mountings on the
 condenser and storages. Scrubbers will be connected to the
vents and irrigated by
 98% sulfuric acid for absorbing any SO3 vapors released
from the vents.
 Sulfuric acid is highly corrosive and can burn skin
and eyes severely.
 It can cause blindness and third degree burns on
contact.
 Exposure to sulfuric acid mist can cause other health
problems.
 Workers in sulfuric acid plants can also be exposed
to the acid through breathing air contaminated with
emissions containing oxides of sulfur
 Strict safety procedures including adequate
methods to trap the fumes are required to minimise
the risks to workers and the environment in the case
of accidently release
 Work areas must be well ventilated and employees
wear protective clothing.
 Acid spills are contained using materials such as
earth, clay or sand and then slowly diluted with
water before being neutralised with a base such as
limestone or sodium carbonate
 pulmonary edema ( fluid in lungs )
 burning sensation
 coughing
 wheezing
 shortness of breath
 headache, nausea
 vomiting
 http://en.wikipedia.org/wiki/Sulphuric_acid
 http://www.akerkvaerner.com/Internet/IndustriesAndService
s/Metals/AcidPlants/SulphuricAcidConcentration.htm
 http://www.na-ag.com/NA_en/rohstoffe/roh_schwefel
 http://www.uyseg.org/greener_industry/pages/sulphuric_aci
d/2SulphuricAcidUses.htm
 http://www.pollutionengineering.com/CDA/ArticleInformati
on/products/BNPProductItem/0,6654,150482,00.html
 http://www.noram-eng.com/technologies/sulphuric.html
 http://www.schoolscience.co.uk/content/5/chemistry/catalys
is/catsch3pg4.html
 http://www.ausetute.com.au/sulfacid.html
 http://www.ratson.com/chemicals/sulfuric.htm
Sulphuric acid

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Sulphuric acid

  • 1.
  • 2.  INTRODUCTION  PRODUCTION  PROPERTIES  USES  MANUFATURING PROCESS  ADVANTAGES DISADVANTAGES  WASTE MANAGEMENT  SAFTEY
  • 3.  sulphuric acid is a colourless dense oily corrosive liquid produced by the reaction of sulphur trioxide with water and used in accumulators and in the manufacture of fertilizers, dyes, and explosives. Formula: H2SO4
  • 4. 9th century: Islamic physician and alchemsit Ibn Zakariya al-Razi – discovered dry distillation of vitriol (al-zajat), and alcohol(ethanol). 17th century: German-Dutch chemist Johann Glauber – burned sulphur with saltpeter (potassium nitrate - KNO3) 18th century: Joseph Gay-Lussac, John Glover – lead chamber process 19th century: Peregrine Phillips – contact process
  • 5. Geometrical Shape : Tetrahedral Bond angle : 109.5
  • 6.  King of compounds  Oil of vitriol  Dipping acid  Battery acid  Electrolyte acid  Mattling acid  Dihydrogen sulphate
  • 7.
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  • 11. Sulphuric acid acts as a catalyst in the following reactions: C1 2H22O11 + H2SO4 12C + 11H2O The dehydrating ability of sulfuric acid is often utilised in laboratories to dry gas mixtures that are being prepared or analysed.
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  • 17. 75% of the SulfuricAcid that is produced is used to make fertilizers such as  Superphosphate  Ammonium sulphate and  Ammonium phosphate.  Rock phosphate contains insoluble Calcium Phosphate .To be made available to plants it needs to be converted to a soluble form:  Ca3(PO4)2, (s) + 2H2SO4 (l) + 4H2O  Ca(H2PO4)2 (s) + 2CaSO4 • 2H2O (s)
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  • 25. There are three industrial processes for manufacturing of sulphuric acid.  Contact process  Lead chamber process  Wet Sulfuric Acid Process (WSA)
  • 26.  Sulphur (source sulphide ore .etc )  Water  Air
  • 27.  • Sulfur burning  • Pyrites roasting  • Metal sulfide roasting and smelting  • Metal sulfate roasting  • Combustion of H2S or other sulfur- containing gases
  • 28. H = -296.7 kJ/mole
  • 29.  Sulphurdioxide burner gas contains impurities like CO2 , As , F , N2 , Cl2 and dust.  Also contain moisture which can cause corrosion to equipment.  To remove all these impurities the burner gas is passed through dust filter chamber ,washing tower and then drying tower Dust filter chamber Washing tower Drying tower
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  • 34. V2O5
  • 35.  The conversion of SO2 into SO3 is and exothermic reaction .  It releases -197 kj per mole energy  To remove this extra heat coolers or heat exchangers are adjusted on the outlets of reaction bed  The temperature in the converter is maintained between 400°C and 500°C and the pressure is close to 1 atm.
  • 36.  Using Le Chatelier’s principal, the equilibrium yield of sulfur trioxide will increase: ▪ As temperature decrease. Since the reaction is exothermic a decrease in temperature will favour the forward reaction. ▪ As pressure increases. Since there are more gas particles on the reactants the forward reaction will result in a decreased pressure. ▪ If excess reactants are added.
  • 37.  Direct reaction of SO3 with water is very exothermic which results in the formation of steam .sulphuric acid as gas is very difficult to collect .  SO3(g) + H2O(l) H2SO4(l) H= -103kjper mole  Due to this SO3 is absorbed in H2SO4 to produce oleum  SO3 (g)+ H2O (l ) H2S2O7(l)
  • 38.  Oleum is mixed with water to form sulphuric acid  H2S2O7 + H2O 2H2SO4
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  • 42. ADVANTAGES  Larger amount of sulphuric acid is manufactured  High concentraion of sulphuric acid is obtained as compared to all other processes  Widely used DISADVANTAGES  The biggest problem is that the catalyst can be poisoned if the sulfur dioxide is not fairly pure. Also it could be faster.
  • 43. Advantages  There are little or no waste by-products produced by this process. It is also the most economic way to get rid of sulfurous waste gases. Disadvantages  This process produces an acid with low concentration instead of the high concentrations that the Contact Process yields.
  • 44. Advantages  The original acid to be used can be obtained at any concentration. Disadvantages  The acid in the chamber is between 62% and 68% sulfuric acid.  This process is not used as widely as the Contact Process is today mainly because this process produces a more dilute acid than the Contact Process which yields pure sulfuric acid. The Contact Process also produces a much larger amount of sulfuric acid than the Lead Chamber Process.
  • 45.
  • 46.  Sulfuric acid plants use sulfur or sulfur dioxide that is a by-product from other industries.  To maximise their conversion of sulfur dioxide to sulfur trioxide most plants now use a double absorption process.  Any unreacted gas from the absorption tower is passed over the catalytic beds again and re passed through the absorption tower.  This improves the percentage of sulfur dioxide converted from 98% to better than 99.6%
  • 47.  Improvements in conversion have also been made by adding small amounts of caesium to the vanadium oxide catalyst to increase its efficiency and allow it to operate at lower temperatures
  • 48.  There is relatively little solid waste produced from sulfuric acid manufacturing.  The catalyst is dumped in landfill after recovering the mildly toxic vanadium.  The cooling water is recycled.  Most sulfuric acid plants are located near smelting and refining industries that produce waste sulfur dioxide, a raw material for the production of sulfuric acid
  • 49.  All three processes are exothermic, meaning energy is produced.The heat released is bring to boilers to produce steamThis energy is used to generate its electricity or as a source to produce other chemicals.
  • 50.
  • 51.  Monitoring of Mist Emissions in the Stack  Emissions from S.A. plants generally consist of some unconverted SO2, unabsorbed  SO3, and acid mist escaping from demisters installed in final absorption tower.  These are minimized by the following techniques:  • Providing a continuously operating alkali scrubber for SCSA plants.  • Using a DCDA process instead of SCSA and cesium promoted catalyst in the last  pass of the converter.  • Strict control of process temperatures and SO2 percentages in gases at the inlet to the converter.
  • 52.  • Use of efficient hot gas filters and sulfur filters to minimize the deposition of ash  on the catalyst surfaces.  • Automatic adjustment of dilution water addition to control the strength of the  circulating acid at optimum level (98.0–98.5%).  • Control of temperatures of acid and gas at the inlet to the absorption towers.  • Sufficient flow of acid in all towers.
  • 53.  The SO3 vapors generated by the oleum boiler should be condensed or absorbed  into a suitable medium.Apart from well designed, fabricated, tested, and maintained  storage and condenser plant, operators will find the following practical suggestions  useful for safe operation:  1. Use only pureTeflon PTFE gaskets in SO3 vapor and liquid lines. Conventional  acid resistant gaskets may not be able to withstand attack by SO3.
  • 54.  2. Provide steam tracing lines, i.e., another steam line in contact with or in the near  vicinity of the liquid SO3 pipeline instead of a steam jacket.  3. Maintain a temperature of between 28 and 33 °C in the storage tanks for SO3.  4. Provide a dual pressure gauge on the SO3 condenser, which can indicate pressures  below and above atmospheric.  5. Use a falling film condenser instead of a shell and tube type condenser wherein  cooling water flows under pressure in the tubes.
  • 55.  In the case of a tube leak, no water should enter the SO3 side.The tubes in the  falling film condenser are open to the sky and, in the case of a leak, the pressure  gets released to the top opening.  6. Safety vents, rupture discs, and air vents will form standard mountings on the  condenser and storages. Scrubbers will be connected to the vents and irrigated by  98% sulfuric acid for absorbing any SO3 vapors released from the vents.
  • 56.  Sulfuric acid is highly corrosive and can burn skin and eyes severely.  It can cause blindness and third degree burns on contact.  Exposure to sulfuric acid mist can cause other health problems.  Workers in sulfuric acid plants can also be exposed to the acid through breathing air contaminated with emissions containing oxides of sulfur
  • 57.  Strict safety procedures including adequate methods to trap the fumes are required to minimise the risks to workers and the environment in the case of accidently release  Work areas must be well ventilated and employees wear protective clothing.  Acid spills are contained using materials such as earth, clay or sand and then slowly diluted with water before being neutralised with a base such as limestone or sodium carbonate
  • 58.  pulmonary edema ( fluid in lungs )  burning sensation  coughing  wheezing  shortness of breath  headache, nausea  vomiting
  • 59.  http://en.wikipedia.org/wiki/Sulphuric_acid  http://www.akerkvaerner.com/Internet/IndustriesAndService s/Metals/AcidPlants/SulphuricAcidConcentration.htm  http://www.na-ag.com/NA_en/rohstoffe/roh_schwefel  http://www.uyseg.org/greener_industry/pages/sulphuric_aci d/2SulphuricAcidUses.htm  http://www.pollutionengineering.com/CDA/ArticleInformati on/products/BNPProductItem/0,6654,150482,00.html  http://www.noram-eng.com/technologies/sulphuric.html  http://www.schoolscience.co.uk/content/5/chemistry/catalys is/catsch3pg4.html  http://www.ausetute.com.au/sulfacid.html  http://www.ratson.com/chemicals/sulfuric.htm