Kamar Timbal

Module 4
Lecture: 17 Sulfuric acid
Dr. N. K. Patel
Module: 4
Lecture: 17
SULFURIC ACID
INTRODUCTION
Sulfuric acid (H2SO4) is a highly corrosive strong mineral acid. It is a colorless to
slightly yellow viscous liquid which is soluble in water at all concentrations. It is one of
the most important heavy industrial chemicals due to it has a number of large-scale
uses particularly in the phosphate fertilizer industry. About 60 % of the sulfuric acid
produced is utilized in fertilizer manufacture.
Sulfuric acid was called "oil of vitriol" by Medieval. The study of vitriol began in
ancient times. Sumerians had a list of types of vitriol that classified according to
substance's colour.
Johann Glauber prepared sulfuric acid by burning sulfur together with
saltpeter (potassium nitrate, KNO3), in the presence of steam in the 17th century.
Decomposition of saltpeter followed by oxidation produces SO3, which combines
with water to produce sulfuric acid. Joshua Ward used the method for the first largescale production of sulfuric acid in 1736.
John Roebuck, produce less expensive and stronger sulfuric acid in lead-lined
chambers in 1746. The strength of sulfuric acid by this method is 65%. After several
refinements, this method, called the "lead chamber process" or "chamber process",
remained the standard for sulfuric acid production for almost two centuries.
The process was modified by Joseph Louis Gay-Lussac and John Glover which
improved concentration to 78%. However, the manufacture of some dyes and other
chemical processes require a more concentrated product. Throughout the 18th
century, this could only be made by dry distilling minerals in a technique similar to
the original alchemical processes.
Pyrite (iron disulfide, FeS2) was heated in air to yield iron(II) sulfate, FeSO4,
which was oxidized by further heating in air to form iron(III) sulfate, Fe 2(SO4)3, which,
when heated to 4800C, decomposed to iron(III) oxide and sulfur trioxide, which
could be passed through water to yield sulfuric acid in any concentration. But the
production expenses are very high.
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Dr. N. K. Patel
More economical process i.e. the contact process was patented by

Peregrine Phillips in 1831. Today, nearly all of the world's sulfuric acid is produced
using this method.
MANUFACTURE
The Industrial manufacture of sulfuric acid is done mainly by two processes
1. The Lead Chamber process
2. The Contact process
1. The lead chamber process
The Lead Chamber process for the manufacture of sulfuric acid dates back
about 200 years. Although less efficient than the contact process, it is still of
considerable commercial importance.
Raw Materials
Basis: 1000kg Sulfuric acid (98% yield)
Sulfur
= 400kg
Air
= 399kg
Reaction
S + O2
SO2
4FeS2 + 11O2
SO2 + NO2
SO3 + H2O
H = - 70.9kcals
2Fe2O3+ 8SO2
SO3 + NO
H2SO4
NO + O2
2NO2
NaNO3 + H2SO4
2HNO3 + 2SO2
NO + NO2 + 2H2SO4
H = - 92.0kcals
H = - 27.12kcals
NaHSO4 + HNO3
2SO3 + H2O + NO + NO2
2NO.HSO4 + H2O
2ON.O.SO2OH + H2O
H2SO4 + NO2 + NO
Manufacture
Block diagram of manufacturing process
Diagram with process equipment
Animation
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Module 4
Dr. N. K. Patel
Conc. H2SO4
Nitrated Acid
Chamber Acid
Chamber I
Watrer Spray
Chamber II
Chamber III
Gay - lussac Tower
To Chimney
Nitre Pot
Burners
Conc. Acid
Chamber Acid
Figure: Manufacturing of Sulfuric acid by Chamber process
Sulfur dioxide is obtained by burning sulfur or by roasting pyrites. There are two
function of burner
1. To oxidize sulfur to maximum extent
2. To produce and constant supply of gas containing maximum concentration
of SO2
The burner of the furnace should expose large surface of melted sulfur and
should be provided secondary air in order to burn sublimed burner. This is necessary
due to low heat of combustion and high vapour pressure of sulfur. At about 400 0C,
pyrite (FeS2) decompose in to FeS and sulfur vapour, the later oxidized to SO 2 in
presence of excess air. The residual FeS also oxidizes to Fe2O3 and SO2. Iron oxide
(Fe2O3) slightly catalyzed oxidation of SO2 to SO3. Burner gas should contain sufficient
oxygen for carry out further oxidation of SO2 to SO3.
The burner gases which contain SO2, N2, O2 and dust or fine particle of pyrites
are passed through dust chamber followed by Cottrell electrical precipitator or
centrifugal separator in order to remove dust or fine particle of ore. Dust chambers
are provided with horizontal shelves or baffles followed by filtration through crushed
coke or similar material.
Now, burner gases are passed through niter oven made of cast iron in which
equimolecular proportion of NaNO3 and H2SO4 is heated. Resulting nitric acid reacts
with SO2 to give mixture of nitric oxide (NO) and nitrogen dioxide (NO2) which are
carried with burner gases.
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Dr. N. K. Patel
In modern plant oxides of nitrogen are produced by passing mixture of

ammonia and air through heated platinum gauze acting as catalyst (same as
manufacture of HNO3 by ammonia oxidation process)
After passing burner gases to dust chamber and niter oven, they pass through
5 meter square and 10 -15meter high Glower tower which is packed with flint stone,
quartz, tile or acid resisting bricks. The packing in the tower is loosely stacked at the
bottom to facilitate mixing of hot gases. The hot burner gases passes up this tower is
at 450 - 6500C and dilute H2SO4 from the lead chamber and nitrosyl sulfuric acid from
Gay-Lussac tower are made to trickle down the Glower tower by means of sprayers.
Here, burner gases are cooled down to 70-800C, dilute chamber acid is
concentrated up to 78% and nitrosyl sulfuric acid (nitrous vitriol) is denitrated by
action of water.
The tower acid is drawn off from the bottom of the tower and collected in the
container called acid egg. The acid from base of Glower tower is cooled to 40 0C by
air coolers.
The mixture of SO2, Oxides of nitrogen and air is then passed to series of
rectangular vessels made of lead (lead chamber) having 15-45 meter length,
6-7 meter width and 7 meter length. The number of chambers depends upon the
size of plant, but usually they are 3 to 6 in number. The chambers are arranged in
two parallel rows. Steam from low pressure boiler or pure filtered water is sprayed
from top of the chamber. Mixture of gases is converted into H 2SO4 having 65-70%v
strength is collected at the bottom of the chamber. Dilute sulfuric acid obtained in
any of the chamber is called chamber acid. A part of chamber acid is pumped to
Glower tower, and the rest is sent for concentration.
The unabsorbed remaining gases contain oxides of nitrogen and SO 2 from
lead chamber are then passed through Gay-Lussac tower at the top of which
Glower acid is sprayed to recover oxides of nitrogen.
The oxides of nitrogen recovered in the form of nitroso sulfuric acid are
pumped to Glower tower to again regenerate oxides of nitrogen.
When pyrite is used as raw material, the chamber acid may contain arsenious
oxide (from pyrite), lead sulfate from lead chamber are removed by treatment of
H2S and dilution of acid respectively. Dilute acid may be further concentrated into
Glower tower.
Kinetics and thermodynamics
2NO+O2
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2NO2
H0 =-27.118kcals
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Module 4
Dr. N. K. Patel
Above reaction is rate controlling step in the chamber process. The

exothermic forward reaction is favoured by decrease in temperature. As the
reaction proceeds with decrease in volume, the formation of NO2 would be
favoured by increase in pressure. It has been observed that the rate of oxidation is
slow at ordinary temperature and rate is proportional to the square of the absolute
pressure. At lower temperature, the production of chamber acid has been found to
be greater. All these facts are in good agreement with the fact that the oxidation of
NO to NO2 is the rate controlling step in this process.
The dilution of nitrosyl sulfuric acid within the Glover tower leads to its
decomposition and nitrous fumes produced catalyze the synthesis of sulfuric acid
when they come in contact with sulfur dioxide and water.
2HSO4.NO + H2O
NO + NO2 + SO2 + H2O
2H2SO4 + NO + NO2
H2SO4 + 2NO
---- (1)
---- (2)
Reaction (2) can be shown in chain as follow

NO + NO2
N2O3 + H2O
2HNO2 + SO2
H2SO4 + 2NO
Reaction (2) can be repeated cyclically by the partial reoxidation of the nitric
oxide produced by excess air which forms part of the sulfurous gas coming from the
combustion chamber.
2NO + 1/2 O2
NO + NO2
---- (3)
Reaction (2) and (3) mainly occur in chambers following the Glover tower
until the SO2 has been exhausted.
The recovery of nitrous gases is important task of Gay Lussac towers but it is
difficult. A reverse reaction of reaction (1) is taking place here. This is in effect, a
typical equilibrium reaction which is particularly sensitive to the mass action effect
by water
2H2SO4 + NO + NO2
2HSO4.NO + H2O
or reversible reaction
2HSO4.NO + H2O
2H2SO4 + NO + NO2
Above reaction is displaced to the right in the Glover tower where water is
relatively abundant and to the left in the Gay Lussac tower which is supplied with
sulfuric acid which is transformed into nitrosyl sulfuric acid by absorbing
equimolecular mixture of NO and NO2 on account of its high concentration (78%).
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Module 4
Dr. N. K. Patel
Reason for obsolesce

As discussed above, overall reaction consisting of number of partial reactions
which takes place in liquid phase, the development of surfaces which are covered
in this liquid is a factor of fundamental importance in promoting the synthesis of
sulfuric acid. Maximum strength of sulfuric acid obtained by chamber process is 78%.
However, in manufacture of some dyes and chemical processes require more
concentrated H2SO4. There so, the process is largely replaced by contact process.
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How is sulfuric acid manufactured?

What are the raw materials and reactions involved in the lead chamber process?

Module 4

Lecture: 17 Sulfuric acid

More economical process i.e. the contact process was patented by

Gay - lussac Tower

Figure: Manufacturing of Sulfuric acid by Chamber process

In modern plant oxides of nitrogen are produced by passing mixture of

Above reaction is rate controlling step in the chamber process. The

Reaction (2) can be shown in chain as follow

Reason for obsolesce

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