Process For Technical Nitration

PROCESS FOR
TECHNICAL
NITRATION
MO.SHAHANAWAZ
2200102926
M.PHARM(PHARMACEUTICAL CHEMISTRY)
INTRODUCTION
 Nitration is the process of introduction of one or more nitro groups in a reacting molecule
(called substrate), e.g.
PROCESS FOR TECHNICAL NITRATION
 Technical nitration can be discussed as batch processes and continuous process. Each kind of
process has advantages peculiar to itself.
 BATCH PROCESSES- Batch process refers to a process that involves a sequence of steps
followed in a specific order.
 CONTINUOUS PROCESS- Continuous process refers to the flow of a single unit of product
between every step of the process without any break in time
ADVANTAGE OF BATCH PROCESS
 It is usually easier to introduce process variations into a batch process than into a continuous
process.
 Beginning production of new compound or pilot production is conveniently done by the batch
process because of operating flexibility.
 For high rates of production when large batches are used, the labour efficiency of a batch process
may be equal to a continuous process.
ADVANTAGE OF CONTINUOUS PROCESSES
 For a given rate of production, the equipment needed for a continuous process is smaller than
batch process.
 Because of relatively small size of continuous process equipment, there is less material in process
at any time, than at certain times in a comparable batch process.
 A continuous process is usually a more efficient labour user than a batch process.
 This is particularly true for small or medium scale production and for hazardous products.
BATCH NITRATION
 Nitration is usually done in cast iron or steel vessel. Now a day’s mild carbon steel is used.
 the rate of corrosion on mild steel becomes very rapid because alloy steels are preferred for
construction the nitrator.
 Nitrator consists of an upright cylindrical vessel with cooling surfaces, a means of agitation,
feed inlet or inlets and product outlet lines.
 Most nitrators also have a large diameter thick dumping line for emergency use.
 A common accessory for a nitrator is suction line in the vapour space above the liquid charge to
remove the acid fumes and oxides of nitrogen which may be liberated.
The two factors of prime importance in the design of nitrators are
I. The degree of agitation
II. The control of temperature.
 Cooling or other temperature control in nitrators is accomplished by coils of tubes through

which cold water or brine for cooling may be circulated or hot water or steam is passed for
heating.
 The most common type of agitating system used in nitrator has vertical shaft with one more
propellers mounted on it.
 An actual cylindrical sleeve is sometimes mounted in the center of coil banks to assure that
circulation of nitrator content is as desired.
BATCH NITRATION OF HYDROCARBONS
 Batch nitration of hydrocarbon such as benzene toluene, it has been common past practice to
nitrate by using conc acid.
 Here the common practice involved charging a sleeve and propeller agitator with cycle acid to
above the level of the top of cooling coils.
 Hydrocarbon was than floated in on top of cycle acid. Nitrating acid was fed into the nitrators in
the cycle acid with continuous stirring near the bottom of sleeve under the propeller.
 Nitrating acid was fed into the nitrators in the cycle acid with continuous stirring near the bottom
of sleeve under the propeller.
 This fortified cycle acid then reacted at the inter phase of the hydrocarbon and acid in top of the
nitrator. Nitration was then completed by allowing the temperature to rise and eventually to
emulsify nitrated products and acid.
CONTINUOUS NITRATION
 Continuous nitration is carried out in the same type of vessels as those used for batch nitration
with the exception that an overflow pipe or weir arrangement is provided for continuous
withdrawal of the products and that continuous feed of all the reactants is provided.
SCHMID NITRATOR
 This nitrator has been designed for the German Schmid Meisener system.
 In this nitrator, the material to be nitrator is fed from top of nitrator and immediately drawn
down through sleeve and intimately and thoroughly mixed with the spent acid and reacting
materials.
 In bottom of nitrator, fresh mixed acid is fed and is immediately mixed with the other reactants
by means of high flow rate caused by the agitators and baffles.
 The reacting materials then pass upward with the high velocity through the tubes surrounded by
refrigerated brine circulating in the jacket.
 Products and spent acid are withdrawn continuously from the nitrator through the overflow line.
BIAZZI NITRATOR
It is designed by Swiss form of M. Biazzi.

 There is a turbine type agitator provides intensive agitation. A vortex is formed in the center
about the agitator shaft.
 The reactants, both of which are fed in nitrator through the top are immediately drawn into this
vortex, thoroughly mixed and circulated down through the center of bank of cooling coils and
back up through and around the coils. The high velocity makes mixing and heat transfer very
efficient.
 In any continuous equipment, the designer must be careful to assure that no stagnant areas can
exist. Also it is quite general to specify high finishes on the interior surfaces with complete
freedom from surface pits or pockets which could trap the product.
 It is also important that the apparatus must be completely drainable so that if the contents must
be dumped no product contaminated with acid remains.
MIXED ACID COMPOSITIONS FOR NITRATION
 From the technical stand point of using mixed acid, there are two primary conditions that must
be met. These are;
1. The amount of 100% HNO3- present in nitration must be enough to satisfy stoichiometric
requirement of the reaction. It is usually present in excess to maintain reasonably fast overall
rate of reaction (nitration).
2. The amount of 100% H2SO4- with dissolved SO3 (i.e. Oleum, H2S2O7) if needed must be
sufficient to promote the desired reaction regardless of mechanism of reaction.
 D.V.S.: It is ratio of H2SO4: H2O present at the end of reaction.
 The nitric ratio (R): It is the ratio of wt. of 100% HNO3: wt. of material being nitrated.
NITROBENZENE
Nitrobenzene can be manufactured by
 Batch Nitration with mixed acid

 Continuous nitration with fortified spent acid
REFERENCES
 Slide share
 Wikipedia
THANK YOU

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PROCESS FOR

ADVANTAGE OF BATCH PROCESS

ADVANTAGE OF CONTINUOUS PROCESSES

The two factors of prime importance in the design of nitrators are

I. The degree of agitation

II. The control of temperature.

 Cooling or other temperature control in nitrators is accomplished by coils of tubes through

It is designed by Swiss form of M. Biazzi.

 D.V.S.: It is ratio of H2SO4: H2O present at the end of reaction.

Nitrobenzene can be manufactured by

 Batch Nitration with mixed acid

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