Production of 1200 Metric Tonnes of Phosphoric Acid Per Day Flow Sheet of Dihydrate

Process

PHOSPHORIC ACID PRODUCTION PROCESS OPTIONS

There are three basic types of processes for the production of phosphoric acid:

• Furnace process
• Wet process
• Dihydrate process

DETAILED DESCRIPTION OF DIHYDRATE PROCESS

Manufacturing of phosphoric acid by dihydrate process generally involves the following sections:
1. Rock phosphate grinding section where coarse rock is ground to the fines required for the subsequent
reaction.
2. Reaction Section – here the raw materials, i.e., ground rock phosphate and sulfuric acid are reacted to get
phosphoric acid and gypsum.
3. Filtration section – here the phosphoric aid produced is separate from the by-product, solid gypsum.
4. Evaporation section – here, the weak acid obtained from filter (25- 30% P2O5) is concentrated to higher
levels (45- 54% P2O5) required for subsequent use.

Though there are four major sections, actual conversion of raw materials to products takes place in reaction section
whereas all other sections involve unit operations only.

ROCK PHOSPHATE GRINDING:

Rapid reaction between rock phosphate and sulfuric acid is influenced by particle size of the rock, since the reactions
begins on the surface of the particle. Accordingly, time required for the rock phosphate to dissolve is proportional to
diameter. The secondary purpose of rock grinding is to reduce the power input to the agitators in the reaction section
where in the rock phosphate is required to be suspended as a uniform slurry.
Another factor influencing the degree of fines required is the relative reactivity of the rock. Over-grinding is not
advisable as it can lead to hyper-reactivity, in addition to wasting energy, finally reflecting in increased losses.

CHEMICAL REACTION:
The objective in designing the reaction system is to carry out the reaction between phosphate rock and sulfuric acid
so as to recover a maximum percentage of P2O5 from the rock for the product in the form of phosphoric acid, in the
simplest and least expensive manner. Since filtration is the most critical and expensive step in the process, the
primary objective of the reactor is to form gypsum crystals of such size and shape that the filtration and washing can
be carried out efficiently and rapidly.
Maximum recovery means minimizing losses. Here, three types of P2O5 losses are recognized:
1. Un-reacted phosphate rock
2. P2O5 co-crystallizes with gypsum through isomorphic substitution of HPO4 and SO4, and,
3. Phosphoric acid lost in gypsum due to incomplete washing.

The purpose of the main reaction is not only to extract the phosphate from the rock but also to ensure growth of
gypsum crystals to a relatively large size. To attain this goal, reaction systems are designed to prevent direct contact
between the two reactants, i.e., phosphate rock and sulfuric acid. A high concentration of free sulfuric acid would
result in coating the phosphate rock with calcium sulfate as reaction product, thus blocking further reaction.

A serious case of ‘reaction -blocking’ in a phosphoric acid plant can take several hours or even days to correct. On
the other hand, a high concentration of calcium ions (low sulfate) in the slurry will increase the amount of phosphate
co-crystallized with gypsum. Hence the aim of the designers and operators of reaction system is to maintain a
uniform composition of slurry, avoiding pockets of high sulfate or calcium concentration. The liquid phase usually
consists of phosphoric acid (about 25-30% P2O5) with about 1.5-3% free sulfuric acid. The optimum concentration of
free sulfuric acid varies with rock composition. The solid phase is mainly gypsum. The proportion of the solids in the
slurry is about 35- 45%. Phosphate rock particles introduced into the slurry dissolve rapidly in the liquid phase
phosphoric acid, which causes supersaturating with calcium sulfate and results in growth of gypsum crystals.

To approach this ideal situation, the incoming streams of phosphate rock and sulfuric acid are mixed with slurry as
rapidly and completely as possible and the slurry in the reaction system is agitated to ensure homogeneity. The heat
of dilution of sulfuric acid and the heat of reaction from phosphate rock decomposition is such that most of it has to be
removed from the reactor in order to keep the reacting slurry medium at its optimum reaction temperature. Otherwise,
temperatures in the reaction system would rise above the range desired for the formation of easily filterable gypsum
(75- 850C). The heat is generated by dilution of sulfuric acid feed, if the heat removal system is not efficient, the
slurry will heat up with evident consequences of crystallization, corrosion, filter cloth damage and so on.
The use of cold- water cooling tubes is not practical because of rapid scale formation and corrosion. Current heat
removal practices involve two methods. The first involves air swept cooling where large quantities of air supplied by a
fan make contact with slurry surface in the reactor. In this process, the air picks up heat as both sensible and
evaporative heat. The advantage of this system lies in its simplicity and in the low energy consumption. The second
method is vacuum flash cooling where hot slurry from reactor is pumped into an evaporation chamber under vacuum.
Heat release is achieved by boiling slurry and the evacuated vapor. The vapor is condensed downstream with large
amounts of water. Though this system is technically sophisticated the disadvantage lies in the large quantity of liquid
effluent leaving the system and containing some dissolved fluorides.

FILTRATION:
The function of filtration step is to is to separate the gypsum (and any insoluble materials derived from phosphate
rock or formed in the reaction) from the phosphoric acid product as completely, efficiently and economically as
possible. All modern plants use only continuous horizontal vacuum filters.
The most popular filters are the tilting-pan rotary table filters and belt filters. In each of these filters, the cycle
proceeds through the following steps:
1. Deposition of phosphoric acid- gypsum slurry on the filter
2. Collection of product acid by application of vacuum
3. Two or three counter-current washes to complete the removal of phosphoric acid from gypsum
4. Discharge of washed gypsum
5. Washing of the filter cloth to prevent accumulations of scale- forming materials.

A good filter vacuum is therefore vital. Generally the vacuum system usually operates with 200-250 mm of mercury –
absolute pressure.
Filtration rates depend on the design of filter, amount of vacuum and numerous other factors such as the solid
content of the slurry, the quality of the crystals; which in turn depend on size and shape, viscosity of the acid and
temperature of the slurry.

EVAPORATION:
The concentration operation is accomplished by evaporation under vacuum, normally using the by-product steam
generated during sulfuric acid production as a source of energy.
A phosphoric acid concentration unit consists of a heat exchanger, a boiler chamber (or vapor body) condenser,
vacuum pump, acid circulation pump and connecting pipes. Though the system is very simple, corrosion and scaling
problems encountered while handling phosphoric acid prohibit the use of sophisticated designs and equipment.

To provide evaporation two objectives have to be achieved:

1. Thermal energy has to be transferred to the acid to make it possible to generate vapor.
2. Vapor must be separated from the liquid in such a manner as to avoid entrainment of acid.

Because of the scaling problems it is essential that the heat transfer takes place under circumstances of low ∆T,
without the liquid being allowed to boil within the tubes of the heat exchanger. This is achieved by maintaining the
vacuum level at the vapor separator so that the liquid will boil at this surface at around 85-950C while maintaining the
hydrostatic head of liquid in the separator so that the absolute pressure in the heat exchanger tubes is above the
vapor pressure.
Also, to ensure the boiling in tubes, it is necessary to ensure that the temperature of the acid does not rise greatly
between the inlet and the outlet of the heat exchanger. This is achieved by large recirculation of acid from the boiling
chamber. The resulting high velocity in the heat exchanger also improves the heat coefficient and in maintaining the
small ∆T required between tube inlet and outlet.
PROCESS CHEMISTRY
The main chemical reaction in the wet process for phosphoric acid production using
Sulfuric acid and dihydrate production route may be represented by equation 1 given below using tricalcium
phosphate to represent phosphate rock. The reaction represents the net result of two stages. In the first stage,
phosphoric acid reacts with rock phosphate forming monocalcium phosphate, as given in the reaction 1(a). in the
second stage the monocalcium phosphate reacts with sulfuric acid to form phosphoric acid and gypsum, as given in
equation 1(b).

1. Ca3(PO4)2 + 3H2SO4 + 6H2O -------> 3(CaSO4.2H2O) + 2H3PO4

Tricalcium Phosphate Sulfuric acid Water Gypsum Phosphoric acid

1(a) Ca3(PO4)2 + 4H3PO4 ----> 3(CaH2PO4)2

Tricalcium Phosphate Phosphoric acid Monocalcium phosphate

1(b) 3(CaH2PO4)2 + 3H2SO4 + 6H2O ----> 3(CaSO4.2H2O) + 2H3PO4

Monocalcium Phosphate Sulfuric acid Water Gypsum Phosphoric acid

Calcium carbonate in the rock reacts with sulfuric acid to form Gypsum and Carbon dioxide (eqn.2). Most of Carbon
dioxide is evolved in the reactor immediately after the rock comes into contact with re-circulating slurry at point of rock
addition itself.

2. CaCO3 + H2SO4 + H2O -----> CaSO4.2H2O + CO2

Calcium Carbonate Sulfuric acid Water Gypsum carbon dioxide

Points to remember,

1. Cooling tower

2. Heat exchanger

3. Flash point

4. Separation technique

5. Fire protection

6. Work permit