There are three basic processes for the production of phosphoric acid:
2. Wet process
3. Dihydrate process
DETAILED DESCRIPTION OF DIHYDRATE PROCESS
Manufacturing of phosphoric acid by dihydrate process generally involves the following sections:
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 acid produced is separate from the by-product, solid gypsum.
4. Evaporation section – here, the weak acid obtained from the filter (25- 30% P2O5) is concentrated to higher levels (45- 54% P2O5) required for subsequent use.
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| Process flow sheet of Phosphoric acid production |
ROCK PHOSPHATE GRINDING:
A rapid reaction between rock phosphate and sulfuric acid is influenced by the particle size of the rock since the reactions begin on the surface of the particle. Accordingly, the 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 wherein 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:
- Un-reacted phosphate rock
- P2O5 co-crystallizes with gypsum through isomorphic substitution of HPO4 and SO4, and,
- 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 the 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 a 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 the 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 the 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 made contact with the slurry surface in the reactor. In this process, the air picks up the 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 the reactor is pumped into an evaporation chamber under vacuum. Heat release is achieved by boiling slurry and the evacuated vapour. The vapour 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:
- Deposition of phosphoric acid- gypsum slurry on the filter
- Collection of product acid by application of vacuum
- Two or three counter-current washes to complete the removal of phosphoric acid from gypsum
- Discharge of washed gypsum
- 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 the 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, the 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 vapour 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:
2. Vapour must be separated from the liquid in such a manner as to avoid entrainment of acid.
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| Material balance flow diagram of the phosphoric acid production |
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 of PRODUCTION OF PHOSPHORIC ACID
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
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| Energy balance flow sheet of phosphoric acid production |