[0001] The present invention relates to a process for the purification of mercury from metal
impurities contained therein, and more particularly to the purification of the mercury
of electrolytic cells of chlorine-sodium hydroxide and chlorine-potassium hydroxide
plants, to the purification of mercury recovered following leaks, and to the purification
of mercury of industrial origin.
[0002] In chlorine-sodium hydroxide and chlorine-potassium hydroxide plants, one of the
main factors that influence the reliability and safety of the mercury amalgam process
is the purity of the NaCl or KC1 brine introduced into the cell. Impurities such as
iron, calcium and magnesium are normally present in the sodium chloride in quantities
varying from 0.01 to 0.3% by weight, while other heavy metals such as chromium, vanadium,
molybdenum and magnesium are often present in quantities of the order of 0.01 ppm.
[0003] These impurities must be removed from the brine because they tend with time to accumulate
in the mercury, where, if they exceed certain threshold concentrations, they catalyze
the cathodic development of hydrogen which, mixing with the chlorine developed at
the anode, may give rise to explosions.
[0004] The impurities present in the mercury also have other adverse effects on the electrolytic
process. There may, for instance, form an amalgam foam (called "mercury butter") which
disturbs the regular flow of the mercury, as a result of which the cell voltage rises
and there may occur short-circuits which will damage the anodes.
[0005] Moreover, the wettability between the bottom of the cell and the mercury is reduced,
with consequential frequent rupture of the continuity of the amalgam layer, and consequential
corrosion of the bottom which has remained uncovered.
[0006] The accumulation of impurities in the mercury also causes unbalances in the distribution
of the current in the various longitudinal sections as well as cross sections of the
cell.
[0007] In order to limit the introduction of impurities in the mercury, the brine, before
its conveyance to the cells, is subjected to a costly process of chemical and physical
purifications.. Since there remain, however, possible accidental pollutions of the
brine, the mercury tends nonetheless to grow rich in impurities, as a result of which
it is necessary to frequently carry out periodical washings of the cells and purification
of the mercury itself, by means of distillation.
[0008] It has been suggested to purify the mercury by electrolytic treatment after its dis-amalgamation.
To this end the mercury, contacted with an aqueous acid solution, is anodically polarized,
whereby the impurities dissolve in the aqueous solution.
[0009] This process involves, however, constructional complications, in particular because
the mercury which is connected with the negative pole in the electrolysis cell, must
be connected to the positive pole in the purification apparatus.
[0010] Thus, one aim of the present invention is to provide a simple, cheap and effective
process for the purification of mercury from the metal impurities contained in it.
[0011] The present invention provides a process for the purification of mercury from metal
impurities contained therein, wherein the mercury is contacted with an aqueous solution,
characterized in that the mercury and the aqueous solution are fed into a reactor,
in the upper part of which a gas is present, and in that the mercury and the aqueous
solution are circulated by means of a pump installed in an external recirculation
circuit, this pump drawing the liquid phases (mercury and aqueous solution) from the
bottom of the reactor and sending them back into the reactor through a nozzle or a
liquid-gas ejector arranged in the upper part of the reactor, whereby as a consequence
of the dynamic-flow conditions thus created the mercury is dispersed in the form of
minute droplets in the aqueous phase, and is intensely mixed with the aqueous phase,
as a result of which the impurities pass into the aqueous phase.
[0012] The invention will be further described, by way of example only, with reference to
the accompanying drawing, which is a schematic view of an apparatus suitable for carrying
out the process of the invention.
[0013] The drawing shows a reactor 1 which contains in its upper part 2 a gas. Fixed to
the upper end of this reactor is arranged a nozzle 3. Furthermore there may be present
a converging-diverging tube 4 which is so arranged with respect to the nozzle 3 as
to form with this latter a liquid-gas ejector.
[0014] The converging-diverging tube 4 is maintained in the reactor 1 in the most suitable
position with respect to the nozzle by means of any mechanical device suited for this
purpose, for instance by means of fixing spokes fixed to the nozzle itself. The mechanical
device is chosen in such a way as not to hinder the passage of the gas from the upper
part 2 of the reactor to the inside of the converging-diverging tube 4 itself. The
lower part of the tube 4 is immersed in the liquid phases present in the reactor.
[0015] Into the upper part 2 of the reactor are fed in the mercury to be purified via a
line 5, and the aqueous solution via a line 6. Starting from the bottom 7 of the reactor,
there is provided a recirculation line 8-9-10 which leads first to a pump 11 and thereafter
to an optional heat exchanger 12 and returns back to the reactor, entering the nozzle
3. From the upper end of the reactor, the gas produced by the purification reaction
(hydrogen) flows out through a line 13.
[0016] From the part 8 of the recirculation line, between the reactor 1 and the pump 11,
there is a branch line 14, in which is installed a valve 15, which allows the discharge
of the liquid phases.
[0017] The-pump 11 ensures the circulation of the two liquid phases (the mercury and the
aqueous solution) in the reactor and in the external recirculation line. The nozzle
3 causes an agitation (or stirring-up) of the liquid phases and the consequential
dispersion of the mercury in the aqueous solution, in the form of droplets of small
diameter.
[0018] If there is present a liquid-gas ejector, such an ejector sucks gas from the top
of the reactor, still further increasing in this way the turbulence in the jet and
in the reactor, and dispersing gas into the system.
[0019] This dispersed gas reduces the coalescence of the mercury particles and provides
an extensive exchange surface for the removal of the gas produced by the reaction.
[0020] Preferably there is used a liquid-gas ejector, considering the above indicated positive
effects that it produces.
[0021] The aqueous solution may be either acid, neutral or alkaline. It is preferred to
use a mineral acid solution, for example a sulphuric acid solution containing from
0.5% to 10% by weight of H SO . In fact, in the presence of an acid solution, the
impurity dissolving reaction proves to be faster. Using an acid solution, the chemical
reaction that takes place is, for instance in the case of iron:

[0022] There may also be added to the acid solution an oxidizer, for instance H
2O
2 .
[0023] The gas present in the reactor may be at atmospheric pressure; however, it may instead
be at a reduced pressure: that is, the process may be operated under a vacuum, as
a result the only gas present being the gas freed by the reaction (H2 However, it
is also possible to work at a pressure higher than atmospheric pressure. The pressure
of the gaseous phase is for example from about 10 mmHg to about 5 atmospheres absolute.
[0024] When working at atmospheric pressure or above atmospheric pressure, the nature of
the gas present in the reactor is not critical; there may be used various types of
gases, for example air or nitrogen. The use of air is convenient in as much as it
may help to dissolve the impurities because the oxygen contained in the air acts as
an oxidiser.
[0025] The ratio between the volume of liquid phases sent back into the reactor each hour
and the volume of the reactor itself is in general at least 10, more preferably from
50:1 to 150:1. The delivery pressure of the pump is in general at least 0.3 atmospheres,
more preferably from 0.7 to 3 atmospheres.
[0026] The temperature at which the purification reaction takes place is usually from 20°C
to the boiling temperature of the aqueous solution. The purification reaction obviously
proceeds faster when the temperature increases, but at high temperatures, in an acid
medium, there may arise problems of corrosion of the equipment.
[0027] It is useful and convenient to use a pump which will ensure a dispersion of the liquid
phases in each other. The mercury droplets tend, in fact, to coalesce in the part
8 of the external recirculation line.
[0028] If the pump re-disperses the liquid phases, new mercury droplets form again. The
reforming of the mercury droplets accelerates the purification reaction. In fact,
if the size (dimensions) of the droplets remains stable in time, there will form concentration
gradients and the diffusion of the impurities towards the mercury-water interface
will slow down. On the contrary, if the droplets re-coalesce and are formed again
with a new surface, the negative effect of the concentration gradients will be appreciably
reduced.
[0029] Pumps suitable for ensuring an effective dispersion of the liquid phases in each
other are for example gear pumps and rotary pumps as well as particular types of centrifugal
pumps.
[0030] The liquid phases may be discharged through the valve 15 which leads, for instance,
to a tank where the purified mercury and the exhausted aqueous solution are separated
by decanting.
[0031] When purifying the mercury of electrolytic cells, the mercury is subjected to the
purifying process after its dis-amalgamation.
[0032] In the operation of the cells, the mercury purification system in which the process
of the present invention is carried out may be coupled to the conventional purification
of the brine, or the latter purification may be dispensed with, as a result of which
the only purification carried out is that in accordance with the invention.
[0033] It is also possible to carry out a simplified purification of the brine, thus reducing
the costs of this operation.
[0034] According to one specific embodiment of the process of the invention, the whole flow
of mercury which flows out of the dis-amalgamator (disamalgamation apparatus), passes
into the purification apparatus shown in the drawing, during all the time of operation
of the electrolytic cell or at suitable time intervals. The mercury is separated by
decanting from the aqueous phase and then flows back into the cell.
[0035] Instead of passing the whole flow of mercury into the purification apparatus, it
is possible instead to pass only part of the flow either during the whole time of
operation of the cell or at suitable time intervals.
[0036] In these two kinds of operation, the purification apparatus is provided with a circulating
pump of its own. Thus, the plant will have two pumps, one for the circulation of the
mercury in the cell, and one for the purification apparatus. There may instead be
used in the plant only one pump which, besides circulating the mercury in the cell,
will convey part or the whole of it to the purification apparatus. In this latter
case, the mercury will pass only once through the purifying apparatus before being
sent back into the cell.
[0037] The purification process of the present invention may also be used for purifying
the mercury butters gathered during the washing of the cells.
[0038] The invention will be further described with reference to the following illustrative
Examples
EXAMPLE 1
[0039] There was used the apparatus shown in the drawing, equipped with a liquid-gas ejector
3-4, a heat exchanger 12 and a gear pump 11.
[0040] The total volume of the reactor and of the recirculation circuit was about 5 litres.
The process was conducted discontinuously, at room temperature.
[0041] There were introduced into the apparatus 5 litres of a 5% by weight solution of H
2S0
4 which was recirculated at a flow-rate of 500 litres/hour. The delivery pressure of
the pump equalled 1.1 atmospheres.
[0042] Into the reactor were then introduced 500 g of mercury containing 20 ppm of sodium
and 15 ppm of iron. After 30 seconds there was drawn a sample of mercury; the content
of sodium was found to be less than 1 ppm while that of the iron was less than 3ppm.
EXAMPLE 2
[0043] There was used the same apparatus as in example 1 and there were followed the same
procedures, except as otherwise specified.
[0044] At room temperature, there were treated 500 g of mercury containing 42 ppm of iron
with 5 litres of an aqueous solution containing 5% by weight of H
2SO
4 and 0.1% by weight of H
20
28 After less than one minute, the content of iron was found to be below 3 ppm.
EXAMPLE 3
[0045] There was used the same apparatus as in example 1 and there were followed the same
procedures, except as otherwise specified.
[0046] 500 g of mercury, containing 430 ppm of iron, were treated at 70°C with five litres
of an aqueous solution containing 2% by weight of H
2SO
4. After one minute, the content of iron in the mercury had dropped to 10 ppm, and
after a further 2 minutes it was found to be below 3 ppm.
EXAMPLES 4-7
[0047] There was used the same apparatus as in example 1 and there were followed the same
procedures, except as otherwise specified.
[0048] The mercury to be treated came from end boxes (examples 4 and 5) and from feed boxes
of electrolytic cells of a chlorine-sodium hydroxide plant.
[0049] 500 g of mercury were treated at room temperature with 3 litres of an aqueous solution
containing 2% by weight of H
2SO
4. The initial composition of the mercury and its composition after 5 and 10 minutes
of treatment are given in the following table.

1. A process for the purification of mercury from metal impurities contained therein,
wherein the mercury is contacted with an aqueous solution, characterized in that the
mercury and the aqueous solution are fed into a reactor (1), in the upper part (2)
of which a gas is present, in that the mercury and the aqueous solution are circulated
by means of a pump (11) installed in an external recirculation circuit (8,9,10), the
said pump drawing the liquid phases from the bottom of the reactor and sending them
back into the reactor through a nozzle (3) or a liquid-gas ejector (3.4) arranged
in the upper part (2) of the reactor, whereby as a consequence of the dynamic-flow
conditions thus created the mercury is dispersed in the aqueous phase in the form
of minute droplets and is intensely mixed with the said aqueous phase, as a result
of which the impurities pass into the aqueous phase.
2. A process as claimed in claim 1, characterized in that the aqueous solution is
a mineral acid solution.
3. A process as claimed in claim 2, characterized in that the mineral acid solution
contains an oxidizer.
4. A process as claimed in any of claims 1 to 3, characterized in that the gas present
in the reactor is air.
5. A process as claimed in any of claims I to 4, characterized in that the ratio of
the volume of the liquid phases sent back into the reactor every hour to the volume
of the reactor is at least 10.
6. A process as claimed in any of claims 1 to 5, characterized in that the delivery
pressure of the pump (11) is at least 0.3 atmospheres.
7. A process as claimed in any of claims 1 to 6, characterized in that the pump (11)
is such as to ensure an effective dispersion of the liquid phases in each other.
8. A process as claimed in any of claims 1 to 7 for the purification of mercury of
electrolytic cells of chlorine-sodium hydroxide and chlorine-potassium- hydroxide
plants, characterized in that the mercury is subjected to purification after its dis-amalgamation.
9. Mercury purified from its metal impurities according to the process as claimed
in any of claims 1 to 8.