This invention relates to the electroltic preparation of Perchlorates directly from Sodium
Chloride using Lead Dioxide anode.
Hitherto it has been the practice to employ a two stage process for the production of
perchlorates from chlorides , the first stage being the oxidation of chloride
to Chlorate using Graphite, Magnetite or Lead Dioxide anodes and the second stage consisting
of the oxidation of Chlorate to Perchlorate, using Platinum or Lead Dioxide anodes. This
conventional process has various drawbacks, such as:
(i) that in between the two stages the solutions have to be processed to isolate the Chlorate
and recover the unconverted Chloride:
(ii) that Graphite gets desintegrated to a considerable extent and Magnetite to a lesser extent
when used in the production of Chlorates and
(iii) that there is an inevitable loss of Platinum due to corrosion in the Perchlorate cell.
With a view to avoiding the intermediate step of the processing of the liquor after the said
first stage of the conventional process, it has been proposed that the effluent from the
chlorate cell should be treated under different electrolytic conditions from thoses in
which the sodium chloride solution was treated in the chlorate cell during the first stage
of the process. But this proposed process also is a two stage process and the processing of
the effluent from the chlorate cell introduces complications in the method.
This invention has for its main object an improved method which will obviate the drawbacks
of known methods, and whereby the perchlorates may be prepared directly from sodium chloride
in a single step of electrolytic oxidation, the conditions of electrolysis being maintained
constant at predetermined levels throughout the period. Another object of this invention is to
avoid the use of graphite, magnetite or platinum as the anode.
With these and other objects in view , this invention broadly consists of a process of preparing
sodium perchlorate directly from sodium chloride in a single step of electrolytic oxidation,
which consists in passing a direct current through a bath of sodium chloride solution containing
fluoride ions.
The improved process according to this invention may be carried out into practice under the
following conditions:
(i) The said fluoride ions may be provided by adding sodium fluoride ou hydrogen fluoride to the
bath.
(ii) About 0.5 to 5 grams per liter of sodium fluoride may be added; but about 2g/L is ok.
(iii) The electrolytic oxidation may be carried out in a cell having a stainless steel cathode
and a lead dioxide anode.
(iv) The said anode may consist of a massive lead dioxide or a GSLD.
(v) The current density may be in range 5 to 40 amps per square decimeter.
(vi) The electrolyte oxidation may be carried out at a temperature of 30 to 60 C.
(vii) The process may be carried until all the chloride is converted into perchlorate, the
conditions being maintained constant at predetermined levels throughout the process.
The following Table I. gives the particulars of three different examples illustrating the
invention.
EXAMPLE | 1 | 2 | 3 |
Concentration of electrolYte (initial) g/L NaCl | 290.8 | 291 | 308.1 |
Sodium fluoride g/L | 2 | 2 | 2 |
Anode | GSLD | GSLD | GSLD |
Cathode | SS | SS | SS |
Current density (amps /dm^2) | 10 | 25 | 19 |
Current concentration (amp/L) | 18.75 | 25 | 10 |
Temperature | 40 | 40 | 45 |
Cell voltage ( volts) | 3.0 to 3.9 | 3.7 to 4.5 | 3.9 to 4.5 |
Current efficiency % | 52.2 | 53.2 | 57.5 |
Energy consumption (kwh/kg of NaClO4) | 13.3 | 13.9 | 13.2 |
Current passed Amps | 15 | 20 | 800 |
Duration (hrs) | 105 | 78 | 223 |
Quantity of NaClO4 present in solution (gms) | 544 | 546 | 61KG |
Table II shows other benificeal effects of using NaF.
Experimental conditions | Without NaF | With NaF |
Anode | GSLD | GSLD |
Cathode | SS | SS |
Anode current density (amps / dm squared) | 20 | 20 |
Current concentration (amp/L) | 25 | 25 |
Temperature C. | 3.5 TO 3.8 | 3.5 TO 4.0 |
Current efficienct % (with ref. to NaClO4 formed) | 39.5 | 53.4 |
Energy consumption (kwh/kg of NaCl04) | 16.2 | 12.3 |
Snip of most of the text repeating the claims above except:
Claim (3): Current density is in the range 5 to 40 Amps per dm^2.
Claim (4): Temperature is in the range 30 to 60 C.
Other patents sited:
2,813,825 11/1957 Miller et al
2,840,519 6/1958 Stern et al
2,872,405 2/1959 Miller et al
3,020,124 2/1962 Bravo et al
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