US1143586A - Process of producing chlorates of alkalis and alkaline earths. - Google Patents

Process of producing chlorates of alkalis and alkaline earths. Download PDF

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Publication number
US1143586A
US1143586A US86139514A US1914861395A US1143586A US 1143586 A US1143586 A US 1143586A US 86139514 A US86139514 A US 86139514A US 1914861395 A US1914861395 A US 1914861395A US 1143586 A US1143586 A US 1143586A
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cell
platinum
graphite
alkalis
anode
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US86139514A
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Walter Laib
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OHIO SALT Co
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OHIO SALT Co
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/34Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis
    • C25B1/46Simultaneous production of alkali metal hydroxides and chlorine, oxyacids or salts of chlorine, e.g. by chlor-alkali electrolysis in diaphragm cells

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  • the object of this invention is to provide for the manufacture of chlorates of alkalis and alkaline earths by electrolysis, and more particularly the manufacture of potassium chlorate.
  • electrolysis in connection with the application of extraneous heat as a subsequent step in conversion, has been used in the production of chlorates, but in the present invention electrolysis alone is used.
  • the invention consists in exposing a solution of potassium chlorid to a preliminary electrolysis, at a relatively low temperature, in electrolytic cell having a graphite or other carbon anode, and a suitable durable cathode, such as iron, and then further electrolyzing the thus electrolyzed solution in another electrolytic cell having a platinum or equivalent permanent anode, and an iron or other durable cathode, in the presence of a higher temperature due to the electric current, and then conveying the electrolyzed solution to a cool crystallizing tank, from which the crystals are removed from time to time, and the liquor run thence into a storage tank, where it is refreshed or resaturated, whence it may be conveyed to a feed tank and delivered to the graphite cell and the process continued, as I will proceed now to explain and finally claim.
  • 1 is a feed tank in which the solution to be electrolyzed is placed.
  • This tank is provided with any suitable means 2 for discharging the contents of the tank into the electrolytic cell 3 having an anode 4 of carbon, such as graphite, and a cathode 5 of iron or other suitable durable material.
  • the anode and cathode in this cell are suitably supplied with an electric current which acting upon the electrolyte therein serves to electrolyze this solution for the partial production of the desired product.
  • the electrolyzed solution overflows from the cell 3 through pipe 6, or other means, to the cell 7 in which the anode 8 is of platinum, or some alloy thereof, and the cathode 9 is of iron or other suitable durable material, and these electrodes in this cell are supplied with electric current in any suitable way, and the electrolysis is continued in such a manner that sutlicient heat will be generated by the electric current to accelerate the formation of chlorate to such an extent that the final concentration of the desired product in the electrolyte or solution will be obtained by direct formation and conversion in this cell.
  • the cell 3 will be herein referred to as the graphite cell, and the cell 7 as the platinum cell.
  • the electrolyte will be removed, as by pipe 10, to a cooling tank 11 in which the product is crystallized. Crystallization may be accelerated by use of any suitable cooling agent, and I have indicated by dotted lines 12, a coil arranged in the bottom of the crystallizing tank which may be supplied with refrigerating brine, or any other suitable cooling agent, circulated therethrough.
  • a coil arranged in the bottom of the crystallizing tank which may be supplied with refrigerating brine, or any other suitable cooling agent, circulated therethrough.
  • the mother liquor is taken away, as through pipe 13, to a storage tank 14 and there refreshed or enriched with additional salts.
  • This tank 14 may be connected by a pipe 15 'with a pump 16 by which this mother Aliquor may bereturned to the feed tank 1, through the pipe 17, to continue the process.
  • potassium chlorate For the manufacture of potassium chlorate, I use a nearly saturated aqueous solution of potassium chlorid, to which may be added a small quantity of potassium chromate or potassium bichromate for the purpose of improving the efficiency of the subsequent'electrolytic conversion.
  • This solution contained in the feed tank is fed continuously therefrom into the graphite cell and the electric current supplied.
  • the ⁇ temperature of the electrolyte in this cell is maintained in any suitable way below 35, centigrade, and the electrolysis continued until the electrolyte is nearly saturated, at the temperature of the cell, with potassium 5 chlorate, formed therein by the action of the electric current.
  • the thus electrolyzed solution is then conveyed into the platinum cell and the electric current supplied to that cell,
  • the electrolyte is raised to a considerably higher temperature, preferably above 7 0, centigrade.
  • the effect of the current in the platinum cell is to increase the quantity of chlorate contained yin the electrolyte or solution, through its direct action on the potassium chlorid and by efficiently converting to chlorate, the hypochlorite which remained in the liquor coming over from the graphite cell.
  • the invention is not limited to the use of a single graphite cell and a single platinum cell, or to the employment of the same relative numbers ofeach, but I do esteem it of importance that in all cases the liquor after leaving the final graphite cell shall enter one of the platinum cells.
  • the number of platinum cells Will be regulated by the final temperature of the electrolyte which it is desired to obtain.
  • the source of current for each type of cell may be independent.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Description

W. LAIB.
PROCESS 0F PRODUCING CHLORATES 0F ALKALIS AND ALKALINE EARTHS.
APPLICATION FILED SEPT. 12, 1914.
Patented June 15, 1915.
" ITNIME.
WALTER LAIB, OF RITTMAN, OHIO, ASSIGNOR TO THE OHIO SALT COMPANY, O13' WADSWORTH, OHIO, A CORPORATION 0F OHIO.
Specication of Letters Patent.
Patenteddfunc 15, 1915.
Application led September 12, 1914. Serial No. 861,395.
T0 all whom it may concern Be it known that I, WALTER LAIB, a citizen of the United States, residing at Rittman, in the county of Wayne and State of Ohio, have invented a certain new and useful Improvement in Processes of Producing Chlorates of Alkalis and Alkaline Earths, of which the following is a full, clear, and eX- act description.
The object of this invention is to provide for the manufacture of chlorates of alkalis and alkaline earths by electrolysis, and more particularly the manufacture of potassium chlorate.
Prior to this invention, electrolysis, in connection with the application of extraneous heat as a subsequent step in conversion, has been used in the production of chlorates, but in the present invention electrolysis alone is used.
While theinvention may be utilized in the production of various chlorates, I will describe it as applied to the production of potassium chlorate.
The invention consists in exposing a solution of potassium chlorid to a preliminary electrolysis, at a relatively low temperature, in electrolytic cell having a graphite or other carbon anode, and a suitable durable cathode, such as iron, and then further electrolyzing the thus electrolyzed solution in another electrolytic cell having a platinum or equivalent permanent anode, and an iron or other durable cathode, in the presence of a higher temperature due to the electric current, and then conveying the electrolyzed solution to a cool crystallizing tank, from which the crystals are removed from time to time, and the liquor run thence into a storage tank, where it is refreshed or resaturated, whence it may be conveyed to a feed tank and delivered to the graphite cell and the process continued, as I will proceed now to explain and finally claim.
The accompanying drawing is a diagrammatic elevation illustrating the apparatus in its simplest form, by which the process may be practised.
In the drawing, 1 is a feed tank in which the solution to be electrolyzed is placed. This tank is provided with any suitable means 2 for discharging the contents of the tank into the electrolytic cell 3 having an anode 4 of carbon, such as graphite, and a cathode 5 of iron or other suitable durable material. The anode and cathode in this cell are suitably supplied with an electric current which acting upon the electrolyte therein serves to electrolyze this solution for the partial production of the desired product. The electrolyzed solution overflows from the cell 3 through pipe 6, or other means, to the cell 7 in which the anode 8 is of platinum, or some alloy thereof, and the cathode 9 is of iron or other suitable durable material, and these electrodes in this cell are supplied with electric current in any suitable way, and the electrolysis is continued in such a manner that sutlicient heat will be generated by the electric current to accelerate the formation of chlorate to such an extent that the final concentration of the desired product in the electrolyte or solution will be obtained by direct formation and conversion in this cell. For convenience the cell 3 will be herein referred to as the graphite cell, and the cell 7 as the platinum cell. From the platinum cell the electrolyte will be removed, as by pipe 10, to a cooling tank 11 in which the product is crystallized. Crystallization may be accelerated by use of any suitable cooling agent, and I have indicated by dotted lines 12, a coil arranged in the bottom of the crystallizing tank which may be supplied with refrigerating brine, or any other suitable cooling agent, circulated therethrough. As the product crystallizes in this tank it is removed, and the mother liquor is taken away, as through pipe 13, to a storage tank 14 and there refreshed or enriched with additional salts. This tank 14 may be connected by a pipe 15 'with a pump 16 by which this mother Aliquor may bereturned to the feed tank 1, through the pipe 17, to continue the process.
For the manufacture of potassium chlorate, I use a nearly saturated aqueous solution of potassium chlorid, to which may be added a small quantity of potassium chromate or potassium bichromate for the purpose of improving the efficiency of the subsequent'electrolytic conversion. This solution contained in the feed tank is fed continuously therefrom into the graphite cell and the electric current supplied. The `temperature of the electrolyte in this cell is maintained in any suitable way below 35, centigrade, and the electrolysis continued until the electrolyte is nearly saturated, at the temperature of the cell, with potassium 5 chlorate, formed therein by the action of the electric current. The thus electrolyzed solution is then conveyed into the platinum cell and the electric current supplied to that cell,
and by action of the current in this platinum cell, the electrolyte is raised to a considerably higher temperature, preferably above 7 0, centigrade. The effect of the current in the platinum cell is to increase the quantity of chlorate contained yin the electrolyte or solution, through its direct action on the potassium chlorid and by efficiently converting to chlorate, the hypochlorite which remained in the liquor coming over from the graphite cell.
It is to be understood, of course, that the invention is not limited to the use of a single graphite cell and a single platinum cell, or to the employment of the same relative numbers ofeach, but I do esteem it of importance that in all cases the liquor after leaving the final graphite cell shall enter one of the platinum cells. The number of platinum cells Will be regulated by the final temperature of the electrolyte which it is desired to obtain. Nor do I limit the invention to the electric connectionsshown, but it is important that graphite and platinum anode respectively be embodied in the two types of cells. Furthermore, the source of current for each type of cell may be independent.
Among other advantages of my combined process I may mention the following First. A very great saving in the cost of apparatus necessary to manufacture a ixed quantity of chlorate, over the use of platinum anodes alone, since a great partof the necessary electrolysis is conducted With the very much cheaper graphite anodes, thus necessitating a smaller vplatinum equipment.
Second. The process of subsequent electrolysis with platinum anodes and at a higher temperature proves the most-eicient method of converting to chlorates any hypochlorites remaining in the electrolyte which is carried over from those cells which have graphite anodes and'which are operated at a. lower temperature. Third. A decided advantage Iof the combined process over the use of graphite anodes alone is the greater final concentration of electrolyte due to the elevated temperature of the subsequent electrolysis in the platinum cell. This results in the handling-of much smaller quantities of elec- A trolyte, with its consequent saving of storage subsequently further electrolyzing chlorate possible in theV capacities, and the greater ease of cooling the electrolyte for crystallization purposes.
What I claim is 1. The process of producing chlorates of 85 alkalis o1' alkaline earths, which consists in subjecting an aqueous solution of the chlorid of the base Whose chlorate is to be formed,
'to electrolysis in a cell having a graphite anode, at a relatively low temperature, and
the thus electrolyzed solution in a cell having a platinum anode, at a higher temperature.
2. lThe process of producing chlorates of alkalis or alkaline earths, which consists in subjecting an aqueous solution of the chlorid of a base Whose chlorate is to be formed, to electrolysis in a cell having a graphite anode, at a relatively low temperature, and subsequently further electrolyzing the thus electrolyzed solutionin a cell having a platinum anode, at a higher temperature, the higher ntemperature being produced by the electric current lowing through the cell with the platinum anode.
3. The process of producing chlorates of alkalis or alkaline earths, which consists in subjecting an aqueous solution of the chlorid of a base Whose chlorate is to be produced, to a primary electrolysis in a cell having a graphite anode, in the presence of a relatively low temperature, then further elec-l trolyzing the thus electrolyzed solution in a cell having a platinum anode and in which a relatively high heat is maintained, then removing the liquor and crytallizing it.
4. The process of producing potassium chlorate, Which consists in primarily electrolyzing an aqueous solution of potassium chlorid in the presence of a graphite anode and at a relatively low temperature, and subsequently further electrolyzing the thus electrolyzed solution in the presence of a platinum anode at a relatively high temperature.
5. The process of producing potassium chlorate, consisting in subjecting an aqueous solution of potassium ychlorid and a potassium derivative of chromic acid to electrolysis in the presence of a graphite anode and loW temperature, and thereafter further electrolyzing it in the presence of a platinum anode and higher temperature generated in the cell.
In testimony whereof I have hereunto set my hand this tenth day of September A. D. 1914.
' WALTER LAIB.
Witnesses:
W. G. BowMAN, A. M. BECK.
US86139514A 1914-09-12 1914-09-12 Process of producing chlorates of alkalis and alkaline earths. Expired - Lifetime US1143586A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2511516A (en) * 1945-10-31 1950-06-13 Western Electrochemical Compan Process for making sodium chlorate
US3043757A (en) * 1959-07-08 1962-07-10 Olin Mathieson Electrolytic production of sodium chlorate
US3427236A (en) * 1965-03-16 1969-02-11 Mo Och Domsjoe Ab Process for the preparation of an alkali metal chlorate solution for use in a chlorine dioxide generation process
US4434033A (en) 1982-05-27 1984-02-28 Olin Corporation Process for producing concentrated solutions containing alkali metal chlorates and alkali metal chlorides

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2511516A (en) * 1945-10-31 1950-06-13 Western Electrochemical Compan Process for making sodium chlorate
US3043757A (en) * 1959-07-08 1962-07-10 Olin Mathieson Electrolytic production of sodium chlorate
US3427236A (en) * 1965-03-16 1969-02-11 Mo Och Domsjoe Ab Process for the preparation of an alkali metal chlorate solution for use in a chlorine dioxide generation process
US4434033A (en) 1982-05-27 1984-02-28 Olin Corporation Process for producing concentrated solutions containing alkali metal chlorates and alkali metal chlorides

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