US633272A - Process of manufacturing chlorates by electrolysis. - Google Patents
Process of manufacturing chlorates by electrolysis. Download PDFInfo
- Publication number
- US633272A US633272A US66306997A US1897663069A US633272A US 633272 A US633272 A US 633272A US 66306997 A US66306997 A US 66306997A US 1897663069 A US1897663069 A US 1897663069A US 633272 A US633272 A US 633272A
- Authority
- US
- United States
- Prior art keywords
- chlorates
- electrolysis
- cell
- cathode
- manufacturing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
- C25B1/26—Chlorine; Compounds thereof
- C25B1/265—Chlorates
Definitions
- This invention relates to electrolytic production of the chlorat'es of sodium and potassium; and it has for its object to insure a means ordinarily employed in the production of such chlorates.
- the tank A which is the cathode, is mad of sheet or thin plate metal, conveniently iron.
- the top edge of the tank is surrounded by an angle-metal stiffener a, which serves also to support longitudinal bearers b,of wood.
- These bearers I) support cross-bearers 0, upon which rest longitudinal copper rods d, to which the pieces of carbon B forming the anode are connected by means of hook-bolts e.
- the hinder ends of these bolts are hooked over the bars at and their forward ends are passed through the respective pieces of carbon and have wing-nuts f screwed thereon to tighten the carbons against the bars 01. Any carbon B may thus be readily removed and replaced without interfering with the working of the cell.
- the tank itself forms, as above stated, the cathode, and the surface area of the oathode may be increased by the introduction adjacent rows of the carbons indicated in-the drawings. As shownin the drawings, the cell becomes a double one. If two or more metal I plates, such as C, be placed within the tank, each by itself between two adjacent rows .of carbons, the'cell becomes triple, quadruple, 850., "according to the number of plates used. The plate or plates 0 are provided with holes Serial No. 663,069. (No specimens.) I
- the solution D, Fig. 3, in the cell is'sodium or potassium chlorid or a solution of these chlorids mixed and is free from alkaline carbonates by preference.
- a diaphragm is omitted altogether and the solution is covered with a thick layer of some buoyant non-conducting substance E, Fig. 3, as pumice-stone, cork, or the like, preferably pumice-stone in bits of about the size of a hazelnut, the layer being about oneinch deep.
- the purpose of this pumice or floating material is to scrub the escaping gases, and thereby prevent them from carrying off any portion of the solution forming the electrolyte.
- the surface areas of the anode (at the surface of which the chlorin is liberated) and of the cathode will be of course arranged to insure a current density suitable for economical workingthat is to say, about twenty amperes per square foot of the superficial area of the cathode.
- the carbons B shown in the drawings are bits of gas-carbon; but molded or prepared carbons may be used as well, or platinum may be used in lieu of. carbon for the anodes.
- An important feature of the invention consists in the maintenance of the temperature of the cell at about 30 to 40centigrade during the Working, and this is most conveniently effected by regulating the current density, as above stated, at about twenty amperes per square foot of cathode area.
- the advantage gained by maintaining such low temperature in the cell is'this: In ordinary working with the usual apparatus there is a small anode and cathode area, and consequently a relatively high current density at their surfaces, with the result that the electrolyte'is heated, and thus current is wasted in raising the temperature of the electrolyte.
- Thepresent invention provides a large anode and cathode area, and thus permits a lower current density to be used, and this insures a low temperature in working, no current being wasted in heating the electrolyte.
- the advantage lies in avoiding against loss of current, and the construction of the apparatus employed permits of effecting this saving.
- the anode-surfaces are separated from the cathode-s11 rfaces by the electrolyte only, no porous protecting material being interposed, as in ordinary cases. Where such material is employed, the apparatus cannot be worked at as low a voltage as where it is not required, and consequently the use of such an intermediate to some extent impairs the eificiency of the apparatus.
- This apparatus requires no protective lining for the cell, as the metal liberated at the cathodesuriace is in itself a suflicient protection.
- Any suitable generator of electricity may be employed in the operation, the anodes and cathodes forming, of course, parts of the circuit.
- an electrolyte consisting of an aqueous solution of an alkali-metal chlorid, which consists in passing a current of electricity through said solution while the latter is covered with a layer of some buoyant nonconducting material, whereby the gases disengaged are scrubbed, and maintaining the current density during the operation, at about twenty ampe'res per square foot, substantially as set forth.
Description
No. 633,272. Patented Sept. l9, I899.
T. PARKER. I
PROCESS OF MANUFACTURING CHLOBATES BY ELECTBOLYSIS.
(Apylics-tion filed Dec. 22, 1897.)
ikmyv w greatly increased efficiency compared with the of one or more metal plates 0 between two UNITE STATES PATENT OFFICE.
THOMAS PARKER, or TETTENHALL, ENGLAND.
PROCESS OF MANUFACTURING CHLORATES BY ELECTROLYSIS.
srncrrmarmn forming pea of Letters Patent No. 633,272, dated September 19, 1899.
Application at DecemberZZ, 1897- To all whom it may concern:
Be it known that I, THOMAS PARKER, a subject of the Queen of Great Britain, residing at Tettenhall, near Wolverhampton, in the county of Stafford, England, have invented certain new and useful Improvements in the Electrolytic Production of the Ohlorates of Sodium and Potassium, of which the following is a specification.
This invention relates to electrolytic production of the chlorat'es of sodium and potassium; and it has for its object to insure a means ordinarily employed in the production of such chlorates.
The invention consists in the method of procedure employed in the electrolytic operation, and the construction of the cell employed is illustrated in the accompanying drawings, wherein- Figure 1 is a longitudinal section, Fig. 2 a plan, and Fig. 3 a transverse section, of a double cell constructed and constituted according to this invention. I
The tank A, which is the cathode, is mad of sheet or thin plate metal, conveniently iron. The top edge of the tank is surrounded by an angle-metal stiffener a, which serves also to support longitudinal bearers b,of wood. These bearers I) support cross-bearers 0, upon which rest longitudinal copper rods d, to which the pieces of carbon B forming the anode are connected by means of hook-bolts e. The hinder ends of these boltsare hooked over the bars at and their forward ends are passed through the respective pieces of carbon and have wing-nuts f screwed thereon to tighten the carbons against the bars 01. Any carbon B may thus be readily removed and replaced without interfering with the working of the cell. The tank itself forms, as above stated, the cathode, and the surface area of the oathode may be increased by the introduction adjacent rows of the carbons indicated in-the drawings. As shownin the drawings, the cell becomes a double one. If two or more metal I plates, such as C, be placed within the tank, each by itself between two adjacent rows .of carbons, the'cell becomes triple, quadruple, 850., "according to the number of plates used. The plate or plates 0 are provided with holes Serial No. 663,069. (No specimens.) I
g' therethrough, or theyare otherwise of such character as to allow free communication between the solution or liquid on opposite sides thereof, and the plate or plates are of course electrically connected with the metal tank in a manner which constitutes it part of the cathode. If no plate 0 is inserted within the tank, one row only of carbons is used and the cell is then a simple or single cell. In practice any desired number of single, double, treble, &c., cells may of course be worked together in series.
The solution D, Fig. 3, in the cell is'sodium or potassium chlorid or a solution of these chlorids mixed and is free from alkaline carbonates by preference. A diaphragm is omitted altogether and the solution is covered with a thick layer of some buoyant non-conducting substance E, Fig. 3, as pumice-stone, cork, or the like, preferably pumice-stone in bits of about the size of a hazelnut, the layer being about oneinch deep. The purpose of this pumice or floating material is to scrub the escaping gases, and thereby prevent them from carrying off any portion of the solution forming the electrolyte.
' The surface areas of the anode (at the surface of which the chlorin is liberated) and of the cathode will be of course arranged to insure a current density suitable for economical workingthat is to say, about twenty amperes per square foot of the superficial area of the cathode.
The carbons B shown in the drawings are bits of gas-carbon; but molded or prepared carbons may be used as well, or platinum may be used in lieu of. carbon for the anodes.
An important feature of the invention consists in the maintenance of the temperature of the cell at about 30 to 40centigrade during the Working, and this is most conveniently effected by regulating the current density, as above stated, at about twenty amperes per square foot of cathode area. The advantage gained by maintaining such low temperature in the cell is'this: In ordinary working with the usual apparatus there is a small anode and cathode area, and consequently a relatively high current density at their surfaces, with the result that the electrolyte'is heated, and thus current is wasted in raising the temperature of the electrolyte. Thepresent invention provides a large anode and cathode area, and thus permits a lower current density to be used, and this insures a low temperature in working, no current being wasted in heating the electrolyte. Obviously the advantage lies in avoiding against loss of current, and the construction of the apparatus employed permits of effecting this saving. It will be observed also that in carrying out this invention the anode-surfaces are separated from the cathode-s11 rfaces by the electrolyte only, no porous protecting material being interposed, as in ordinary cases. Where such material is employed, the apparatus cannot be worked at as low a voltage as where it is not required, and consequently the use of such an intermediate to some extent impairs the eificiency of the apparatus. This apparatus requires no protective lining for the cell, as the metal liberated at the cathodesuriace is in itself a suflicient protection.
Any suitable generator of electricity may be employed in the operation, the anodes and cathodes forming, of course, parts of the circuit.
Having thus described my invention, I claim 1. The herein-described method of carrying on the prod nction by electrolysis of chlorates,
directly from an electrolyte consisting of an aqueous solution of an alkali-metal chlorid, which consists in passing a current of electricity through said solution while the latter is covered with a layer of some buoyant nonconducting material, whereby the gases disengaged are scrubbed, and maintaining the current density during the operation, at about twenty ampe'res per square foot, substantially as set forth.
2. The herein-described method of carrying on the production by electrolysis of chlorates, directly from an electrolyte consisting of a solution of an alkali-metal chlorid, which consists in passing a current of electricity through said electrolytefrom the anode to the cathode, separated only by the electrolyte, said solution being covered with a layer of some buoyant non-conducting material whereby the gases disengaged are scrubbed, substantially as set forth.
In witness whereof I have hereunto signed my name in the presence of two subscribing witnesses.
THOMAS PARKER.
\Vitnesses:
STEPHEN \VATKINS, ROBERT M. LESTER.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66306997A US633272A (en) | 1897-12-22 | 1897-12-22 | Process of manufacturing chlorates by electrolysis. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66306997A US633272A (en) | 1897-12-22 | 1897-12-22 | Process of manufacturing chlorates by electrolysis. |
Publications (1)
Publication Number | Publication Date |
---|---|
US633272A true US633272A (en) | 1899-09-19 |
Family
ID=2701864
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US66306997A Expired - Lifetime US633272A (en) | 1897-12-22 | 1897-12-22 | Process of manufacturing chlorates by electrolysis. |
Country Status (1)
Country | Link |
---|---|
US (1) | US633272A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2515614A (en) * | 1945-10-31 | 1950-07-18 | Western Electrochemical Compan | Electrolytic cell |
US3451906A (en) * | 1965-10-29 | 1969-06-24 | Electric Reduction Co | Respacing of electrodes in electrolytic cells for the production of the halates,perhalates or hypohalites of alkali metals |
US3948747A (en) * | 1975-05-09 | 1976-04-06 | Amax Inc. | Elimination or control of acid mists over electrolytic cells |
US20030137427A1 (en) * | 2001-12-11 | 2003-07-24 | Tichborne Frank George | Signal lamps and apparatus |
US20030230239A1 (en) * | 2002-06-17 | 2003-12-18 | Applied Materials, Inc. | Gas flow division in a wafer processing system having multiple chambers |
US6805787B2 (en) | 2001-09-07 | 2004-10-19 | Severn Trent Services-Water Purification Solutions, Inc. | Method and system for generating hypochlorite |
US20100116787A1 (en) * | 2005-03-25 | 2010-05-13 | Tokyo Electron Limited | Etching method and apparatus |
-
1897
- 1897-12-22 US US66306997A patent/US633272A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2515614A (en) * | 1945-10-31 | 1950-07-18 | Western Electrochemical Compan | Electrolytic cell |
US3451906A (en) * | 1965-10-29 | 1969-06-24 | Electric Reduction Co | Respacing of electrodes in electrolytic cells for the production of the halates,perhalates or hypohalites of alkali metals |
US3948747A (en) * | 1975-05-09 | 1976-04-06 | Amax Inc. | Elimination or control of acid mists over electrolytic cells |
US6805787B2 (en) | 2001-09-07 | 2004-10-19 | Severn Trent Services-Water Purification Solutions, Inc. | Method and system for generating hypochlorite |
US20030137427A1 (en) * | 2001-12-11 | 2003-07-24 | Tichborne Frank George | Signal lamps and apparatus |
US20030230239A1 (en) * | 2002-06-17 | 2003-12-18 | Applied Materials, Inc. | Gas flow division in a wafer processing system having multiple chambers |
US20100116787A1 (en) * | 2005-03-25 | 2010-05-13 | Tokyo Electron Limited | Etching method and apparatus |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3676315A (en) | Production of sodium chlorate | |
US633272A (en) | Process of manufacturing chlorates by electrolysis. | |
US2987463A (en) | High amperage diaphragm cell for the electrolysis of brine | |
US3268427A (en) | Electrolysis of alkaline chloride solutions | |
US3390072A (en) | Diaphragm electrolytic alkali halogen cell | |
US1847435A (en) | Electrolytic manufacture of chlorine | |
GB861978A (en) | Improvements in or relating to a process for the electrolytic production of fluorineand apparatus therefor | |
US3772201A (en) | Electrode for electrolytic conversion cells including passage means in the electrode for electrolyte flow through the electrode | |
US2693445A (en) | Electrolytic method for production of fluorine | |
US3796648A (en) | Electrolytic cell having self-aligning anodes | |
US555511A (en) | Method of converting potential energy of carbon into electrical energy | |
US1446736A (en) | Manufacture of hydrogen and oxygen | |
US2959527A (en) | Self-restoring anode in multi-cell furnaces particularly for the electrolytic production of aluminum | |
US1176551A (en) | Apparatus for decomposing alkali-chlorid solutions. | |
US2786810A (en) | Anodes and cover of electrolytic cells | |
US1863661A (en) | Manufacture of fluorine | |
US1143586A (en) | Process of producing chlorates of alkalis and alkaline earths. | |
US655343A (en) | Electrolytic cell. | |
US2624703A (en) | Electrolytic fluorine cell | |
US1092369A (en) | Process of making chlorates and apparatus therefor. | |
US3251756A (en) | Electrolytic process for making phosphine | |
GB190022406A (en) | Improvements in the Decomposition of Alkaline Salts by Electrolysis and in Apparatus therefor | |
US2285858A (en) | Electrolytic process for the production of quinone and hydroquinone | |
Murray et al. | Carbon-Anode Fluorine Cell | |
US1347088A (en) | Electrolytic apparatus |