US809089A - Process of making caustic alkali. - Google Patents
Process of making caustic alkali. Download PDFInfo
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- US809089A US809089A US25981905A US1905259819A US809089A US 809089 A US809089 A US 809089A US 25981905 A US25981905 A US 25981905A US 1905259819 A US1905259819 A US 1905259819A US 809089 A US809089 A US 809089A
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- alkali
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- 239000003513 alkali Substances 0.000 title description 18
- 238000000034 method Methods 0.000 title description 16
- 230000008569 process Effects 0.000 title description 16
- 239000003518 caustics Substances 0.000 title description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 48
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 48
- 229910052753 mercury Inorganic materials 0.000 description 48
- 229910052783 alkali metal Inorganic materials 0.000 description 32
- 229910001338 liquidmetal Inorganic materials 0.000 description 31
- 150000001340 alkali metals Chemical class 0.000 description 26
- 230000001590 oxidative effect Effects 0.000 description 25
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 23
- 229910052708 sodium Inorganic materials 0.000 description 23
- 239000011734 sodium Substances 0.000 description 23
- 238000005868 electrolysis reaction Methods 0.000 description 22
- 230000005484 gravity Effects 0.000 description 17
- 235000002639 sodium chloride Nutrition 0.000 description 17
- 235000011121 sodium hydroxide Nutrition 0.000 description 17
- 239000007788 liquid Substances 0.000 description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 12
- 229910000497 Amalgam Inorganic materials 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- -1 sodium chlorid Chemical compound 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- SURLGNKAQXKNSP-DBLYXWCISA-N chlorin Chemical compound C\1=C/2\N/C(=C\C3=N/C(=C\C=4NC(/C=C\5/C=CC/1=N/5)=CC=4)/C=C3)/CC\2 SURLGNKAQXKNSP-DBLYXWCISA-N 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 4
- 238000007599 discharging Methods 0.000 description 4
- MJGFBOZCAJSGQW-UHFFFAOYSA-N mercury sodium Chemical compound [Na].[Hg] MJGFBOZCAJSGQW-UHFFFAOYSA-N 0.000 description 4
- 229910001023 sodium amalgam Inorganic materials 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 150000003388 sodium compounds Chemical class 0.000 description 4
- 238000004891 communication Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000528 Na alloy Inorganic materials 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- GFVUWETXLKDTIO-UHFFFAOYSA-J [C+4].[SH-].[SH-].[SH-].[SH-] Chemical compound [C+4].[SH-].[SH-].[SH-].[SH-] GFVUWETXLKDTIO-UHFFFAOYSA-J 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/12—Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper
Definitions
- the object of my invention is to make caustic alkali by electrolytic action in such a manner as to effect a saving in time and expense together with a larger yield with less power in an automatic manner than has been obtained hitherto; and it consists of certain new and novel features, as hereinafter set forth.
- My invention relates particularly to the production of caustic soda and chlorin from aqueous solutions of common salt, but is not limited thereto, as it may be applied to the production of many other alkalis, such as potassa or lithia and other salts or compounds of alkali than the chlorid, such as sodium chlorid,- as em ployed in the specific example of my process herein set forth.
- alkalis such as potassa or lithia
- other salts or compounds of alkali than the chlorid such as sodium chlorid,- as em ployed in the specific example of my process herein set forth.
- the apparatus consists of the following parts: a vessel 1 communicates by bottom outlet 2 with a chamber 3. Within chamber 3 is a ball-float4, communicating by rod 5, lever 6, and link? with avalve 8 in outlet 2. This float-feed mechanism serves to maintain a col.- umn of mercury at uniform level in chamber 3. An outlet-pipe 9, leading from the bottom of chamber 3, opens into a manifold 10, which in turn hasseveral outlet-pipes 11, opening into the bottom of electrolytic cell 12. The layer of mercury13 thus introduced uponthe bottom of electrolytic cell is connected to act as cathode by contact 13f.
- a strip 17 of insulating material which serves to support the stems 18 of anodes 19.
- the cover 15 has also a number of vertical outlet-pipes 20 for chlorin leading into a manifold.
- a receptacle 22 for solid sodium chlorid or other substances to beelectrolyzed.
- These receptacles are in open communication with the electrolyte in cell 13 by openings 23 and serve to maintain it in a saturated condition.
- From the side. of cell 13 one or more sets of pipes 24: 25 lead into one or more vessels 26, from the bottom of which in turn a valve-pipe 27 leads into the oxidizing vessel 28.
- Pipe 24 serves to put the electrolyte into-open communication with a similar body of liquid 29 in vessel 26, while pipe 25 is arranged to draw off the liquid amalgam produced by electrolysis as soon as the same rises above the normal level of the cathode.
- the oxidizing vessel 28 is divided into a number of parallel compartments alternately communicating at opposite ends by vertical baffle-plates 31.
- the liquid amalgam is introduced by pipe 27 into one end of the compartments and flows back and forth through the succeeding compartments to an inlet-pipe 32.
- Adjacent to but above outlet 32 is an inlet-pipe 33 for water or other oxidizing agents.
- the introduced water flows over the surface of the amalgam and serves to remove therefrom the sodium or other easily-oxidizable metals, the resulting sodiumhydrate escaping through the valved outlet-pipe 34.
- the rate of oxidation of the sodium may be increased by placing electrodes 35, of carbon or other relatively electronegative material, in the water and putting them in electrical communication with the amalgam below either directly or by connecting the amalgam with the positive lead of the electrolyzing-current 43 and the carbon electrodes with the negative lead, thereby utilizing the electrical energy generated in the oxidizing-cell to furnish current to the electrolyzing-cell.
- Pipe 32 serves to carry the depleted alloy. metal from the oxidizing-cell into. an adjoining vertical cylinder 36, in the bottom of whichis a valve-outlet 37 controlled by a float 38.
- A-pipe 39 leads from outlet 37 into a receiving vessel 40.
- the mercury col lected in vessel 40 is returned by pipes 4:1, including pump 42, or otherwise to the reservoir 1.
- the movement of mercury and amalgam through the various vessels is efiected solely by the differences of level of the vari- ICC .
- the maintenance of the electrolyte in a saturated condition tends to prevent the absorption of chlorin by it and prevents the changes of level which would otherwise occur.
- the outlet-pipe 34: for sodium hydrate should besomewhat larger than the water-inlet pipe 33 and serves to maintain a constant level of the water in the oxidizing-chambers.
- the apparatus may be adapted for the electrolysis of molten sodium chlorid upon a cathode of molten metal, such as lead, any suitable means being employed for oxidizing and removing the sodium, such as a stream of molten sodium hydrate flowing in contact with the lead-sodium alloy or injected into the body of the alloy, the resulting sodium oxid being regenerated, if desired, by the action of steam.
- molten sodium chlorid upon a cathode of molten metal, such as lead
- any suitable means being employed for oxidizing and removing the sodium, such as a stream of molten sodium hydrate flowing in contact with the lead-sodium alloy or injected into the body of the alloy, the resulting sodium oxid being regenerated, if desired, by the action of steam.
- alloy as used in the claims is intended to cover a solution of an oxidizable .metal in any alloying metal, whether mercury or lead.
- sel or cell 12 is at a higher level than the liquid metal in the oxidizing vessel or cell 28 and that metallic connection between the metal in the electrolytic vessel and the oxidizing vessel is prevented by the interposition of a liquid compound which is either a non-conductor of electricity, such as carbon bisulfld or carbon tetrachlorid, or a liquid or a liquefied compound not a conductor of the first degree to the electric current employed in the electrolytic vessel for the purpose of electrolysis, by which means the electric current is prevented from short-circuiting between the liquid metal in the oxidizing vessel, which is electrically connected as cathode, and the liquid metal in the oxidizing-chamber,which is electrically connected as anode.
- a liquid compound which is either a non-conductor of electricity, such as carbon bisulfld or carbon tetrachlorid, or a liquid or a liquefied compound not a conductor of the first degree to the electric current employed in the electrolytic vessel for the purpose
- the sodium amalgam passing from the electrolytic vessel as it is formed into the oxidizing vessel through a liquid breaking its metallic connection admits of the alkali-metal amalgam passing from one vessel to the other in such a manner that the short-circuiting of electric currents is prevented, and also being accomplished below the surface of the metal contact breaking liquid compound the oxidation of the mercury which would otherwise occur in the presence of atmospheric oxygen is prevented.
- TheChlorinliberated at the anodes passes up and out through the outlet-pipes 20 and 21, while the sodium unites superficially with the mercury, and thus increases the bulk thereof until it rises above the level of the outlet-pipe 25, whereupon it overflows and drops through the layer of carbon tetrachlorid in vessel-26 and accumulates and passes out into the oxidizing vessel 28 through the connecting-pipe 27.
- this sodium amalgam is connected as anode, while suspended in the weak solution of caustic soda floating upon the sodium amalgam is the copper cathode 35.
- a current of electricity is then passed through the cathode and the liquid-metal anode, whereupon the sodium therein becomes oxidized and is separated therefrom, dissolving in the weak alkali solution, while the mercury depleted of its sodium as it accumulates gradually raises the valve 38 and passes out into the cistern or reservoir 40-, from which it is returned to reservoir 1 to be reused.
- the caustic soda produced in the oxidizingchamber 28 is gradually withdrawn through the pipe 34:, controlled by a valve therein, while a corresponding amount of water is allowed to pass in and over the mercury amalgam during electrolytic action .through pipe 33.
- the water is gradually passed through the oxidizing-cell over the sodium amalgam, the sodium in which is being oxidized and dissolved in water with the formation of caustic soda in a tortuous manner and with such a speed with relation to electrolytic action in the cell that a solution of caustic soda of calculated strength may be withdrawn through pipe 34 accordingly as the water is supplied through pipe 33.
- caustic alkali from salts of alkali metal, which consists in introducing mercury into a cell containing an aqueous solution of the alkali-metal salt to be decomposed, liberating the alkali metal in juxtaposition to the mercury, causing the mercury containing the alkali metal to pass into a separate or oxidizing cell through a liquid compound breaking its metallic connection between the mercury in the electrolytic cell and the mercury in the oxidizing-cell, by gravity, oxidizing the alkali metal contained in the mercury in the oxidizing-cell with the formation of caustic alkali, by electrolysis, and causing the mercury depleted of alkali to pass from the oxidizing-cell by gravity.
- the process of making caustic alkali from salts of alkali metals which consists in passing mercury through an electrolytic cell containing an aqueous solution of the alkali-metal salt to be decomposed during electrolysis, decreasing the density and increasing the bulk of the mercury in the said electrolytic cell by causing it to unite with the alkali metal libcrated by electrolysis therein, and causing it to overflow into a separate or oxidizing cell through a liquid compound capable of breaking metallic contact of the mercury in the separate cells from each other, by gravity, increasing the density of the mercury in the oxidizing-cell by separating the alkali metal therefrom by electrolytic oxidation, and dis charging the mercury, thus separated from alkali metal, by gravity.
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Electrolytic Production Of Metals (AREA)
Description
No. 909,099. PATENTED JAN. 2, 1906.
H. s. BLAGKMORB.
PROGESSOF MAKING GAUSTIO ALKALI.
APPLICATION FILED MAY 10, 1905.
@"W MUZML UNITED STATES PATENT OFFICE.
PROCESS OF MAKING CAUSTIC ALKALI.
Specification of Letters Patent.
Patented Jan. 2, 1906.
Application filed May 10, 1905 Serial No. 259,819.
To all whom, it may concern:
Be it known that I, HENRY SPnNoER BLACK- MORE, a citizen of the United States, residing at Mount Vernon, in the county of VVestchester and State of New York, have invented certain new and useful Improvements in Processes of Making Caustic Alkali, ofwhich the following is a specification.
The object of my invention is to make caustic alkali by electrolytic action in such a manner as to effect a saving in time and expense together with a larger yield with less power in an automatic manner than has been obtained hitherto; and it consists of certain new and novel features, as hereinafter set forth.
My invention relates particularly to the production of caustic soda and chlorin from aqueous solutions of common salt, but is not limited thereto, as it may be applied to the production of many other alkalis, such as potassa or lithia and other salts or compounds of alkali than the chlorid, such as sodium chlorid,- as em ployed in the specific example of my process herein set forth.
In carrying out my invention for the production of caustic soda from an aqueous solution of common salt (sodium chlorid) I proceed as follows, reference being had to the accompanying drawings, in which+ Figure 1 is a longitudinal vertical section of the apparatus, taken on line I I of Fig. 2. Fig. 2 is a plan view, partly in horizontal section; and Fig. 3 illustrates a modification,using asiphon 25 to draw off the alloy from the electrolytic cell, a body of liquid other than the electrolyte being used in the intermediate vessel 28for example, carbon bisulfid, carbon tetrachlorid, &c.
The apparatus consists of the following parts: a vessel 1 communicates by bottom outlet 2 with a chamber 3. Within chamber 3 is a ball-float4, communicating by rod 5, lever 6, and link? with avalve 8 in outlet 2. This float-feed mechanism serves to maintain a col.- umn of mercury at uniform level in chamber 3. An outlet-pipe 9, leading from the bottom of chamber 3, opens into a manifold 10, which in turn hasseveral outlet-pipes 11, opening into the bottom of electrolytic cell 12. The layer of mercury13 thus introduced uponthe bottom of electrolytic cell is connected to act as cathode by contact 13f.
Supported upon Above each row of openings is a strip 17 of insulating material which serves to support the stems 18 of anodes 19. The cover 15 has also a number of vertical outlet-pipes 20 for chlorin leading into a manifold. Upon each end of the electrolytic cell is arranged a receptacle 22 for solid sodium chlorid or other substances to beelectrolyzed. These receptacles are in open communication with the electrolyte in cell 13 by openings 23 and serve to maintain it in a saturated condition. From the side. of cell 13 one or more sets of pipes 24: 25 lead into one or more vessels 26, from the bottom of which in turn a valve-pipe 27 leads into the oxidizing vessel 28. Pipe 24 serves to put the electrolyte into-open communication with a similar body of liquid 29 in vessel 26, while pipe 25 is arranged to draw off the liquid amalgam produced by electrolysis as soon as the same rises above the normal level of the cathode.
The oxidizing vessel 28 is divided into a number of parallel compartments alternately communicating at opposite ends by vertical baffle-plates 31. The liquid amalgam is introduced by pipe 27 into one end of the compartments and flows back and forth through the succeeding compartments to an inlet-pipe 32. Adjacent to but above outlet 32 is an inlet-pipe 33 for water or other oxidizing agents. The introduced water flows over the surface of the amalgam and serves to remove therefrom the sodium or other easily-oxidizable metals, the resulting sodiumhydrate escaping through the valved outlet-pipe 34. The rate of oxidation of the sodium may be increased by placing electrodes 35, of carbon or other relatively electronegative material, in the water and putting them in electrical communication with the amalgam below either directly or by connecting the amalgam with the positive lead of the electrolyzing-current 43 and the carbon electrodes with the negative lead, thereby utilizing the electrical energy generated in the oxidizing-cell to furnish current to the electrolyzing-cell. Pipe 32 serves to carry the depleted alloy. metal from the oxidizing-cell into. an adjoining vertical cylinder 36, in the bottom of whichis a valve-outlet 37 controlled by a float 38. A-pipe 39 leads from outlet 37 into a receiving vessel 40. The mercury col lected in vessel 40 is returned by pipes 4:1, including pump 42, or otherwise to the reservoir 1. The movement of mercury and amalgam through the various vessels is efiected solely by the differences of level of the vari- ICC . slight vacuum over the electrolyte and facilitate the escape of chlorin. The maintenance of the electrolyte in a saturated condition tends to prevent the absorption of chlorin by it and prevents the changes of level which would otherwise occur. The outlet-pipe 34: for sodium hydrate should besomewhat larger than the water-inlet pipe 33 and serves to maintain a constant level of the water in the oxidizing-chambers.
By the use of vessels which are provided with heating means the apparatus may be adapted for the electrolysis of molten sodium chlorid upon a cathode of molten metal, such as lead, any suitable means being employed for oxidizing and removing the sodium, such as a stream of molten sodium hydrate flowing in contact with the lead-sodium alloy or injected into the body of the alloy, the resulting sodium oxid being regenerated, if desired, by the action of steam.
The term alloy, as used in the claims is intended to cover a solution of an oxidizable .metal in any alloying metal, whether mercury or lead.
As is well known, the addition of a comparatively small amount of alkali or an alkaline-earth metal to mercury converts the latter into a pasty condition in which it does not readily flow. This difflulty may be avoided When mercury is employed as a cathode by applying heat to it, thereby maintaining the amalgam produced by electrolysis in fluent condition and enabling larger percentages of sodium to be absorbed without interforcing with the continuous overflow of amalgam into the oxidizing vessel. Such heat may be supplied by a gas-burner 4E4. beneath the electrolytic cell, as indicated by dotted lines in Fig. 1.
It will be noted that the alkali-metal amalgam or alloy produced in the electrolytic ves.
sel or cell 12 is at a higher level than the liquid metal in the oxidizing vessel or cell 28 and that metallic connection between the metal in the electrolytic vessel and the oxidizing vessel is prevented by the interposition of a liquid compound which is either a non-conductor of electricity, such as carbon bisulfld or carbon tetrachlorid, or a liquid or a liquefied compound not a conductor of the first degree to the electric current employed in the electrolytic vessel for the purpose of electrolysis, by which means the electric current is prevented from short-circuiting between the liquid metal in the oxidizing vessel, which is electrically connected as cathode, and the liquid metal in the oxidizing-chamber,which is electrically connected as anode. It will also be noted that the sodium amalgam passing from the electrolytic vessel as it is formed into the oxidizing vessel through a liquid breaking its metallic connection admits of the alkali-metal amalgam passing from one vessel to the other in such a manner that the short-circuiting of electric currents is prevented, and also being accomplished below the surface of the metal contact breaking liquid compound the oxidation of the mercury which would otherwise occur in the presence of atmospheric oxygen is prevented.
In carrying out my invention for producing caustic soda from common salt (sodium chlorid) I place in the electrolytic vessel 12 a quantity of water and saturate the same with common salt, (sodium chlorid,) which is dissolved into the water from the receptacles 22, in which it is placed. I also place Water in vessel 28 and introduce below the same a layer or stratum of mercury. I then place in vessel 26 upon the mercury therein a quantity of carbon tetrachlorid sufficient to reach the connecting-pipe and then feed mercury from receptacle or reservoir 1 through the metalregulating chamber or balancing-chamber 3 into the electrolytic cell 12 until it nearly reaches the outlet-pipe 25, the float checkvalve in vessel 3 being regulated to check the flow of mercury at that level. I then pass a current of electricity through the anodes 19, connecting the mercury in the bottom of electrolytic vessel 12 as cathode, whereupon the sodium chlorid in solution above the mercury cathode becomes electrolyzed and chlorin and sodium liberated therefrom. TheChlorinliberated at the anodes passes up and out through the outlet-pipes 20 and 21, while the sodium unites superficially with the mercury, and thus increases the bulk thereof until it rises above the level of the outlet-pipe 25, whereupon it overflows and drops through the layer of carbon tetrachlorid in vessel-26 and accumulates and passes out into the oxidizing vessel 28 through the connecting-pipe 27. In the oxidizing vessel this sodium amalgam is connected as anode, while suspended in the weak solution of caustic soda floating upon the sodium amalgam is the copper cathode 35. A current of electricity is then passed through the cathode and the liquid-metal anode, whereupon the sodium therein becomes oxidized and is separated therefrom, dissolving in the weak alkali solution, while the mercury depleted of its sodium as it accumulates gradually raises the valve 38 and passes out into the cistern or reservoir 40-, from which it is returned to reservoir 1 to be reused.
During the continuous operation of the process it will be seen that the whole process is operated in an automatic manner by grav- IIO ity actuated by the increase and decrease in bulk of the liquid metal actuated by electrolytic action.
The caustic soda produced in the oxidizingchamber 28 is gradually withdrawn through the pipe 34:, controlled by a valve therein, while a corresponding amount of water is allowed to pass in and over the mercury amalgam during electrolytic action .through pipe 33. In this manner the water is gradually passed through the oxidizing-cell over the sodium amalgam, the sodium in which is being oxidized and dissolved in water with the formation of caustic soda in a tortuous manner and with such a speed with relation to electrolytic action in the cell that a solution of caustic soda of calculated strength may be withdrawn through pipe 34 accordingly as the water is supplied through pipe 33.
Having now described my invention, What I claim as new, and desire to secure by Letters Patent, is
1. The process of making caustic alkali from salts of alkali-metals, which consists in introducing into a cell containing an aqueous solution of the alkali metal salt to be decomposed, a liquid metal, liberating the alkali metal in juxtaposition to the liquid metal by electrolysis, causing the liquid metal containing the alkali metal to pass into a separate or oxidizing cell through a liquid compound breaking its metallic connection between the liquid metal in the electrolytic .cell' and the liquid metal in the oxidizing-cell, by gravity, oxidizing the alkali metal contained in the liquid metal inthe oxidizing-cell with the formation of caustic alkali, by electrolysis, and cansing the liquid metal depleted of alkali to pass from the oxidizing-cell by gravity.
2. The process of making caustic alkali from salts of alkali metals. which consists in passing a liquid metal through an electrolytic cell con taining an aqueous solution of the alkali-metal salt to be decomposed during electrolysis, decreasing the density and increasing the bulk of the liquid metal in the said electrolytic cell by causing itto unite with the alkali metal liberated by electrolysis therein, and. causing it to overflow into a separate or oxidizing cell through a liquid compound capable of breaking metallic contact of the liquid metal in the separate cells from each other, by gravity, increasing the density of the liquid metal in the oxidizing-cell by separating the alkali metal therefrom by electrolytic oxidation, and discharging the liquid metal, thus separated from alkali metal, therefrom, by gravity.
3. The process of making caustic soda from sodium compounds, which consists in introducing into a cell containing an aqueous solution of the sodium compound to be decomposed, a liquid metal, liberating the sodium in juxtaposition to the liquid metal by electrolysis, causing the liquid metal containing the sodium to pass into a separate or oxidizing cell through a liquid compound breaking its metallic connection between the liquid metal in the electrolytic cell, and the liquid metal in the oxidizing-cell, by gravity, oxidizing the sodium contained in the liquid metal in the oxidizing-cell with the formation of caustic soda by electrolysis and causing the liquid metal depleted of sodium to pass from the oxidizing-cell, by gravity.
4. The process of making caustic soda from sodium chlorid, which consists in introducing into a cell containing an aqueous solution of the sodium chlorid to be decomposed, a liquid metal, liberating the sodium in juxtaposition to the liquid metal by electrolysis, causing the liquid metal containing the sodium to pass into a separate or oxidizing cell through a liquid compound breaking its metallic connection between the liquid metal in the electrolytic cell, and the liquid metal in the oxidizing-cell, by gravity, oxidizing the sodium contained in the liquid metal in the oxidizing-cell with the formation of caustic soda by electrolysis and causing the liquid metal depleted of sodium to pass from the oxidizing-cell, by gravity.
5. The process of making caustic alkali from salts of alkali metal, which consists in introducing mercury into a cell containing an aqueous solution of the alkali-metal salt to be decomposed, liberating the alkali metal in juxtaposition to the mercury, causing the mercury containing the alkali metal to pass into a separate or oxidizing cell through a liquid compound breaking its metallic connection between the mercury in the electrolytic cell and the mercury in the oxidizing-cell, by gravity, oxidizing the alkali metal contained in the mercury in the oxidizing-cell with the formation of caustic alkali, by electrolysis, and causing the mercury depleted of alkali to pass from the oxidizing-cell by gravity.
6, The process of making caustic soda from sodium compounds, which consists in introducing mercury into a cell containing an aqueous solution of the sodium compound to position to the mercury by electrolysis, causing the mercury containing the sodium to pass into a separate or oxidizing cell through aliquid compound breaking its metallic connection between the mercury in the electrolytic cell, and the mercury in the oxidizing-cell, by gravity, oxidizing the sodium contained in the' mercury in the oxidizing-cell with the formation of caustic soda by electrolysis and causing the mercury depleted of sodium to pass from the oxidizing-cell, by gravity.
7. The process of making caustic soda from sodium chlorid, which consists in introducing mercury into a cell containing an aqueous so lution of the sodium chlorid to be decomposed, liberating the sodium in juxtaposition to the mercury by electrolysis, causing the mercury containing the sodium to pass into a separate or oxidizing cell through a liquid compound be decomposed liberating the sodium in juxta- 8. The process of making caustic alkali from salts of alkali metals, which consists in passing mercury through an electrolytic cell containing an aqueous solution of the alkali-metal salt to be decomposed during electrolysis, decreasing the density and increasing the bulk of the mercury in the said electrolytic cell by causing it to unite with the alkali metal libcrated by electrolysis therein, and causing it to overflow into a separate or oxidizing cell through a liquid compound capable of breaking metallic contact of the mercury in the separate cells from each other, by gravity, increasing the density of the mercury in the oxidizing-cell by separating the alkali metal therefrom by electrolytic oxidation, and dis charging the mercury, thus separated from alkali metal, by gravity.
9. The process of making caustic alkali from salts of alkali metals, which consists in passing mercury through an electrolytic cell containing an aqueous solution of an alkali-metal salt to be decomposed during electrolysis, decreasing the density and increasing the bulk of the mercury in the said electrolytic cell by causing it to unite with the alkali metal liberated by electrolysis therein, causing it to over" flow into a separate or oxidizing cell through an electrically non-conductive liquid capable of breaking metallic contact of the mercury in the separate cells from each other, by gravity, increasing the density of the mercury in the oxidizing-cell by separating the alkali metal therefrom by electrolytic oxidation, and discharging the mercury, thus separated from the alkali metal, therefrom, by gravity.
10. The process of making caustic alkali from salts of alkali metals, which consists in passing mercury through an electrolytic cell containing an aqueous solution of an alkali-metal salt to be decomposed during electrolysis, decreasing the densityand increasing the bulk of the mercury in the said electrolytic cell by causing it to unite with the alkali metal liberated by electrolysis therein, causing it to overflow into a separate or oxidizing cell through carbon tetrachlorid thereby breaking metallic contact of the mercury in the separate cells from each other, increasing the density of the mercury in the oxidizing-cell by separating the alkali metal therefrom by electrolytic oxidation, and discharging the mercury, thus separated from the alkali metal, by gravity.
In testimony whereof I affix my signature in presence of two witnesses.
HENRY SPENCER BLACKMORE.
Witnesses:
H. N. JENKINS, ALBERT W. SIoUssA.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25981905A US809089A (en) | 1905-05-10 | 1905-05-10 | Process of making caustic alkali. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25981905A US809089A (en) | 1905-05-10 | 1905-05-10 | Process of making caustic alkali. |
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| Publication Number | Publication Date |
|---|---|
| US809089A true US809089A (en) | 1906-01-02 |
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ID=2877570
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US25981905A Expired - Lifetime US809089A (en) | 1905-05-10 | 1905-05-10 | Process of making caustic alkali. |
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| Country | Link |
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| US (1) | US809089A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2477579A (en) * | 1945-12-01 | 1949-08-02 | California Research Corp | Electrolytic process for the production of cyclohexadiene dicarboxylic acids |
| US2584824A (en) * | 1946-01-31 | 1952-02-05 | Solvay | Electrolytic preparation of alkali metal chlorites |
| US2970095A (en) * | 1954-10-07 | 1961-01-31 | Ludwig Kandler | Method and apparatus for electrolytic decomposition of amalgams |
| US2989450A (en) * | 1958-01-30 | 1961-06-20 | Dow Chemical Co | Preparation of alkali metal halides |
| US3068157A (en) * | 1958-12-22 | 1962-12-11 | Accumulatoren Fabrik Ag | Process for using the decomposition energy of amalgams for electrolysis of metal salts by using reversible hydrogen electrodes |
| US3092516A (en) * | 1960-05-06 | 1963-06-04 | Standard Oil Co | Electrochemical reaction apparatus |
| US3104213A (en) * | 1957-12-02 | 1963-09-17 | Chlormetals Inc | Electrolytic cell and process thereof |
-
1905
- 1905-05-10 US US25981905A patent/US809089A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2477579A (en) * | 1945-12-01 | 1949-08-02 | California Research Corp | Electrolytic process for the production of cyclohexadiene dicarboxylic acids |
| US2584824A (en) * | 1946-01-31 | 1952-02-05 | Solvay | Electrolytic preparation of alkali metal chlorites |
| US2970095A (en) * | 1954-10-07 | 1961-01-31 | Ludwig Kandler | Method and apparatus for electrolytic decomposition of amalgams |
| US3104213A (en) * | 1957-12-02 | 1963-09-17 | Chlormetals Inc | Electrolytic cell and process thereof |
| US2989450A (en) * | 1958-01-30 | 1961-06-20 | Dow Chemical Co | Preparation of alkali metal halides |
| US3068157A (en) * | 1958-12-22 | 1962-12-11 | Accumulatoren Fabrik Ag | Process for using the decomposition energy of amalgams for electrolysis of metal salts by using reversible hydrogen electrodes |
| US3092516A (en) * | 1960-05-06 | 1963-06-04 | Standard Oil Co | Electrochemical reaction apparatus |
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