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- US583513A US583513A US583513DA US583513A US 583513 A US583513 A US 583513A US 583513D A US583513D A US 583513DA US 583513 A US583513 A US 583513A
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- United States
- Prior art keywords
- anode
- cathode
- parchment
- apertures
- frame
- Prior art date
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- 239000007788 liquid Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 14
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 11
- 235000011941 Tilia x europaea Nutrition 0.000 description 11
- 239000004571 lime Substances 0.000 description 11
- 239000012528 membrane Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 7
- 238000005868 electrolysis reaction Methods 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 6
- 239000011575 calcium Substances 0.000 description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- -1 halogen alkali metals Chemical class 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 239000012266 salt solution Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229940072033 potash Drugs 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- 235000015320 potassium carbonate Nutrition 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 208000025814 Inflammatory myopathy with abundant macrophages Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 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 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 235000004879 dioscorea Nutrition 0.000 description 1
- 229910052571 earthenware Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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
- C25B13/00—Diaphragms; Spacing elements
- C25B13/04—Diaphragms; Spacing elements characterised by the material
- C25B13/05—Diaphragms; Spacing elements characterised by the material based on inorganic materials
- C25B13/07—Diaphragms; Spacing elements characterised by the material based on inorganic materials based on ceramics
Definitions
- This invention relates to a process for the production of diaphragms for use in electrolytic processes by the electrolytic process itself with the preliminary aid of an endosmotic vegetable, animal, or mineral membranesuch as parchment, asbestos, &c.
- membranes of this invention were to be used in the electrolysis of halogen alkali metals by one of the known processes, they would in a short time be destroyed by the ohlorin, this being the reason why it has hitherto been necessary to use diaphragms made of clay or other similar mineral substance in electrolytic processes of this kind.
- a membrane of a substance that is easily destroyed-parchment, for example-4s by a particular electrolytic process furnished with a firm, adhesive, and porous coating forming with the parchment-membrane a firm plate of any suitable dimensions.
- Iemploya bath of any suitable construction separate the cathode and anode spaces with parchment, charge the anode space with a solution of chlorid of potassium made alkaline by lime, and use caustic-potash lye as the cathode liquid. It now the bath be placed in communication with the source of electricity, hypochlorite will be formed at the anode or positive pole.
- the diaphragm of this invention is notattacked by. hypochlorite, greatly resists the action of chlorin, and may therefore be used in the decomposition of halogen alkali metals and in the electrolysis of watery solutions.
- the composition consists of lime, respectively, magnesia, and at the same time chlorids.
- the same process may be performed by employing magnesia, other alkaline earth metals, and similar oxyhydrates instead of lime, also instead of chlorid of potassium, other halogen alkali metalschlorid of sodium, for example.
- the anode solution contains sufficient lime in solution, this precipitate cannot again dissolve therein, and thus forms the first portion of the coating. This keeps on increasing in thickness and so prevents any attack of the hypochlorite on the parchment.
- the coating has become sufficiently thick, the supply of fresh lime to the anode liquid is diminished to a certain extent, say by about twenty per cent, so that said liquid is capable of dissolving further quantities of lime, and from this time the coating remains of the thickness already given to it.
- the parchment on the cathode side with a firm bearing-surface to prevent the bulging out of the same and the fracture of the unfinished diaphragm, and so that this latter shall be formed in one solid inseparable whole.
- the parchment which is to serve as the substratum for a diaphragm is firmly fixed to the edges of a perforated metal plate serving as a cathode, against the perforated surface of which the parchment bears, and in the course of the building up of the diaphragm becomes firmly attached.
- Perforated plates are necessary to prevent increase of resistance and to allow of the passage of the potash solution formed at the cathode and also that of the hydrogen, or the cathode-plates maybe constructed of several pieces of metal with open spaces between them.
- FIG. 1 is a side view, partly in section, of a cathode-frame with a portion broken away to show a perforated sheet-metal plate which, inserted in the cathode-frame, serves as cathode.
- Fig. 1 is a side view of a perforated sheet-metal plate serving as cathode.
- Fig. 2 is a vertical section taken through line A B of Fig. 1; Fig. 3, a side view, partly in section, of an anode-frame; Fig. 4, a vertical section through line C D of Fig. 3; Fig.
- Fig. 4 a plan view of Fig. Fig. 5 is a vertical section, through line E F of Fig. 3, of a portion of the complete apparatus.
- Figs. 6 and 7 are similar sections, respectively, through line C D and through line G H of Fig. 3.
- Figs. 8 and 9 are sectional views showing the method of suspending the anodes in the anodeframe.
- Fig. 10 is a section through line C D of Fig. 3 on a larger scale.
- the apparatus is constructed of cathode-frames h and anode-frames a in the following manner: Upon a cathode-frame k is laid a perforated sheet-metal plate 1', then upon the latter a number of parchment-sheets 1), upon these an anode-frame a, then again a number of parchment-sheets p, succeeded by a perforated sheet-metal plate t, then a cathode frame a perforated sheet-metal plate '6 parchment-sheets p, anode-frame a, and so on.
- the cathode and anode frames thus combined are held together by two locking-plates s s, fastened by screw-bolts t t i &c., in the manner of a filter-press.
- the iron cathode frames 70 are provided with apertures" 12 b and c c, Fig. 1, and serve for the reception of the perforated sheet-metal plates i, acting as cathodes.
- the anode-frames to are pro-- vided with apertures g g and 71, h, corresponding precisely in position and shape to the apertures 19 Z) and c c of the cathodeframes 70.
- the apertures g g form.
- the apertures h 7L correspond in position and shape to the apertures b b of the cathode-frames 7c, and with these apertures form, when the apparatus is put together, channels for the passage of the cathode liquid. From the apertures 19 aslot d in the frame it leads to the inside of the oathode-space 70, which is shut off on both sides by the perforated sheet-metal plates 1'. From the apertures b a slot (1 in the frame 70 leads to the inside of the cathode-space 7c.
- slots Z Z in the anode-frame a connect the apertures g g with the inside of the anode-space a.
- the apertures 79 b h h and c c g g give four channels, which, through slots d cl and Z Z, permit the supply of the cathode and anode liquids to their compartments 70 6& or the discharge of said liquids therefrom.
- the cathode liquid is passed through a funnel T, communicating with the channel formed by the apertures b of the cathode-frame k and the apertures h of the anode-frame a, into said channel and filling the same and the cathode-spaces 70 through the slots cl, and, further, filling through the slots 01 the channel formed by the apertures 19 of the cathodeframe 70 and the apertures 71. of the anodeframe a.
- the anode liquid is passed through a funnel T, Fig.
- P are rods of lead.
- All the cathode-frames are connected together by themselves and all the anode-frames by themselves, each set by an electric conductor, the cathode-frames being connected with each other at their projecting part gby means of a conducting-rod o, placed so as to bear upon all the projecting parts q, and the anode-frames being connected with each other at their projecting part g by means of a conducting-rod '0.
- the rod 1 is in connection with one pole and the rod 1) in connection with the other pole of a source of electricity, so that the current is conducted through the anode and cathode liquid presentin the whole of the anode and cathode spaces, which are only separated from one another by the parchment-membranes p.
- the liquids pass through the membranes in contact and the diaphragm now forms on the parchment-membranes p.
- the process for the production of endosmotic membranes for use in the electrolysis by the electrolysis itself, which process consists in separating by means of a membrane serving as a foundation-diaphragm, an alkaline-cathode solution from an anode solution consisting of a mixture of the chlorids of the alkali metals and calcium holding the corresponding oxyhydrate, caustic lime, in solution and causing a solid porous coating to be firmly attached to said foundation-membrane on the side of the anode-space by passing an electric current through the bath, substantially as described.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
Description
(No Model.) 8 Sheets-Sheet 1.
w W. SPILKER. ELEGTROLYSIS 0F WATERY SALT SOLUTIONS. No. 583,513. Patented June 1,1897.
.OOOOOOOOOOOOOOOQOO OQOOOOOOQOOOOOOOOD OOOOOOOOOOO Q OOOOO 00000 00199000 00 0. GOOOO0 000000 00000 0,00090000000000000 OOOOOQOOOOOOOOOOOO ooooo ooooooooeooo oooooo o eooooooso 0000000 00 00 ooooo o OOQOQOOG Q O O GOO o oooo 0 0000000000 OG OOOQ O 0000GOOO OOOOGOOOO OOOOOOO OQQOOQOOOOQO O GO Z 06000000000000 0000 m: Nqlms #21: co. rnoruumou WrJNINGTON. n. c
060000 60 DO QQO OO u a o o 000 o o o o o o 00 0 00000000 0006 ooo W f 0 oooooooooeeoeeoeo ooooooooopo oooo uooooooeooooeoooo ooooooaoo o mm ooo voooaeooooeeoo 00 00000000000060 l\||| oqooooowooooeooeo OOGG QOOGOOOQOO OO ll 0 o oo o e a a o a e oo o o o o oooo ooooooo ooo m l 4 ooooaooooboooeooe ooooeoooaoooeooooo lvl 2 l oaoeeooooo aaoeo 000000000000000000 f oaaaoaoaoaooooboo 00000060006000000 J 8 R E K L T P S ELEGTROLYSIS 0F WATERY SALT SOLUTIONS.
Patented June 1.1897.
mm duke/v MWwY/m/ (imam qwv We (MN l0 mzm 04: minus yams no, morowmou vusnmamu, o. (z,
(No Model.) 3 Sheets,Sheet 3.
W. SPILKER] ELEGTROLYSIS 0F WA'TERY SALT SOLUTIONS. No. 583,513. Patented June 1,1897.
.5 i I I w u I a & a R i a Q g a n v R m g c9 Q Q ag g g UNITED STATES EEicE.
PATENT VVILHELM SPILKER, OF BERLIN/GERMANY.
SPECIFICATION forming part of Letters Patent N 0. 583,513, dated June 1, 1897. Application filed August 15, 1891. Serial No. 402,716. (Specimens) To aZZ whom it may concern:
Be it known that I, WILHELM SPILKER, a subject of the King of Prussia, German Emperor, and a resident of the city of Berlin, in the German Empire, have invented certain new and useful Improvements in the Electrolysis of WVatery Salt Solutions; and I do hereby declare that the following is a full, clear, and exact description of the invention, which will enable others skilled in the art to which it appertains to make and use the same.
This invention relates to a process for the production of diaphragms for use in electrolytic processes by the electrolytic process itself with the preliminary aid of an endosmotic vegetable, animal, or mineral membranesuch as parchment, asbestos, &c.
- In the greater number of electrolytic processes carried out with the use of diaphragms, as in the decomposition of halogen alkali metals, acid solutions or lyes are employed,which rapidly destroyendosmoticmembranes-such as parchment, & c.so that in all these cases it has hitherto been necessary to use expensive fragile clay diaphragms, which is difticult on a large scale; and the object of the invention is to supersede diaphragms of this kind by other and inexpensive membranes suitable for operations on a large scale.
If the membranes of this invention were to be used in the electrolysis of halogen alkali metals by one of the known processes, they would in a short time be destroyed by the ohlorin, this being the reason why it has hitherto been necessary to use diaphragms made of clay or other similar mineral substance in electrolytic processes of this kind.
In carrying out the invention a membrane of a substance that is easily destroyed-parchment, for example-4s by a particular electrolytic process furnished with a firm, adhesive, and porous coating, forming with the parchment-membrane a firm plate of any suitable dimensions. Iemploya bath of any suitable construction, separate the cathode and anode spaces with parchment, charge the anode space with a solution of chlorid of potassium made alkaline by lime, and use caustic-potash lye as the cathode liquid. It now the bath be placed in communication with the source of electricity, hypochlorite will be formed at the anode or positive pole. This would in a very short time destroy the toughest parchment, so that the anode and cathode liquids would mix together and render the apparatus useless. If, however, previous to the passage of the electric current a certain suitable quantity, say about two per cent, of chlorid of calcium be added to the anode liquid, a firm, adhesive, and even coating consistin g mainly of lime will, after the electric current has been in operation a short time, be formed on the parchment on the anode side, while the parchment on the cathode side remains free from the coating. If now so much lime be added to the anode solution as to keep the same constantly nearly saturated with lime, the quantity of Ca() employed for the purpose being about one per cent, the
coating will continue to increase, the process being carried on until it attains a thickness of about ten millimeters. It has the form of a firm even plate fixed to the parchment and gives out a sound similar to that given out by burnt clay or earthenware, which it also resembles in firmness or tenacity. If the electric current did not pass through the bath,
the parchment would merely show a pasty lime precipitate which could not protect it from injury.
, The diaphragm of this invention is notattacked by. hypochlorite, greatly resists the action of chlorin, and may therefore be used in the decomposition of halogen alkali metals and in the electrolysis of watery solutions. The composition consists of lime, respectively, magnesia, and at the same time chlorids. The same process may be performed by employing magnesia, other alkaline earth metals, and similar oxyhydrates instead of lime, also instead of chlorid of potassium, other halogen alkali metalschlorid of sodium, for example.
The formation of the firm, even, porous diaphragm, of any suitable thickness, inseparable from the parchment, and of only slight resistance, is explained by the fact that in employing such parchment -membranes the potash contents never mount in the same measure as the employed ampere hours generally do, but somewhat less. A portion of the potash formed in the electrolysis, therefore, in consequence of endosmotic action, passes over into the parchment, remaining therein instead of uniting with the cathode liquid, and at the boundary-that is to say, toward the anode side-is, with the chlorid of calcium there present, transformed into lime and chlorid of potassium or also to fixed basic chlorid of calcium and chlorid of potassium. If now the anode solution contains sufficient lime in solution, this precipitate cannot again dissolve therein, and thus forms the first portion of the coating. This keeps on increasing in thickness and so prevents any attack of the hypochlorite on the parchment. When the coating has become sufficiently thick, the supply of fresh lime to the anode liquid is diminished to a certain extent, say by about twenty per cent, so that said liquid is capable of dissolving further quantities of lime, and from this time the coating remains of the thickness already given to it.
In the performance of the process on a large scale it is desirable to provide the parchment on the cathode side with a firm bearing-surface to prevent the bulging out of the same and the fracture of the unfinished diaphragm, and so that this latter shall be formed in one solid inseparable whole. For this purpose the parchment which is to serve as the substratum for a diaphragm is firmly fixed to the edges of a perforated metal plate serving as a cathode, against the perforated surface of which the parchment bears, and in the course of the building up of the diaphragm becomes firmly attached. Perforated plates are necessary to prevent increase of resistance and to allow of the passage of the potash solution formed at the cathode and also that of the hydrogen, or the cathode-plates maybe constructed of several pieces of metal with open spaces between them.
In carrying out the process commercially I employ an apparatus constructed in the manner of a filter-press, as shown in the accom panying drawings, in which- Figure 1 is a side view, partly in section, of a cathode-frame with a portion broken away to show a perforated sheet-metal plate which, inserted in the cathode-frame, serves as cathode. Fig. 1 is a side view of a perforated sheet-metal plate serving as cathode. Fig. 2 is a vertical section taken through line A B of Fig. 1; Fig. 3, a side view, partly in section, of an anode-frame; Fig. 4, a vertical section through line C D of Fig. 3; Fig. 4:, a plan view of Fig. Fig. 5 is a vertical section, through line E F of Fig. 3, of a portion of the complete apparatus. Figs. 6 and 7 are similar sections, respectively, through line C D and through line G H of Fig. 3. Figs. 8 and 9 are sectional views showing the method of suspending the anodes in the anodeframe. Fig. 10 is a section through line C D of Fig. 3 on a larger scale.
The apparatus, as shown in Figs. 5, G, and 7, is constructed of cathode-frames h and anode-frames a in the following manner: Upon a cathode-frame k is laid a perforated sheet-metal plate 1', then upon the latter a number of parchment-sheets 1), upon these an anode-frame a, then again a number of parchment-sheets p, succeeded by a perforated sheet-metal plate t, then a cathode frame a perforated sheet-metal plate '6 parchment-sheets p, anode-frame a, and so on. The cathode and anode frames thus combined are held together by two locking-plates s s, fastened by screw-bolts t t i &c., in the manner of a filter-press. The iron cathode frames 70 are provided with apertures" 12 b and c c, Fig. 1, and serve for the reception of the perforated sheet-metal plates i, acting as cathodes. The anode-frames to are pro-- vided with apertures g g and 71, h, corresponding precisely in position and shape to the apertures 19 Z) and c c of the cathodeframes 70. The apertures g g form. with the apertures c 0, when the apparatus is put together, channels for the passage of the anode liquid, Figs. 5 and 7. The apertures h 7L correspond in position and shape to the apertures b b of the cathode-frames 7c, and with these apertures form, when the apparatus is put together, channels for the passage of the cathode liquid. From the apertures 19 aslot d in the frame it leads to the inside of the oathode-space 70, which is shut off on both sides by the perforated sheet-metal plates 1'. From the apertures b a slot (1 in the frame 70 leads to the inside of the cathode-space 7c. The
slots Z Z in the anode-frame a connect the apertures g g with the inside of the anode-space a. The apertures 79 b h h and c c g g give four channels, which, through slots d cl and Z Z, permit the supply of the cathode and anode liquids to their compartments 70 6& or the discharge of said liquids therefrom.
Then the cathode and anode frames are placed together, as shown in Figs. 5, 6, and '7, the cathode liquid is passed through a funnel T, communicating with the channel formed by the apertures b of the cathode-frame k and the apertures h of the anode-frame a, into said channel and filling the same and the cathode-spaces 70 through the slots cl, and, further, filling through the slots 01 the channel formed by the apertures 19 of the cathodeframe 70 and the apertures 71. of the anodeframe a. The anode liquid is passed through a funnel T, Fig. 5, into the channel formed by the apertures g of the anode-frame aand the apertures c of the cathode-frame 70, said anode liquid then passing through the slots Z into the anode-spaces a and filling the same and through the slots Z into the channel formed by the apertures g of the anode-frame a and the apertures c of the cathode-frame 7.; and filling this channel. a is an aperture for the discharge of the cathode liquid and .2 an aperture for the discharge of the anode liquid. These apertures are normally closed by plugs or stoppers. In the upper edge of the anode-frames a are slots m, through which the carbon bodies 1?. of the anodes are suspended in the anode-spaces a. The carbon bodies-in the form of rods or bars, for instance-are cast in a lead plate 0, to the top of which is fixed a brass plate m, having an area greater than that of the slot m, thereby permitting the carbon bodies to be held suspended from the anode-frame a.
P are rods of lead.
All the cathode-frames are connected together by themselves and all the anode-frames by themselves, each set by an electric conductor, the cathode-frames being connected with each other at their projecting part gby means of a conducting-rod o, placed so as to bear upon all the projecting parts q, and the anode-frames being connected with each other at their projecting part g by means of a conducting-rod '0. The rod 1; is in connection with one pole and the rod 1) in connection with the other pole of a source of electricity, so that the current is conducted through the anode and cathode liquid presentin the whole of the anode and cathode spaces, which are only separated from one another by the parchment-membranes p. The liquids pass through the membranes in contact and the diaphragm now forms on the parchment-membranes p.
What I claim as my invention, and desire to secure by Letters Patent, is
In the electrolysis of watery salt solutions, the process for the production of endosmotic membranes for use in the electrolysis, by the electrolysis itself, which process consists in separating by means of a membrane serving as a foundation-diaphragm, an alkaline-cathode solution from an anode solution consisting of a mixture of the chlorids of the alkali metals and calcium holding the corresponding oxyhydrate, caustic lime, in solution and causing a solid porous coating to be firmly attached to said foundation-membrane on the side of the anode-space by passing an electric current through the bath, substantially as described.
In testimony whereof I have signed this specification in the presence of two subscribing Witnesses.
WILHELM SPILKER.
Witnesses:
W. H. EDWARDS, W. HAUPT.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US583513A true US583513A (en) | 1897-06-01 |
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|---|---|---|---|
| US583513D Expired - Lifetime US583513A (en) | Qoooooooo |
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| Country | Link |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2543059A (en) * | 1948-07-19 | 1951-02-27 | William T Rawles | Apparatus for electrowining or electroplating of metals |
| USRE30409E (en) * | 1978-12-22 | 1980-09-30 | Powered contaminant evacuator | |
| US4705614A (en) * | 1986-05-12 | 1987-11-10 | The Dow Chemical Company | Cell with improved electrolyte flow distributor |
| US8486236B1 (en) * | 2010-06-17 | 2013-07-16 | Walter B. Warning | Electrolysis chamber |
| RU2606240C2 (en) * | 2011-07-15 | 2017-01-10 | Астриум Гмбх | Platform relative navigation using range measurements |
-
0
- US US583513D patent/US583513A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2543059A (en) * | 1948-07-19 | 1951-02-27 | William T Rawles | Apparatus for electrowining or electroplating of metals |
| USRE30409E (en) * | 1978-12-22 | 1980-09-30 | Powered contaminant evacuator | |
| US4705614A (en) * | 1986-05-12 | 1987-11-10 | The Dow Chemical Company | Cell with improved electrolyte flow distributor |
| US8486236B1 (en) * | 2010-06-17 | 2013-07-16 | Walter B. Warning | Electrolysis chamber |
| RU2606240C2 (en) * | 2011-07-15 | 2017-01-10 | Астриум Гмбх | Platform relative navigation using range measurements |
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