US1516326A - Manufacture of electrolytic iron - Google Patents
Manufacture of electrolytic iron Download PDFInfo
- Publication number
- US1516326A US1516326A US507352A US50735221A US1516326A US 1516326 A US1516326 A US 1516326A US 507352 A US507352 A US 507352A US 50735221 A US50735221 A US 50735221A US 1516326 A US1516326 A US 1516326A
- Authority
- US
- United States
- Prior art keywords
- solution
- air
- iron
- electrolytic iron
- manufacture
- 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 23
- 238000004519 manufacturing process Methods 0.000 title description 7
- 239000000243 solution Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 11
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 7
- 239000003792 electrolyte Substances 0.000 description 7
- 239000008151 electrolyte solution Substances 0.000 description 7
- 239000006260 foam Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000005868 electrolysis reaction Methods 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000002999 depolarising effect Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229960002089 ferrous chloride Drugs 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 241001527902 Aratus Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010961 commercial manufacture process Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 208000017482 infantile neuronal ceroid lipofuscinosis Diseases 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- C25C1/06—Electrolytic production, recovery or refining of metals by electrolysis of solutions or iron group metals, refractory metals or manganese
Definitions
- the present invention has for its object a process for the commercial manufacture of electrolytic iron. In order that such manufacture may be conducted on a truly commercial scale, it is necessary to be able to operate with a current of high density, while obtaining a product of very good quality and a maximum yield.
- the electrolyte is prepared, which is constituted by a solution of ferrous chloride or of ferrous sulfate or a mixture of ferrous salts. If the electrolyte is used without any previous treatment, and which has then a green color, there will 'be obtained merely a deposit of wholly irregular form and w thout commercial. value.
- the proper temperature isfrom 75 to 77 C.
- electrolytic deposits always contain a certain proportion of different gases which give rise to rather high tensions in the body of the metal itself.
- the facture o' electrolytic iron which consists in preparing an electrolyte solution of solpresence of. air until it assumes a bro colour 'and ceases to team, electrolyzing said solution by means "of insoluble anodes, and,
- the recess for theindustrial -manufact-are o electrolytic iron which consists in preparing an electrolyte solution of solpresence of air until it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, and causing said solution to circulate around said anodes at as high a speed as possible.
Landscapes
- Chemical & Material Sciences (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
- a ized after a slig Patented Nov. 18, 1924.
UNITED STATES PATENT OFFICE.
AUGUS'IE BOUCHAYER, OF GEE-NOBLE, FRANCE, ASSIGNOR, BY HESNE ASSIGNMENTS,
1'0 ELECTROLYTIC IRON, INCL, OF DOVER, DELAWARE, A CORPORATION OF DELA- wane.
No Drawing.
To all whom it may concern.-
Be it known that I, Auous'rn Boucnarna, a citizen of the Republic of France, and resident of Grenoble France, post-ofiice ad- 5 dress 8 Rue Les 'guieres, have invented new and useful Improvements in the Mannfacture of Electrolytic Iron, which im rove-.
ments are fully set forth in the fol owing specification. 10 The present invention has for its object a process for the commercial manufacture of electrolytic iron. In order that such manufacture may be conducted on a truly commercial scale, it is necessary to be able to operate with a current of high density, while obtaining a product of very good quality and a maximum yield.
Consequently, it-is necessary to' observe various special conditions.
First of all, the electrolyte is prepared, which is constituted by a solution of ferrous chloride or of ferrous sulfate or a mixture of ferrous salts. If the electrolyte is used without any previous treatment, and which has then a green color, there will 'be obtained merely a deposit of wholly irregular form and w thout commercial. value.
In order to obtain aneven, com act and homogeneous de osit capable of bemg utilht reheating, it is advisable at the start to agitate the electrolyte in a receptacle, which may or may not be spe-.
ciall constructed, by merely rotating the ano e, for example, in such a way as to produce an oxidizing action of the air at the same time as the phenomenon of electrolysis properly speaking. As the iron salts are very easily oxidized in air, the composition of the'bath becomes changed and there is 40 formed, in particular, oxychloride of iron,
which reacts on the hydro en bubbles collected on the cathode, an thereby eliminates the cause of the poor quality of the deposits. p Concurrentl with this formation of oxychloride, t e oxygen of the air likewise produces ferric chloride which, at theexpense of the apparatus itself or of the de- 't of iron on the cathode, is again converted into ferrous chloride. In order to avoid this loss of yield, as well as the corrosion of the apparatus, the electrolyte is caused to circulate through a mass of iron filings in a. separate receptacle.
MAITUFACTURE 0F ELECTROLYTIC IRON.
' Application filed October 12,1921. Serial No. 507,352..
It will be observed that the solution is in good condition when it has attained a bright rown color and no longer foams. It can then be used commercially in the regular way; this foaming being due to the oxidation of the ferrous salts to ferric.
It is, moreove necessary to observe the following operating conditions:
1. To rotate the cathode at a tangential speed which varies according to the density of the current. When operating under very low amperages, it is'possible to rotate the electrode very slowly or even not at all; but with high current densities, it is necessary. to increase the speed; the more the amperage increases the faster it is necessary to turn the cathode, without, however, exceeding a practical speed in order to avoid complications .of apparatus, the inconveniences of centrifugal force, etc. By way of'example, it may be stated that at 800 amperes per square meter the advisable tangential speed is 120 meters per minute.
2. To re ulate the temperature according to the density of the particular current used and to maintain this temperature absolutely constant. It is possible to obtain a good yield operating in the cold with a Very low current density, but if the amperage increases, it is necessary to equally increase the tem erature, without, however, reaching the boi mg point of the liquid, for at that moment there are formed in the interior of the electrolyte bubbles of gas or steam which interfere with the regularity of the deposit.
At 1000 amperes per square meter, for example, the proper temperature isfrom 75 to 77 C. Moreover, and above all, it is necessary to maintain the temperature absolutely constant in order to obtain an extremely regulardeposit; in fact, electrolytic deposits always contain a certain proportion of different gases which give rise to rather high tensions in the body of the metal itself. By varying the temperature these internal tensions are caused to vary, and there very often results a cracking and separation of the deposit which renders it worthless.
3. To regulate the concentration in accordance with the depolarizing power of the liquid and to maintain this concentration absolutely constant. In order to regulate the,concentration, it is necessary to. take into account the depolarizing power of the 'did - ociet Le For, assignee of the present liquid. In fact, when the concentration of the liquid varies, there is a variable electrolysis of the water; in other words, the quantity of hydrogen varies at the cathode, and the hydrogen has an action which is harmful or not according to the depolarizing power of the liquid. It is necessary, then, for any particular ap aratus, to adopt a suitable concentration, or example, 20 B., and'to maintain this concentration constant; otherwise, irregularities will take place in the deposit and the iron is no longer utilizable commercially. It is possible to replace the losses of liquid by continuously circulatin in the apparatus a stream of fresh liquid instead of adding this liquid to the electrolyte from time to time and in relatively unimportant quantities.
t. Finally. it is advisable to maintain a speed of circulation as high as possible for t e electrolyte around the anode. It has been established, indeed, that the more the speed of circulation increases, the more the phosphorus content is lowered.
By observing the above-mentioned conditions, excellent results are obtained.
In order to keep the liquid at the proper degree of oxidation,which is readily recognized, as has already been stated above, by the bright brown color and the absence of foaming-it has been usual, heretofore, to blowair into the liquid, re ulating the blast by means of a valve. In t is way, the difiiculties are avoided which result from the employment of scaled vessels-i. a, vessels absolutely deprived of air-which necessitate the constant addition of a special depolarizer, as well as those resulting from the employment of open vessels which leave the entire surface of the electrolytic liquid in contact with atmospheric air.
By regulating-the action of the air, the formation of a certain quantity of oxychloride of iron results, which acts as a depolarizer; and on the other hand, the formation of an excess of ferric salts, which would lower the yield, is avoided. it is possible, under these conditions, to operate at it current density of 1000 amperes and above'per square meter, and to obtain an extremely homogeneous product, with a mean yield of 98% of the ampere's. a
Now, the above-described process, which is primaril that disclosed in United States patent to nthelme Bouchenllo. 1,086,132, ranted February 3, 1914:, and assignedto case, is open to the objection that it requires the supply of a large volume of air, which necessitate the provision of considerable motive'power and which, moreover, entails the further drawback of cooling the bath.
lhe resent invention com letely evercomes t e disadvantages above indicated, by
dispensing with the air blast or controlled retained.
action of the air and re lacing the soluble anodes in one or more 0 ,the vats or vessels by insoluble anodes, graphite for example;
lized to effect a depolarizing action which is' extremely similar to that produced by the controlled introduction of air. All of the other phases of the process, however, are
What I claim and desire to secure by Letters Patent is:
1. The process for the industrial manufacture ofelectrolytic iron which consists in preparing an electrolyte solution of soluble ferrous salts, stirring the same in the presence of air until it assumes abrown colour and ceases to foam, andelectrolyzing said solution by means of insoluble anodes.
2. The process for the industrial manufacture of electrolytic iron which consists in preparing an electrolyte solution of soluble ferrous salts, stirring the same in the presence of airuntil it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, and allowing access of air thereto during elec= trolysis.
3. The recess. for the industrial manu facture o electrolytic iron which consists in preparing an electrolyte solution of solubleferrous salts, stirring the same inthe presence of air until it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, and
maintaining the temperature and concern tration of said solution at a constant value during electrolysis l. The facture o' electrolytic iron which consists in preparing an electrolyte solution of solpresence of. air until it assumes a bro colour 'and ceases to team, electrolyzing said solution by means "of insoluble anodes, and,
recess for the industrial menulid . uble ferrous salts, stirring the same in the maintaining at a constant value the tempera-- ture and concentration oi said solution dur= ing electrolysis while allowingaccess oi air thereto. 1 a q 5.. The recess for theindustrial -manufact-are o electrolytic iron which consists in preparing an electrolyte solution of solpresence of air until it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, and causing said solution to circulate around said anodes at as high a speed as possible.
6. The process for the industrial manufacture of electrolytic iron which consists in preparingan electrolyte solution of soluble ferrous salts, stirring the same in the presence of air until it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, circulatin said solution around said anodes at as .high a speed as possible, and allowing access of air to said solution during electrolysis.
7. The process for the industrial manufacture of electrolytic iron which consists in preparing an electrolyte solution of s01- uble ferrous salts, stirring the same in the presence of air until it assumes a brown colour and ceases to foam, electrolyzing said solution by means of insoluble anodes, circulating said solution around said anodes at as high a speed as possible, and maintaining at a constant value the temperature and concentration of said solution during electrolysis while allowing access of air thereto.
In testimony whereof I have signed this specification in the presence of two subscribing witnesses.
AUGUSTE BOUGHAYER.
Witnesses:
JULIAN KEMBLE Lonnnns, LuomNNn BnUnRLT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US507352A US1516326A (en) | 1921-10-12 | 1921-10-12 | Manufacture of electrolytic iron |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US507352A US1516326A (en) | 1921-10-12 | 1921-10-12 | Manufacture of electrolytic iron |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1516326A true US1516326A (en) | 1924-11-18 |
Family
ID=24018309
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US507352A Expired - Lifetime US1516326A (en) | 1921-10-12 | 1921-10-12 | Manufacture of electrolytic iron |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1516326A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2516515A (en) * | 1948-01-22 | 1950-07-25 | American Metal Co Ltd | Method for making iron powder |
| US2745800A (en) * | 1953-01-16 | 1956-05-15 | Horst Corp Of America V D | Electroplating with iron |
-
1921
- 1921-10-12 US US507352A patent/US1516326A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2516515A (en) * | 1948-01-22 | 1950-07-25 | American Metal Co Ltd | Method for making iron powder |
| US2745800A (en) * | 1953-01-16 | 1956-05-15 | Horst Corp Of America V D | Electroplating with iron |
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