US753875A - Electrical manufacture of iron alloys. - Google Patents
Electrical manufacture of iron alloys. Download PDFInfo
- Publication number
- US753875A US753875A US11466102A US1902114661A US753875A US 753875 A US753875 A US 753875A US 11466102 A US11466102 A US 11466102A US 1902114661 A US1902114661 A US 1902114661A US 753875 A US753875 A US 753875A
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- US
- United States
- Prior art keywords
- oxid
- iron
- alkaline
- electrical
- iron alloys
- 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
- 238000004519 manufacturing process Methods 0.000 title description 9
- 229910000640 Fe alloy Inorganic materials 0.000 title description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 239000003513 alkali Substances 0.000 description 8
- 229910052742 iron Inorganic materials 0.000 description 7
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 6
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 6
- 229910001864 baryta Inorganic materials 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 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 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 229910017361 Fe2Si Inorganic materials 0.000 description 1
- 229910000616 Ferromanganese Inorganic materials 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241000876852 Scorias Species 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229910000754 Wrought iron Inorganic materials 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052916 barium silicate Inorganic materials 0.000 description 1
- HMOQPOVBDRFNIU-UHFFFAOYSA-N barium(2+);dioxido(oxo)silane Chemical compound [Ba+2].[O-][Si]([O-])=O HMOQPOVBDRFNIU-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
Definitions
- the present invention has for its object the electrical production of iron alloys, such as ferrosilicon or ferrornanganese, with the simultaneous production of alkaline oxidsor alkaline earths.
- the reaction is very rapid and presents no electric energy is expensive.
- the barium-slag is reduced on a second electric furnace after being mixed with a proportion of oxid of iron or wrought or cast iron according to the amount-of silicon to be obtained in the iron alloy and of a quantity of carbon regulated according to the quantity of oxygen to be eliminated, but not'sufficient to reduce the baryta and form carbid of barium.
- ferrosilicon containing about twenty per cent. of silicon, one will operate on the mixtures according to the following equations:
- SiO3Ba+2Fe+2C Fe2Si+BaO+2CO.
- the operation is readily effected with a current having a tension'of between twenty-five and thirty-five volts and a limitation of expenditure of energy of between fifty and sixty watts per square centimeter of section of the electrode. Under these conditions only an insignificant quantity of carbid of barium is produced and the volatilization of the baryta is not great. However, to prevent loss the furnaces gases are directed to a chamber where one can recover the volatile or trapped materials. These materials can be treated with boiling water, and one can separate by crystallization the baryta in the form of hydrate. The course followed for ferromanganese is identical.
- the electric reduction takes place in the furnace A.
- the sulfurous gases escape from the furnace through a pipe, through which they pass into an apparatus B, adapted to change the temperature and in which they are then passed into a disare cooled.
- solution-chamber C where they are dissolved in cold water injected through an atomizer.
- the solution is sucked up by the pump D and passed into the apparatus B, where it is first atomized in order to subsequently pass through a mass of coke into which hot air is forced.
- a mixture of air and sulfurous anhydrid is disengaged from the solution and passes into the chamber E, where it is dried by contact with the sulfuric acid. It is then passed into an apparatus F, adapted to change the temperature, in which it is heated by contact with the oxidated gases coming from the catalytic apparatus G.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
PATENTBD MA R. "is
' G. Gm. ELECTRICAL MANUFAGTURHOF IRON ALLOYS.
APPLICATION FILED JULY 7, 1902.
N0 MODEL.
WY/nesses:
Patented March 8, 1904.
OFFICE.
GUSTAVE GIN, OF PARIS, FRANCE.
ELECTRICAL-MANUFACTURE OF IRONALLOYS.
SPECIFICATION forming part of Letters Patent No. 753,875, dated March 8, I904.
' Application filed July 7, 1902. Serial No. 114,661. (No specimens.)
' To all whom it may concern:
- Be it known that I. GUsTAvE GIN, a citizen of the French Republic, and a resident of Paris, France, have invented certain new and useful Improvements in the Electrical Manufacture of Iron Alloys, with the Simultaneous Production ofAlkaline Oxids and Alkaline Earths,
of which the following is a specification.
The present invention-has for its object the electrical production of iron alloys, such as ferrosilicon or ferrornanganese, with the simultaneous production of alkaline oxidsor alkaline earths.
p In the first place, respecting ferrosilicon, my process consists in treating by silicic acid in the presence of a suitable proportion of carbon the sulfate of the metallic iron or the oxid of iron that it is desired to combine with silicon insuch a manner as to form a silicate of this oxid alkaline or earth-like alkaline while it disengages itself from the sulfurous anhydrid and carbonic oxid. The alkaline silicateor alkaline earth is introduced into a sec ond electric furnace after having had added to it in calculated proportions carbon and oxid of iron or metallic iron.- Ferrosilicon is formed at the same time that the alkaline oxid or alkaline-earth oxid is set free. It can be recovered in the form of scoria or by sublimation if it is volatile at the temperature of the reaction.
If in the preceding operations the silicic acid is replaced by dioxid of manganese, it is expedient inthe case of volatile alkaline oxids not to employ electric heat for the first operation and to substitute for the alkaline sulfate the corresponding sulfid.
In order that my invention may be the better understood, I shall now proceed to describe how I operate in the particular cases of ferrosilicon and baryta.
To effect the formation of barium silicate, I introduce into an electric furnace adapted for the smelting and casting of founding materials a mixture of broken quartz or nonclayey sand, barium sulfate, and charcoal in the proportions determined by the following equation:
The reaction is very rapid and presents no electric energy is expensive. The barium-slag is reduced on a second electric furnace after being mixed with a proportion of oxid of iron or wrought or cast iron according to the amount-of silicon to be obtained in the iron alloy and of a quantity of carbon regulated according to the quantity of oxygen to be eliminated, but not'sufficient to reduce the baryta and form carbid of barium. To obtain, for example, ferrosilicon containing about twenty per cent. of silicon, one will operate on the mixtures according to the following equations:
i or, what is better with metallic iron,
SiO3Ba+2Fe+2C=Fe2Si+BaO+2CO.
The operation is readily effected with a current having a tension'of between twenty-five and thirty-five volts and a limitation of expenditure of energy of between fifty and sixty watts per square centimeter of section of the electrode. Under these conditions only an insignificant quantity of carbid of barium is produced and the volatilization of the baryta is not great. However, to prevent loss the furnaces gases are directed to a chamber where one can recover the volatile or trapped materials. These materials can be treated with boiling water, and one can separate by crystallization the baryta in the form of hydrate. The course followed for ferromanganese is identical. If it is desired to produce it at the same time as the baryta, one introduces into a convenient electric furnace a mixture of dioxid of manganese and sulfate of barium in such a manner as'to produce the oxid mangano-barium according to the following formula:
One thus realizes the electrical reduction as explained and according to the formula:
This latter reaction is exothermic and is carried out in any ordinary furnace. The electrical reduction 1s effected according to the following formula:
When it is desired to produce an iron alloy at the same time as oxid of sodium, this oxid is volatilized in an electric furnace and can be collected by sublimation in a dust-chamber or by means of steam. The condensed product is recovered, which possesses very great purity.
All the operations ought to be carried on in closed furnaces, for the dust of the oxids of the alkalies and of the alkali earths are irritating to the respiratory organs and in some cases are poisonous.
It will be understood that what has been described with regard to baryta and oxid of sodium applies equally to alkali or alkali-earth oxids.
In order to render the invention more clear, a general view of the apparatus used for simultaneously carrying out the various operations, as herein described, is shown in the accompanying drawing.
The electric reduction takes place in the furnace A. The sulfurous gases escape from the furnace through a pipe, through which they pass into an apparatus B, adapted to change the temperature and in which they They are then passed into a disare cooled.
solution-chamber C, where they are dissolved in cold water injected through an atomizer. The solution is sucked up by the pump D and passed into the apparatus B, where it is first atomized in order to subsequently pass through a mass of coke into which hot air is forced. Under the simultaneous action of the furnace heat and injected air a mixture of air and sulfurous anhydrid is disengaged from the solution and passes into the chamber E, where it is dried by contact with the sulfuric acid. It is then passed into an apparatus F, adapted to change the temperature, in which it is heated by contact with the oxidated gases coming from the catalytic apparatus G. It passes subsequently into the latter apparatus, where the sulfurous anhydrid is transformed into sulfuric anhydrid, which is collected in a suitable condenser, (indicated in the drawings at H H.) These arrangements are chosen in the present case; but it is clear that they may be modified and that other-means can be used for the production of the sulfuric acid.
Having now fully described my invention, what I claim, and desire to secure by Letters Patent, is
The herein-described process for electrically producing an alloy of iron with the simultaneous production of oxids of alkalies, consisting of mixing a silicic acid with the sulfate of the alkali, adding carbon to the mixture heating the same in an electric fur nace with the production of the silicate of the alkali, then introducing this alkali silicate into a second furnace, adding an oxid of iron, and carbon thereto, heating the same with the production of ferrosilicon and oxid of the alkali, and collecting the oxid of the alkali in the form of a sublimate of the same, substantially as described.
In testimony whereof Ihave hereunto set my hand in presence of two witnesses.
GUSTAVE GIN.
Witnesses:
ADoLPHE STURM, EDWARD P. MAGLEAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11466102A US753875A (en) | 1902-07-07 | 1902-07-07 | Electrical manufacture of iron alloys. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11466102A US753875A (en) | 1902-07-07 | 1902-07-07 | Electrical manufacture of iron alloys. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US753875A true US753875A (en) | 1904-03-08 |
Family
ID=2822368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11466102A Expired - Lifetime US753875A (en) | 1902-07-07 | 1902-07-07 | Electrical manufacture of iron alloys. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US753875A (en) |
-
1902
- 1902-07-07 US US11466102A patent/US753875A/en not_active Expired - Lifetime
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