US40472A - Improvement in purifying iron and steel - Google Patents
Improvement in purifying iron and steel Download PDFInfo
- Publication number
- US40472A US40472A US40472DA US40472A US 40472 A US40472 A US 40472A US 40472D A US40472D A US 40472DA US 40472 A US40472 A US 40472A
- Authority
- US
- United States
- Prior art keywords
- steel
- iron
- improvement
- purifying iron
- same
- 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 28
- 229910052742 iron Inorganic materials 0.000 title description 15
- 229910000831 Steel Inorganic materials 0.000 title description 14
- 239000010959 steel Substances 0.000 title description 14
- 230000006872 improvement Effects 0.000 title description 6
- 238000000034 method Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 230000008569 process Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000005864 Sulphur Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005262 decarbonization Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-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
- 240000003936 Plumbago auriculata Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 229910000754 Wrought iron Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Inorganic materials O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 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
- C21C7/0056—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00 using cored wires
Definitions
- my invention consists in a peculiar method of introducing oxides of iron or other solid substances containing oxygen into molten iron for the purpose of decarbonizing the same, in order to strengthen it or to reduce it to cast-steel or wrought-iron, in the manner here below fully specified.
- Figure I of the annexed drawings shows one modification of the apparatus, which I prefer to use when I desire to produce a quick decarbonization of cast-iron or a softer modification of steel.
- A is a short cylinder, in which the tubea can he slid up and down.
- This inner tube contains a wire, 0, on the lower end of which is attached a cup or cover, E, supporting the sheet-iron cylinder B, which closes around A.
- I When the lower wire, cap, and tube have burned away, I push the oxidizing material contained in the tube slowly down until all of it shall have been expelled, when the tube is withdrawn.
- the iron or steel to be decarbonized contains sulphur or otherimpurities, I mix with the oxides such substance or substances as can combine with the same, pass off as vapor, or unite with the covering flux.
- the oxides such substance or substances as can combine with the same, pass off as vapor, or unite with the covering flux.
- the chlorine will abstract the sulphur, pass off par-. tially as chloride of sulphur,while the rest will be kept by the flux covering the steel or iron. It is of the highest importance to,free steel and iron from sulphur. The most intimate contact with the material that should act upon it is required. This can only be accomplished by such means as I have adopted in my process.
- Fig. 'II of the drawings. It consists in the vessel A, covered with a lid, a, of convenient shape and size, constructed of fire-clay, magnesia, or
- This vessel or crucible is pierced with numerous holes, and is'attached to a handle, B, by the clamp or ring 0.
- This vessel is filled with black oxide of manganese, oxide of iron, or other solid substance containing oxygen, and then placed into the crucible or vessel containing the steel or castiron, detached, and the handle withdrawn.
- the lid of the steel crucible or cover of the vessel ill hold the small vesselbelow the surface of the metal, allowing the slow escape of the oxygen through small holes into the steel or iron, whereby the gradual decarboniza-tion is effected.
- the advantage of this apparatus consists in using the pure oxygen-gas, keeping the remaining substance from comingin contact with the steel or iron.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
w. GERHARDT. Refining IrOn, and Shah].
Patented Nov. 3. 1863.
N. PUEHS Plwlo-l lthwwphur. Washington, D. (L
ilmrnn STATES WILLIAM GERHARDT,
PATENT @rmcn.
OF NEW YORK, N. Y.
IMPROVEMENT IN 'PURIFYIN'G IRON AND STEEL.
Specification forming part of Letters Patent No. 10,4 72, dated November 3, 1863.
To all whom it may concern.-
Be it known that I, WILLIAM GERHARDT, of the city, county, and State of New York, have invented a new and useful Improvement in the Manufacture of Steel and Iron 5 and I do hereby declare that the following is afull and exact description thereof, reference being had to the accompanying drawings, and to letters of reference marked thereon.
The nature of my invention consists in a peculiar method of introducing oxides of iron or other solid substances containing oxygen into molten iron for the purpose of decarbonizing the same, in order to strengthen it or to reduce it to cast-steel or wrought-iron, in the manner here below fully specified. I
The advantages that results from the use of my improvements are manifold. As it is very important to obtain cast-iron of great strength and close texture, many means have been resorted to to increase the compactness and resistance of the same. The most successful of all devices invented for this purposethat of abstracting carbon by injection of airrequires complicated arrangements, and conse-' quently great outlay. At the same time this process is not without danger, involving considerable loss, and it canthercfore only be conducted bymen of intelligence. In my process I accomplish the same resultthe partial decarbonization of the cast-iron-in much less time, with a mere nominal, expense,without danger, and with a precision that none of the known processes can offer. The amount of carbon that has to be oxidized in order to obtainiron of a certain strength can previously be ascertained, and the corresponding quantity of oxygen present, in exact calculated proportions inthe oxides, subsequently added, as claimed in my improvement, introduced. When, further, my process is applied to steel, the same can be rendered softer, even during the last heating moments in the crucible, because the reducing material, as well as that to be reduced, can fully be controlled and calculated to a fraction-an advantage that has never before been obtained. It it well known to steel-melters that the plumbago-crucibles,when exposed to very intense heat, give off their carbon to the molten steel, and render thereby the intended soft steel too high. This is too highly carbonized, and therefore too short or brittle. 7
, Thecomparatively trifling cost ofthe process, the facility with which it can be applied at any time, in small as well as large quantities, the absence of loss, and the perfect control of the product are ad vantages that every practical steel andiron manufacturer willfreely admit.
Having described the mostimportant advantages of my process, I will, to enable others skilled in the art to construct and use my improvements, describe the apparatus used in the same and the modus operandi.
Figure I of the annexed drawings shows one modification of the apparatus, which I prefer to use when I desire to produce a quick decarbonization of cast-iron or a softer modification of steel.
A is a short cylinder, in which the tubea can he slid up and down. This inner tube contains a wire, 0, on the lower end of which is attached a cup or cover, E, supporting the sheet-iron cylinder B, which closes around A. Between the cover E and the sliding cap D, Iplace the oxide of iron'or other decarbonizing substance, and, holding up the upper part of the wire 0, I dip the sheet-iron tube B into the crucible or other vessel containing the molten metal. When the lower wire, cap, and tube have burned away, I push the oxidizing material contained in the tube slowly down until all of it shall have been expelled, when the tube is withdrawn. If the iron or steel to be decarbonized contains sulphur or otherimpurities, I mix with the oxides such substance or substances as can combine with the same, pass off as vapor, or unite with the covering flux. Forinstance, if asmall portion of chloride of sodium or calcium or lime, or any other substance having the desired properties, be mixed with the oxides, the chlorine will abstract the sulphur, pass off par-. tially as chloride of sulphur,while the rest will be kept by the flux covering the steel or iron. It is of the highest importance to,free steel and iron from sulphur. The most intimate contact with the material that should act upon it is required. This can only be accomplished by such means as I have adopted in my process.
The other modification, to be used when a slower oxidationis desirable, is shown in Fig. 'II of the drawings. It consists in the vessel A, covered with a lid, a, of convenient shape and size, constructed of fire-clay, magnesia, or
other fireproof material,which,however,-1nust be free from any carbonaceous substance, such as plumbago, coke, &c. This vessel or crucible is pierced with numerous holes, and is'attached to a handle, B, by the clamp or ring 0. This vessel is filled with black oxide of manganese, oxide of iron, or other solid substance containing oxygen, and then placed into the crucible or vessel containing the steel or castiron, detached, and the handle withdrawn. The lid of the steel crucible or cover of the vessel ill hold the small vesselbelow the surface of the metal, allowing the slow escape of the oxygen through small holes into the steel or iron, whereby the gradual decarboniza-tion is effected.
The advantage of this apparatus consists in using the pure oxygen-gas, keeping the remaining substance from comingin contact with the steel or iron.
Ade
It is understood that, as otherwise constructed apparatus may be used to accomplish the same purpose, I do not confine myself to the exact shape of one or the other of the modifications described,'and illustrated in my drawingshere attached. I have described these apparatus only as the way or means by which the most intimate contact of the respective materials can be obtained, as is required by the lay A of chemical afiinity. I
Having fully described my-invention, I claim for me as new and desire to secure by Letters Patent- The method herein fully described, and for the purposes specified.
WILLIAM GERHARDT.
In presence of- N. DAVENPORT, J AS. T. O. GooDFELLow.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US40472A true US40472A (en) | 1863-11-03 |
Family
ID=2110042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US40472D Expired - Lifetime US40472A (en) | Improvement in purifying iron and steel |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US40472A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3917125A (en) * | 1974-04-01 | 1975-11-04 | Rockwell International Corp | Apparatus and method for dispensing materials into a melt composition |
| US3942775A (en) * | 1973-04-02 | 1976-03-09 | Labate Michael D | Submerged desulphurization device and method |
| US4143866A (en) * | 1976-02-02 | 1979-03-13 | Mannesmann Aktiengesellschaft | Deoxidizing and/or desulfurizing of steel |
| US4625950A (en) * | 1985-07-12 | 1986-12-02 | General Motors Corporation | Lead alloying apparatus |
| US4699764A (en) * | 1985-07-12 | 1987-10-13 | General Motors Corporation | Method for alloying metals having significantly different melting points |
-
0
- US US40472D patent/US40472A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3942775A (en) * | 1973-04-02 | 1976-03-09 | Labate Michael D | Submerged desulphurization device and method |
| US3917125A (en) * | 1974-04-01 | 1975-11-04 | Rockwell International Corp | Apparatus and method for dispensing materials into a melt composition |
| US4143866A (en) * | 1976-02-02 | 1979-03-13 | Mannesmann Aktiengesellschaft | Deoxidizing and/or desulfurizing of steel |
| US4625950A (en) * | 1985-07-12 | 1986-12-02 | General Motors Corporation | Lead alloying apparatus |
| US4699764A (en) * | 1985-07-12 | 1987-10-13 | General Motors Corporation | Method for alloying metals having significantly different melting points |
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