US229308A - Casting metal - Google Patents
Casting metal Download PDFInfo
- Publication number
- US229308A US229308A US229308DA US229308A US 229308 A US229308 A US 229308A US 229308D A US229308D A US 229308DA US 229308 A US229308 A US 229308A
- Authority
- US
- United States
- Prior art keywords
- metal
- iron
- steel
- oxygen
- casting
- 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
- 229910052751 metal Inorganic materials 0.000 title description 38
- 239000002184 metal Substances 0.000 title description 38
- 238000005266 casting Methods 0.000 title description 15
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 40
- 229910052742 iron Inorganic materials 0.000 description 20
- 229910000831 Steel Inorganic materials 0.000 description 18
- 239000010959 steel Substances 0.000 description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 15
- 239000001301 oxygen Substances 0.000 description 15
- 229910052760 oxygen Inorganic materials 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 11
- 239000007789 gas Substances 0.000 description 8
- 239000002893 slag Substances 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 5
- 230000000266 injurious effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- 229910001296 Malleable iron Inorganic materials 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 241000364057 Peoria Species 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 229910000754 Wrought iron Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 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 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000007514 turning Methods 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 208000027418 Wounds and injury Diseases 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
- 238000000576 coating method Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
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
- C21C7/0025—Adding carbon material
Definitions
- any ordinary crucible steel-furnace may be used and the metal melted, as is ordinarily done in such furnaces.
- the deoxidizing is accomplished by putting the deoxidizing compound hereinafter described into the crucible with the metal. This may be done before melting or at any stage of the melting process. I prefer putting it in before and in the bottom of the crucible, or the melted metal may be poured upon the mixture.
- the metal should be retained in a liquid state, after the compound is put in, until the metallic oxide and other oxides existing in the metal are entirely absorbed by the deoxidizing agent and have had time to rise to.
- the lid of the crucible should be kept closed as much as possible from the beginning of the melting until the metal is ready to be poured, in order to keep air and carbonic-acid and carbonic-oxide, or other oxidizing gases, from coming in contact with the heated metal, and the slag hereinafter described should be used as directed.
- the molds are of such a size and shape as to make it probable that the metal will not readily flow into all the parts it may be heated several degrees hotter than the melting-point just before pouring without injury to the metal, as it is never exposed to oxidation during the heated state in casting by my process.
- the deoxidizing compound which I use is and other oxidizing gases.
- Steel and iron containing a considerable per cent. of carbon, silicon, manganese, or other (leoxidizin g agent, may be deoxidized by maintaining it in its molten state while protected by the slag hereinafter described, or other similar slag, and as much as possible by the lid of the crucible.
- the pouring-chamber is constructed as described in a patent issued to me hearing date the 28th day of May, A.D. 1878; butother pouring-chambers may be constructed to accomplish the same purpose.
- the metal issuingto said molding-chamber and poured into the molds as described in that patent.
- Iron and steel should be poured in an atmosphere of nitrogen gas. Any gas that does not contain oxygen, or does not have a direct affinity for the metal in its heated state to form a salt, may be used. Nitrogen is the best, according to my present knowledge and experience, it being odorless, not injurious to the lungs of the workmen, not explosive, and not injurious to the metal.
- gases not containing oxygen which may be successfully used are hydrogen and carbureted hydrogen.
Landscapes
- 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
UNITED STATES PATENT OFFICE.
JAMES DUFF, OF PEORIA, ILLINOIS.
CASTING METAL.
SPECIFICATION forming part of Letters Patent No. 229,308, dated June 29, 1880. Application filed October 16, 1879.
To all whom it may concern:
Be it known that I, JAMES DUFF, of the city and county of Peoria, and State of Illinois, have invented a new and useful Improvement in Casting Metals; and I do hereby declare that the following is a full, clear, and exact description of the same.
To get rid of blow-holes and points of weakness caused by particles of oxide has long been a desideratum in the working of iron and steel. As the cause of the former I have discovered that a part of the small quantities of oxygen which remain in and are taken up by the hot iron and steel and their alloys, as they have heretofore been manufactured and east, leaves its union with the metals during the casting process and unites with the carbon contained in the metal, and forms small quantities of carbonic-oxide or other gas, which is imprisoned by the cooling metal, thereby making it porous when cast and destroying its solidity and strength. The gas-cells or blow-holes which are thus formed in the ingots or castings can seldom be entirely worked out, so as to make the metal as strong, homogeneous, and solid as if they had never existed. Otherjparts of the small quantities of oxygen so retained or taken up by the metal in its molten state, or by substances mixed or combined with the metal, remain in the metal in the form of metallic and other oxides, and are not and cannot be removed entirely by forging or any process of manufacture now in use, being simply flattened or lengthened out by such treatment to form lines of weakness. Such being the character of the ordinary merchantable malleable iron and steel, it renders them less homogeneous, more difficult to cast and manufacture, and less solid and strong when cast and manufactured, and, Ibelieve, more liable to further and future oxidation. These objections do not apply to such an extent to ordinary cast-iron, for the reason that the presence of silicon in large quantities permits solidity to be more frequently obtained, and from which fact cast-iron is in practice successfully cast into form direct. These objections apply to steel and malleable iron, however, to such an extent as to practically preclude the casting of these metals into form direct, necessitating, instead, the casting into ingots first, and then My complete process consists in first deoxi- I dizing the molten metal beneath a surface which shall protect it from the air, and then, while in this melted condition, pouring or castin g the metal into form in an atmosphere containin g no oxygen.
In the deoxidizin g process any ordinary crucible steel-furnace may be used and the metal melted, as is ordinarily done in such furnaces.
The deoxidizing is accomplished by putting the deoxidizing compound hereinafter described into the crucible with the metal. This may be done before melting or at any stage of the melting process. I prefer putting it in before and in the bottom of the crucible, or the melted metal may be poured upon the mixture. The metal should be retained in a liquid state, after the compound is put in, until the metallic oxide and other oxides existing in the metal are entirely absorbed by the deoxidizing agent and have had time to rise to.
the surface and be liberated from theiron or steel. This will be indicated by the ebullition ceasing and not recurring when the crucible is shaken or moved. The lid of the crucible should be kept closed as much as possible from the beginning of the melting until the metal is ready to be poured, in order to keep air and carbonic-acid and carbonic-oxide, or other oxidizing gases, from coming in contact with the heated metal, and the slag hereinafter described should be used as directed.
If the molds are of such a size and shape as to make it probable that the metal will not readily flow into all the parts it may be heated several degrees hotter than the melting-point just before pouring without injury to the metal, as it is never exposed to oxidation during the heated state in casting by my process.
The deoxidizing compound which I use is and other oxidizing gases.
composed of the following ingredients in the following proportions oxide of silicon, (clean sand,) five ounces; carbon, (pulverized charcoal,) two ounces; pulverized iron, (fine iron turnings,) thirty ounces. This should be well mixed together and placed in the bottom of the crucible, and will ordinarily be the proper quantity for a melt consisting of sixty pounds of ordinary scrap-steel comparatively free from coatings of rust and ten pounds of wroughtiron reasonably free from exterior rust or oxide. A greater proportion of wrought-iron, as compared with the steel, and a greater quantity of rust on the iron and steel,will make a greater quantity of the compound advisable. If an excess of the compound is used-that is, if more silicon is disengaged by the decomposition of the compound than can be taken up by the oxygen of the metals-it may unite with the metal. A small quantity of silicon is not usually considered injurious to the metal. This depends somewhat upon the purpose for which the metal is to be used.
By my process of casting the presence of silicon and ofmanganese and some other alloys of a like nature, if injurious at all, is rendered less injurious than when the metals are cast by other processes. It is not so much the presence of these substances that injures the iron or steel as the presence of the oxides of them imprisoned in the cooling metal before they have time to rise to the surface. If the compound is not used in excess the silicon will not unite with the iron or steel, but will ounces; carbon, (pulverized charcoal,) one and one-half ounce; oxide of manganese, (black,) two ounces; pulverized iron, (fine iron turnings,) twenty ounces. Mix these well together. Use this quantity as a substitute for the foregoing quantity of the first compound, and use in the same way.
, Steel and iron containing a considerable per cent. of carbon, silicon, manganese, or other (leoxidizin g agent, may be deoxidized by maintaining it in its molten state while protected by the slag hereinafter described, or other similar slag, and as much as possible by the lid of the crucible.
I place upon the metal in the crucible a compound composed of one pound of aluminous clay and one or two ounces of lime, as it may be desired to have the slag more or less liquid. The larger portion of lime makes the more liquid slag. This compound will melt and form a complete protection to the metal from contact with the air, carbonic acid, Small globules of the metal'will be thrown into the slag, and by the ebullition be carried to the top of the slag, and for this reason it is desirable to keep the cover of the crucible closed as much as possi- 1016 during the process. This slag will remain After thorough deoxidation, as before described, the metal is carried to the pouringchamber, conveniently situated near the meltin g-furnace.
The pouring-chamber is constructed as described in a patent issued to me hearing date the 28th day of May, A.D. 1878; butother pouring-chambers may be constructed to accomplish the same purpose. The metal is putinto said molding-chamber and poured into the molds as described in that patent.
Iron and steel should be poured in an atmosphere of nitrogen gas. Any gas that does not contain oxygen, or does not have a direct affinity for the metal in its heated state to form a salt, may be used. Nitrogen is the best, according to my present knowledge and experience, it being odorless, not injurious to the lungs of the workmen, not explosive, and not injurious to the metal.
Among other gases not containing oxygen which may be successfully used are hydrogen and carbureted hydrogen. Such gases as chlorine, although not containing oxygen, could not be used on account of their direct affinity for the metal.
Great care must be taken to have the molding-chamber and the gas free from dampness and the molds perfectly dry and free from oxide of iron and every other substance that will be decomposed by the heat or heated iron or the carbon in the iron, and give off oxygen. Iron molds must be, and it is better that all molds should be, carefully luted with some substance entirely free from oxygen. A mixture of lamp-black and spirits of turpentine is good.
In defining my invention more clearly, I would state that I do not claim, broadly, deoxidizing iron or steel by the compositiondescribed, 'as I am aware that substantially similar deoxidizing compounds havebeen heretofore employed. 1 am aware also of the English Patent to Bessemer, N 0. 1,292 of 1856, and the United States Patent to Ghubb, No. 65,473, granted June 4, 1867. I therefore do not claim, broadly, casting iron or steel in an atmosphere containing no oxygen. I do not know, however, that iron and steel have ever been deoxidized and then, while in the same melted condition in which said deoxidation took place, immediately poured or cast in an atmosphere containing no oxygen, and from these successiveand coacting steps there results the perfect product which has not been. heretofore obtained-4. 0., a perfectly dense homogeneous casting of steel or malleable iron entirely free from holes, particles of oxide, and lines of weakness, which renders practical the casting of such metals into form direct. That these two steps, practiced under the same melt, do coact to produce this result is evidenced by the fact that neither of these steps, conducted separately, can give such result, For if, leaving out the first step, we pour iron or steel containing more or less oxide in an atmosphere containing no oxygen, the particles of oxide decompose at the high heat at which these metals are poured and the oxygen of said oxide unites with the carbon in the steel or iron and forms in little globules a gas (carbonic-oxide) which is im prisoned in the casting, and renders it porous,
notwithstanding the fact that no air or oxygen had access to it during the melting and, casting. On the other hand, if the second step of casting in an atmosphere containing no oxygen is dispensed with, no matter how thorough the deoxidation is, if the metal has any
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US229308A true US229308A (en) | 1880-06-29 |
Family
ID=2298685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US229308D Expired - Lifetime US229308A (en) | Casting metal |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US229308A (en) |
-
0
- US US229308D patent/US229308A/en not_active Expired - Lifetime
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