US282118A - Production of ferro-phosphorus - Google Patents
Production of ferro-phosphorus Download PDFInfo
- Publication number
- US282118A US282118A US282118DA US282118A US 282118 A US282118 A US 282118A US 282118D A US282118D A US 282118DA US 282118 A US282118 A US 282118A
- Authority
- US
- United States
- Prior art keywords
- phosphorus
- ferro
- metal
- slag
- iron
- 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
- 229910052698 phosphorus Inorganic materials 0.000 title description 102
- 239000011574 phosphorus Substances 0.000 title description 102
- 238000004519 manufacturing process Methods 0.000 title description 28
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 82
- 235000014786 phosphorus Nutrition 0.000 description 78
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 72
- 229910052751 metal Inorganic materials 0.000 description 50
- 239000002184 metal Substances 0.000 description 50
- 239000002893 slag Substances 0.000 description 40
- 229910052742 iron Inorganic materials 0.000 description 36
- 238000000034 method Methods 0.000 description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 22
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 18
- 229910052710 silicon Inorganic materials 0.000 description 18
- 239000010703 silicon Substances 0.000 description 18
- 229910000831 Steel Inorganic materials 0.000 description 16
- 239000010959 steel Substances 0.000 description 16
- JNRQHASIGICJBU-UHFFFAOYSA-N iron(3+);phosphorus(3-) Chemical class [P-3].[Fe+3] JNRQHASIGICJBU-UHFFFAOYSA-N 0.000 description 12
- 235000021317 phosphate Nutrition 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- FZTWZIMSKAGPSB-UHFFFAOYSA-N phosphide(3-) Chemical compound [P-3] FZTWZIMSKAGPSB-UHFFFAOYSA-N 0.000 description 8
- 238000003723 Smelting Methods 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- PWHULOQIROXLJO-UHFFFAOYSA-N manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
- 229910052748 manganese Inorganic materials 0.000 description 6
- 239000011572 manganese Substances 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 6
- 229910000906 Bronze Inorganic materials 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 235000015450 Tilia cordata Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000010974 bronze Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000001066 destructive Effects 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 210000002370 ICC Anatomy 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N Silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 241000282898 Sus scrofa Species 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
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 object of this invention is the production of a metal composed chiefly of iron and phosphorus, and containing not less than ten (10) per cent. and not more than thirty-five (35) per cent; of phosphorus.
- This ferrophosphide will be of great advantage in the production of ingot iron and steel by the basic process, as will be more fully explained hereinafter. It will also be useful for the production of phosphor -bronze and other metallic compounds in which phosphorus is an element.
- silicon is relied on as the principal caloric-producing agent.
- standard Bessemer metal is required to contain from two (2) to three (3) per cent.
- silicon while in the practice of the Bessemer basic process silicon is avoided, as its combustion produces silicic acid, which is destructive to the basic linings, and otherwise retards dephosphorization, and as two or three per cent.
- phosphorus may be as readily eliminated as one-tenth of that amount, and as phosphoric acid resulting from the oxidation of ph osph orus is not destructive on the lining in thebasic process, silicon is displaced and phosphorus sub stituted in its place in the metal as a calorific power as far as convenient.
- the amount of phosphorus required in order to supply the amount of caloric lost by the absence of silicon, and to meet other requirements, will be from one (1) to three (3) per cent, according to the conditions and amount of silicon with drawn; and as the phosphorus is eliminated at the period known as the overblow, it is exceedingly desirable that an exact and uniform amount of phosphorus may be present in each of a series of successive charges, in order that a definite relative amount of oxygen may be blown in, which will be just sufficient to oxidize all of the phosphorus, and that the overblow may be ended at that juncture, and thus prevent the oxidation of the iron, which and upward; and in order to utilize any and all of such metal in the manufacture of ingot iron and steel by the basic process, it is desirable that the amount of phosphorus in the initial charges should conform to a determined standard,- and, in order to meet this requirement, I have produced a metal containing from ten (10) to thirty-five (35) per cent. of phosphorus, which I call ferrophosphorus.
- the essential conditions for the production of ferro-phosphorus are bringing iron and phosphorus together while in a molten state in the presence of a silicious slag and avapor of carbonic oxide, (00,) or either of them.
- One means of securing these conditions is by smelting ores of iron and a phosphoritic slag in a blast-furnace. In such case as little lime should be used as consistent with the proper working of the furnace, so as to keep the slag highly silicious; or, when the ores contain sui ficicnt phosphorus in themselves, the phosphoritic slag may be'omitted.
- ferro-phosphidc Another means of producing ferro-phosphidc is by smelting cast-iron in a cupola provided with a hearth of sufficient capacity to hold the metal, and from six to twelve inches of slag below the line where the blast enters the cupola, and then melting phosphoritic ores or phosphoritic slag, and causing it to flow and rest upon the face of the metal. Then injecting into the metal or slag a vapor of hydrocarbon or carbonic oxide, whereby the carbon so injected will abstract the oxygen from the phosphate of'the slag or ore and reduce the phosphate to a phosphide, which will immediately unite with the metal.
- This ferro-phosphorus is designed to be used by mixing it with iron, which contains less than two per cent. of phosphorus, so as to bring up the average per cent. of phosphorus in the mixture to the requirement of the basic dephosphorizing process; and even. where suf ficient amount of metal containing from two to three per cent.
- the duration of the overblow cannot be readily determined, owing to the varying content of phosphorus inthe metal, and if the overblow is not continued sufficiently long, then the phosphorus is not sufficiently eliminated, and if it is continued too long, an extra portion of the iron is oxidized, and not only lost, but leaves an increased amount of oxygen in the metal.
- This invention being the production of iron containing phosphorus in a larger degree than has hitherto been produced for commercial purposes by the processes herein set forth, I do not wish to confine or limit the processes to any form of apparatus referred to in my explanation of practice, and I do not herein claim the substitution of phosphorus instead of sili con in the basic process, nor the special use of phosphoritic metal with metal low in phosphorus to secure a definite duration of the overblow or for the utilization of scrap, as I have filed applications for said inventions.
Description
UNITED STATES PATENT 'GFFICEQ JACOB REESE, OF PITTSBURG, PENNSYLVANIA.
PRODUCTION OF FERRO-PHOSPHORUS.
SPECIFICATION forming part of Letters Patent No. 282,118, dated July 31,1883.
Application filed September 27,1881. (No specimens.)
To allwhom it may concern.-
Be it known that I, JACOB REESE, a citizen of the United States, residing in the city of Pittsburg, county of Allegheny, and State of Pennsylvania, have invented a new and useful Improvement in the Production of Ferro-Phosphorus, and I do hereby declare the followingto be a full, clear, and exact specification thereof.
The object of this invention is the production of a metal composed chiefly of iron and phosphorus, and containing not less than ten (10) per cent. and not more than thirty-five (35) per cent; of phosphorus. This ferrophosphide will be of great advantage in the production of ingot iron and steel by the basic process, as will be more fully explained hereinafter. It will also be useful for the production of phosphor -bronze and other metallic compounds in which phosphorus is an element. In the Bessemer acid process silicon is relied on as the principal caloric-producing agent. Hence standard Bessemer metal is required to contain from two (2) to three (3) per cent. of silicon, while in the practice of the Bessemer basic process silicon is avoided, as its combustion produces silicic acid, which is destructive to the basic linings, and otherwise retards dephosphorization, and as two or three per cent. of phosphorus may be as readily eliminated as one-tenth of that amount, and as phosphoric acid resulting from the oxidation of ph osph orus is not destructive on the lining in thebasic process, silicon is displaced and phosphorus sub stituted in its place in the metal as a calorific power as far as convenient. The amount of phosphorus required in order to supply the amount of caloric lost by the absence of silicon, and to meet other requirements, will be from one (1) to three (3) per cent, according to the conditions and amount of silicon with drawn; and as the phosphorus is eliminated at the period known as the overblow, it is exceedingly desirable that an exact and uniform amount of phosphorus may be present in each of a series of successive charges, in order that a definite relative amount of oxygen may be blown in, which will be just sufficient to oxidize all of the phosphorus, and that the overblow may be ended at that juncture, and thus prevent the oxidation of the iron, which and upward; and in order to utilize any and all of such metal in the manufacture of ingot iron and steel by the basic process, it is desirable that the amount of phosphorus in the initial charges should conform to a determined standard,- and, in order to meet this requirement, I have produced a metal containing from ten (10) to thirty-five (35) per cent. of phosphorus, which I call ferrophosphorus.
The essential conditions for the production of ferro-phosphorus are bringing iron and phosphorus together while in a molten state in the presence of a silicious slag and avapor of carbonic oxide, (00,) or either of them. One means of securing these conditions is by smelting ores of iron and a phosphoritic slag in a blast-furnace. In such case as little lime should be used as consistent with the proper working of the furnace, so as to keep the slag highly silicious; or, when the ores contain sui ficicnt phosphorus in themselves, the phosphoritic slag may be'omitted. Another means of producing ferro-phosphidc is by smelting cast-iron in a cupola provided with a hearth of sufficient capacity to hold the metal, and from six to twelve inches of slag below the line where the blast enters the cupola, and then melting phosphoritic ores or phosphoritic slag, and causing it to flow and rest upon the face of the metal. Then injecting into the metal or slag a vapor of hydrocarbon or carbonic oxide, whereby the carbon so injected will abstract the oxygen from the phosphate of'the slag or ore and reduce the phosphate to a phosphide, which will immediately unite with the metal. In the latter case care should be taken to keep the ores or slag as highly silicious as consistent with their fluidity. In producing a ferro-phosphide by the cupola process, as just described, when a metal high in phos phorus is desired, I construct the cupola with a tymp or sla'g notch just below the blast-line, and continue to melt the phosphoritic slag until a suificient quantity of phosphorus will be deposited in the metal, the excess of slag escaping out of the hearth through the tymp.
'i n silicon.
By this method Ihave been able to abstract phosphorus from puddle-furnace slag and produce a ferro-phosphide of a high grade. It is a well-known fact that the elements unite with each other in certain relative equivalents, and as a phosphide of iron consists of thirty-one (31) parts, by weight, of phosphorus, and fiftysix (56) parts of iron, it will be seen that if a ferro-phosphorus metal was a pure ferro-phos phide its composition would be phosphorus, 35.63 per cent; iron, 64.37 per cent. It therefore follows that a ferro-phosphide cannot con tain over thirty-five (85) per cent. of phosphorus, owing to a trace of other matter than 1ron.
In the production of ferro-phosphorus by means of the cupola, I line the cupola in the ordinary manner with a silicious lining, charge it with coke, and after it has become properly heated, pig-metal or scrap-steel is charged and melted. I prefer scrap-steel, as it is low I then charge the phosphoritic slag from time to time, keeping up a brisk fire by blowing in the airblast, and depositing the phosphorus in the metal by injecting the carbonaceous vapor into the bath. By this means I am able to produce a metal containing from ten (10) to thirty-five (35) per cent. of phosphorus, depending uponthe quality of the slag and the time of treatment.
This ferro-phosphorus is designed to be used by mixing it with iron, which contains less than two per cent. of phosphorus, so as to bring up the average per cent. of phosphorus in the mixture to the requirement of the basic dephosphorizing process; and even. where suf ficient amount of metal containing from two to three per cent. of phosphorus is easily obtained, the fei'rophosphorus will be of great advantage, as a Bessemer works producing one hundred thousand tons of steel per annum will also produce twelve thousand tons of scrap in the form of sculls,- bloom ends, and rail (illtlS5fL11d as all this scrap is low in silicon, carbon, and phosphorus, it could not be used in the basic process unless it was admixed with a caloric agent. This I do by admixing such scrap with a sufficient amount of the ferro-phosphide and melting the mixture in the cupola and running it into the converter, or by throwing. the scrap and phosphide into the converter, as is now done with scrap in the acid process. By the use of the phosphide all the scrap may thus be used and again put into serviceable ingots.
It is well known that phosphorus tends to make cast-iron very fluid, and by the admixture of a small portion of the ferro phos phorus with pig metal in foundry practice, the iron will run more freely and smoother and finer castings can be produced. Phosphorus also tends to harden iron and strengthens it in the absence of concussive blows or sudden strains. The ferro-phosporus will, therefore, be of great service in producing phosphor bronze, and all castings in which phosphorus is found to be desirable, as I purpose to furnish it as a regular article of manufacture, the same as ferroananganese is now supplied.
I11 the basic dephosphorizing process as at present practiced, the duration of the overblow cannot be readily determined, owing to the varying content of phosphorus inthe metal, and if the overblow is not continued sufficiently long, then the phosphorus is not sufficiently eliminated, and if it is continued too long, an extra portion of the iron is oxidized, and not only lost, but leaves an increased amount of oxygen in the metal. Consequently when it is deoxidized a less amount of manganese is left in the steel, and as it is of great importance to have no more and no less than the required amount of manganese in the resulting steel, the advantage of using the ferro-phosphorus will readily be seen, as by its use the amount of phosphorus may be definitely determined and the duration of the blow and amount of oxygen in the metal calculated, and I can thus produce steel free from phosphorus and containing a definite and desired percentage of manganese. For these reasons I conceive that the ferro-phosphorus will prove to be of great value in the practice of the basic dephosphorizing process.
In the production of ferro-phosphorus the more silicious the slag is the more readily the phosphorus will be deposited in the metal. Therefore but little lime, if any, should be used in the cupola, and when the calcarious phosphoritic slag is used, it should be admixed with silicious matter to as great a degree as it will remain in a fluid state while in the cupola, and in the use of phosphoritic ores I preferto use those containing at least fifteen per cent. of silica.
This invention being the production of iron containing phosphorus in a larger degree than has hitherto been produced for commercial purposes by the processes herein set forth, I do not wish to confine or limit the processes to any form of apparatus referred to in my explanation of practice, and I do not herein claim the substitution of phosphorus instead of sili con in the basic process, nor the special use of phosphoritic metal with metal low in phosphorus to secure a definite duration of the overblow or for the utilization of scrap, as I have filed applications for said inventions.
I am aware that in the recovery of phosphorus from fossil phosphates and the manufacture of alkaline phosphates a phosphuret of iron has been produced by smelting a mixture of iron, silica, and the fossil phosphates, and do not herein claim such a process.
Having thus described the invention, what I claim, and wish to secure by Letters Patent,
1. The process herein described for the production of ferro-phosphorus, which consists in subjecting molten iron while in a cupola to the action of a phosphoritic and silicious'slag and to the action of a carbonaceous vapor or ICC gas, substantially as and for the purposes slag is reduced and the phosphorus is taken specified. up by the metal, substantia11y as and for the 2. As a step in the process for the producpurpose set forth.
tion of ferro-phosphorus, covering inolten iron J AOOB REESE.
with a phosphoritic slag, and then'injecting' Witnesses:
into the molten metal or slag a carbonaceous JAMEs'H. FORTE,
vapor or gag-whereby the phosphate of the FRANK M. REEsE.
Publications (1)
Publication Number | Publication Date |
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US282118A true US282118A (en) | 1883-07-31 |
Family
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Family Applications (1)
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US282118D Expired - Lifetime US282118A (en) | Production of ferro-phosphorus |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2467039A (en) * | 1945-05-26 | 1949-04-12 | Stowell | Recovery of vanadium concentrate |
US3381113A (en) * | 1964-09-29 | 1968-04-30 | Albright & Wilson Mfg Ltd | Heat storage apparatus |
US4009024A (en) * | 1975-09-26 | 1977-02-22 | Koppers Company, Inc. | Process for regeneration and reuse of steelmaking slag |
US20040250455A1 (en) * | 2003-06-10 | 2004-12-16 | Wheeler Thomas J. | Hangtag with tool securing mechanism |
-
0
- US US282118D patent/US282118A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2467039A (en) * | 1945-05-26 | 1949-04-12 | Stowell | Recovery of vanadium concentrate |
US3381113A (en) * | 1964-09-29 | 1968-04-30 | Albright & Wilson Mfg Ltd | Heat storage apparatus |
US4009024A (en) * | 1975-09-26 | 1977-02-22 | Koppers Company, Inc. | Process for regeneration and reuse of steelmaking slag |
US20040250455A1 (en) * | 2003-06-10 | 2004-12-16 | Wheeler Thomas J. | Hangtag with tool securing mechanism |
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