US1127163A - Method of treating mill-scale. - Google Patents

Method of treating mill-scale. Download PDF

Info

Publication number
US1127163A
US1127163A US83041814A US1914830418A US1127163A US 1127163 A US1127163 A US 1127163A US 83041814 A US83041814 A US 83041814A US 1914830418 A US1914830418 A US 1914830418A US 1127163 A US1127163 A US 1127163A
Authority
US
United States
Prior art keywords
scale
tungsten
mill
iron
phosphorus
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
Application number
US83041814A
Inventor
Frederick M Becket
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Electro Metallurgical Co USA
Original Assignee
Electro Metallurgical Co USA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Electro Metallurgical Co USA filed Critical Electro Metallurgical Co USA
Priority to US83041814A priority Critical patent/US1127163A/en
Application granted granted Critical
Publication of US1127163A publication Critical patent/US1127163A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00

Definitions

  • g is materially higher than in the unreduced material.
  • the present invention relates to the application of processes of this kind to the oxidized material known as high-speed millscale.
  • This scale is produced in considerable quantities as a by-product in the manufacture of high-speed steel, and consists, essentially, of oxid compounds of iron and tungsten, usually with smaller proportions of chromium and vanadium and containing also considerable quantities of cobalt when derived from the so-called cobalt steels.
  • the metals are present in the scale in the form of oxid, but are not, in all cases at least, in their highest state of oxidation.
  • composition ot a typical high-speed mill-scale Iron 57.66 per cent' Tungsten 12.25 Chromium 3.23 Vanadium 0.43 Manganese 0.47 Silicon, 0.75 Carbon 0.35
  • this scale By smelting this scale with silicon as a reducing agent, in an electric furnace and in accordance .with the methods disclosed in my prior patents, it may be reduced to an alloy having approximately the composition of the steel from which the scale was originally derived. For example, partial analyses of a mill-scale and the alloy obtained there- Spaciflcatto'n 01' Letters intent.
  • the mill-scale is subjected to a reducing operation before removing the phosphorus and concentrating its tungstencontents.
  • An illustrative example in accordance with the present invention is as follows : The scale is ground to pass an eight-mesh screen and is mixed with about the theoretical proportion of charcoal or other carbonaceous reducing-agent, calculated upon its contents of wads of iron and tungsten.
  • Theproportion of charcoal used should be so restricted as to avoid substantial contamination of the reduced roduct by carbon, while efi'ecting as near y complete reduction of the iron and tungsten 'as may be practicable without such contaminainto a bath of sulfuric acid of 1.2 to 1.4 specific gravity and digested for some hours, preferably with agitation. Following this digestion, the residue is'washed to remove the soluble sulfate, dried, and smelted with a small proportion of silicon inthe electric furnace. Silicon is added in approximately the theoretical proportions required for the reduction of such oxids as may have remained unreduced as a result of the first treatment, avoiding such excess of silicon as would yield a reduced product undesirably high in silicon. Lime or other flux may be added in proportion to form with .the silica a suitable slag, as is well understood in this art.
  • the totaliron-content may be extracted without entailing material losses of tungsten.
  • the resulting alloys may contain up to sixty-five per cent. of tungsten or more according to the amount of iron removed-and are, for practical purposes, free from phosphorus.
  • the herein-described method of preparing tungsten or its alloys from highspeed mill-scale containing tungsten which consists in subjecting the scale to a reducing-operation at a temperature below the melting-point of the reduced product, concentrating the tungsten in such reduced product and removing phosphorus therefrom by an acid reagent, and fusing the resulting purified concentrate in an electric furnace in presence of silicon.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

UNITED s 'rnrns PATENT our-ionrnnnnmcx M. menu, or unease ram-s. new roan, gssronon 'ro nnncrno METALLURGICAL comrmx, 0!." MAG or WEST VIRGINIA.
Ana mus, new Yong, A, qoaronarron METHOD 0! TREATING MILL-SCALE.
No Drawing.
Niagara and State of New York, have in- I vented certain new and useful Improvements in Methods of Treating Mill-Scale, of which the following is a specification.
In my prior Patents Numbers 1,081,566 and 1,081,570, patented December 16, 1913, I have described certain processes applicable to the treatment of ores, concentrates, or like products, of the iron-tungstate type, to
. obtain therefrom tungsten or its alloys in which the ratio of tungsten to phosphorus,
expressed as g is materially higher than in the unreduced material.
The present invention relates to the application of processes of this kind to the oxidized material known as high-speed millscale. This scale is produced in considerable quantities as a by-product in the manufacture of high-speed steel, and consists, essentially, of oxid compounds of iron and tungsten, usually with smaller proportions of chromium and vanadium and containing also considerable quantities of cobalt when derived from the so-called cobalt steels. The metals are present in the scale in the form of oxid, but are not, in all cases at least, in their highest state of oxidation.
The following is the composition ot a typical high-speed mill-scale Iron 57.66 per cent' Tungsten 12.25 Chromium 3.23 Vanadium 0.43 Manganese 0.47 Silicon, 0.75 Carbon 0.35
Phorphorus 0.015 to 0.030
By smelting this scale with silicon as a reducing agent, in an electric furnace and in accordance .with the methods disclosed in my prior patents, it may be reduced to an alloy having approximately the composition of the steel from which the scale was originally derived. For example, partial analyses of a mill-scale and the alloy obtained there- Spaciflcatto'n 01' Letters intent.
Amman m d, 4 x;; 8.1914. Serial a. $30.41;.
Patented Feb. 2, 1915.
from by known processes of silicon reduction, are as follows MilLacale. Reduced alloy. Tungsten 11.90 15.60 Qhromium 2.90 3.40 Vanadium 0.49, 0.43
The alloy so, obtained is utilizable as such, or, with appropriate additions, it is available for themanufacture of steels of modified composition. I have found, however, that such high-speed mill-scales usually contain a proportion of phosphoruswhich is distinctly objectionable. Moreover, the product of direct reduction of the scale is comparatively low in tungsten: this of course necessitates the use of a relatively large proportion of the allo in compounding a given steel, fromv whic it results that the phosphorus-content of the steel is not much less than that of the alloy. These dificulties are avoided by treating a millscale, before reduction, with an acid reagent which serves the double purpose of removing iron, and thereb concentrating the tungsten-content, an of removing phosphorus, and thereby increasing the ratio I have to nd that these mill-scales yield a large proportion of their iron, together with substantially all of their phosphorus, to acids, such as sulfuric acid, even in the cold. In other words, the very high temperature to which they have been subjected in the course of their production has not resulted, as might be expected, in converting the iron into such an insoluble condition as occurs when iron-tungstate ores are ignited or calcined. The process involving such acidtreatment of the mill-scale is claimed in my copending application Serial No. 830,417, filed concurrently herewith.
According to the present modification of the invention, the mill-scale is subjected to a reducing operation before removing the phosphorus and concentrating its tungstencontents. An illustrative example in accordance with the present invention is as follows :The scale is ground to pass an eight-mesh screen and is mixed with about the theoretical proportion of charcoal or other carbonaceous reducing-agent, calculated upon its contents of wads of iron and tungsten. Theproportion of charcoal used should be so restricted as to avoid substantial contamination of the reduced roduct by carbon, while efi'ecting as near y complete reduction of the iron and tungsten 'as may be practicable without such contaminainto a bath of sulfuric acid of 1.2 to 1.4 specific gravity and digested for some hours, preferably with agitation. Following this digestion, the residue is'washed to remove the soluble sulfate, dried, and smelted with a small proportion of silicon inthe electric furnace. Silicon is added in approximately the theoretical proportions required for the reduction of such oxids as may have remained unreduced as a result of the first treatment, avoiding such excess of silicon as would yield a reduced product undesirably high in silicon. Lime or other flux may be added in proportion to form with .the silica a suitable slag, as is well understood in this art.
According to this method, up to ninety per cent. of the totaliron-content may be extracted without entailing material losses of tungsten. The resulting alloys may contain up to sixty-five per cent. of tungsten or more according to the amount of iron removed-and are, for practical purposes, free from phosphorus.
I claim:--
1. The herein-described method of preparing tungsten or its alloys from highspeed mill-scale containing tungsten, whichconsists in subjecting the scale to a reducing-operation at a temperature below the melting-point of the reduced product, ex-
tracting a portion of the iron and thereby concentrating the tungsten in such reduced product, and fusing the concentrate in an electric furnace.
2. The herein-described method of preparing tungsten or its alloys from highspeed mill-scale containing tungstem-which consists in subjecting the scale to a reducing-operation at a temperature below the product and removing phosphorus therefrom, and fusing the concentrate in an electric'furnace in presence of a non-carbon reducing-agent.
Y 4. The herein-described method of preparing tungsten or its alloys from highspeed mill-scale containing tungsten, which consists in subjecting the scale to a reducing-operation at a temperature below the melting-point of the reduced product, concentrating the tungsten in such reduced product and removing phosphorus therefrom by an acid reagent, and fusing the concentrate in an electric furnace in presence of a non-carbon reducing-agent.
5. The herein-described method of preparing tungsten or its alloys from highspeed mill-scale containing tungsten, which consists in subjecting the scale to a reducing-operation at a temperature below the melting-point of the reduced product, concentrating the tungsten in such reduced product and removing phosphorus therefrom by an acid reagent, and fusing the resulting purified concentrate in an electric furnace in presence of silicon.
6. The method of preparing low-phosphorus tungsten or ferrotungsten from high-speed mill-scale, which consists in partially reducing said mill-scale, treating the reduced product to increase the ratio of tungsten to phosphorus, and thereafter completing the reduction.
In testimony whereof I aflix my signature in presence of two witnesses.
FREDERICK M. BECKET.
Witnesses:
J. A. HOLLADAY, G. C. FURNESS.
US83041814A 1914-04-08 1914-04-08 Method of treating mill-scale. Expired - Lifetime US1127163A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US83041814A US1127163A (en) 1914-04-08 1914-04-08 Method of treating mill-scale.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US83041814A US1127163A (en) 1914-04-08 1914-04-08 Method of treating mill-scale.

Publications (1)

Publication Number Publication Date
US1127163A true US1127163A (en) 1915-02-02

Family

ID=3195316

Family Applications (1)

Application Number Title Priority Date Filing Date
US83041814A Expired - Lifetime US1127163A (en) 1914-04-08 1914-04-08 Method of treating mill-scale.

Country Status (1)

Country Link
US (1) US1127163A (en)

Similar Documents

Publication Publication Date Title
US2476453A (en) Titaniferous material for producing titanium dioxide
US2424866A (en) Process for the treatment of matte to recover metallic salts
US4398945A (en) Process for producing a ferronickel alloy from nickel bearing laterites
CN113234880A (en) Method for smelting vanadium-rich pig iron from vanadium-containing steel slag and vanadium extraction tailings
US1127163A (en) Method of treating mill-scale.
US1835925A (en) Smelting process
US2203214A (en) Method of making alloys
US3699213A (en) Dephosphorization of ferrophosphorus
JPS63500873A (en) Vanadium slag and its manufacturing method
US1745360A (en) Direct production of steel or steel alloys from titaniferous ores and iron sands
US1820998A (en) Smelting of ores
US3460937A (en) Method for recovering vanadium from iron-base alloys
US3677741A (en) Method of processing ferrophosphorus
US1363657A (en) Method for producing manganese or alloys of manganese
US2687952A (en) Cyclic process for producing high grade synthetic manganese ores by oxidation of molten iron-manganese alloys
US1127162A (en) Method of treating mill-scale.
CN110117746A (en) A kind of manufacturing method of high-performance magnetism-free stainless steel
US855157A (en) Process of reducing metallic sulfids.
US858325A (en) Process of producing vanadium and its alloys.
US2791501A (en) Vanadium-carbon-iron alloy
US2883278A (en) Process for preparing a sintered agglomerate
US891898A (en) Process of making low-carbon metals or alloys.
US2616797A (en) Alloy for the preparation of titanium-boron steel
US1913833A (en) Method of producing and refining tungsten steel
US1537997A (en) Method of making iron and steel